scholarly article | Q13442814 |
P50 | author | Alpha Yap | Q37377160 |
Annette M Shewan | Q58828273 | ||
P2093 | author name string | Madhavi P Maddugoda | |
Matthew S Crampton | |||
P2860 | cites work | The localization of myosin VI at the golgi complex and leading edge of fibroblasts and its phosphorylation and recruitment into membrane ruffles of A431 cells after growth factor stimulation | Q22008538 |
Myosin VI is an actin-based motor that moves backwards | Q22010643 | ||
Myosin VI isoform localized to clathrin-coated vesicles with a role in clathrin-mediated endocytosis | Q24291429 | ||
Myo6 facilitates the translocation of endocytic vesicles from cell peripheries | Q24307920 | ||
F-actin binding site masked by the intramolecular association of vinculin head and tail domains | Q24309102 | ||
alpha-Catenin-vinculin interaction functions to organize the apical junctional complex in epithelial cells | Q24322872 | ||
Vezatin, a novel transmembrane protein, bridges myosin VIIA to the cadherin-catenins complex | Q24597349 | ||
Deconstructing the cadherin-catenin-actin complex | Q24609677 | ||
Myosin VI: two distinct roles in endocytosis | Q28191412 | ||
The role of the cell adhesion molecule uvomorulin in the formation and maintenance of the epithelial junctional complex | Q28289033 | ||
Cortactin is necessary for E-cadherin-mediated contact formation and actin reorganization | Q30443460 | ||
Myosin 2 is a key Rho kinase target necessary for the local concentration of E-cadherin at cell-cell contacts | Q30476214 | ||
Ena/VASP proteins can regulate distinct modes of actin organization at cadherin-adhesive contacts | Q30476860 | ||
Differential roles for actin polymerization and a myosin II motor in assembly of the epithelial apical junctional complex | Q33841357 | ||
Cadherin-directed actin assembly: E-cadherin physically associates with the Arp2/3 complex to direct actin assembly in nascent adhesive contacts | Q34117282 | ||
The ins and outs of E-cadherin trafficking | Q34340762 | ||
folded gastrulation, cell shape change and the control of myosin localization. | Q34445867 | ||
Myosin VI stabilizes an actin network during Drosophila spermatid individualization | Q34662188 | ||
Myosin VI, an actin motor for membrane traffic and cell migration | Q35009595 | ||
Interaction of alpha-actinin and vinculin with actin: opposite effects on filament network formation | Q35362231 | ||
Vinculin is part of the cadherin-catenin junctional complex: complex formation between alpha-catenin and vinculin | Q36255361 | ||
Mechanisms of epithelial cell-cell adhesion and cell compaction revealed by high-resolution tracking of E-cadherin-green fluorescent protein | Q36255689 | ||
Vinculin, an intracellular protein localized at specialized sites where microfilament bundles terminate at cell membranes | Q36398107 | ||
Regulation of cell-cell junctions by the cytoskeleton. | Q36564376 | ||
Characterization of two F-actin-binding and oligomerization sites in the cell-contact protein vinculin | Q38343794 | ||
Myosin VI plays a role in cell-cell adhesion during epithelial morphogenesis | Q38449026 | ||
Loss of myosin VI reduces secretion and the size of the Golgi in fibroblasts from Snell's waltzer mice | Q39698975 | ||
Myosin VI is required for sorting of AP-1B-dependent cargo to the basolateral domain in polarized MDCK cells | Q39735805 | ||
Rac-WAVE-mediated actin reorganization is required for organization and maintenance of cell-cell adhesion. | Q40197369 | ||
Dynamic microtubules regulate the local concentration of E-cadherin at cell-cell contacts | Q40293778 | ||
Characterization of an F-actin-binding domain in the cytoskeletal protein vinculin | Q42770908 | ||
Three-dimensional structure of vinculin bound to actin filaments | Q44718700 | ||
The mechanism of myosin VI translocation and its load-induced anchoring | Q44790017 | ||
Myosin VI altered at threonine 406 stabilizes actin filaments in vivo | Q46044406 | ||
Myosin VI is required for E-cadherin-mediated border cell migration | Q47070917 | ||
Arp2/3 activity is necessary for efficient formation of E-cadherin adhesive contacts | Q47438183 | ||
Minimal mutation of the cytoplasmic tail inhibits the ability of E-cadherin to activate Rac but not phosphatidylinositol 3-kinase: direct evidence of a role for cadherin-activated Rac signaling in adhesion and contact formation | Q47996855 | ||
Two-headed binding of a processive myosin to F-actin. | Q52863984 | ||
Actin activates a cryptic dimerization potential of the vinculin tail domain | Q73316721 | ||
A role for myosin VII in dynamic cell adhesion | Q73670214 | ||
Actin cable dynamics and Rho/Rock orchestrate a polarized cytoskeletal architecture in the early steps of assembling a stratified epithelium | Q78319031 | ||
P4510 | describes a project that uses | ImageJ | Q1659584 |
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | morphogenesis | Q815547 |
P1104 | number of pages | 12 | |
P304 | page(s) | 529-540 | |
P577 | publication date | 2007-07-01 | |
P1433 | published in | Journal of Cell Biology | Q1524550 |
P1476 | title | Myosin VI and vinculin cooperate during the morphogenesis of cadherin cell cell contacts in mammalian epithelial cells | |
P478 | volume | 178 |
Q33373673 | A Myo6 mutation destroys coordination between the myosin heads, revealing new functions of myosin VI in the stereocilia of mammalian inner ear hair cells |
Q36433801 | A WAVE2-Arp2/3 actin nucleator apparatus supports junctional tension at the epithelial zonula adherens. |
Q53148839 | A bigger picture: classical cadherins and the dynamic actin cytoskeleton. |
Q37159012 | A mechanobiological perspective on cadherins and the actin-myosin cytoskeleton |
Q42085205 | A negative modulatory role for rho and rho-associated kinase signaling in delamination of neural crest cells |
Q38991878 | Actin dynamics modulate mechanosensitive immobilization of E-cadherin at adherens junctions |
Q88547133 | Adherens junctions influence tight junction formation via changes in membrane lipid composition |
Q35642916 | An association between type Iγ PI4P 5-kinase and Exo70 directs E-cadherin clustering and epithelial polarization |
Q35195321 | Apical protein transport and lumen morphogenesis in polarized epithelial cells |
Q33675805 | Bacillus cereus Certhrax ADP-ribosylates vinculin to disrupt focal adhesion complexes and cell adhesion |
Q36588911 | Balancing forces: architectural control of mechanotransduction |
Q37333596 | Cadherins and cancer: how does cadherin dysfunction promote tumor progression? |
Q40641225 | Calcium binding protects E-cadherin from cleavage by Helicobacter pylori HtrA. |
Q30499464 | Cardiac myocyte remodeling mediated by N-cadherin-dependent mechanosensing. |
Q30438289 | Cell adhesion receptors in mechanotransduction |
Q37035184 | Coiled-coil-mediated dimerization is not required for myosin VI to stabilize actin during spermatid individualization in Drosophila melanogaster |
Q37781561 | Conserved F-actin dynamics and force transmission at cell adhesions |
Q37135682 | Diverse functions of myosin VI elucidated by an isoform-specific α-helix domain |
Q38211486 | Dynamic contacts: rearranging adherens junctions to drive epithelial remodelling. |
Q38449977 | E-cadherin junctions as active mechanical integrators in tissue dynamics |
Q36423364 | EPLIN mediates linkage of the cadherin catenin complex to F-actin and stabilizes the circumferential actin belt |
Q47749975 | Epithelial Monolayers Coalesce on a Viscoelastic Substrate through Redistribution of Vinculin |
Q38206254 | Force measurement tools to explore cadherin mechanotransduction |
Q36665969 | Genetic characterization of the Drosophila jaguar322 mutant reveals that complete myosin VI loss of function is not lethal |
Q37857739 | Intercellular and extracellular mechanotransduction in cardiac myocytes |
Q34147630 | Intercellular mechanotransduction during multicellular morphodynamics |
Q35747240 | Involvement of unconventional myosin VI in myoblast function and myotube formation. |
Q27330739 | Multicomponent analysis of junctional movements regulated by myosin II isoforms at the epithelial zonula adherens |
Q30009836 | Myosin 1e is a component of the glomerular slit diaphragm complex that regulates actin reorganization during cell-cell contact formation in podocytes |
Q34067428 | Myosin II activity dependent and independent vinculin recruitment to the sites of E-cadherin-mediated cell-cell adhesion |
Q36191191 | Myosin II isoforms identify distinct functional modules that support integrity of the epithelial zonula adherens |
Q34575273 | Myosin VI and optineurin are required for polarized EGFR delivery and directed migration |
Q33957293 | Myosin VI contributes to synaptic transmission and development at the Drosophila neuromuscular junction. |
Q34094507 | Myosin VI is differentially regulated by DNA damage in p53- and cell type-dependent manners |
Q50502817 | Myosin VI regulates actin dynamics and melanosome biogenesis. |
Q27329752 | Myosin VI regulates actin structure specialization through conserved cargo-binding domain sites |
Q38088529 | Myosin motors at neuronal synapses: drivers of membrane transport and actin dynamics. |
