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- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- A novel missense mutation (C622G) in the zinc‐finger domain of the human hairless gene associated with congenital atrichia with papular lesions
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- Arabidopsis ZINC FINGER PROTEIN1 Acts Downstream of GL2 to Repress Root Hair Initiation and Elongation by Directly Suppressing bHLH Genes
- Large Scale Gene Expression Profiles of Regenerating Inner Ear Sensory Epithelia
- Basonuclin is associated with the ribosomal RNA genes on human keratinocyte mitotic chromosomes
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Dynamic expression of the zinc-finger transcription factor Trps1 during hair follicle morphogenesis and cycling
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