-
1
-
-
0017558067
-
Albinism in Icelandic sheep.
-
Adalsteinsson, S. (1977). Albinism in Icelandic sheep. Journal of Heredity 68, 347-349.
-
(1977)
Journal of Heredity
, vol.68
, pp. 347-349
-
-
Adalsteinsson, S.1
-
2
-
-
0033866632
-
Tyrosinase gene variants indifferent rabbit strains.
-
Aigner, B., Besenfelder, U., Müller, M. & Brem, G. (2000). Tyrosinase gene variants indifferent rabbit strains. Mammalian Genome 11, 700-702.
-
(2000)
Mammalian Genome
, vol.11
, pp. 700-702
-
-
Aigner, B.1
Besenfelder, U.2
Müller, M.3
Brem, G.4
-
3
-
-
68949198769
-
Genetic architecture of tameness in a rat model of animal domestication.
-
Albert, F. W., Carlborg, Ö., Plyusnina, I., Besnier, F., Hedwig, D., Lautenschläger, S., Lorenz, D., McIntosh, J., Neumann, C., Richter, H., Zeising, C., Kozhemyakina, R., Shchepina, O., Kratsch, J., Trut, L., Teupser, D., Thiery, J., Schöneberg, T., Andersson, L. & Pääbo, S. (2009). Genetic architecture of tameness in a rat model of animal domestication. Genetics 182, 541-554.
-
(2009)
Genetics
, vol.182
, pp. 541-554
-
-
Albert, F.W.1
Carlborg, O.2
Plyusnina, I.3
Besnier, F.4
Hedwig, D.5
Lautenschläger, S.6
Lorenz, D.7
McIntosh, J.8
Neumann, C.9
Richter, H.10
Zeising, C.11
Kozhemyakina, R.12
Shchepina, O.13
Kratsch, J.14
Trut, L.15
Teupser, D.16
Thiery, J.17
Schöneberg, T.18
Andersson, L.19
Pääbo, S.20
more..
-
4
-
-
0035425773
-
Melanosomal pH controls rate of melanogenesis, eumelanin/phaeomelanin ratio and melanosome maturation in melanocytes and melanoma cells.
-
Ancans, J., Tobin, D. J., Hoogduijn, M. J., Smit, N. P., Wakamatsu, K. & Thody, A. J. (2001). Melanosomal pH controls rate of melanogenesis, eumelanin/phaeomelanin ratio and melanosome maturation in melanocytes and melanoma cells. Experimental Cell Research 268, 26-35.
-
(2001)
Experimental Cell Research
, vol.268
, pp. 26-35
-
-
Ancans, J.1
Tobin, D.J.2
Hoogduijn, M.J.3
Smit, N.P.4
Wakamatsu, K.5
Thody, A.J.6
-
5
-
-
62149151949
-
Molecular and evolutionary history of melanism in North American gray wolves.
-
Anderson, T. M., Von Holdt, B. M., Candille, S. I., Musiani, M., Greco, C., Stahler, D. R., Smith, D. W., Padhukasahasram, B., Randi, E., Leonard, J. A., Bustamante, C. D., Ostrander, E. A., Tang, H., Wayne, R. K. & Barsh, G. S. (2009). Molecular and evolutionary history of melanism in North American gray wolves. Science 323, 1339-1343.
-
(2009)
Science
, vol.323
, pp. 1339-1343
-
-
Anderson, T.M.1
Von Holdt, B.M.2
Candille, S.I.3
Musiani, M.4
Greco, C.5
Stahler, D.R.6
Smith, D.W.7
Padhukasahasram, B.8
Randi, E.9
Leonard, J.A.10
Bustamante, C.D.11
Ostrander, E.A.12
Tang, H.13
Wayne, R.K.14
Barsh, G.S.15
-
6
-
-
0038389317
-
Melanocortin receptor variants with phenotypic effects in horse, pig, and chicken.
-
Andersson, L. (2003). Melanocortin receptor variants with phenotypic effects in horse, pig, and chicken. Annals of the New York Academy of Sciences 994, 313-318.
-
(2003)
Annals of the New York Academy of Sciences
, vol.994
, pp. 313-318
-
-
Andersson, L.1
-
7
-
-
55949127974
-
Albinism in the American mink (Neovison vison) is associated with a tyrosinase nonsense mutation.
-
Anistoroaei, R., Fredholm, M., Christensen, K. & Leeb, T. (2008). Albinism in the American mink (Neovison vison) is associated with a tyrosinase nonsense mutation. Animal Genetics 39, 645-648.
-
(2008)
Animal Genetics
, vol.39
, pp. 645-648
-
-
Anistoroaei, R.1
Fredholm, M.2
Christensen, K.3
Leeb, T.4
-
8
-
-
33744462059
-
The origin of European cattle: Evidence from modern and ancient DNA.
-
Beja-Pereira, A., Caramellic, D., Lalueza-Foxe, C., Vernesif, C., Ferranda, N., Casolih, A., Goyachei, F., Royoi, L. J., Contid, S., Larid, M., Martinij, A., Ouraghk, L., Magid, A., Atash, A., Zsolnaim, A., Boscaton, P., Triantaphlidiso, C., Ploumip, K., Sineoq, L., Mallegnir, F., Taberlet, P., Erhardts, G., Sampietrot, L., Bertranpetitt, J., Barbujaniu, G., Luikart, G. & Bertorelle, G. (2006). The origin of European cattle: Evidence from modern and ancient DNA. Proceedings of the National Academy of Sciences 103, 8113-8118.
-
(2006)
Proceedings of the National Academy of Sciences
, vol.103
, pp. 8113-8118
-
-
Beja-Pereira, A.1
Caramellic, D.2
Lalueza-Foxe, C.3
Vernesif, C.4
Ferranda, N.5
Casolih, A.6
Goyachei, F.7
Royoi, L.J.8
Contid, S.9
Larid, M.10
Martinij, A.11
Ouraghk, L.12
Magid, A.13
Atash, A.14
Zsolnaim, A.15
Boscaton, P.16
Triantaphlidiso, C.17
Ploumip, K.18
Sineoq, L.19
Mallegnir, F.20
Taberlet, P.21
Erhardts, G.22
Sampietrot, L.23
Bertranpetitt, J.24
Barbujaniu, G.25
Luikart, G.26
Bertorelle, G.27
more..
-
9
-
-
55749100524
-
Differential gene expression of TRPM1, the potential cause of congenital stationary night blindness and coat spotting patterns (LP) in the Appaloosa horse (Equus caballus).
-
Bellone, R. R., Brooks, S. A., Sandmayer, L., Murphy, B. A., Forsyth, G., Archer, S., Bailey, E. & Grahn, B. (2008). Differential gene expression of TRPM1, the potential cause of congenital stationary night blindness and coat spotting patterns (LP) in the Appaloosa horse (Equus caballus). Genetics 179, 1861-1870.
-
(2008)
Genetics
, vol.179
, pp. 1861-1870
-
-
Bellone, R.R.1
Brooks, S.A.2
Sandmayer, L.3
Murphy, B.A.4
Forsyth, G.5
Archer, S.6
Bailey, E.7
Grahn, B.8
-
10
-
-
77953926968
-
Fine-mapping and mutation analysis of TRPMI: a candidate gene for leopard complex (LP) spotting and congenital stationary night blindness in horse.
-
Bellone, R. R., Forsyth, G., Leeb, T. Archer, S. Sigurdsson, S., Imsland, F., Mauceli, E., Engensteiner, M., Bailey, E., Sandmeyer, L., Grahn, B., Lindblad-Toh, K. & Wade, C. M. (2010). Fine-mapping and mutation analysis of TRPMI: a candidate gene for leopard complex (LP) spotting and congenital stationary night blindness in horse. Briefings in Functional Genomics 9, 193-207.
-
(2010)
Briefings in Functional Genomics
, vol.9
, pp. 193-207
-
-
Bellone, R.R.1
Forsyth, G.2
Leeb, T.3
Archer, S.4
Sigurdsson, S.5
Imsland, F.6
Mauceli, E.7
Engensteiner, M.8
Bailey, E.9
Sandmeyer, L.10
Grahn, B.11
Lindblad-Toh, K.12
Wade, C.M.13
-
11
-
-
78549245590
-
Pleiotropic effects of pigmentation genes in horses.
-
Bellone, R. R. (2010). Pleiotropic effects of pigmentation genes in horses. Animal Genetics 41, 100-110.
-
(2010)
Animal Genetics
, vol.41
, pp. 100-110
-
-
Bellone, R.R.1
-
12
-
-
64949123876
-
Molecular characterization of the Himalayan mink.
-
Benkel, B. F., Rouvinen-Watt, K., Farid, H. & Anistoroaei, R. (2009). Molecular characterization of the Himalayan mink. Mammalian Genome 20, 256-259.
-
(2009)
Mammalian Genome
, vol.20
, pp. 256-259
-
-
Benkel, B.F.1
Rouvinen-Watt, K.2
Farid, H.3
Anistoroaei, R.4
-
13
-
-
8644243850
-
Chicken W: A genetically uniform chromosome in a highly variable genome.
-
Berlin, S. & Ellegren, H. (2004). Chicken W: A genetically uniform chromosome in a highly variable genome. Proceedings of the National Academy of Sciences 101, 15967-15969.
-
(2004)
Proceedings of the National Academy of Sciences
, vol.101
, pp. 15967-15969
-
-
Berlin, S.1
Ellegren, H.2
-
14
-
-
80053981037
-
-
Genetic studies of coat colors and length in Highland cattle. Plant and Animal Genomes XV Conference 13-17 January.
-
Berryere, T. G., Oulmouden, A. & Schmutz, S. M. (2007). Genetic studies of coat colors and length in Highland cattle. Plant and Animal Genomes XV Conference 13-17 January.
-
(2007)
-
-
Berryere, T.G.1
Oulmouden, A.2
Schmutz, S.M.3
-
15
-
-
0038724134
-
TYRP1 is associated with dun coat colour in Dexter cattle or how now brown cow?
-
Berryere, T. G., Schmutz, S. M., Schimpf, R. J., Cowan, C. M. & Potter, J. (2003). TYRP1 is associated with dun coat colour in Dexter cattle or how now brown cow? Animal Genetics 34, 169-175.
-
(2003)
Animal Genetics
, vol.34
, pp. 169-175
-
-
Berryere, T.G.1
Schmutz, S.M.2
Schimpf, R.J.3
Cowan, C.M.4
Potter, J.5
-
16
-
-
0027812323
-
-
The kit-ligand (steel factor) and its receptor c-kit/W: pleiotropic roles in gametogenesis and melanogenesis. Development
-
Besmer, P., Manova, K., Duttlinger, R., Huang E. J., Packer, A., Gyssler, C. & Bachvarova, R. F. (1993). The kit-ligand (steel factor) and its receptor c-kit/W: pleiotropic roles in gametogenesis and melanogenesis. Development Suppl. S, 125-137.
-
(1993)
, Issue.SUPPL. S
, pp. 125-137
-
-
Besmer, P.1
Manova, K.2
Duttlinger, R.3
Huang, E.J.4
Packer, A.5
Gyssler, C.6
Bachvarova, R.F.7
-
17
-
-
34547098573
-
Identification of a tyrosinase (TYR) exon 4 deletion in albino ferrets (Mustela putorius furo).
-
Blaszczyk, W. M., Distler, C., Dekomien, G., Arning, L., Hoffmann, K.-P. & Epplen, J. T. (2007). Identification of a tyrosinase (TYR) exon 4 deletion in albino ferrets (Mustela putorius furo). Animal Genetics 38, 421-423.
-
(2007)
Animal Genetics
, vol.38
, pp. 421-423
-
-
Blaszczyk, W.M.1
Distler, C.2
Dekomien, G.3
Arning, L.4
Hoffmann, K.-P.5
Epplen, J.T.6
-
18
-
-
27744434902
-
Exon skipping in the KIT gene causes a sabino spotting pattern in horses.
-
Brooks, S. A. & Bailey, E. (2005). Exon skipping in the KIT gene causes a sabino spotting pattern in horses. Mammalian Genome 16, 893-902.
-
(2005)
Mammalian Genome
, vol.16
, pp. 893-902
-
-
Brooks, S.A.1
Bailey, E.2
-
19
-
-
39049123708
-
A chromosome inversion near the KIT gene and the tobiano spotting pattern in horses.
-
Brooks, S. A., Lear, T. L., Adelson, D. L. & Bailey, E. (2007). A chromosome inversion near the KIT gene and the tobiano spotting pattern in horses. Cytogenetic and Genome Research 119, 225-230.
-
(2007)
Cytogenetic and Genome Research
, vol.119
, pp. 225-230
-
-
Brooks, S.A.1
Lear, T.L.2
Adelson, D.L.3
Bailey, E.4
-
20
-
-
77952378278
-
Whole-genome SNP association in the horse: identification of a deletion in myosine Va responsible for Lavender Foal Syndrome.
-
Brooks, S. A., Gabreski, N., Miller, D., Brisbin, A., Brown, H. E., Streeter, C., Mezey, J., Cook, D. & Antczak, D. F. (2010). Whole-genome SNP association in the horse: identification of a deletion in myosine Va responsible for Lavender Foal Syndrome. Public Library of Science Genetics 6(4), e1000909.
-
(2010)
Public Library of Science Genetics
, vol.6
, Issue.4
-
-
Brooks, S.A.1
Gabreski, N.2
Miller, D.3
Brisbin, A.4
Brown, H.E.5
Streeter, C.6
Mezey, J.7
Cook, D.8
Antczak, D.F.9
-
21
-
-
33750603074
-
A missense mutation in PMEL17 is associated with the silver coat color in the horse.
-
Brunberg, E., Andersson, L., Cothran, G., Sandberg, K., Mikko, S. & Lindgren, G. (2006). A missense mutation in PMEL17 is associated with the silver coat color in the horse. BioMed Central Genetics 7, 46.
-
(2006)
BioMed Central Genetics
, vol.7
, pp. 46
-
-
Brunberg, E.1
Andersson, L.2
Cothran, G.3
Sandberg, K.4
Mikko, S.5
Lindgren, G.6
-
22
-
-
0029098575
-
Structure of the mouse tyrosinase-related protein-2/dopachrome tautomerase (Tyrp2/Dct) gene and sequence of two novel slaty alleles.
-
Budd, P. S. & Jackson, I. J. (1995). Structure of the mouse tyrosinase-related protein-2/dopachrome tautomerase (Tyrp2/Dct) gene and sequence of two novel slaty alleles. Genomics 29, 35-43.
-
(1995)
Genomics
, vol.29
, pp. 35-43
-
-
Budd, P.S.1
Jackson, I.J.2
-
23
-
-
36749008499
-
A β-defensin mutation causes black coat colour in domestic dogs.
-
Candille, S. I., Kaelin, C. B., Cattanach, B. M., Yu, B., Thompson, D. A., Nix, M. A., Kerns, J. A., Schmutz, S. M., Millhauser, G. L. & Barsh, G. S. (2007). A β-defensin mutation causes black coat colour in domestic dogs. Science 318, 1418-1423.
-
(2007)
Science
, vol.318
, pp. 1418-1423
-
-
Candille, S.I.1
Kaelin, C.B.2
Cattanach, B.M.3
Yu, B.4
Thompson, D.A.5
Nix, M.A.6
Kerns, J.A.7
Schmutz, S.M.8
Millhauser, G.L.9
Barsh, G.S.10
-
24
-
-
19344363306
-
Dorsoventral patterning of the mouse coat by Tbx15.
-
Candille, S. I., Van Raansdonk, C. D., Chen, C., Kuijper, S., Chen-Tsai, Y., Russ, A., Meijlink, F. & Barsh, S. G. (2004). Dorsoventral patterning of the mouse coat by Tbx15. Public Library of Science Biology 2(1), 0031.
-
(2004)
Public Library of Science Biology
, vol.2
, Issue.1
, pp. 0031
-
-
Candille, S.I.1
Van Raansdonk, C.D.2
Chen, C.3
Kuijper, S.4
Chen-Tsai, Y.5
Russ, A.6
Meijlink, F.7
Barsh, S.G.8
-
25
-
-
33144487646
-
Complete association between a retroviral insertion in the tyrosinase gene and the recessive white mutation in chickens.
-
Chang, C. M., Coville, J. L., Coquerelle, G., Gourichon, D., Oulmouden, A. & Tixier-Boichard, M. (2006). Complete association between a retroviral insertion in the tyrosinase gene and the recessive white mutation in chickens. BioMed Central Genomics 7, 19.
-
(2006)
BioMed Central Genomics
, vol.7
, pp. 19
-
-
Chang, C.M.1
Coville, J.L.2
Coquerelle, G.3
Gourichon, D.4
Oulmouden, A.5
Tixier-Boichard, M.6
-
26
-
-
78650885878
-
Origin and history of mitochondrial DNA lineages in domestic horses.
-
Cieslak, M., Pruvost, M., Benecke, N., Hofreiter, M., Morales, A., Reissmann, M. & Ludwig, A. (2010). Origin and history of mitochondrial DNA lineages in domestic horses. Public Library of Science ONE 5(12), e15311.
-
(2010)
Public Library of Science ONE
, vol.5
, Issue.12
-
-
Cieslak, M.1
Pruvost, M.2
Benecke, N.3
Hofreiter, M.4
Morales, A.5
Reissmann, M.6
Ludwig, A.7
-
27
-
-
31944436548
-
Retrotransposon insertion in SILV is responsible for merle patterning of the domestic dog.
-
Clark, L. A., Wahl, J. M., Rees, C. A. & Murphy, K. E. (2006). Retrotransposon insertion in SILV is responsible for merle patterning of the domestic dog. Proceedings of the National Academy of Sciences 103, 1376-1381.
-
(2006)
Proceedings of the National Academy of Sciences
, vol.103
, pp. 1376-1381
-
-
Clark, L.A.1
Wahl, J.M.2
Rees, C.A.3
Murphy, K.E.4
-
28
-
-
52949086463
-
Missense mutation in exon 2 of SLC36A1 responsible for Champagne dilution in horses.
-
Cook, D., Brooks, S., Bellone, R., & Bailey, E. (2008). Missense mutation in exon 2 of SLC36A1 responsible for Champagne dilution in horses. Public Library of Science Genetics 4(9), e1000195.
-
(2008)
Public Library of Science Genetics
, vol.4
, Issue.9
-
-
Cook, D.1
Brooks, S.2
Bellone, R.3
Bailey, E.4
-
29
-
-
33645227840
-
White spotting in the domestic cat (Felis catus) maps near KIT on feline chromosome B1.
-
Cooper, M. P., Fretwell, N., Bailey, S. J. & Lyons, L. A. (2005). White spotting in the domestic cat (Felis catus) maps near KIT on feline chromosome B1. Animal Genetics 37, 163-165.
-
(2005)
Animal Genetics
, vol.37
, pp. 163-165
-
-
Cooper, M.P.1
Fretwell, N.2
Bailey, S.J.3
Lyons, L.A.4
-
31
-
-
36749007954
-
β-Defensin Repertoire Expands.
-
Dorin, J. R. & Jackson, I. J. (2007). β-Defensin Repertoire Expands. Science 318, 1395.
-
(2007)
Science
, vol.318
, pp. 1395
-
-
Dorin, J.R.1
Jackson, I.J.2
-
32
-
-
77955010419
-
A new mutationin MCIR explains a coat color phenotype in 2 "old" breeds: Saluki and Afghan hound.
-
Dreger, D. L. & Schmutz, S. M. (2010a). A new mutationin MCIR explains a coat color phenotype in 2 "old" breeds: Saluki and Afghan hound. Journal of Heredity 101, 644-649.
-
(2010)
Journal of Heredity
, vol.101
, pp. 644-649
-
-
Dreger, D.L.1
Schmutz, S.M.2
-
33
-
-
73849086569
-
The variant red coat colour phenotype of Holstein cattle maps to BTA27.
-
Dreger, D. L. & Schmutz, S. M. (2010b). The variant red coat colour phenotype of Holstein cattle maps to BTA27. Animal Genetics 41, 109-112.
-
(2010)
Animal Genetics
, vol.41
, pp. 109-112
-
-
Dreger, D.L.1
Schmutz, S.M.2
-
34
-
-
34547566897
-
The near Eastern origin of cat domestication.
-
Driscoll, C. A., Menotti-Raymond, M., Roca, A. L., Hupe, K., Johnson, W. E., Geffen, E., Harley, E., Delibes, M., Pontier, D., Kitchener, A. C., Yamaguchi, N., O'Brien, S. & McDonald, D. (2007). The near Eastern origin of cat domestication. Science 317, 519-523.
-
(2007)
Science
, vol.317
, pp. 519-523
-
-
Driscoll, C.A.1
Menotti-Raymond, M.2
Roca, A.L.3
Hupe, K.4
Johnson, W.E.5
Geffen, E.6
Harley, E.7
Delibes, M.8
Pontier, D.9
Kitchener, A.C.10
Yamaguchi, N.11
O'Brien, S.12
McDonald, D.13
-
35
-
-
67650341019
-
From wild animals to domestic pets, an evolutionary view of domestication.
-
Driscoll, C. A., McDonald, D. & O'Brien, S. (2009). From wild animals to domestic pets, an evolutionary view of domestication. Proceedings of the National Academy of Sciences 106, 9971-9978.
-
(2009)
Proceedings of the National Academy of Sciences
, vol.106
, pp. 9971-9978
-
-
Driscoll, C.A.1
McDonald, D.2
O'Brien, S.3
-
36
-
-
30744442765
-
The mutation causing the black-and-tan pigmentation phenotype of Mangalitza pigs maps to the porcine ASIP locus but does not affect its coding sequence.
-
Drögemüller, C., Giese, A., Martins-Wess, F., Wiedemann, S., Andersson, L., Breng, B., Fries, R. & Leeb, T. (2006). The mutation causing the black-and-tan pigmentation phenotype of Mangalitza pigs maps to the porcine ASIP locus but does not affect its coding sequence. Mammalian Genome 17, 58-66.
-
(2006)
Mammalian Genome
, vol.17
, pp. 58-66
-
-
Drögemüller, C.1
Giese, A.2
Martins-Wess, F.3
Wiedemann, S.4
Andersson, L.5
Breng, B.6
Fries, R.7
Leeb, T.8
-
37
-
-
0032054272
-
Down-Regulation of the Novel Gene Melastatin Correlates with Potential for Melanoma Metastasis.
-
Duncan, L. M., Deeds, J., Hunter, J., Shao, J., Holmgren, L. M., Woolf, E. A., Tepper, R. I. & Shyjan, A. W. (1998). Down-Regulation of the Novel Gene Melastatin Correlates with Potential for Melanoma Metastasis. Cancer Research 58, 1515-1520.
-
(1998)
Cancer Research
, vol.58
, pp. 1515-1520
-
-
Duncan, L.M.1
Deeds, J.2
Hunter, J.3
Shao, J.4
Holmgren, L.M.5
Woolf, E.A.6
Tepper, R.I.7
Shyjan, A.W.8
-
38
-
-
0037418588
-
Molecular genetics and evolution of melanism in the cat family.
-
Eizirik, E., Yuhki, N., Johnson, W. E., Menotti-Raymond, M., Hannah, S. S. & O'brien, S. J. (2003). Molecular genetics and evolution of melanism in the cat family. Current Biology 13, 448-453.
-
(2003)
Current Biology
, vol.13
, pp. 448-453
-
-
Eizirik, E.1
Yuhki, N.2
Johnson, W.E.3
Menotti-Raymond, M.4
Hannah, S.S.5
O'brien, S.J.6
-
39
-
-
40149109370
-
Identification of the yellow skin gene reveals a hybrid origin of the domestic chicken.
-
Eriksson, J., Larson, G., Gunnarsson, U. Bed'Hom, B., Tixier-Boichard, M., Strömstedt, L., Wright, D., Jungerius, A., Vereijken, A., Randi, E., Jensen, P. & Andersson, L. (2008). Identification of the yellow skin gene reveals a hybrid origin of the domestic chicken. Public Library of Science Genetics 4(2), e1000010.
-
(2008)
Public Library of Science Genetics
, vol.4
, Issue.2
-
-
Eriksson, J.1
Larson, G.2
Gunnarsson, U.3
Bed'Hom, B.4
Tixier-Boichard, M.5
Strömstedt, L.6
Wright, D.7
Jungerius, A.8
Vereijken, A.9
Randi, E.10
Jensen, P.11
Andersson, L.12
-
40
-
-
33645236759
-
Characterization of OCA2 cDNA in different porcine breeds and analysis of its potential effect on skin pigmentation in a red Iberian strain.
-
Fernandez, A., Silio, L., Rodrigez, C. & Ovilo, C. (2006). Characterization of OCA2 cDNA in different porcine breeds and analysis of its potential effect on skin pigmentation in a red Iberian strain. Animal Genetics 37, 166-170.
-
(2006)
Animal Genetics
, vol.37
, pp. 166-170
-
-
Fernandez, A.1
Silio, L.2
Rodrigez, C.3
Ovilo, C.4
-
41
-
-
77954064730
-
A composite six bp in-frame deletion in the melanocortin 1 receptor (MC1R) gene is associated with the Japanese brindling coat colour in rabbits (Oryctolagus cuniculus).
-
Fontanesi, L., Scotti, E., Colombo, M., Beretti, F., Forestier, L., Dall'olio, S., Deretz, S., Russo, V., Allain, D. & Oulmouden, A. (2010). A composite six bp in-frame deletion in the melanocortin 1 receptor (MC1R) gene is associated with the Japanese brindling coat colour in rabbits (Oryctolagus cuniculus). BioMed Central Genetics 11, 59.
-
(2010)
BioMed Central Genetics
, vol.11
, pp. 59
-
-
Fontanesi, L.1
Scotti, E.2
Colombo, M.3
Beretti, F.4
Forestier, L.5
Dall'olio, S.6
Deretz, S.7
Russo, V.8
Allain, D.9
Oulmouden, A.10
-
42
-
-
33748797926
-
Mutations in the melanocortin 1 receptor (MC1R) gene are associated with coat colours in the domestic rabbit (Oryctolagus cuniculus).
-
Fontanesi, L., Tazzoli, M., Beretti, F. & Russo, V. (2006). Mutations in the melanocortin 1 receptor (MC1R) gene are associated with coat colours in the domestic rabbit (Oryctolagus cuniculus). Animal Genetics 37, 489-493.
-
(2006)
Animal Genetics
, vol.37
, pp. 489-493
-
-
Fontanesi, L.1
Tazzoli, M.2
Beretti, F.3
Russo, V.4
-
43
-
-
60249097293
-
Y chromosome haplotype analysis in Portuguese cattle breeds using SNPs and STRs.
-
Ginja, C. L., Da Gama, T. & Penedo, M. C. T. (2009). Y chromosome haplotype analysis in Portuguese cattle breeds using SNPs and STRs. Journal of Heredity 100, 148-157.
-
(2009)
Journal of Heredity
, vol.100
, pp. 148-157
-
-
Ginja, C.L.1
Da Gama, T.2
Penedo, M.C.T.3
-
44
-
-
0032700355
-
The belt mutation in pigs is an allele at the dominant white (I/KIT) locus.
-
Giuffra, E., Evans, G., Törnsten, A., Wales, R., Day, A., Looft, H., Plastow, G. & Andersson, L. (1999). The belt mutation in pigs is an allele at the dominant white (I/KIT) locus. Mammalian Genome 10, 1132-1136.
-
(1999)
Mammalian Genome
, vol.10
, pp. 1132-1136
-
-
Giuffra, E.1
Evans, G.2
Törnsten, A.3
Wales, R.4
Day, A.5
Looft, H.6
Plastow, G.7
Andersson, L.8
-
45
-
-
0034117004
-
The origin of the domestic pig: Independent domestication and subsequent introgression.
-
Giuffra, E., Kijasa, J. M. H., Amargera, V., Carlborga, Ö., Jeona, J.-T. & Andersson, L. (2000). The origin of the domestic pig: Independent domestication and subsequent introgression. Genetics 154, 1785-1791.
-
(2000)
Genetics
, vol.154
, pp. 1785-1791
-
-
Giuffra, E.1
Kijasa, J.M.H.2
Amargera, V.3
Carlborga, O.4
Jeona, J.-T.5
Andersson, L.6
-
46
-
-
33947516238
-
Compelling evidence that a single nucleotide substitution in TYRP1 is responsible for coat-colour polymorphism in a free-living population of Soay sheep.
-
Gratten, J., Beraldi, D., Lowder, B. V., Mcrae, A. F., Visscher, P. M., Pemberton, J. M. & Slate, J. (2006). Compelling evidence that a single nucleotide substitution in TYRP1 is responsible for coat-colour polymorphism in a free-living population of Soay sheep. Proceedings of the Royal Society B-Biological Sciences 274, 619-626.
-
(2006)
Proceedings of the Royal Society B-Biological Sciences
, vol.274
, pp. 619-626
-
-
Gratten, J.1
Beraldi, D.2
Lowder, B.V.3
Mcrae, A.F.4
Visscher, P.M.5
Pemberton, J.M.6
Slate, J.7
-
47
-
-
75549089708
-
The genetic basis of recessive self-colour pattern in a wild sheep population.
-
Gratten, J., Pilkington, J. G., Brown, E. A., Beraldi, D., Pemberton, J. M. & Slate, J. (2010). The genetic basis of recessive self-colour pattern in a wild sheep population. Heredity 104, 206-214.
-
(2010)
Heredity
, vol.104
, pp. 206-214
-
-
Gratten, J.1
Pilkington, J.G.2
Brown, E.A.3
Beraldi, D.4
Pemberton, J.M.5
Slate, J.6
-
48
-
-
34247854954
-
Mutations in SLC45A2 cause plumage color variation in chicken and Japanese quail.
-
Gunnarsson, U., Hellström, A. R., Tixier-Boichard, M., Minvielle, F., Bed'Hom, B., Ito, S., Jensen, P., Rattink, A., Vereijken, A. & Andersson, L. (2007). Mutations in SLC45A2 cause plumage color variation in chicken and Japanese quail. Genetics 175, 867-877.
-
(2007)
Genetics
, vol.175
, pp. 867-877
-
-
Gunnarsson, U.1
Hellström, A.R.2
Tixier-Boichard, M.3
Minvielle, F.4
Bed'Hom, B.5
Ito, S.6
Jensen, P.7
Rattink, A.8
Vereijken, A.9
Andersson, L.10
-
49
-
-
34848903930
-
Genetic effects on coat colour in cattle: dilution of eumelanin and phaeomelanin pigments in an F2-Backcross Charolais × Holstein population.
-
Gutiérrez-Gil, B., Wiener, P. & Williams, J. L. (2007). Genetic effects on coat colour in cattle: dilution of eumelanin and phaeomelanin pigments in an F2-Backcross Charolais × Holstein population. BioMed Central Genetics 8, 56.
-
(2007)
BioMed Central Genetics
, vol.8
, pp. 56
-
-
Gutiérrez-Gil, B.1
Wiener, P.2
Williams, J.L.3
-
50
-
-
1842505318
-
Melanocytes and pigmentation are affected in dopachrome tautomerase knockout mice.
-
Guyonneau, L., Murisier, F., Rossier, A., Moulin, A. & Beermann, F. (2004). Melanocytes and pigmentation are affected in dopachrome tautomerase knockout mice. Molecular and Cellular Biology 24, 3396-3403.
-
(2004)
Molecular and Cellular Biology
, vol.24
, pp. 3396-3403
-
-
Guyonneau, L.1
Murisier, F.2
Rossier, A.3
Moulin, A.4
Beermann, F.5
-
51
-
-
77952879494
-
Molecular tracking of jaguar melanism using faecal DNA.
-
Haag, T., Santos, A. S., Valdez, F. P., Sana, D. A., Silveira, L., Cullen Jr., L., De Angelo, C., Morato, R. G., Crawshaw Jr., P. G., Salzano, F. M. & Ezirik, E. (2009). Molecular tracking of jaguar melanism using faecal DNA. Conservation Genetics 11, 1239-1242.
-
(2009)
Conservation Genetics
, vol.11
, pp. 1239-1242
-
-
Haag, T.1
Santos, A.S.2
Valdez, F.P.3
Sana, D.A.4
Silveira, L.5
Cullen Jr., L.6
De Angelo, C.7
Morato, R.G.8
Crawshaw Jr., P.G.9
Salzano, F.M.10
Ezirik, E.11
-
52
-
-
37349023135
-
Allelic heterogeneity at the equine KIT Locus in dominant white (W) horses.
-
Haase, B., Brooks, S. A., Schlumbaum, A., Azor, P. J., Bailey, E., Alaeddine, F., Mevissen, M., Burger, D., Poncet, P-A., Rieder, S. & Leeb, T. (2007). Allelic heterogeneity at the equine KIT Locus in dominant white (W) horses. Public Library of Science Genetics 3(11), e195.
-
(2007)
Public Library of Science Genetics
, vol.3
, Issue.11
-
-
Haase, B.1
Brooks, S.A.2
Schlumbaum, A.3
Azor, P.J.4
Bailey, E.5
Alaeddine, F.6
Mevissen, M.7
Burger, D.8
Poncet, P.-A.9
Rieder, S.10
Leeb, T.11
-
53
-
-
69949166667
-
Seven novel KIT mutations in horses with white coat colour phenotypes.
-
Haase, B., Brooks, S. A., Tozaki, T., Burger, D., Poncet, P-A., Rieder, S., Hasegawa, T., Penedo, C. & Leeb, T. (2009). Seven novel KIT mutations in horses with white coat colour phenotypes. Animal Genetics 40, 623-629.
-
(2009)
Animal Genetics
, vol.40
, pp. 623-629
-
-
Haase, B.1
Brooks, S.A.2
Tozaki, T.3
Burger, D.4
Poncet, P.-A.5
Rieder, S.6
Hasegawa, T.7
Penedo, C.8
Leeb, T.9
-
54
-
-
44049090321
-
An equine chromosome 3 inversion is associated with the tobiano spotting pattern in German horse breeds.
-
Haase, B., Jude, R., Brooks, S. A. & Leeb, T. (2008). An equine chromosome 3 inversion is associated with the tobiano spotting pattern in German horse breeds. Animal Genetics 339, 306-309.
-
(2008)
Animal Genetics
, vol.339
, pp. 306-309
-
-
Haase, B.1
Jude, R.2
Brooks, S.A.3
Leeb, T.4
-
55
-
-
17344384767
-
Genomic, transcriptional and mutational analysis of the mouse microphthalmia locus.
-
Hallsson, J. H., Favor, J., Hodgkinson, C., Glaser, T., Lamoreux, M. L., Magnúsdlóttir, R., Gunnarsson, G. J., Sweet, H. O., Copeland, N. G., Jenkins, N. A. & Steingrimsson, E. (2000). Genomic, transcriptional and mutational analysis of the mouse microphthalmia locus. Genetics 155, 291-300.
-
(2000)
Genetics
, vol.155
, pp. 291-300
-
-
Hallsson, J.H.1
Favor, J.2
Hodgkinson, C.3
Glaser, T.4
Lamoreux, M.L.5
Magnúsdlóttir, R.6
Gunnarsson, G.J.7
Sweet, H.O.8
Copeland, N.G.9
Jenkins, N.A.10
Steingrimsson, E.11
-
56
-
-
0031968476
-
Analysis of mitochondrial DNA indicates that domestic sheep are derived from two different ancestral maternal sources. No evidence for contributions from urial and argali sheep.
-
Hiendleder, S., Mainz, K., Plante, Y. & Lewalski, H. (1998). Analysis of mitochondrial DNA indicates that domestic sheep are derived from two different ancestral maternal sources. No evidence for contributions from urial and argali sheep. Journal of Heredity 89, 113-120.
-
(1998)
Journal of Heredity
, vol.89
, pp. 113-120
-
-
Hiendleder, S.1
Mainz, K.2
Plante, Y.3
Lewalski, H.4
-
57
-
-
40849098896
-
Recessive black is allelic to the yellow plumage locus in Japanese quail and associated with a frame shift deletion in the ASIP Gene.
-
Hiragaki, T., Inoue-Murayama, M., Miwa, M., Fujiwara, A., Mizutani, M., Minvielle, F., Ito, S. (2008). Recessive black is allelic to the yellow plumage locus in Japanese quail and associated with a frame shift deletion in the ASIP Gene. Genetics 178, 771-775.
-
(2008)
Genetics
, vol.178
, pp. 771-775
-
-
Hiragaki, T.1
Inoue-Murayama, M.2
Miwa, M.3
Fujiwara, A.4
Mizutani, M.5
Minvielle, F.6
Ito, S.7
-
58
-
-
33745911143
-
A single amino acid mutation contributes to adaptive beach mouse color pattern.
-
Hoekstra, H. E., Hirschmann, R. J., Bundey, R. A., Insel, P. A. & Crossland, J. P. (2006). A single amino acid mutation contributes to adaptive beach mouse color pattern. Science 313, 101-104.
-
(2006)
Science
, vol.313
, pp. 101-104
-
-
Hoekstra, H.E.1
Hirschmann, R.J.2
Bundey, R.A.3
Insel, P.A.4
Crossland, J.P.5
-
59
-
-
78449267934
-
De novo mutation of KIT discovered as a result of a non-hereditary white coat colour pattern.
-
Holl, H., Brooks, S. & Bailey, E. (2010). De novo mutation of KIT discovered as a result of a non-hereditary white coat colour pattern. Animal Genetics 41(S2), 196-198.
-
(2010)
Animal Genetics
, vol.41
, Issue.S2
, pp. 196-198
-
-
Holl, H.1
Brooks, S.2
Bailey, E.3
-
60
-
-
77951931078
-
Vertebrate pigmentation: from underlying genes to adaptive function.
-
Hubbard, J. K., Uy, J. A. C., Hauber, M. E., Hoekstra, H. E. & Safran, R. J. (2010). Vertebrate pigmentation: from underlying genes to adaptive function. Trends in Genetics 26, 231-239.
