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Research 571–600 of 1000+
- Association between angiotensin‐converting enzyme gene insertion deletion polymorphism and androgenetic alopecia susceptibility among Egyptian patients: A preliminary case‐controlled study
- Glutathione S-transferase gene polymorphism, total antioxidant status, and blood pressure changes in androgenic alopecia
- Tru9I Variant as a Novel Genetic Marker for Vitamin D Deficiency in Alopecia Areata
- Androgenic Effects on Ventricular Repolarization
- Sulphation catalysed by the human cytosolic sulphotransferases - chemical defence or molecular terrorism?
- Testosterone levels in relation to oral contraceptive use and the androgen receptor CAG and GGC length polymorphisms in healthy young women
- Hemorrhagic cystitis in allogeneic stem cell transplantation: a role for age and prostatic hyperplasia
- Hormonal Control of Cardiac Action Potential Phase 1 Currents in the Brugada Syndrome
- Associations between sun sensitive pigmentary genes and serum prostate specific antigen levels
- Evidence of a Causal Relationship Between Body Mass Index and Immune-Mediated and Inflammatory Skin Diseases and Biomarkers: A Mendelian Randomization Study
- NUDT15 polymorphism explains serious toxicity to azathioprine in Indian patients with chronic immune thrombocytopenia and autoimmune hemolytic anemia: a case series
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- Selenium or No Selenium- That Is the Question in Tumor Patients: A New Controversy
- Ischemic Stroke in a Young Adult Male During Finasteride Therapy
- Faculty Opinions recommendation of Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.
- Drug-associated insomnia: A pharmacovigilance study based on FDA adverse event reporting system
- Analyzing the role of ACE2, AR, MX1 and TMPRSS2 genetic markers for COVID-19 severity
- RETRACTED: Gut microbiota, skin microbiota, and alopecia areata: A Mendelian randomization study
- Association of single nucleotide polymorphisms in the <i>RAB5B</i> gene 3′UTR region with polycystic ovary syndrome in Chinese Han women
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- Pharmacogenomic variation and chemotherapy-related toxicity profiles in pediatric patients with cancer in Tanzania: a cross-sectional study
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- Genomic Analysis of Trichotillomania
- Association between <i>IL16</i> gene polymorphisms and susceptibility to alopecia areata in the Korean population
- Association between genetically predicted leukocyte telomere length and non-scarring alopecia: A two-sample Mendelian randomization study
- Interleukin gene polymorphisms and alopecia areata: A systematic review and meta-analysis
- Genetic analysis of 5 α reductase type 2 enzyme in relation to oxidative stress in cases of androgenetic alopecia in a sample of egyptian population
- Detection of a Second KAP22 Family Member in Sheep and Analysis of Its Genetic Variation and Associations with Selected Wool Fibre Traits
- Causal relationship between gut microbiota and androgenetic alopecia: A Mendelian randomization study