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Research 151–180 of 1000+
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases
- Regulation of Mitochondrial Oxidative Metabolism by Tumor Suppressor FLCN
- Understanding autoimmunity of vitiligo and alopecia areata
- Divergent roles of HDAC1 and HDAC2 in the regulation of epidermal development and tumorigenesis
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- Characterization of the Human Hair Keratin–Associated Protein 2 (KRTAP2) Gene Family
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- An update on alopecia areata
- Association Between Interleukin 18 Polymorphisms and Alopecia Areata in Koreans
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Mutations in the Serum/Glucocorticoid Regulated Kinase 3 (Sgk3) Are Responsible for the Mouse Fuzzy (fz) Hair Phenotype
- Lack of association between Vitamin D receptor FokI polymorphism and alopecia areata.
- Clinical Manifestations of Hyperandrogenism and Ovulatory Dysfunction Are Not Associated with His1058 C/T SNP (rs1799817) Polymorphism of Insulin Receptor Gene Tyrosine Kinase Domain in Kashmiri Women with PCOS
- CTLA4 +49AG (rs231775) and CT60 (rs3087243) gene variants are not associated with alopecia areata in a Mexican population from Monterrey Mexico
- Osteopontin Gene Polymorphisms rs1126616 C>T and rs1126772 A>G are Associated with Atopic Dermatitis in Polish Population
- Vitamin D Receptor gene polymorphisms taq-1 and cdx-1 in female pattern hair loss
- Cardiac biopsy in myocarditis
- Novel genes and variants associated with longevity in Bulgarian centenarians revealed by whole exome sequencing DNA pools: a pilot study
- Alopecia Areata is associated with MICA and an extended HLA haplotype
- Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- Interleukin 15 Gene Polymorphism in patients with Alopecia Areata
- Association of eNOS and STAT6 Gene Polymorphisms with the Susceptibility of Polycystic Ovary Syndrome in South Indian Women
- Alopecia areata susceptibility variant identified by MHC risk haplotype sequencing reproduces symptomatic patched hair loss in mice
- Mutations in the Desmoglein 4 Gene Are Associated with Monilethrix-like Congenital Hypotrichosis
- Cutaneous consequences of inhibiting EGF receptor signaling in vivo: Normal hair follicle development, but retarded hair cycle induction and inhibition of adipocyte growth in EgfrWa5 mice
- 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