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Research 271–300 of 1000+
- Role of the ABCA4 Gene Expression in the Clearance of Toxic Vitamin A Derivatives in Human Hair Follicle Stem Cells and Keratinocytes
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Influence of TRPV3 mutation on hair growth cycle in mice
- Clock genes, hair growth and aging
- Hoxc-Dependent Mesenchymal Niche Heterogeneity Drives Regional Hair Follicle Regeneration
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Mimicking Senescence Factors to Characterize the Mechanisms Responsible for Hair Regression and Hair Loss: An In Vitro Study
- Forkhead/winged-helix transcription factor whn regulates hair keratin gene expression: Molecular analysis of theNude skin phenotype
- Modeling Oxidative Stress-Linked Telogen Effluvium Using Monte Carlo Simulation of Published Trichoscopy Norms and Cannabis Exposure Distributions
- Evaluating the Role of Thyroid Stimulating Hormone and Ferritin Levels with Hair Loss among Patients with COVID-19: Case-Control Study
- Transcriptome meta-analysis reveals the hair genetic rules in six animal breeds and genes associated with wool fineness
- Association of metabolic syndrome with female pattern hair loss in women: A case-control study
- The clock gene brain and muscle Arnt-like protein-1 (BMAL1) is involved in hair growth
- Stromal Vascular Fraction and Platelet-Rich Plasma Upregulate Vascular Endothelial Growth Factor Expression to Promote Hair Growth via the Wnt/β-Catenin Signaling Pathway
- The GPR30 agonist G-1 promotes hair growth via Wnt/Hedgehog signaling in mice
- AN UPDATE OF HAIR SHAFT DISORDERS
- Pictorial Essay on Hair Loss; the Result of Head Bones Displacement
- The effect of COVID‐19 on development of hair and nail disorders: a Turkish multicenter, controlled study
- Genetic prediction of male pattern baldness
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Integration of Biochemical and Mechanical Signals at the Nuclear Periphery: Impacts on Skin Development and Disease
- Main Plenary Sessions: Summaries of Papers
- Local Artemis dysfunction may be one molecular mechanism for androgenetic alopecia via telomere shortening
- Polycystic Ovary Syndrome, Insulin Resistance, and Obesity: Navigating the Pathophysiologic Labyrinth
- Maternal PPARγ protects nursing neonates by suppressing the production of inflammatory milk
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia