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Research 30 of 542
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Immunolocalization of junctional proteins in human hairs indicates that the membrane complex stabilizes the inner root sheath while desmosomes contact the companion layer through specific keratins
- Desmosomes in Developing Human Epidermis
- A desmosomal cadherin controls multipotent hair follicle stem cell quiescence and orchestrates regeneration through adhesion signaling
- LB1076 Using the frog embryonic epidermis as a model to study desmosome function during development
- USING THE FROG EPIDERMIS TO UNCOVER DESMOSOME FUNCTION AND REGULATION IN THE DEVELOPING EMBRYO
- 876 Imaging nanoscale changes in desmosome protein organization
- 441 RPGRIP1L facilitates desmosomal adhesion through suppressing PKCβII-mediated desmoglein endocytosis: Implication in pemphigus
- 1422 Uncoupling desmosomal cadherin adhesion activates quiescent hair follicle stem cells and orchestrates self-organized regeneration through outside-in signaling
- Patterns of desmocollin synthesis in human epithelia: immunolocalization of desmocollins 1 and 3 in special epithelia and in cultured cells.
- Increased expression of keratin 16 causes anomalies in cytoarchitecture and keratinization in transgenic mouse skin.
- Biology and Genetics of Hair
- Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children
- Ultrastructural Resemblance of Basal Cell Epithelioma to Primary Epithelial Germ
- Congenital hair loss disorders: Rare, but not too rare
- Against the Rules: Human Keratin K80
- Ichthyosis follicularis with alopecia and photophobia in a mother and daughter
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Growth of human hair follicle keratinocytes in vitro
- A case of monilethrix caused by novel compound heterozygous mutations in the desmoglein 4 (DSG4) gene
- Regulation of Hair Shedding by the Type 3 IP3 Receptor
- Structural and biochemical changes underlying a keratoderma-like phenotype in mice lacking suprabasal AP1 transcription factor function
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Bikunin, a Serine Protease Inhibitor, is Present on the Cell Boundary of Epidermis
- Hair Loss in Autoimmune Cutaneous Bullous Disorders
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Molecular Genetics of Alopecias
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- Hereditary mucoepithelial dysplasia: unique histopathological findings in skin lesions