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- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- HR Gene Variants Identified in Mexican Patients with Alopecia Areata
- A newly identified missense mutation of the HR gene is associated with a novel, unusual phenotype of Marie Unna Hereditary Hypotrichosis 1 including limb deformities
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- 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
- Biology and Genetics of Hair
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Characterization of hairless (Hr) and FGF5genes provides insights into the molecular basis of hair loss in cetaceans
- 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
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Atrichia with papular lesions resulting from mutations in the rhesus macaque (<i>Macaca mulatta</i>) <i>hairless</i> 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
- Genetics of Structural Hair Disorders
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approach
- 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>)
- Molecular Genetics of Alopecias
- The Near-Naked Hairless (Hr) Mutation Disrupts Hair Formation but Is Not Due to a Mutation in the Hairless Coding Region
- Disease causing homozygous variants in the human hairless gene
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Identification of a recurrent nonsense mutation in <i>HR</i> gene responsible for atrichia with papular lesions in two Kashmiri families
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus