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- The Near-Naked Hairless (Hr) Mutation Disrupts Hair Formation but Is Not Due to a Mutation in the Hairless Coding Region
- 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
- The “Bald Mill Hill” Mutation in the Mouse Is Associated with an Abnormal, Mislocalized HR bmh Protein
- 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 in a Taiwanese patient without hairless (HR) gene mutation
- The role of vitamin D receptor mutations in the development of alopecia
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- 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>)
- Hypomorphic mutation in the hairless gene accelerates pruritic atopic skin caused by feeding a special diet to mice
- Atrichia with Papular Lesions in a Chinese Family Caused by Novel Compound Heterozygous Mutations and Literature Review
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Identification of novel mutation in the<i>HR</i>gene responsible for atrichia with papular lesions in a Pakistani family
- Identification of a recurrent nonsense mutation in <i>HR</i> gene responsible for atrichia with papular lesions in two Kashmiri families
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Atrichia with papular lesions resulting from mutations in the rhesus macaque (<i>Macaca mulatta</i>) <i>hairless</i> gene
- The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approach
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Human Hairless Protein Roles in Skin/Hair and Emerging Connections to Brain and Other Cancers
- Alopecia: Association with Resistance to Thyroid Hormones
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus