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Research 691–720 of 1000+
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
- Lineage Analysis of Epidermal Stem Cells
- Characterization of hairless (Hr) and FGF5genes provides insights into the molecular basis of hair loss in cetaceans
- The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defects
- Gene variants associated with acne vulgaris presentation and severity: a systematic review and meta-analysis
- Hair follicle and interfollicular epidermal stem cells make varying contributions to wound regeneration
- 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
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Androgenetic alopecia and coronary artery disease in women
- The Female Pattern Hair Loss: Review of Etiopathogenesis and Diagnosis
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- A review of cutaneous lupus erythematosus: improving outcomes with a multidisciplinary approach
- The Implication of Neuroactive Steroids in Tourette's Syndrome Pathogenesis: A Role for 5α‐Reductase?
- Hair shaft miniaturization causes stem cell depletion through mechanosensory signals mediated by a Piezo1-calcium-TNF-α axis
- Bone vs. fat: Embryonic origin of progenitors determines response to androgen in adipocytes and osteoblasts
- Human Hair Graying Revisited: Principles, Misconceptions, and Key Research Frontiers
- New developments in the molecular treatment of ichthyosis: review of the literature
- New approach to the understanding of keloid: psychoneuroimmune–endocrine aspects
- A Comprehensive Review of Mammalian Pigmentation: Paving the Way for Innovative Hair Colour-Changing Cosmetics
- Molecular characterization of HOXC8 gene and methylation status analysis of its exon 1 associated with the length of cashmere fiber in Liaoning cashmere goat
- Report from the Cicatricial Alopecia Colloquium
- The Search for the Causes of Common Hyperandrogenism, 1965 to Circa 2015
- The Complexity of the Ovine and Caprine Keratin-Associated Protein Genes
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- Single‐cell transcriptomics reveals a senescence‐associated IL ‐6/ CCR6 axis driving radiodermatitis
- Frontal fibrosing alopecia: a disease that remains enigmatic