Huang W - Search Results

1

Inversa acne (hidradenitis suppurativa): a case report and identification of the locus at chromosome 1p21.1-1q25.3.

Gao M, Wang PG, Cui Y, Yang S, Zhang YH, Lin D, Zhang KY, Liang YH, Sun LD, Yan KL, Xiao FL, Huang W, Zhang XJ. Gao M, et al. Among authors: huang w. J Invest Dermatol. 2006 Jun;126(6):1302-6. doi: 10.1038/sj.jid.5700272. J Invest Dermatol. 2006. PMID: 16543891 Free article.

2

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: huang w. 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.

3

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: huang w. 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.

4

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: huang w. 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.

5

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: huang w. Arch Dermatol. 2005 Feb;141(2):193-6. doi: 10.1001/archderm.141.2.193. Arch Dermatol. 2005. PMID: 15724015

6

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: huang w. 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.

7

Identification of a novel mutation in the DSRAD gene in a Chinese pedigree with dyschromatosis symmetrica hereditaria.

Cui Y, Wang J, Yang S, Gao M, Chen JJ, Yan KL, Xiao FL, Huang W, Zhang XJ. Cui Y, et al. Among authors: huang w. Arch Dermatol Res. 2005 May;296(11):543-5. doi: 10.1007/s00403-005-0546-z. Epub 2005 Mar 15. Arch Dermatol Res. 2005. PMID: 15844011

8

Identification of a novel locus for Marie Unna hereditary hypotrichosis to a 17.5 cM interval at 1p21.1-1q21.3.

Yang S, Gao M, Cui Y, Yan KL, Ren YQ, Zhang GL, Wang PG, Xiao FL, Du WH, Liang YH, Sun LD, Xu SJ, Huang W, Zhang XJ. Yang S, et al. Among authors: huang w. J Invest Dermatol. 2005 Oct;125(4):711-4. doi: 10.1111/j.0022-202X.2005.23874.x. J Invest Dermatol. 2005. PMID: 16185270 Free article.

9

The gene for a rare autosomal dominant form of pompholyx maps to chromosome 18q22.1-18q22.3.

Chen JJ, Liang YH, Zhou FS, Yang S, Wang J, Wang PG, Du WH, Xu SJ, Huang W, Zhang XJ. Chen JJ, et al. Among authors: huang w. J Invest Dermatol. 2006 Feb;126(2):300-4. doi: 10.1038/sj.jid.5700103. J Invest Dermatol. 2006. PMID: 16374448 Free article.

10

A novel MGST2 non-synonymous mutation in a Chinese pedigree with psoriasis vulgaris.

Yan KL, Zhang XJ, Wang ZM, Yang S, Zhang GL, Wang J, Xiao FL, Gao M, Cui Y, Chen JJ, Fan X, Sun LD, Xia Q, Zhang KY, Niu ZM, Xu SJ, Tzschach A, Ropers H, Huang W, Liu JJ. Yan KL, et al. Among authors: huang w. J Invest Dermatol. 2006 May;126(5):1003-5. doi: 10.1038/sj.jid.5700186. J Invest Dermatol. 2006. PMID: 16498398 Free article.

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