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Research 481–510 of 1000+
- Global Adiposity and Thickness of Intraperitoneal and Mesenteric Adipose Tissue Depots Are Increased in Women With Polycystic Ovary Syndrome (PCOS)
- Oestrogen functions in skin and skin appendages
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- Targeting lymphoid-derived IL-17 signaling to delay skin aging
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Androgen receptor gene CAG repeat polymorphism in women with polycystic ovary syndrome
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- Identification of potential key genes and pathways associated with the Pashmina fiber initiation using RNA-Seq and integrated bioinformatics analysis
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Comparative Transcriptome Analysis Reveals that a Ubiquitin-Mediated Proteolysis Pathway Is Important for Primary and Secondary Hair Follicle Development in Cashmere Goats
- <i>WNT10A</i> , dermatology and dentistry
- CAG Repeat Testing of Androgen Receptor Polymorphism: Is This Necessary for the Best Clinical Management of Hypogonadism?
- The VEGF +405 G>C 5' untranslated region polymorphism and risk of PCOS: a study in the South Indian Women
- The metabolic syndrome- associated small G protein ARL15 plays a role in adipocyte differentiation and adiponectin secretion
- Defining the identity of mouse embryonic dermal fibroblasts
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- A curated catalog of canine and equine keratin genes
- The quality of European dermatological guidelines: critical appraisal of the quality of EDF guidelines using the AGREE II instrument
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Discovery of Natural Steroid 5 Alpha-Reductase Inhibitors
- Minoxidil Sulfotransferase Enzyme (SULT1A1) genetic variants predicts response to oral minoxidil treatment for female pattern hair loss
- HSD3B1 gene polymorphism and female pattern hair loss in women with polycystic ovary syndrome
- Novel <i>ABCD1</i> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Urinary 5-ene-steroid excretion in non-classical congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase deficiency (NC-3BHSD)
- Biotechs target stagnant baldness market
- H2AK119ub dynamics control hair follicle stem cell quiescence
- Sexually dimorphic sail feathers in the Mandarin duck as a model for lifelong developmental modulation