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Research 151–180 of 211
- Current Genetics in Hair Diseases
- Dynamic remodeling of skin microbiota during healthy homeostatic and wound repair conditions
- Peptide-Based Approaches for Pain Relief and Healing in Wounds
- Research Progress on the Molecular Mechanism of Poultry Feather Follicle Development
- Supraphysiological Dose of Testosterone Impairs the Expression and Distribution of Sex Steroid Receptors during Endometrial Receptivity Development in Female Sprague–Dawley Rats
- Phase-specific differential regulation of mechanical allodynia in a murine model of neuropathic pain by progesterone
- Evolution and mechanistic insights of platelet-derived products in temporomandibular joint regeneration
- Painful thickened skin on the soles of the feet
- Leveraging nature’s nanocarriers: Translating insights from extracellular vesicles to biomimetic synthetic vesicles for biomedical applications
- Two- and Three-Dimensional Culture of Keratinocyte Stem and Precursor Cells Derived from Primary Murine Epidermal Cultures
- Cellular response of keratinocytes to the entry and accumulation of nanoplastic particles
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- Understanding sex and gender disparities in COVID-19 mortality: a narrative review beyond biology
- A State-of-the-Art Overview on (Epi)Genomics and Personalized Skin Rejuvenating Strategies
- 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 43 expression in the testes during postnatal development of finasteride-treated male rat offspring
- 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
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- Gap junctions in Turing-type periodic feather pattern formation
- Clouston’s syndrome: a rare case report
- 918 Skin morphogenesis by coupling biochemical-bioelectric signals: Calcium oscillations coordinate dermal cell movement by epidermis-derived SHH signaling during feather bud orientation
- 478 Mutation-specific siRNA Knockdown of GJB2 − Potential gene therapy for Keratitis-ichthyosis-deafness Syndrome
- 882 Syndactyly type III and hypotrichosis in oculodentodigital syndrome with GJA1 mutation
- Clinical Snippets