Zhang XJ - Search Results

1

Multiple variants in 5q31.1 are associated with systemic lupus erythematosus susceptibility and subphenotypes in the Han Chinese population.

Wen LL, Zhu ZW, Yang C, Liu L, Zuo XB, Morris DL, Dou JF, Ye L, Cheng YY, Guo HM, Huang HQ, Lin Y, Zhu CH, Tang LL, Chen MY, Zhou Y, Ding YT, Liang B, Zhou FS, Gao JP, Tang XF, Zheng XD, Wang WJ, Yin XY, Tang HY, Sun LD, Yang S, Zhang XJ, Sheng YJ, Cui Y. Wen LL, et al. Among authors: zhang xj. Br J Dermatol. 2017 Sep;177(3):801-808. doi: 10.1111/bjd.15362. Epub 2017 Jun 12. Br J Dermatol. 2017. PMID: 28144936

2

Guillain-Barré syndrome or "new" Chinese paralytic syndrome in northern China?

Tang XF, Zhang XJ. Tang XF, et al. Among authors: zhang xj. Electroencephalogr Clin Neurophysiol. 1996 Apr;101(2):105-9. doi: 10.1016/0924-980x(95)00236-e. Electroencephalogr Clin Neurophysiol. 1996. PMID: 8647015

3

A new glycine substitution mutation in the COL7A1 gene in a Chinese family with dominant dystrophic epidermolysis bullosa.

Zhang XJ, Song YX, Zhang XQ, Yang S, Li M, Li CR, Yang CJ, Yang J. Zhang XJ, et al. Among authors: zhang xq. Clin Exp Dermatol. 2003 Jul;28(4):437-9. doi: 10.1046/j.1365-2230.2003.01317.x. Clin Exp Dermatol. 2003. PMID: 12823310

4

Identification of a locus for porokeratosis palmaris et plantaris disseminata to a 6.9-cM region at chromosome 12q24.1-24.2.

Wei SC, Yang S, Li M, Song YX, Zhang XQ, Bu L, Zheng GY, Kong XY, Zhang XJ. Wei SC, et al. Among authors: zhang xq, zhang xj. Br J Dermatol. 2003 Aug;149(2):261-7. doi: 10.1046/j.1365-2133.2003.05461.x. Br J Dermatol. 2003. PMID: 12932230

5

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: zhang xj. 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.

6

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: zhang xj. Br J Dermatol. 2004 May;150(5):837-42. doi: 10.1111/j.1365-2133.2004.05913.x. Br J Dermatol. 2004. PMID: 15149494

7

The genetic epidemiology of alopecia areata in China.

Yang S, Yang J, Liu JB, Wang HY, Yang Q, Gao M, Liang YH, Lin GS, Lin D, Hu XL, Fan L, Zhang XJ. Yang S, et al. Among authors: zhang xj. Br J Dermatol. 2004 Jul;151(1):16-23. doi: 10.1111/j.1365-2133.2004.05915.x. Br J Dermatol. 2004. PMID: 15270868

8

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: zhang xj. Clin Exp Dermatol. 2004 Sep;29(5):460-3. doi: 10.1111/j.1365-2230.2004.01570.x. Clin Exp Dermatol. 2004. PMID: 15347323

9

A novel mutation of the DSRAD gene in a Chinese family with dyschromatosis symmetrica hereditaria.

Li M, Jiang YX, Liu JB, Yang S, He PP, Gao M, Wei SC, Yan KL, Huang W, Zhang XJ. Li M, et al. Among authors: zhang xj. Clin Exp Dermatol. 2004 Sep;29(5):533-5. doi: 10.1111/j.1365-2230.2004.01548.x. Clin Exp Dermatol. 2004. PMID: 15347341

10

The effect of mizolastine on expression of vascular endothelial cell growth factor, tumour necrosis factor-alpha and keratinocyte-derived chemokine in murine mast cells, compared with dexamethasone and loratadine.

Xia Q, Yang S, Zhang SQ, Chen B, Wang DB, Zhu QX, Wang Y, Yan KL, He PP, Zhang XJ. Xia Q, et al. Among authors: zhang sq, zhang xj. Clin Exp Dermatol. 2005 Mar;30(2):165-70. doi: 10.1111/j.1365-2230.2005.01721.x. Clin Exp Dermatol. 2005. PMID: 15725247

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