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- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- 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
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Atrichia with papular lesions resulting from a novel homozygous missense mutation in the hairless gene
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approach
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- Androgenetic alopecia in heterozygous carriers of a mutation in the human hairless gene
- Disease causing homozygous variants in the human hairless gene
- ‘Atrichosis’, a new hairless gene with cyst formation in rats
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus
- Hypomorphic mutation in the hairless gene accelerates pruritic atopic skin caused by feeding a special diet to mice
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Androgenetic alopecia in heterozygous carriers of a mutation in the human hairless gene
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- Analyse de la régulation du gène Hairless et identification des voies de signalisation affectées chez les mutants «bald Mill Hill».
- [Molecular cloning of full-long cDNA sequences encoding hairless gene in the Kunming mouse].
- The Effect of Hairless Mutant Gene on The Thymus and Skin Under The C_(57)BL/6 Genetic Background