-
(2010)
Trends in Genetics
, vol.26
, pp. 231-239
-
-
Hubbard, J.K.1
Uy, J.A.C.2
Hauber, M.E.3
Hoekstra, H.E.4
Safran, R.J.5
-
61
-
-
34948826453
-
Rab27a and MyoVa are the primary Mlph interactors regulating melanosome transport in melanocytes.
-
Hume, A. N., Ushakov, D. S., Tarafder, A. K., Ferenczi, M. A. & Seabra, M. C. (2007). Rab27a and MyoVa are the primary Mlph interactors regulating melanosome transport in melanocytes. Journal of Cell Science 120, 3111-3122.
-
(2007)
Journal of Cell Science
, vol.120
, pp. 3111-3122
-
-
Hume, A.N.1
Ushakov, D.S.2
Tarafder, A.K.3
Ferenczi, M.A.4
Seabra, M.C.5
-
62
-
-
34047158078
-
Analysis of auction data for horses and influence factors on pricing.
-
Icken, W., Bennewitz, J., & Kalm, E. (2007). Analysis of auction data for horses and influence factors on pricing. Zuchtungskunde 79, 111-118.
-
(2007)
Zuchtungskunde
, vol.79
, pp. 111-118
-
-
Icken, W.1
Bennewitz, J.2
Kalm, E.3
-
63
-
-
33645210498
-
Albinism in the domestic cat (Felis catus) is associated with a tyrosinase (TYR) mutation.
-
Imes, D. L., Geary, L. A., Grahn, R. A. & Lyons, L. A. (2006). Albinism in the domestic cat (Felis catus) is associated with a tyrosinase (TYR) mutation. Animal Genetics 37, 175-178.
-
(2006)
Animal Genetics
, vol.37
, pp. 175-178
-
-
Imes, D.L.1
Geary, L.A.2
Grahn, R.A.3
Lyons, L.A.4
-
64
-
-
33751084845
-
A homozygous single-base deletion in MLPH causes the dilute coat color phenotype in the domestic cat.
-
Ishida, Y., David, V. A., Eizirik, E., Schäffer, A. A., Neelam, B. A., Roelke, M. E., Hannah, S. S., O'Brien, S. J. & Menotti-Raymond, M. (2006). A homozygous single-base deletion in MLPH causes the dilute coat color phenotype in the domestic cat. Genomics 88, 698-705.
-
(2006)
Genomics
, vol.88
, pp. 698-705
-
-
Ishida, Y.1
David, V.A.2
Eizirik, E.3
Schäffer, A.A.4
Neelam, B.A.5
Roelke, M.E.6
Hannah, S.S.7
O'Brien, S.J.8
Menotti-Raymond, M.9
-
65
-
-
0021235085
-
Characterization of melanogenesis in mouse and Guinie pig hair by chemical analysis of melanins and of free and bound Dopa and 5-S-Cysteinyldopa.
-
Ito, S., Fujita, K., Takahashi, H. & Jimbow, K. (1984). Characterization of melanogenesis in mouse and Guinie pig hair by chemical analysis of melanins and of free and bound Dopa and 5-S-Cysteinyldopa. Investigative Dermatology 83, 12-14.
-
(1984)
Investigative Dermatology
, vol.83
, pp. 12-14
-
-
Ito, S.1
Fujita, K.2
Takahashi, H.3
Jimbow, K.4
-
66
-
-
0042733275
-
Quantitative analysis of eumelanin and pheomelanin in humans, mice, and other animals: a comparative review.
-
Ito, S. & Wakamatsu, K. (2003). Quantitative analysis of eumelanin and pheomelanin in humans, mice, and other animals: a comparative review. Pigment Cell Research 16, 523-531.
-
(2003)
Pigment Cell Research
, vol.16
, pp. 523-531
-
-
Ito, S.1
Wakamatsu, K.2
-
67
-
-
42549092546
-
Chemistry of mixed melanogenesis-pivotal roles of dopaquinone.
-
Ito, S & Wakamatsu, K. (2008). Chemistry of mixed melanogenesis-pivotal roles of dopaquinone. Photochemistry and Photobiology 84, 582-592.
-
(2008)
Photochemistry and Photobiology
, vol.84
, pp. 582-592
-
-
Ito, S.1
Wakamatsu, K.2
-
68
-
-
0026567071
-
A second tyrosinase-related protein, TRP-2, maps to and is mutated at the mouse slaty locus.
-
Jackson, I. J., Chambers, D. M., Tsukamoto, K., Copeland, N. G., Gilbert, D. J., Jenkins, N. A. & Hearing, V. (1992). A second tyrosinase-related protein, TRP-2, maps to and is mutated at the mouse slaty locus. European Molecular Biology Organisation Journal 11, 527-535.
-
(1992)
European Molecular Biology Organisation Journal
, vol.11
, pp. 527-535
-
-
Jackson, I.J.1
Chambers, D.M.2
Tsukamoto, K.3
Copeland, N.G.4
Gilbert, D.J.5
Jenkins, N.A.6
Hearing, V.7
-
69
-
-
0036679199
-
Mitochondrial DNA and the origins of the domestic horse.
-
Jansen, T., Forster, P., Levine, M. A., Oelke, H., Hurles, M., Renfrew, C., Weber, J. & Olek, K. (2002). Mitochondrial DNA and the origins of the domestic horse. Proceedings of the National Academy of Sciences 99, 10905-10910.
-
(2002)
Proceedings of the National Academy of Sciences
, vol.99
, pp. 10905-10910
-
-
Jansen, T.1
Forster, P.2
Levine, M.A.3
Oelke, H.4
Hurles, M.5
Renfrew, C.6
Weber, J.7
Olek, K.8
-
70
-
-
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. (1996). Red coat color in Holstein cattle is associated with a deletion in the MSHR gene. Mammalian Genome 7, 317-318.
-
(1996)
Mammalian Genome
, vol.7
, pp. 317-318
-
-
Joerg, H.1
Fries, H.R.2
Meijerink, E.3
Stranzinger, G.F.4
-
71
-
-
35648953308
-
Efficient mapping of Mendelian traits in dogs through genome-wide association.
-
Karlsson, E. K., Baranowska, I., Wade, C. M., Salmon Hillbertz, N. H. C., Zody, M. C., Anderson, N., Biagi, T. M., Patterson, N., Pielberg, G. R., Kulbokas, E. J., Comstock, K. E., Keller, E. T., Mesirov, J. P., Von Euler, H., Kämpe, O., Hedhammer, A., Lander, E. S., Andersson, G., Andersson, L. & Lindlbad-Toh, K. (2007). Efficient mapping of Mendelian traits in dogs through genome-wide association. Nature Genetics 39, 1321-1328.
-
(2007)
Nature Genetics
, vol.39
, pp. 1321-1328
-
-
Karlsson, E.K.1
Baranowska, I.2
Wade, C.M.3
Salmon Hillbertz, N.H.C.4
Zody, M.C.5
Anderson, N.6
Biagi, T.M.7
Patterson, N.8
Pielberg, G.R.9
Kulbokas, E.J.10
Comstock, K.E.11
Keller, E.T.12
Mesirov, J.P.13
Von Euler, H.14
Kämpe, O.15
Hedhammer, A.16
Lander, E.S.17
Andersson, G.18
Andersson, L.19
Lindlbad-Toh, K.20
more..
-
72
-
-
0035142015
-
Spontaneous mutation in Mitf gene causes osteopetrosis in silver homozygote quail.
-
Kawaguchi, N., Ono, T., Mochii, M. & Noda, M. (2001). Spontaneous mutation in Mitf gene causes osteopetrosis in silver homozygote quail. Developmental Dynamics 220, 133-140.
-
(2001)
Developmental Dynamics
, vol.220
, pp. 133-140
-
-
Kawaguchi, N.1
Ono, T.2
Mochii, M.3
Noda, M.4
-
73
-
-
0014751425
-
Melanin, adrenalin and the legacy of fear.
-
Keeler, C., Mellinger, T., Fromm, E. & Wade, L. (1970). Melanin, adrenalin and the legacy of fear. Journal of Heredity 61, 81-88.
-
(1970)
Journal of Heredity
, vol.61
, pp. 81-88
-
-
Keeler, C.1
Mellinger, T.2
Fromm, E.3
Wade, L.4
-
74
-
-
19944361828
-
The dominant white, dun and smoky color variants in chicken are associated with insertion/deletion polymorphisms in the PMEL17.
-
Kerje, S., Sharma, P., Gunnarsson, U., Kim, H., Bagchi, S., Fredriksson, R., Schütz, K., Jensen, P., Heinje, G. v., Okimoto, R. & Andersson, L. (2004). The dominant white, dun and smoky color variants in chicken are associated with insertion/deletion polymorphisms in the PMEL17. Molecular and General Genetics 168, 1507-1518.
-
(2004)
Molecular and General Genetics
, vol.168
, pp. 1507-1518
-
-
Kerje, S.1
Sharma, P.2
Gunnarsson, U.3
Kim, H.4
Bagchi, S.5
Fredriksson, R.6
Schütz, K.7
Jensen, P.8
Heinje, G.9
Okimoto, R.10
Andersson, L.11
-
75
-
-
34547097033
-
Linkage and segregation analysis of black and brindle coat color in domestic dogs.
-
Kerns, J. A., Cargill, E. J., Clark, L. A., Candill, S. I., Berryere, T. G., Olivier, M., Lust, G., Todhunter, R. J., Schmutz, S. M., Murphy, K. E. & Barsh, G. S. (2007). Linkage and segregation analysis of black and brindle coat color in domestic dogs. Genetics 176, 1979-89.
-
(2007)
Genetics
, vol.176
, pp. 1979-1989
-
-
Kerns, J.A.1
Cargill, E.J.2
Clark, L.A.3
Candill, S.I.4
Berryere, T.G.5
Olivier, M.6
Lust, G.7
Todhunter, R.J.8
Schmutz, S.M.9
Murphy, K.E.10
Barsh, G.S.11
-
76
-
-
10944272602
-
Characterization of the dog Agouti gene and a nonagoutimutation in German shepherd dogs.
-
Kerns, J. A., Newton, J., Berryere, T. G., Rubin, E. M., Cheng, J. F., Schmutz, S. M. & Barsh, G. S. (2004). Characterization of the dog Agouti gene and a nonagoutimutation in German shepherd dogs. Mammalian Genome 15, 798-808.
-
(2004)
Mammalian Genome
, vol.15
, pp. 798-808
-
-
Kerns, J.A.1
Newton, J.2
Berryere, T.G.3
Rubin, E.M.4
Cheng, J.F.5
Schmutz, S.M.6
Barsh, G.S.7
-
77
-
-
0034971184
-
A frameshift mutation in MC1R and a high frequency of somatic reversions cause black spotting in pigs.
-
Kijas, J. M., Moller, M., Plastow, G. & Andersson, L. (2001). A frameshift mutation in MC1R and a high frequency of somatic reversions cause black spotting in pigs. Genetics 158, 779-785.
-
(2001)
Genetics
, vol.158
, pp. 779-785
-
-
Kijas, J.M.1
Moller, M.2
Plastow, G.3
Andersson, L.4
-
78
-
-
0031737430
-
Melanocortin Receptor 1 (MC1R) mutations and coat color in pigs.
-
Kijas, J. M., Wales, R., Törnsten, A., Chardon, P., Moller, M. & Anedersson, L. (1998). Melanocortin Receptor 1 (MC1R) mutations and coat color in pigs. Genetics 150, 1177-1185.
-
(1998)
Genetics
, vol.150
, pp. 1177-1185
-
-
Kijas, J.M.1
Wales, R.2
Törnsten, A.3
Chardon, P.4
Moller, M.5
Anedersson, L.6
-
79
-
-
68149087809
-
Melanism in Peromyscus is caused by independent mutations in Agouti.
-
Kingsley, E. P., Manceau, M., Wiley, C. D. & Hoekstra, H. E. (2009). Melanism in Peromyscus is caused by independent mutations in Agouti. Public Library of Science ONE 4(7), e6435.
-
(2009)
Public Library of Science ONE
, vol.4
, Issue.7
-
-
Kingsley, E.P.1
Manceau, M.2
Wiley, C.D.3
Hoekstra, H.E.4
-
81
-
-
0029360495
-
The role of melanocyte-stimulating hormone (MSH) receptor in bovine coat color determination.
-
Klungland, H., Våge, D. I., Gomez-Raya, L., Adalsteinsson, S. & Lien, S. (1995). The role of melanocyte-stimulating hormone (MSH) receptor in bovine coat color determination. Mammalian Genome 6, 636-639.
