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Research 781–810 of 1000+
- Topical Finasteride: A Comprehensive Review of Androgenetic Alopecia Management for Men and Women
- Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report
- New Target for Minoxidil in the Treatment of Androgenetic Alopecia
- Hair-Cycle-Associated Remodeling of the Peptidergic Innervation of Murine Skin, and Hair Growth Modulation by Neuropeptides
- Biotinidase Deficiency: Prevalence, Impact And Management Strategies.
- Role of FGFR2-signaling in the pathogenesis of acne
- Lysophospholipid Mediators in Health and Disease
- CD34 defines melanocyte stem cell subpopulations with distinct regenerative properties
- Disruption of tubular Flcn expression as a mouse model for renal tumor induction
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Skin transcriptome profiling of Changthangi goats highlights the relevance of genes involved in Pashmina production
- Pseudofolliculitis barbae; current treatment options
- Skin-specific regulation of SREBP processing and lipid biosynthesis by glycerol kinase 5
- Epidermolysis Bullosa Simplex Caused by Distal Truncation of BPAG1-e: An Intermediate Generalized Phenotype with Prurigo Papules
- Prevention of Male Late-Onset Hypogonadism by Natural Polyphenolic Antioxidants
- Skin tissue engineering
- Differential distribution and genetic determination of eccrine sweat glands and hair follicles in the volar skin of C57BL/6 mice and SD rats
- Reduced plakoglobin increases the risk of sodium current defects and atrial conduction abnormalities in response to androgenic anabolic steroid abuse
- Gender-Difference in Hair Length as Revealed by Crispr-Based Production of Long-Haired Mice with Dysfunctional FGF5 Mutations
- GWASs Identify Genetic Loci Associated with Human Scalp Hair Whorl Direction
- Steroidogenic Factor-1 Lineage Origin of Skin Lesions in Carney Complex Syndrome
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- Apoptosis in Hair and Skin: A Review
- Generation of iPS-derived model cells for analyses of hair shaft differentiation
- DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma
- Hirsutism Beyond PCOS: Genome-wide Evidence for Genetic Factors
- Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant