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Research 691–720 of 1000+
- SAT-210 When Acne, Hirsutism and Menstrual Irregularities Are More Than PCOS
- 879 Molecular network of Smads and Id2 genes in hair follicle stem cells regulation
- 839 Spatiotemporal antagonism in mesenchymal-epithelial Signaling in sweat versus hair fate decision
- 837 From genotoxic stresses to skin damage: Distinct, novel mechanisms of skin and hair damage in chemo/radiation therapy
- Genetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation
- Mesenchymal-epidermal interactions in hair follicle cycling and regeneration
- Regenerative Medicine of Epidermal Structures
- Editors' Picks
- A Novel Gene Homologous to Teashirt is Differentially Expressed in Neonatal Mouse Skin During Development of Hair Follicles
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Hairless triggers reactivation of hair growth by promoting Wnt signaling
- Melanocytes: The new Black
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- HRT for women with premature ovarian insufficiency: a comprehensive review
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Asian Hair: A Review of Structures, Properties, and Distinctive Disorders
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- The VEGF +405 G>C 5' untranslated region polymorphism and risk of PCOS: a study in the South Indian Women
- Whole Genome Scan and Selection Signatures for Climate Adaption in Yanbian Cattle
- Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets
- Development of Autoimmune Hair Loss Disease Alopecia Areata Is Associated with Cardiac Dysfunction in C3H/HeJ Mice
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Genetics of Structural Hair Disorders
- The relationship among androgens, insulin resistanceand ghrelin polymorphisms in post-adolescent malepatients with severe acne vulgaris
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Comparison of mitochondrial transplantation by using a stamp-type multineedle injector and platelet-rich plasma therapy for hair aging in naturally aging mice
- The association between rs2476601 polymorphism in PTPN22 gene and risk of alopecia areata
- Allopregnanolone Alters the Gene Expression Profile of Human Glioblastoma Cells