-
1
-
-
0038879019
-
Analyse généalogique des races bovines laitières françaises
-
Boichard D, Maignel L, Verrier E, (1996) Analyse généalogique des races bovines laitières françaises. INRA Prod Anim 9: 323-335.
-
(1996)
INRA Prod Anim
, vol.9
, pp. 323-335
-
-
Boichard, D.1
Maignel, L.2
Verrier, E.3
-
3
-
-
0026646217
-
Identification and prevalence of a genetic defect that causes leukocyte adhesion deficiency in Holstein cattle
-
Shuster DE, Kehrli ME, Ackermann MR, Gilbert RO, (1992) Identification and prevalence of a genetic defect that causes leukocyte adhesion deficiency in Holstein cattle. Proc Nat Acad Sci USA 89: 9225-9229.
-
(1992)
Proc Nat Acad Sci USA
, vol.89
, pp. 9225-9229
-
-
Shuster, D.E.1
Kehrli, M.E.2
Ackermann, M.R.3
Gilbert, R.O.4
-
4
-
-
0035406096
-
Complex vertebral malformation in Holstein calves
-
Agerholm JS, Bendixen C, Andersen O, Arnbjerg J, (2001) Complex vertebral malformation in Holstein calves. Journal of Veterinary Diagnostic Investigation 13: 283-289.
-
(2001)
Journal of Veterinary Diagnostic Investigation
, vol.13
, pp. 283-289
-
-
Agerholm, J.S.1
Bendixen, C.2
Andersen, O.3
Arnbjerg, J.4
-
5
-
-
33749632800
-
Identification of a doublet missense substitution in the bovine LRP4 gene as a candidate causal mutation for syndactyly in Holstein cattle
-
Duchesne A, Gautier M, Chadi S, Grohs C, Floriot S, et al. (2006) Identification of a doublet missense substitution in the bovine LRP4 gene as a candidate causal mutation for syndactyly in Holstein cattle. Genomics 88: 610-621.
-
(2006)
Genomics
, vol.88
, pp. 610-621
-
-
Duchesne, A.1
Gautier, M.2
Chadi, S.3
Grohs, C.4
Floriot, S.5
-
6
-
-
34347255335
-
Familial occurrence of Danish and Dutch cases of the bovine brachyspina syndrome
-
Agerholm JS, Peperkamp K, (2007) Familial occurrence of Danish and Dutch cases of the bovine brachyspina syndrome. BMC Vet Res 3: 8.
-
(2007)
BMC Vet Res
, vol.3
, pp. 8
-
-
Agerholm, J.S.1
Peperkamp, K.2
-
7
-
-
84865578249
-
A deletion in the bovine FANCI gene compromises fertility by causing fetal death and brachyspina
-
Charlier C, Agerholm JS, Coppieters W, Karlskov-Mortensen P, Li W, et al. (2012) A deletion in the bovine FANCI gene compromises fertility by causing fetal death and brachyspina. PLoS One 7: e43085.
-
(2012)
PLoS One
, vol.7
-
-
Charlier, C.1
Agerholm, J.S.2
Coppieters, W.3
Karlskov-Mortensen, P.4
Li, W.5
-
10
-
-
0023239442
-
Homozygosity mapping - a way to map human recessive traits with the dna of inbred children
-
Lander ES, Botstein D, (1987) Homozygosity mapping- a way to map human recessive traits with the dna of inbred children. Science 236: 1567-1570.
-
(1987)
Science
, vol.236
, pp. 1567-1570
-
-
Lander, E.S.1
Botstein, D.2
-
11
-
-
40849110768
-
Highly effective SNP-based association mapping and management of recessive defects in livestock
-
Charlier C, Coppieters W, Rollin F, Desmecht D, Agerholm JS, et al. (2008) Highly effective SNP-based association mapping and management of recessive defects in livestock. Nat Genet 40: 449-454.
-
(2008)
Nat Genet
, vol.40
, pp. 449-454
-
-
Charlier, C.1
Coppieters, W.2
Rollin, F.3
Desmecht, D.4
Agerholm, J.S.5
-
12
-
-
77955879880
-
Female Fertility in French Dairy Breeds: Current Situation and Strategies for Improvement
-
Barbat A, Le Mezec P, Ducrocq V, Mattalia S, Fritz S, et al. (2010) Female Fertility in French Dairy Breeds: Current Situation and Strategies for Improvement. J Reprod Dev 56: S15-S21.
-
(2010)
J Reprod Dev
, vol.56
-
-
Barbat, A.1
Le Mezec, P.2
Ducrocq, V.3
Mattalia, S.4
Fritz, S.5
-
13
-
-
82155170576
-
Harmful recessive effects on fertility detected by absence of homozygous haplotypes
-
VanRaden PM, Olson KM, Null DJ, Hutchison JL, (2011) Harmful recessive effects on fertility detected by absence of homozygous haplotypes. J Dairy Sci 94: 6153-6161.
