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国际皮肤性病学杂志 2004 30 (2): 91-94 ISSN: 2096-5540 CN: 32-1880/R |
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白癜风相关基因研究进展 |
章一近, 许爱娥 |
杭州市第三人民医院皮肤科, 杭州 310009 |
收稿日期 2003-06-16 修回日期 null 网络版发布日期 null |
参考文献 [1] Njoo MD, Westerhof W. Vitiligo. Pathogenesis and treatment. Am J Clin Dermatol, 2001, 2(3):167-181. [2] Kwon BS. Pigmentation genes:the tyrosinase gene family and the pmel 7 gene family. J Invest Dermatol, 1993, 100(2 Suppl):S134. [3] Nishioka E, Funasaka Y, Kondoh H, et al. Expression of tyrosinase,TRP1 and TRP2 in ultraviolet-irradiated human melanomas and melanocytes:TRP2 protects melanoma cells from ultraviolet B induced apoptosis. Melanoma Res, 1999, 9(5):433-443. [4] Manga P, Sato K, Ye L, et al. Mutational analysis of the modulation of tyrosinase by tyrosinase-related proteins 1 and 2 in vitro. Pigment Cell Res, 2000, 13(5):364-374. [5] Sarangarajan R, Zhao Y, Babcock G, et al. Mutant alleles at the brown locus encoding tyrosinase-related protein-1(TRP-1)affect proliferation of mouse melanocytes in culture. Pigment Cell Res,2000, 13(5):337-344. [6] Lee YM, Ha M J, Ryu MS, et al. Assignments of the tyrosinase related protein-I and-2 genes to human chromosome bands 9p23 and 13q32.1 by in situ hybridization. Yonsei Med J, 2000, 41(3):398. [7] Jimbow K, Chen H, Park JS, et al. Increased sensitivity of melanocytes to oxidative stress and abnormal expression of tyrosinase-related protein in vitiligo. Br J Dermatol, 2001, 144(1):55-65. [8] Amae S,Yasumoto K,Takeda K, et al. Identification of a composite enhancer of the human tyrosinase-related protein 2/DOPA chrome tautomerase gene. Biochim Biophys Acta, 2000, 1492(2-3):505. [9] Boissy RE, Nordlund JJ. Molecular basis of congenital hypopigmentary disorders in humans:a review. Pigment Cell Res, 1997, 10(1-2):12-24. [10] Tripathi RK, Flanders DJ,Young TL, et al. Microphthalmia-associated transcription factor(MITF)locus lacks linkage to human vitiligo or osteopetrosis:an evaluation. Pigment Cell Res, 1999, 12(3):187. [11] Smith SB, Zhou BK, Orlow SJ. Expression of tyrosinase and the tyrosinase related proteins in the Mitfvit(vitiligo)mouse eye:implications for the function of the microphthalmia transcription factor. Exp Eye Res, 1998, 66(4):403-410. [12] Lamoreux ML, Boissy RE, Womack JE, et al. The vit gene maps to the mi(microphthalmia)locus of the laboratory mouse. J Hered,1992, 83(6):435-439. [13] Richards KA, Fukai K, Oiso N, et al. A novel KIT mutation results in piebaldism with progressive depigmentation. J Am Acad Dermatol,2001,44(2):288-292. [14] Norris A, Todd C, Graham A, et al. The expression of the c-kit receptor by epidermal melanocytes may be reduced in vitiligo. Br J Dermatol, 1996, 134(2):299-306. [15] Dippel E, Haas N, Grabbe J, et al. Expression of the c-kit receptor in hypomelanosis:a comparative study between piebaldism, naevus depigmentosus and vitiligo. Br J Dermatol, 1995, 132(2):182. [16] Casp CB, She JX, McCormack WT. Genetic association of the catalase gene(CAT)with vitiligo susceptibility. Pigment Cell Res,2002, 15(1):62-66. [17] Nath SK, Kelly JA, Namjou B, et al. Evidence for a susceptibility gene, SLEV1, on chromosome 17p13 in families with vitiligo-related systemic lupus erythematosus. Am J Hum Genet, 2001, 69(6):1401. [18] Grimes PE, Sevall JS, Vojdani A. Cytomegalovirus DNA identified in skin biopsy specimens of patients with vitiligo. J Am Acad Dermatol,1996, 35(1):21-26. [19] Sreekumar GP, Smyth JR Jr, Ambady S, et al. Analysis of the effect of endogenous viral genes in the Smyth line chicken model for autoimmune vitiligo. Am J Patrol, 2000, 156(3):1099-1107. [20] Le Poole IC, Sarangarajan R, Zhao Y, et al. "VIT1", a novel gene associated with vitiligo. Pigment Cell Res, 2001, 14(6):475-484. |
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