Cui Y - Search Results

1

Exome sequencing identified a missense mutation of EPS8L3 in Marie Unna hereditary hypotrichosis.

Zhang X, Guo BR, Cai LQ, Jiang T, Sun LD, Cui Y, Hu JC, Zhu J, Chen G, Tang XF, Sun GQ, Tang HY, Liu Y, Li M, Li QB, Cheng H, Gao M, Li P, Yang X, Zuo XB, Zheng XD, Wang PG, Wang J, Wang J, Liu JJ, Yang S, Li YR, Zhang XJ. Zhang X, et al. Among authors: cui y. J Med Genet. 2012 Dec;49(12):727-30. doi: 10.1136/jmedgenet-2012-101134. Epub 2012 Oct 25. J Med Genet. 2012. PMID: 23099647 Free PMC article.

2

Identification of a locus for dyschromatosis symmetrica hereditaria at chromosome 1q11-1q21.

Zhang XJ, Gao M, Li M, Li M, Li CR, Cui Y, He PP, Xu SJ, Xiong XY, Wang ZX, Yuan WT, Yang S, Huang W. Zhang XJ, et al. Among authors: cui y. J Invest Dermatol. 2003 May;120(5):776-80. doi: 10.1046/j.1523-1747.2003.12130.x. J Invest Dermatol. 2003. PMID: 12713580 Free article.

3

A mutation in the connexin 30 gene in Chinese Han patients with hidrotic ectodermal dysplasia.

Zhang XJ, Chen JJ, Yang S, Cui Y, Xiong XY, He PP, Dong PL, Xu SJ, Li YB, Zhou Q, Wang Y, Huang W. Zhang XJ, et al. Among authors: cui y. J Dermatol Sci. 2003 Jun;32(1):11-7. doi: 10.1016/s0923-1811(03)00033-1. J Dermatol Sci. 2003. PMID: 12788524

4

Association of HLA class I alleles with psoriasis vulgaris in southeastern Chinese Hans.

Zhang XJ, Zhang AP, Yang S, Gao M, Wei SC, He PP, Wang HY, Song YX, Cui Y, Chen JJ. Zhang XJ, et al. Among authors: cui y. J Dermatol Sci. 2003 Oct;33(1):1-6. doi: 10.1016/s0923-1811(03)00157-9. J Dermatol Sci. 2003. PMID: 14527733

5

Identification of the cylindromatosis tumor-suppressor gene responsible for multiple familial trichoepithelioma.

Zhang XJ, Liang YH, He PP, Yang S, Wang HY, Chen JJ, Yuan WT, Xu SJ, Cui Y, Huang W. Zhang XJ, et al. Among authors: cui y. J Invest Dermatol. 2004 Mar;122(3):658-64. doi: 10.1111/j.0022-202X.2004.22321.x. J Invest Dermatol. 2004. PMID: 15086550 Free article.

6

Identification of a locus for punctate palmoplantar keratodermas at chromosome 8q24.13-8q24.21.

Zhang XJ, Li M, Gao TW, He PP, Wei SC, Liu JB, Li CR, Cui Y, Yang S, Yuan WT, Li CY, Liu YF, Xu SJ, Huang W. Zhang XJ, et al. Among authors: cui y. J Invest Dermatol. 2004 May;122(5):1121-5. doi: 10.1111/j.0022-202X.2004.22507.x. J Invest Dermatol. 2004. PMID: 15140213 Free article.

7

Seven novel mutations of the ADAR gene in Chinese families and sporadic patients with dyschromatosis symmetrica hereditaria (DSH).

Zhang XJ, He PP, Li M, He CD, Yan KL, Cui Y, Yang S, Zhang KY, Gao M, Chen JJ, Li CR, Jin L, Chen HD, Xu SJ, Huang W. Zhang XJ, et al. Among authors: cui y. Hum Mutat. 2004 Jun;23(6):629-30. doi: 10.1002/humu.9246. Hum Mutat. 2004. PMID: 15146470

8

Association of HLA class I alleles with vitiligo in Chinese Hans.

Zhang XJ, Liu HS, Liang YH, Sun LD, Wang JY, Yang S, Liu JB, Gao M, He PP, Cui Y, Yang Q. Zhang XJ, et al. Among authors: cui y. J Dermatol Sci. 2004 Aug;35(2):165-8. doi: 10.1016/j.jdermsci.2004.05.003. J Dermatol Sci. 2004. PMID: 15265531 No abstract available.

9

Two frameshift mutations in the RNA-specific adenosine deaminase gene associated with dyschromatosis symmetrica hereditaria.

Gao M, Wang PG, Yang S, Hu XL, Zhang KY, Zhu YG, Ren YQ, Du WH, Zhang GL, Cui Y, Chen JJ, Yan KL, Xiao FL, Xu SJ, Huang W, Zhang XJ. Gao M, et al. Among authors: cui y. Arch Dermatol. 2005 Feb;141(2):193-6. doi: 10.1001/archderm.141.2.193. Arch Dermatol. 2005. PMID: 15724015

10

A novel linkage to generalized vitiligo on 4q13-q21 identified in a genomewide linkage analysis of Chinese families.

Chen JJ, Huang W, Gui JP, Yang S, Zhou FS, Xiong QG, Wu HB, Cui Y, Gao M, Li W, Li JX, Yan KL, Yuan WT, Xu SJ, Liu JJ, Zhang XJ. Chen JJ, et al. Among authors: cui y. Am J Hum Genet. 2005 Jun;76(6):1057-65. doi: 10.1086/430279. Epub 2005 Apr 4. Am J Hum Genet. 2005. PMID: 15809929 Free PMC article.

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