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Research 27
- Calcium blockers protect against sensory epithelial damage and hearing loss in Cx26-cKO mice
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Epidermal Stem Cells do not Communicate Through Gap Junctions
- Connexin 26 (<i>GJB2</i>) mutations in keratitis–ichthyosis–deafness syndrome presenting with squamous cell carcinoma
- Connexin mutations in human disease
- 478 Mutation-specific siRNA Knockdown of GJB2 − Potential gene therapy for Keratitis-ichthyosis-deafness Syndrome
- Mutant Cx43 in Skin Differentiation and Disease
- Clinical Snippets
- Oral Presentations
- 475 Paraoxonase 1 (PON1) L55M and Q192R polymorphisms, lipid profiles and psoriasis
- 476 Development of an intrinsic skin sensor for blood glucose level with CRISPR-mediated genome editing in epidermal stem cells
- Clinical Snippets
- Defining stem cell dynamics and migration during wound healing in mouse skin epidermis
- Pannexin 3 regulates skin development via Epiprofin
- Sebaceous carcinoma arising at a chronic candidiasis skin lesion of a patient with keratitis-ichthyosis-deafness (KID) syndrome
- 9. Immunology and Genetics
- Porokeratotic eccrine ostial and dermal duct nevus and porokeratotic eccrine and hair follicle nevus: Is nomenclature “porokeratotic adnexal ostial nevus” more appropriate?
- Case Report of Wound Treatment with Hyiodine Gel in an Occasional KID Syndrome Patient
- Porokeratotic adnexal ostial nevus: a paradigm of cutaneous mosaicism
- An Integrated Transcriptome Atlas of Embryonic Hair Follicle Progenitors, Their Niche, and the Developing Skin
- Defining the Cellular Environment in the Organ of Corti following Extensive Hair Cell Loss: A Basis for Future Sensory Cell Replacement in the Cochlea
- Genetically modified laboratory mice with sebaceous glands abnormalities
- New developments in the molecular treatment of ichthyosis: review of the literature
- The Role of Nrf2 in Hearing Loss
- Desmosomes in Developing Human Epidermis
- Developmentally regulated expression of integrin alpha-6 distinguishes neural crest derivatives in the skin
- Current Genetics in Hair Diseases