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Research 391–420 of 1000+
- Evolution of long scalp hair in humans
- Androgenetic alopecia: An update
- Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta
- SAT-210 When Acne, Hirsutism and Menstrual Irregularities Are More Than PCOS
- Palatogenesis and cutaneous repair: A two‐headed coin
- Hair Follicle Pigmentation
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- Janus kinase inhibition in Down syndrome: 2 cases of therapeutic benefit for alopecia areata
- Therapeutics of premature hair graying: A long journey ahead
- Hidradenitis suppurativa and Mediterranean fever gene mutations
- Deletion of an Enhancer in FGF5 is Associated With Ectopic Expression in Goat Hair Follicles and the Cashmere Growth Phenotype
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- Gene expression of FOXA1 and CCL2 in different phenotypes of infertile women with polycystic ovarian syndrome
- Enhancing the diagnostic yield of monogenic diabetes in unresolved cases with early-onset hyperglycemia
- Microbial allies in skin trauma recovery: from immune modulation to engineered probiotic therapeutics
- Prospects of integrated multi-omics-driven biomarkers for efficient hair loss therapy from systems biology perspective
- Genome-Wide Association Studies for Immunoglobulins in Colostrum and Serum in Chinese Holstein
- Spatiotemporal control of CRISPR/Cas9 gene editing
- RNA sequencing reveals lncRNA-mediated non-mendelian inheritance of feather growth change in chickens
- Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient with Androgen Insensitivity Syndrome
- Correlation Analysis of BLTP1 (KIAA1109) and KIF27 Gene Polymorphisms with Wool Traits in Subo Merino Sheep
- Selection signatures in goats reveal a novel deletion mutant underlying cashmere yield and diameter
- ODP398 A Novel NR5A1 Gene Mutation Causing 46, XY DSD Without Adrenal Insufficiency in an Immigrant Boy from Dominican Republic
- The Organizer and Beyond
- Angiogenesis: a Dynamic Balance of Stimulators and Inhibitors
- Different phenotypes in a family with androgen insensitivity caused by the same M780I point mutation in the androgen receptor gene.
- Non-nutritional rickets: Approach, precision medicine, and outcomes
- The laboratory in the multidisciplinary diagnosis of differences or disorders of sex development (DSD)
- Immunohistochemical localization of fatty acid transporters and MCT1 in the sebaceous glands of mouse skin
- Expanding the Senior-Løken syndrome spectrum: Combined Rothmund-Thomson features unveil the distinct Teelwani Syndrome phenotype