[1]NEWTON J M,COHEN B O,FLAGIWARA N.Mutations in the human orthologue of the mouse underwhite gene(uw) underlie a new form of oculocutaneous albinism[J].Am J Hum Genet,2001,69:981-988.
[2]HARADA M,LI Y F,EL-GAMIL M.Use of an in vitro immunoselected tumor line to identify shared melanoma antigens recognized by HLA-A*0201-restricted T cells[J].Cancer Res,2001,61:1089-1094.
[3]FUKAMACHI S,SHIMADA A,SHIMA A.Mutations in the gene encoding B,a novel transporter protein,reduce melanin content in Medaka[J].Nat Genet,2001,28(4):381-385.
[4]BAXTER L L,PAVAN W J.The oculocutaneous albinism type IV gene MATP is a new marker of pigment cell precursors during mouse embryonic development[J].Mech Dev,2002,116(1-2):209-212.
[5]LOFTUS S K,LARSON D M,BAXTER L L.Mutation of melanosome protein RAB38 in Chocolate mice[J].Proc Natl Acad Sci U S A,2002,99:4471-4476.
[6]INAGAKI K,SUZUKI T,SHIMIZU H.Oculocutaneous albinism type 4 is one of the most common types of albinism in Japan[J].Am J Hum Genet,2004,74:466-471.
[7]LIVAK K J,SCHMITTGEN T D.Analysis of relativegene expression data using real time quantitative PCR and the 2(Delta DeltaC(T)) method[J].Methods,2001,25(4):402-408.
[8]STURM R A,TEASDELE R D,BOX N F.Human pigmentation genes:Identification structure and consequences of polymorphic variation [J].Gene,2001,277:49-62.
[9]GRAF J,HODGSON R,VAN DAAL A.Single nucleotide polymorphisms in the MATP gene are associated with normal human pigmentation variation[J].Hum Mutat,2005,25:278-284.
[10]NORDLUMD J J,BIOSSY R E,HEARING V J,et al.The pigment system-physiological and pathophysiology[M].Oxford:Oxford University Press,1998.
[11]MOORE K J.Insight into the microphthalmia gene[M].Trends Genet,1995,11(11):442-448.
[12]SPRITZ R A,HEARING V J.Genetic disorders of pigmentation[J].Adv Hum Genet,1994,22:1-45.
[13]LEHMAN A L,SILVERS W K,PURI N,et al.The underwhite(uw) locus acts autonomously and reduces the production of melanin[J].Invest Dermatol,2000,10(115):601-606.
[14]COSTIN G E,VALENCIA J C,VIEIRA W D,et al.Tyrosinase processing and intracellular trafficking is disrupted in mouse primary melanocytes carrying the underwhite(uw) mutation.A model for oculocutaneous albinism(OCA) type 4[J].Cell Sci,2003,116:3203-3212.
[15]TOMITA Y,SUZUKI T.Genetics of pigmentary disorders[J].Am J Med Genet C Semin Med Genet,2004,15:75-81.
[16]SCHEPSKY A,BRUSER K,GUNNARSSON G J.The microphthalmia-associated transcription factor Mitf interacts with β-catenin to determine target gene expression[J].Mol Cell Biol,2006,26(23):8914-8927.
[17]NISHIMURA E K,GRANTER S R,FISHER D E.Mechanisms of hair graying:incomplete melanocyte stem cell maintenance in the niche [J].Science,2005,307(5710):720-724.
[18]于秀菊,董常生,范阔海,等.β-catenin 在不同毛色羊驼皮肤中的表达和定位[J].畜牧兽医学报,2010,41(3):235-240.
[19]杨磊,董常生,王海东,等.Lef-1 基因在棕色和白色羊驼皮肤差异表达[J].中国生物化学与分子生物学报,2011,27(11):1061-1066.
[20]LEVY C,KHALED M,FISHER D E.MITF:master regulator of melanocyte development and melanoma oncogene[J].Trends Mol Med,2006,12(9):406-414.
[21]高莉,董常生,赫晓燕,等.羊驼酪氨酸酶基因家族在不同毛色个体中的基因表达水平[J].畜牧兽医学报,2008,39(7):895-899.
[22]TAKEDA K,YASUMOTO K,TAKADA R.Induction of melanocyte-specific microphthalmia-associated transcription factor by wnt3a[J].J Biol Chem,2000,275(19):14013-14016.
[23]LIN J Y,FISHER D E.Melanocyte biology and skin pigmentation[J].Nature,2007,442:843-850. |