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Research 361–390 of 1000+
- Genomic Inbreeding and Runs of Homozygosity Analysis of Cashmere Goat
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- Exomic Sequencing of Immune-Related Genes Reveals Novel Candidate Variants Associated with Alopecia Universalis
- Premature hair graying: a multifaceted phenomenon
- Androgenetic Alopecia in Men: An Update On Genetics
- The causal relationship between androgenetic alopecia and serum uric acid: A bidirectional Mendelian randomization analysis
- Ophthalmologic Comorbidities in Alopecia Areata
- Drug Repositioning with GraphSAGE and Clustering Constraints Based on Drug and Disease Networks
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Polycystic Ovary Syndrome: An Updated Overview Foregrounding Impacts of Ethnicities and Geographic Variations
- Loss of the Y Chromosome: A Review of Molecular Mechanisms, Age Inference, and Implications for Men’s Health
- Causal effects of glutamine and lipid-related metabolites on alopecia areata: A 2-sample Mendelian randomization study
- A replication study confirmed the EDAR gene to be a major contributor to population differentiation regarding head hair thickness in Asia
- S100A6 Protein—Expression and Function in Norm and Pathology
- Evolution and genetic architecture of sex-limited polymorphism in cuckoos
- Novel genes and variants associated with longevity in Bulgarian centenarians revealed by whole exome sequencing DNA pools: a pilot study
- Serum levels of vitamin C, vitamin E, and total antioxidant capacity in premature graying hair
- Integrated analysis of coding genes and non-coding RNAs during hair follicle cycle of cashmere goat (Capra hircus)
- Skin Manifestations Associated with Autoimmune Liver Diseases: a Systematic Review
- Screening of Protein Related to Wool Development and Fineness in Gansu Alpine Fine-Wool Sheep
- Risk factors for prostate cancer: An umbrella review of prospective observational studies and mendelian randomization analyses
- Data-driven strategies for drug repurposing: insights, recommendations, and case studies
- Pharmacogenomic variation and chemotherapy-related toxicity profiles in pediatric patients with cancer in Tanzania: a cross-sectional study
- 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
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Alopecia areata and risk of atopic and autoimmune conditions: population-based cohort study
- Is age at puberty associated with semen quality and reproductive hormones in young adult life?
- Genetic analysis of interleukin 18 gene polymorphisms in alopecia areata
- Genotype Triad for HOTAIR rs10783618, LINC-ROR rs1942347, and MALAT1 rs3200401 as Molecular Markers in Systemic Lupus Erythematous
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults