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Research 31–60 of 1000+
- An Australian family with macular dystrophy linked to autosomal recessive alopecia universalis
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- Papular atrichia
- Cultured follicles offer hope for beating baldness
- Hairless controls hair fate decision via Wnt/β–catenin signaling
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Atrichia with papular lesions resulting from mutations in the rhesus macaque (<i>Macaca mulatta</i>) <i>hairless</i> gene
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Hypomorphic mutation in the hairless gene accelerates pruritic atopic skin caused by feeding a special diet to mice
- Biology and Genetics of Hair
- Mutation des menschlichen hairless -Gens bei Atrichia universalis
- Hairless protein of Jumonji family and hair loss
- Hair Follicle Disruption Facilitates Pathogenesis to UVB-Induced Cutaneous Inflammation and Basal Cell Carcinoma Development in Ptch+/− Mice
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development
- Le gène<i>hairless</i>de la souris
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Hairless is a nuclear receptor corepressor essential for skin function
- Hairless: A nuclear receptor corepressor essential for skin function
- Stem Cells and their Niches
- Congenital atrichia with papular lesions
- Handbook of Mouse Mutations with Skin and Hair Abnormalities: Animal Models and Biomedical Tools
- Congenital Atrichia: A Case Report
- Lateral plate mesoderm directs human amnion and ventral skin organoid formation
- The Mammalian Hairless Protein as a DNA Binding Phosphoprotein
- Vitamin D receptor: molecular signaling and actions of nutritional ligands in disease prevention
- A mutation in MAP2 is associated with prenatal hair follicle density
- Analysis of hairless corepressor mutants to characterize molecular cooperation with the vitamin D receptor in promoting the mammalian hair cycle
- The Photoprotective Effect of S-Methylmethionine Sulfonium in Skin