-
1
-
-
0028261705
-
Genetic mapping of quantitative trait loci for growth and fatness in pigs
-
Andersson, L., Haley, C.S., Ellegren, H., Knott, S.A., Johansson, M., Andersson, K., Andersson-Eklund, L., Edfors-Lilja, I., Fredholm, M., Hansson, J., Hakansson, J., Lundström, K. Genetic mapping of quantitative trait loci for growth and fatness in pigs. Science 1994, 263: 1771-1774.
-
(1994)
Science
, vol.263
, pp. 1771-1774
-
-
Andersson, L.1
Haley, C.S.2
Ellegren, H.3
Knott, S.A.4
Johansson, M.5
Andersson, K.6
Andersson-Eklund, L.7
Edfors-Lilja, I.8
Fredholm, M.9
Hansson, J.10
Hakansson, J.11
Lundström, K.12
-
2
-
-
0029961325
-
Livestock genomics comes of age
-
Georges, M., Andersson, L. Livestock genomics comes of age. Genome Res. 1996, 6: 907-921.
-
(1996)
Genome Res.
, vol.6
, pp. 907-921
-
-
Georges, M.1
Andersson, L.2
-
3
-
-
0033592988
-
Genetic epidemiology of single-nucleotide polymorphisms
-
Collins, A., Lonjou, C., Morton, N.E. Genetic epidemiology of single-nucleotide polymorphisms. Proc. Natl. Acad. Sci. USA 1999, 96: 15173-15177.
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 15173-15177
-
-
Collins, A.1
Lonjou, C.2
Morton, N.E.3
-
4
-
-
0032954497
-
Utilization of gene mapping information in livestock animals
-
Kappes, S.M. Utilization of gene mapping information in livestock animals. Theriogenology 1999, 51: 135-147.
-
(1999)
Theriogenology
, vol.51
, pp. 135-147
-
-
Kappes, S.M.1
-
5
-
-
0027433315
-
Genomic organization of the porcine skeletal muscle ryanodine receptor (RYR1) gene coding region 4624 to 7929
-
Leeb, T., Schmolzl, S., Brem, G., Brenig, B. Genomic organization of the porcine skeletal muscle ryanodine receptor (RYR1) gene coding region 4624 to 7929. Genomics 1993, 18: 349-354.
-
(1993)
Genomics
, vol.18
, pp. 349-354
-
-
Leeb, T.1
Schmolzl, S.2
Brem, G.3
Brenig, B.4
-
6
-
-
0027410910
-
Anchored reference loci for comparative genome mapping in mammals
-
O'Brien, S.J., Womack, J.E., Lyons, L.A., Moore, K.J., Jenkins, N.A., Copeland, N.G. Anchored reference loci for comparative genome mapping in mammals. Nat. Genet. 1993, 3: 103-112.
-
(1993)
Nat. Genet.
, vol.3
, pp. 103-112
-
-
O'Brien, S.J.1
Womack, J.E.2
Lyons, L.A.3
Moore, K.J.4
Jenkins, N.A.5
Copeland, N.G.6
-
7
-
-
0028877463
-
Genetic dissection of complex traits, guideline for interpreting and reporting linkage results
-
Lander, E., Kruglyak, L. Genetic dissection of complex traits, guideline for interpreting and reporting linkage results. Nat. Genet. 1995, 11: 241-247.
-
(1995)
Nat. Genet.
, vol.11
, pp. 241-247
-
-
Lander, E.1
Kruglyak, L.2
-
8
-
-
0032053208
-
Moving from QTL experimental results to the utilization of QTL in breeding programmes
-
Spelman, R.J., Bovenhuis, H. Moving from QTL experimental results to the utilization of QTL in breeding programmes. Anim. Genet. 1998, 29: 77-84.
-
(1998)
Anim. Genet.
, vol.29
, pp. 77-84
-
-
Spelman, R.J.1
Bovenhuis, H.2
-
9
-
-
0027507643
-
Construction of a bovine genomic library of large artificial chromosome clones
-
Libbert, F., Lefort, A., Okimoto, R., Georges, M. Construction of a bovine genomic library of large artificial chromosome clones. Genomics 1993, 18: 270-276.
-
(1993)
Genomics
, vol.18
, pp. 270-276
-
-
Libbert, F.1
Lefort, A.2
Okimoto, R.3
Georges, M.4
-
10
-
-
0029167578
-
Construction of a porcine YAC library and mapping of the cardiac-muscle ryanodine receptor gene to chromosome 14q22-23
-
Leeb, T., Rettenberger, G., Hameister, H., Brem, G., Brenig, B. Construction of a porcine YAC library and mapping of the cardiac-muscle ryanodine receptor gene to chromosome 14q22-23. Mamm. Genome 1995, 6: 37-41.
-
(1995)
Mamm. Genome
, vol.6
, pp. 37-41
-
-
Leeb, T.1
Rettenberger, G.2
Hameister, H.3
Brem, G.4
Brenig, B.5
-
11
-
-
0032529138
-
An improved approach for construction of bacterial artificial chromosome libraries
-
Osoegawa, K., Woon, P.Y., Zhao, B., Frengen, E., Tateno, M., Catanese, J.J., de Jong, P.J. An improved approach for construction of bacterial artificial chromosome libraries. Genomics 1998, 52: 1-8.
-
(1998)
Genomics
, vol.52
, pp. 1-8
-
-
Osoegawa, K.1
Woon, P.Y.2
Zhao, B.3
Frengen, E.4
Tateno, M.5
Catanese, J.J.6
de Jong, P.J.7
-
12
-
-
0030846891
-
A whole-genome radiation hybrid panel for bovine gene mapping
-
Womack, J.E., Johnson, J.S., Owens, E.K., Rexroad, C.E., Schlapfer, J., Yang, Y.P. A whole-genome radiation hybrid panel for bovine gene mapping. Mamm. Genome 1997, 8: 854-856.
-
(1997)
Mamm. Genome
, vol.8
, pp. 854-856
-
-
Womack, J.E.1
Johnson, J.S.2
Owens, E.K.3
Rexroad, C.E.4
Schlapfer, J.5
Yang, Y.P.6
-
13
-
-
0032797067
-
A radiation hybrid map of the RN region in pigs demonstrates conserved gene order compared with the human and mouse genomes
-
Robic, A., Seroude, V., Jeon, J.T., Yerle, M., Wasungu, L., Andersson, L., Gellin, J., Milan, D. A radiation hybrid map of the RN region in pigs demonstrates conserved gene order compared with the human and mouse genomes. Mamm. Genome 1999, 10: 565-568.
-
(1999)
Mamm. Genome
, vol.10
, pp. 565-568
-
-
Robic, A.1
Seroude, V.2
Jeon, J.T.3
Yerle, M.4
Wasungu, L.5
Andersson, L.6
Gellin, J.7
Milan, D.8
-
14
-
-
0030811399
-
Targeted development of microsatellite markers from the defined region of bovine chromosome 6q21-31
-
Weikard, R., Goldammer, T., Kuhn, C., Barendse, W., Schwerin, M. Targeted development of microsatellite markers from the defined region of bovine chromosome 6q21-31. Mamm. Genome 1997, 8: 836-840.
-
(1997)
Mamm. Genome
, vol.8
, pp. 836-840
-
-
Weikard, R.1
Goldammer, T.2
Kuhn, C.3
Barendse, W.4
Schwerin, M.5
-
15
-
-
0033557826
-
High-resolution human/goat comparative map of the goat polled/intersex syndrome (PIS), the human homologue is contained in a human YAC from HSA3q23
-
Vaiman, D., Schibler, L., Oustry-Vaiman, A., Pailhoux, E., Goldammer, T., Stevanovic, M., Furet, J.P., Schwerin, M., Cotinot, C., Fellous, M., Cribiu, E.P. High-resolution human/goat comparative map of the goat polled/intersex syndrome (PIS), the human homologue is contained in a human YAC from HSA3q23. Genomics 1999, 56: 31-39.
-
(1999)
Genomics
, vol.56
, pp. 31-39
-
-
Vaiman, D.1
Schibler, L.2
Oustry-Vaiman, A.3
Pailhoux, E.4
Goldammer, T.5
Stevanovic, M.6
Furet, J.P.7
Schwerin, M.8
Cotinot, C.9
Fellous, M.10
Cribiu, E.P.11
-
16
-
-
0033975420
-
A major effect QTL determined by multiple genes in epileptic EL mice
-
Legare, M.E., Bartlett, F.S. 2n., Frankel, W.N. A major effect QTL determined by multiple genes in epileptic EL mice. Genome Res. 2000, 10: 42-48.
-
(2000)
Genome Res.
, vol.10
, pp. 42-48
-
-
Legare, M.E.1
Bartlett F.S. II2
Frankel, W.N.3
-
17
-
-
0033780652
-
Guilt by association
-
Altshuler, D., Daly, M., Kruglyak, L. Guilt by association. Nat. Genet. 2000, 26: 135-137.
-
(2000)
Nat. Genet.
, vol.26
, pp. 135-137
-
-
Altshuler, D.1
Daly, M.2
Kruglyak, L.3
-
18
-
-
16944364045
-
A deletion in the bovine myostatin gene causes the double-muscled phenotype in cattle
-
Grobet, L., Martin, L.J., Poncelet, D., Pirottin, D., Brouwers, B., Riquet, J., Schoeberlein, A., Dunner, S., Menissier, F., Massabanda, J., Fries, R., Hanset, R., Georges, M. A deletion in the bovine myostatin gene causes the double-muscled phenotype in cattle. Nat. Genet. 1997, 17: 71-74.
-
(1997)
Nat. Genet.
, vol.17
, pp. 71-74
-
-
Grobet, L.1
Martin, L.J.2
Poncelet, D.3
Pirottin, D.4
Brouwers, B.5
Riquet, J.6
Schoeberlein, A.7
Dunner, S.8
Menissier, F.9
Massabanda, J.10
Fries, R.11
Hanset, R.12
Georges, M.13
-
19
-
-
0034685949
-
A mutation in PRKAG3 associated with excess glycogen content in pig skeletal muscle
-
Milan, D., Jeon, J.T., Looft, C., Amarger, V., Robic, A., Thelander, M., Rogel-Gaillard, C., Paul, S., Iannuccelli, N., Rask, L., Ronne, H., Lundstrom, K., Reinsch, N., Gellin, J., Kalm, E., Roy, P.L., Chardon, P., Andersson, L. A mutation in PRKAG3 associated with excess glycogen content in pig skeletal muscle. Science 2000, 288: 1248-1251.
-
(2000)
Science
, vol.288
, pp. 1248-1251
-
-
Milan, D.1
Jeon, J.T.2
Looft, C.3
Amarger, V.4
Robic, A.5
Thelander, M.6
Rogel-Gaillard, C.7
Paul, S.8
Iannuccelli, N.9
Rask, L.10
Ronne, H.11
Lundstrom, K.12
Reinsch, N.13
Gellin, J.14
Kalm, E.15
Roy, P.L.16
Chardon, P.17
Andersson, L.18
-
20
-
-
0034425606
-
The roads from phenotypic variation to gene discovery, mutagenesis versus QTL
-
Nadeau, J.H., Frankel, W.N. The roads from phenotypic variation to gene discovery, mutagenesis versus QTL. Nat. Genet. 2000, 25: 381-384.
-
(2000)
Nat. Genet.
, vol.25
, pp. 381-384
-
-
Nadeau, J.H.1
Frankel, W.N.2
-
21
-
-
0032837860
-
Mouse ENU mutagenesis
-
Justice, M.J., Noveroske, J.K., Weber, J.S., Zheng, B., Bradley, A. Mouse ENU mutagenesis. Hum. Mol. Genet. 1999, 8: 1955-1963.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 1955-1963
-
-
Justice, M.J.1
Noveroske, J.K.2
Weber, J.S.3
Zheng, B.4
Bradley, A.5
-
22
-
-
0031975307
-
Experimental strategies for the genetic dissection of complex traits in animal models
-
Darvasi, A. Experimental strategies for the genetic dissection of complex traits in animal models. Nat. Genet. 1998, 18: 19-24.
-
(1998)
Nat. Genet.
, vol.18
, pp. 19-24
-
-
Darvasi, A.1
-
23
-
-
0034659898
-
Genomics, gene expression and DNA arrays
-
Lockhart, D.J., Winzeler, E.A. Genomics, gene expression and DNA arrays. Nature 2000, 405: 827-836.
-
(2000)
Nature
, vol.405
, pp. 827-836
-
-
Lockhart, D.J.1
Winzeler, E.A.2
-
24
-
-
0030724420
-
From expressed sequence tags to 'epigenomics', an understanding of disease processes
-
Zweiger, G., Scott, R.W. From expressed sequence tags to 'epigenomics', an understanding of disease processes. Curr. Opin. Biotechnol. 1997, 8: 684-687.
-
(1997)
Curr. Opin. Biotechnol.
, vol.8
, pp. 684-687
-
-
Zweiger, G.1
Scott, R.W.2
-
25
-
-
0030895722
-
2006 expressed-sequence tags derived from human chromosome 7-enriched cDNA libraries
-
Touchman, J.W., Bouffard, G.G., Weintraub, L.A., Idol, J.R., Wang, L., Robbins, C.M., Nussbaum, J.C., Lovett, M., Green, E.D. 2006 expressed-sequence tags derived from human chromosome 7-enriched cDNA libraries. Genome Res. 1997, 7: 281-292.
-
(1997)
Genome Res.
, vol.7
, pp. 281-292
-
-
Touchman, J.W.1
Bouffard, G.G.2
Weintraub, L.A.3
Idol, J.R.4
Wang, L.5
Robbins, C.M.6
Nussbaum, J.C.7
Lovett, M.8
Green, E.D.9
-
26
-
-
0026664464
-
A preliminary linkage map of the chicken genome
-
Bumstead, N., Palyga, J. A preliminary linkage map of the chicken genome. Genomics 1992, 13: 690-697.
-
(1992)
Genomics
, vol.13
, pp. 690-697
-
-
Bumstead, N.1
Palyga, J.2
-
27
-
-
0000629096
-
Characterization of a Red Jungle Fowl by White Leghorn Backcross Reference Population for Molecular Mapping of the Chicken Genome
-
Crittenden, L.B. Characterization of a Red Jungle Fowl by White Leghorn Backcross Reference Population for Molecular Mapping of the Chicken Genome. Poult. Sci. 1993, 72: 334-348.
-
(1993)
Poult. Sci.
, vol.72
, pp. 334-348
-
-
Crittenden, L.B.1
-
28
-
-
0032522150
-
A comprehensive microsatellite linkage map of the chicken genome
-
Groenen, M.A., Crooijmans, R.P., Veenendaal, A., Cheng, H.H., Siwek, M., van der, Po.J. A comprehensive microsatellite linkage map of the chicken genome. Genomics 1998, 49: 265-274.
-
(1998)
Genomics
, vol.49
, pp. 265-274
-
-
Groenen, M.A.1
Crooijmans, R.P.2
Veenendaal, A.3
Cheng, H.H.4
Siwek, M.5
van der, Po.J.6
-
29
-
-
0033962741
-
A consensus linkage map of the chicken genome
-
Groenen, M.A., Cheng, H.H., Bumstead, N., Benkel, B.F., Briles, W.E., Burke, T., Burt, D.W., Crittenden, L.B., Dodgson, J., Hillel, J., Lamont, S., de Leon, A.P., Soller, M., Takahashi, H., Vignal, A. A consensus linkage map of the chicken genome. Genome Res. 2000, 10: 137-147.
-
(2000)
Genome Res.
, vol.10
, pp. 137-147
-
-
Groenen, M.A.1
Cheng, H.H.2
Bumstead, N.3
Benkel, B.F.4
Briles, W.E.5
Burke, T.6
Burt, D.W.7
Crittenden, L.B.8
Dodgson, J.9
Hillel, J.10
Lamont, S.11
de Leon, A.P.12
Soller, M.13
Takahashi, H.14
Vignal, A.15
-
30
-
-
0034534753
-
Bu. First report on chicken genes and chromosomes 2000
-
Schmid, M., Nanda, I., Guttenbach, M., Steinlein, C., Hoehn, M., Schartl, M., Haaf, T., Weigend, S., Fries, R., Buerstedde, J.M., Wimmers, K., Burt, D.W., Smith, J., A'Hara, S., Law, A., Griffin, D.K., Bumstead, N., Kaufman, J., Thomson, P.A., Bu. First report on chicken genes and chromosomes 2000. Cytogenet. Cell Genet. 2000, 90: 169-218.
-
(2000)
Cytogenet. Cell Genet.
, vol.90
, pp. 169-218
-
-
Schmid, M.1
Nanda, I.2
Guttenbach, M.3
Steinlein, C.4
Hoehn, M.5
Schartl, M.6
Haaf, T.7
Weigend, S.8
Fries, R.9
Buerstedde, J.M.10
Wimmers, K.11
Burt, D.W.12
Smith, J.13
A'Hara, S.14
Law, A.15
Griffin, D.K.16
Bumstead, N.17
Kaufman, J.18
Thomson, P.A.19
-
31
-
-
0034756444
-
Partial deletion of the bovine ED1 gene causes anhidrotic ectodermal dysplasia in cattle
-
Drögemüller, C., Disti, O., Leeb, T. Partial deletion of the bovine ED1 gene causes anhidrotic ectodermal dysplasia in cattle. Genome Res. 2001, 11: 1699-1705.
-
(2001)
Genome Res.
, vol.11
, pp. 1699-1705
-
-
Drögemüller, C.1
Disti, O.2
Leeb, T.3
-
32
-
-
0015029599
-
Ectodermal dysplasia in cattle, analogues in man
-
Selmanowitz, V. Ectodermal dysplasia in cattle, analogues in man. British Journal of Dermatology 1971, 84: 258-265.
-
(1971)
British Journal of Dermatology
, vol.84
, pp. 258-265
-
-
Selmanowitz, V.1
-
33
-
-
0036012801
-
A single point mutation within the ED1 gene disrupts correct splicing at two different splice sites and leads to anhidrotic ectodermal dysplasia in cattle
-
Drogemuller, C., Peters, M., Pohlenz, J., Distl, O., Leeb, T. A single point mutation within the ED1 gene disrupts correct splicing at two different splice sites and leads to anhidrotic ectodermal dysplasia in cattle. J. Mol. Med. 2002, 80: 319-323.
-
(2002)
J. Mol. Med.
, vol.80
, pp. 319-323
-
-
Drogemuller, C.1
Peters, M.2
Pohlenz, J.3
Distl, O.4
Leeb, T.5
-
34
-
-
0032743842
-
Cloning of bovine LYST gene and identification of a missense mutation associated with Chediak-Higashi syndrome of cattle
-
Kunieda, T., Nakagiri, M., Takami, M., Ide, H., Ogawa, H. Cloning of bovine LYST gene and identification of a missense mutation associated with Chediak-Higashi syndrome of cattle. Mamm. Genome 1999, 10: 1146-1149.
-
(1999)
Mamm. Genome
, vol.10
, pp. 1146-1149
-
-
Kunieda, T.1
Nakagiri, M.2
Takami, M.3
Ide, H.4
Ogawa, H.5
-
35
-
-
0034090840
-
Localization of the locus responsible for Chediak-Higashi syndrome in cattle to bovine chromosome 28
-
Kunieda, T., Ide, H., Nakagiri, M., Yoneda, K., Konfortov, B., Ogawa, H. Localization of the locus responsible for Chediak-Higashi syndrome in cattle to bovine chromosome 28. Anim. Genet. 2000, 31: 87-90.
-
(2000)
Anim. Genet.
, vol.31
, pp. 87-90
-
-
Kunieda, T.1
Ide, H.2
Nakagiri, M.3
Yoneda, K.4
Konfortov, B.5
Ogawa, H.6
-
36
-
-
0024330416
-
Molecular definition of bovine arginosuccinate synthetase deficiency
-
Dennis, J.A., Healey, P.J., Beaudetal. O'Brien, W.E. Molecular definition of bovine arginosuccinate synthetase deficiency. Proc. Natl. Acad. Sci. USA 1989, 86: 7947-7951.
-
(1989)
Proc. Natl. Acad. Sci. USA
, vol.86
, pp. 7947-7951
-
-
Dennis, J.A.1
Healey, P.J.2
Beaudetal, A.3
O'Brien, W.E.4
-
37
-
-
0028031239
-
Mapping the bovine albino locus
-
Foreman, M.E., Lamoreux, M.L., Kwon, B., Womack, J.E. Mapping the bovine albino locus. J. Hered. 1994, 85: 318-320.
-
(1994)
J. Hered.
, vol.85
, pp. 318-320
-
-
Foreman, M.E.1
Lamoreux, M.L.2
Kwon, B.3
Womack, J.E.4
-
38
-
-
0029360495
-
The role of melanocyte-stimulating hormone (MSH) receptor in bovine coat color determination
-
Klungland, H., Vage, D.I., Gomez-Raya, L., Adalsteinsson, S., Lien, S. The role of melanocyte-stimulating hormone (MSH) receptor in bovine coat color determination. Mamm. Genome 1995, 6: 636-639.
-
(1995)
Mamm. Genome
, vol.6
, pp. 636-639
-
-
Klungland, H.1
Vage, D.I.2
Gomez-Raya, L.3
Adalsteinsson, S.4
Lien, S.5
-
39
-
-
0030120492
-
Red coat color in Holstein cattle is associated with a deletion in the MSHR gene
-
Joerg, H., Fries, H.R., Meijerink, E., Stranzinger, G.F. Red coat color in Holstein cattle is associated with a deletion in the MSHR gene. Mamm. Genome 1996, 7: 317-318.
-
(1996)
Mamm. Genome
, vol.7
, pp. 317-318
-
-
Joerg, H.1
Fries, H.R.2
Meijerink, E.3
Stranzinger, G.F.4
-
40
-
-
0035406096
-
Complex vertebral malformation in holstein calves
-
Agerholm, J.S., Bendixen, C., Andersen, O., Arnbjerg, J. Complex vertebral malformation in holstein calves. J. Vet. Diagn. Invest. 2001, 13: 283-289.
-
(2001)
J. Vet. Diagn. Invest.
, vol.13
, pp. 283-289
-
-
Agerholm, J.S.1
Bendixen, C.2
Andersen, O.3
Arnbjerg, J.4
-
41
-
-
0027273318
-
DUMPS cattle carry a point mutation in the uridine monophosphate synthase gene
-
Schwenger, B., Schober, S., Simon, D. DUMPS cattle carry a point mutation in the uridine monophosphate synthase gene. Genomics 1993, 16: 241-244.
-
(1993)
Genomics
, vol.16
, pp. 241-244
-
-
Schwenger, B.1
Schober, S.2
Simon, D.3
-
42
-
-
0025412574
-
Deficiency of uridine monophosphate synthase among Holstein cattle
-
Shanks, R.D., Robinson, J.L. Deficiency of uridine monophosphate synthase among Holstein cattle. Cornell Vet. 1990, 80: 119-122.
-
(1990)
Cornell Vet.
, vol.80
, pp. 119-122
-
-
Shanks, R.D.1
Robinson, J.L.2
-
43
-
-
0027730167
-
A genetic map of DNA loci on bovine chromosome 1
-
Barendse, W., Armitage, S.M., Ryan, A.M., Moore, S.S., Clayton, D., Georges, M., Womack, J.E., Hetzel, J. A genetic map of DNA loci on bovine chromosome 1. Genomics 1993, 18: 602-608.
-
(1993)
Genomics
, vol.18
, pp. 602-608
-
-
Barendse, W.1
Armitage, S.M.2
Ryan, A.M.3
Moore, S.S.4
Clayton, D.5
Georges, M.6
Womack, J.E.7
Hetzel, J.8
-
44
-
-
0027950623
-
Assignment of the bovine uridine monophosphate synthase gene to the bovine chromosome region 1q34-36 by FISH
-
Friedl, R., Rottmann, O.J. Assignment of the bovine uridine monophosphate synthase gene to the bovine chromosome region 1q34-36 by FISH. Mamm. Genome 1994, 5: 38-40.
-
(1994)
Mamm. Genome
, vol.5
, pp. 38-40
-
-
Friedl, R.1
Rottmann, O.J.2
-
45
-
-
0034103658
-
Obesity resistance and multiple mechanisms of triglyceride synthesis in mice lacking Dgat
-
Smith, S.J., Cases, S., Jensen, D.R., Chen, H.C., Sande, E., Tow, B., Sanan, D.A., Raber, J., Eckel, R.H., Farese, R.V. Jr. Obesity resistance and multiple mechanisms of triglyceride synthesis in mice lacking Dgat. Nat. Genet. 2000, 25: 87-90.
-
(2000)
Nat. Genet.
, vol.25
, pp. 87-90
-
-
Smith, S.J.1
Cases, S.2
Jensen, D.R.3
Chen, H.C.4
Sande, E.5
Tow, B.6
Sanan, D.A.7
Raber, J.8
Eckel, R.H.9
Farese R.V., Jr.10
-
46
-
-
0037047067
-
Association of a lysine-232/alanine polymorphism in a bovine gene encoding acyl-CoA, diacylglycerol acyltransferase (DGAT1) with variation at a quantitative trait locus for milk fat content
-
Winter, A., Kramer, W., Werner, F.A., Kollers, S., Kata, S., Durstewitz, G., Buitkamp, J., Womack, J.E., Thaller, G., Fries, R. Association of a lysine-232/alanine polymorphism in a bovine gene encoding acyl-CoA, diacylglycerol acyltransferase (DGAT1) with variation at a quantitative trait locus for milk fat content. Proc. Natl. Acad. Sci. USA 2002, 99: 9300-9305.
-
(2002)
Proc. Natl. Acad. Sci. USA
, vol.99
, pp. 9300-9305
-
-
Winter, A.1
Kramer, W.2
Werner, F.A.3
Kollers, S.4
Kata, S.5
Durstewitz, G.6
Buitkamp, J.7
Womack, J.E.8
Thaller, G.9
Fries, R.10
-
47
-
-
0036175484
-
Positional candidate cloning of a QTL in dairy cattle, identification of a missense mutation in the bovine DGAT1 gene with major effect on milk yield and composition
-
Grisart, B., Coppieters, W., Farnir, F., Karim, L., Ford, C., Berzi, P., Cambisano, N., Mni, M., Reid, S., Simon, P., Spelman, R., Georges, M., Snell, R. Positional candidate cloning of a QTL in dairy cattle, identification of a missense mutation in the bovine DGAT1 gene with major effect on milk yield and composition. Genome Res. 2002, 12: 222-231.
-
(2002)
Genome Res.
, vol.12
, pp. 222-231
-
-
Grisart, B.1
Coppieters, W.2
Farnir, F.3
Karim, L.4
Ford, C.5
Berzi, P.6
Cambisano, N.7
Mni, M.8
Reid, S.9
Simon, P.10
Spelman, R.11
Georges, M.12
Snell, R.13
-
48
-
-
0033126177
-
Gene defect of dermatan sulfate proteoglycan of cattle affected with a variant form of Ehlers-Danlos syndrome
-
Tajima, M., Miyake, S., Takehana, K., Kobayashi, A., Yamato, O., Maede, Y. Gene defect of dermatan sulfate proteoglycan of cattle affected with a variant form of Ehlers-Danlos syndrome. J. Vet. Intern. Med. 1999, 13: 202-205.
-
(1999)
J. Vet. Intern. Med.
, vol.13
, pp. 202-205
-
-
Tajima, M.1
Miyake, S.2
Takehana, K.3
Kobayashi, A.4
Yamato, O.5
Maede, Y.6
-
49
-
-
0033358540
-
Human Ehlers-Danlos syndrome type VII C and bovine dermatosparaxis are caused by mutations in the procollagen I N-proteinase gene
-
Colige, A., Sieron, A.L., Li, S.W., Schwarze, U., Petty, E., Wertelecki, W., Wilcox, W., Krakow, D., Cohn, D.H., Reardon, W., Byers, P.H., Lapiere, C.M., Prockop, D.J., Nusgens, B.V. Human Ehlers-Danlos syndrome type VII C and bovine dermatosparaxis are caused by mutations in the procollagen I N-proteinase gene. Am. J. Hum. Genet. 1999, 65: 308-317.
-
(1999)
Am. J. Hum. Genet.
, vol.65
, pp. 308-317
-
-
Colige, A.1
Sieron, A.L.2
Li, S.W.3
Schwarze, U.4
Petty, E.5
Wertelecki, W.6
Wilcox, W.7
Krakow, D.8
Cohn, D.H.9
Reardon, W.10
Byers, P.H.11
Lapiere, C.M.12
Prockop, D.J.13
Nusgens, B.V.14
-
50
-
-
0034050816
-
The bovine alpha-glucosidase gene, coding region, genomic structure, and mutations that cause bovine generalized glycogenosis
-
Dennis, J.A., Moran, C., Healy, P.J. The bovine alpha-glucosidase gene, coding region, genomic structure, and mutations that cause bovine generalized glycogenosis. Mamm. Genome 2000, 11: 206-212.
-
(2000)
Mamm. Genome
, vol.11
, pp. 206-212
-
-
Dennis, J.A.1
Moran, C.2
Healy, P.J.3
-
51
-
-
0029037248
-
Myophosphorylase deficiency associated with rhabdomyolysis and exercise intolerance in 6 related Charolais cattle
-
Angelos, S., Valberg, S.J., Smith, B.P., McQuarrie, P.S., Shanske, S., Tsujino, S., DiMauro, S., Cardinet, G.H. Myophosphorylase deficiency associated with rhabdomyolysis and exercise intolerance in 6 related Charolais cattle. Muscle and Nerve 1995, 18: 736-740.
-
(1995)
Muscle and Nerve
, vol.18
, pp. 736-740
-
-
Angelos, S.1
Valberg, S.J.2
Smith, B.P.3
McQuarrie, P.S.4
Shanske, S.5
Tsujino, S.6
DiMauro, S.7
Cardinet, G.H.8
-
52
-
-
0030064815
-
Cloning of bovine muscle glycogen phosphorylase cDNA and identification of a mutation in cattle with myophosphorylase deficiency, an animal model for McArdle's disease
-
Tsujino, S., Shanske, S., Valberg, S.J., Cardinet, G.H. 3r., Smith, B.P., DiMauro, S. Cloning of bovine muscle glycogen phosphorylase cDNA and identification of a mutation in cattle with myophosphorylase deficiency, an animal model for McArdle's disease. Neuromuscul. Disord 1996, 6: 19-26.
-
(1996)
Neuromuscul. Disord.
, vol.6
, pp. 19-26
-
-
Tsujino, S.1
Shanske, S.2
Valberg, S.J.3
Cardinet G.H. III4
Smith, B.P.5
DiMauro, S.6
-
53
-
-
0023256564
-
A nonsense mutation causes hereditary goitre in the Afrikander cattle and unmasks alternative splicing of thyroglobulin transcripts
-
Ricketts, M.H., Simons, M.J., Parma, J., Mercken, L., Dong, Q., Vassart, G. A nonsense mutation causes hereditary goitre in the Afrikander cattle and unmasks alternative splicing of thyroglobulin transcripts. Proc. Natl. Acad. Sci. USA 1987, 84: 3181-3184.
-
(1987)
Proc. Natl. Acad. Sci. USA
, vol.84
, pp. 3181-3184
-
-
Ricketts, M.H.1
Simons, M.J.2
Parma, J.3
Mercken, L.4
Dong, Q.5
Vassart, G.6
-
54
-
-
0026646217
-
Identification and prevalence of a genetic defect that causes leukocyte adhesion deficiency in Holstein cattle
-
Shuster, D.E., Kehrli, M.E., Ackermann, M.R., Gilbert, R.O. Identification and prevalence of a genetic defect that causes leukocyte adhesion deficiency in Holstein cattle. Proc. Natl. Acad. Sci. USA 1992, 89: 9225-9229.
-
(1992)
Proc. Natl. Acad. Sci. USA
, vol.89
, pp. 9225-9229
-
-
Shuster, D.E.1
Kehrli, M.E.2
Ackermann, M.R.3
Gilbert, R.O.4
-
55
-
-
0030940335
-
alpha-Mannosidosis, functional cloning of the lysosomal alpha-mannosidase cDNA and identification of a mutation in two affected siblings
-
Nilssen, O., Berg, T., Riise, H.M., Ramachandran, U., Evjen, G., Hansen, G.M., Malm, D., Tranebjaerg, L., Tollersrud, O.K. alpha-Mannosidosis, functional cloning of the lysosomal alpha-mannosidase cDNA and identification of a mutation in two affected siblings. Hum. Mol. Genet. 1997, 6: 717-726.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 717-726
-
-
Nilssen, O.1
Berg, T.2
Riise, H.M.3
Ramachandran, U.4
Evjen, G.5
Hansen, G.M.6
Malm, D.7
Tranebjaerg, L.8
Tollersrud, O.K.9
-
56
-
-
0030921264
-
Purification of bovine lysosomal alpha-mannosidase, characterization of its gene and determination of two mutations that cause alpha-mannosidosis
-
Tollersrud, O.K., Berg, T., Healy, P., Evjen, G., Ramachandran, U., Nilssen, O. Purification of bovine lysosomal alpha-mannosidase, characterization of its gene and determination of two mutations that cause alpha-mannosidosis. Eur. J. Biochem. 1997, 246: 410-419.
-
(1997)
Eur. J. Biochem.
, vol.246
, pp. 410-419
-
-
Tollersrud, O.K.1
Berg, T.2
Healy, P.3
Evjen, G.4
Ramachandran, U.5
Nilssen, O.6
-
57
-
-
0031265930
-
Molecular heterogeneity for bovine alpha-mannosidosis, PCR based assays for detection of breed-specific mutations
-
Berg, T., Healy, P.J., Tollersrud, O.K., Nilssen, O. Molecular heterogeneity for bovine alpha-mannosidosis, PCR based assays for detection of breed-specific mutations. Res. Vet. Sci. 1997, 63: 279-282.
-
(1997)
Res. Vet. Sci.
, vol.63
, pp. 279-282
-
-
Berg, T.1
Healy, P.J.2
Tollersrud, O.K.3
Nilssen, O.4
-
58
-
-
0025845834
-
Maple syrup urine disease caused by a partial deletion in the inner E2 core domain of the branched chain alpha-keto acid dehydrogenase complex due to aberrant splicing. A single base deletion at a 5′-splice donor site of an intron of the E2 gene disr
-
Mitsubuchi, H., Nobukuni, Y., Akaboshi, I., Indo, Y., Endo, F., Matsuda, I. Maple syrup urine disease caused by a partial deletion in the inner E2 core domain of the branched chain alpha-keto acid dehydrogenase complex due to aberrant splicing. A single base deletion at a 5′-splice donor site of an intron of the E2 gene disr. J. Clin. Invest. 1991, 87: 1207-1211.
-
(1991)
J. Clin. Invest.
, vol.87
, pp. 1207-1211
-
-
Mitsubuchi, H.1
Nobukuni, Y.2
Akaboshi, I.3
Indo, Y.4
Endo, F.5
Matsuda, I.6
-
59
-
-
0033172914
-
Definition of the mutation responsible for maple syrup urine disease in Poll Shorthorns and genotyping Poll Shorthorns and Poll Herefords for maple syrup urine disease alleles
-
Dennis, J.A., Healy, P.J. Definition of the mutation responsible for maple syrup urine disease in Poll Shorthorns and genotyping Poll Shorthorns and Poll Herefords for maple syrup urine disease alleles. Res. Vet. Sci. 1999, 67: 1-6.
-
(1999)
Res. Vet. Sci.
, vol.67
, pp. 1-6
-
-
Dennis, J.A.1
Healy, P.J.2
-
60
-
-
0029400485
-
The mh gene causing double-muscling in cattle maps to bovine Chromosome 2. Mamm
-
Charlier, C., Coppieters, W., Farnir, F., Grobet, L., Leroy, P.L., Michaux, C., Mni, M., Schwers, A., anmanshoven, P., Hanset, R., Georges, M. The mh gene causing double-muscling in cattle maps to bovine Chromosome 2. Mamm. Genome 1995, 6: 788-792.
-
(1995)
Genome
, vol.6
, pp. 788-792
-
-
Charlier, C.1
Coppieters, W.2
Farnir, F.3
Grobet, L.4
Leroy, P.L.5
Michaux, C.6
Mni, M.7
Schwers, A.8
Anmanshoven, P.9
Hanset, R.10
Georges, M.11
-
61
-
-
0030818314
-
Mutations in myostatin (GDF8) in double-muscled Belgian Blue and Piedmontese cattle
-
Kambadur, R., Sharma, M., Smith, T.P., Bass, J.J. Mutations in myostatin (GDF8) in double-muscled Belgian Blue and Piedmontese cattle. Genome Res. 1997, 7: 910-916.
-
(1997)
Genome Res.
, vol.7
, pp. 910-916
-
-
Kambadur, R.1
Sharma, M.2
Smith, T.P.3
Bass, J.J.4
-
62
-
-
0030840359
-
Double muscling in cattle due to mutations in the myostatin gene
-
McPherron, A.C., Lee, S.J. Double muscling in cattle due to mutations in the myostatin gene. Proc. Natl. Acad. Sci. USA 1997, 94: 12457-12461.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 12457-12461
-
-
McPherron, A.C.1
Lee, S.J.2
-
63
-
-
15644381757
-
Molecular definition of an allelic series of mutations disrupting the myostatin function and causing double-muscling in cattle
-
Grobet, L., Poncelet, D., Royo, L.J., Brouwers, B., Pirottin, D., Michaux, C., Menissier, F., Zanotti, M., Dunner, S., Georges, M. Molecular definition of an allelic series of mutations disrupting the myostatin function and causing double-muscling in cattle. Mamm. Genome 1998, 9: 210-213.
-
(1998)
Mamm. Genome
, vol.9
, pp. 210-213
-
-
Grobet, L.1
Poncelet, D.2
Royo, L.J.3
Brouwers, B.4
Pirottin, D.5
Michaux, C.6
Menissier, F.7
Zanotti, M.8
Dunner, S.9
Georges, M.10
-
64
-
-
0013676285
-
Positional candidate cloning of the bovine mh locus identifies an allelic series of mutations disrupting the myostatin function and causing double-muscling in cattle
-
Presented in
-
Georges, M., Grobet, L., Poncelet, D., Royo, L.J., Pirottin, D., Brouwers, B. Positional candidate cloning of the bovine mh locus identifies an allelic series of mutations disrupting the myostatin function and causing double-muscling in cattle. Presented in, Congress on Genetics Applied to Livestock Production 1998, 26: 195-204.
-
(1998)
Congress on Genetics Applied to Livestock Production
, vol.26
, pp. 195-204
-
-
Georges, M.1
Grobet, L.2
Poncelet, D.3
Royo, L.J.4
Pirottin, D.5
Brouwers, B.6
-
65
-
-
0034745729
-
A nonsense mutation in the alpha1 subunit of the inhibitory glycine receptor associated with bovine myoclonus
-
Pierce, K.D., Handford, C.A., Morris, R., Vafa, B., Dennis, J.A., Healy, P.J., Schofield, P.R. A nonsense mutation in the alpha1 subunit of the inhibitory glycine receptor associated with bovine myoclonus. Mol. Cell Neurosci. 2001, 17: 354-363.
-
(2001)
Mol. Cell Neurosci.
, vol.17
, pp. 354-363
-
-
Pierce, K.D.1
Handford, C.A.2
Morris, R.3
Vafa, B.4
Dennis, J.A.5
Healy, P.J.6
Schofield, P.R.7
-
66
-
-
0015130992
-
Hereditary neuraxial oedema of calves
-
Blood, D., Gay, C. Hereditary neuraxial oedema of calves. Aust. Vet. J. 1971, 47: 520.
-
(1971)
Aust. Vet. J.
, vol.47
, pp. 520
-
-
Blood, D.1
Gay, C.2
-
67
-
-
0029384526
-
Use of hair root as a source of DNA for the detection of heterozygotes for recessive defects in cattle
-
Healy, P.J., Dennis, J.A., Moule, J.F. Use of hair root as a source of DNA for the detection of heterozygotes for recessive defects in cattle. Aust. Vet. J. 1995, 72: 392.
-
(1995)
Aust. Vet. J.
, vol.72
, pp. 392
-
-
Healy, P.J.1
Dennis, J.A.2
Moule, J.F.3
-
68
-
-
0031789155
-
A novel stop codon mutation (X417L) of the ferrochelatase gene in bovine protoporphyria, a natural animal model of the human disease
-
1408
-
Jenkins, M.M., LeBoeuf, R.D., Ruth, G.R., Bloomer, J.R. A novel stop codon mutation (X417L) of the ferrochelatase gene in bovine protoporphyria, a natural animal model of the human disease. Biochim. Biophys. Acta 1998, 1408: 18-24.
-
(1998)
Biochim. Biophys. Acta
, pp. 18-24
-
-
Jenkins, M.M.1
LeBoeuf, R.D.2
Ruth, G.R.3
Bloomer, J.R.4
-
69
-
-
0036010110
-
A new deletion mutation in bovine Claudin-16 (CL-16) deficiency and diagnosis
-
Hirano, T., Hirotsune, S., Sasaki, S., Kikuchi, T., Sugimoto, Y. A new deletion mutation in bovine Claudin-16 (CL-16) deficiency and diagnosis. Anim. Genet. 2002, 33: 118-122.
-
(2002)
Anim. Genet.
, vol.33
, pp. 118-122
-
-
Hirano, T.1
Hirotsune, S.2
Sasaki, S.3
Kikuchi, T.4
Sugimoto, Y.5
-
70
-
-
0033159013
-
Multicystic renal dysplasia in a Japanese black bull
-
Ushigaki, K., Uchida, K., Murakami, T., Yamaguchi, R., Tateyama, S. Multicystic renal dysplasia in a Japanese black bull. J. Vet. Med. Sci. 1999, 61: 839-842.
-
(1999)
J. Vet. Med. Sci.
, vol.61
, pp. 839-842
-
-
Ushigaki, K.1
Uchida, K.2
Murakami, T.3
Yamaguchi, R.4
Tateyama, S.5
-
71
-
-
0034063708
-
Homozygosity mapping of the locus responsible for renal tubular dysplasia of cattle on bovine chromosome 1
-
Ohba, Y., Kitagawa, H., Kitoh, K., Asahina, S., Nishimori, K., Yoneda, K., Kunieda, T., Sasaki, Y. Homozygosity mapping of the locus responsible for renal tubular dysplasia of cattle on bovine chromosome 1. Mamm. Genome 2000, 11: 316-319.
-
(2000)
Mamm. Genome
, vol.11
, pp. 316-319
-
-
Ohba, Y.1
Kitagawa, H.2
Kitoh, K.3
Asahina, S.4
Nishimori, K.5
Yoneda, K.6
Kunieda, T.7
Sasaki, Y.8
-
72
-
-
0034068924
-
Null mutation of PCLN-1/Claudin-16 results in bovine chronic interstitial nephritis
-
Hirano, T., Kobayashi, N., Itoh, T., Takasuga, A., Nakamaru, T., Hirotsune, S., Sugimoto, Y. Null mutation of PCLN-1/Claudin-16 results in bovine chronic interstitial nephritis. Genome Res. 2000, 10: 659-663.
-
(2000)
Genome Res.
, vol.10
, pp. 659-663
-
-
Hirano, T.1
Kobayashi, N.2
Itoh, T.3
Takasuga, A.4
Nakamaru, T.5
Hirotsune, S.6
Sugimoto, Y.7
-
73
-
-
0029944734
-
Deletion of the SRY region on the Y chromosome detected in bovine gonadal hypoplasia (XY female) by PCR
-
Kawakura, K., Miyake, Y.I., Murakami, R.K., Kondoh, S., Hirata, T.I., Kaneda, Y. Deletion of the SRY region on the Y chromosome detected in bovine gonadal hypoplasia (XY female) by PCR. Cytogenet. Cell Genet. 1996, 72: 183-184.
-
(1996)
Cytogenet. Cell Genet.
, vol.72
, pp. 183-184
-
-
Kawakura, K.1
Miyake, Y.I.2
Murakami, R.K.3
Kondoh, S.4
Hirata, T.I.5
Kaneda, Y.6
-
74
-
-
15844377239
-
Defective anion transport and marked spherocytosis with membrane instability caused by hereditary total deficiency of red cell band 3 in cattle due to a nonsense mutation
-
Inaba, M., Yawata, A., Koshino, I., Sato, K., Takeuchi, M., Takakuwa, Y., Manno, S., Yawata, Y., Kanzaki, A. Defective anion transport and marked spherocytosis with membrane instability caused by hereditary total deficiency of red cell band 3 in cattle due to a nonsense mutation. J. Clin. Invest. 1996, 97: 1804-1817.
-
(1996)
J. Clin. Invest.
, vol.97
, pp. 1804-1817
-
-
Inaba, M.1
Yawata, A.2
Koshino, I.3
Sato, K.4
Takeuchi, M.5
Takakuwa, Y.6
Manno, S.7
Yawata, Y.8
Kanzaki, A.9
-
75
-
-
0032805203
-
Localization of a locus responsible for the bovine chondrodysplastic dwarfism (bcd) on chromosome 6
-
Yoneda, K., Moritomo, Y., Takami, M., Hirata, S., Kikukawa, Y., Kunieda, T. Localization of a locus responsible for the bovine chondrodysplastic dwarfism (bcd) on chromosome 6. Mamm. Genome 1999, 10: 597-600.
-
(1999)
Mamm. Genome
, vol.10
, pp. 597-600
-
-
Yoneda, K.1
Moritomo, Y.2
Takami, M.3
Hirata, S.4
Kikukawa, Y.5
Kunieda, T.6
-
76
-
-
0038314055
-
Spider and other major Genes im Farm Livestock
-
Owen JB, Axford RFE (eds.), (CAB International, Wallingford Oxon, United Kingdom
-
Owen, J.B. Spider and other major Genes im Farm Livestock, in Owen JB, Axford RFE (eds.), Breeding for Disease Resistance in Farm Animals, (CAB International, Wallingford Oxon, United Kingdom 1991, pp 439-448.
-
(1991)
Breeding for Disease Resistance in Farm Animals
, pp. 439-448
-
-
Owen, J.B.1
-
77
-
-
18244415748
-
Genetic mapping of a locus associated with bovine chronic interstitial nephritis to chromosome 1
-
Kobayashi, N., Hirano, T., Maruyama, S., Matsuno, H., Mukoujima, K., Morimoto, H., Noike, H., Tomimatsu, H., Hara, K., Itoh, T., Imakawa, K., Nakayama, H., Nakamaru, T., Sugimoto, Y. Genetic mapping of a locus associated with bovine chronic interstitial nephritis to chromosome 1. Anim. Genet. 2000, 31: 91-95.
-
(2000)
Anim. Genet.
