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Research 30 of 566
- A desmosomal cadherin controls multipotent hair follicle stem cell quiescence and orchestrates regeneration through adhesion signaling
- 1422 Uncoupling desmosomal cadherin adhesion activates quiescent hair follicle stem cells and orchestrates self-organized regeneration through outside-in signaling
- 876 Imaging nanoscale changes in desmosome protein organization
- Congenital hair loss disorders: Rare, but not too rare
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Intercellular junctions in normal epidermis
- Biology and Genetics of Hair
- A function for Rac1 in the terminal differentiation and pigmentation of hair
- Transcriptome Profiling of Pilosebaceous Units in Male Androgenetic Alopecia Reveals Altered Junctional Networks
- Patterns of desmocollin synthesis in human epithelia: immunolocalization of desmocollins 1 and 3 in special epithelia and in cultured cells.
- 320 Desmoglein 3-mediated mechanical transadhesion controls epithelial stem cell quiescence
- Pseudo Pemphigus Phenotypes in Mice with Inactivated Desmoglein 3
- 875 A novel animal model of Desmoglein 1 (Dsg1) deficiency reveals an essential role for Dsg1 in epidermal barrier formation
- Inherited Disorders of the Hair
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children
- 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
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Molecular Genetics of Alopecias
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Desmosomes in Developing Human Epidermis
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Genetics of Structural Hair Disorders
- Role of vitamin D and calcium signaling in epidermal wound healing
- DHT deficiency perturbs the integrity of the rat seminiferous epithelium by disrupting tight and adherens junctions
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis