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Research 481–510 of 1000+
- B-Raf and C-Raf Are Required for Melanocyte Stem Cell Self-Maintenance
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- The sheep KAP8-2 gene, a new KAP8 family member that is absent in humans
- Functional redundancy of <i>Frizzled 3</i> and <i>Frizzled 6</i> in planar cell polarity control of mouse hair follicles
- Hair Growth Cycle Is Arrested in SCD1 Deficiency by Impaired Wnt3a-Palmitoleoylation and Retrieved by the Artificial Lipid Barrier
- DNA Damage-Inducible Transcript 4 Is an Innate Surveillant of Hair Follicular Stress in Vitamin D Receptor Knockout Mice and a Regulator of Wound Re-Epithelialization
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- Converging physiological roles of the anthrax toxin receptors
- Directed Expression of a Chimeric Type II Keratin Partially Rescues Keratin 5-null Mice
- Basal cell carcinomas acquire secondary mutations to overcome dormancy and progress from microscopic to macroscopic disease
- Essential Role for Integrin-Linked Kinase in Melanoblast Colonization of the Skin
- Treatment of Cystathionine β-Synthase Deficiency in Mice Using a Minicircle-Based Naked DNA Vector
- No Evidence That Human Papillomavirus Is Responsible for the Aggressive Nature of Recessive Dystrophic Epidermolysis Bullosa–Associated Squamous Cell Carcinoma
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- The Wound Reporting in Animal and Human Preclinical Studies (WRAHPS) Guidelines
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Evolution, classification, structure, and functional diversification of steroid 5α-reductase family in eukaryotes
- A homozygous missense mutation in the fibroblast growth factor 5 gene is associated with the long-hair trait in Angora rabbits
- Case Report:Pregnancy and birth in a mild phenotype of Alström syndrome
- Read-Through for Nonsense Mutations in Type XVII Collagen‒Deficient Junctional Epidermolysis Bullosa
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- Expression of Signaling Components in Embryonic Eyelid Epithelium
- The Rho guanosine nucleotide exchange factors Vav2 and Vav3 modulate epidermal stem cell function
- PNKP is required for maintaining the integrity of progenitor cell populations in adult mice
- Wound healing with topical BRAF inhibitor therapy in a diabetic model suggests tissue regenerative effects
- Proteolysis‐targeting chimeras in cancer therapy: Targeted protein degradation for next‐generation treatment
- Ear pinna growth and differentiation is conserved in murids and requires BMP signaling for chondrocyte proliferation
- Exploring the clinical implications of novel SRD5A2 variants in 46,XY disorders of sex development
- TRPV3 Ion Channel: From Gene to Pharmacology