Associated Papers
Atrichia with papular lesions in a chinese family caused by novel compound heterozygous mutations and literature review.
Wang S et al.
Dermatology (basel, Switzerland), 2013
Analysis of hairless corepressor mutants to characterize molecular cooperation with the vitamin D receptor in promoting the mammalian hair cycle.
Hsieh JC et al.
Journal of Cellular Biochemistry, 2010
A novel deletion mutation in the human hairless (HR) gene in an Iranian family with atrichia and papular lesions.
Balighi K et al.
Clinical and Experimental Dermatology, 2009
Interactions of the vitamin D receptor with the corepressor hairless: analysis of hairless mutants in atrichia with papular lesions.
Wang J et al.
The Journal of Biological Chemistry, 2007
Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene.
Wali A et al.
Clinical and Experimental Dermatology, 2006
Hairless and Wnt signaling: allies in epithelial stem cell differentiation.
Thompson CC et al.
Cell Cycle (georgetown, Tex.), 2006
Atrichia Congenita with Papular Lesions: A Report of Rare Case Showing "Cluster of Stars' Appearance on Dermoscopy".
Sarojadevi HS et al.
International Journal of Trichology, 0
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