Arp2/3 activity is necessary for efficient formation of E-cadherin adhesive contacts.
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Get to grips: steering local actin dynamics with IQGAPsWAVE2 regulates epithelial morphology and cadherin isoform switching through regulation of Twist and AblbFGF regulates PI3-kinase-Rac1-JNK pathway and promotes fibroblast migration in wound healingNeogenin recruitment of the WAVE regulatory complex maintains adherens junction stability and tension.Integrated biochemical and mechanical signals regulate multifaceted human embryonic stem cell functions.Myosin 2 is a key Rho kinase target necessary for the local concentration of E-cadherin at cell-cell contactsArp2/3 complex-deficient mouse fibroblasts are viable and have normal leading-edge actin structure and functionEna/VASP proteins can regulate distinct modes of actin organization at cadherin-adhesive contacts.N- and E-cadherins in Xenopus are specifically required in the neural and non-neural ectoderm, respectively, for F-actin assembly and morphogenetic movements.Zyxin-mediated actin assembly is required for efficient wound closure.Adherens junctions determine the apical position of the midbody during follicular epithelial cell division.A common clathrin-mediated machinery co-ordinates cell-cell adhesion and bacterial internalizationFormin-mediated actin polymerization at cell-cell junctions stabilizes E-cadherin and maintains monolayer integrity during wound repair.Differential roles for actin polymerization and a myosin II motor in assembly of the epithelial apical junctional complex.IQGAP1 stimulates actin assembly through the N-WASP-Arp2/3 pathway.The Arp2/3 complex has essential roles in vesicle trafficking and transcytosis in the mammalian small intestineE-cadherin adhesion activates c-Src signaling at cell-cell contacts.Myosin VI and vinculin cooperate during the morphogenesis of cadherin cell cell contacts in mammalian epithelial cells.Crossroads of integrins and cadherins in epithelia and stroma remodeling.Myosin II isoforms identify distinct functional modules that support integrity of the epithelial zonula adherens.A WAVE2-Arp2/3 actin nucleator apparatus supports junctional tension at the epithelial zonula adherens.Molecular components of the adherens junction.Relaxing the actin cytoskeleton for adhesion and movement with Ena/VASP.Tissue organization by cadherin adhesion molecules: dynamic molecular and cellular mechanisms of morphogenetic regulationNeural Wiskott-Aldrich syndrome protein (N-WASP)-mediated p120-catenin interaction with Arp2-Actin complex stabilizes endothelial adherens junctions.Mycolactone activation of Wiskott-Aldrich syndrome proteins underpins Buruli ulcer formation.N-cadherin as a therapeutic target in cancer.Making and breaking contacts: the cellular biology of cadherin regulationTropomodulin 1 Regulation of Actin Is Required for the Formation of Large Paddle Protrusions Between Mature Lens Fiber Cells.Actin-related protein2/3 complex regulates tight junctions and terminal differentiation to promote epidermal barrier formation.Cortactin is a functional target of E-cadherin-activated Src family kinases in MCF7 epithelial monolayersFSGS3/CD2AP is a barbed-end capping protein that stabilizes actin and strengthens adherens junctions.Tension-sensitive actin assembly supports contractility at the epithelial zonula adherens.DAAM1 stabilizes epithelial junctions by restraining WAVE complex-dependent lateral membrane motility.Profilin-1 overexpression restores adherens junctions in MDA-MB-231 breast cancer cells in R-cadherin-dependent manner.Centralspindlin and α-catenin regulate Rho signalling at the epithelial zonula adherens.Molecular bases of cell-cell junctions stability and dynamics.Vinculin, cadherin mechanotransduction and homeostasis of cell-cell junctions.Patterns in space: coordinating adhesion and actomyosin contractility at E-cadherin junctions.Correlation between liver metastasis of the colocalization of actin-related protein 2 and 3 complex and WAVE2 in colorectal carcinoma.
P2860
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P2860
Arp2/3 activity is necessary for efficient formation of E-cadherin adhesive contacts.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年学术文章
@wuu
2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
@yue
2004年學術文章
@zh
2004年學術文章
@zh-hant
name
Arp2/3 activity is necessary for efficient formation of E-cadherin adhesive contacts.
@en
Arp2/3 activity is necessary for efficient formation of E-cadherin adhesive contacts.
@nl
type
label
Arp2/3 activity is necessary for efficient formation of E-cadherin adhesive contacts.
@en
Arp2/3 activity is necessary for efficient formation of E-cadherin adhesive contacts.
@nl
prefLabel
Arp2/3 activity is necessary for efficient formation of E-cadherin adhesive contacts.
@en
Arp2/3 activity is necessary for efficient formation of E-cadherin adhesive contacts.
@nl
P2093
P2860
P50
P356
P1476
Arp2/3 activity is necessary for efficient formation of E-cadherin adhesive contacts.
@en
P2093
Falak M Helwani
Hiroaki Miki
Jeanie A Scott
Suzie Verma
Tadaomi Takenawa
P2860
P304
34062-34070
P356
10.1074/JBC.M404814200
P407
P577
2004-05-24T00:00:00Z