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Research 31–60 of 747
- Epidermolysis bullosa in animals: a review
- Dermatopathology and molecular genetics
- Skin structure
- Identification of somatic and germline mosaicism for a keratin 5 mutation in epidermolysis bullosa simplex in a family of which the proband was previously regarded as a sporadic case
- Unraveling the ECM-Immune Cell Crosstalk in Skin Diseases
- Wnt/β-Catenin Signaling Stabilizes Hemidesmosomes in Keratinocytes
- The importance and use of stem cells in dermatology
- Clinical Snippets
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Review of the Latest Methods of Epidermolysis Bullosa and Other Chronic Wounds Treatment Including BIOOPA Dressing
- Inherited Epidermolysis Bullosa: A Clinical Case
- A homozygous nonsense mutation identified in <i>COL7A1</i> in a family with autosomal recessive dystrophic epidermolysis bullosa
- P‐35 Nonlethal junctional epidermolysis bullosa in a dog
- Dominant dystrophic epidermolysis bullosa: Seven familial cases
- Skin Development and Disease: A Molecular Perspective
- 572 Defining chronic wound types in recessive dystrophic epidermolysis bullosa patients for clinical outcome assessment
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- Characterization of the epidermal-dermal junction in hiPSC-derived skin organoids
- Advances in a rapidly emerging field of hair follicle stem cell research.
- 1435 Dynamic morphogen-p63 chromatin interactions that guide epigenetic changes and p63 activity in surface ectoderm commitment
- Life before and beyond blistering: The role of collagen XVII in epidermal physiology
- Hair Loss in Autoimmune Cutaneous Bullous Disorders
- First symposium on natural gene therapy of the skin
- 474 Stabilizing mutations of KLHL24 ubiquitin ligase cause loss of keratin 14 and human skin fragility
- Research Snippets
- A Neonate with Blisters
- TERMIS ‐ AMERICAS Toronto, Ontario, Canada July 10–13, 2022
- From molecular biology to therapeutics