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Research 631–660 of 1000+
- Hairless Modulates Ligand-Dependent Activation of the Vitamin D Receptor-Retinoid X Receptor Heterodimer
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Analysis of hairless corepressor mutants to characterize molecular cooperation with the vitamin D receptor in promoting the mammalian hair cycle
- 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
- Insertional mutation of the hairless locus on mouse Chromosome 14
- Modulation of Vitamin D Receptor Activity by the Corepressor Hairless: Differential Effects of Hairless Isoforms
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- Catagen in the hairless house mouse
- Human Hairless Protein Roles in Skin/Hair and Emerging Connections to Brain and Other Cancers
- The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approach
- Hairless down-regulates expression of Msx2 and its related target genes in hair follicles
- Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript
- Adam10 haploinsufficiency causes freckle-like macules in Hairless mice
- Successful Hair Transplantation for Treatment of Acquired Temporal Triangular Alopecia
- Hair loss
- Hairless Up‐Regulates <i>Tgf‐β2</i> Expression via Down‐Regulation of miR‐31 in the Skin of “Hairpoor” (<i>Hr</i><sup><i>Hp</i></sup>) Mice
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Skin morphology of the mutant hairless USP mouse
- Hairless and the polyamine putrescine form a negative regulatory loop in the epidermis
- Androgenetic alopecia in heterozygous carriers of a mutation in the human hairless gene
- Pathobiology of the hairless phenotype: Dysregulation of hair follicle apoptosis and topobiology during the initiation of follicle cycling
- Comparison of the acute ultraviolet photoresponse in congenic albino hairless C57BL/6J mice relative to outbred SKH1 hairless mice
- The Near-Naked Hairless (Hr) Mutation Disrupts Hair Formation but Is Not Due to a Mutation in the Hairless Coding Region
- Experimental cutaneous Bacillus anthracis infections in hairless HRS/J mice
- Disease causing homozygous variants in the human hairless gene
- The hairless mouse as a model for evaluating promoters of hair growth
- Diagnostic Value of VDR in Bone Metastasis and Prognosis of Patients with Breast Cancer and Expression Correlation between Vitamin D Receptor and Hairless Protein