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Research 61–90 of 564
- The relationship between keratin 18 and epithelial-derived tumors: as a diagnostic marker, prognostic marker, and its role in tumorigenesis
- DataSheet1_Single-Cell Transcriptomics Reveals the Molecular Anatomy of Sheep Hair Follicle Heterogeneity and Wool Curvature.zip
- 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
- 441 RPGRIP1L facilitates desmosomal adhesion through suppressing PKCβII-mediated desmoglein endocytosis: Implication in pemphigus
- 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
- 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.
- Biology and Genetics of Hair
- Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Against the Rules: Human Keratin K80
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Regulation of Hair Shedding by the Type 3 IP3 Receptor
- Genetics of Structural Hair Disorders
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Hair Loss in Autoimmune Cutaneous Bullous Disorders
- A function for Rac1 in the terminal differentiation and pigmentation of hair
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Recent advances in congenital ichthyoses
- Molecular Genetics of Alopecias
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- Pili Trianguli et Canaliculi Is a Defect of Inner Root Sheath Keratinization
- Reduced plakoglobin increases the risk of sodium current defects and atrial conduction abnormalities in response to androgenic anabolic steroid abuse
- Dysfunction of keratinocyte adhesion
- Intercellular junctions in normal epidermis
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Inherited Disorders of the Hair