Search
for
Sort by
Research 181–210 of 1000+
- Miz1 is required for hair follicle structure and hair morphogenesis
- Hair regrowth treatment efficacy and resistance in androgenetic alopecia: A systematic review and continuous Bayesian network meta-analysis
- Calcium and Vitamin D Supplementation with and Without Collagen on Bone Density and Skin Elasticity in Menopausal Women—A Randomized Controlled Study
- Can oral minoxidil be the game changer in androgenetic alopecia? A comprehensive review and meta-analysis comparing topical and oral minoxidil for treating androgenetic alopecia
- Genomic Surveillance Reveals the Rapid Expansion of the XBB Lineage among Circulating SARS-CoV-2 Omicron Lineages in Southeastern Wisconsin, USA
- The Impact of Vitamin D Receptor Gene Polymorphisms (FokI, ApaI, TaqI) in Correlation with Oxidative Stress and Hormonal and Dermatologic Manifestations in Polycystic Ovary Syndrome
- Structural perspectives on the androgen receptor, the elusive shape-shifter
- A Novel Model System to Identify Cellular and Molecular Defects Underlying Rare Genetic Disorders
- One Transgene: Two Outcomes
- Formation of regulator/target gene relationships during evolution
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Intramembrane Proteolysis of Astrotactins
- Specific receptor detection by a functional keratinocyte growth factor-immunoglobulin chimera.
- Carbon, nitrogen, and sulfur elemental and isotopic variations in mouse hair and bone collagen during short-term graded calorie restriction
- Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex
- Regulation of Receptor Binding Specificity of FGF9 by an Autoinhibitory Homodimerization
- An LRH-RSL4 feedback regulatory loop controls the determinate growth of root hairs in Arabidopsis
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Dermoscopic features of follicular mycosis fungoides of nonscalp areas: Report of 11 cases and literature review
- Calreticulin: non‐endoplasmic reticulum functions in physiology and disease
- Bidirectional binding property of high glycine–tyrosine keratin-associated protein contributes to the mechanical strength and shape of hair
- Mechanisms of proton inhibition and sensitization of the cation channel TRPV3
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- The susceptibility of disulfide bonds to modification in keratin fibers undergoing tensile stress
- Complete Structure of an Epithelial Keratin Dimer: Implications for Intermediate Filament Assembly
- The Mixed Lineage Kinase Leucine-Zipper Protein Kinase Exhibits a Differentiation-Associated Localization in Normal Human Skin and Induces Keratinocyte Differentiation upon Overexpression
- Enzymes
- Epidermal Notch signalling: differentiation, cancer and adhesion
- Analysis of Apoptotic Cell Death in Human Hair Follicles In Vivo andIn Vitro