-
(1995)
Mammalian Genome
, vol.6
, pp. 636-639
-
-
Klungland, H.1
Våge, D.I.2
Gomez-Raya, L.3
Adalsteinsson, S.4
Lien, S.5
-
82
-
-
0028561876
-
Tyrosinase related protein 1 (TRP1) functions as a DHICA oxidase in melanin biosynthesis.
-
Kobayashi, T., Urabe, K., Winder, A., Jiménez-Cervantes, C., Imokawa, G., Brewington, T., Solano, F., García-Borrón, J. C. & Hearing, V. J. (1994). Tyrosinase related protein 1 (TRP1) functions as a DHICA oxidase in melanin biosynthesis. EMBO Journal 13, 5818-5825.
-
(1994)
EMBO Journal
, vol.13
, pp. 5818-5825
-
-
Kobayashi, T.1
Urabe, K.2
Winder, A.3
Jiménez-Cervantes, C.4
Imokawa, G.5
Brewington, T.6
Solano, F.7
García-Borrón, J.C.8
Hearing, V.J.9
-
83
-
-
0033610797
-
Tyrosinase Stabilization by Tyrp1 (the brown Locus Protein).
-
Kobayashi, T., Imokawa, G., Bennett, D. C. & Hearing, V. J. (1998). Tyrosinase Stabilization by Tyrp1 (the brown Locus Protein). Journal of Biological Chemistry 273, 31801-31805.
-
(1998)
Journal of Biological Chemistry
, vol.273
, pp. 31801-31805
-
-
Kobayashi, T.1
Imokawa, G.2
Bennett, D.C.3
Hearing, V.J.4
-
84
-
-
77957162897
-
TRPM1: A vertebrate TRP channel responsible for retinal on bipolar function.
-
Koike, C., Numata, T., Ueda, H., Mori, Y. & Furukawa, T. (2010). TRPM1: A vertebrate TRP channel responsible for retinal on bipolar function. Cell Calcium 48, 95-101.
-
(2010)
Cell Calcium
, vol.48
, pp. 95-101
-
-
Koike, C.1
Numata, T.2
Ueda, H.3
Mori, Y.4
Furukawa, T.5
-
85
-
-
34047110250
-
An investigation into the genetic background of coat colour dilution in a Charolais × German Holstein F2 resource population.
-
Kühn, C. H. & Weikard, R. (2007). An investigation into the genetic background of coat colour dilution in a Charolais × German Holstein F2 resource population. Animal Genetics 38, 109-113.
-
(2007)
Animal Genetics
, vol.38
, pp. 109-113
-
-
Kühn, C.H.1
Weikard, R.2
-
86
-
-
40049103814
-
Measurement of segregating behaviors in experimental silver fox pedigrees.
-
Kukekova, A. V., Trut, L. N., Chase, K., Shepeleva, D. V., Vladimirova, A. V., Kharlamova, A. V., Oskina, I., Stepika, N., Klebanov, A. S., Erb, H. N. & Acland, G. M. (2008). Measurement of segregating behaviors in experimental silver fox pedigrees. Behaviour Genetics 38, 185-194.
-
(2008)
Behaviour Genetics
, vol.38
, pp. 185-194
-
-
Kukekova, A.V.1
Trut, L.N.2
Chase, K.3
Shepeleva, D.V.4
Vladimirova, A.V.5
Kharlamova, A.V.6
Oskina, I.7
Stepika, N.8
Klebanov, A.S.9
Erb, H.N.10
Acland, G.M.11
-
87
-
-
0035091825
-
Interaction of major color gene functions in mice as studied by chemical analysis of eumelanin and pheomelanin.
-
Lamoreux, M. L., Wakamatsu, K. & Ito, S. (2001). Interaction of major color gene functions in mice as studied by chemical analysis of eumelanin and pheomelanin. Pigment Cell Research 14, 23-31.
-
(2001)
Pigment Cell Research
, vol.14
, pp. 23-31
-
-
Lamoreux, M.L.1
Wakamatsu, K.2
Ito, S.3
-
88
-
-
0031989593
-
Die Fellfarbe beim Hund. Teil 1: Grundlagen der Farbgenese.
-
K
-
Laukner, A. (1998). Die Fellfarbe beim Hund. Teil 1: Grundlagen der Farbgenese. Tierärztliche Praxis 26(K), 49-54.
-
(1998)
Tierärztliche Praxis
, vol.26
, pp. 49-54
-
-
Laukner, A.1
-
89
-
-
0002930176
-
Genetics of colour variation
-
edited by M. F. Rothschild and A. Ruvinsky. CAB International, Oxon, UK.
-
Legault, C. (1998). Genetics of colour variation, pp. 51-69 in The Genetics of the Pig, edited by M. F. Rothschild and A. Ruvinsky. CAB International, Oxon, UK.
-
(1998)
The Genetics of the Pig
, pp. 51-69
-
-
Legault, C.1
-
90
-
-
85047681855
-
It's a bull market.
-
Lewin, H. A. (2009). It's a bull market. Science 324, 478-479.
-
(2009)
Science
, vol.324
, pp. 478-479
-
-
Lewin, H.A.1
-
91
-
-
12144288614
-
Limited number of patrilines in horse domestication.
-
Lindgren, G., Backström, N., Swinburne, J., Hellborg, L., Einarsson, A., Sandberg, K., Cothran, G., Vila, C., Binns, M. & Ellegren, H. (2004). Limited number of patrilines in horse domestication. Nature Genetics 36, 335-336.
-
(2004)
Nature Genetics
, vol.36
, pp. 335-336
-
-
Lindgren, G.1
Backström, N.2
Swinburne, J.3
Hellborg, L.4
Einarsson, A.5
Sandberg, K.6
Cothran, G.7
Vila, C.8
Binns, M.9
Ellegren, H.10
-
92
-
-
77954969837
-
Identification of y chromosome genetic variations in Chinese indigenous horse breeds.
-
Ling, Y., Ma, Y., Guan, W., Cheng, Y., Wang, Y., Han, J., Jin, D., Mang, L. & Mahmut, H. (2010) Identification of y chromosome genetic variations in Chinese indigenous horse breeds. Journal of Heredity 101, 639-43.
-
(2010)
Journal of Heredity
, vol.101
, pp. 639-643
-
-
Ling, Y.1
Ma, Y.2
Guan, W.3
Cheng, Y.4
Wang, Y.5
Han, J.6
Jin, D.7
Mang, L.8
Mahmut, H.9
-
93
-
-
69549110251
-
On the origin and spread of an adaptive allele in deer mice.
-
Linnen, C. R., Kingsley, E. P., Jensen, J. D. & Hoekstra, H. E. (2009). On the origin and spread of an adaptive allele in deer mice. Science 325, 1095.
-
(2009)
Science
, vol.325
, pp. 1095
-
-
Linnen, C.R.1
Kingsley, E.P.2
Jensen, J.D.3
Hoekstra, H.E.4
-
94
-
-
28844500831
-
Multiple maternal origins of chickens: Out of the Asian jungles.
-
Liu, Y., Wu, G-S., Yao, Y-G., Miao, Y-W., Luikart, G., Baig, M., Beja-Pereira, A., Ding, Z-L., Palanichamy, M. G. & Zhang, Y-P. (2006). Multiple maternal origins of chickens: Out of the Asian jungles. Molecular Phylogenetics and Evolution 38, 12-19.
-
(2006)
Molecular Phylogenetics and Evolution
, vol.38
, pp. 12-19
-
-
Liu, Y.1
Wu, G.-S.2
Yao, Y.-G.3
Miao, Y.-W.4
Luikart, G.5
Baig, M.6
Beja-Pereira, A.7
Ding, Z.-L.8
Palanichamy, M.G.9
Zhang, Y.-P.10
-
95
-
-
40549111313
-
MC1R variants correlate with thinhorn sheep colour cline but not individual colour.
-
Loehr, J., Worley, K., Moe, J., Carey, J. & Coltman, D. W. (2008). MC1R variants correlate with thinhorn sheep colour cline but not individual colour. Canadian Journal of Zoology 86, 147-150.
-
(2008)
Canadian Journal of Zoology
, vol.86
, pp. 147-150
-
-
Loehr, J.1
Worley, K.2
Moe, J.3
Carey, J.4
Coltman, D.W.5
-
96
-
-
65449148743
-
Coat color variation at the beginning of horse domestication.
-
Ludwig, A., Pruvost, M., Reissmann, M., Benecke, N., Brockmann, G. A., Castanos, P., Cieslak, M., Lippold, S., Llorente, L., Malaspinas, A-S., Slatkin, M. & Hofreiter, M. (2009). Coat color variation at the beginning of horse domestication. Science 324, 485.
-
(2009)
Science
, vol.324
, pp. 485
-
-
Ludwig, A.1
Pruvost, M.2
Reissmann, M.3
Benecke, N.4
Brockmann, G.A.5
Castanos, P.6
Cieslak, M.7
Lippold, S.8
Llorente, L.9
Malaspinas, A.-S.10
Slatkin, M.11
Hofreiter, M.12
-
97
-
-
0035826870
-
Multiple maternal origins and weak phylogeographic structure in domestic goats.
-
Luikart, G., Gielly, L., Excoffier, L., Vigne, J-D., Bouvet, J. & Taberlet, P. (2001). Multiple maternal origins and weak phylogeographic structure in domestic goats. Proceedings of the National Academy of Sciences 98, 5927-5932.
-
(2001)
Proceedings of the National Academy of Sciences
, vol.98
, pp. 5927-5932
-
-
Luikart, G.1
Gielly, L.2
Excoffier, L.3
Vigne, J.-D.4
Bouvet, J.5
Taberlet, P.6
-
98
-
-
23844535500
-
Chocolate coated cats: TYRP1 mutations for brown color in domestic cats.
-
Lyons, L. A., Foe, I. T., Rah, H. C. & Grahn, R. A. (2005a). Chocolate coated cats: TYRP1 mutations for brown color in domestic cats. Mammalian Genome 16, 356-66.
-
(2005)
Mammalian Genome
, vol.16
, pp. 356-366
-
-
Lyons, L.A.1
Foe, I.T.2
Rah, H.C.3
Grahn, R.A.4
-
99
-
-
17144394138
-
Tyrosinase mutations associated with Siamese and Burmese patterns in the domestic cat (Felis catus).
-
Lyons, L. A., Imes, D. L., Rah, H. C. & Grahn, R. A. (2005b). Tyrosinase mutations associated with Siamese and Burmese patterns in the domestic cat (Felis catus). Animal Genetics 36, 119-126.
-
(2005)
Animal Genetics
, vol.36
, pp. 119-126
-
-
Lyons, L.A.1
Imes, D.L.2
Rah, H.C.3
Grahn, R.A.4
-
100
-
-
0026648110
-
Genetic and molecular analysis of recessive alleles at the pink-eyed dilution (p) locus of the mouse.
-
Lyon, M. F., King, T. R., Gondo, Y., Gardner, J. M., Nakatsu, Y., Eicher, E. M. & Brilliant, M. H. (1992). Genetic and molecular analysis of recessive alleles at the pink-eyed dilution (p) locus of the mouse. Proceedings of the National Academy of Sciences 89, 6968-6972.
-
(1992)
Proceedings of the National Academy of Sciences
, vol.89
, pp. 6968-6972
-
-
Lyon, M.F.1
King, T.R.2
Gondo, Y.3
Gardner, J.M.4
Nakatsu, Y.5
Eicher, E.M.6
Brilliant, M.H.7
-
101
-
-
0038713136
-
A mutation in the MATP gene causes the cream coat colour in the horse.
-
Mariat, D., Taourit, S. & Guerin, G. (2003). A mutation in the MATP gene causes the cream coat colour in the horse. Genetics Selection Evolution 35, 119-133.
-
(2003)
Genetics Selection Evolution
, vol.35
, pp. 119-133
-
-
Mariat, D.1
Taourit, S.2
Guerin, G.3
-
102
-
-
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. (1996). A missense mutation in the gene for melanocyte-stimulating hormone receptor (MC1R) is associated with the chestnut coat color in horses. Mammalian Genome 7, 895-899.
-
(1996)
Mammalian Genome
, vol.7
, pp. 895-899
-
-
Marklund, L.1
Moller, M.J.2
Sandberg, K.3
Andersson, L.4
-
103
-
-
0032806006
-
Close association between sequence polymorphism in the KIT gene and the roan coat color in horses.
-
Marklund, S., Moller, M., Sandberg, K. & Andersson, L. (1999). Close association between sequence polymorphism in the KIT gene and the roan coat color in horses. Mammalian Genome 10, 283-288.
-
(1999)
Mammalian Genome
, vol.10
, pp. 283-288
-
-
Marklund, S.1
Moller, M.2
Sandberg, K.3
Andersson, L.4
-
104
-
-
0036134088
-
A mouse model of Waardenburg syndrome type 4 with a new spontaneous mutation of the endothelin-B receptor gene.
-
Matsushima, Y., Shinkai, Y., Kobayashi, Y, Sakamoto, M., Kunieda, T. & Tachibana, M. (2002). A mouse model of Waardenburg syndrome type 4 with a new spontaneous mutation of the endothelin-B receptor gene. Mammalian Genome 13, 30-35.
-
(2002)
Mammalian Genome
, vol.13
, pp. 30-35
-
-
Matsushima, Y.1
Shinkai, Y.2
Kobayashi, Y.3
Sakamoto, M.4
Kunieda, T.5
Tachibana, M.6
-
106
-
-
70349257590
-
Mapping of the domestic cat "SILVER" coat color locus identifies a unique genomic location for silver in mammals.
-
Menotti-Raymond, M., David, V. A., Eizirik, E., Roelke, M. E., Ghaffari, H. & O'Brien, S. J. (2009). Mapping of the domestic cat "SILVER" coat color locus identifies a unique genomic location for silver in mammals. Journal of Heredity 100, S8-S13.
-
(2009)
Journal of Heredity
, vol.100
-
-
Menotti-Raymond, M.1
David, V.A.2
Eizirik, E.3
Roelke, M.E.4
Ghaffari, H.5
O'Brien, S.J.6
-
107
-
-
0031828292
-
A missense mutation in the endothelin-B receptor gene is associated with lethal white foal syndrome: an equine version of Hirschsprung disease.
-
Metallinos, D. L., Bowling, A. T. & Rine, J. (1998). A missense mutation in the endothelin-B receptor gene is associated with lethal white foal syndrome: an equine version of Hirschsprung disease. Mammalian Genome 9, 426-431.
-
(1998)
Mammalian Genome
, vol.9
, pp. 426-431
-
-
Metallinos, D.L.1
Bowling, A.T.2
Rine, J.3
-
108
-
-
77950500935
-
The "silver" Japanese quail and the MITF gene: causal mutation, associated traits and homology with the "blue" chicken plumage.
-
Minvielle, F., Bed'Hom, B., Coville, J-L., Ito, S., Inoue-Murayama, M. & Gourichon, D. (2010). The "silver" Japanese quail and the MITF gene: causal mutation, associated traits and homology with the "blue" chicken plumage. BioMed Central Genetics 11, 15.
-
(2010)
BioMed Central Genetics
, vol.11
, pp. 15
-
-
Minvielle, F.1
Bed'Hom, B.2
Coville, J.-L.3
Ito, S.4
Inoue-Murayama, M.5
Gourichon, D.6
-
109
-
-
34047190879
-
Endothelin receptor B2 (EDNRB2) is associated with the panda plumage colour mutation in Japanese quail.
-
Miwa, M., Inoue-Murayama, M., Aoki, H., Kunisada, T., Hiragaki, T., Mizutani, M. & Ito, S. (2007). Endothelin receptor B2 (EDNRB2) is associated with the panda plumage colour mutation in Japanese quail. Animal Genetics 38, 103-108.
-
(2007)
Animal Genetics
, vol.38
, pp. 103-108
-
-
Miwa, M.1
Inoue-Murayama, M.2
Aoki, H.3
Kunisada, T.4
Hiragaki, T.5
Mizutani, M.6
Ito, S.7
-
111
-
-
26244436635
-
A window on the genetics of evolution: MC1R and plumage colouration in birds.
-
Mundy, N. (2005). A window on the genetics of evolution: MC1R and plumage colouration in birds. Proceedings of the Royal Society B-Biological Sciences 272, 1633-1640.
-
(2005)
Proceedings of the Royal Society B-Biological Sciences
, vol.272
, pp. 1633-1640
-
-
Mundy, N.1
-
112
-
-
40849121008
-
Characterization of Japanese quail yellow as a genomic deletion upstream of the avian homolog of the mammalian ASIP (agouti) gene.
-
Nadeau, N. J., Minvielle, F., Ito, S., Inoue-Murayama, M., Gourichon, D., Folett, S. A., Burke, T. & Mundy, N. I. (2008). Characterization of Japanese quail yellow as a genomic deletion upstream of the avian homolog of the mammalian ASIP (agouti) gene. Genetics 178, 777-786.
-
(2008)
Genetics
, vol.178
, pp. 777-786
-
-
Nadeau, N.J.1
Minvielle, F.2
Ito, S.3
Inoue-Murayama, M.4
Gourichon, D.5
Folett, S.A.6
Burke, T.7
Mundy, N.I.8
-
113
-
-
33744478894
-
Association of a Glu92Lys substitution in MC1R with extended brown in Japanese quail (Coturnix japonica).
-
Nadeau, N. J., Minvielle, F. & Mundy, N. I. (2006). Association of a Glu92Lys substitution in MC1R with extended brown in Japanese quail (Coturnix japonica). Animal Genetics 37, 287-289.
-
(2006)
Animal Genetics
, vol.37
, pp. 287-289
-
-
Nadeau, N.J.1
Minvielle, F.2
Mundy, N.I.3
-
114
-
-
36749013028
-
Association of a single-nucleotide substitution in TYRP1 with roux in Japanese quail (Coturnix japonica).
-
Nadeau, N. J., Mundy, N. I., Gourichon, D. & Minvielle, F. (2007). Association of a single-nucleotide substitution in TYRP1 with roux in Japanese quail (Coturnix japonica). Animal Genetics 38, 609-613.
-
(2007)
Animal Genetics
, vol.38
, pp. 609-613
-
-
Nadeau, N.J.1
Mundy, N.I.2
Gourichon, D.3
Minvielle, F.4
-
115
-
-
0033961998
-
Melanocortin 1 receptor variation in the domestic dog.
-
Newton, J. M., Wilkie, A. L., He, L., Jordan, S. A., Mettalinos, D. L., Holmes, N. G., Jackson, I. J. & Barsh, G. S. (2000). Melanocortin 1 receptor variation in the domestic dog. Mammalian Genome 11, 24-30.
-
(2000)
Mammalian Genome
, vol.11
, pp. 24-30
-
-
Newton, J.M.1
Wilkie, A.L.2
He, L.3
Jordan, S.A.4
Mettalinos, D.L.5
Holmes, N.G.6
Jackson, I.J.7
Barsh, G.S.8
-
116
-
-
70349236419
-
TRPM1 forms ion channels associated with melanin content in melanocytes.
-
Oancea, E., Vriene, J., Brauchi, S., Jun, J., Splawski, I. & Clapham, D. E. (2009). TRPM1 forms ion channels associated with melanin content in melanocytes. Science Signaling 2, ra21-ra21.
-
(2009)
Science Signaling
, vol.2
-
-
Oancea, E.1
Vriene, J.2
Brauchi, S.3
Jun, J.4
Splawski, I.5
Clapham, D.E.6
-
117
-
-
0031262856
-
Clinical, morphologic, and biochemical characteristics of Chediak-Higashi syndrome in fifty-six Japanese black cattle.
-
Ogawa, H., Tu, C. H., Kagamizono, H., Soki, K., Inoue, Y., Akatsuka, H., Nagata, S., Wada, T., Ikeya, M., Makimura, S., Uchida, K., Yamaguchi, R. & Otsuka, H. (1997). Clinical, morphologic, and biochemical characteristics of Chediak-Higashi syndrome in fifty-six Japanese black cattle. American Journal of Veterinary Research 58, 1221-1226.
-
(1997)
American Journal of Veterinary Research
, vol.58
, pp. 1221-1226
-
-
Ogawa, H.1
Tu, C.H.2
Kagamizono, H.3
Soki, K.4
Inoue, Y.5
Akatsuka, H.6
Nagata, S.7
Wada, T.8
Ikeya, M.9
Makimura, S.10
Uchida, K.11
Yamaguchi, R.12
Otsuka, H.13
-
118
-
-
62149112479
-
The earliest horse harnessing and milking.
-
Outram, A. K., Stear, N. A., Bendrey, R., Olsen, S., Kasparov, A., Zaibert, V., Thorpe, N. & Evershed, R. P. (2009). The earliest horse harnessing and milking. Science 323, 1332-1335.
-
(2009)
Science
, vol.323
, pp. 1332-1335
-
-
Outram, A.K.1
Stear, N.A.2
Bendrey, R.3
Olsen, S.4
Kasparov, A.5
Zaibert, V.6
Thorpe, N.7
Evershed, R.P.8
-
119
-
-
70450227389
-
mtDNA data indicate a single origin for dogs South of Yangtze River, less than 16,300 years ago, from numerous wolves.
-
Pang, J.-F., Kluetsch, C., Zou, X.-J., Zhang, A-B., Luo, L-Y., Angleby, H., Ardalan, A., Ekström, C., Sköllermo, A., Lundeberg, J., Matsumura, S., Leitner, T., Zhang, Y.-P. & Savolainen, P. (2009). mtDNA data indicate a single origin for dogs South of Yangtze River, less than 16, 300 years ago, from numerous wolves. Molecular Biology and Evolution 26, 2849-2864.
-
(2009)
Molecular Biology and Evolution
, vol.26
, pp. 2849-2864
-
-
Pang, J.-F.1
Kluetsch, C.2
Zou, X.-J.3
Zhang, A.-B.4
Luo, L.-Y.5
Angleby, H.6
Ardalan, A.7
Ekström, C.8
Sköllermo, A.9
Lundeberg, J.10
Matsumura, S.11
Leitner, T.12
Zhang, Y.-P.13
Savolainen, P.14
-
120
-
-
26944496413
-
Evidence of three maternal lineages in near eastern sheep supporting multiple domestication events.
-
Pedrosa, S., Uzun, M., Arranz, J-J., Gutierrez-Gil, B., San Primitivo, F. & Bayon, Y. (2005). Evidence of three maternal lineages in near eastern sheep supporting multiple domestication events. Proceedings of the Royal Society B-Biological Sciences 272, 2211-2217.
-
(2005)
Proceedings of the Royal Society B-Biological Sciences
, vol.272
, pp. 2211-2217
-
-
Pedrosa, S.1
Uzun, M.2
Arranz, J.-J.3
Gutierrez-Gil, B.4
San Primitivo, F.5
Bayon, Y.6
-
121
-
-
70450231699
-
Tracing the history of goat pastoralism: New clues from mitochondrial and Y chromosome DNA in North Africa.
-
Pereira, F., Queirós, S., Gusmão, L., Nijman, I. J., Cuppen, E., Lenstra, J. A., Econogene Consortium, Davis, S. M. J., Nejmeddine, F. & Amorim, A. (2009). Tracing the history of goat pastoralism: New clues from mitochondrial and Y chromosome DNA in North Africa. Molecular Biology and Evolution 26, 2765-2773.
-
(2009)
Molecular Biology and Evolution
, vol.26
, pp. 2765-2773
-
-
Pereira, F.1
Queirós, S.2
Gusmão, L.3
Nijman, I.J.4
Cuppen, E.5
Lenstra, J.A.6
Econogene Consortium Davis, S.M.J.7
Nejmeddine, F.8
Amorim, A.9
-
122
-
-
26444448038
-
Polymorphisms within the canine MLPH gene are associated with diluted coat color in dogs.
-
Philipp, U., Hamann, H., Mecklenburg, L., Nishino, S., Mignot, E., Günzel-Apel, A. R., Schmutz, S. M. & Leeb, T. (2005). Polymorphisms within the canine MLPH gene are associated with diluted coat color in dogs. BioMed Central Genetics 6, 34.
-
(2005)
BioMed Central Genetics
, vol.6
, pp. 34
-
-
Philipp, U.1
Hamann, H.2
Mecklenburg, L.3
Nishino, S.4
Mignot, E.5
Günzel-Apel, A.R.6
Schmutz, S.M.7
Leeb, T.8
-
123
-
-
48349098128
-
A cis-acting regulatory mutation causes premature hair graying and susceptibility to melanoma in the horse.
-
Pielberg, G. R., Golovko, A., Sundström, E., Curik, I., Lennartsson, J., Seltenhammer, M. H., Druml, T., Binns, M., Fitzsimmons, C., Lindgren, G., Sandberg, K., Baumung, R., Vetterlein, M., Strömberg, S., Grabherr, M., Wade, C., Lindblad-Toh, K., Ponten, F., Heldin, C., Sölkner, J. & Andersson, L. (2008). A cis-acting regulatory mutation causes premature hair graying and susceptibility to melanoma in the horse. Nature Genetics 40, 1004-1009.
-
(2008)
Nature Genetics
, vol.40
, pp. 1004-1009
-
-
Pielberg, G.R.1
Golovko, A.2
Sundström, E.3
Curik, I.4
Lennartsson, J.5
Seltenhammer, M.H.6
Druml, T.7
Binns, M.8
Fitzsimmons, C.9
Lindgren, G.10
Sandberg, K.11
Baumung, R.12
Vetterlein, M.13
Strömberg, S.14
Grabherr, M.15
Wade, C.16
Lindblad-Toh, K.17
Ponten, F.18
Heldin, C.19
Sölkner, J.20
Andersson, L.21
more..
-
124
-
-
0036165284
-
Unexpectedly high allelic diversity at the KIT locus causing dominant white color in the domestic pig.
-
Pielberg, G., Olsson, C., Syvänen, A. C. & Andersoon, L. (2002). Unexpectedly high allelic diversity at the KIT locus causing dominant white color in the domestic pig. Genetics 160, 305-311.
-
(2002)
Genetics
, vol.160
, pp. 305-311
-
-
Pielberg, G.1
Olsson, C.2
Syvänen, A.C.3
Andersoon, L.4
-
125
-
-
65649102307
-
Maternal methyl supplements affect the phenotypic variation of the agouti gene in the offspring of rats with different behavioral types.
-
Prasolova, L. A., Os'Kina, I. N., Plyusnina, I. Z. & Trut, L. N. (2009). Maternal methyl supplements affect the phenotypic variation of the agouti gene in the offspring of rats with different behavioral types. Russian Journal of Genetics 45, 587-592.
-
(2009)
Russian Journal of Genetics
, vol.45
, pp. 587-592
-
-
Prasolova, L.A.1
Os'Kina, I.N.2
Plyusnina, I.Z.3
Trut, L.N.4
-
126
-
-
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., Forster, M., Reents, R. & Averdunk, G. (1999). A QTL for the degree of spotting in cattle shows synteny with the KIT locus on chromosome 6. Journal of Heredity 90, 629-634.
-
(1999)
Journal of Heredity
, 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
Forster, M.16
Reents, R.17
Averdunk, G.18
-
127
-
-
33846566400
-
Two SNPs in the SILV gene are associated with silver coat colour in ponies.
-
Reissmann, M., Bierwolf, J. & Brockmann, G. A. (2007). Two SNPs in the SILV gene are associated with silver coat colour in ponies. Animal Genetics 38, 1-6.
-
(2007)
Animal Genetics
, vol.38
, pp. 1-6
-
-
Reissmann, M.1
Bierwolf, J.2
Brockmann, G.A.3
-
128
-
-
0035008008
-
Mutations in the agouti (ASIP), the extension (MC1R), and the brown (TYRP1) loci and their association to coat colour phenotypes in horses (Equus caballus).
-
Rieder, S., Taourit, S., Mariat, D., Langlois, B. & Guerin, G. (2001). Mutations in the agouti (ASIP), the extension (MC1R), and the brown (TYRP1) loci and their association to coat colour phenotypes in horses (Equus caballus). Mammalian Genome 12, 450-455.
-
(2001)
Mammalian Genome
, vol.12
, pp. 450-455
-
-
Rieder, S.1
Taourit, S.2
Mariat, D.3
Langlois, B.4
Guerin, G.5
-
129
-
-
0035908915
-
Inheritance and population structure of the white-phased "Kermode" black bear.
-
Ritland, K., Newton, C. & Marshall, H. D. (2001). Inheritance and population structure of the white-phased "Kermode" black bear. Current Biology 11, 1468-1472.
-
(2001)
Current Biology
, vol.11
, pp. 1468-1472
-
-
Ritland, K.1
Newton, C.2
Marshall, H.D.3
-
130
-
-
33745926818
-
Nuclear gene indicates coat color polymorphism in mammoths.
-
Rompler, H., Rohland, N., Lalueza-Fox, C., Willerslev, E., Kuznetsova, T., Rabeder, G., Bertranpetit, J., Schöneberg, T. & Hofreiter, M. (2006). Nuclear gene indicates coat color polymorphism in mammoths. Science 313, 62.
-
(2006)
Science
, vol.313
, pp. 62
-
-
Rompler, H.1
Rohland, N.2
Lalueza-Fox, C.3
Willerslev, E.4
Kuznetsova, T.5
Rabeder, G.6
Bertranpetit, J.7
Schöneberg, T.8
Hofreiter, M.9
-
131
-
-
41649119205
-
Domestication of the donkey: Timing, processes, and indicators.
-
Rossel, S., Marshall, F., Peters, J., Pilgram, T., Adams, M. D. & O'Connor, D. (2008). Domestication of the donkey: Timing, processes, and indicators. Proceedings of the National Academy of Sciences 105, 3715-3720.
-
(2008)
Proceedings of the National Academy of Sciences
, vol.105
, pp. 3715-3720
-
-
Rossel, S.1
Marshall, F.2
Peters, J.3
Pilgram, T.4
Adams, M.D.5
O'Connor, D.6
-
132
-
-
44049099086
-
Differences in the expression of the ASIP gene are involved in the recessive black coat colour pattern in sheep: evidence from the rare Xalda sheep breed.
-
Royo, L. J., Alvarez, I., Arranz, J. J., Fernández, I., Rodriguez, A., Pérez-Pardal, L. & Goyache, F. (2008). Differences in the expression of the ASIP gene are involved in the recessive black coat colour pattern in sheep: evidence from the rare Xalda sheep breed. Animal Genetics 39, 290-293.
-
(2008)
Animal Genetics
, vol.39
, pp. 290-293
-
-
Royo, L.J.1
Alvarez, I.2
Arranz, J.J.3
Fernández, I.4
Rodriguez, A.5
Pérez-Pardal, L.6
Goyache, F.7
-
133
-
-
0032053530
-
Endothelin receptor B polymorphism associated with lethal white foal syndrome in horses.
-
Santchi, E. M., Purdy, A. K., Valberg, S, J., Vrotsos, P. D., Kaese, H. & Mickelson, N. R. (1998). Endothelin receptor B polymorphism associated with lethal white foal syndrome in horses. Mammalian Genome 9, 306-309.
-
(1998)
Mammalian Genome
, vol.9
, pp. 306-309
-
-
Santchi, E.M.1
Purdy, A.K.2
Valberg, S.J.3
Vrotsos, P.D.4
Kaese, H.5
Mickelson, N.R.6
-
134
-
-
2242463993
-
Genetic evidence for an East Asian origin of domestic dogs.
-
Savolainen, P., Zhang, Y., Luo, J., Lundeberg, J. & Leitner, T. (2002). Genetic evidence for an East Asian origin of domestic dogs. Science 298, 1610-1613.
-
(2002)
Science
, vol.298
, pp. 1610-1613
-
-
Savolainen, P.1
Zhang, Y.2
Luo, J.3
Lundeberg, J.4
Leitner, T.5
-
135
-
-
36749093467
-
Genes affecting coat colour and pattern in domestic dogs: a review.
-
Schmutz, S. M. & Berryere, T. G. (2007). Genes affecting coat colour and pattern in domestic dogs: a review. Animal Genetics 38, 539-549.
-
(2007)
Animal Genetics
, vol.38
, pp. 539-549
-
-
Schmutz, S.M.1
Berryere, T.G.2
-
136
-
-
0347931983
-
A form of albinism in cattle is caused by a tyrosinase frameshift mutation.
-
Schmutz, S. M., Berryere, T. G., Ciobanu, D. C., Mileham, A. J., Schmidtz, B. H. & Fredholm, M. (2004). A form of albinism in cattle is caused by a tyrosinase frameshift mutation. Mammalian Genome 15, 62-67.
-
(2004)
Mammalian Genome
, vol.15
, pp. 62-67
-
-
Schmutz, S.M.1
Berryere, T.G.2
Ciobanu, D.C.3
Mileham, A.J.4
Schmidtz, B.H.5
Fredholm, M.6
-
137
-
-
78149427289
-
MITF and White Spotting in Dogs: A Population Study.
-
Schmutz, S. M., Berryere, T. G. & Dreger, D. L. (2009). MITF and White Spotting in Dogs: A Population Study. Journal of Heredity 100, 66-74.
-
(2009)
Journal of Heredity
, vol.100
, pp. 66-74
-
-
Schmutz, S.M.1
Berryere, T.G.2
Dreger, D.L.3
-
138
-
-
0346217088
-
MC1R studies in dogs with melanistic mask or Brindle patterns.
-
Schmutz, S. M., Berryere, T. G., Ellinwood, N. M., Kerns, J. A. & Barsh, G. S. (2003). MC1R studies in dogs with melanistic mask or Brindle patterns. Journal of Heredity 94, 69-73.
-
(2003)
Journal of Heredity
, vol.94
, pp. 69-73
-
-
Schmutz, S.M.1
Berryere, T.G.2
Ellinwood, N.M.3
Kerns, J.A.4
Barsh, G.S.5
-
139
-
-
0036017944
-
TYRP1 and MC1R genotypes and their effects on coat color in dogs
-
Schmutz, S. M., Berryere, T. G. & Goldfinch, A. D. (2002). TYRP1 and MC1R genotypes and their effects on coat color in dogs, Mammalian Genome 13, 380-387.
-
(2002)
Mammalian Genome
, vol.13
, pp. 380-387
-
-
Schmutz, S.M.1
Berryere, T.G.2
Goldfinch, A.D.3
-
140
-
-
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. (1999). A missense mutation in the bovine MGF gene is associated with the roan phenotype in Belgian Blue and Shorthorn cattle. Mammalian Genome 10, 710-712.
-
(1999)
Mammalian Genome
, vol.10
, pp. 710-712
-
-
Seitz, J.J.1
Schmutz, S.M.2
Thue, T.D.3
Buchanan, F.C.4
-
141
-
-
0036091788
-
Melanosomal proteins-role in melanin polymerization.
-
Sharma, S., Wagh, S. & Govindarajan, R. (2002). Melanosomal proteins-role in melanin polymerization. Pigment Cell Research 15, 127-133.
-
(2002)
Pigment Cell Research
, vol.15
, pp. 127-133
-
-
Sharma, S.1
Wagh, S.2
Govindarajan, R.3
-
142
-
-
0141749482
-
Investigation of KIT gene mutations in women with 46 XX spontaneous premature ovarian failure.
-
Shibanuma, K., Tong, Z-B., Vanderhoof, V. H., Vanevski, K. & Nelson, L. N. (2002). Investigation of KIT gene mutations in women with 46 XX spontaneous premature ovarian failure. BioMed Central Womens Health 2, 8.
-
(2002)
BioMed Central Womens Health
, vol.2
, pp. 8
-
-
Shibanuma, K.1
Tong, Z.-B.2
Vanderhoof, V.H.3
Vanevski, K.4
Nelson, L.N.5
-
143
-
-
69449104505
-
Current challenges in understanding melanogenesis: bridging chemistry, biological control, morphology, and function.
-
Simon, J. D., Peles, D., Wakamatsu, K. & Ito, S. (2009). Current challenges in understanding melanogenesis: bridging chemistry, biological control, morphology, and function. Pigment Cell Melanoma Research 22, 563-579.
-
(2009)
Pigment Cell Melanoma Research
, vol.22
, pp. 563-579
-
-
Simon, J.D.1
Peles, D.2
Wakamatsu, K.3
Ito, S.4
-
144
-
-
58849134980
-
A role of the microphthalmia-associated transcription factor in congenital sensorineural deafness and eye pigmentation in Dalmatian dogs.
-
Stritzel, S., Wöhlke, A. & Distel, O. (2009). A role of the microphthalmia-associated transcription factor in congenital sensorineural deafness and eye pigmentation in Dalmatian dogs. Journal of Animal Breeding and Genetics 126, 59-62.
-
(2009)
Journal of Animal Breeding and Genetics
, vol.126
, pp. 59-62
-
-
Stritzel, S.1
Wöhlke, A.2
Distel, O.3
-
145
-
-
25444456658
-
The Silver locus product Pmel17/gp100/Silv/ME20: conreoversial in name and function.
-
Theos, A. C., Truschel, S. T., Raposo, G. & Marks, M. S. (2005). The Silver locus product Pmel17/gp100/Silv/ME20: conreoversial in name and function. Pigment Cell Research 18, 322-336.
-
(2005)
Pigment Cell Research
, vol.18
, pp. 322-336
-
-
Theos, A.C.1
Truschel, S.T.2
Raposo, G.3
Marks, M.S.4
-
146
-
-
0033627949
-
Autosomal albino chicken mutation (ca/ca) deletes hexanucleotide (-delta GACTGG817) at a copper-binding site of the tyrosinase gene.
-
Tobita-Teramoto, T., Jang, G. Y., Kino, K., Salter, D. W., Brumbaugh, J. & Akiyama, T. (2000). Autosomal albino chicken mutation (ca/ca) deletes hexanucleotide (-delta GACTGG817) at a copper-binding site of the tyrosinase gene. Poultry Science 79, 46-50.
-
(2000)
Poultry Science
, vol.79
, pp. 46-50
-
-
Tobita-Teramoto, T.1
Jang, G.Y.2
Kino, K.3
Salter, D.W.4
Brumbaugh, J.5
Akiyama, T.6
-
147
-
-
0001227499
-
Early canid domestication: the farm-fox experiment.