, vol.31
, pp. 91-95
-
-
Kobayashi, N.1
Hirano, T.2
Maruyama, S.3
Matsuno, H.4
Mukoujima, K.5
Morimoto, H.6
Noike, H.7
Tomimatsu, H.8
Hara, K.9
Itoh, T.10
Imakawa, K.11
Nakayama, H.12
Nakamaru, T.13
Sugimoto, Y.14
-
78
-
-
0022626874
-
A new acute transforming feline retrovirus and relationship of its oncogene v-kit with the protein kinase gene family
-
Besmer, P., Murphy, J.E., George, P.C., Qiu, F.H., Bergold, P.J., Lederman, L., Snyder, H.W. Jr., Brodeur, D., Zuckerman, E.E., Hardy, W.D. A new acute transforming feline retrovirus and relationship of its oncogene v-kit with the protein kinase gene family. Nature 1986, 320: 415-421.
-
(1986)
Nature
, vol.320
, pp. 415-421
-
-
Besmer, P.1
Murphy, J.E.2
George, P.C.3
Qiu, F.H.4
Bergold, P.J.5
Lederman, L.6
Snyder H.W., Jr.7
Brodeur, D.8
Zuckerman, E.E.9
Hardy, W.D.10
-
79
-
-
0023919865
-
Localization of the human c-kit protooncogene on the q11-q12 region of chromosome 4
-
d'Auriol, L., Mattei, M.G., Andre, C., Galibert, F. Localization of the human c-kit protooncogene on the q11-q12 region of chromosome 4. Hum. Genet. 1988, 78: 374-376.
-
(1988)
Hum. Genet.
, vol.78
, pp. 374-376
-
-
d'Auriol, L.1
Mattei, M.G.2
Andre, C.3
Galibert, F.4
-
80
-
-
0023694835
-
The proto-oncogene c-kit encoding a transmembrane tyrosine kinase receptor maps to the mouse W locus
-
Chabot, B., Stephenson, D.A., Chapman, V.M., Besmer, P., Bernstein, A. The proto-oncogene c-kit encoding a transmembrane tyrosine kinase receptor maps to the mouse W locus. Nature 1988, 335: 88-89.
-
(1988)
Nature
, vol.335
, pp. 88-89
-
-
Chabot, B.1
Stephenson, D.A.2
Chapman, V.M.3
Besmer, P.4
Bernstein, A.5
-
81
-
-
0025940323
-
Mutation of the KIT (mast/stem cell growth factor receptor) protooncogene in human piebaldism
-
Giebel, L.B., Spritz, R.A. Mutation of the KIT (mast/stem cell growth factor receptor) protooncogene in human piebaldism. Proc. Natl. Acad. Sci. USA 1991, 88: 8696-8699.
-
(1991)
Proc. Natl. Acad. Sci. USA
, vol.88
, pp. 8696-8699
-
-
Giebel, L.B.1
Spritz, R.A.2
-
82
-
-
0034141324
-
A DNA polymorphism in the bovine c-kit gene
-
Olsen, H.G., Vage, D.I., Lien, S., Klungland, H. A DNA polymorphism in the bovine c-kit gene. Anim. Genet. 2000, 31: 71.
-
(2000)
Anim. Genet.
, vol.31
, pp. 71
-
-
Olsen, H.G.1
Vage, D.I.2
Lien, S.3
Klungland, H.4
-
83
-
-
0030074569
-
Microsatellite mapping of the bovine roan locus, a major determinant of White Heifer disease
-
Charlier, C., Denys, B., Belanche, J.I., Coppieters, W., Grobet, L., Mni, M., Womack, J., Hanset, R., Georges, M. Microsatellite mapping of the bovine roan locus, a major determinant of White Heifer disease. Mamm. Genome 1996, 7: 138-142.
-
(1996)
Mamm. Genome
, vol.7
, pp. 138-142
-
-
Charlier, C.1
Denys, B.2
Belanche, J.I.3
Coppieters, W.4
Grobet, L.5
Mni, M.6
Womack, J.7
Hanset, R.8
Georges, M.9
-
84
-
-
0032863308
-
A missense mutation in the bovine MGF gene is associated with the roan phenotype in Belgian Blue and Shorthorn cattle
-
Seitz, J.J., Schmutz, S.M., Thue, T.D., Buchanan, F.C. A missense mutation in the bovine MGF gene is associated with the roan phenotype in Belgian Blue and Shorthorn cattle. Mamm. Genome 1999, 10: 710-712.
-
(1999)
Mamm. Genome
, vol.10
, pp. 710-712
-
-
Seitz, J.J.1
Schmutz, S.M.2
Thue, T.D.3
Buchanan, F.C.4
-
85
-
-
0032928739
-
The "spotted" locus maps to bovine chromosome 6 in a Hereford-Cross population
-
Grosz, M.D., MacNeil, M.D. The "spotted" locus maps to bovine chromosome 6 in a Hereford-Cross population. J. Hered. 1999, 90: 233-236.
-
(1999)
J. Hered.
, vol.90
, pp. 233-236
-
-
Grosz, M.D.1
MacNeil, M.D.2
-
86
-
-
0029970420
-
The polled locus maps to BTA1 in a Bos indicus x Bos taurus cross
-
Brenneman, R.A., Davis, S.K., Sanders, J.O., Burns, B.M., Wheeler, T.C., Turner, J.W., Taylor, J.F. The polled locus maps to BTA1 in a Bos indicus x Bos taurus cross. J. Hered. 1996, 87: 156-161.
-
(1996)
J. Hered.
, vol.87
, pp. 156-161
-
-
Brenneman, R.A.1
Davis, S.K.2
Sanders, J.O.3
Burns, B.M.4
Wheeler, T.C.5
Turner, J.W.6
Taylor, J.F.7
-
87
-
-
0348198490
-
A comparison of production traits and welfare implications between horned and polled beef bulls
-
Stookey, J.M., Goonewardene, L.A. A comparison of production traits and welfare implications between horned and polled beef bulls. Can. J. Anim. Sci. 1996, 76: 1-5.
-
(1996)
Can. J. Anim. Sci.
, vol.76
, pp. 1-5
-
-
Stookey, J.M.1
Goonewardene, L.A.2
-
88
-
-
0029381884
-
DNA marker-assisted selection of the polled condition in Charolais cattle
-
Schmutz, S.M., Marquess, F.L., Berryere, T.G., Moker. J.S. DNA marker-assisted selection of the polled condition in Charolais cattle. Mamm. Genome 1995, 6: 710-713.
-
(1995)
Mamm. Genome
, vol.6
, pp. 710-713
-
-
Schmutz, S.M.1
Marquess, F.L.2
Berryere, T.G.3
Moker, J.S.4
-
89
-
-
0031109650
-
New markers on bovine chromosome 1 are closely linked to the polled gene in Simmental and Pinzgauer cattle
-
Harlizius, B., Tammen, I., Eichler, K., Eggen, A., Hetzel, D.J. New markers on bovine chromosome 1 are closely linked to the polled gene in Simmental and Pinzgauer cattle. Mamm. Genome 1997, 8: 255-257.
-
(1997)
Mamm. Genome
, vol.8
, pp. 255-257
-
-
Harlizius, B.1
Tammen, I.2
Eichler, K.3
Eggen, A.4
Hetzel, D.J.5
-
90
-
-
0037638673
-
The A.I. dilemma
-
anonymous
-
anonymous. The A.I. dilemma. Holstein-Friesian World 1967, 64: 1394-1395.
-
(1967)
Holstein-Friesian World
, vol.64
, pp. 1394-1395
-
-
-
91
-
-
0038653053
-
Syndactyly in cattle
-
Leipold, H.W., Dennis, S.M., Huston, K. Syndactyly in cattle. Vet. Bulletin 1973, 43: 399-403.
-
(1973)
Vet. Bulletin
, vol.43
, pp. 399-403
-
-
Leipold, H.W.1
Dennis, S.M.2
Huston, K.3
-
92
-
-
0019159497
-
Progeny testing for bovine syndactyly
-
Johnson, J.L., Leipold, H.W., Snider, G.W., Baker, R.D. Progeny testing for bovine syndactyly. J. Am. Vet. Med. Assoc. 1980, 176: 549-550.
-
(1980)
J. Am. Vet. Med. Assoc.
, vol.176
, pp. 549-550
-
-
Johnson, J.L.1
Leipold, H.W.2
Snider, G.W.3
Baker, R.D.4
-
94
-
-
0029792636
-
Identity-by-descent mapping of recessive traits in livestock, application to map the bovine syndactyly locus to chromosome 15
-
Charlier, C., Farnir, F., Berzi, P., Vanmanshoven, P., Brouwers, B., Vromans, H., Georges, M. Identity-by-descent mapping of recessive traits in livestock, application to map the bovine syndactyly locus to chromosome 15. Genome Res. 1996, 6: 580-589.
-
(1996)
Genome Res.
, vol.6
, pp. 580-589
-
-
Charlier, C.1
Farnir, F.2
Berzi, P.3
Vanmanshoven, P.4
Brouwers, B.5
Vromans, H.6
Georges, M.7
-
95
-
-
0027398362
-
Microsatellite mapping of the gene causing weaver disease in cattle will allow the study of an associated quantitative trait locus
-
Georges, M., Dietz, A.B., Mishra, A., Nielsen, D., Sargeant, L.S., Sorensen, A., Steele, M.R., Zhao, X., Leipold, H.W., Womack, J., Lathorp, M. Microsatellite mapping of the gene causing weaver disease in cattle will allow the study of an associated quantitative trait locus. Proc. Natl. Acad. Sci. USA 1993, 90: 1058-1062.
-
(1993)
Proc. Natl. Acad. Sci. USA
, vol.90
, pp. 1058-1062
-
-
Georges, M.1
Dietz, A.B.2
Mishra, A.3
Nielsen, D.4
Sargeant, L.S.5
Sorensen, A.6
Steele, M.R.7
Zhao, X.8
Leipold, H.W.9
Womack, J.10
Lathorp, M.11
-
96
-
-
0030215528
-
A high-density molecular genetic map around the weaver locus
-
Millonig, J.H., Millen, K.J., Hatten, M.E. A high-density molecular genetic map around the weaver locus. Mamm. Genome 1996, 7: 616-618.
-
(1996)
Mamm. Genome
, vol.7
, pp. 616-618
-
-
Millonig, J.H.1
Millen, K.J.2
Hatten, M.E.3
-
97
-
-
0018675836
-
Evidence for a new lethal gene causing cardiomyopathy in Japanese black calves
-
Watanabe, S., Akita, T., Itakura, C., Goto, M. Evidence for a new lethal gene causing cardiomyopathy in Japanese black calves. J. Hered. 1979, 70: 255-258.
-
(1979)
J. Hered.
, vol.70
, pp. 255-258
-
-
Watanabe, S.1
Akita, T.2
Itakura, C.3
Goto, M.4
-
98
-
-
0032110404
-
Evidence for autosomal recessive inheritance of a major gene for bovine dilated cardiomyopathy
-
Dolf, G., Stricker, C., Tontis, A., Martig, J., Gaillard, C. Evidence for autosomal recessive inheritance of a major gene for bovine dilated cardiomyopathy. J. Anim. Sci. 1998, 76: 1824-1829.
-
(1998)
J. Anim. Sci.
, vol.76
, pp. 1824-1829
-
-
Dolf, G.1
Stricker, C.2
Tontis, A.3
Martig, J.4
Gaillard, C.5
-
99
-
-
84964146634
-
Neuronal lipodystrophy. Occurrence in an inbred strain of cattle
-
Read, W.K., Bridges, C.H. Neuronal lipodystrophy. Occurrence in an inbred strain of cattle. Pathol. Vet. 1969, 6: 235-243.
-
(1969)
Pathol. Vet.
, vol.6
, pp. 235-243
-
-
Read, W.K.1
Bridges, C.H.2
-
100
-
-
0025983474
-
Bovine ceroid-lipofuscinosis (Batten's disease), the major component stored is the DCCD-reactive proteolipid, subunit C, of mitochondrial ATP synthase
-
Martinus. R.D., Harper, P.A., Jolly, R.D., Bayliss, S.L., Midwinter, G.G., Shaw, G.J., Palmer, D.N. Bovine ceroid-lipofuscinosis (Batten's disease), the major component stored is the DCCD-reactive proteolipid, subunit C, of mitochondrial ATP synthase. Vet. Res. Commun. 1991, 15: 85-94.
-
(1991)
Vet. Res. Commun.
, vol.15
, pp. 85-94
-
-
Martinus, R.D.1
Harper, P.A.2
Jolly, R.D.3
Bayliss, S.L.4
Midwinter, G.G.5
Shaw, G.J.6
Palmer, D.N.7
-
101
-
-
0038314095
-
The genetics of Dexter cattle
-
Curran, P.L. The genetics of Dexter cattle. The Ark. 1986, 13: 199-202.
-
(1986)
The Ark.
, vol.13
, pp. 199-202
-
-
Curran, P.L.1
-
102
-
-
0031612068
-
Patterns of ovarian growth and development in cattle with a growth hormone receptor deficiency
-
Chase, C.C., Kirby, C.J., Hammond, A.C., Olson, T.A., Lucy, M.C. Patterns of ovarian growth and development in cattle with a growth hormone receptor deficiency. J. Anim. Sci. 1998, 76: 212-219.
-
(1998)
J. Anim. Sci.
, vol.76
, pp. 212-219
-
-
Chase, C.C.1
Kirby, C.J.2
Hammond, A.C.3
Olson, T.A.4
Lucy, M.C.5
-
103
-
-
0015807464
-
Beta-galactosidase deficiency in GM1 gangliosidosis of Friesian calves
-
Donnelly, W.J.C., Sheahan, B.J., Kelly, M. Beta-galactosidase deficiency in GM1 gangliosidosis of Friesian calves. Res. Vet. Sci. 1973, 15: 139-141.
-
(1973)
Res. Vet. Sci.
, vol.15
, pp. 139-141
-
-
Donnelly, W.J.C.1
Sheahan, B.J.2
Kelly, M.3
-
104
-
-
0038314096
-
Bovine GM1 gangliosidosis, an inborn lysosomal disease
-
Donnelly, W.J.C., Sheahan, B.J. Bovine GM1 gangliosidosis, an inborn lysosomal disease. Vet. Sci. Comm. 1977, 1: 65-74.
-
(1977)
Vet. Sci. Comm.
, vol.1
, pp. 65-74
-
-
Donnelly, W.J.C.1
Sheahan, B.J.2
-
105
-
-
0037638672
-
An inherited defect in Friesian calves
-
McPherson, E.A., Beattie, I.S., Young, G.B. An inherited defect in Friesian calves. Nordisk Veterinaermedicin 1964, 16: 533-540.
-
(1964)
Nordisk Veterinaermedicin
, vol.16
, pp. 533-540
-
-
McPherson, E.A.1
Beattie, I.S.2
Young, G.B.3
-
106
-
-
0030113674
-
Bovine hereditary zinc deficiency, lethal trait A 46
-
Machen, M., Montgomery, T., Holland, R., Braselton, E., Dunstan, R., Brewer, G., Yuzbasiyan-Gurkan, V. Bovine hereditary zinc deficiency, lethal trait A 46. J. Vet. Diagn. Invest. 1996, 8: 219-227.
-
(1996)
J. Vet. Diagn. Invest.
, vol.8
, pp. 219-227
-
-
Machen, M.1
Montgomery, T.2
Holland, R.3
Braselton, E.4
Dunstan, R.5
Brewer, G.6
Yuzbasiyan-Gurkan, V.7
-
107
-
-
0038314060
-
A suggested control gene mechanism for the excessive production of types I and III porphyrins in congenital erythropoietic porphyria
-
Watson, C.J., Runge, W., Taddeini, L., Bossenmaier, I., Cardinal, R. A suggested control gene mechanism for the excessive production of types I and III porphyrins in congenital erythropoietic porphyria. Proc. Natl. Acad. Sci. USA 1964, 52: 478-485.
-
(1964)
Proc. Natl. Acad. Sci. USA
, vol.52
, pp. 478-485
-
-
Watson, C.J.1
Runge, W.2
Taddeini, L.3
Bossenmaier, I.4
Cardinal, R.5
-
108
-
-
0025239016
-
The lack of protamine 2 (P2) in boar and bull spermatozoa is due to mutations within the P2 gene
-
Maier, W.M., Nussbaum, G., Domenjoud, L., Klemm, U., Engel, W. The lack of protamine 2 (P2) in boar and bull spermatozoa is due to mutations within the P2 gene. Nucl. Acids Res. 1990, 18: 1249-1254.
-
(1990)
Nucl. Acids Res.
, vol.18
, pp. 1249-1254
-
-
Maier, W.M.1
Nussbaum, G.2
Domenjoud, L.3
Klemm, U.4
Engel, W.5
-
109
-
-
84984002370
-
Spinal muscular atrophy in Brown Swiss calves
-
el-Hamidi, M., Leipold, H.W., Vestweber, J.G., Saperstein, G. Spinal muscular atrophy in Brown Swiss calves. Zentralbl. Veterinarmed. A 1989, 36: 731-738.
-
(1989)
Zentralbl. Veterinarmed. A
, vol.36
, pp. 731-738
-
-
el-Hamidi, M.1
Leipold, H.W.2
Vestweber, J.G.3
Saperstein, G.4
-
110
-
-
0019875536
-
Testicular feminisation in a Ayrshire cow
-
Long, S.E., David, J.S.E. Testicular feminisation in a Ayrshire cow. Vet. Rec. 1981, 109: 116-118.
-
(1981)
Vet. Rec.
, vol.109
, pp. 116-118
-
-
Long, S.E.1
David, J.S.E.2
-
111
-
-
21144480386
-
Male Pseudohermaphroditism of the Testicular Feminization Type in a Heifer
-
Peter, A.T., Scheidt, A., Campell, J., Hahn, K. Male Pseudohermaphroditism of the Testicular Feminization Type in a Heifer. Can. Vet. J. 1993, 34: 304-305.
-
(1993)
Can. Vet. J.
, vol.34
, pp. 304-305
-
-
Peter, A.T.1
Scheidt, A.2
Campell, J.3
Hahn, K.4
-
112
-
-
0000221991
-
Inheritance of coat colour in swine
-
Spillmann, W.J. Inheritance of coat colour in swine. Science Sci. 1906, 24: 441-443.
-
(1906)
Science Sci.
, vol.24
, pp. 441-443
-
-
Spillmann, W.J.1
-
113
-
-
0027083269
-
The gene for dominant white color in the pig is closely linked to ALB and PDGRFRA on chromosome 8
-
Johansson, M., Ellegren, H., Marklund, L., Gustavsson, U., Ringmar-Cederberg, E., Andersson, K., Edfors-Lilja, I., Andersson, L. The gene for dominant white color in the pig is closely linked to ALB and PDGRFRA on chromosome 8. Genomics 1992, 14: 965-969.
-
(1992)
Genomics
, vol.14
, pp. 965-969
-
-
Johansson, M.1
Ellegren, H.2
Marklund, L.3
Gustavsson, U.4
Ringmar-Cederberg, E.5
Andersson, K.6
Edfors-Lilja, I.7
Andersson, L.8
-
114
-
-
0030281363
-
Pigs with the dominant white coat color phenotype carry a duplication of the KIT gene encoding the mast/stem cell growth factor receptor
-
Moller, M.J., Chaudhary, R., Hellmen, E., Hoyheim. B., Chowdhary, B., Andersson, L. Pigs with the dominant white coat color phenotype carry a duplication of the KIT gene encoding the mast/stem cell growth factor receptor. Mamm. Genome 1996, 7: 822-830.
-
(1996)
Mamm. Genome
, vol.7
, pp. 822-830
-
-
Moller, M.J.1
Chaudhary, R.2
Hellmen, E.3
Hoyheim, B.4
Chowdhary, B.5
Andersson, L.6
-
115
-
-
0031668527
-
Molecular basis for the dominant white phenotype in the domestic pig
-
Marklund, S., Kijas, J., Rodriguez-Martinez, H., Ronnstrand, L., Funa, K.., Moller, M., Lange, D., Edfors-Lilja, I., Andersson, L. Molecular basis for the dominant white phenotype in the domestic pig. Genome Res. 1998, 8: 826-833.
-
(1998)
Genome Res.
, vol.8
, pp. 826-833
-
-
Marklund, S.1
Kijas, J.2
Rodriguez-Martinez, H.3
Ronnstrand, L.4
Funa, K.5
Moller, M.6
Lange, D.7
Edfors-Lilja, I.8
Andersson, L.9
-
116
-
-
0038653054
-
Comparative positional cloning, KIT as a candidate gene for the Hereford coat colour phenotype
-
Grosz, M.D., Fahrenkrug, S., Macneil, M.D. Comparative positional cloning, KIT as a candidate gene for the Hereford coat colour phenotype. Archiv für Tierzucht - Arch. Anim. Breed. 1999, 42: 160-162.
-
(1999)
Archiv für Tierzucht - Arch. Anim. Breed.
, vol.42
, pp. 160-162
-
-
Grosz, M.D.1
Fahrenkrug, S.2
Macneil, M.D.3
-
117
-
-
0033212795
-
A single nucleotide polymorphism in the bovine kit oncogene (Hardy-Zuckerman 4 feline sarcoma viral (v-kit) oncogene homolog)
-
Grosz, M.D., Stone, R.T. A single nucleotide polymorphism in the bovine kit oncogene (Hardy-Zuckerman 4 feline sarcoma viral (v-kit) oncogene homolog). Anim. Genet. 1999, 30: 394.
-
(1999)
Anim. Genet.
, vol.30
, pp. 394
-
-
Grosz, M.D.1
Stone, R.T.2
-
118
-
-
0032735314
-
A QTL for the degree of spotting in cattle shows synteny with the KIT locus on chromosome 6
-
Reinsch, N., Thomsen, H., Xu, N., Brink, M., Looft, C., Kalm, E., Brockmann, G.A., Grupe, S., Kuhn, C., Schwerin, M., Leyhe, B., Hiendleder, S., Erhardt, G., Medjugorac, I., Russ, I., Förster, M., Reents, R., Averdunk, G. A QTL for the degree of spotting in cattle shows synteny with the KIT locus on chromosome 6. J. Hered. 1999, 90: 629-634.
-
(1999)
J. Hered.
, vol.90
, pp. 629-634
-
-
Reinsch, N.1
Thomsen, H.2
Xu, N.3
Brink, M.4
Looft, C.5
Kalm, E.6
Brockmann, G.A.7
Grupe, S.8
Kuhn, C.9
Schwerin, M.10
Leyhe, B.11
Hiendleder, S.12
Erhardt, G.13
Medjugorac, I.14
Russ, I.15
Förster, M.16
Reents, R.17
Averdunk, G.18
-
119
-
-
0032513567
-
Identification of a mutation in the low density lipoprotein receptor gene associated with recessive familial hypercholesterolemia in swine
-
Hasler-Rapacz, J., Ellegren, H., Fridolfsson, A.K., Kirkpatrick, B., Kirk, S., Andersson, L., Rapacz, J. Identification of a mutation in the low density lipoprotein receptor gene associated with recessive familial hypercholesterolemia in swine. Am. J. Med. Genet. 1998, 76: 379-386.
-
(1998)
Am. J. Med. Genet.
, vol.76
, pp. 379-386
-
-
Hasler-Rapacz, J.1
Ellegren, H.2
Fridolfsson, A.K.3
Kirkpatrick, B.4
Kirk, S.5
Andersson, L.6
Rapacz, J.7
-
120
-
-
0026319058
-
Identification of a mutation in porcine ryanodine receptor associated with malignant hyperthermia
-
Fujii, J., Otsu, K., Zorzato, F., de Leon, S., Khanna, V.K., Weiler, J.E., O'Brien, P.J., MacLennan, D.H. Identification of a mutation in porcine ryanodine receptor associated with malignant hyperthermia. Science 1991, 253: 448-451.
-
(1991)
Science
, vol.253
, pp. 448-451
-
-
Fujii, J.1
Otsu, K.2
Zorzato, F.3
de Leon, S.4
Khanna, V.K.5
Weiler, J.E.6
O'Brien, P.J.7
MacLennan, D.H.8
-
121
-
-
0025354344
-
Evidence for a new major gene influencing meat quality in pigs
-
Le Roy, P., Naveau, J., Elsen, J.M., Sellier, P. Evidence for a new major gene influencing meat quality in pigs. Genet. Res. 1990, 55: 33-40.
-
(1990)
Genet. Res.
, vol.55
, pp. 33-40
-
-
Le Roy, P.1
Naveau, J.2
Elsen, J.M.3
Sellier, P.4
-
122
-
-
0029678479
-
Accurate mapping of the "acid meat" RN gene on genetic and physical maps of pig chromosome 15
-
Milan, D., Woloszyn, N., Yerle, M., Le Roy, P., Bonnet, M., Riquet, J., Lahbib-Mansais, Y., Caritez, J.C., Robic, A., Sellier, P., Elsen, J.M., Gellin, J. Accurate mapping of the "acid meat" RN gene on genetic and physical maps of pig chromosome 15. Mamm. Genome 1996, 7: 47-51.
-
(1996)
Mamm. Genome
, vol.7
, pp. 47-51
-
-
Milan, D.1
Woloszyn, N.2
Yerle, M.3
Le Roy, P.4
Bonnet, M.5
Riquet, J.6
Lahbib-Mansais, Y.7
Caritez, J.C.8
Robic, A.9
Sellier, P.10
Elsen, J.M.11
Gellin, J.12
-
123
-
-
85005626128
-
Recessive mode of inheritance in progressive ataxia and incoordination in Yorkshire pigs
-
Rimaila-Parnanen, E. Recessive mode of inheritance in progressive ataxia and incoordination in Yorkshire pigs. Hereditas 1982, 97: 305-306.
-
(1982)
Hereditas
, vol.97
, pp. 305-306
-
-
Rimaila-Parnanen, E.1
-
124
-
-
0032887583
-
Congenital progressive ataxia and spastic paresis, a hereditary disease in swine, maps to Chromosome 3 by linkage analysis
-
Kratzsch, A., Stricker, C., Gmur, C., Rieder, S., Jorg, H., Ossent, P., Burgi, E., Zimmermann, W., Stranzinger, G. Congenital progressive ataxia and spastic paresis, a hereditary disease in swine, maps to Chromosome 3 by linkage analysis. Mamm. Genome 1999, 10: 1036-1038.
-
(1999)
Mamm. Genome
, vol.10
, pp. 1036-1038
-
-
Kratzsch, A.1
Stricker, C.2
Gmur, C.3
Rieder, S.4
Jorg, H.5
Ossent, P.6
Burgi, E.7
Zimmermann, W.8
Stranzinger, G.9
-
125
-
-
0029347206
-
The porcine intestinal receptor for Escherichia coli K88ab, K88ac, regional localization on chromosome 13 and influence of IgG response to the K88 antigen
-
Edfors-Lilja, I., Gustafsson, U., Duval-Iflah, Y., Ellergren, H., Johansson, M., Juneja, R.K., Marklund, L., Andersson, L. The porcine intestinal receptor for Escherichia coli K88ab, K88ac, regional localization on chromosome 13 and influence of IgG response to the K88 antigen. Anim. Genet. 1995, 26: 237-242.
-
(1995)
Anim. Genet.
, vol.26
, pp. 237-242
-
-
Edfors-Lilja, I.1
Gustafsson, U.2
Duval-Iflah, Y.3
Ellergren, H.4
Johansson, M.5
Juneja, R.K.6
Marklund, L.7
Andersson, L.8
-
126
-
-
0037638670
-
A positional cloning study to identify the gene causing the 'Campus syndrome', a hereditary high frequency tremor in pigs
-
Tammen, I., Harlizius, B. A positional cloning study to identify the gene causing the 'Campus syndrome', a hereditary high frequency tremor in pigs. Anim. Genet. 1996, 27: 83.
-
(1996)
Anim. Genet.
, vol.27
, pp. 83
-
-
Tammen, I.1
Harlizius, B.2
-
127
-
-
0022295532
-
Arthrogryposis and associated defects in pigs, indication of simple recessive inheritance
-
Lomo, O.M. Arthrogryposis and associated defects in pigs, indication of simple recessive inheritance. Acta Vet. Scand. 1985, 26: 419-422.
-
(1985)
Acta Vet. Scand.
, vol.26
, pp. 419-422
-
-
Lomo, O.M.1
-
128
-
-
9444295985
-
The extension coat color locus and the loci for blood group O and tyrosine aminotransferase are on pig chromosome 6
-
Mariani, P., Moller, M.J., Hoyheim, B., Marklund, L., Davies, W., Ellegren, H., Andersson, L. The extension coat color locus and the loci for blood group O and tyrosine aminotransferase are on pig chromosome 6. J. Hered. 1996, 87: 272-276.
-
(1996)
J. Hered.
, vol.87
, pp. 272-276
-
-
Mariani, P.1
Moller, M.J.2
Hoyheim, B.3
Marklund, L.4
Davies, W.5
Ellegren, H.6
Andersson, L.7
-
129
-
-
0021309509
-
Hereditary dwarfism in pigs
-
Jensen, P.T., Nielsen, D.H., Jensen, P., Bille, N. Hereditary dwarfism in pigs. Nord. Vet. Med. 1984, 36: 32-37.
-
(1984)
Nord. Vet. Med.
, vol.36
, pp. 32-37
-
-
Jensen, P.T.1
Nielsen, D.H.2
Jensen, P.3
Bille, N.4
-
130
-
-
0018120341
-
Clinical and biochemical abnormalities in porcine GM2-gangliosidosis
-
Kosanke, S.D Pierce, K.R., Bay, W.W. Clinical and biochemical abnormalities in porcine GM2-gangliosidosis. Vet. Pathol. 1978, 15: 685-699.
-
(1978)
Vet. Pathol.
, vol.15
, pp. 685-699
-
-
Kosanke, S.D.1
Pierce, K.R.2
Bay, W.W.3
-
131
-
-
0029909770
-
The cDNA and derived amino acid sequence of porcine factor VIII
-
Healey, J., Lubin, I., Lollar, P. The cDNA and derived amino acid sequence of porcine factor VIII. Blood 1996, 88: 4209-4214.
-
(1996)
Blood
, vol.88
, pp. 4209-4214
-
-
Healey, J.1
Lubin, I.2
Lollar, P.3
-
132
-
-
0029907935
-
In vivo studies of activated porcine factor VIII
-
Littlewood, J.D., Bevan, S.A., Kemball-Cook, G., Barrowcliffe, T.W. In vivo studies of activated porcine factor VIII. Thromb. Haemost. 1996, 76: 43-748.
-
(1996)
Thromb. Haemost.
, vol.76
, pp. 43-748
-
-
Littlewood, J.D.1
Bevan, S.A.2
Kemball-Cook, G.3
Barrowcliffe, T.W.4
-
133
-
-
0036207147
-
Porcine factor VIII, current status and future developments
-
Hay, C.R. Porcine factor VIII, current status and future developments. Haemophilia 2002, 8: 24-27.
-
(2002)
Haemophilia
, vol.8
, pp. 24-27
-
-
Hay, C.R.1
-
134
-
-
0037976620
-
The inheritance of paralysed hind legs, scrotal hernia and atresia ani in pigs
-
Berge, S. The inheritance of paralysed hind legs, scrotal hernia and atresia ani in pigs. J. Hered. 1941, 32: 271-274.
-
(1941)
J. Hered.
, vol.32
, pp. 271-274
-
-
Berge, S.1
-
136
-
-
0010835492
-
The inheritance of hairlessness in swine
-
Roberts, E., Carroll, E. The inheritance of hairlessness in swine. J. Hered. 1931, 22: 125-132.
-
(1931)
J. Hered.
, vol.22
, pp. 125-132
-
-
Roberts, E.1
Carroll, E.2
-
137
-
-
0038314081
-
"Legless", a new lethal in swine
-
Johnson, D.H., Lush, J.L. "Legless", a new lethal in swine. Genetics 1939, 24: 79.
-
(1939)
Genetics
, vol.24
, pp. 79
-
-
Johnson, D.H.1
Lush, J.L.2
-
138
-
-
2742598826
-
The genetics of hereditary lymphosarcoma of pigs
-
McTaggart, H.S., Laing, A.H., Head, K.W., Brownlie, S.E. The genetics of hereditary lymphosarcoma of pigs. Vet. Rec. 1979, 105: 36.
-
(1979)
Vet. Rec.
, vol.105
, pp. 36
-
-
McTaggart, H.S.1
Laing, A.H.2
Head, K.W.3
Brownlie, S.E.4
-
139
-
-
0029633133
-
Porcine membranoproliferative glomerulonephritis type II, an autosomal recessive deficiency of factor H
-
Jansen, J.H., Hogasen, K., Grondahl, A.M. Porcine membranoproliferative glomerulonephritis type II, an autosomal recessive deficiency of factor H. Vet. Rec. 1995, 137: 240-244.
-
(1995)
Vet. Rec.
, vol.137
, pp. 240-244
-
-
Jansen, J.H.1
Hogasen, K.2
Grondahl, A.M.3
-
140
-
-
0026731355
-
Nucleoside transport-deficient mutants of PK-15 pig kidney cell line
-
1110
-
Aran, J.M., Plagemann, P.G. Nucleoside transport-deficient mutants of PK-15 pig kidney cell line. Biochim. Biophys. Acta 1992, 1110: 51-58.
-
(1992)
Biochim. Biophys. Acta
, pp. 51-58
-
-
Aran, J.M.1
Plagemann, P.G.2
-
141
-
-
0010638031
-
Congenital porphyria in swine and cattle in Denmark
-
Jorgensen, S.K., With, T.K. Congenital porphyria in swine and cattle in Denmark. Nature 1955, 176: 156-158.
-
(1955)
Nature
, vol.176
, pp. 156-158
-
-
Jorgensen, S.K.1
With, T.K.2
-
142
-
-
0010629870
-
Congenital porphyria in pigs
-
Clare, T., Stephens, E.H. Congenital porphyria in pigs. Nature 1944, 153: 252-253.
-
(1944)
Nature
, vol.153
, pp. 252-253
-
-
Clare, T.1
Stephens, E.H.2
-
143
-
-
0037976619
-
Pietrain creeper syndrome, a primary myopathy of the pig?
-
Wells, G.A.H., Bradley, R. Pietrain creeper syndrome, a primary myopathy of the pig? Neuropathol. Appl. Neurobiol. 1978, 4: 237-238.
-
(1978)
Neuropathol. Appl. Neurobiol.
, vol.4
, pp. 237-238
-
-
Wells, G.A.H.1
Bradley, R.2
-
144
-
-
0014232702
-
An inherited disorder of calcium metabolism in the pig (hereditary rickets)
-
Meyer, H., Plonait, H. [An inherited disorder of calcium metabolism in the pig (hereditary rickets)]. Zentralbl. Veterinarmed. A 1968, 15: 481-493.
-
(1968)
Zentralbl. Veterinarmed. A
, vol.15
, pp. 481-493
-
-
Meyer, H.1
Plonait, H.2
-
145
-
-
0019330984
-
Inherited renal cysts in pigs, results of breeding experiments
-
Wijeratne, W.V., Wells, G.A. Inherited renal cysts in pigs, results of breeding experiments. Vet. Rec. 1980, 107: 484-488.
-
(1980)
Vet. Rec.
, vol.107
, pp. 484-488
-
-
Wijeratne, W.V.1
Wells, G.A.2
-
146
-
-
0027270009
-
Inheritance of resistance to oedema disease in the pig, experiments with an Escherichia coli strain expressing fimbriae 107
-
Bertschinger, H.U., Stamm, M., Vögeli, P. Inheritance of resistance to oedema disease in the pig, experiments with an Escherichia coli strain expressing fimbriae 107. Vet. Microbiol. 1993, 35: 79-89.
-
(1993)
Vet. Microbiol.
, vol.35
, pp. 79-89
-
-
Bertschinger, H.U.1
Stamm, M.2
Vögeli, P.3
-
147
-
-
0030266225
-
Genes specifying receptors for F18 fimbriated Escherichia coli, causing oedema disease and postweaning diarrhoea in pigs, map to chromosome 6
-
Vögeli, P., Bertschinger, H.U., Stamm, M., Stricker, C., Hagger, C., Fries, R., Rapacz, J., Stranzinger, G. Genes specifying receptors for F18 fimbriated Escherichia coli, causing oedema disease and postweaning diarrhoea in pigs, map to chromosome 6. Anim. Genet. 1996, 27: 321-328.
-
(1996)
Anim. Genet.
, vol.27
, pp. 321-328
-
-
Vögeli, P.1
Bertschinger, H.U.2
Stamm, M.3
Stricker, C.4
Hagger, C.5
Fries, R.6
Rapacz, J.7
Stranzinger, G.8
-
148
-
-
0028519145
-
Genetic analysis of 38XX males with genital ambiguities and true hermaphrodites in pigs
-
Pailhoux, E., Popescu, P.C., Parma, P., Boscher, J., Legault, C., Molteni, L., Fellous, M., Cotinot, C. Genetic analysis of 38XX males with genital ambiguities and true hermaphrodites in pigs. Anim. Genet. 1994, 25: 299-305.
-
(1994)
Anim. Genet.
, vol.25
, pp. 299-305
-
-
Pailhoux, E.1
Popescu, P.C.2
Parma, P.3
Boscher, J.4
Legault, C.5
Molteni, L.6
Fellous, M.7
Cotinot, C.8
-
149
-
-
0015453561
-
Lipid deficiency in the central nervous system of Landrace piglets affected with congenital tremor A3. A form of cerebrospinal hypomyelinogenesis
-
Patterson, D.S., Sweasey, D., Harding, J.D. Lipid deficiency in the central nervous system of Landrace piglets affected with congenital tremor A3. A form of cerebrospinal hypomyelinogenesis. J. Neurochem. 1972, 19: 2791-2799.
-
(1972)
J. Neurochem.
, vol.19
, pp. 2791-2799
-
-
Patterson, D.S.1
Sweasey, D.2
Harding, J.D.3
-
150
-
-
0030255096
-
The role of proteolipid proteins in the development of congenital tremors type AIII, a review
-
Baumgartner, B.G., Brenig, B. The role of proteolipid proteins in the development of congenital tremors type AIII, a review. Dtsch. Tierarztl. Wochenschr. 1996, 103: 404-407.
-
(1996)
Dtsch. Tierarztl. Wochenschr.
, vol.103
, pp. 404-407
-
-
Baumgartner, B.G.1
Brenig, B.2
-
151
-
-
0008951845
-
A hemophilia-like disease in swine
-
Hogan, A.G., Muehrer, M.E., Bogart, R. A hemophilia-like disease in swine. Proc. Soc. Exp. Biol. Med. 1941, 48: 217.
-
(1941)
Proc. Soc. Exp. Biol. Med.
, vol.48
, pp. 217
-
-
Hogan, A.G.1
Muehrer, M.E.2
Bogart, R.3
-
152
-
-
0023806920
-
Molecular genetic analysis of porcine von Willebrand disease, tight linkage to the von Willebrand factor locus
-
Bahou, W.F., Bowie, E.J., Fass, D.N., Ginsburg, D. Molecular genetic analysis of porcine von Willebrand disease, tight linkage to the von Willebrand factor locus. Blood 1988, 72: 308-313.
-
(1988)
Blood
, vol.72
, pp. 308-313
-
-
Bahou, W.F.1
Bowie, E.J.2
Fass, D.N.3
Ginsburg, D.4
-
153
-
-
0026553792
-
Porcine von Willebrand disease and atherosclerosis. Influence of polymorphism in apolipoprotein B100 genotype
-
Nichols, T.C., Bellinger, D.A., Davis, K.E., Koch, G.G., Reddick, R.L., Read, M.S., Rapacz, J., Hasler-Rapacz, J. Porcine von Willebrand disease and atherosclerosis. Influence of polymorphism in apolipoprotein B100 genotype. Am. J. Pathol. 1992, 140: 403-415.
-
(1992)
Am. J. Pathol.
, vol.140
, pp. 403-415
-
-
Nichols, T.C.1
Bellinger, D.A.2
Davis, K.E.3
Koch, G.G.4
Reddick, R.L.5
Read, M.S.6
Rapacz, J.7
Hasler-Rapacz, J.8
-
154
-
-
0029844837
-
FISH mapping of the porcine vWF gene to chromosome 5q21 extends synteny homology with human chromosome 12
-
Sjoberg, A., Seaman, W.T., Bellinger, D.A., Griggs, T.R., Nichols, T.C., Chowdhary, B. FISH mapping of the porcine vWF gene to chromosome 5q21 extends synteny homology with human chromosome 12. Hereditas 1996, 124: 199-202.
-
(1996)
Hereditas
, vol.124
, pp. 199-202
-
-
Sjoberg, A.1
Seaman, W.T.2
Bellinger, D.A.3
Griggs, T.R.4
Nichols, T.C.5
Chowdhary, B.6
-
155
-
-
0010905451
-
Woolly hair in swine
-
Rhoad, A.O. Woolly hair in swine. J. Hered. 1934, 25: 371-375.
-
(1934)
J. Hered.
, vol.25
, pp. 371-375
-
-
Rhoad, A.O.1
-
156
-
-
0031846129
-
Ovine neuronal ceroid lipofuscinosis, a large animal model syntenic with the human neuronal ceroid lipofuscinosis variant CLN6
-
Broom, M.F., Zhou, C., Broom, J.E., Barwell, K.J., Jolly, R.D., Hill, D.F. Ovine neuronal ceroid lipofuscinosis, a large animal model syntenic with the human neuronal ceroid lipofuscinosis variant CLN6. J. Med. Genet. 1998, 35: 717-721.
-
(1998)
J. Med. Genet.
, vol.35
, pp. 717-721
-
-
Broom, M.F.1
Zhou, C.2
Broom, J.E.3
Barwell, K.J.4
Jolly, R.D.5
Hill, D.F.6
-
157
-
-
0032812173
-
Splicing variants in sheep CLN3, the gene underlying juvenile neuronal ceroid lipofuscinosis
-
Oswald, M.J., Palmer, D.N., Damak, S. Splicing variants in sheep CLN3, the gene underlying juvenile neuronal ceroid lipofuscinosis. Mol. Genet. Metab. 1999, 67: 169-175.
-
(1999)
Mol. Genet. Metab.
, vol.67
, pp. 169-175
-
-
Oswald, M.J.1
Palmer, D.N.2
Damak, S.3
-
158
-
-
4243785350
-
Identification of the causative mutation in ovine hereditary chondroplasia
-
Beever, J.E., Shay, T.L., Albretson, J., Maciulis, A., Bunch, T.D., Holyoak, G.R., Cockett, N.E. Identification of the causative mutation in ovine hereditary chondroplasia. Plant Anim. Genome 1998, V1, W21.
-
(1998)
Plant Anim. Genome
, vol.6
-
-
Beever, J.E.1
Shay, T.L.2
Albretson, J.3
Maciulis, A.4
Bunch, T.D.5
Holyoak, G.R.6
Cockett, N.E.7
-
159
-
-
0012571197
-
Molecular Biology, Therapeutic Trials and Animal Models of Lysosomal Storage Disease - Type II Glycogenesis as an Example
-
Reuser, A.J.J. Molecular Biology, Therapeutic Trials and Animal Models of Lysosomal Storage Disease - Type II Glycogenesis as an Example. Annales de Biologie Clinique. 1993, 51: 218-219.
-
(1993)
Annales de Biologie Clinique
, vol.51
, pp. 218-219
-
-
Reuser, A.J.J.1
-
160
-
-
0002894305
-
The single gene inheritance of the prolificacy of the Booroola Merino
-
Land R, Robinson D (eds.), (Butterworths, London)
-
Piper, L., Bindon, B., Davis, G. The single gene inheritance of the prolificacy of the Booroola Merino, in Land R, Robinson D (eds.), The Genetics of Reproduction in Sheep, (Butterworths, London) 1984 pp, 115-125.
-
(1984)
The Genetics of Reproduction in Sheep
, pp. 115-125
-
-
Piper, L.1
Bindon, B.2
Davis, G.3
-
161
-
-
0027198581
-
The ovine Booroola fecundity gene (FecB) is linked to markers from a region of human chromosome 4q
-
Montgomery, G.W., Crawford, A.M., Penty, J.M., Dodds, K.G., Ede, A.J., Henry, H.M., Pierson, C.A., Lord, E.A. The ovine Booroola fecundity gene (FecB) is linked to markers from a region of human chromosome 4q. Nat. Genet. 1993, 4: 410-414.
-
(1993)
Nat. Genet.
, vol.4
, pp. 410-414
-
-
Montgomery, G.W.1
Crawford, A.M.2
Penty, J.M.3
Dodds, K.G.4
Ede, A.J.5
Henry, H.M.6
Pierson, C.A.7
Lord, E.A.8
-
162
-
-
0028168691
-
The Booroola fecundity (FecB) gene maps to sheep chromosome 6
-
Montgomery, G.W., Lord, E.A., Penty, J.M., Dodds, K.G., Broad, T.E., Cambridge, L., Sunden, S.L., Stone, R. The Booroola fecundity (FecB) gene maps to sheep chromosome 6. Genomics 1994, 22: 148-153.
-
(1994)
Genomics
, vol.22
, pp. 148-153
-
-
Montgomery, G.W.1
Lord, E.A.2
Penty, J.M.3
Dodds, K.G.4
Broad, T.E.5
Cambridge, L.6
Sunden, S.L.7
Stone, R.8
-
163
-
-
0029962686
-
Mapping the Horns (Ho) locus in sheep, a further locus controlling horn development in domestic animals
-
Montgomery, G.W., Henry, H.M., Dodds, K.G., Beattie A.E., Wuliji, T., Crawford, A.M. Mapping the Horns (Ho) locus in sheep, a further locus controlling horn development in domestic animals. J. Hered. 1996, 87: 358-363.
-
(1996)
J. Hered.
, vol.87
, pp. 358-363
-
-
Montgomery, G.W.1
Henry, H.M.2
Dodds, K.G.3
Beattie, A.E.4
Wuliji, T.5
Crawford, A.M.6
-
164
-
-
0025273876
-
Two alleles of a neural protein gene linked to scrapie in sheep
-
Goldmann, W., Hunter, N., Foster, J.D., Salbaum, J.M., Beyreuther, K., Hope, J. Two alleles of a neural protein gene linked to scrapie in sheep. Proc. Natl. Acad. Sci. USA 1990, 87: 2476-2480.
-
(1990)
Proc. Natl. Acad. Sci. USA
, vol.87
, pp. 2476-2480
-
-
Goldmann, W.1
Hunter, N.2
Foster, J.D.3
Salbaum, J.M.4
Beyreuther, K.5
Hope, J.6
-
165
-
-
0026001588
-
Different scrapie-associated fibril proteins (PrP) are encoded by lines of sheep selected for different alleles of the Sip gene
-
Goldmann, W., Hunter, N., Benson, G., Foster, J.D., Hope, J.
