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Research 331–360 of 1000+
- Ageratum Conyzoides L. Extract Inhibits 5α-Reductase Gene Expression and Prostaglandin D2 Release in Human Hair Dermal Papilla Cells and Improves Symptoms of Hair Loss in Otherwise Healthy Males and Females in an Open Label Pilot Study
- Nonclassic adrenal hyperplasia
- Progeroide Syndrome
- Screening for 21-hydroxylase–deficient nonclassic adrenal hyperplasia among hyperandrogenic women: a prospective study
- A variant of the glucocorticoid receptor gene is not associated with adrenal androgen excess in women with polycystic ovary syndrome
- How to diagnose a lipodystrophy syndrome
- Coordinated Activation of Wnt in Epithelial and Melanocyte Stem Cells Initiates Pigmented Hair Regeneration
- From gene to therapy in spinal and bulbar muscular atrophy: Are we there yet?
- COVID‐19, androgens, and androgenic alopecia
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus
- Global expression profile and global genome methylation signatures in male patients with androgenetic alopecia
- A curated catalog of canine and equine keratin genes
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- Cloning of the human phenol sulfotransferase gene family: three genes implicated in the metabolism of catecholamines, thyroid hormones and drugs
- Targets to treat androgen excess in polycystic ovary syndrome
- Androgens and hair: a biological paradox
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- A newly identified missense mutation of the HR gene is associated with a novel, unusual phenotype of Marie Unna Hereditary Hypotrichosis 1 including limb deformities
- Phenotypic Heterogeneity in 5 Japanese Patients with an Identical Point Mutation in the Vitamin D Receptor Gene
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- Virilizing insulinoma
- Riboflavin-responsive glutaryl CoA dehydrogenase deficiency
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Trichorhinophalangeal syndrome with low expression of TRPS1 on epidermal and hair follicle epithelial cells
- Significance of iron status in hair loss in women
- Recombinant Goat VEGF164 Increases Hair Growth by Painting Process on the Skin of Shaved Mouse
- Association of eNOS and STAT6 Gene Polymorphisms with the Susceptibility of Polycystic Ovary Syndrome in South Indian Women
- Control of hair growth and follicle size by VEGF-mediated angiogenesis
- Vitamin D metabolism and function in the skin