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Research 91–120 of 1000+
- Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- Use of genetics in the prediction of success in male pattern hair loss therapy and mechanistic studies
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Comparative study of efficacy of excimer light therapy vs. intralesional triamcinolone vs. topical 5% minoxidil for alopecia areata: an observational study
- Alisertib is active as single agent in recurrent atypical teratoid rhabdoid tumors in 4 children
- What does acne genetics teach us about disease pathogenesis?
- Premature Greying of Hair (Premature Canities): A Concern for Parent and Child
- Molecular heterogeneity of quiescent melanocyte stem cells revealed by single-cell RNA-sequencing
- IV Międzynarodowe Sympozjum Studenckich Kół Naukowych Środowisko – Roślina – Zwierzę – Produkt Streszczenia
- Neuroendocrine Controls of Keratin Expression in Human Skin
- Australasian Society for Dermatology Research Meeting, May 2006
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Orchestration of tissue‐scale mechanics and fate decisions by polarity signalling
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- The nude gene and the skin
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Stereological Quantification of Cell-Cycle Kinetics and Mobilization of Epithelial Stem Cells during Wound Healing
- Mechanism-Based Strategies for Prevention of Taxane-Induced Hair Follicle Damage in Cancer Chemotherapy
- The analysis of genetics and associated autoimmune diseases in Chinese vitiligo patients
- Type II Epithelial Keratin 6hf (K6hf) Is Expressed in the Companion Layer, Matrix, and Medulla in Anagen-Stage Hair Follicles