-
(1991)
J. Gen. Virol.
, vol.72
, pp. 2411-2417
-
-
Goldmann, W.1
Hunter, N.2
Benson, G.3
Foster, J.D.4
Hope, J.5
-
166
-
-
0027108686
-
Natural scrapie in British sheep, breeds, ages and PrP gene polymorphisms
-
Hunter, N., Foster, J.D., Hope, J. Natural scrapie in British sheep, breeds, ages and PrP gene polymorphisms. Vet. Rec. 1992, 130: 389-392.
-
(1992)
Vet. Rec.
, vol.130
, pp. 389-392
-
-
Hunter, N.1
Foster, J.D.2
Hope, J.3
-
167
-
-
0028010396
-
The association of a codon 136 PrP gene variant with the occurrence of natural scrapie
-
Hunter, N., Goldmann, W., Smith, G., Hope, J. The association of a codon 136 PrP gene variant with the occurrence of natural scrapie. Arch. Virol. 1994, 137: 171-177.
-
(1994)
Arch. Virol.
, vol.137
, pp. 171-177
-
-
Hunter, N.1
Goldmann, W.2
Smith, G.3
Hope, J.4
-
168
-
-
0028928171
-
Identification of five allelic variants of the sheep PrP gene and their association with natural scrapie
-
Belt, P.B., Muileman, I.H., Schreuder, B.E., Bos-de Ruijter, J., Gielkens, A.L., Smits, M.A. Identification of five allelic variants of the sheep PrP gene and their association with natural scrapie. J. Gen. Virol, 1995, 76: 509-517.
-
(1995)
J. Gen. Virol.
, vol.76
, pp. 509-517
-
-
Belt, P.B.1
Muileman, I.H.2
Schreuder, B.E.3
Bos-de Ruijter, J.4
Gielkens, A.L.5
Smits, M.A.6
-
169
-
-
0029161777
-
Different allelic effects of the codons 136 and 171 of the prion protein gene in sheep with natural scrapie
-
Clouscard, C., Beaudry, P., Elsen, J.M., Milan, D., Dussaucy, M., Bounneau, C., Schelcher, F., Chatelain, J., Launay, J.M., Laplanche, J.L. Different allelic effects of the codons 136 and 171 of the prion protein gene in sheep with natural scrapie. J. Gen. Virol. 1995, 76: 2097-2101.
-
(1995)
J. Gen. Virol.
, vol.76
, pp. 2097-2101
-
-
Clouscard, C.1
Beaudry, P.2
Elsen, J.M.3
Milan, D.4
Dussaucy, M.5
Bounneau, C.6
Schelcher, F.7
Chatelain, J.8
Launay, J.M.9
Laplanche, J.L.10
-
170
-
-
0032490201
-
Guidance on the use of PrP genotyping as an aid to the control of clinical scrapie
-
Scrapie Information Group
-
Dawson, M., Hoinville, L.J., Hosie, B.D., Hunter, N. Guidance on the use of PrP genotyping as an aid to the control of clinical scrapie. Scrapie Information Group. Vet. Rec. 1998, 142: 623-625.
-
(1998)
Vet. Rec.
, vol.142
, pp. 623-625
-
-
Dawson, M.1
Hoinville, L.J.2
Hosie, B.D.3
Hunter, N.4
-
171
-
-
0038314082
-
An inherited arginase deficiency in sheep erthrocytes
-
Wright, P.C., Young, J.D., Mangan, J.L., Tucker, E.M. An inherited arginase deficiency in sheep erthrocytes. Journal of Agriculture Science 1977, 88: 765-767.
-
(1977)
Journal of Agriculture Science
, vol.88
, pp. 765-767
-
-
Wright, P.C.1
Young, J.D.2
Mangan, J.L.3
Tucker, E.M.4
-
172
-
-
84936324530
-
Heritable characters of the red blood cells of sheep
-
Evans, J.V., Phillipson, A.T. Heritable characters of the red blood cells of sheep. N. Z. Vet. J. 1958, 6: 12-14.
-
(1958)
N. Z. Vet. J.
, vol.6
, pp. 12-14
-
-
Evans, J.V.1
Phillipson, A.T.2
-
173
-
-
25044459174
-
Loci for blood polymorphism in sheep and goats, red cell blood groups and lymphocyte antigens
-
Presented in, COGNOSAG Workshop
-
Nguyen, T.C. Loci for blood polymorphism in sheep and goats, red cell blood groups and lymphocyte antigens. Presented in, COGNOSAG Workshop 1986, 53-56.
-
(1986)
, pp. 53-56
-
-
Nguyen, T.C.1
-
174
-
-
0038653085
-
Blood groups in sheep. III. The A, C, D and M systems
-
Rasmusen, B.A., Stormont, C., Suzuki, Y. Blood groups in sheep. III. The A, C, D and M systems. Genetics 1960, 45: 1595-1603.
-
(1960)
Genetics
, vol.45
, pp. 1595-1603
-
-
Rasmusen, B.A.1
Stormont, C.2
Suzuki, Y.3
-
175
-
-
0026480180
-
Sheep blood polymorphism and genetic divergence between French Rambouillet and Spanish Merino, role of genetic drift
-
Nguyen, T.C., Morera, L., Llanes, D., Leger, P. Sheep blood polymorphism and genetic divergence between French Rambouillet and Spanish Merino, role of genetic drift. Anim. Genet. 1992, 23: 325-332.
-
(1992)
Anim. Genet.
, vol.23
, pp. 325-332
-
-
Nguyen, T.C.1
Morera, L.2
Llanes, D.3
Leger, P.4
-
176
-
-
0037638619
-
Blood groups and evolutionary relationships among domestic sheep (Ovis aries), domestic goat (Capra hircus), aoudad (Ammotragus lervia) and european mouflon (Ovis musimon)
-
Nguyen, T.C., Bunch, T.D. Blood groups and evolutionary relationships among domestic sheep (Ovis aries), domestic goat (Capra hircus), aoudad (Ammotragus lervia) and european mouflon (Ovis musimon). Annales de Genetique et de Selection Animale 1980, 12: 169-180.
-
(1980)
Annales de Genetique et de Selection Animale
, vol.12
, pp. 169-180
-
-
Nguyen, T.C.1
Bunch, T.D.2
-
177
-
-
0038314084
-
Linkage between the C and I blood group loci in sheep
-
Rasmusen, B.A. Linkage between the C and I blood group loci in sheep. Genetics 1966, 54: 356.
-
(1966)
Genetics
, vol.54
, pp. 356
-
-
Rasmusen, B.A.1
-
178
-
-
0021807630
-
Evaluation of linkage between the R-O-i and C blood group systems in sheep
-
Nguyen, T.C. Evaluation of linkage between the R-O-i and C blood group systems in sheep. Anim. Blood Groups Biochem. Genet. 1985, 16: 13-17.
-
(1985)
Anim. Blood Groups Biochem. Genet.
, vol.16
, pp. 13-17
-
-
Nguyen, T.C.1
-
179
-
-
0038653086
-
Inheritance of R-O-I blood groups and alkaline phosphatase polymorphism in sheep
-
Rasmusen, B.A. Inheritance of R-O-I blood groups and alkaline phosphatase polymorphism in sheep. Genetics 1965, 51: 767-770.
-
(1965)
Genetics
, vol.51
, pp. 767-770
-
-
Rasmusen, B.A.1
-
180
-
-
0037976647
-
Blood groups in sheep. I. The X-Z system
-
Rasmusen, B.A. Blood groups in sheep. I. The X-Z system. Genetics 1958, 43: 814-821.
-
(1958)
Genetics
, vol.43
, pp. 814-821
-
-
Rasmusen, B.A.1
-
181
-
-
0028189954
-
Juvenile-onset neuronal ceroid-lipofuscinosis in Rambouillet sheep
-
Edwards, J.F., Storts, R.W., Joyce, J.R., Shelton, J.M., Menzies, C.S. Juvenile-onset neuronal ceroid-lipofuscinosis in Rambouillet sheep. Vet. Pathol. 1994, 31: 48-54.
-
(1994)
Vet. Pathol.
, vol.31
, pp. 48-54
-
-
Edwards, J.F.1
Storts, R.W.2
Joyce, J.R.3
Shelton, J.M.4
Menzies, C.S.5
-
182
-
-
0033255269
-
Isolation of the ovine agouti coding sequence
-
Parsons, Y.M., Fleet, M.R., Cooper, D.W. Isolation of the ovine agouti coding sequence. Pigment Cell Res. 1999, 12: 394-397.
-
(1999)
Pigment Cell Res.
, vol.12
, pp. 394-397
-
-
Parsons, Y.M.1
Fleet, M.R.2
Cooper, D.W.3
-
183
-
-
0032818124
-
The Agouti gene, a positional candidate for recessive self-colour pigmentation in Australian Merino sheep
-
Parsons, Y.M., Fleet, M.R., Cooper, D.W. The Agouti gene, a positional candidate for recessive self-colour pigmentation in Australian Merino sheep. Aust. J. Agricult. Res. 1999, 50: 1099-1103.
-
(1999)
Aust. J. Agricult. Res.
, vol.50
, pp. 1099-1103
-
-
Parsons, Y.M.1
Fleet, M.R.2
Cooper, D.W.3
-
184
-
-
0017558067
-
Albinism in Icelandic sheep
-
Adalsteinsson, S. Albinism in Icelandic sheep. J. Hered. 1977, 68: 347-349.
-
(1977)
J. Hered.
, vol.68
, pp. 347-349
-
-
Adalsteinsson, S.1
-
185
-
-
0023930818
-
A defective cell surface collagen-binding protein in dermatosparactic sheep fibroblasts
-
Mauch, C., van der Mark, K., Helle, O., Mollenhauer, J., Pfaffle, M., Krieg, T. A defective cell surface collagen-binding protein in dermatosparactic sheep fibroblasts. J. Cell Biol. 1988, 106: 205-211.
-
(1988)
J. Cell Biol.
, vol.106
, pp. 205-211
-
-
Mauch, C.1
van der Mark, K.2
Helle, O.3
Mollenhauer, J.4
Pfaffle, M.5
Krieg, T.6
-
186
-
-
0015451579
-
A hereditary skin defect in sheep
-
Helle, O., Nes, N.N. A hereditary skin defect in sheep. Acta Vet. Scand. 1972, 13: 443-445.
-
(1972)
Acta Vet. Scand.
, vol.13
, pp. 443-445
-
-
Helle, O.1
Nes, N.N.2
-
187
-
-
0025896587
-
Animal model for dermolytic mechanobullous disease, sheep with recessive dystrophic epidermolysis bullosa lack collagen VII
-
Bruckner-Tuderman, L., Guscetti, F., Ehrensperger, F. Animal model for dermolytic mechanobullous disease, sheep with recessive dystrophic epidermolysis bullosa lack collagen VII. J. Invest. Dermatol. 1991, 96: 452-458.
-
(1991)
J. Invest. Dermatol.
, vol.96
, pp. 452-458
-
-
Bruckner-Tuderman, L.1
Guscetti, F.2
Ehrensperger, F.3
-
188
-
-
0014906614
-
Epitheliogenesis imperfecta in lambs and kittens
-
Munday, B.L. Epitheliogenesis imperfecta in lambs and kittens. Br. Vet. J. 1970, 126.
-
(1970)
Br. Vet. J.
, pp. 126
-
-
Munday, B.L.1
-
189
-
-
84972055120
-
Expected Consequences of the Segregation of a Major Gene in a Sheep Population in Relation to Observations on the Ovulation Rate of a Flock of Cambridge Sheep
-
Owen, J.B., Whitaker, C.J., Axford, R.F.E., Dewi, I.A. Expected Consequences of the Segregation of a Major Gene in a Sheep Population in Relation to Observations on the Ovulation Rate of a Flock of Cambridge Sheep. Anim. Prod. 1990, 51: 277-282.
-
(1990)
Anim. Prod.
, vol.51
, pp. 277-282
-
-
Owen, J.B.1
Whitaker, C.J.2
Axford, R.F.E.3
Dewi, I.A.4
-
190
-
-
0034597320
-
Pre-ovulatory follicular characteristics and ovulation rates in different breed crosses, carriers or non-carriers of the Booroola or Cambridge fecundity gene
-
Mandiki, S.N., Noel, B., Bister, J.L., Peeters, R., Beerlandt, G., Decuypere, E., Visscher, A., Suess, R. Pre-ovulatory follicular characteristics and ovulation rates in different breed crosses, carriers or non-carriers of the Booroola or Cambridge fecundity gene. Anim. Reprod. Sci. 2000, 63: 77-88.
-
(2000)
Anim. Reprod. Sci.
, vol.63
, pp. 77-88
-
-
Mandiki, S.N.1
Noel, B.2
Bister, J.L.3
Peeters, R.4
Beerlandt, G.5
Decuypere, E.6
Visscher, A.7
Suess, R.8
-
191
-
-
0034967562
-
Genes controlling ovulation rate in sheep
-
Montgomery, G.W., Galloway, S.M., Davis, G.H., McNatty, K.P. Genes controlling ovulation rate in sheep. Reproduction 2001, 121: 843-852.
-
(2001)
Reproduction
, vol.121
, pp. 843-852
-
-
Montgomery, G.W.1
Galloway, S.M.2
Davis, G.H.3
McNatty, K.P.4
-
192
-
-
0000508296
-
Single genes for fecundity in Icelandic sheep
-
Land, R., Robinson, D. (eds.). (Butterworths, London)
-
Jonmundsson, J.V., Adalsteinsson, S. Single genes for fecundity in Icelandic sheep, in Land, R., Robinson, D. (eds.). Genetics of Reproduction in Sheep, (Butterworths, London 1985) pp. 159-168.
-
(1985)
Genetics of Reproduction in Sheep
, pp. 159-168
-
-
Jonmundsson, J.V.1
Adalsteinsson, S.2
-
193
-
-
0031505544
-
The effect of the introduction of the thoka gene for fecundity on lamb production from Cheviot ewes
-
Russel, A.J.F., Alexieva, S.A., Elston, D.A. The effect of the introduction of the thoka gene for fecundity on lamb production from Cheviot ewes. Anim. Sci. (1997), 64: 503-507.
-
(1997)
Anim. Sci.
, vol.64
, pp. 503-507
-
-
Russel, A.J.F.1
Alexieva, S.A.2
Elston, D.A.3
-
194
-
-
0025903923
-
Evidence for the presence of a major gene influencing ovulation rate on the X chromosome of sheep
-
Davis, G.H., McEwan, J.C., Fennessy, P.F., Dodds, K.G., Farquhar, P.A. Evidence for the presence of a major gene influencing ovulation rate on the X chromosome of sheep. Biol. Reprod. 1991, 44: 620-624.
-
(1991)
Biol. Reprod.
, vol.44
, pp. 620-624
-
-
Davis, G.H.1
McEwan, J.C.2
Fennessy, P.F.3
Dodds, K.G.4
Farquhar, P.A.5
-
195
-
-
0026754074
-
Physiology and molecular genetics of mutations that increase ovulation rate in sheep
-
Montgomery, G.W., McNatty, K.P., Davis, G.H. Physiology and molecular genetics of mutations that increase ovulation rate in sheep. Endocr. Rev. 1992, 13: 309-328.
-
(1992)
Endocr. Rev.
, vol.13
, pp. 309-328
-
-
Montgomery, G.W.1
McNatty, K.P.2
Davis, G.H.3
-
196
-
-
0022764358
-
Reproduction in Javanese sheep, evidence for a gene with large effect on ovulation rate and litter size
-
Bradford, G.E., Quirke, J.F., Sitorus, P., Inounu, I., Tiesnamurti, B., Bell, F.L., Fletcher, I.C., Torell, D.T. Reproduction in Javanese sheep, evidence for a gene with large effect on ovulation rate and litter size. J. Anim. Sci. 1986, 63: 418-431.
-
(1986)
J. Anim. Sci.
, vol.63
, pp. 418-431
-
-
Bradford, G.E.1
Quirke, J.F.2
Sitorus, P.3
Inounu, I.4
Tiesnamurti, B.5
Bell, F.L.6
Fletcher, I.C.7
Torell, D.T.8
-
197
-
-
25044450130
-
An inherited lysosomal storage disease of sheep associated with deficiencies of beta-galactosidase and alpha-neuraminidase
-
(Abstract)
-
Ahern-Rindell, A.J., Prieur, D.J., Murnane, R.D. An inherited lysosomal storage disease of sheep associated with deficiencies of beta-galactosidase and alpha-neuraminidase (Abstract). Am. J. Hum. Genet. 1986, 39: A3.
-
(1986)
Am. J. Hum. Genet.
, vol.39
-
-
Ahern-Rindell, A.J.1
Prieur, D.J.2
Murnane, R.D.3
-
198
-
-
0014328651
-
Lipidoses of the hepatic reticuloendothelial cells in a sheep
-
Laws, L., Saal, J.R. Lipidoses of the hepatic reticuloendothelial cells in a sheep. Aust. Vet. J. 1968, 44: 416-417.
-
(1968)
Aust. Vet. J.
, vol.44
, pp. 416-417
-
-
Laws, L.1
Saal, J.R.2
-
199
-
-
0030774756
-
A splice-site mutation causing ovine McArdle's-disease
-
Tan, P., Allen, J.G., Wilton, S.D., Akkari, P.A., Huxtable, C.R., Laing, N.G. A splice-site mutation causing ovine McArdle's-disease. Neuromuscul. Disord. 1997, 7: 336-342.
-
(1997)
Neuromuscul. Disord.
, vol.7
, pp. 336-342
-
-
Tan, P.1
Allen, J.G.2
Wilton, S.D.3
Akkari, P.A.4
Huxtable, C.R.5
Laing, N.G.6
-
200
-
-
84970555858
-
Inheritance of congenital goitre due to a thyroid defect in Merino sheep
-
Mayo, G.M.E., Mulhearn, C.J. Inheritance of congenital goitre due to a thyroid defect in Merino sheep. Aust. J. Agricult. Res. 1969, 20: 533-547.
-
(1969)
Aust. J. Agricult. Res.
, vol.20
, pp. 533-547
-
-
Mayo, G.M.E.1
Mulhearn, C.J.2
-
201
-
-
0017173842
-
Congenital goitre in sheep, isolation of the iodoproteins which replace thyroglobulin
-
Dolling, C.E., Good, B.F. Congenital goitre in sheep, isolation of the iodoproteins which replace thyroglobulin. J. Endocrinol. 1976, 71: 179-192.
-
(1976)
J. Endocrinol.
, vol.71
, pp. 179-192
-
-
Dolling, C.E.1
Good, B.F.2
-
202
-
-
0028032511
-
Carrier detection of ovine hemophilia A using an RFLP marker, and mapping of the factor VIII gene on the ovine X-chromosome
-
Backfisch, W., Neuenschwander, S., Giger, U., Stranzinger, G., Pliska, V. Carrier detection of ovine hemophilia A using an RFLP marker, and mapping of the factor VIII gene on the ovine X-chromosome. J. Hered. 1994, 85: 474-478.
-
(1994)
J. Hered.
, vol.85
, pp. 474-478
-
-
Backfisch, W.1
Neuenschwander, S.2
Giger, U.3
Stranzinger, G.4
Pliska, V.5
-
203
-
-
0012940807
-
A Mendelian situation in the birthcoat of the New Zealand Romney lamb
-
Dry, F.W., McMahon, P.R., Sutherland, J.A. A Mendelian situation in the birthcoat of the New Zealand Romney lamb. Nature 1940, 145: 390-391.
-
(1940)
Nature
, vol.145
, pp. 390-391
-
-
Dry, F.W.1
McMahon, P.R.2
Sutherland, J.A.3
-
204
-
-
84970564758
-
The dominant N gene in New Zealand Romney sheep
-
Dry, F.W. The dominant N gene in New Zealand Romney sheep. Aust. J. Agricult. Res. (1955), 6: 725-769.
-
(1955)
Aust. J. Agricult. Res.
, vol.6
, pp. 725-769
-
-
Dry, F.W.1
-
205
-
-
0037976651
-
The gentics of carpet wool production, the Elliotdale breed
-
Presented in, Sixth Conference
-
Sides, R.H., Banks, R.G. The gentics of carpet wool production, the Elliotdale breed. Presented in, Sixth Conference, Aust. Assoc. Anim. Breed. Genet. 1987, 356-359.
-
(1987)
Aust. Assoc. Anim. Breed. Genet.
, pp. 356-359
-
-
Sides, R.H.1
Banks, R.G.2
-
206
-
-
0037976646
-
Photosensitivity diseases in New Zealand. I. Facial eczema, its clinical, pathological and biochemical characteristics
-
Cunningham, T.J., Hopkirk, C.S.M., Filmer, J.E. Photosensitivity diseases in New Zealand. I. Facial eczema, its clinical, pathological and biochemical characteristics. N.Z. J. Sci. Tech. 1942, 24A, 185-198.
-
(1942)
N.Z. J. Sci. Tech.
, vol.24 A
, pp. 185-198
-
-
Cunningham, T.J.1
Hopkirk, C.S.M.2
Filmer, J.E.3
-
207
-
-
0037976659
-
A mutation in Southdown sheep affecting the hepatic uptake of sulfobromophthalein (BSP) indocyanine green, rose bengal, sodium cholate and phylloerythrin from blood
-
Cornelius, C.E., Gronwall, R.R. A mutation in Southdown sheep affecting the hepatic uptake of sulfobromophthalein (BSP) indocyanine green, rose bengal, sodium cholate and phylloerythrin from blood. Fed. Proc. 1979, 24: 144.
-
(1979)
Fed. Proc.
, vol.24
, pp. 144
-
-
Cornelius, C.E.1
Gronwall, R.R.2
-
208
-
-
0037638669
-
Congenital photosensitivity in Southdown sheep, a new sublethal factor in sheep
-
Hancock, J. Congenital photosensitivity in Southdown sheep, a new sublethal factor in sheep. N.Z. J. Sci. Tech. 1950, 32A, 16-24.
-
(1950)
N.Z. J. Sci. Tech.
, vol.32 A
, pp. 16-24
-
-
Hancock, J.1
-
209
-
-
0018564911
-
Animal model of human disease, intrarenal obstructive uropathy with proximal ectasia, cystic kidney disease
-
Cuppage, F.W., McGavin, M.D., Strafuss, A.C. Animal model of human disease, intrarenal obstructive uropathy with proximal ectasia, cystic kidney disease. Am. J. Pathol. 1979, 97: 207-210.
-
(1979)
Am. J. Pathol.
, vol.97
, pp. 207-210
-
-
Cuppage, F.W.1
McGavin, M.D.2
Strafuss, A.C.3
-
210
-
-
0037638647
-
Black liver disease in Corriedale sheep, a new mutation affecting hepatic excretory function
-
Arias, I., Bernstein, L., Toffler, R., Cornelius, C., Novikoff, A.B., Essner, E. Black liver disease in Corriedale sheep, a new mutation affecting hepatic excretory function. J. Clin. Invest. 1964, 43: 1249-1250.
-
(1964)
J. Clin. Invest.
, vol.43
, pp. 1249-1250
-
-
Arias, I.1
Bernstein, L.2
Toffler, R.3
Cornelius, C.4
Novikoff, A.B.5
Essner, E.6
-
211
-
-
0037976648
-
Hepatic pigmentation with photosensitivity, a syndrome in Corriedale sheep resembling Dubin-Johnson syndrome in man
-
Cornelius, C., Arias, I., Osburn, B.I. Hepatic pigmentation with photosensitivity, a syndrome in Corriedale sheep resembling Dubin-Johnson syndrome in man. J. Am. Vet. Med. Assoc. 1965, 146: 709-713.
