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Research 451–480 of 1000+
- Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles
- Selenium for preventing cancer
- The pathophysiology of polycystic ovary syndrome
- Common variants in the sex hormone-binding globulin gene (SHBG) and polycystic ovary syndrome (PCOS) in Mediterranean women
- Epidemiological study of prostate cancer (EPICAP): a population-based case–control study in France
- Thyroid diseases and skin autoimmunity
- PSEUDOPELADE: AN INHERITED ALOPECIA
- Compilation of a comprehensive gene panel for systematic assessment of genes that govern an individual’s drug responses
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Exploring Variation in Ovine KRTAP19-5 and Its Effect on Fine Wool Fibre Curvature in Chinese Tan Sheep
- Familial patterns of alopecia areata: A systematic review and meta-analysis
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Co-occurrence of monilethrix and Type 1 diabetes mellitus
- Polycystic Ovarian Syndrome: A Breakthrough Etiology, Symptoms and Therapy
- SÍNDROME PÓS-FINASTERIDA E O IMPACTO DOS INIBIDORES DA 5-ALFA REDUTASE NOS EIXOS NEUROENDÓCRINO E METABÓLICO
- Immunogenetic and metabolic risk factors in male androgenetic alopecia: the role of HLA-DRB1 alleles and vitamin D3 deficiency
- PA30 Evaluation of markers of inflammation and oxidative stress in patients with premature canities
- Recent Advances in Understanding of the Etiopathogenesis, Diagnosis, and Management of Hair Loss Diseases
- An Unusual Cause of Primary Amenorrhea
- Clinical Snippets
- Fertility and Sterility Vol 101 No 4, April 2014
- Tricholemmoma and tricholemmal carcinoma and Cowden syndrome
- Correction: Androgenic Alopecia Is Associated with Less Dietary Soy, Higher Blood Vanadium and rs1160312 1 Polymorphism in Taiwanese Communities
- Frontal Fibrosing Alopecia
- Differential impact of environmental factors on systemic and localized autoimmunity
- Research Snippets
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- Birt-Hogg-Dube Syndrome with a Novel Mutation in the <i>FLCN</i> Gene