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Research 451–480 of 1000+
- Resistance to the Insulin and Elevated Level of Androgen: A Major Cause of Polycystic Ovary Syndrome
- Madarosis: A marker of many Maladies
- Understanding the role of prostaglandin E2 in regulating human platelet activity in health and disease
- Sarcoidosis: Are there differences in your skin of color patients?
- Pathophysiology of the Behçet's Disease
- Mouse Intestinal Krt15+ Crypt Cells Are Radio-Resistant and Tumor Initiating
- Rare and common genetic determinants of metabolic individuality and their effects on human health
- Genetic Variants Associated with Hyperandrogenemia in PCOS Pathophysiology
- Male infertility and genitourinary birth defects: there is more than meets the eye
- Genetic Hair Disorders: A Review
- Activation of TRPV3 Inhibits Lipogenesis and Stimulates Production of Inflammatory Mediators in Human Sebocytes—A Putative Contributor to Dry Skin Dermatoses
- Alopecia and Associated Toxic Agents: A Systematic Review
- Isolation and Characterization of a Putative Keratin-Associated Protein Gene Expressed in Embryonic Skin of Mice
- Alopecia Areata: Pathogenesis, Diagnosis, and Therapies
- Cronkhite–Canada syndrome: from clinical features to treatment
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- The role of ultrasound and Doppler analysis in the diagnosis of polycystic ovary syndrome
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- The ATP sensitive potassium channel (KATP) is a novel target for migraine drug development
- Comparison of pemetrexed and docetaxel as salvage chemotherapy for the treatment for nonsmall-cell lung cancer after the failure of epidermal growth factor receptor-tyrosine kinase inhibitors
- Lrig1-expression confers suppressive function to CD4+ cells and is essential for averting autoimmunity via the Smad2/3/Foxp3 axis
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- The Search for the Causes of Common Hyperandrogenism, 1965 to Circa 2015
- Clinical Management of Prostate Cancer in High-Risk Genetic Mutation Carriers
- Nivolumab-Induced Alopecia Areata: A Case Report and Literature Review
- Suppression of FGF5 and FGF18 Expression by Cholesterol-Modified siRNAs Promotes Hair Growth in Mice
- Hair follicle aging is driven by transepidermal elimination of stem cells via COL17A1 proteolysis
- Biliary fibrosis is an important but neglected pathological feature in hepatobiliary disorders: from molecular mechanisms to clinical implications
- The quality of sexual life after vaginal surgical interventions