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Research 811–840 of 1000+
- [Association of eight single nucleotide polymorphisms of chromosomes 20 and X with androgenetic alopecia among ethnic Han Chinese from Yunnan].
- Common Variants in the Sex Hormone-Binding Globulin (SHBG) Gene Influence SHBG Levels in Women with Polycystic Ovary Syndrome
- A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation
- Alopecia areata susceptibility variant identified by MHC risk haplotype sequencing reproduces symptomatic patched hair loss in mice
- Identification of 736T>A mutation of lipase H in Japanese siblings with autosomal recessive woolly hair
- Association Between Interleukin 18 Polymorphisms and Alopecia Areata in Koreans
- Association of methionine synthase gene polymorphisms with wool production and quality traits in Chinese Merino population12
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- AKT2 Gene Polymorphisms, sRANKL/OPG and Hormone Measurements in Polycystic Ovarian Syndrome (PCOS) Women
- Genetic and Environmental Factors Affecting Hair Density in East Asian Populations
- Gene-Environment Interaction Between <i>CYP1B1</i> and Oral Contraception on Frontal Fibrosing Alopecia
- 268 Male-pattern baldness and its association with coronary heart disease
- Pilot study: genetic distribution of AR, FGF5, SULT1A1 and CYP3A5 polymorphisms in male Mexican population with androgenetic alopecia.
- Novel genes and variants associated with longevity in Bulgarian centenarians revealed by whole exome sequencing DNA pools: a pilot study
- Efficacy of metformin therapy in adolescent girls with androgen excess: relation to sex hormone–binding globulin and androgen receptor polymorphisms
- Cardiac biopsy in myocarditis
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- Alopecia Areata is associated with MICA and an extended HLA haplotype
- Regulation of Mitochondrial Oxidative Metabolism by Tumor Suppressor FLCN
- THE PATHOGENESIS OF ALOPECIA AREATA
- The Genetic Architecture of Alopecia Areata
- CTLA4 +49AG (rs231775) and CT60 (rs3087243) gene variants are not associated with alopecia areata in a Mexican population from Monterrey Mexico
- Effects of <i>KISS1</i> structural polymorphism on the risk of polycystic ovary syndrome and reproductive hormones in Iraqi women who take metformin
- Distinct genotype-phenotype patterns in non-syndromic hereditary hypotrichosis: a multicenter Chinese cohort
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- FGFR2 is associated with hair thickness in Asian populations
- Validation and casework testing of the BioPlex-11 for STR typing of telogen hair roots
- Genetic Single Nucleotide Polymorphisms of IL-16 and its Concentration of Patients Infected with Alopecia Areata in Diyala Province, Iraq
- Recent Advances in the Pathogenesis of Autoimmune Hair Loss Disease Alopecia Areata
- 9. Immunology and Genetics