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Research 30 of 1000+
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Disease causing homozygous variants in the human hairless gene
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- Androgenetic alopecia in heterozygous carriers of a mutation in the human hairless gene
- Androgenetic alopecia in heterozygous carriers of a mutation in the human hairless gene
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- A novel missense mutation (C622G) in the zinc‐finger domain of the human hairless gene associated with congenital atrichia with papular lesions
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript
- Loss of ‘Epidermal Melanin Unit’ Integrity in Human Skin During Melanoma-Genesis
- Hair Today
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>
- The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approach
- Molecular basis of congenital atrichia in humans and mice.
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus
- ‘Atrichosis’, a new hairless gene with cyst formation in rats
- Growth retardation and hair loss in transgenic mice overexpressing human H-ferritin gene
- Atrichia with papular lesions