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Research 181–210 of 1000+
- 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
- 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
- Catagen in the hairless house mouse
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- 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
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- Vitamin D receptor-mediated control of Soggy, Wise, and Hairless gene expression in keratinocytes
- 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
- 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>)
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>
- 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
- Parathyroid hormone-related peptide and the hair cycle - is it the agonists or the antagonists that cause hair growth?
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- Comparison of the acute ultraviolet photoresponse in congenic albino hairless C57BL/6J mice relative to outbred SKH1 hairless mice
- Hair Follicle Disruption Facilitates Pathogenesis to UVB-Induced Cutaneous Inflammation and Basal Cell Carcinoma Development in Ptch+/− 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