Q30416190 | Myosin-1c regulates the dynamic stability of E-cadherin-based cell-cell contacts in polarized Madin-Darby canine kidney cells. |
Q30513859 | Myosin-X functions in polarized epithelial cells |
Q26749344 | Myosins as fundamental components during tumorigenesis: diverse and indispensable |
Q27004163 | Myosins in cell junctions |
Q37768293 | Neighborly relations: cadherins and mechanotransduction. |
Q35591684 | New insights into vinculin function and regulation |
Q83230501 | Non-canonical Wnt signaling regulates junctional mechanocoupling during angiogenic collective cell migration |
Q34207052 | Non-muscle myosins in tumor progression, cancer cell invasion, and metastasis |
Q52321911 | Nonmuscle myosin IIA is involved in recruitment of apical junction components through activation of α-catenin. |
Q27015094 | Normal morphogenesis of epithelial tissues and progression of epithelial tumors |
Q39783600 | Overexpression of myosin VI in prostate cancer cells enhances PSA and VEGF secretion, but has no effect on endocytosis |
Q38160892 | Patterns in space: coordinating adhesion and actomyosin contractility at E-cadherin junctions. |
Q50436014 | Phospholipase Cδ3 is a novel binding partner of myosin VI and functions as anchoring of myosin VI on plasma membrane |
Q37597342 | Potential roles of myosin VI in cell motility |
Q37671129 | Rap1, a mercenary among the Ras-like GTPases |
Q39665584 | Role for Traf4 in polarizing adherens junctions as a prerequisite for efficient cell shape changes |
Q38747970 | Role of vinculin in cellular mechanotransduction |
Q34036844 | SAX-7/L1CAM and HMR-1/cadherin function redundantly in blastomere compaction and non-muscle myosin accumulation during Caenorhabditis elegans gastrulation |
Q50539828 | Secreted autotransporter toxin (Sat) triggers autophagy in epithelial cells that relies on cell detachment. |
Q37780682 | Spatial organization of adhesion: force-dependent regulation and function in tissue morphogenesis |
Q35534690 | Spectrin-adducin membrane skeleton: A missing link between epithelial junctions and the actin cytoskeletion? |
Q33647855 | Strength dependence of cadherin-mediated adhesions |
Q37406209 | Tension-sensitive actin assembly supports contractility at the epithelial zonula adherens |
Q27678448 | The Cytoskeletal Protein -Catenin Unfurls upon Binding to Vinculin |
Q37267715 | The Drosophila afadin homologue Canoe regulates linkage of the actin cytoskeleton to adherens junctions during apical constriction. |
Q97520547 | The Expressions and Mechanisms of Sarcomeric Proteins in Cancers |
Q38155160 | The cortical acto-Myosin network: from diffusion barrier to functional gateway in the transport of neurosecretory vesicles to the plasma membrane |
Q36965073 | The juxtamembrane domain of the E-cadherin cytoplasmic tail contributes to its interaction with Myosin VI. |
Q30493646 | The motor protein myosin-X transports VE-cadherin along filopodia to allow the formation of early endothelial cell-cell contacts. |
Q36567245 | Tissue organization by cadherin adhesion molecules: dynamic molecular and cellular mechanisms of morphogenetic regulation |
Q92156441 | Unconventional Myosins: How Regulation Meets Function |
Q36929781 | Unconventional myosins acting unconventionally. |
Q38946365 | VERO cells harbor a poly-ADP-ribose belt partnering their epithelial adhesion belt. |
Q35099507 | Vinculin activators target integrins from within the cell to increase melanoma sensitivity to chemotherapy. |
Q27009352 | Vinculin and metavinculin: oligomerization and interactions with F-actin |
Q35839771 | Vinculin associates with endothelial VE-cadherin junctions to control force-dependent remodeling |
Q30577227 | Vinculin phosphorylation differentially regulates mechanotransduction at cell-cell and cell-matrix adhesions |
Q33950292 | Vinculin potentiates E-cadherin mechanosensing and is recruited to actin-anchored sites within adherens junctions in a myosin II-dependent manner. |
Q24296424 | Vinculin regulates cell-surface E-cadherin expression by binding to beta-catenin |
Q37775233 | Vinculin, an adapter protein in control of cell adhesion signalling |
Q38070294 | Vinculin, cadherin mechanotransduction and homeostasis of cell-cell junctions |
Q36425571 | Vinculin-dependent Cadherin mechanosensing regulates efficient epithelial barrier formation. |
Q36620828 | α-Catenin and vinculin cooperate to promote high E-cadherin-based adhesion strength |
Q35801858 | α-Catenin uses a novel mechanism to activate vinculin |
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