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Research 211–240 of 1000+
- COVID-19: The question of genetic diversity and therapeutic intervention approaches
- Hair, Hormones, and High-Risk Prostate Cancer
- Abstracts
- Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium
- Repurposing With Purpose: Treatment of Bachmann–Bupp Syndrome With Eflornithine and Implications for Other Polyaminopathies
- Genetic association of wool quality characteristics in United States Rambouillet sheep
- The Predictive Value of Midscalp Hair Density and Terminal Hair Percentage in the Severity Evaluation of FPHL Assessed by Trichoscan in a Sample of Chinese Population
- The Polycystic Ovary Syndrome - Challenges and Opportunities in Adolescent Medicine
- Genetic Variation in CYP2B6, UGT1A4 and Sulfotransferases Is Associated with Disease-Free Survival in South African Breast Cancer Patients Treated with Tamoxifen
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- Case report: Exploring autosomal recessive woolly hair: genetic and scanning electron microscopic perspectives on a Japanese patient
- Fibrosing Frontal Alopecia: A comprehensive study to understand its etiology
- Factors associated with early-onset androgenetic alopecia: A scoping review
- 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
- Phenotypic heterogeneity in human genetic diseases: ultrasensitivity-mediated threshold effects as a unifying molecular mechanism
- Female Pattern Hair Loss: An Overview with Focus on the Genetics
- Dermatological diseases from a genetic perspective
- Meeting report: The 15thannual meeting of the European hair research society
- Risk factors for prostate cancer: a case-control study investigating selected key exposures and their interactions with predisposition genes
- Genetics of Diabetes in Childhood
- Genetic architecture of thermotolerance traits in beef cattle: a novel integration of SNP and breed-of-origin effects
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- Biology of the wool follicle: an excursion into a unique tissue interaction system waiting to be re‐discovered
- Genome-wide association study identifies a new locus JMJD1C at 10q21 that may influence serum androgen levels in men
- The genetics of alopecia areata: New approaches, new findings, new treatments
- Genetic Variants Associated with Hyperandrogenemia in PCOS Pathophysiology
- The diagnosis of nonclassic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, based on serum basal or post-ACTH stimulation 17-hydroxyprogesterone, can lead to false-positive diagnosis
- Emerging concepts about prenatal genesis, aberrant metabolism and treatment paradigms in polycystic ovary syndrome