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Research 121–150 of 1000+
- Molecular basis of congenital atrichia in humans and mice.
- Handbook of Mouse Mutations with Skin and Hair Abnormalities: Animal Models and Biomedical Tools
- Stem Cells and their Niches
- A missense mutation in Lama3 causes androgen alopecia
- 毛乳頭細胞と毛包上皮細胞間の細胞内・細胞外情報伝達
- Cultured follicles offer hope for beating baldness
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- Supplementary Material for: Effects of Food-Derived Collagen Peptides on the Expression of Keratin and Keratin-Associated Protein Genes in the Mouse Skin
- Supplementary Material for: Effects of Food-Derived Collagen Peptides on the Expression of Keratin and Keratin-Associated Protein Genes in the Mouse Skin
- Adam10 haploinsufficiency causes freckle-like macules in Hairless mice
- Effects of Food-Derived Collagen Peptides on the Expression of Keratin and Keratin-Associated Protein Genes in the Mouse Skin
- The Mammalian Hairless Protein as a DNA Binding Phosphoprotein
- Identification of differentially expressed genes affecting hair and cashmere growth in the Laiwu black goat by microarray
- Genetic and Environmental Factors that Control Merkel Cell Development and Survival
- Growth retardation and hair loss in transgenic mice overexpressing human H-ferritin gene
- Correlation of trichoscopic findings with clinico-epidemiological factors in male pattern&nbsp;<span style="font-size: 1rem;">hairloss: A cross-sectional study from a tertiary care center in Chengalpattu</span>
- 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>)
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- The role of vitamin D receptor mutations in the development of alopecia
- A mutation in MAP2 is associated with prenatal hair follicle density
- Decision letter: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Author response: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Congenital Atrichia: A Case Report
- Recent advances in the genetics of alopecia areata
- Gender differences in scalp hair growth rates are maintained but reduced in pattern hair loss compared to controls
- Fractal Pattern in the Premature Graying of Hair: A Case Report
- Hairless and the polyamine putrescine form a negative regulatory loop in the epidermis
- Comparison of the acute ultraviolet photoresponse in congenic albino hairless C57BL/6J mice relative to outbred SKH1 hairless mice