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Research 301–330 of 1000+
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- Differential sensitivity of epidermal cell subpopulations to β-catenin-induced ectopic hair follicle formation
- Reduced plakoglobin increases the risk of sodium current defects and atrial conduction abnormalities in response to androgenic anabolic steroid abuse
- Impact of Combined Baricitinib and FTI Treatment on Adipogenesis in Hutchinson–Gilford Progeria Syndrome and Other Lipodystrophic Laminopathies
- Zinc and Zinc Transporters in Dermatology
- Case Report of Wound Treatment with Hyiodine Gel in an Occasional KID Syndrome Patient
- Molecular Genetics of Human Hair Diseases
- Targeted Inactivation of Gh/Tissue Transglutaminase II
- Activation of TRPV3 Regulates Inflammatory Actions of Human Epidermal Keratinocytes
- Targeting Superficial or Nodular Basal Cell Carcinoma with Topically Formulated Small Molecule Inhibitor of Smoothened
- The Roles of Keratinocytes in the Initiation, Progression and Maintenance of Hidradenitis Suppurativa
- Anti-Graying Effects of External and Internal Treatments with Luteolin on Hair in Model Mice
- Role of the ABCA4 Gene Expression in the Clearance of Toxic Vitamin A Derivatives in Human Hair Follicle Stem Cells and Keratinocytes
- Hair Follicle Stem Cells Provide a Functional Niche for Melanocyte Stem Cells
- Dermal fibroblast in cutaneous development and healing
- 5-α-Reductase type 2 deficiency: is there a genotype-phenotype correlation? A review
- Recently Identified Forms of Epidermolysis Bullosa
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Histopathology of aging of the hair follicle
- Developmental genetics of color pattern establishment in cats
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- Effects of Androgen Treatment on Growth in Patients with 5-α-Reductase Type 2 Deficiency
- Congenital Adrenal Hyperplasia
- Hair & Cutaneous Development
- Identification of a link between Wnt/β-catenin signalling and the cell fusion pathway
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Dynamic regulation of retinoic acid-binding proteins in developing, adult and neoplastic skin reveals roles for β-catenin and Notch signalling
- SHISA6 Confers Resistance to Differentiation-Promoting Wnt/β-Catenin Signaling in Mouse Spermatogenic Stem Cells
- The keratin 19 promoter is potent for cell-specific targeting of genes in transgenic mice