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Research 211–240 of 1000+
- Atopic dermatitis and risk of autoimmune diseases: a systematic review and meta-analysis
- Intraethnic variation in steroid-5-alpha-reductase polymorphisms in prostate cancer patients: a potential factor implicated in 5-alpha-reductase inhibitor treatment
- RETRACTED: Genetic association between asthma and alopecia areata: A two‐sample Mendelian randomization study
- SNP variation in male pattern hair loss in Russians with different dihydrotestosterone levels
- Abstracts
- The genetic link between thyroid dysfunction and alopecia areata: a bidirectional two-sample Mendelian randomization study
- Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium
- Genetic Upregulation of Activated Protein C Mitigates Delayed Effects of Acute Radiation Exposure in the Mouse Plasma
- Analysis of Various Factors Responsible for Hair Loss and Awareness Level in Delhi and the National Capital Region of India
- Hirsutism Beyond PCOS: Genome-wide Evidence for Genetic Factors
- Genetic Variation in CYP2B6, UGT1A4 and Sulfotransferases Is Associated with Disease-Free Survival in South African Breast Cancer Patients Treated with Tamoxifen
- Research progress on mechanisms of skin aging and anti-aging strategies
- Tangled Causes, Targeted Solutions: A Comprehensive Review of Alopecia.
- Genetic Variant of the Canine FGF5 Gene for the Hair Length Trait in the Akita: Utility for Hair Coat Variations and Welfare in Conservation Breeding
- Maternal Melatonin Contributes to Offspring Hair Follicle Development Through Transcriptional Regulation of the AP-1 Complex and MAPK Pathway
- Comprehensive Administrative and Engineering Strategies for Radiation Protection and Occupational Health Safety
- Genetic Variants and Lifestyle Factors in Androgenetic Alopecia Patients: A Case–Control Study of Single Nucleotide Polymorphisms and Their Contribution to Baldness Risk
- Genetic Differences between Male and Female Pattern Hair Loss in a Korean Population
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Genetic Upregulation of Activated Protein C Mitigates Delayed Effects of Acute Radiation Exposure in the Mouse Plasma
- Progress in Research and Prospects for Application of Precision Gene-Editing Technology Based on CRISPR–Cas9 in the Genetic Improvement of Sheep and Goats
- Genetic Association Between Polycystic Ovary Syndrome and the <i>APOA5</i> rs662799 and <i>PLIN1</i> rs894160 Metabolic Variants in the Western Saudi Population: A Case-Control Study
- Pediatric Features of Genetic Predisposition to Polycystic Ovary Syndrome
- Maternal androgen excess significantly impairs sexual behavior in male and female mouse offspring: Perspective for a biological origin of sexual dysfunction in PCOS
- QSAR Analysis of a Series of Hydantoin‐based Androgen Receptor Modulators and Corresponding Binding Affinities
- Human Pigmentation: A Review of Molecular Mechanisms, Genetic Architecture, Evolution, Forensic DNA Phenotyping and Health Implications
- Phenotypic heterogeneity in human genetic diseases: ultrasensitivity-mediated threshold effects as a unifying molecular mechanism
- Maternal iron status in early pregnancy and DNA methylation in offspring: an epigenome-wide meta-analysis
- Polycystic ovarian syndrome: current understanding of pathogenesis, diagnosis and treatment
- COVID-19: The question of genetic diversity and therapeutic intervention approaches