305 related articles for article (PubMed ID: 18410476)
1. An equine chromosome 3 inversion is associated with the tobiano spotting pattern in German horse breeds.
Haase B; Jude R; Brooks SA; Leeb T
Anim Genet; 2008 Jun; 39(3):306-9. PubMed ID: 18410476
[TBL] [Abstract][Full Text] [Related]
2. A chromosome inversion near the KIT gene and the Tobiano spotting pattern in horses.
Brooks SA; Lear TL; Adelson DL; Bailey E
Cytogenet Genome Res; 2007; 119(3-4):225-30. PubMed ID: 18253033
[TBL] [Abstract][Full Text] [Related]
3. Seven novel KIT mutations in horses with white coat colour phenotypes.
Haase B; Brooks SA; Tozaki T; Burger D; Poncet PA; Rieder S; Hasegawa T; Penedo C; Leeb T
Anim Genet; 2009 Oct; 40(5):623-9. PubMed ID: 19456317
[TBL] [Abstract][Full Text] [Related]
4. A PCR-RFLP for KIT associated with tobiano spotting pattern in horses.
Brooks SA; Terry RB; Bailey E
Anim Genet; 2002 Aug; 33(4):301-3. PubMed ID: 12139510
[TBL] [Abstract][Full Text] [Related]
5. Tobiano spotting pattern in horses: linkage of To with AlA and linkage disequilibrium.
Duffield DA; Goldie PL
J Hered; 1998; 89(1):104-6. PubMed ID: 9487684
[TBL] [Abstract][Full Text] [Related]
6. Whole genome sequencing reveals a novel deletion variant in the KIT gene in horses with white spotted coat colour phenotypes.
Dürig N; Jude R; Holl H; Brooks SA; Lafayette C; Jagannathan V; Leeb T
Anim Genet; 2017 Aug; 48(4):483-485. PubMed ID: 28444912
[TBL] [Abstract][Full Text] [Related]
7. Exon skipping in the KIT gene causes a Sabino spotting pattern in horses.
Brooks SA; Bailey E
Mamm Genome; 2005 Nov; 16(11):893-902. PubMed ID: 16284805
[TBL] [Abstract][Full Text] [Related]
8. Chinese white Rongchang pig does not have the dominant white allele of KIT but has the dominant black allele of MC1R.
Lai F; Ren J; Ai H; Ding N; Ma J; Zeng D; Chen C; Guo Y; Huang L
J Hered; 2007; 98(1):84-7. PubMed ID: 17150979
[TBL] [Abstract][Full Text] [Related]
9. 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
BMC Genet; 2006 Oct; 7():46. PubMed ID: 17029645
[TBL] [Abstract][Full Text] [Related]
10. Fine-mapping and mutation analysis of TRPM1: a candidate gene for leopard complex (LP) spotting and congenital stationary night blindness in horses.
Bellone RR; Forsyth G; Leeb T; Archer S; Sigurdsson S; Imsland F; Mauceli E; Engensteiner M; Bailey E; Sandmeyer L; Grahn B; Lindblad-Toh K; Wade CM
Brief Funct Genomics; 2010 May; 9(3):193-207. PubMed ID: 20353955
[TBL] [Abstract][Full Text] [Related]
11. Identification of W13 in the American Miniature Horse and Shetland Pony Populations.
Esdaile E; Kallenberg A; Avila F; Bellone RR
Genes (Basel); 2021 Dec; 12(12):. PubMed ID: 34946933
[TBL] [Abstract][Full Text] [Related]
12. Novel variants in the KIT and PAX3 genes in horses with white-spotted coat colour phenotypes.
Hauswirth R; Jude R; Haase B; Bellone RR; Archer S; Holl H; Brooks SA; Tozaki T; Penedo MC; Rieder S; Leeb T
Anim Genet; 2013 Dec; 44(6):763-5. PubMed ID: 23659293
[TBL] [Abstract][Full Text] [Related]
13. Two variants in the KIT gene as candidate causative mutations for a dominant white and a white spotting phenotype in the donkey.
Haase B; Rieder S; Leeb T
Anim Genet; 2015 Jun; 46(3):321-4. PubMed ID: 25818843
[TBL] [Abstract][Full Text] [Related]
14. Variant in the RFWD3 gene associated with PATN1, a modifier of leopard complex spotting.
Holl HM; Brooks SA; Archer S; Brown K; Malvick J; Penedo MC; Bellone RR
Anim Genet; 2016 Feb; 47(1):91-101. PubMed ID: 26568529
[TBL] [Abstract][Full Text] [Related]
15. Sequence analysis of the equine SLC26A2 gene locus on chromosome 14q15-->q21.
Hansen M; Knorr C; Hall AJ; Broad TE; Brenig B
Cytogenet Genome Res; 2007; 118(1):55-62. PubMed ID: 17901700
[TBL] [Abstract][Full Text] [Related]
16. A complex structural variant at the KIT locus in cattle with the Pinzgauer spotting pattern.
Küttel L; Letko A; Häfliger IM; Signer-Hasler H; Joller S; Hirsbrunner G; Mészáros G; Sölkner J; Flury C; Leeb T; Drögemüller C
Anim Genet; 2019 Oct; 50(5):423-429. PubMed ID: 31294880
[TBL] [Abstract][Full Text] [Related]
17. A missense mutation in the endothelin-B receptor gene is associated with Lethal White Foal Syndrome: an equine version of Hirschsprung disease.
Metallinos DL; Bowling AT; Rine J
Mamm Genome; 1998 Jun; 9(6):426-31. PubMed ID: 9585428
[TBL] [Abstract][Full Text] [Related]
18. Five novel KIT mutations in horses with white coat colour phenotypes.
Haase B; Rieder S; Tozaki T; Hasegawa T; Penedo MC; Jude R; Leeb T
Anim Genet; 2011 Jun; 42(3):337-9. PubMed ID: 21554354
[No Abstract] [Full Text] [Related]
19. Allelic heterogeneity at the equine KIT locus in dominant white (W) horses.
Haase B; Brooks SA; Schlumbaum A; Azor PJ; Bailey E; Alaeddine F; Mevissen M; Burger D; Poncet PA; Rieder S; Leeb T
PLoS Genet; 2007 Nov; 3(11):e195. PubMed ID: 17997609
[TBL] [Abstract][Full Text] [Related]
20. [Effect study of white locus (I) on coat color inheritance in Chinese native pig breeds].
Shi KR; Wang AG; Li N; Deng XM
Yi Chuan Xue Bao; 2005 Mar; 32(3):275-81. PubMed ID: 15931788
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]