Cui Y - Search Results

1

The familial risk of acne vulgaris in Chinese Hans - a case-control study.

Xu SX, Wang HL, Fan X, Sun LD, Yang S, Wang PG, Xiao FL, Gao M, Cui Y, Ren YQ, Du WH, Quan C, Zhang XJ. Xu SX, et al. Among authors: cui y. J Eur Acad Dermatol Venereol. 2007 May;21(5):602-5. doi: 10.1111/j.1468-3083.2006.02022.x. J Eur Acad Dermatol Venereol. 2007. PMID: 17447973

2

Two mixed-metal carboxylate-base adducts.

Cui Y, Zhang X, Zheng F, Ren J, Chen G, Qian Y, Huang J. Cui Y, et al. Acta Crystallogr C. 2000 Oct;56 (Pt 10):1198-200. doi: 10.1107/s0108270100009999. Acta Crystallogr C. 2000. PMID: 11025294

3

Refined localization of dyschromatosis symmetrica hereditaria gene to a 9.4-cM region at 1q21-22 and a literature review of 136 cases reported in China.

He PP, He CD, Cui Y, Yang S, Xu HH, Li M, Yuan WT, Gao M, Liang YH, Li CR, Xu SJ, Chen JJ, Chen HD, Huang W, Zhang XJ. He PP, et al. Among authors: cui y. Br J Dermatol. 2004 Apr;150(4):633-9. doi: 10.1111/j.0007-0963.2004.05861.x. Br J Dermatol. 2004. PMID: 15099357 Review.

4

Refinement of a locus for Marie Unna hereditary hypotrichosis to a 1.1-cM interval at 8p21.3.

He PP, Zhang XJ, Yang Q, Li M, Liang YH, Yang S, Yan KL, Cui Y, Shen YY, Wang HY, Sun LD, Du WH, Shen YJ, Xu SJ, Huang W. He PP, et al. Among authors: cui y. Br J Dermatol. 2004 May;150(5):837-42. doi: 10.1111/j.1365-2133.2004.05913.x. Br J Dermatol. 2004. PMID: 15149494

5

Marie Unna hereditary hypotrichosis: report of a Chinese family and evidence for genetic heterogeneity.

Yan KL, He PP, Yang S, Li M, Yang Q, Ren YQ, Cui Y, Gao M, Xiao FL, Huang W, Zhang XJ. Yan KL, et al. Among authors: cui y. Clin Exp Dermatol. 2004 Sep;29(5):460-3. doi: 10.1111/j.1365-2230.2004.01570.x. Clin Exp Dermatol. 2004. PMID: 15347323

6

Refined localization of a punctate palmoplantar keratoderma gene to a 5.06-cM region at 15q22.2-15q22.31.

Gao M, Yang S, Li M, Yan KL, Jiang YX, Cui Y, Xiao FL, Shen YJ, Chen JJ, Liu JB, Xu SJ, Huang W, Zhang XJ. Gao M, et al. Among authors: cui y. Br J Dermatol. 2005 May;152(5):874-8. doi: 10.1111/j.1365-2133.2005.06488.x. Br J Dermatol. 2005. PMID: 15888140

7

Two novel CYLD gene mutations in Chinese families with trichoepithelioma and a literature review of 16 families with trichoepithelioma reported in China.

Liang YH, Gao M, Sun LD, Liu LJ, Cui Y, Yang S, Fan X, Wang J, Xiao FL, Zhang XJ. Liang YH, et al. Among authors: cui y. Br J Dermatol. 2005 Dec;153(6):1213-5. doi: 10.1111/j.1365-2133.2005.06960.x. Br J Dermatol. 2005. PMID: 16307661 Review. No abstract available.

8

Genetic heterogeneity in acrokeratosis verruciformis of Hopf.

Wang PG, Gao M, Lin GS, Yang S, Lin D, Liang YH, Zhang GL, Zhu YG, Cui Y, Zhang KY, Huang W, Zhang XJ. Wang PG, et al. Among authors: cui y. Clin Exp Dermatol. 2006 Jul;31(4):558-63. doi: 10.1111/j.1365-2230.2006.02134.x. Clin Exp Dermatol. 2006. PMID: 16716163

9

Follow-up analysis of 180 Chinese Han families: identification of a novel locus for psoriasis at 2p22.3-11.2.

Sun LD, Yang S, Liu JJ, Ren YQ, Fan X, Xu SX, Zhou L, Yang CJ, Xiao FL, Gao M, Cui Y, Du WH, Huang W, Zhang XJ. Sun LD, et al. Among authors: cui y. Br J Dermatol. 2008 Mar;158(3):512-7. doi: 10.1111/j.1365-2133.2007.08417.x. Epub 2008 Jan 30. Br J Dermatol. 2008. PMID: 18241272

10

Novel and recurrent keratin 6A (KRT6A) mutations in Chinese patients with pachyonychia congenita type 1.

Lv YM, Yang S, Zhang Z, Cui Y, Quan C, Zhou FS, Fang QY, Du WH, Zhang FR, Chang JM, Tao XP, Zhang AL, Kang RH, Du WD, Zhang XJ. Lv YM, et al. Among authors: cui y. Br J Dermatol. 2009 Jun;160(6):1327-9. doi: 10.1111/j.1365-2133.2009.09062.x. Epub 2009 Mar 11. Br J Dermatol. 2009. PMID: 19416275 No abstract available.

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