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Research 151–180 of 1000+
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- No difference in the proteome of racially and geometrically classified scalp hair sample from a South African cohort: Preliminary findings
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- Androgen Regulation of the Human Hair Follicle: The Type I Hair Keratin hHa7 Is a Direct Target Gene in Trichocytes
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Male infertility and genitourinary birth defects: there is more than meets the eye
- Increased rate of hair keratin gene loss in the cetacean lineage
- Molecular Genetics of Human Hair Diseases
- The relationship between keratin 18 and epithelial-derived tumors: as a diagnostic marker, prognostic marker, and its role in tumorigenesis
- Adverse effects of 5α-reductase inhibitors: What do we know, don’t know, and need to know?
- Genetic Hair Disorders: A Review
- Evolution, classification, structure, and functional diversification of steroid 5α-reductase family in eukaryotes
- DNA dioxygenases Tet2/3 regulate gene promoter accessibility and chromatin topology in lineage-specific loci to control epithelial differentiation
- Beta Human Papillomavirus and Merkel Cell Polyomavirus in Skin Neoplasms
- Role of Sulfur Metabolism Gene and High-Sulfur Gene Expression in Wool Growth Regulation in the Cashmere Goat
- Fast Motions in 5 Alpha Reductase and Its Impact on Enzyme Kinetics
- Immune and Non-immune Interactions in the Pathogenesis of Androgenetic Alopecia
- Wokeness in Our Practice
- Genetic Variants and Lifestyle Factors in Androgenetic Alopecia Patients: A Case–Control Study of Single Nucleotide Polymorphisms and Their Contribution to Baldness Risk
- Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix
- Construction of the coexpression network involved in the pathogenesis of thyroid eye disease via bioinformatics analysis
- Polycystic ovary syndrome
- The Catalog of Human Hair Keratins
- Recent Advances in the Pathogenesis of Autoimmune Hair Loss Disease Alopecia Areata
- K25 (K25irs1), K26 (K25irs2), K27 (K25irs3), and K28 (K25irs4) Represent the Type I Inner Root Sheath Keratins of the Human Hair Follicle
- A Novel Epithelial Keratin, hK6irs1, is Expressed Differentially in All Layers of the Inner Root Sheath, Including Specialized Huxley Cells (Flügelzellen) of the Human Hair Follicle
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Mammalian keratin associated proteins (KRTAPs) subgenomes: disentangling hair diversity and adaptation to terrestrial and aquatic environments