-
(1965)
J. Am. Vet. Med. Assoc.
, vol.146
, pp. 709-713
-
-
Cornelius, C.1
Arias, I.2
Osburn, B.I.3
-
212
-
-
0018952525
-
Globoid cell leucodystrophy in polled Dorset sheep
-
Pritchard, D.H., apthine, D.V., Sinclair, A.J. Globoid cell leucodystrophy in polled Dorset sheep. Vet. Pathol. 1980, 17: 399-405.
-
(1980)
Vet. Pathol.
, vol.17
, pp. 399-405
-
-
Pritchard, D.H.1
Apthine, D.V.2
Sinclair, A.J.3
-
213
-
-
0037638668
-
A dominant felting lustre mutant fleece type in the Australian Merino sheep
-
Short, B.F. A dominant felting lustre mutant fleece type in the Australian Merino sheep. Nature 1958, 181: 1414-1415.
-
(1958)
Nature
, vol.181
, pp. 1414-1415
-
-
Short, B.F.1
-
214
-
-
85047694966
-
Inheritance of a Major Gene for Excessively Lustrous Wool in Sheep
-
Blair, H.T. Inheritance of a Major Gene for Excessively Lustrous Wool in Sheep. J. Hered. 1990, 81: 220-222.
-
(1990)
J. Hered.
, vol.81
, pp. 220-222
-
-
Blair, H.T.1
-
215
-
-
0029242770
-
Serum swainsonine concentration and alpha-mannosidase activity in cattle and sheep ingesting Oxytropis sericea and Astragalus lentiginosus (locoweeds)
-
Stegelmeier, B.L., James, L.F., Panter, K.E., Molyneux, R.J. Serum swainsonine concentration and alpha-mannosidase activity in cattle and sheep ingesting Oxytropis sericea and Astragalus lentiginosus (locoweeds). Am. J. Vet. Res. 1995, 56: 149-154.
-
(1995)
Am. J. Vet. Res.
, vol.56
, pp. 149-154
-
-
Stegelmeier, B.L.1
James, L.F.2
Panter, K.E.3
Molyneux, R.J.4
-
216
-
-
19244382300
-
An EcoRV polymorphism at the ovine Menkes disease locus (ATP7A)
-
Potts, M.D., Hanrahan, V., Hill, D.F. An EcoRV polymorphism at the ovine Menkes disease locus (ATP7A). Anim. Genet. 1994, 25: 293.
-
(1994)
Anim. Genet.
, vol.25
, pp. 293
-
-
Potts, M.D.1
Hanrahan, V.2
Hill, D.F.3
-
217
-
-
84964186322
-
A congenital progressive ovine muscular dystrophy
-
McGavin, M.D., Baynes, I.D. A congenital progressive ovine muscular dystrophy. Pathol. Vet. 1969, 6: 513-524.
-
(1969)
Pathol. Vet.
, vol.6
, pp. 513-524
-
-
McGavin, M.D.1
Baynes, I.D.2
-
218
-
-
0028264793
-
Chromosomal localization of the callipyge gene in sheep (Ovis aries) using bovine DNA markers
-
Cockett, N.E., Jackson, S.P., Shay, T.L., Nielsen, D., Moore, S.S., Steele, M.R., Barendse, W., Green, R.D., Georges, M. Chromosomal localization of the callipyge gene in sheep (Ovis aries) using bovine DNA markers. Proc. Natl. Acad. Sci. USA 1994, 91: 3019-3023.
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 3019-3023
-
-
Cockett, N.E.1
Jackson, S.P.2
Shay, T.L.3
Nielsen, D.4
Moore, S.S.5
Steele, M.R.6
Barendse, W.7
Green, R.D.8
Georges, M.9
-
219
-
-
0029443229
-
A muscle hypertrophy condition in lamb (callipyge), characterization of effects on muscle growth and meat quality traits
-
Koohmaraie, M., Shackelford, S.D., Wheeler, T.L., Lonergan, S.M., Doumit, M.E. A muscle hypertrophy condition in lamb (callipyge), characterization of effects on muscle growth and meat quality traits. J. Anim. Sci. 1995, 73: 3596-3607.
-
(1995)
J. Anim. Sci.
, vol.73
, pp. 3596-3607
-
-
Koohmaraie, M.1
Shackelford, S.D.2
Wheeler, T.L.3
Lonergan, S.M.4
Doumit, M.E.5
-
220
-
-
0030076302
-
Histology and composition of muscles from normal and callipyge lambs
-
Carpenter, C.E., Rice, O.D., Cockett, N.E., Snowder, G.D. Histology and composition of muscles from normal and callipyge lambs. J. Anim. Sci. 1996, 74: 388-393.
-
(1996)
J. Anim. Sci.
, vol.74
, pp. 388-393
-
-
Carpenter, C.E.1
Rice, O.D.2
Cockett, N.E.3
Snowder, G.D.4
-
221
-
-
0030638548
-
Phenotypic characterization of rambouillet sheep expressing the callipyge gene, I. Inheritance of the condition and production characteristics
-
Jackson, S.P., Green, R.D., Miller, M.F. Phenotypic characterization of rambouillet sheep expressing the callipyge gene, I. Inheritance of the condition and production characteristics. J. Anim. Sci. 1997, 75: 14-18.
-
(1997)
J. Anim. Sci.
, vol.75
, pp. 14-18
-
-
Jackson, S.P.1
Green, R.D.2
Miller, M.F.3
-
222
-
-
0030635511
-
Phenotypic characterization of rambouillet sheep expression the callipyge gene, III. Muscle weights and muscle weight distribution
-
Jackson, S.P., Miller, M.F., Green, R.D. Phenotypic characterization of rambouillet sheep expression the callipyge gene, III. Muscle weights and muscle weight distribution. J. Anim. Sci. 1997, 75: 133-138.
-
(1997)
J. Anim. Sci.
, vol.75
, pp. 133-138
-
-
Jackson, S.P.1
Miller, M.F.2
Green, R.D.3
-
223
-
-
0035125220
-
Fine-mapping and construction of a bovine contig spanning the ovine callipyge locus
-
Shay, T.L., Berghmans, S., Segers, K., Meyers, S., Beever, J.E., Womack, J.E., Georges, M., Charlier, C. Fine-mapping and construction of a bovine contig spanning the ovine callipyge locus. Mamm. Genome 2001, 12: 141-149.
-
(2001)
Mamm. Genome
, vol.12
, pp. 141-149
-
-
Shay, T.L.1
Berghmans, S.2
Segers, K.3
Meyers, S.4
Beever, J.E.5
Womack, J.E.6
Georges, M.7
Charlier, C.8
-
224
-
-
0035069170
-
The callipyge mutation enhances the expression of coregulated imprinted genes in cis without affecting their imprinting status
-
Charlier, C., Segers, K., Karim, L., Shay, T., Gyapay, G., Cockett, N., Georges, M. The callipyge mutation enhances the expression of coregulated imprinted genes in cis without affecting their imprinting status. Nat. Genet. 2001, 27: 367-369.
-
(2001)
Nat. Genet.
, vol.27
, pp. 367-369
-
-
Charlier, C.1
Segers, K.2
Karim, L.3
Shay, T.4
Gyapay, G.5
Cockett, N.6
Georges, M.7
-
225
-
-
0030802414
-
Autosomal recessive myotonia congenita in sheep
-
Moore, G.A., Dyer, K.R., Dyer, R.M., Sponenberg, D.P. Autosomal recessive myotonia congenita in sheep. Genet. Select. Evol. 1997, 29: 291-294.
-
(1997)
Genet. Select. Evol.
, vol.29
, pp. 291-294
-
-
Moore, G.A.1
Dyer, K.R.2
Dyer, R.M.3
Sponenberg, D.P.4
-
226
-
-
0037976650
-
Red cell amino acid and nucleoside transport, inherited lesions and related enzyme deficiencies in sheep
-
Belton, N.R., Toothill, C. (eds.). (MTP Press Limited, Lancaster)
-
Young, J.D., Jarvis, S.M. Red cell amino acid and nucleoside transport, inherited lesions and related enzyme deficiencies in sheep, in Belton, N.R., Toothill, C. (eds.). Transport and Inherited Disease, (MTP Press Limited, Lancaster 1981) pp, 347-368.
-
(1981)
Transport and Inherited Disease
, pp. 347-368
-
-
Young, J.D.1
Jarvis, S.M.2
-
227
-
-
0037976649
-
Genetic control of sodium and potassium concentrations in the red blood cells of sheep
-
Evans, J.V., King, J.W.B. Genetic control of sodium and potassium concentrations in the red blood cells of sheep. Nature 1955, 176: 171.
-
(1955)
Nature
, vol.176
, pp. 171
-
-
Evans, J.V.1
King, J.W.B.2
-
228
-
-
0002467481
-
Cation transport in red blood cells
-
Agar, N.S., Board, P.G. (eds.). (Elsevier, Amsterdam)
-
Ellory, J.C., Tucker, E.M. Cation transport in red blood cells, in Agar, N.S., Board, P.G. (eds.). Red Blood Cells of Domestic Mammals, (Elsevier, Amsterdam 1983), pp 291-314.
-
(1983)
Red Blood Cells of Domestic Mammals
, pp. 291-314
-
-
Ellory, J.C.1
Tucker, E.M.2
-
229
-
-
0004116699
-
The blood groups of domestic mammals
-
Agar, N.S., Board, P.G. (eds.). (Elsevier, Amsterdam)
-
Bell, K. The blood groups of domestic mammals, in Agar, N.S., Board, P.G. (eds.). Red Blood Cells of Domestic Mammals, (Elsevier, Amsterdam 1983), pp 133-164.
-
(1983)
Red Blood Cells of Domestic Mammals
, pp. 133-164
-
-
Bell, K.1
-
230
-
-
0005061519
-
Erythrocyte amino acid and nucleoside transport
-
Agar, N.S., Board, P.G. (eds.). (Elsevier, Amsterdam)
-
Young, J.D. Erythrocyte amino acid and nucleoside transport, in Agar, N.S., Board, P.G. (eds.). Red Blood Cells of Domestic Mammals, (Elsevier, Amsterdam 1983), pp 271-290.
-
(1983)
Red Blood Cells of Domestic Mammals
, pp. 271-290
-
-
Young, J.D.1
-
231
-
-
0002774682
-
Glutathione metabolism in erythrocytes
-
N.S., Board, P.G. (eds.). (Elsevier, Amsterdam)
-
Board, P.G., Agar, N.S. Glutathione metabolism in erythrocytes, in Agar, N.S., Board, P.G. (eds.). Red Blood Cells of Domestic Mammals, (Elsevier, Amsterdam 1983), pp 253-270.
-
(1983)
Red Blood Cells of Domestic Mammals
, pp. 253-270
-
-
Board, P.G.1
Agar, N.S.2
-
232
-
-
0023955198
-
The inheritance of non-response to noradrenaline in newborn Scottish blackface lambs
-
Simpson, S.P., Slee, J. The inheritance of non-response to noradrenaline in newborn Scottish blackface lambs. Genet. Res. 1988, 51: 65-69.
-
(1988)
Genet. Res.
, vol.51
, pp. 65-69
-
-
Simpson, S.P.1
Slee, J.2
-
233
-
-
0033006635
-
Hereditary deficiency of vitamin-K-dependent coagulation factors in Rambouillet sheep
-
Baker, D.C., Robbe, S.L., Jacobson, L., Manco-Johnson, M.J., Holler, L., Lefkowitz, J. Hereditary deficiency of vitamin-K-dependent coagulation factors in Rambouillet sheep. Blood Coagul Fibrinolysis 1999, 10: 75-80.
-
(1999)
Blood Coagul. Fibrinolysis
, vol.10
, pp. 75-80
-
-
Baker, D.C.1
Robbe, S.L.2
Jacobson, L.3
Manco-Johnson, M.J.4
Holler, L.5
Lefkowitz, J.6
-
234
-
-
0030337794
-
A missense mutation in the gene for melanocyte-stimulating hormone receptor (MC1R) is associated with the chestnut coat color in horses
-
Marklund, L., Moller, M.J., Sandberg, K., Andersson, L. A missense mutation in the gene for melanocyte-stimulating hormone receptor (MC1R) is associated with the chestnut coat color in horses. Mamm. Genome 1996, 7: 895-899.
-
(1996)
Mamm. Genome
, vol.7
, pp. 895-899
-
-
Marklund, L.1
Moller, M.J.2
Sandberg, K.3
Andersson, L.4
-
235
-
-
0032053530
-
Endothelin receptor B polymorphism associated with lethal white foal syndrome in horses
-
Santschi, E.M., Purdy, A.K., Valberg, S.J., Vrotsos, P.D., Kaese, H., Mickelson, J.R. Endothelin receptor B polymorphism associated with lethal white foal syndrome in horses. Mamm. Genome 1998, 9: 306-309.
-
(1998)
Mamm. Genome
, vol.9
, pp. 306-309
-
-
Santschi, E.M.1
Purdy, A.K.2
Valberg, S.J.3
Vrotsos, P.D.4
Kaese, H.5
Mickelson, J.R.6
-
236
-
-
23044529268
-
Genetic cause of overo lethal white foal syndrome
-
anonymous
-
anonymous, Genetic cause of overo lethal white foal syndrome. J. Equine Vet. Sci. 2001, 21: 381-382.
-
(2001)
J. Equine Vet. Sci.
, vol.21
, pp. 381-382
-
-
-
237
-
-
0008469716
-
An episodic weakness in four horses associated with intermittent serum hyperkalemia and the similarity of the diesease to hyperkalemic periodic paresis in man
-
Presented in, American Association of Equine Practioners
-
Cox, J.H. An episodic weakness in four horses associated with intermittent serum hyperkalemia and the similarity of the diesease to hyperkalemic periodic paresis in man. Presented in, American Association of Equine Practioners 1985, 21: 383-391.
-
(1985)
, vol.21
, pp. 383-391
-
-
Cox, J.H.1
-
238
-
-
0038653089
-
Episodic muscle tremors in a quarter horse, resemblance to hyperkalemic periodic paralysis
-
Steiss, J.E., Naylor, J.M. Episodic muscle tremors in a quarter horse, resemblance to hyperkalemic periodic paralysis. Can. Vet. J. 1986, 27: 332-335.
-
(1986)
Can. Vet. J.
, vol.27
, pp. 332-335
-
-
Steiss, J.E.1
Naylor, J.M.2
-
239
-
-
0026456095
-
Linkage of hyperkalaemic periodic paralysis in quarter horses to the horse adult skeletal muscle sodium channel gene
-
Rudolph, J.A., Spier, S.J., Byrns, G., Hoffman, E.P. Linkage of hyperkalaemic periodic paralysis in quarter horses to the horse adult skeletal muscle sodium channel gene. Anim. Genet. 1992, 23: 241-250.
-
(1992)
Anim. Genet.
, vol.23
, pp. 241-250
-
-
Rudolph, J.A.1
Spier, S.J.2
Byrns, G.3
Hoffman, E.P.4
-
240
-
-
0029911215
-
The equine periodic paralysis Na+ channel mutation alters molecular transitions between the open and inactivated states
-
Hanna, W.J., Tsushima, R.G., Sah, R., McCutcheon, L.J., Marban, E., Backx, P.H. The equine periodic paralysis Na+ channel mutation alters molecular transitions between the open and inactivated states. J. Physiol. 1996, 497: 349-364.
-
(1996)
J. Physiol.
, vol.497
, pp. 349-364
-
-
Hanna, W.J.1
Tsushima, R.G.2
Sah, R.3
McCutcheon, L.J.4
Marban, E.5
Backx, P.H.6
-
241
-
-
0031569608
-
A kinase-negative mutation of DNA-PK(CS) in equine SCID results in defective coding and signal joint formation
-
Shin, E.K., Perryman, L.E., Meek, K. A kinase-negative mutation of DNA-PK(CS) in equine SCID results in defective coding and signal joint formation. J. Immunol. 1997, 158: 3565-3569.
-
(1997)
J. Immunol.
, vol.158
, pp. 3565-3569
-
-
Shin, E.K.1
Perryman, L.E.2
Meek, K.3
-
242
-
-
0031213931
-
Linkage of the gene for equine combined immunodeficiency disease to microsatellite markers HTG8 and HTG4; synteny and FISH mapping to ECA9
-
Bailey, E., Reid, R.C., Skow, L.C., Mathiason, K., Lear, T.L., McGuire, T.C. Linkage of the gene for equine combined immunodeficiency disease to microsatellite markers HTG8 and HTG4; synteny and FISH mapping to ECA9. Anim. Genet. 1997, 28: 268-273.
-
(1997)
Anim. Genet.
, vol.28
, pp. 268-273
-
-
Bailey, E.1
Reid, R.C.2
Skow, L.C.3
Mathiason, K.4
Lear, T.L.5
McGuire, T.C.6
-
243
-
-
0031572948
-
Evaluation of a test for identification of Arabian horses heterozygous for the severe combined immunodeficiency trait
-
Shin, E.K., Perryman, L.E., Meek, K. Evaluation of a test for identification of Arabian horses heterozygous for the severe combined immunodeficiency trait. J. Am. Vet. Med. Assoc. 1997, 211: 1268-1270.
-
(1997)
J. Am. Vet. Med. Assoc.
, vol.211
, pp. 1268-1270
-
-
Shin, E.K.1
Perryman, L.E.2
Meek, K.3
-
244
-
-
0022536023
-
XY sex-reversal syndrome in the domestic horse
-
Kent, M.G., Shoffner, R.N., Buoen, L., Weber, A.F. XY sex-reversal syndrome in the domestic horse. Cytogenet. Cell Genet. 1986, 42: 8-18.
-
(1986)
Cytogenet. Cell Genet.
, vol.42
, pp. 8-18
-
-
Kent, M.G.1
Shoffner, R.N.2
Buoen, L.3
Weber, A.F.4
-
245
-
-
0033158820
-
Deletion of the Sry region on the Y chromosome detected in a case of equine gonadal hypoplasia (XY female) with abnormal hormonal profiles
-
Abe, S., Miyake, Y.I., Kageyama, S.I., Watanabe, G., Taya, K., Kawakura, K. Deletion of the Sry region on the Y chromosome detected in a case of equine gonadal hypoplasia (XY female) with abnormal hormonal profiles. Equine Vet. J. 1999, 31: 336-338.
-
(1999)
Equine Vet. J.
, vol.31
, pp. 336-338
-
-
Abe, S.1
Miyake, Y.I.2
Kageyama, S.I.3
Watanabe, G.4
Taya, K.5
Kawakura, K.6
-
246
-
-
0034056348
-
The horse homolog of congenital aniridia conforms to codominant inheritance
-
Ewart, S.L., Ramsey, D.T., Xu, J.., Meyers, D. The horse homolog of congenital aniridia conforms to codominant inheritance. J. Hered. 2000, 91: 93-98.
-
(2000)
J. Hered.
, vol.91
, pp. 93-98
-
-
Ewart, S.L.1
Ramsey, D.T.2
Xu, J.3
Meyers, D.4
-
247
-
-
0030114587
-
Unequivocal identification of the equine Dcfmqr phenogroup
-
Bell, K., Colling, D.T. Unequivocal identification of the equine Dcfmqr phenogroup. Anim. Genet. 1996, 27: 103-104.
-
(1996)
Anim. Genet.
, vol.27
, pp. 103-104
-
-
Bell, K.1
Colling, D.T.2
-
248
-
-
0030473443
-
Champagne, a dominant colour dilution of horses
-
Sponenberg, D.P., Bowling, A.T. Champagne, a dominant colour dilution of horses. Genet. Sel. Evol. 1996, 28: 457-462.
-
(1996)
Genet. Sel. Evol.
, vol.28
, pp. 457-462
-
-
Sponenberg, D.P.1
Bowling, A.T.2
-
249
-
-
0018439810
-
Growth rate of thoroughbreds, effect of age of dam, year and month of birth, and sex of foal
-
Hintz, H.F., Hintz, R.L., Van Vleck, L.D. Growth rate of thoroughbreds, effect of age of dam, year and month of birth, and sex of foal. J. Anim. Sci. 1979, 48: 480-487.
-
(1979)
J. Anim. Sci.
, vol.48
, pp. 480-487
-
-
Hintz, H.F.1
Hintz, R.L.2
Van Vleck, L.D.3
-
250
-
-
0020073636
-
A linkage group composed of 3 coat colour genes and 3 serum protein loci in horses
-
Andersson, L., Sandberg, K. A linkage group composed of 3 coat colour genes and 3 serum protein loci in horses. J. Hered. 1982, 73: 91-94.
-
(1982)
J. Hered.
, vol.73
, pp. 91-94
-
-
Andersson, L.1
Sandberg, K.2
-
251
-
-
0028370008
-
Parentage testing and linkage analysis in the horse using a set of highly polymorphic microsatellites
-
Marklund, S., Ellegren, H., Eriksson, S., Sandberg, K., Andersson, L. Parentage testing and linkage analysis in the horse using a set of highly polymorphic microsatellites. Anim. Genet. 1994, 25: 19-23.
-
(1994)
Anim. Genet.
, vol.25
, pp. 19-23
-
-
Marklund, S.1
Ellegren, H.2
Eriksson, S.3
Sandberg, K.4
Andersson, L.5
-
252
-
-
25044479874
-
Applied molecular genetics in domestic animals with particular focus on the horse
-
PhD Thesis
-
Marklund, S. Applied molecular genetics in domestic animals with particular focus on the horse. PhD Thesis, Acta Universitatis agriculturae Sueciae Agraria 1997, 79: 92s.
-
(1997)
Acta Universitatis Agriculturae Sueciae Agraria
, vol.79
-
-
Marklund, S.1
-
253
-
-
0014489913
-
Lethal dominant white in horses
-
Pulos, W.L., Hutt, F.B. Lethal dominant white in horses. J. Hered. (1969), 60: 59-63.
-
(1969)
J. Hered.
, vol.60
, pp. 59-63
-
-
Pulos, W.L.1
Hutt, F.B.2
-
255
-
-
0037638667
-
Hereditary multiple exostosis in the horse
-
Morgan, J.P., Carlson, W.D., Adams, O.R. Hereditary multiple exostosis in the horse. J. Am. Vet. Med. Assoc. 1962, 140: 1320-1322.
-
(1962)
J. Am. Vet. Med. Assoc.
, vol.140
, pp. 1320-1322
-
-
Morgan, J.P.1
Carlson, W.D.2
Adams, O.R.3
-
256
-
-
0028510509
-
Equine glucose-6-phosphate dehydrogenase deficiency
-
Stockham, S.L., Harvey, J.W., Kinden, D.A. Equine glucose-6-phosphate dehydrogenase deficiency. Vet. Pathol. 1994, 3: 518-527.
-
(1994)
Vet. Pathol.
, vol.3
, pp. 518-527
-
-
Stockham, S.L.1
Harvey, J.W.2
Kinden, D.A.3
-
257
-
-
0013658798
-
True haemophilia (haemophilia A) in a thoroughbred foal
-
Archer, R.K. True haemophilia (haemophilia A) in a thoroughbred foal. Vet. Rec. 1961, 73: 338-340.
-
(1961)
Vet. Rec.
, vol.73
, pp. 338-340
-
-
Archer, R.K.1
-
258
-
-
21844486541
-
Persistent hyperbilirubinemia in a horse - A case report
-
Deprez, P., Sustronck, B., Van Loon, G., Muylle, E. [Persistent hyperbilirubinemia in a horse - a case report]. Vlaams Diergeneeskundig Tijdschrift 1995, 64: 212-215.
