Xu SJ - Search Results

1

KCNQ1 gain-of-function mutation in familial atrial fibrillation.

Chen YH, Xu SJ, Bendahhou S, Wang XL, Wang Y, Xu WY, Jin HW, Sun H, Su XY, Zhuang QN, Yang YQ, Li YB, Liu Y, Xu HJ, Li XF, Ma N, Mou CP, Chen Z, Barhanin J, Huang W. Chen YH, et al. Among authors: xu wy, xu hj, xu sj. Science. 2003 Jan 10;299(5604):251-4. doi: 10.1126/science.1077771. Science. 2003. PMID: 12522251

2

[Mapping studies of type 2 diabetes mellitus gene in one family].

Li Y, Lu H, Liu W, Zhang C, Xiong X, Xu S, Huang W. Li Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003 Apr;20(2):123-6. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003. PMID: 12673580 Chinese.

3

Evidence for a major psoriasis susceptibility locus at 6p21(PSORS1) and a novel candidate region at 4q31 by genome-wide scan in Chinese hans.

Zhang XJ, He PP, Wang ZX, Zhang J, Li YB, Wang HY, Wei SC, Chen SY, Xu SJ, Jin L, Yang S, Huang W. Zhang XJ, et al. Among authors: xu sj. J Invest Dermatol. 2002 Dec;119(6):1361-6. doi: 10.1046/j.1523-1747.2002.19612.x. J Invest Dermatol. 2002. PMID: 12485440 Free article.

4

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: xu sj. J Dermatol Sci. 2003 Jun;32(1):11-7. doi: 10.1016/s0923-1811(03)00033-1. J Dermatol Sci. 2003. PMID: 12788524

5

A gene for freckles maps to chromosome 4q32-q34.

Zhang XJ, He PP, Liang YH, Yang S, Yuan WT, Xu SJ, Huang W. Zhang XJ, et al. Among authors: xu sj. J Invest Dermatol. 2004 Feb;122(2):286-90. doi: 10.1046/j.0022-202X.2004.22244.x. J Invest Dermatol. 2004. PMID: 15009706 Free article.

6

Fine mapping and identification of a candidate gene SSH1 in disseminated superficial actinic porokeratosis.

Zhang Z, Niu Z, Yuan W, Liu W, Xiang L, Zhang J, Chu X, Zhao J, Jiang F, Chai B, Cui F, Wang Y, Zhang K, Wang Y, Xu S, Xia L, Gu J, Zhang S, Meng X, Wang S, Gao S, Fan M, Nie L, Zheng Z, Huang W. Zhang Z, et al. Hum Mutat. 2004 Nov;24(5):438. doi: 10.1002/humu.9283. Hum Mutat. 2004. PMID: 15459975

7

Divergence of the genes on human chromosome 21 between human and other hominoids and variation of substitution rates among transcription units.

Shi J, Xi H, Wang Y, Zhang C, Jiang Z, Zhang K, Shen Y, Jin L, Zhang K, Yuan W, Wang Y, Lin J, Hua Q, Wang F, Xu S, Ren S, Xu S, Zhao G, Chen Z, Jin L, Huang W. Shi J, et al. Proc Natl Acad Sci U S A. 2003 Jul 8;100(14):8331-6. doi: 10.1073/pnas.1332748100. Epub 2003 Jun 25. Proc Natl Acad Sci U S A. 2003. PMID: 12826612 Free PMC article.

8

Refinement of DSAP1 locus and mutation detection for candidate genes.

Zhang ZH, Niu ZM, Yuan WT, Zhao JJ, Jiang FX, Zhang J, Chai B, Xiong XY, Xiang LH, Wang Y, Xu SJ, Liu WD, Zheng ZZ, Huang W. Zhang ZH, et al. Among authors: xu sj. Yi Chuan Xue Bao. 2005 Jul;32(7):667-74. Yi Chuan Xue Bao. 2005. PMID: 16078733

9

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: xu sj. 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.

10

Autosomal dominant coralliform cataract related to a missense mutation of the gammaD-crystallin gene.

Xu WZ, Zheng S, Xu SJ, Huang W, Yao K, Zhang SZ. Xu WZ, et al. Among authors: xu sj. Chin Med J (Engl). 2004 May;117(5):727-32. Chin Med J (Engl). 2004. PMID: 15161542

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