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Research 91–120 of 1000+
- Tissue engineering strategies combining molecular targets against inflammation and fibrosis, and umbilical cord blood stem cells to improve hampered muscle and skin regeneration following cleft repair
- Tp63-expressing adult epithelial stem cells cross lineages boundaries revealing latent hairy skin competence
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- [Association of a pediatric bullous eruption, cutaneous and muscular atrophy, hyperpigmentation and dysmorphism. A new entity?].
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- TONGUE, RED
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- Extra-Intestinal Manifestation of Celiac Disease in Children
- Odontogenic Keratocysts Arise from Quiescent Epithelial Rests and Are Associated with Deregulated Hedgehog Signaling in Mice and Humans
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Congenital insensitivity to pain with anhidrosis and progressing acro-osteolysis: a case report with 7-year follow-up
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Drug-associated gingival disorders: a retrospective pharmacovigilance assessment using disproportionality analysis
- P326: Cardiovascular features in adult individuals affected with Tatton-Brown-Rahman syndrome
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- <i>egfl6</i> expression in the pharyngeal pouch is dispensable for craniofacial development
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Stabilization of epithelial β-catenin compromises mammary cell fate acquisition and branching morphogenesis
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- The Parathyroid Hormone Second Receptor PTH2R and its Ligand Tuberoinfundibular Peptide of 39 Residues TIP39 Regulate Intracellular Calcium and Influence Keratinocyte Differentiation
- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice
- Commitment of Oral-Derived Stem Cells in Dental and Maxillofacial Applications
- KGF and EGF signalling block hair follicle induction and promote interfollicular epidermal fate in developing mouse skin
- Genetic Hair Disorders: A Review
- The Autoimmune Regulator (AIRE), Which Is Defective in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Patients, Is Expressed in Human Epidermal and Follicular Keratinocytes and Associates With the Intermediate Filament Protein Cytokeratin 17
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma