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Research 181–210 of 1000+
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks
- Current Genetics in Hair Diseases
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities
- Polycystic ovary syndrome
- Genetically Altered Expression of Spermidine/Spermine N1-Acetyltransferase Affects Fat Metabolism in Mice via Acetyl-CoA
- Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
- Genetic predictors of testosterone and their associations with cardiovascular disease and risk factors: A Mendelian randomization investigation
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Genetic Variants Associated with Hyperandrogenemia in PCOS Pathophysiology
- Identification of key genes induced by platelet-rich plasma in human dermal papilla cells using bioinformatics methods
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- IL-15 in alopecia areata: the immune tolerance mechanistic insights and translational perspectives
- Molecular Mechanisms and Targeted Therapeutics in Androgenetic Alopecia: From Signaling Pathways to Regenerative Approaches
- Current understanding and treatment of sex hormone-related hair diseases
- Male-pattern hair loss: Comprehensive identification of the associated genes as a basis for understanding pathophysiology
- Regulation of adult stem cell quiescence and its functions in the maintenance of tissue integrity
- Developing Human Skin Contains Lymphocytes Demonstrating a Memory Signature
- Desmoplastic Trichoepithelioma: Histopathologic and Immunohistochemical Criteria for Differentiation of a Rare Benign Hair Follicle Tumor From Other Cutaneous Adnexal Tumors
- The human type I keratin gene family: Characterization of new hair follicle specific members and evaluation of the chromosome 17q21.2 gene domain
- Sequence Data and Chromosomal Localization of Human Type I and Type II Hair Keratin Genes
- Congenital Generalized Hypertrichosis Terminalis with Gingival Hyperplasia and a Coarse Face: a Case Report
- A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type
- Genomic Organization and Amplification of the Human Keratin 15 and Keratin 19 Genes
- Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.
- Hair follicle-specific keratins and their diseases
- Terrestrial vertebrates have two keratin gene clusters; striking differences in teleost fish
- Novel Type I Hair Keratins K39 and K40 Are the Last to be Expressed in Differentiation of the Hair: Completion of the Human Hair Keratin Catalog