-
(1995)
Vlaams Diergeneeskundig Tijdschrift
, vol.64
, pp. 212-215
-
-
Deprez, P.1
Sustronck, B.2
Van Loon, G.3
Muylle, E.4
-
259
-
-
0027372715
-
Deficit of inhibitory glycine receptors in spinal cord from Peruvian Pasos, evidence for an equine form of inherited myoclonus
-
Gundlach, A.L., Kortz, G., Burazin, T.C., Madigan, J., Higgins, R.J. Deficit of inhibitory glycine receptors in spinal cord from Peruvian Pasos, evidence for an equine form of inherited myoclonus. Brain Res. 1993, 628: 263-270.
-
(1993)
Brain Res.
, vol.628
, pp. 263-270
-
-
Gundlach, A.L.1
Kortz, G.2
Burazin, T.C.3
Madigan, J.4
Higgins, R.J.5
-
260
-
-
0027600611
-
Hypercoagulable state associated with a deficiency of protein C in a thoroughbred colt
-
Edens, L.M., Morris, D.D., Prasse, K.W., Anver, M.R. Hypercoagulable state associated with a deficiency of protein C in a thoroughbred colt. J. Vet. Intern. Med. 1993, 7: 190-193.
-
(1993)
J. Vet. Intern. Med.
, vol.7
, pp. 190-193
-
-
Edens, L.M.1
Morris, D.D.2
Prasse, K.W.3
Anver, M.R.4
-
261
-
-
0016881242
-
Male pseudohermaphroditism of the testicular feminizing type in a horse
-
Kieffer, N.M., Burns, S.J., Judge, N.C. Male pseudohermaphroditism of the testicular feminizing type in a horse. Equine Vet. J. 1976, 8: 38-41.
-
(1976)
Equine Vet. J.
, vol.8
, pp. 38-41
-
-
Kieffer, N.M.1
Burns, S.J.2
Judge, N.C.3
-
262
-
-
0025985831
-
Bleeding disorder (von Willebrand disease) in a quarter horse
-
Brooks, M., Leith, G.S., Allen, A.K., Woods, P.R., Benson, R.E., Dodds, W.J. Bleeding disorder (von Willebrand disease) in a quarter horse. J. Am. Vet. Med. Assoc. 1991, 198: 114-116.
-
(1991)
J. Am. Vet. Med. Assoc.
, vol.198
, pp. 114-116
-
-
Brooks, M.1
Leith, G.S.2
Allen, A.K.3
Woods, P.R.4
Benson, R.E.5
Dodds, W.J.6
-
263
-
-
0028106553
-
Dysfunctional growth hormone receptor in a strain of sex-linked dwarf chicken, evidence for a mutation in the intracellular domain
-
Agarwal, S.K., Cogburn, L.A., Burnside, J. Dysfunctional growth hormone receptor in a strain of sex-linked dwarf chicken, evidence for a mutation in the intracellular domain. J. Endocrinol. 1994, 142: 427-434.
-
(1994)
J. Endocrinol.
, vol.142
, pp. 427-434
-
-
Agarwal, S.K.1
Cogburn, L.A.2
Burnside, J.3
-
264
-
-
0033627949
-
Autosomal albino chicken mutation (ca/ca) deletes hexanucleotide (-deltaGACTGG817) at a copper-binding site of the tyrosinase gene
-
Tobita-Teramoto, T., ang, G.Y., Kino, K., Salter, D.W., Brumbaugh, J., Akiyama, T. Autosomal albino chicken mutation (ca/ca) deletes hexanucleotide (- deltaGACTGG817) at a copper-binding site of the tyrosinase gene. Poult. Sci. 2000, 79: 46-50.
-
(2000)
Poult. Sci.
, vol.79
, pp. 46-50
-
-
Tobita-Teramoto, T.1
Ang, G.Y.2
Kino, K.3
Salter, D.W.4
Brumbaugh, J.5
Akiyama, T.6
-
265
-
-
0023957713
-
Association of the slow feathering (K) and an endogenous viral (ev21) gene on the Z chromosome of chickens
-
Bacon, L.D., Smith, E., Crittenden, L.B., Havenstein, G.B. Association of the slow feathering (K) and an endogenous viral (ev21) gene on the Z chromosome of chickens. Poult. Sci. 1988, 67: 191-197.
-
(1988)
Poult. Sci.
, vol.67
, pp. 191-197
-
-
Bacon, L.D.1
Smith, E.2
Crittenden, L.B.3
Havenstein, G.B.4
-
266
-
-
0025518252
-
Molecular analysis of endogenous virus ev21-slow feathering complex of chickens. 1. Cloning of proviral-cell junction fragment and unoccupied integration site
-
Levin, I., Smith, E.J. Molecular analysis of endogenous virus ev21-slow feathering complex of chickens. 1. Cloning of proviral-cell junction fragment and unoccupied integration site. Poult. Sci. 1990, 69: 2017-2026.
-
(1990)
Poult. Sci.
, vol.69
, pp. 2017-2026
-
-
Levin, I.1
Smith, E.J.2
-
267
-
-
0026456258
-
The endogenous retroviral ev21 locus in commercial chicken lines and its relationship with the slow-feathering phenotype (K)
-
Boulliou, A., Le Pennec, J.P., Hubert, G., Donal, R., Smiley, M. The endogenous retroviral ev21 locus in commercial chicken lines and its relationship with the slow-feathering phenotype (K). Poult. Sci. 1992, 71: 38-46.
-
(1992)
Poult. Sci.
, vol.71
, pp. 38-46
-
-
Boulliou, A.1
Le Pennec, J.P.2
Hubert, G.3
Donal, R.4
Smiley, M.5
-
268
-
-
0025094771
-
Inheritance of the henny feathering trait in the golden Campine chicken, evidence for allelism with the gene that causes henny feathering in the Sebright bantam
-
George, F.W., Matsumine, H., McPhaul, M.J., Somes, R.G., Wilson, J.D. Inheritance of the henny feathering trait in the golden Campine chicken, evidence for allelism with the gene that causes henny feathering in the Sebright bantam. J. Hered. 1990, 81: 107-110.
-
(1990)
J. Hered.
, vol.81
, pp. 107-110
-
-
George, F.W.1
Matsumine, H.2
McPhaul, M.J.3
Somes, R.G.4
Wilson, J.D.5
-
269
-
-
0025724095
-
Aromatase mRNA in the extragonadal tissues of chickens with the henny-feathering trait is derived from a distinctive promoter structure that contains a segment of a retroviral long terminal repeat. Functional organization of the Sebright, Leghorn, and Campine aromalase genes
-
Matsumine, H., Herbst, M.A., Ou, S.H., Wilson, J.D., McPhaul, M.J. Aromatase mRNA in the extragonadal tissues of chickens with the henny-feathering trait is derived from a distinctive promoter structure that contains a segment of a retroviral long terminal repeat. Functional organization of the Sebright, Leghorn, and Campine aromalase genes. J. Biol. Chem. 1991, 266: 19900-19907.
-
(1991)
J. Biol. Chem.
, vol.266
, pp. 19900-19907
-
-
Matsumine, H.1
Herbst, M.A.2
Ou, S.H.3
Wilson, J.D.4
McPhaul, M.J.5
-
270
-
-
0026360772
-
The gene for aromatase (P450arom) in the chicken is located on the long arm of chromosome 1
-
Tereba, A., McPhaul, M.J., Wilson, J.D. The gene for aromatase (P450arom) in the chicken is located on the long arm of chromosome 1. J. Hered. 1991, 82: 80-81.
-
(1991)
J. Hered.
, vol.82
, pp. 80-81
-
-
Tereba, A.1
McPhaul, M.J.2
Wilson, J.D.3
-
271
-
-
0009756329
-
Nanomelia, a lethal mutation of the fowl
-
Landauer, W. Nanomelia, a lethal mutation of the fowl. J. Hered. 1965, 56: 131-138.
-
(1965)
J. Hered.
, vol.56
, pp. 131-138
-
-
Landauer, W.1
-
272
-
-
0027983560
-
Molecular basis of nanomelia, a heritable chondrodystrophy of chicken
-
Primorac, D., Stover, M.L., Clark, S.H., Rowe, D.W. Molecular basis of nanomelia, a heritable chondrodystrophy of chicken. Matrix Biol. 1994, 14: 297-305.
-
(1994)
Matrix Biol.
, vol.14
, pp. 297-305
-
-
Primorac, D.1
Stover, M.L.2
Clark, S.H.3
Rowe, D.W.4
-
273
-
-
0031947867
-
The CAR1 gene encoding a cellular receptor specific for subgroup B and D avian leukosis viruses maps to the chicken tvb locus
-
Smith, E.J., Brojatsch, J., Naughton, J., Young, J.A. The CAR1 gene encoding a cellular receptor specific for subgroup B and D avian leukosis viruses maps to the chicken tvb locus. J. Virol. 1998, 72: 3501-3503.
-
(1998)
J. Virol.
, vol.72
, pp. 3501-3503
-
-
Smith, E.J.1
Brojatsch, J.2
Naughton, J.3
Young, J.A.4
-
274
-
-
0037976660
-
Inherited riboflavin deficiency in chicken eggs
-
Maw, A.J.G. Inherited riboflavin deficiency in chicken eggs. Poult. Sci. 1954, 33: 216-217.
-
(1954)
Poult. Sci.
, vol.33
, pp. 216-217
-
-
Maw, A.J.G.1
-
275
-
-
0028229868
-
Effects of rRNA gene copy number and nucleolar variation on early development, inhibition of gastrulation in rDNA-deficient chick embryos
-
Delany, M.E., Muscarella, D.E., Bloom, S.E. Effects of rRNA gene copy number and nucleolar variation on early development, inhibition of gastrulation in rDNA-deficient chick embryos. J. Hered. 1994, 85: 211-217.
-
(1994)
J. Hered.
, vol.85
, pp. 211-217
-
-
Delany, M.E.1
Muscarella, D.E.2
Bloom, S.E.3
-
276
-
-
0023432358
-
Characterization of ribosomal RNA synthesis in a gene dosage mutant, the relationship of topoisomerase I and chromatin structure to transcriptional activity
-
Muscarella, D.E., Vogt, V.M., Bloom, S.E. Characterization of ribosomal RNA synthesis in a gene dosage mutant, the relationship of topoisomerase I and chromatin structure to transcriptional activity. J. Cell Biol. 1987, 105: 1501-1513.
-
(1987)
J. Cell Biol.
, vol.105
, pp. 1501-1513
-
-
Muscarella, D.E.1
Vogt, V.M.2
Bloom, S.E.3
-
277
-
-
0037976658
-
Contribution to the study of sex-linked diplopodia and Creeper achondroplasia in the chick embryo, in vitro culture of the cartilaginous primordia of the tibio-tarsus and the fibula
-
Kieny, M., Abbott, U.K. Contribution to the study of sex-linked diplopodia and Creeper achondroplasia in the chick embryo, in vitro culture of the cartilaginous primordia of the tibio-tarsus and the fibula. Dev. Biol. 1962, 4: 473-488.
-
(1962)
Dev. Biol.
, vol.4
, pp. 473-488
-
-
Kieny, M.1
Abbott, U.K.2
-
278
-
-
0027649902
-
Association of dominant marker traits and metric traits in chickens
-
Shoffner, R.N., Otis, J.S., Garwood, V.A. Association of dominant marker traits and metric traits in chickens. Poult. Sci. 1993, 72: 1405-1410.
-
(1993)
Poult. Sci.
, vol.72
, pp. 1405-1410
-
-
Shoffner, R.N.1
Otis, J.S.2
Garwood, V.A.3
-
279
-
-
0014085292
-
A gene for partial feather achromatosis in the fowl
-
Washburn, K.W., Smyth, J.R. A gene for partial feather achromatosis in the fowl. J. Hered. 1967, 58: 130-134.
-
(1967)
J. Hered.
, vol.58
, pp. 130-134
-
-
Washburn, K.W.1
Smyth, J.R.2
-
280
-
-
0014089236
-
Ametapodia, a dominant mutation in the fowl
-
Cole, R.K. Ametapodia, a dominant mutation in the fowl. J. Hered. 1967, 58: 141-146.
-
(1967)
J. Hered.
, vol.58
, pp. 141-146
-
-
Cole, R.K.1
-
281
-
-
0033920467
-
A new recessive ametapodia mutation in the chicken (Gallus domesticus)
-
Smyth, J.R., Sreekumar, G.P., Coyle, C.A, Bitgood, J.J. A new recessive ametapodia mutation in the chicken (Gallus domesticus). J. Hered. 2000, 91: 340-342.
-
(2000)
J. Hered.
, vol.91
, pp. 340-342
-
-
Smyth, J.R.1
Sreekumar, G.P.2
Coyle, C.A.3
Bitgood, J.J.4
-
282
-
-
0025375053
-
Spontaneous high density lipoprotein deficiency syndrome associated with a Z-linked mutation in chickens
-
Poernama, F., Schreyer, S.A., Bitgood, J.J., Cook, M.E., Attie, A.D. Spontaneous high density lipoprotein deficiency syndrome associated with a Z-linked mutation in chickens. J. Lipid Res. 1990, 31: 955-963.
-
(1990)
J. Lipid Res.
, vol.31
, pp. 955-963
-
-
Poernama, F.1
Schreyer, S.A.2
Bitgood, J.J.3
Cook, M.E.4
Attie, A.D.5
-
283
-
-
0024958383
-
Hereditary congenital baldness, a sex-linked trait in the domestic fowl
-
Somes, R.G. Hereditary congenital baldness, a sex-linked trait in the domestic fowl. J. Hered. 1989, 80: 493-496.
-
(1989)
J. Hered.
, vol.80
, pp. 493-496
-
-
Somes, R.G.1
-
284
-
-
0026199561
-
Use of the sex-linked barring (B) gene for chick sexing on an eumelanotic columbian background
-
Campo, J.L. Use of the sex-linked barring (B) gene for chick sexing on an eumelanotic columbian background. Poult. Sci. 1991, 70: 1469-1473.
-
(1991)
Poult. Sci.
, vol.70
, pp. 1469-1473
-
-
Campo, J.L.1
-
285
-
-
0027054929
-
Blastoderm degeneration, an early embryonic failure in dwarf Single Comb White Leghorn chickens
-
Savage, T.F., Mirosh, L.W., Jones, J.L., Schneiderman, E.T., Blastoderm degeneration, an early embryonic failure in dwarf Single Comb White Leghorn chickens. J. Hered. 1992, 83: 249-254.
-
(1992)
J. Hered.
, vol.83
, pp. 249-254
-
-
Savage, T.F.1
Mirosh, L.W.2
Jones, J.L.3
Schneiderman, E.T.4
-
286
-
-
0037638650
-
Refined linkage value for Pea comb and Blue Eggs, lack of effect of pea comb, blue egg, and naked neck on age at first egg in the domestic fowl
-
Bitgood, J.J., Otis, J.S., Shoffner, R.N. Refined linkage value for Pea comb and Blue Eggs, lack of effect of pea comb, blue egg, and naked neck on age at first egg in the domestic fowl. Poult. Sci. 1983, 62: 235-238.
-
(1983)
Poult. Sci.
, vol.62
, pp. 235-238
-
-
Bitgood, J.J.1
Otis, J.S.2
Shoffner, R.N.3
-
287
-
-
0347018128
-
Effect of the Na (Naked Neck) and O (Blue Eggshell) Genes on Egg Production, Egg Traits and Female Reproductive Performances According to the Ambient Temperature
-
Merat, P., Bordas, A., Coquerelle, G., Monvoisin, J.L. Effect of the Na (Naked Neck) and O (Blue Eggshell) Genes on Egg Production, Egg Traits and Female Reproductive Performances According to the Ambient Temperature. Arch. Geflügelk. 1991, 55: 130-133.
-
(1991)
Arch. Geflügelk.
, vol.55
, pp. 130-133
-
-
Merat, P.1
Bordas, A.2
Coquerelle, G.3
Monvoisin, J.L.4
-
288
-
-
0028021480
-
Tissue-specific expression of mouse tyrosinase gene in cultured chicken cells
-
Akiyama, T., Whitaker, B., Federspiel, M., Hughes, S.H., Yamamoto, H., Takeuchi, T., Brumbaugh, J. Tissue-specific expression of mouse tyrosinase gene in cultured chicken cells. Exp. Cell Res. 1994, 214: 154-162.
-
(1994)
Exp. Cell Res.
, vol.214
, pp. 154-162
-
-
Akiyama, T.1
Whitaker, B.2
Federspiel, M.3
Hughes, S.H.4
Yamamoto, H.5
Takeuchi, T.6
Brumbaugh, J.7
-
289
-
-
0014802705
-
Sex-linked coloboma in the chicken
-
Abbott, U.K., Craig, R.M., Bennett, E.B. Sex-linked coloboma in the chicken. J. Hered. 1970, 61: 95-105.
-
(1970)
J. Hered.
, vol.61
, pp. 95-105
-
-
Abbott, U.K.1
Craig, R.M.2
Bennett, E.B.3
-
290
-
-
0029775054
-
Shh, HoxD, Bmp-2, and Fgf-4 gene expression during development of the polydactylous talpid2, diplopodial, and diplopodia4 mutant chick limb buds
-
Rodriguez, C., Kos, R., Macias, D., Abbott, U.K., Izpisua Belmonte, J.C. Shh, HoxD, Bmp-2, and Fgf-4 gene expression during development of the polydactylous talpid2, diplopodial, and diplopodia4 mutant chick limb buds. Dev. Genet. 1996, 19: 26-32.
-
(1996)
Dev. Genet.
, vol.19
, pp. 26-32
-
-
Rodriguez, C.1
Kos, R.2
Macias, D.3
Abbott, U.K.4
Izpisua Belmonte, J.C.5
-
291
-
-
0015352765
-
Further studies on diplopodia. V. Diplopodia-3
-
Taylor, L.W. Further studies on diplopodia. V. Diplopodia-3. Can. J. Genet. Cytol. 1972, 14: 417-422.
-
(1972)
Can. J. Genet. Cytol.
, vol.14
, pp. 417-422
-
-
Taylor, L.W.1
-
292
-
-
0026708381
-
Role of the chicken homeobox-containing genes GHox-4.6 and GHox-8 in the specification of positional identities during the development of normal and polydactylous chick limb buds
-
Coelho, C.N., Upholt, W.B., Kosher, R.A. Role of the chicken homeobox-containing genes GHox-4.6 and GHox-8 in the specification of positional identities during the development of normal and polydactylous chick limb buds. Development 1992, 115: 629-637.
-
(1992)
Development
, vol.115
, pp. 629-637
-
-
Coelho, C.N.1
Upholt, W.B.2
Kosher, R.A.3
-
293
-
-
0031845674
-
The HMGI-C gene is a likely candidate for the autosomal dwarf locus in the chicken
-
Ruyter-Spira, C.P., de Groof, A.J., van der Poel, J.J., Herbergs, J., Masabanda, J., Fries, R., Groenen, M.A. The HMGI-C gene is a likely candidate for the autosomal dwarf locus in the chicken. J. Hered. 1998, 89: 295-300.
-
(1998)
J. Hered.
, vol.89
, pp. 295-300
-
-
Ruyter-Spira, C.P.1
de Groof, A.J.2
van der Poel, J.J.3
Herbergs, J.4
Masabanda, J.5
Fries, R.6
Groenen, M.A.7
-
294
-
-
84981839229
-
Crooked neck dwarf lethal syndrome in domestic fowl
-
Pun, C.F. Crooked neck dwarf lethal syndrome in domestic fowl. J. Exp. Zool. 1954, 126: 101-133.
-
(1954)
J. Exp. Zool.
, vol.126
, pp. 101-133
-
-
Pun, C.F.1
-
295
-
-
0029913716
-
Linkage analysis of endogenous viral element 1: Blue eggshell, and pea comb loci in chickens
-
Bartlett, J.R., Jones, C.P., Smith, E.J. Linkage analysis of endogenous viral element 1: blue eggshell, and pea comb loci in chickens. J. Hered. 1996, 87: 67-70.
-
(1996)
J. Hered.
, vol.87
, pp. 67-70
-
-
Bartlett, J.R.1
Jones, C.P.2
Smith, E.J.3
-
296
-
-
0037976653
-
A new mutant causing epileptiform seizures in domestic fowl
-
Crawford, R.D. A new mutant causing epileptiform seizures in domestic fowl. Poult. Sci. 1969, 48: 1799.
-
(1969)
Poult. Sci.
, vol.48
, pp. 1799
-
-
Crawford, R.D.1
-
297
-
-
0025488073
-
Test for linkage between the eumelanin dilution blue (B1), the extended black (E) allele at the E-locus and the linked pea comb (P) and eumelanin extension (M1) genes in the domestic fowl
-
Carefoot, W.C. Test for linkage between the eumelanin dilution blue (B1), the extended black (E) allele at the E-locus and the linked pea comb (P) and eumelanin extension (M1) genes in the domestic fowl. Br. Poult. Sci. 1990, 31: 465-472.
-
(1990)
Br. Poult. Sci.
, vol.31
, pp. 465-472
-
-
Carefoot, W.C.1
-
298
-
-
0023300903
-
Test for linkage between the eumelanin restrictor (Db) and the eumelanin extension (M1) genes in the domestic fowl
-
Carefoot, W.C. Test for linkage between the eumelanin restrictor (Db) and the eumelanin extension (M1) genes in the domestic fowl. Br. Poult. Sci. 1987, 28: 69-73.
-
(1987)
Br. Poult. Sci.
, vol.28
, pp. 69-73
-
-
Carefoot, W.C.1
-
299
-
-
0023352329
-
Relative positions of the loci of the peacomb (P), eumelanin restrictor (Db), eumelanin extension (M1) and plumage pattern (Pg) genes of the domestic fowl
-
Carefoot, W.C. Relative positions of the loci of the peacomb (P), eumelanin restrictor (Db), eumelanin extension (M1) and plumage pattern (Pg) genes of the domestic fowl. Br. Poult. Sci. 1987, 28: 347-350.
-
(1987)
Br. Poult. Sci.
, vol.28
, pp. 347-350
-
-
Carefoot, W.C.1
-
300
-
-
0037513601
-
Linkage Relationship Between the Pea Comb (P) and Extended Black (E) Loci of the Chicken
-
Smyth, J.R., Deleon, F.A.P. Linkage Relationship Between the Pea Comb (P) and Extended Black (E) Loci of the Chicken. Poult. Sci. 1992, 71: 208-210.
-
(1992)
Poult. Sci.
, vol.71
, pp. 208-210
-
-
Smyth, J.R.1
Deleon, F.A.P.2
-
301
-
-
0023003282
-
Faded shaker, a lethal pigment and neurological mutation in the chicken
-
Silversides, F.G., Smyth, J.R. Faded shaker, a lethal pigment and neurological mutation in the chicken. J. Hered. 1986, 77: 295-300.
-
(1986)
J. Hered.
, vol.77
, pp. 295-300
-
-
Silversides, F.G.1
Smyth, J.R.2
-
302
-
-
0026215935
-
Albinism in White Leghorn chickens
-
Bitgood, J.J., Smyth, J.R. Albinism in White Leghorn chickens. Poult. Sci. 1991, 70: 1861-1863.
-
(1991)
Poult. Sci.
, vol.70
, pp. 1861-1863
-
-
Bitgood, J.J.1
Smyth, J.R.2
-
304
-
-
0038653090
-
Genetic Aspects of a New Mutation (Sal-S) to Sex-Linked Imperfect Albinism in Chickens
-
Silversides, F.G., Crawford, R.D. Genetic Aspects of a New Mutation (Sal-S) to Sex-Linked Imperfect Albinism in Chickens. Genet. Sel. Evol. 1990, 22: 447-455.