-
Trut, L. N. (1999). Early canid domestication: the farm-fox experiment. American Scientist 87, 160-169.
-
(1999)
American Scientist
, vol.87
, pp. 160-169
-
-
Trut, L.N.1
-
148
-
-
0345507904
-
-
eds Ruvinsky, A., Sampson, J., CABI Publishing, New York
-
Trut, L. N., Ruvinsky, A. & Sampson, J. (2001). The genetics of the dog, experimental studies in early canid domestication. eds Ruvinsky, A., Sampson, J., CABI Publishing, New York, pp 15-41.
-
(2001)
The genetics of the dog, experimental studies in early canid domestication.
, pp. 15-41
-
-
Trut, L.N.1
Ruvinsky, A.2
Sampson, J.3
-
149
-
-
77954649705
-
"Transcription physiology" of pigment formation in melanocytes: central role of MITF.
-
Vachtenheim, J. & Borovanský, J. (2010). "Transcription physiology" of pigment formation in melanocytes: central role of MITF. Experimental Dermatology 19, 617-627.
-
(2010)
Experimental Dermatology
, vol.19
, pp. 617-627
-
-
Vachtenheim, J.1
Borovanský, J.2
-
150
-
-
39549107341
-
A single point-mutation within the melanophilin gene causes the lavender plumage colour dilution phenotype in the chicken.
-
Vaez, M., Follet, S. A., Bed'Hom, B., Gourichon, D., Tixier-Boichard, M. & Burke, T. (2008). A single point-mutation within the melanophilin gene causes the lavender plumage colour dilution phenotype in the chicken. BioMed Central Genetics 9, 7.
-
(2008)
BioMed Central Genetics
, vol.9
, pp. 7
-
-
Vaez, M.1
Follet, S.A.2
Bed'Hom, B.3
Gourichon, D.4
Tixier-Boichard, M.5
Burke, T.6
-
151
-
-
1842339332
-
A non-epistatic interaction of agouti and extension in the fox, Vulpes vulpes.
-
Våge, D. I., Lu, D., Klungland, H., Lien, S., Adalsteinsson, S. & Cone, R. D. (1997). A non-epistatic interaction of agouti and extension in the fox, Vulpes vulpes. Nature Genetics 15, 311-315.
-
(1997)
Nature Genetics
, vol.15
, pp. 311-315
-
-
Våge, D.I.1
Lu, D.2
Klungland, H.3
Lien, S.4
Adalsteinsson, S.5
Cone, R.D.6
-
152
-
-
0032775886
-
Molecular and pharmacological characterization of dominant black coat color in sheep.
-
Våge, D. I., Klungland, H. & Cone, R. D. (1999). Molecular and pharmacological characterization of dominant black coat color in sheep. Mammalian Genome 10, 39-43.
-
(1999)
Mammalian Genome
, vol.10
, pp. 39-43
-
-
Våge, D.I.1
Klungland, H.2
Cone, R.D.3
-
153
-
-
71849117485
-
Mutations in TRPM1 are a common cause of complete congenital stationary night blindness.
-
Van Genderen, A. A., Bijveld, M. M., Claassen, Y. B., Florijn, R. J., Pearring, J. N., Meire, F. M., McCall, M. A., Riemslag, F. C., Gregg, R. G., Bergen, A. A. & Kamermans, M. (2009). Mutations in TRPM1 are a common cause of complete congenital stationary night blindness. American Journal of Human Genetics 85, 730-736.
-
(2009)
American Journal of Human Genetics
, vol.85
, pp. 730-736
-
-
Van Genderen, A.A.1
Bijveld, M.M.2
Claassen, Y.B.3
Florijn, R.J.4
Pearring, J.N.5
Meire, F.M.6
McCall, M.A.7
Riemslag, F.C.8
Gregg, R.G.9
Bergen, A.A.10
Kamermans, M.11
-
154
-
-
1842482431
-
Early taming of the cat in Cyprus.
-
Vigne, J. D., Guilaine, J., Debue, K., Haye, L. & Gerad, P. (2004). Early taming of the cat in Cyprus. Science 304, 259.
-
(2004)
Science
, vol.304
, pp. 259
-
-
Vigne, J.D.1
Guilaine, J.2
Debue, K.3
Haye, L.4
Gerad, P.5
-
155
-
-
0035910491
-
Widespread origins of domestic horse lineages.
-
Vila, C., Leonard, J. A., Götherström, A., Marklund, S., Sandberg, K., Lidén, K., Wayne, R. K. & Ellegren, H. (2001). Widespread origins of domestic horse lineages. Science 291, 474-477.
-
(2001)
Science
, vol.291
, pp. 474-477
-
-
Vila, C.1
Leonard, J.A.2
Götherström, A.3
Marklund, S.4
Sandberg, K.5
Lidén, K.6
Wayne, R.K.7
Ellegren, H.8
-
156
-
-
0030616576
-
Multiple and ancient origins of the domestic dog.
-
Vila, C., Savolainen, P., Maldonado, J. E., Amorim, I. R. Rice, J. E. Honeycutt, R. L., Crandall, K. A., Lundeberg, J. & Wayne, R. K. (1997). Multiple and ancient origins of the domestic dog. Science 276, 1687-1689.
-
(1997)
Science
, vol.276
, pp. 1687-1689
-
-
Vila, C.1
Savolainen, P.2
Maldonado, J.E.3
Amorim, I.R.4
Rice, J.E.5
Honeycutt, R.L.6
Crandall, K.A.7
Lundeberg, J.8
Wayne, R.K.9
-
157
-
-
0035999728
-
Agouti: From mouse to man, from skin to fat.
-
Voisey, J. & Van Daal, A. (2002). Agouti: From mouse to man, from skin to fat. Pigment Cell Research 15, 10-18.
-
(2002)
Pigment Cell Research
, vol.15
, pp. 10-18
-
-
Voisey, J.1
Van Daal, A.2
-
158
-
-
70449379045
-
Genome sequence, comparative analysis, and population genetics of the domestic horse.
-
Broad Institute Genome Sequencing Platform; Broad Institute Whole Genome Assembly Team
-
Wade, C. M., Giulotto, E., Sigurdsson, S., Zoli, M., Gnerre, S., Imsland, F., Lear, T. L., Adelson, D. L., Bailey, E., Bellone, R. R., Blöcker, H., Distl, O., Edgar, R. C., Garber, M., Leeb, T., Mauceli, E., MacLeod, J. N., Penedo, M. C., Raison, J. M., Sharpe, T., Vogel, J., Andersson, L., Antczak, D. F., Biagi, T., Binns, M. M., Chowdhary, B. P., Coleman, S. J., Della Valle, G., Fryc, S., Guérin, G., Hasegawa, T., Hill, E. W., Jurka, J., Kiialainen, A., Lindgren, G., Liu, J., Magnani, E., Mickelson, J. R., Murray, J., Nergadze, S. G., Onofrio, R., Pedroni, S., Piras, M. F., Raudsepp, T., Rocchi, M., Røed, K. H., Ryder, O. A., Searle, S., Skow, L., Swinburne, J. E., Syvänen, A. C., Tozaki, T., Valberg, S. J., Vaudin, M., White, J. R. & Zody, M. C.; Broad Institute Genome Sequencing Platform; Broad Institute Whole Genome Assembly Team, Lander, E. S. & Lindblad-Toh, K. (2009). Genome sequence, comparative analysis, and population genetics of the domestic horse. Science 326, 865-867.
-
(2009)
Science
, vol.326
, pp. 865-867
-
-
Wade, C.M.1
Giulotto, E.2
Sigurdsson, S.3
Zoli, M.4
Gnerre, S.5
Imsland, F.6
Lear, T.L.7
Adelson, D.L.8
Bailey, E.9
Bellone, R.R.10
Blöcker, H.11
Distl, O.12
Edgar, R.C.13
Garber, M.14
Leeb, T.15
Mauceli, E.16
MacLeod, J.N.17
Penedo, M.C.18
Raison, J.M.19
Sharpe, T.20
Vogel, J.21
Andersson, L.22
Antczak, D.F.23
Biagi, T.24
Binns, M.M.25
Chowdhary, B.P.26
Coleman, S.J.27
Della Valle, G.28
Fryc, S.29
Guérin, G.30
Hasegawa, T.31
Hill, E.W.32
Jurka, J.33
Kiialainen, A.34
Lindgren, G.35
Liu, J.36
Magnani, E.37
Mickelson, J.R.38
Murray, J.39
Nergadze, S.G.40
Onofrio, R.41
Pedroni, S.42
Piras, M.F.43
Raudsepp, T.44
Rocchi, M.45
Røed, K.H.46
Ryder, O.A.47
Searle, S.48
Skow, L.49
Swinburne, J.E.50
Syvänen, A.C.51
Tozaki, T.52
Valberg, S.J.53
Vaudin, M.54
White, J.R.55
Zody, M.C.56
Lander, E.S.57
Lindblad-Toh, K.58
more..
-
159
-
-
1942476015
-
Isolation of Y chromosome-specific microsatellites in the horse and cross-species amplification in the genus Equus.
-
Wallner, B., Piumi, F., Brem, G., Müller, M. & Achmann, R. (2004). Isolation of Y chromosome-specific microsatellites in the horse and cross-species amplification in the genus Equus. Journal of Heredity 95, 158-164.
-
(2004)
Journal of Heredity
, vol.95
, pp. 158-164
-
-
Wallner, B.1
Piumi, F.2
Brem, G.3
Müller, M.4
Achmann, R.5
-
160
-
-
79952427563
-
MLPH Genotype-Melanin Phenotype Correlation in Dilute Dogs.
-
Welle, M., Phillipp, U., Rüfenacht, S., Roosje, P., Scharfenstein, M., Schütz, E., Brenig, B., Linek, M., Mecklenburg, L., Grest, P., Drögemüller, M., Haase, B., Leeb, T. & Drögemüller, C. (2009). MLPH Genotype-Melanin Phenotype Correlation in Dilute Dogs. Journal of Heredity 100, 75-79.
-
(2009)
Journal of Heredity
, vol.100
, pp. 75-79
-
-
Welle, M.1
Phillipp, U.2
Rüfenacht, S.3
Roosje, P.4
Scharfenstein, M.5
Schütz, E.6
Brenig, B.7
Linek, M.8
Mecklenburg, L.9
Grest, P.10
Drögemüller, M.11
Haase, B.12
Leeb, T.13
Drögemüller, C.14
-
161
-
-
34548587654
-
Cellular defects in Chediak-Higashi syndrome correlate with the molecular genotype and clinical phenotype.
-
Westbroek, W., Adams, D., Huizing, M., Koshoffer, A., Dorward, H., Tinloy, B., Parkes, J., Helip-Wooley, A., Kleta, R., Tsilou, E., Duvernay, P., Digre, K. B., Creel, D. J., White, J. G., Boissy, R. E. & Gahl, W. A. (2007). Cellular defects in Chediak-Higashi syndrome correlate with the molecular genotype and clinical phenotype. Journal of Investigative Dermatology 127, 2674-2677.
-
(2007)
Journal of Investigative Dermatology
, vol.127
, pp. 2674-2677
-
-
Westbroek, W.1
Adams, D.2
Huizing, M.3
Koshoffer, A.4
Dorward, H.5
Tinloy, B.6
Parkes, J.7
Helip-Wooley, A.8
Kleta, R.9
Tsilou, E.10
Duvernay, P.11
Digre, K.B.12
Creel, D.J.13
White, J.G.14
Boissy, R.E.15
Gahl, W.A.16
-
162
-
-
0031831546
-
A dinucleotide mutation in the endothelin-B receptor gene is associated with lethal white foal syndrome (LWFS), a horse variant of Hirschsprung disease.
-
Yang, G. C., Croacker, D., Zhang, A. L., Manglick, P., Cartmill, T. & Cass, D. (1998). A dinucleotide mutation in the endothelin-B receptor gene is associated with lethal white foal syndrome (LWFS), a horse variant of Hirschsprung disease. Human Molecular Genetics 7, 1047-1052.
-
(1998)
Human Molecular Genetics
, vol.7
, pp. 1047-1052
-
-
Yang, G.C.1
Croacker, D.2
Zhang, A.L.3
Manglick, P.4
Cartmill, T.5
Cass, D.6
-
163
-
-
0034708628
-
The initial domestication of goats (Capra hircus) in the Zagros Mountains 10,000 years ago.
-
Zeder, M. A. & Hesse, B. (2000). The initial domestication of goats (Capra hircus) in the Zagros Mountains 10, 000 years ago. Science 287, 2254-2257.
-
(2000)
Science
, vol.287
, pp. 2254-2257
-
-
Zeder, M.A.1
Hesse, B.2
|