-
(2011)
J Dairy Sci
, vol.94
, pp. 6153-6161
-
-
VanRaden, P.M.1
Olson, K.M.2
Null, D.J.3
Hutchison, J.L.4
-
14
-
-
84897661193
-
Identification of a Nonsense Mutation in APAF1 that is Causal for a Decrease in Reproductive Efficiency in Dairy Cattle
-
June 14-18 2012, San Diego
-
Adams HA, Sonstegard T, VanRaden PM, Null DJ, Van Tassell C, et al. (2012) Identification of a Nonsense Mutation in APAF1 that is Causal for a Decrease in Reproductive Efficiency in Dairy Cattle. Plant and Animal Genome Meeting, Poster P0555, June 14-18 2012, San Diego.
-
(2012)
Plant and Animal Genome Meeting, Poster P0555
-
-
Adams, H.A.1
Sonstegard, T.2
VanRaden, P.M.3
Null, D.J.4
Van Tassell, C.5
-
15
-
-
84872803971
-
Identification of a nonsense mutation in CWC15 associated with decreased reproductive efficiency in Jersey cattle
-
Sonstegard TS, Cole JB, VanRaden PM, Van Tassell CP, Null DJ, et al. (2013) Identification of a nonsense mutation in CWC15 associated with decreased reproductive efficiency in Jersey cattle. PLoS ONE 8: e54872.
-
(2013)
PLoS ONE
, vol.8
-
-
Sonstegard, T.S.1
Cole, J.B.2
VanRaden, P.M.3
Van Tassell, C.P.4
Null, D.J.5
-
16
-
-
65149096757
-
A whole-genome assembly of the domestic cow, Bos taurus
-
Zimin AV, Delcher AL, Florea L, Kelley DR, Schatz MC, et al. (2009) A whole-genome assembly of the domestic cow, Bos taurus. Genome Biology 10: R42.
-
(2009)
Genome Biology
, vol.10
-
-
Zimin, A.V.1
Delcher, A.L.2
Florea, L.3
Kelley, D.R.4
Schatz, M.C.5
-
17
-
-
67349209683
-
Loss of AND-34/BCAR3 expression in mice results in rupture of the adult lens
-
Near RI, Smith RS, Toselli PA, Freddo TF, Bloom AB, et al. (2009) Loss of AND-34/BCAR3 expression in mice results in rupture of the adult lens. Mol Vis 15: 685-699.
-
(2009)
Mol Vis
, vol.15
, pp. 685-699
-
-
Near, R.I.1
Smith, R.S.2
Toselli, P.A.3
Freddo, T.F.4
Bloom, A.B.5
-
18
-
-
77951640946
-
A method and server for predicting damaging missense mutations
-
Adzhubei IA, Schmidt S, Peshkin L, Ramensky VE, Gerasimova A, et al. (2010) A method and server for predicting damaging missense mutations. Nature methods 7: 248-249.
-
(2010)
Nature Methods
, vol.7
, pp. 248-249
-
-
Adzhubei, I.A.1
Schmidt, S.2
Peshkin, L.3
Ramensky, V.E.4
Gerasimova, A.5
-
19
-
-
68149165614
-
Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm
-
Kumar P, Henikoff S, Ng PC, (2009) Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm. Nature protocols 4: 1073-1081.
-
(2009)
Nature Protocols
, vol.4
, pp. 1073-1081
-
-
Kumar, P.1
Henikoff, S.2
Ng, P.C.3
-
20
-
-
84878747346
-
-
UniProtKB/Swiss-Prot database. Available:. Accessed 2013 Jan 15
-
UniProtKB/Swiss-Prot database. Available: http://www.uniprot.org/uniprot/. Accessed 2013 Jan 15.
-
-
-
-
21
-
-
84878756729
-
-
GART in NCBI Gene database. Available:. Accessed 2013 Jan 15
-
GART in NCBI Gene database. Available: http://www.ncbi.nlm.nih.gov/gene/2618. Accessed 2013 Jan 15.
-
-
-
-
22
-
-
84860759279
-
Roles of Mis18α in epigenetic regulation of centromeric chromatin and CENP-A loading
-
Kim IS, Lee M, Park KC, Jeon Y, Park JH, et al. (2012) Roles of Mis18α in epigenetic regulation of centromeric chromatin and CENP-A loading. Mol Cell 46: 260-273.
