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Research 151–180 of 1000+
- Cardiometabolic and neuroimaging correlates of cognitive function in polycystic ovary syndrome
- Pediatric Endocrine-Disrupting Chemical Exposure Produces Irreversible Organizational Injury: Biomarker Evidence Necessitating a Precautionary Public Health Framework
- The Clinical Presentation of Systemic Lupus Erythematosus
- 毛乳頭細胞と毛包上皮細胞間の細胞内・細胞外情報伝達
- COVID-19: Understanding Inter-Individual Variability and Implications for Precision Medicine
- Hair Follicle Disruption Facilitates Pathogenesis to UVB-Induced Cutaneous Inflammation and Basal Cell Carcinoma Development in Ptch+/− Mice
- Associations between genetically predicted sex and growth hormones and facial aging in the UK Biobank: a two−sample Mendelian randomization study
- Interventions for androgenic alopecia in women
- A regenerative stem cell-derived matrix accelerates functional dermal wound repair in a preclinical diabetic model
- Optimizing hair transplant outcomes: integration of AI, robotics, and stem cell therapies
- Association between SQSTM1 dysregulation and risk in alopecia areata: a Mendelian randomization study
- Gut Microbiota and Its Association with Alopecia Areata: Insights from a Two-Sample Mendelian Randomization Study
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Linking Morphogen and Chromatin in the Hair Follicle
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- Identifying causal genes in alopecia areata using integrative analysis of differential expression and Mendelian randomization
- The Androgen Excess and PCOS Society criteria for the polycystic ovary syndrome: the complete task force report
- Nonalcoholic fatty liver disease and polycystic ovary syndrome
- A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females
- Steroid Biomarkers and Genetic Studies Reveal Inactivating Mutations in Hexose-6-Phosphate Dehydrogenase in Patients with Cortisone Reductase Deficiency
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Convergent Evolution of Cysteine-Rich Keratins in Hard Skin Appendages of Terrestrial Vertebrates
- The Genetics of Human Skin Disease
- Alopecia Areata
- Defining the identity of mouse embryonic dermal fibroblasts
- The endocrinology of baldness
- Effectiveness and Safety of Botulinum Toxin Type A in the Treatment of Androgenetic Alopecia
- SNP variation in male pattern hair loss in Russians with different dihydrotestosterone levels
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Understanding Polycystic Ovary Syndrome