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Research 30 of 1000+
- Receptor tyrosine kinase Kit action in skin melanocytes: is it exclusively cell autonomous?
- Hair Depigmentation Is a Biological Readout for Pharmacological Inhibition of KIT in Mice and Humans
- Upregulation of interfollicular epidermal and hair infundibulum β-catenin expression in Gsdma3 mutant mice
- Analysis of the function of ADAM17 in iRhom2 curly-bare and tylosis with esophageal cancer mutant mice
- Delayed hair cycle in mnd2 mutant mice lacking HtrA2 serine protease activity
- Transgenic mice display hair loss and regrowth overexpressing mutant <i>Hr</i> gene
- Gender-Difference in Hair Length as Revealed by Crispr-Based Production of Long-Haired Mice with Dysfunctional FGF5 Mutations
- Skin morphology of the mutant hairless USP mouse
- Engineering a New Mouse Model for Vitiligo
- An Extended Epidermal Response Heals Cutaneous Wounds in the Absence of a Hair Follicle Stem Cell Contribution
- Local circadian clock gates cell cycle progression of transient amplifying cells during regenerative hair cycling
- Premature aging and cancer development in transgenic mice lacking functional CYLD
- The Critical Roles of Serum/Glucocorticoid-Regulated Kinase 3 (SGK3) in the Hair Follicle Morphogenesis and Homeostasis
- Alopecia in a Viable Phospholipase C Delta 1 and Phospholipase C Delta 3 Double Mutant
- Reversing wrinkled skin and hair loss in mice by restoring mitochondrial function
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- B-Raf and C-Raf Are Required for Melanocyte Stem Cell Self-Maintenance
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- The disruption of Sox21-mediated hair shaft cuticle differentiation causes cyclic alopecia in mice
- HtrA1L364P leads to cognitive dysfunction and vascular destruction through TGF‐β/Smad signaling pathway in CARASIL model mice
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Genetic Ablation of the <i>CDP/Cux</i> Protein C Terminus Results in Hair Cycle Defects and Reduced Male Fertility
- A pair of transmembrane receptors essential for the retention and pigmentation of hair
- β-catenin Activity in the Dermal Papilla Regulates Morphogenesis and Regeneration of Hair
- Gsdma3 regulates hair follicle differentiation via Wnt5a-mediated non-canonical Wnt signaling pathway
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- A missense mutation in Lama3 causes androgen alopecia