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Research 30 of 45
- CPC14 Blaschko-linear trichoepitheliomas: unveiling type 1 segmental mosaicism
- The Genetics of Human Skin Disease
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities
- Long-Term Survival of Type XVII Collagen Revertant Cells in an Animal Model of Revertant Cell Therapy
- Acne Syndromes and Mosaicism
- Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Nuclear Topology, Epigenetics, and Keratinocyte Differentiation
- Molecular pathology of skin adnexal tumours
- An updated review of the sebaceous gland and its role in health and diseases Part 2: Pathophysiological clinical disorders of sebaceous glands
- Acquired trichomegaly of the eyelashes and hypertrichosis induced by bimatoprost
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter
- Loss of the Y Chromosome: A Review of Molecular Mechanisms, Age Inference, and Implications for Men’s Health
- Understanding autoimmunity of vitiligo and alopecia areata
- Poster Presentations
- Vitiligo and Its Mimics in Childhood: A Diagnostic Framework for Hypopigmented Disorders
- Sperm aneuploidy in infertile male patients: a systematic review of the literature
- Highlights from the Field of Pediatric Dermatology Research from the 2023 PeDRA Annual Conference
- Postzygotic Mutations in Beta-Actin Are Associated with Becker’s Nevus and Becker’s Nevus Syndrome
- Postzygotic KRAS G12C mutation, associated with various malignancies, is also underling epidermal nevus syndrome
- Double-Lined Frontoparietal Scleroderma en coup de sabre
- Becker's Nevus Syndrome
- The Molecular Basis of Androgen Insensitivity
- PA15 Becker naevus syndrome associated with a mosaic pathogenic variant in <i>ACTB</i>
- Morpho-Regulation of Ectodermal Organs
- 312 CRISPR/Cas9-based targeted genome editing for correction of recessive dystrophic epidermolysis bullosa using iPS cells
- A Case of Basal Cell Carcinoma Arising in Congenital Triangular Alopecia
- 314 Molecular genetic dissection of ILVEN leads to successful targeted therapy