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Research 181–210 of 229
- A State-of-the-Art Overview on (Epi)Genomics and Personalized Skin Rejuvenating Strategies
- Harnessing mesenchymal aggregation for engineered organ‐level regeneration: Recent progress and perspective
- Transcriptome Profiling of Pilosebaceous Units in Male Androgenetic Alopecia Reveals Altered Junctional Networks
- Multifunctional Self-Assembled Peptide Hydrogels for Biomedical Applications
- JMJD3 and NF-κB-dependent activation of Notch1 gene is required for keratinocyte migration during skin wound healing
- A Scarless Healing Tale: Comparing Homeostasis and Wound Healing of Oral Mucosa With Skin and Oesophagus
- Dedicator of Cytokinesis 5 Regulates Keratinocyte Function and Promotes Diabetic Wound Healing
- Innovative Functional Biomaterials as Therapeutic Wound Dressings for Chronic Diabetic Foot Ulcers
- Reductive Stress Selectively Disrupts Collagen Homeostasis and Modifies Growth Factor-independent Signaling Through the MAPK/Akt Pathway in Human Dermal Fibroblasts
- Role of regeneration in tissue repairing and therapies
- The Role of Natural Hydrogels in Enhancing Wound Healing: From Biomaterials to Bioactive Therapies
- Fascia Layer—A Novel Target for the Application of Biomaterials in Skin Wound Healing
- Current Insight of Peptide-Based Hydrogels for Chronic Wound Healing Applications: A Concise Review
- Electroosmotic pore transport in human skin.
- Genetic targeting of lymphatic endothelial cells in mice: current strategies and future perspectives
- A novel mutation in the connexin 26 gene (<i>GJB2</i>) in a child with clinical and histological features of keratitis–ichthyosis–deafness (KID) syndrome
- Connexin 30, a new marker of hyperproliferative epidermis
- Connexin 26 (<i>GJB2</i>) mutations in keratitis–ichthyosis–deafness syndrome presenting with squamous cell carcinoma
- Connexin mutations in human disease
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient
- Severe form of keratitis–ichthyosis–deafness (KID) syndrome associated with septic complications
- Gap junctions in Turing-type periodic feather pattern formation
- Clinical Snippets
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- Gap junctions in Turing-type periodic feather pattern formation
- 478 Mutation-specific siRNA Knockdown of GJB2 − Potential gene therapy for Keratitis-ichthyosis-deafness Syndrome
- Clinical Snippets
- Porokeratotic eccrine ostial and dermal duct nevus and porokeratotic eccrine and hair follicle nevus: Is nomenclature “porokeratotic adnexal ostial nevus” more appropriate?
- Clinical Snippets