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Research 331–360 of 1000+
- Intrinsic and Extrinsic Factors Associated with Hair Graying (Canities) and Therapeutic Potential of Plant Extracts and Phytochemicals
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Editor's evaluation: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Decision letter: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Molecular Mechanisms Regulating Hair Follicle Development
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- ROOT HAIR DEFECTIVE SIX‐LIKE4 (RSL4) promotes root hair elongation by transcriptionally regulating the expression of genes required for cell growth
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Lineage Analysis of Epidermal Stem Cells
- Hair follicle and interfollicular epidermal stem cells make varying contributions to wound regeneration
- Hunting the genes in male‐pattern alopecia: how important are they, how close are we and what will they tell us?
- Deciphering the Complex Immunopathogenesis of Alopecia Areata
- A powerful method for pleiotropic analysis under composite null hypothesis identifies novel shared loci between Type 2 Diabetes and Prostate Cancer
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Distinct Phenotypic and Genomic Signatures Underlie Contrasting Pathogenic Potential of Staphylococcus epidermidis Clonal Lineages
- Divergent neuroactive steroid responses to stress and ethanol in rat and mouse strains: relevance for human studies
- A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients
- Gsdma3 is required for hair follicle differentiation in mice
- Gata6 promotes hair follicle progenitor cell renewal by genome maintenance during proliferation
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Hair shaft miniaturization causes stem cell depletion through mechanosensory signals mediated by a Piezo1-calcium-TNF-α axis
- Immunology of alopecia areata
- Stem Cell Therapies for Epidermolysis Bullosa Treatment
- A Comprehensive Review of Mammalian Pigmentation: Paving the Way for Innovative Hair Colour-Changing Cosmetics