Associated Papers
Human Hairless Protein Roles in Skin/Hair and Emerging Connections to Brain and Other Cancers.
Maatough A et al.
Journal of Cellular Biochemistry, 2018
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
Cross-comparison of the genome sequences from human, chimpanzee, Neanderthal and a Denisovan hominin identifies novel potentially compensated mutations.
Zhang G et al.
Human Genomics, 2011
PhenoHM: human-mouse comparative phenome-genome server.
Sardana D et al.
Nucleic Acids Research, 2010
20507906 (PubMed )
Supplement: gkq472_nar-00429-web-b-2010-File006.xls › MPO_to_OMIM_allelic_Variants
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
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
The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approach.
Hillmer AM et al.
The British Journal of Dermatology, 2002
Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia.
Cichon S et al.
Human Molecular Genetics, 1998
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