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Research 91–120 of 1000+
- AP-2α/AP-2β transcription factors are key regulators of epidermal homeostasis
- Insulin resistance and β-cell dysfunction and the relationship with cardio-metabolic disorders among women with polycystic ovary syndrome
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- Transforming growth factor-β in stem cells and tissue homeostasis
- The Role of Hormonal Imbalances in Amenorrhea
- An essential role for <i>Rxrα</i> in the development of Th2 responses
- DNA dioxygenases Tet2/3 regulate gene promoter accessibility and chromatin topology in lineage-specific loci to control epithelial differentiation
- Updates to Male Infertility: AUA/ASRM Guideline (2024)
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Delayed epidermal permeability barrier formation and hair follicle aberrations in Inv-Cldn6 mice
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- Skin-specific regulation of SREBP processing and lipid biosynthesis by glycerol kinase 5
- Mesenchymal Stem Cells With Modification of Junctional Adhesion Molecule A Induce Hair Formation
- Prevalence and Risk Factors Associated with the Occurrence of Autoimmune Diseases in Patients with Alopecia Areata
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- Adrenal and Gonadal Activity, Androgen Concentrations, and Adult Height Outcomes in Boys With Silver-Russell Syndrome
- The Molecular Pathogenesis of Trichilemmal Carcinoma
- The Molecular Pathogenesis of Trichilemmal Carcinoma
- Genetics of Structural Hair Disorders
- Spinal and bulbar muscular atrophy: pathogenesis and clinical management
- Drug-induced male infertility: a real-world study using FAERS and EudraVigilance databases
- Pregnancy, hair loss, and the pill.
- Anaesthetics and platelets.
- Group IID, IIE, IIF and III secreted phospholipase A2s
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- Advances in Hair Diseases
- Disorders of ovulation
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development