-
(1990)
Genet. Sel. Evol.
, vol.22
, pp. 447-455
-
-
Silversides, F.G.1
Crawford, R.D.2
-
305
-
-
0030226691
-
Chocolate, a sex-linked recessive plumage colour mutant of the domestic fowl
-
Carefoot, W.C. Chocolate, a sex-linked recessive plumage colour mutant of the domestic fowl. Br. Poult. Sci. 1996, 37: 867-868.
-
(1996)
Br. Poult. Sci.
, vol.37
, pp. 867-868
-
-
Carefoot, W.C.1
-
306
-
-
0036251707
-
Testing homology of loci for two plumage colors, "lavender" and "recessive white," with chicken and Japanese quail hybrids
-
Minvielle, F., Gourichon, D., Monvoisin, J.L. Testing homology of loci for two plumage colors, "lavender" and "recessive white," with chicken and Japanese quail hybrids. J. Hered. 2002, 93: 73-76.
-
(2002)
J. Hered.
, vol.93
, pp. 73-76
-
-
Minvielle, F.1
Gourichon, D.2
Monvoisin, J.L.3
-
307
-
-
0037976655
-
New loci in the sex chromosome of the fowl
-
Hutt, F.B. New loci in the sex chromosome of the fowl. Heredity 1960, 15: 97-110.
-
(1960)
Heredity
, vol.15
, pp. 97-110
-
-
Hutt, F.B.1
-
308
-
-
0038314089
-
Energy Metabolism of Laying Hens of Different Genotypes Exposed to High Ambient Temperatures. 2. Influence of the Gene for Curling Feathers (F) on Performance and Energy Metabolism of Full vs Partly Feathered Normal and Dwarfed Laying Hens
-
Manner, K. Energy Metabolism of Laying Hens of Different Genotypes Exposed to High Ambient Temperatures. 2. Influence of the Gene for Curling Feathers (F) on Performance and Energy Metabolism of Full vs Partly Feathered Normal and Dwarfed Laying Hens. Arch. Geflügelk. 1992, 56: 8-13.
-
(1992)
Arch. Geflügelk.
, vol.56
, pp. 8-13
-
-
Manner, K.1
-
309
-
-
0038314088
-
Structure of Frizzle mutant feather keratin
-
Krimm, S. Structure of Frizzle mutant feather keratin. J. Mol. Biol. 1960, 2: 247-249.
-
(1960)
J. Mol. Biol.
, vol.2
, pp. 247-249
-
-
Krimm, S.1
-
310
-
-
33750616811
-
Direct and Indirect Effects of the Frizzle Gene (F) for the Productive Adaptability of Layers
-
Haarenkiso, A.V., Horst, P., Zarate, A.V. Direct and Indirect Effects of the Frizzle Gene (F) for the Productive Adaptability of Layers. Arch. Geflügelk. 1994, 58: 248-257.
-
(1994)
Arch. Geflügelk.
, vol.58
, pp. 248-257
-
-
Haarenkiso, A.V.1
Horst, P.2
Zarate, A.V.3
-
311
-
-
0037976652
-
A sex-linked mutation causing low hatchability in the broiler chicken
-
Presented in
-
Sheridan, A.K. A sex-linked mutation causing low hatchability in the broiler chicken. Presented in, Poult. Sci. Conven. 1964, 87-90.
-
(1964)
Poult. Sci. Conven.
, pp. 87-90
-
-
Sheridan, A.K.1
-
312
-
-
0026315619
-
Altered expression of the chicken homeobox-containing genes GHox-7 and GHox-8 in the limb buds of limbless mutant chick embryos
-
Coelho, C.N., Krabbenhoft, K.M., Upholt, W.B., Fallon, J.F., Kosher, R.A. Altered expression of the chicken homeobox-containing genes GHox-7 and GHox-8 in the limb buds of limbless mutant chick embryos. Development 1991, 113: 1487-1493.
-
(1991)
Development
, vol.113
, pp. 1487-1493
-
-
Coelho, C.N.1
Krabbenhoft, K.M.2
Upholt, W.B.3
Fallon, J.F.4
Kosher, R.A.5
-
313
-
-
0037638663
-
An identified micromelia in the domestic fowl
-
Asmundson, V.S. An identified micromelia in the domestic fowl. J. Hered. 1942, 33: 328-330.
-
(1942)
J. Hered.
, vol.33
, pp. 328-330
-
-
Asmundson, V.S.1
-
314
-
-
0008303095
-
Inherited muscle abnormality in the domestic fowl
-
Asmundson, V.S., Julian, L.M. Inherited muscle abnormality in the domestic fowl. J. Hered. 1956, 47: 248-250.
-
(1956)
J. Hered.
, vol.47
, pp. 248-250
-
-
Asmundson, V.S.1
Julian, L.M.2
-
315
-
-
0018616841
-
Genetic analyses of an immunodeficiency in hereditary muscular dystrophic chickens
-
Kline, K., Morton, C.J., Sanders, B.G. Genetic analyses of an immunodeficiency in hereditary muscular dystrophic chickens. J. Hered. 1979, 70: 354-356.
-
(1979)
J. Hered.
, vol.70
, pp. 354-356
-
-
Kline, K.1
Morton, C.J.2
Sanders, B.G.3
-
316
-
-
0036173682
-
Localization of the muscular dystrophy AM locus using a chicken linkage map constructed with the Kobe University resource family
-
Lee, E.J., Yoshizawa, K., Mannen, H., Kikuchi, H., Kikuchi, T., Mizutani, M., Tsuji, S. Localization of the muscular dystrophy AM locus using a chicken linkage map constructed with the Kobe University resource family. Anim. Genet. 2002, 33: 42-48.
-
(2002)
Anim. Genet.
, vol.33
, pp. 42-48
-
-
Lee, E.J.1
Yoshizawa, K.2
Mannen, H.3
Kikuchi, H.4
Kikuchi, T.5
Mizutani, M.6
Tsuji, S.7
-
317
-
-
0011985466
-
Naked neck gene, laing performance and food efficiency according to temperature in the fowl
-
Bordas, A., Monnet, L.E., Merat, P. Naked neck gene, laing performance and food efficiency according to temperature in the fowl. Annales de Genetique et de Selection Animale 1980, 12: 343-361.
-
(1980)
Annales de Genetique et de Selection Animale
, vol.12
, pp. 343-361
-
-
Bordas, A.1
Monnet, L.E.2
Merat, P.3
-
318
-
-
0033820174
-
Mapping the Naked Neck (NA) and Polydactyly (PO) mutants of the chicken with microsatellite molecular markers
-
Pitel, F., Berge, R., Coquerelle, G., Crooijmans, R.P.M.A., Groenen, M.A., Vignal, A., Tixier-Boichard, M. Mapping the Naked Neck (NA) and Polydactyly (PO) mutants of the chicken with microsatellite molecular markers. Genetics Selection Evolution 2000, 32: 73-86.
-
(2000)
Genetics Selection Evolution
, vol.32
, pp. 73-86
-
-
Pitel, F.1
Berge, R.2
Coquerelle, G.3
Crooijmans, R.P.M.A.4
Groenen, M.A.5
Vignal, A.6
Tixier-Boichard, M.7
-
319
-
-
0037638662
-
Paroxysm - A sex linked lethal in the fowl
-
Cole, R.K. Paroxysm - a sex linked lethal in the fowl. Poult. Sci. 1958, 37: 1194-1195.
-
(1958)
Poult. Sci.
, vol.37
, pp. 1194-1195
-
-
Cole, R.K.1
-
320
-
-
0037638659
-
The effect of comb-type genotypes on six metric traits in apopulation of meat-type chickens
-
Kan, J., Manasco, B.D., Gyles, N.R., Smith, R.M. The effect of comb-type genotypes on six metric traits in apopulation of meat-type chickens. Poult. Sci. 1959, 38: 826-828.
-
(1959)
Poult. Sci.
, vol.38
, pp. 826-828
-
-
Kan, J.1
Manasco, B.D.2
Gyles, N.R.3
Smith, R.M.4
-
321
-
-
0014516350
-
Genetic perosis in the domestic fowl
-
Somes, R.G. Genetic perosis in the domestic fowl. J. Hered. 1969, 60: 163-166.
-
(1969)
J. Hered.
, vol.60
, pp. 163-166
-
-
Somes, R.G.1
-
322
-
-
0023473644
-
Evidence that the mottled (mo) and pied (pi) plumage genes of the domestic fowl are identical
-
Carefoot WC, Evidence that the mottled (mo) and pied (pi) plumage genes of the domestic fowl are identical. Br. Poult. Sci. 1987, 28: 753-754.
-
(1987)
Br. Poult. Sci.
, vol.28
, pp. 753-754
-
-
Carefoot, W.C.1
-
323
-
-
0030229302
-
Close linkage relationship of the Z-linked pop-eye and silver plumage color loci in the chicken
-
Bitgood, J.J., Rozum, J.J., Rozum, J.J. Close linkage relationship of the Z-linked pop-eye and silver plumage color loci in the chicken. Poult. Sci. 1996, 75: 1067-1068.
-
(1996)
Poult. Sci.
, vol.75
, pp. 1067-1068
-
-
Bitgood, J.J.1
Rozum, J.J.2
Rozum, J.J.3
-
324
-
-
0014035834
-
Prenatal, a sex-linked lethal mutation of the fowl
-
Somes, R.G., Smyth, J.R. Prenatal, a sex-linked lethal mutation of the fowl. J. Hered. 1967, 58: 2529.
-
(1967)
J. Hered.
, vol.58
, pp. 2529
-
-
Somes, R.G.1
Smyth, J.R.2
-
325
-
-
0037638661
-
The effect of a protoporphyrin mutant on some economic traits of the chicken
-
Shoffner, R.N., Shuman, R., Otis, J.S., Bitgood, J.J., Garwood, V.A., Lowe, P. The effect of a protoporphyrin mutant on some economic traits of the chicken. Poult. Sci. 1982, 61: 817-820.
-
(1982)
Poult. Sci.
, vol.61
, pp. 817-820
-
-
Shoffner, R.N.1
Shuman, R.2
Otis, J.S.3
Bitgood, J.J.4
Garwood, V.A.5
Lowe, P.6
-
326
-
-
0024509492
-
Oocytes from the Mutant Restricted Ovulator Hen Lack Receptor for Very Low Density Lipoprotein
-
Nimpf, J., Radosavljevic, M.J., Schneider, W.J. Oocytes from the Mutant Restricted Ovulator Hen Lack Receptor for Very Low Density Lipoprotein. J. Biol. Chem. 1989, 264: 1393-1398.
-
(1989)
J. Biol. Chem.
, vol.264
, pp. 1393-1398
-
-
Nimpf, J.1
Radosavljevic, M.J.2
Schneider, W.J.3
-
327
-
-
0030227862
-
A rapid, polymerase chain reaction-based procedure for identifying mutant restricted ovulator chickens
-
Bujo, H., Elkin, R.G., Lindstedt, K.A., Nimpf, J., Bitgood, J.J., Schneider, W.J. A rapid, polymerase chain reaction-based procedure for identifying mutant restricted ovulator chickens. Poult. Sci. 1996, 75: 1113-1117.
-
(1996)
Poult. Sci.
, vol.75
, pp. 1113-1117
-
-
Bujo, H.1
Elkin, R.G.2
Lindstedt, K.A.3
Nimpf, J.4
Bitgood, J.J.5
Schneider, W.J.6
-
328
-
-
0029884378
-
Expression of GCAP1 and GCAP2 in the retinal degeneration (rd) mutant chicken retina
-
Semple-Rowland, S.L., Gorczyca, W.A., Buczylko, J., Helekar, B.S., Ruiz, C.C., Subbaraya, I., Palczewski, K., Baehr, W. Expression of GCAP1 and GCAP2 in the retinal degeneration (rd) mutant chicken retina. FEBS Letters 1996, 385: 47-52.
-
(1996)
FEBS Letters
, vol.385
, pp. 47-52
-
-
Semple-Rowland, S.L.1
Gorczyca, W.A.2
Buczylko, J.3
Helekar, B.S.4
Ruiz, C.C.5
Subbaraya, I.6
Palczewski, K.7
Baehr, W.8
-
329
-
-
0032703824
-
rd and rc chickens carry the same GC1 null allele (GUCY1)
-
Semple-Rowland, S.L., Cheng, K.M. rd and rc chickens carry the same GC1 null allele (GUCY1). Exp. Eye Res. 1999, 69: 579-581.
-
(1999)
Exp. Eye Res.
, vol.69
, pp. 579-581
-
-
Semple-Rowland, S.L.1
Cheng, K.M.2
-
330
-
-
0033612647
-
Characterization of the chicken GCAP gene array and analyses of GCAP1, GCAP2, and GC1 gene expression in normal and rd chicken pineal
-
Semple-Rowland, S.L., Larkin, P., Bronson, J.D., Nykamp, K., Streit, W.J., Baehr, W. Characterization of the chicken GCAP gene array and analyses of GCAP1, GCAP2, and GC1 gene expression in normal and rd chicken pineal. Mol. Vis. 1999, 5: 7-14.
-
(1999)
Mol. Vis.
, vol.5
, pp. 7-14
-
-
Semple-Rowland, S.L.1
Larkin, P.2
Bronson, J.D.3
Nykamp, K.4
Streit, W.J.5
Baehr, W.6
-
331
-
-
0027381381
-
Riboflavinuria in the rd Chicken - 5′-Splice Site Mutation in the Gene for Riboflavin-Binding Protein
-
MacLachlan, I., Nimpf, J., White, H.B., Schneider, W.J. Riboflavinuria in the rd Chicken - 5′-Splice Site Mutation in the Gene for Riboflavin-Binding Protein. J. Biol. Chem. 1993, 268: 23222-23226.
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 23222-23226
-
-
MacLachlan, I.1
Nimpf, J.2
White, H.B.3
Schneider, W.J.4
-
332
-
-
0037976657
-
The relationship between rose comb and reproduction in the domestic fowl
-
Crawford, R.D., Merritt, E.S. The relationship between rose comb and reproduction in the domestic fowl. Can. J. Genet. Cytol. 1963, 5: 89-95.
-
(1963)
Can. J. Genet. Cytol.
, vol.5
, pp. 89-95
-
-
Crawford, R.D.1
Merritt, E.S.2
-
333
-
-
0013637993
-
Scaleless, an inherited ectodermal defect in the domestic fowl
-
Abbott, U.K., Asmundson, V.S. Scaleless, an inherited ectodermal defect in the domestic fowl. J. Hered. 1957, 46: 63-70.
-
(1957)
J. Hered.
, vol.46
, pp. 63-70
-
-
Abbott, U.K.1
Asmundson, V.S.2
-
334
-
-
0026453448
-
Analysis of Seminal Plasma from Roosters Carring the Sd (Sperm Degeneration) Allele
-
Alaghbari, A., Engel, H.N., Froman, D.P. Analysis of Seminal Plasma from Roosters Carring the Sd (Sperm Degeneration) Allele. Biol. Reprod. 1992, 47: 1059-1063.
-
(1992)
Biol. Reprod.
, vol.47
, pp. 1059-1063
-
-
Alaghbari, A.1
Engel, H.N.2
Froman, D.P.3
-
335
-
-
0037638660
-
A second talpidlike mutation in the fowl
-
Abbott, U.K., Taylor, L.W., Abplanalp, H. A second talpidlike mutation in the fowl. Poult. Sci. 1959, 38: 1185-1262.
-
(1959)
Poult. Sci.
, vol.38
, pp. 1185-1262
-
-
Abbott, U.K.1
Taylor, L.W.2
Abplanalp, H.3
-
336
-
-
0037638664
-
Developmental abnormalities in the trunk and limbs of the talpid-3 mutant of the fowl
-
Ede, D.A., Kelly, W.A. Developmental abnormalities in the trunk and limbs of the talpid-3 mutant of the fowl. J. Embryol. Exp. Morphol. 1964, 12: 339-356.
-
(1964)
J. Embryol. Exp. Morphol.
, vol.12
, pp. 339-356
-
-
Ede, D.A.1
Kelly, W.A.2
-
337
-
-
0019536413
-
White skin, a Z-linked recessive mutation in the fowl
-
McGibbon, W.H. White skin, a Z-linked recessive mutation in the fowl. J. Hered. 1981, 72: 139-140.
-
(1981)
J. Hered.
, vol.72
, pp. 139-140
-
-
McGibbon, W.H.1
-
338
-
-
0001230798
-
Wingless poultry
-
Pease, M.S. Wingless poultry. J. Hered. 1962, 53: 109-110.
-
(1962)
J. Hered.
, vol.53
, pp. 109-110
-
-
Pease, M.S.1
-
339
-
-
0026848621
-
Chromosome substitution effects associated with kappa-casein and beta-lactoglobulin in Holstein cattle
-
Cowan, C.M., Dentine, M.R., Coyle, T. Chromosome substitution effects associated with kappa-casein and beta-lactoglobulin in Holstein cattle. J. Dairy Sci. 1992, 75: 1097-1104.
-
(1992)
J. Dairy Sci.
, vol.75
, pp. 1097-1104
-
-
Cowan, C.M.1
Dentine, M.R.2
Coyle, T.3
-
340
-
-
0025827079
-
Molecular defects in the E1 alpha subunit of the branched-chain alpha-ketoacid dehydrogenase complex that cause maple syrup urine disease
-
Zhang, B., Zhao, Y., Harris, R.A., Crabb, D.W. Molecular defects in the E1 alpha subunit of the branched-chain alpha-ketoacid dehydrogenase complex that cause maple syrup urine disease. Mol. Biol. Med. 1991, 8: 39-47.
-
(1991)
Mol. Biol. Med.
, vol.8
, pp. 39-47
-
-
Zhang, B.1
Zhao, Y.2
Harris, R.A.3
Crabb, D.W.4
-
341
-
-
0033727551
-
Physical and linkage mapping of the bovine acidic alpha-glucosidase gene to chromosome 19
-
Tammen, I., Larsson, U., Bergknut, N., Barendse, W., Moran, C., Dennis, J.A. Physical and linkage mapping of the bovine acidic alpha-glucosidase gene to chromosome 19. Anim. Genet. 2000, 31: 285-286.
-
(2000)
Anim. Genet.
, vol.31
, pp. 285-286
-
-
Tammen, I.1
Larsson, U.2
Bergknut, N.3
Barendse, W.4
Moran, C.5
Dennis, J.A.6
-
342
-
-
0034141661
-
Chediak-Higashi syndrome mutation and genetic testing in Japanese black cattle (Wagyu)
-
Yamakuchi, H., Agaba, M., Hirano, T., Hara, K., Todoroki, J., Mizoshita, K., Kubota, C., Tabara, N., Sugimoto, Y. Chediak-Higashi syndrome mutation and genetic testing in Japanese black cattle (Wagyu). Anim. Genet. 2000, 31: 13-19.
-
(2000)
Anim. Genet.
, vol.31
, pp. 13-19
-
-
Yamakuchi, H.1
Agaba, M.2
Hirano, T.3
Hara, K.4
Todoroki, J.5
Mizoshita, K.6
Kubota, C.7
Tabara, N.8
Sugimoto, Y.9
-
343
-
-
0033251627
-
SSCP analysis at the bovine CSN3 locus discriminates six alleles corresponding to known protein variants (A, B, C, E, F, G) and three new DNA polymorphisms (H, I, A1)
-
Prinzenberg, E.M., Krause, I., Erhardt, G. SSCP analysis at the bovine CSN3 locus discriminates six alleles corresponding to known protein variants (A, B, C, E, F, G) and three new DNA polymorphisms (H, I, A1). Anim. Biotechnol. 1999, 10: 49-62.
-
(1999)
Anim. Biotechnol.
, vol.10
, pp. 49-62
-
-
Prinzenberg, E.M.1
Krause, I.2
Erhardt, G.3
-
344
-
-
0034433421
-
A DNA polymorphism influencing alpha(1,2)fucosyltransferase activity of the pig FUT1 enzyme determines susceptibility of small intestinal epithelium to Escherichia coli F18 adhesion
-
Meijerink, E., Neuenschwander, S., Fries, R., Dinter, A., Bertschinger, H.U., Stranzinger, G., Vögeli, P. A DNA polymorphism influencing alpha(1,2)fucosyltransferase activity of the pig FUT1 enzyme determines susceptibility of small intestinal epithelium to Escherichia coli F18 adhesion. Immunogenetics 2000, 52: 129-136.
-
(2000)
Immunogenetics
, vol.52
, pp. 129-136
-
-
Meijerink, E.1
Neuenschwander, S.2
Fries, R.3
Dinter, A.4
Bertschinger, H.U.5
Stranzinger, G.6
Vögeli, P.7
-
345
-
-
0034153456
-
Rapid communication, linkage and physical mapping of the porcine melanocortin-4 receptor (MC4R) gene
-
Kim, K.S., Larsen, N.J., Rothschild, M.F. Rapid communication, linkage and physical mapping of the porcine melanocortin-4 receptor (MC4R) gene. J. Anim. Sci. 2000, 78: 791-792.
-
(2000)
J. Anim. Sci.
, vol.78
, pp. 791-792
-
-
Kim, K.S.1
Larsen, N.J.2
Rothschild, M.F.3
-
346
-
-
0030174243
-
Linkage mapping of the retinoic acid receptor-gamma gene to porcine chromosome 5
-
Messer. L., Wang, L., Yelich, J., Pomp, D., Geisert, R., Rothschild, M.F. Linkage mapping of the retinoic acid receptor-gamma gene to porcine chromosome 5. Anim. Genet. 1996, 27: 175-177.
-
(1996)
Anim. Genet.
, vol.27
, pp. 175-177
-
-
Messer, L.1
Wang, L.2
Yelich, J.3
Pomp, D.4
Geisert, R.5
Rothschild, M.F.6
-
347
-
-
0031889436
-
A comprehensive evolutionary analysis based on nucleotide and amino acid sequences of the alpha-and beta-subunits of glycoprotein hormone gene family
-
Li, M.D., Ford, J.J. A comprehensive evolutionary analysis based on nucleotide and amino acid sequences of the alpha-and beta-subunits of glycoprotein hormone gene family. J. Endocrinol. 1998, 156: 529-542.
-
(1998)
J. Endocrinol.
, vol.156
, pp. 529-542
-
-
Li, M.D.1
Ford, J.J.2
-
348
-
-
0026018717
-
Immunochemical studies of ferrochelatase protein, characterization of the normal and mutant protein in bovine and human protoporphyria
-
Straka, J.G., Hill, H.D., Krikava, J.M., Kools, A.M., Bloomer, J.R. Immunochemical studies of ferrochelatase protein, characterization of the normal and mutant protein in bovine and human protoporphyria. Am. J. Hum. Genet. 1991, 48: 72-78.
-
(1991)
Am. J. Hum. Genet.
, vol.48
, pp. 72-78
-
-
Straka, J.G.1
Hill, H.D.2
Krikava, J.M.3
Kools, A.M.4
Bloomer, J.R.5
-
349
-
-
0028908970
-
Molecular cloning and characterization of bovine beta-mannosidase
-
Chen, H., Leipprandt, J.R., Traviss, C.E., Sopher, B.L., Jones, M.Z., Cavanagh, K.T., Friderici, K.H. Molecular cloning and characterization of bovine beta-mannosidase. J. Biol. Chem. 1995, 270: 3841-3848.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 3841-3848
-
-
Chen, H.1
Leipprandt, J.R.2
Traviss, C.E.3
Sopher, B.L.4
Jones, M.Z.5
Cavanagh, K.T.6
Friderici, K.H.7
|