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Research 61–90 of 590
- Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA
- Epidemiological study of prostate cancer (EPICAP): a population-based case–control study in France
- GENOTYPE ? PHENOTYPE CORRELATIONS IN CUTANEOUS MELANOMA PATIENTS CARRIER OF THE MITF p.E318K PATHOGENIC VARIANT
- Transcriptomic crossroads: Decoding genes and pathways that connect alopecia areata with chronic inflammatory skin disorders
- Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing
- Fibrodysplasia Ossificans Progressiva (FOP): A Segmental Progeroid Syndrome
- 2022 Update on Prostate Cancer Epidemiology and Risk Factors—A Systematic Review
- Uncovering novel biomarkers and drug targets for androgenetic alopecia via metabolite regulation and multi-tissue validation
- Birt–Hogg–Dubé syndrome
- Prostate Cancer Early Detection, Version 2.2015
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Hair & Cutaneous Development
- Comedonal and Cystic Fibrofolliculomas in Birt-Hogg-Dube Syndrome
- Research Techniques Made Simple: Zebrafish Models for Human Dermatologic Disease
- Regulatory T cell dysfunction and immunotherapeutic breakthroughs in type 1 diabetes
- Comprehensive Genomic Profiling of Cutaneous Adnexal Carcinomas: A Genomic Landscape Study
- A Short Report on Melanocyte/Melanoma Culture, Senescence, and Reproducibility
- Unmet Medical Needs in Chronic, Non-communicable Inflammatory Skin Diseases
- Disruption of tubular Flcn expression as a mouse model for renal tumor induction
- Engineering molecular imaging strategies for regenerative medicine
- Merkel cell carcinoma: updates in tumor biology, emerging therapies, and preclinical models
- Evolution of long scalp hair in humans
- Trailing the Path to Preventive Oncology
- Coronavirus 2019 Infectious Disease Epidemic: Where We Are, What Can Be Done and Hope For
- Stem Cell Use to Treat Dermatological Disorders
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Short-term Efficacy of Tofacitinib, a JAK Inhibitor, in IFIH1-related Aicardi-Goutières Syndrome