Interactions between actin filaments and between actin filaments and membranes in quick-frozen and deeply etched hair cells of the chick ear
about
Vezatin, a novel transmembrane protein, bridges myosin VIIA to the cadherin-catenins complexZO-3, a novel member of the MAGUK protein family found at the tight junction, interacts with ZO-1 and occludinSynaptopodin couples epithelial contractility to α-actinin-4-dependent junction maturationActin-interacting protein 1 controls assembly and permeability of intestinal epithelial apical junctionsLocalization and differential expression of two isoforms of the tight junction protein ZO-1Supervillin Is a Component of the Hair Cell's Cuticular Plate and the Head Plates of Organ of Corti Supporting CellsSupporting cells eliminate dying sensory hair cells to maintain epithelial integrity in the avian inner ear.Reinforcement of cell junctions correlates with the absence of hair cell regeneration in mammals and its occurrence in birds.In vivo and in vitro effects of two novel gamma-actin (ACTG1) mutations that cause DFNA20/26 hearing impairment.Actin filaments, stereocilia, and hair cells of the bird cochlea. II. Packing of actin filaments in the stereocilia and in the cuticular plate and what happens to the organization when the stereocilia are bent.Myosin-X functions in polarized epithelial cells.Filopodial initiation and a novel filament-organizing center, the focal ringThe spatial organization of apical junctional complex-associated proteins in feline and human corneal endothelium.A complex of ZO-1 and the BAR-domain protein TOCA-1 regulates actin assembly at the tight junction.Apically exposed, tight junction-associated beta1-integrins allow binding and YopE-mediated perturbation of epithelial barriers by wild-type Yersinia bacteria.Actin cores of hair-cell stereocilia support myosin motility.Mutations in the gamma-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26).Inner ear tissue preservation by rapid freezing: improving fixation by high-pressure freezing and hybrid methods.Architecture of tight junctions and principles of molecular composition.Structure, regulation, and pathophysiology of tight junctions in the gastrointestinal tractThe suprabasal layer of corneal epithelial cells represents the major barrier site to the passive movement of small molecules and trafficking leukocytes.Genetic insights into the morphogenesis of inner ear hair cells.Regulation of epithelial permeability by the actin cytoskeleton.F-actin binding protein, anillin, regulates integrity of intercellular junctions in human epithelial cells.Characterization of the 110-kdalton actin-calmodulin-, and membrane-binding protein from microvilli of intestinal epithelial cells.Mechanism of brush border contractility studied by the quick-freeze, deep-etch methodIn vivo co-distribution of fibronectin and actin fibers in granulation tissue: immunofluorescence and electron microscope studies of the fibronexus at the myofibroblast surface.Distribution of epinemin in colloidal gold-labelled, quick-frozen, deep-etched cytoskeletons.Effects of cytochalasin D on occluding junctions of intestinal absorptive cells: further evidence that the cytoskeleton may influence paracellular permeability and junctional charge selectivity.Cytoskeletal reorganization of human platelets after stimulation revealed by the quick-freeze deep-etch technique.Structures linking microfilament bundles to the membrane at focal contacts.Nonredundant roles of cytoplasmic β- and γ-actin isoforms in regulation of epithelial apical junctionsCa2+-ATPase of the sarcoplasmic reticulum shares a common domain with a membrane glycoprotein associated with the cytoskeleton of microvilli.Unconventional myosins in inner-ear sensory epitheliaIdentification of a tight junction-associated guanine nucleotide exchange factor that activates Rho and regulates paracellular permeabilityObservations on how actin filaments become organized in cellsA membrane cytoskeleton from Dictyostelium discoideum. III. Plasma membrane fragments bind predominantly to the sides of actin filaments.High-purity isolation of bullfrog hair bundles and subcellular and topological localization of constituent proteinsThree different actin filament assemblies occur in every hair cell: each contains a specific actin crosslinking protein.Binding of actin to liver cell membranes: the state of membrane-bound actin.
P2860
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P2860
Interactions between actin filaments and between actin filaments and membranes in quick-frozen and deeply etched hair cells of the chick ear
description
1982 nî lūn-bûn
@nan
1982 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1982 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1982年の論文
@ja
1982年論文
@yue
1982年論文
@zh-hant
1982年論文
@zh-hk
1982年論文
@zh-mo
1982年論文
@zh-tw
1982年论文
@wuu
name
Interactions between actin fil ...... ed hair cells of the chick ear
@ast
Interactions between actin fil ...... ed hair cells of the chick ear
@en
type
label
Interactions between actin fil ...... ed hair cells of the chick ear
@ast
Interactions between actin fil ...... ed hair cells of the chick ear
@en
prefLabel
Interactions between actin fil ...... ed hair cells of the chick ear
@ast
Interactions between actin fil ...... ed hair cells of the chick ear
@en
P2860
P356
P1476
Interactions between actin fil ...... ed hair cells of the chick ear
@en
P2093
L G Tilney
N Hirokawa
P2860
P304
P356
10.1083/JCB.95.1.249
P407
P577
1982-10-01T00:00:00Z