-
(2012)
Mol Cell
, vol.46
, pp. 260-273
-
-
Kim, I.S.1
Lee, M.2
Park, K.C.3
Jeon, Y.4
Park, J.H.5
-
23
-
-
84878752018
-
-
SHBG in NCBI Gene database. Available:. Accessed 2013 Jan 15
-
SHBG in NCBI Gene database. Available: www.ncbi.nlm.nih.gov/gene/6462. Accessed 2013 Jan 15.
-
-
-
-
24
-
-
2942619075
-
Deletion of the mouse P450c17 gene causes early embryonic lethality
-
Bair SR, Mellon SH, (2004) Deletion of the mouse P450c17 gene causes early embryonic lethality. Mol Cell Biol 24: 5383-5390.
-
(2004)
Mol Cell Biol
, vol.24
, pp. 5383-5390
-
-
Bair, S.R.1
Mellon, S.H.2
-
25
-
-
40849113345
-
Placenta defects and embryonic lethality resulting from disruption of mouse hydroxysteroid (17-beta) dehydrogenase 2 gene
-
Rantakari P, Strauss L, Kiviranta R, Lagerbohm H, Paviala J, et al. (2008) Placenta defects and embryonic lethality resulting from disruption of mouse hydroxysteroid (17-beta) dehydrogenase 2 gene. Mol Endocrinol 3: 665-675.
-
(2008)
Mol Endocrinol
, vol.3
, pp. 665-675
-
-
Rantakari, P.1
Strauss, L.2
Kiviranta, R.3
Lagerbohm, H.4
Paviala, J.5
-
26
-
-
0344875503
-
The orphan steroid receptor Nur77 family member Nor-1 is essential for early mouse embryogenesis
-
DeYoung RA, Baker JC, Cado D, Winoto A, (2003) The orphan steroid receptor Nur77 family member Nor-1 is essential for early mouse embryogenesis. J Biol Chem 278: 47104-47109.
-
(2003)
J Biol Chem
, vol.278
, pp. 47104-47109
-
-
DeYoung, R.A.1
Baker, J.C.2
Cado, D.3
Winoto, A.4
-
27
-
-
70349656483
-
Lack of Protein S in mice causes embryonic lethal coagulopathy and vascular dysgenesis
-
Burstyn-Cohen T, Heeb MJ, Lemke G, (2009) Lack of Protein S in mice causes embryonic lethal coagulopathy and vascular dysgenesis. J Clin Invest 119: 2942-2953.
-
(2009)
J Clin Invest
, vol.119
, pp. 2942-2953
-
-
Burstyn-Cohen, T.1
Heeb, M.J.2
Lemke, G.3
-
28
-
-
1242340323
-
The ABCs of solute carriers: physiological, pathological and therapeutic implications of human membrane transport proteins: Introduction
-
Hediger MA, Romero MF, Peng JB, Rolfs A, Takanaga H, et al. (2004) The ABCs of solute carriers: physiological, pathological and therapeutic implications of human membrane transport proteins: Introduction. Pflugers Arch 447: 465-468.
-
(2004)
Pflugers Arch
, vol.447
, pp. 465-468
-
-
Hediger, M.A.1
Romero, M.F.2
Peng, J.B.3
Rolfs, A.4
Takanaga, H.5
-
29
-
-
84878765309
-
-
Online Mendelian Inheritance in Animal. Available:. Accessed 2013 Jan 15
-
Online Mendelian Inheritance in Animal. Available: http://omia.angis.org.au. Accessed 2013 Jan 15.
-
-
-
-
30
-
-
80052960191
-
SLC37A1 and SLC37A2 are phosphate-linked, glucose-6-phosphate antiporters
-
Pan CJ, Chen SY, Jun HS, Lin SR, Mansfield BC, et al. (2011) SLC37A1 and SLC37A2 are phosphate-linked, glucose-6-phosphate antiporters. PLoS One 6: e23157.
-
(2011)
PLoS One
, vol.6
-
-
Pan, C.J.1
Chen, S.Y.2
Jun, H.S.3
Lin, S.R.4
Mansfield, B.C.5
-
31
-
-
18544369618
-
Maternally transmitted severe glucose 6-phosphate dehydrogenase deficiency is an embryonic lethal
-
Longo L, Vanegas OC, Patel M, Rosti V, Li H, et al. (2002) Maternally transmitted severe glucose 6-phosphate dehydrogenase deficiency is an embryonic lethal. EMBO J 21: 4229-4239.
-
(2002)
EMBO J
, vol.21
, pp. 4229-4239
-
-
Longo, L.1
Vanegas, O.C.2
Patel, M.3
Rosti, V.4
Li, H.5
-
32
-
-
0029449972
-
Sequence characterization of ENU-induced mutants of glucose phosphate isomerase in mouse
-
Pearce SR, Peters J, Ball S, Morgan MJ, Walker JI, et al. (1995) Sequence characterization of ENU-induced mutants of glucose phosphate isomerase in mouse. Mamm Genome 6: 858-861.
-
(1995)
Mamm Genome
, vol.6
, pp. 858-861
-
-
Pearce, S.R.1
Peters, J.2
Ball, S.3
Morgan, M.J.4
Walker, J.I.5
-
33
-
-
0029155957
-
Animal model for maturity-onset diabetes of the young generated by disruption of the mouse glucokinase gene
-
Bali D, Svetlanov A, Lee HW, Fusco-DeMane D, Leiser M, et al. (1995) Animal model for maturity-onset diabetes of the young generated by disruption of the mouse glucokinase gene. J Biol Chem 270: 21464-21467.
-
(1995)
J Biol Chem
, vol.270
, pp. 21464-21467
-
-
Bali, D.1
Svetlanov, A.2
Lee, H.W.3
Fusco-DeMane, D.4
Leiser, M.5
-
34
-
-
84858111040
-
Genomic Selection in French Dairy Cattle
-
Boichard D, Guillaume F, Baur A, Croiseau P, Rossignol MN, et al. (2012) Genomic Selection in French Dairy Cattle. Anim Prod Sci 52: 115-120.
-
(2012)
Anim Prod Sci
, vol.52
, pp. 115-120
-
-
Boichard, D.1
Guillaume, F.2
Baur, A.3
Croiseau, P.4
Rossignol, M.N.5
-
35
-
-
77950613737
-
A Hidden Markov Model Combining Linkage and Linkage Disequilibrium Information for Haplotype Reconstruction and Quantitative Trait Locus Fine Mapping
-
Druet T, Georges M, (2010) A Hidden Markov Model Combining Linkage and Linkage Disequilibrium Information for Haplotype Reconstruction and Quantitative Trait Locus Fine Mapping. Genetics 184: 789-798.
-
(2010)
Genetics
, vol.184
, pp. 789-798
-
-
Druet, T.1
Georges, M.2
-
36
-
-
67649884743
-
Fast and accurate short read alignment with Burrows-wheeler transform
-
Li H, Durbin R, (2009) Fast and accurate short read alignment with Burrows-wheeler transform. Bioinformatics 25: 1754-1760.
-
(2009)
Bioinformatics
, vol.25
, pp. 1754-1760
-
-
Li, H.1
Durbin, R.2
-
37
-
-
68549104404
-
The Sequence Alignment/Map format and SAMtools
-
Li H, Handsaker B, Wysoker A, Fennell T, Ruan J, et al. (2009) The Sequence Alignment/Map format and SAMtools. Bioinformatics 25: 2078-2079.
-
(2009)
Bioinformatics
, vol.25
, pp. 2078-2079
-
-
Li, H.1
Handsaker, B.2
Wysoker, A.3
Fennell, T.4
Ruan, J.5
-
38
-
-
77956295988
-
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
-
McKenna A, Hanna M, Banks E, Sivachenko A, Cibulskis K, et al. (2010) The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data. Genome Res 20: 1297-1303.
-
(2010)
Genome Res
, vol.20
, pp. 1297-1303
-
-
McKenna, A.1
Hanna, M.2
Banks, E.3
Sivachenko, A.4
Cibulskis, K.5
-
39
-
-
70350694443
-
Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads
-
Ye K, Schulz MH, Long Q, Apweiler R, Ning Z, (2009) Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads. Bioinformatics 25: 2865-2871.
-
(2009)
Bioinformatics
, vol.25
, pp. 2865-2871
-
-
Ye, K.1
Schulz, M.H.2
Long, Q.3
Apweiler, R.4
Ning, Z.5
-
40
-
-
84878757183
-
-
Ensembl genome browser. Available:. Accessed 2013 Jan 15
-
Ensembl genome browser. Available: http://www.ensembl.org. Accessed 2013 Jan 15.
-
-
-
-
42
-
-
0033990048
-
Primer3 on the WWW for general users and for biologist programmers
-
Rozen S, Skaletsky H, (2000) Primer3 on the WWW for general users and for biologist programmers. Methods Mol Biol 132: 365-386.
-
(2000)
Methods Mol Biol
, vol.132
, pp. 365-386
-
-
Rozen, S.1
Skaletsky, H.2
-
43
-
-
15544369976
-
NovoSNP, a novel computational tool for sequence variation discovery
-
Weckx S, Del-Favero J, Rademakers R, Claes L, Cruts M, et al. (2005) NovoSNP, a novel computational tool for sequence variation discovery. Genome Res 15: 436-442.
-
(2005)
Genome Res
, vol.15
, pp. 436-442
-
-
Weckx, S.1
Del-Favero, J.2
Rademakers, R.3
Claes, L.4
Cruts, M.5
|