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Research 121–150 of 1000+
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- Prostaglandin-Induced Hair Growth
- 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
- Towards Defining the Pathogenesis of the Hairless Phenotype
- Therapeutic strategy for hair regeneration: hair cycle activation, niche environment modulation, wound-induced follicle neogenesis, and stem cell engineering
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Relation of Skin Polyamines to the Hairless Phenotype in Transgenic Mice Overexpressing Spermidine/Spermine N1-Acetyltransferase
- A novel missense mutation (C622G) in the zinc‐finger domain of the human hairless gene associated with congenital atrichia with papular lesions
- Evaluation of the Hairless Rat as a Model for in Vivo Percutaneous Absorption
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- The character “hairless” in the mouse
- Ion pairs of risedronate for transdermal delivery and enhanced permeation rate on hairless mouse skin
- Intragenic deletion in the Desmoglein 4 gene underlies the skin phenotype in the Iffa Credo “hairless” rat
- The mouse frizzy (<i>fr</i>) and rat ‘hairless’ (<i>fr</i><sup><i>CR</i></sup>) mutations are natural variants of protease serine S1 family member 8 (<i>Prss8</i>)
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Atrichia with papular lesions resulting from a novel homozygous missense mutation in the hairless gene
- Insertional mutation of the hairless locus on mouse Chromosome 14
- 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
- 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
- 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