[1] Haase B, Brooks SA, Schlumbaum A, Azor PJ, Bailey E, Alaeddine F, Mevissen M, Burger D, Poncet PA, Rieder S, Leeb T. Allelic heterogeneity at the equine KIT locus in dominant white (W) horses. PLoS Genet, 2007, 3(11): e195.[2] Haase B, Brooks SA, Tozaki T, Burger D, Poncet PA, Rieder S, Hasegawa T, Penedo C, Leeb T. Seven novel KIT mutations in horses with white coat colour pheno-types. Anim Genet, 2009, 40(5): 623-629.[3] Castle WE. Coat color inheritance in horses and in other mammals. Genetics, 1954, 39(1): 35-44.[4] Pielberg G, Mikko S, Sandberg K, Andersson L. Comparative linkage mapping of the Grey coat colour gene in horses. Anim Genet, 2005, 36(5): 390-395.[5] Brooks SA, Bailey E. Exon skipping in the KIT gene causes a Sabino spotting pattern in horses. Mamm Genome, 2005, 16(11): 893-902.[6] Metallinos DL, Bowling AT, 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, 1998, 9(6): 426-431.[7] Marklund S, Moller M, Sandberg K, Andersson L. Close association between sequence polymorphism in the KIT gene and the roan coat color in horses. Mamm Genome, 1999, 10(3): 283-288.[8] Woolf CM. Multifactorial inheritance of common white markings in the Arabian horse. J Hered, 1990, 81(4): 250-256.[9] Brooks SA, Lear T, Adelson DL, Bailey E. A chromosome inversion near the KIT gene and the Tobiano spotting pattern in horses. Cytogenet Genome Res, 2007, 119(3-4): 225-230.[10] Hwang KC, Cho SK, Lee SH, Park JY, Kwon DN, Choi YJ, Park C, Kim JH, Park KK, Hwang S, Park SB, Kim JH. Depigmentation of skin and hair color in the somatic cell cloned pig. Dev Dyn, 2009, 238(7): 1701-1708.[11] Roskoski R Jr. Structure and regulation of Kit pro-tein-tyrosine kinase-the stem cell factor receptor. Bio-chem Biophys Res Commun, 2005, 338(3): 1307-1315.[12] Roskoski R Jr. Signaling by Kit protein-tyrosine kinase- the stem cell factor receptor. Biochem Biophys Res Commun, 2005, 337(3): 1-13.[13] Blume-Jensen P, Claesson-Welsh L, Siegbahn A, Zsebo KM, Westermark B, Heldin CH. Activation of the human c-kit product by ligand-induced dimerization mediates circular actin reorganization and chemotaxis. EMBO J, 1991, 10(13): 4121-4128.[14] Rönnstrand L. Signal transduction via the stem cell factor receptor/c-Kit. Cell Mol Life Sci, 2004, 61(19-20): 2535-2548.[15] Giebel LB, Spritz RA. Mutation of the KIT (mast/stem cell growth factor receptor) protooncogene in human piebaldism. Proc Natl Acad Sci USA, 1991, 88(19): 8696-8699.[16] Spritz RA. Molecular basis of human piebaldism. J Invest Dermatol, 1994, 103(S5): 137S-140S.[17] Furitsu T, Tsujimura T, Tono T, Ikeda H, Kitayama H, Koshimizu U, Sugahara H, Butterfield JH, Ashman LK, Kanayama Y. Identification of mutations in the coding sequence of the proto-oncogene c-kit in a human mast cell leukemia cell line causing ligand-independent activation of c-kit product. J Clin Invest, 1993, 92(4): 1736-1744.[18] Fleischman RA, Saltman DL, Stastny V, Zneimer S. Deletion of the c-kit protooncogene in the human developmental defect piebald trait. Proc Natl Acad Sci USA, 1991, 88(23): 10885-10889.[19] Santschi EM, Purdy AK, Valberg SJ, Vrotsos PD, Kaese H, Mickelson JR. Endothelin receptor B polymorphism asso-ciated with lethal white foal syndrome in horses. Mamm Genome, 1998, 9(4): 306-309.[20] Castle WE. The ABC of color inheritance in horses. Genetics, 1948, 33(1): 22-35.[21] Pulos WL, Hutt FB. Lethal dominant white in horses. J Hered, 1969, 60(2): 59-63.[22] Haase B, Obexer-Ruff G, Dolf G, Rieder S, Burger D, Poncet PA, Gerber V, Howard J, Leeb T. Haematological parameter |