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Research 91–120 of 1000+
- Genetics and other factors in the aetiology of female pattern hair loss
- The genetics of alopecia areata: What's new and how will it help our patients?
- The association between Interleukin (IL)-4 gene intron 3 VNTR polymorphism and alopecia areata (AA) in Turkish population
- Increased rate of hair keratin gene loss in the cetacean lineage
- Identification of the Ovine Keratin-Associated Protein 22-1 (KAP22-1) Gene and Its Effect on Wool Traits
- Androgen receptor gene polymorphisms and risk for androgenetic alopecia: a meta-analysis
- Epidermal Stem Cells Manipulated by pDNA-VEGF165/CYD-PEI Nanoparticles Loaded Gelatin/β-TCP Matrix as a Therapeutic Agent and Gene Delivery Vehicle for Wound Healing
- Gene Expression of Mouse S100A3, a Cysteine-Rich Calcium-Binding Protein, in Developing Hair Follicle
- Genetic Basis of Alopecia Areata
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Effect of Adenovirus-Mediated Expression of Sonic Hedgehog Gene on Hair Regrowth in Mice With Chemotherapy-Induced Alopecia
- Regulation of a hair follicle keratin intermediate filament gene promoter
- Generation and characterization of hair-bearing skin organoids from human pluripotent stem cells
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Studying the genetic predisposing factors in the pathogenesis of acne vulgaris
- A Group of Type I Keratin Genes on Human Chromosome 17: Characterization and Expression
- Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss
- The Aromatase Inhibitor Fadrozole and the 5-Reductase Inhibitor Finasteride Affect Gonadal Differentiation and Gene Expression in the Frog <i>Silurana tropicalis</i>
- Transgenic mouse models support HCR as an effector gene in the PSORS1 locus
- Genetic studies on the functional relevance of the protein prenyltransferases in skin keratinocytes
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- Genetic hair and nail disorders
- Gene therapy to enhance angiogenesis in chronic wounds
- Genetically-manipulated adult stem cells as therapeutic agents and gene delivery vehicle for wound repair and regeneration
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Genetic association of <i>HLA‐DQB1</i> and <i>HLA‐DRB1</i> polymorphisms with alopecia areata in the Italian population
- Gene Delivery to the Hair Follicle
- Generation of Cashmere Goats Carrying an <i>EDAR</i> Gene Mutant Using CRISPR-Cas9-Mediated Genome Editing
- Gene trajectory inference for single-cell data by optimal transport metrics
- Serum Androgens and Genetic Linkage Analysis in Early Onset Androgenetic Alopecia