-
1
-
-
0026936507
-
Periodic paralysis in quarter horses: a sodium channel mutation disseminated by selective breeding
-
Rudolph J.A., Spier S.J., Byrns G., Rojas C.V., Bernoco D., and Hoffman E.P. Periodic paralysis in quarter horses: a sodium channel mutation disseminated by selective breeding. Nat Genet 2 (1992) 144-147
-
(1992)
Nat Genet
, vol.2
, pp. 144-147
-
-
Rudolph, J.A.1
Spier, S.J.2
Byrns, G.3
Rojas, C.V.4
Bernoco, D.5
Hoffman, E.P.6
-
2
-
-
0033090372
-
Hyperkalaemic periodic paralysis in homozygous and heterozygous horses: a co-dominant genetic condition
-
Naylor J.M., Nickel D.D., Trimino G., Card C., Lightfoot K., and Adams G. Hyperkalaemic periodic paralysis in homozygous and heterozygous horses: a co-dominant genetic condition. Equine Vet J 31 (1999) 153-159
-
(1999)
Equine Vet J
, vol.31
, pp. 153-159
-
-
Naylor, J.M.1
Nickel, D.D.2
Trimino, G.3
Card, C.4
Lightfoot, K.5
Adams, G.6
-
3
-
-
0031569608
-
A kinase-negative mutation of DNA-PK(CS) in equine SCID results in defective coding and signal joint formation
-
Shin E.K., Perryman L.E., and Meek K. A kinase-negative mutation of DNA-PK(CS) in equine SCID results in defective coding and signal joint formation. J Immunol 158 (1997) 3565-3569
-
(1997)
J Immunol
, vol.158
, pp. 3565-3569
-
-
Shin, E.K.1
Perryman, L.E.2
Meek, K.3
-
4
-
-
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., and Rine J. A missense mutation in the endothelin-B receptor gene is associated with Lethal White Foal Syndrome: an equine version of Hirschsprung disease. Mamm Genome 9 (1998) 426-431
-
(1998)
Mamm Genome
, vol.9
, pp. 426-431
-
-
Metallinos, D.L.1
Bowling, A.T.2
Rine, J.3
-
5
-
-
0032053530
-
Endothelin receptor B polymorphism associated with lethal white foal syndrome in horses
-
Santschi E.M., Purdy A.K., Valberg S.J., Vrotsos P.D., Kaese H., and Mickelson J.R. Endothelin receptor B polymorphism associated with lethal white foal syndrome in horses. Mamm Genome 9 (1998) 306-309
-
(1998)
Mamm Genome
, vol.9
, pp. 306-309
-
-
Santschi, E.M.1
Purdy, A.K.2
Valberg, S.J.3
Vrotsos, P.D.4
Kaese, H.5
Mickelson, J.R.6
-
6
-
-
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., Croaker D., Zhang A.L., Manglick P., Cartmill T., and Cass D. A dinucleotide mutation in the endothelin-B receptor gene is associated with lethal white foal syndrome (LWFS); a horse variant of Hirschsprung disease. Hum Mol Genet 7 (1998) 1047-1052
-
(1998)
Hum Mol Genet
, vol.7
, pp. 1047-1052
-
-
Yang, G.C.1
Croaker, D.2
Zhang, A.L.3
Manglick, P.4
Cartmill, T.5
Cass, D.6
-
7
-
-
0036379397
-
Animal models for skin blistering conditions: absence of laminin 5 causes hereditary junctional mechanobullous disease in the Belgian horse
-
Spirito F., Charlesworth A., Linder K., Ortonne J.P., Baird J., and Meneguzzi G. Animal models for skin blistering conditions: absence of laminin 5 causes hereditary junctional mechanobullous disease in the Belgian horse. J Invest Dermatol 119 (2002) 684-691
-
(2002)
J Invest Dermatol
, vol.119
, pp. 684-691
-
-
Spirito, F.1
Charlesworth, A.2
Linder, K.3
Ortonne, J.P.4
Baird, J.5
Meneguzzi, G.6
-
8
-
-
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., and Andersson L. A missense mutation in the gene for melanocyte-stimulating hormone receptor (MC1R) is associated with the chestnut coat color in horses. Mamm Genome 7 (1996) 895-899
-
(1996)
Mamm Genome
, vol.7
, pp. 895-899
-
-
Marklund, L.1
Moller, M.J.2
Sandberg, K.3
Andersson, L.4
-
9
-
-
0035008008
-
Mutations in the agouti (ASIP), the extension (MC1R), and the brown (TYRP1) loci and their association to coat color phenotypes in horses (Equus caballus)
-
Rieder S., Taourit S., Mariat D., Langlois B., and Guerin G. Mutations in the agouti (ASIP), the extension (MC1R), and the brown (TYRP1) loci and their association to coat color phenotypes in horses (Equus caballus). Mamm Genome 12 (2001) 450-455
-
(2001)
Mamm Genome
, vol.12
, pp. 450-455
-
-
Rieder, S.1
Taourit, S.2
Mariat, D.3
Langlois, B.4
Guerin, G.5
-
10
-
-
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., et al. Allelic heterogeneity at the equine KIT locus in dominant white (W) horses. PLoS Genet 3 (2007) e195
-
(2007)
PLoS Genet
, vol.3
-
-
Haase, B.1
Brooks, S.A.2
Schlumbaum, A.3
Azor, P.J.4
Bailey, E.5
Alaeddine, F.6
-
11
-
-
27744434902
-
Exon skipping in the KIT gene causes a Sabino spotting pattern in horses
-
Brooks S.A., and Bailey E. Exon skipping in the KIT gene causes a Sabino spotting pattern in horses. Mamm Genome 16 (2005) 893-902
-
(2005)
Mamm Genome
, vol.16
, pp. 893-902
-
-
Brooks, S.A.1
Bailey, E.2
-
12
-
-
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., and Lindgren G. A missense mutation in PMEL17 is associated with the Silver coat color in the horse. BMC Genet 7 (2006) 46
-
(2006)
BMC Genet
, vol.7
, pp. 46
-
-
Brunberg, E.1
Andersson, L.2
Cothran, G.3
Sandberg, K.4
Mikko, S.5
Lindgren, G.6
-
13
-
-
0018171063
-
Linkage of tobiano coat spotting and albumin markers in a pony family
-
Trommershausen-Smith A. Linkage of tobiano coat spotting and albumin markers in a pony family. J Hered 69 (1978) 214-216
-
(1978)
J Hered
, vol.69
, pp. 214-216
-
-
Trommershausen-Smith, A.1
-
14
-
-
39049123708
-
A chromosome inversion near the KIT gene and the Tobiano spotting pattern in horses
-
Brooks S.A., Lear T.L., Adelson D.L., and Bailey E. A chromosome inversion near the KIT gene and the Tobiano spotting pattern in horses. Cytogenet Genome Res 119 (2007) 225-230
-
(2007)
Cytogenet Genome Res
, vol.119
, pp. 225-230
-
-
Brooks, S.A.1
Lear, T.L.2
Adelson, D.L.3
Bailey, E.4
-
15
-
-
0035543325
-
The cream dilution gene, responsible for the palomino and buckskin coat colours, maps to horse chromosome 21
-
Locke M.M., Ruth L.S., Millon L.V., Penedo M.C., Murray J.D., and Bowling A.T. The cream dilution gene, responsible for the palomino and buckskin coat colours, maps to horse chromosome 21. Anim Genet 32 (2001) 340-343
-
(2001)
Anim Genet
, vol.32
, pp. 340-343
-
-
Locke, M.M.1
Ruth, L.S.2
Millon, L.V.3
Penedo, M.C.4
Murray, J.D.5
Bowling, A.T.6
-
16
-
-
0038713136
-
A mutation in the MATP gene causes the cream coat colour in the horse
-
Mariat D., Taourit S., and Guerin G. A mutation in the MATP gene causes the cream coat colour in the horse. Genet Sel Evol 35 (2003) 119-133
-
(2003)
Genet Sel Evol
, vol.35
, pp. 119-133
-
-
Mariat, D.1
Taourit, S.2
Guerin, G.3
-
17
-
-
0036802655
-
Linkage of the grey coat colour locus to microsatellites on horse chromosome 25
-
Locke M.M., Penedo M.C., Bricker S.J., Millon L.V., and Murray J.D. Linkage of the grey coat colour locus to microsatellites on horse chromosome 25. Anim Genet 33 (2002) 329-337
-
(2002)
Anim Genet
, vol.33
, pp. 329-337
-
-
Locke, M.M.1
Penedo, M.C.2
Bricker, S.J.3
Millon, L.V.4
Murray, J.D.5
-
18
-
-
33644876600
-
Comparative linkage mapping of the Grey coat colour gene in horses
-
Pielberg G., Mikko S., Sandberg K., and Andersson L. Comparative linkage mapping of the Grey coat colour gene in horses. Anim Genet 36 (2005) 390-395
-
(2005)
Anim Genet
, vol.36
, pp. 390-395
-
-
Pielberg, G.1
Mikko, S.2
Sandberg, K.3
Andersson, L.4
-
19
-
-
0036800919
-
Assignment of the horse grey coat colour gene to ECA25 using whole genome scanning
-
Swinburne J.E., Hopkins A., and Binns M.M. Assignment of the horse grey coat colour gene to ECA25 using whole genome scanning. Anim Genet 33 (2002) 338-342
-
(2002)
Anim Genet
, vol.33
, pp. 338-342
-
-
Swinburne, J.E.1
Hopkins, A.2
Binns, M.M.3
-
20
-
-
55749100524
-
Differential gene expression of TRPM1, the potential cause of congenital stationary night blindness (CSNB) and coat spotting patterns (LP) in the Appaloosa horse (Equus caballus)
-
Bellone R.R., Brooks S.A., Sandmeyer L., Murphy B.A., Forsyth G., Archer S., et al. Differential gene expression of TRPM1, the potential cause of congenital stationary night blindness (CSNB) and coat spotting patterns (LP) in the Appaloosa horse (Equus caballus). Genetics (2008)
-
(2008)
Genetics
-
-
Bellone, R.R.1
Brooks, S.A.2
Sandmeyer, L.3
Murphy, B.A.4
Forsyth, G.5
Archer, S.6
-
21
-
-
1842816468
-
Assignment of the appaloosa coat colour gene (LP) to equine chromosome 1
-
Terry R.B., Archer S., Brooks S., Bernoco D., and Bailey E. Assignment of the appaloosa coat colour gene (LP) to equine chromosome 1. Anim Genet 35 (2004) 134-137
-
(2004)
Anim Genet
, vol.35
, pp. 134-137
-
-
Terry, R.B.1
Archer, S.2
Brooks, S.3
Bernoco, D.4
Bailey, E.5
-
22
-
-
48349098128
-
A cis-acting regulatory mutation causes premature hair graying and susceptibility to melanoma in the horse
-
Rosengren Pielberg G., Golovko A., Sundstrom E., Curik I., Lennartsson J., Seltenhammer M.H., et al. A cis-acting regulatory mutation causes premature hair graying and susceptibility to melanoma in the horse. Nat Genet 40 (2008) 1004-1009
-
(2008)
Nat Genet
, vol.40
, pp. 1004-1009
-
-
Rosengren Pielberg, G.1
Golovko, A.2
Sundstrom, E.3
Curik, I.4
Lennartsson, J.5
Seltenhammer, M.H.6
-
24
-
-
34249978971
-
Homozygosity mapping approach identifies a missense mutation in equine cyclophilin B (PPIB) associated with HERDA in the American Quarter Horse
-
Tryon R.C., White S.D., and Bannasch D.L. Homozygosity mapping approach identifies a missense mutation in equine cyclophilin B (PPIB) associated with HERDA in the American Quarter Horse. Genomics 90 (2007) 93-102
-
(2007)
Genomics
, vol.90
, pp. 93-102
-
-
Tryon, R.C.1
White, S.D.2
Bannasch, D.L.3
-
25
-
-
42049111858
-
Glycogen synthase (GYS1) mutation causes a novel skeletal muscle glycogenosis
-
McCue M.E., Valberg S.J., Miller M.B., Wade C., DiMauro S., Akman H.O., et al. Glycogen synthase (GYS1) mutation causes a novel skeletal muscle glycogenosis. Genomics 91 (2008) 458-466
-
(2008)
Genomics
, vol.91
, pp. 458-466
-
-
McCue, M.E.1
Valberg, S.J.2
Miller, M.B.3
Wade, C.4
DiMauro, S.5
Akman, H.O.6
-
26
-
-
56049103427
-
Preliminary analysis of the equine genome sequence
-
Wade C., Gnerre S., Garber M., BIGSaA T., Lander E., Lindblad-Toh K., et al. Preliminary analysis of the equine genome sequence. Plant and Animal Genome Conference XVI (2008)
-
(2008)
Plant and Animal Genome Conference XVI
-
-
Wade, C.1
Gnerre, S.2
Garber, M.3
BIGSaA, T.4
Lander, E.5
Lindblad-Toh, K.6
-
27
-
-
35648953308
-
Efficient mapping of mendelian traits in dogs through genome-wide association
-
Karlsson E.K., Baranowska I., Wade C.M., Salmon Hillbertz N.H., Zody M.C., Anderson N., et al. Efficient mapping of mendelian traits in dogs through genome-wide association. Nat Genet 39 (2007) 1321-1328
-
(2007)
Nat Genet
, vol.39
, pp. 1321-1328
-
-
Karlsson, E.K.1
Baranowska, I.2
Wade, C.M.3
Salmon Hillbertz, N.H.4
Zody, M.C.5
Anderson, N.6
-
29
-
-
0038728292
-
Equine melanoma in a population of 296 grey Lipizzaner horses
-
Seltenhammer M.H., Simhofer H., Scherzer S., Zechner R., Curik I., Solkner J., et al. Equine melanoma in a population of 296 grey Lipizzaner horses. Equine Vet J 35 (2003) 153-157
-
(2003)
Equine Vet J
, vol.35
, pp. 153-157
-
-
Seltenhammer, M.H.1
Simhofer, H.2
Scherzer, S.3
Zechner, R.4
Curik, I.5
Solkner, J.6
|