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Research 31–60 of 590
- Risk factors for prostate cancer: a case-control study investigating selected key exposures and their interactions with predisposition genes
- Lichen Planopilaris and Frontal Fibrosing Alopecia as Model Epithelial Stem Cell Diseases
- Acne
- ACE2 and TMPRSS2 Potential Involvement in Genetic Susceptibility to SARS-COV-2 in Cancer Patients
- Evolution and genetic architecture of sex-limited polymorphism in cuckoos
- Human Pigmentation: A Review of Molecular Mechanisms, Genetic Architecture, Evolution, Forensic DNA Phenotyping and Health Implications
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- The Molecular Pathogenesis of Trichilemmal Carcinoma
- Ichthyosis with confetti: clinics, molecular genetics and management
- SAT-210 When Acne, Hirsutism and Menstrual Irregularities Are More Than PCOS
- Diagnostic approach to low‐renin hypertension
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Muir-torre syndrome in two families in Leicestershire, United Kingdom
- Keratinocyte Cytokine Networks Associated with Human Melanocytic Nevus Development
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Intraovarian platelet-rich plasma administration could improve blastocyst euploidy rates in women undergoing in vitro fertilization
- Prostate cancer and androgenic alopecia
- Perspectives in dermatopathology: telomeres and telomerase in ageing and cancer; with emphasis on cutaneous disease
- Case Report: PTCH1 splice-site mutation and sonidegib treatment in Gorlin-Goltz syndrome: clinical insights from a family case study
- Tumor Mapping in 2 Large Multigenerational Families With CYLD Mutations
- Calcineurin/Nfatc1 signaling links skin stem cell quiescence to hormonal signaling during pregnancy and lactation
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- Cutaneous signals of immune system disease
- Adrenal Disorders and the Paediatric Brain: Pathophysiological Considerations and Clinical Implications
- Sperm aneuploidy in infertile male patients: a systematic review of the literature
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- The molecular pathogenesis of Trichilemmal carcinoma
- Exploring Hirsutism: Epidemiology, Associated Endocrinal Abnormalities, and Societal Challenges in GCC—A Narrative Review
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction