Stressing the limits of focal adhesion mechanosensitivity.
about
Spatiotemporal dynamics of traction forces show three contraction centers in migratory neuronsLocal 3D matrix microenvironment regulates cell migration through spatiotemporal dynamics of contractility-dependent adhesions.ATRA mechanically reprograms pancreatic stellate cells to suppress matrix remodelling and inhibit cancer cell invasion.In-situ coupling between kinase activities and protein dynamics within single focal adhesions.Heading in the Right Direction: Understanding Cellular Orientation Responses to Complex Biophysical EnvironmentsModel-based traction force microscopy reveals differential tension in cellular actin bundlesMechanism of Focal Adhesion Kinase MechanosensingInhibition of αvβ3 integrin induces loss of cell directionality of oral squamous carcinoma cells (OSCC)The mTOR-FAK mechanotransduction signaling axis for focal adhesion maturation and cell proliferation.Cost-benefit analysis of the mechanisms that enable migrating cells to sustain motility upon changes in matrix environments.Geometric guidance of integrin mediated traction stress during stem cell differentiationTalin determines the nanoscale architecture of focal adhesions.Simulation of the cytoskeletal response of cells on grooved or patterned substrates.Overview of the Muscle Cytoskeleton.Actin-Based Adhesion Modules Mediate Cell Interactions with the Extracellular Matrix and Neighboring Cells.In vivo quantitative analysis of Talin turnover in response to force.Effects of substrate stiffness and actomyosin contractility on coupling between force transmission and vinculin-paxillin recruitment at single focal adhesions.Dasatinib inhibits actin fiber reorganization and promotes endothelial cell permeability through RhoA-ROCK pathwayCell-Extracellular Matrix Mechanobiology: Forceful Tools and Emerging Needs for Basic and Translational Research.Phosphorylation of human enhancer filamentation 1 (HEF1) stimulates interaction with Polo-like kinase 1 leading to HEF1 localization to focal adhesions.Molecular Simulations Suggest a Force-Dependent Mechanism of Vinculin Activation.Large Amplitude Oscillatory Shear Rheology of Living Fibroblasts: Path-Dependent Steady States.Buckle up: Membrane tension drives lamellipodial network compression and adhesion deposition.Loss of β-PIX inhibits focal adhesion disassembly and promotes keratinocyte motility via myosin light chain activation.A phenomenological cohesive model for the macroscopic simulation of cell-matrix adhesions.Tug of War at the Cell-Matrix Interface.Nano-mechanical single-cell sensing of cell-matrix contacts.Dynamin Autonomously Regulates Podocyte Focal Adhesion Maturation.Vinculin Force-Sensitive Dynamics at Focal Adhesions Enable Effective Directed Cell Migration.Substrate stiffness-dependent exacerbation of endothelial permeability and inflammation: mechanisms and potential implications in ALI and PH (2017 Grover Conference Series).Focal Adhesions Undergo Longitudinal Splitting into Fixed-Width UnitsCombustion-derived particles inhibit in vitro human lung fibroblast-mediated matrix remodeling
P2860
Q27310707-EE57A482-4077-4400-8CA8-CACB0D0A183EQ27319852-E2B6E64F-5CB8-49C2-AA84-96D68A857D1DQ27330342-6B9921B1-9C21-4783-AAB2-487F99866BEDQ27331739-D3F38D6F-F6F2-4F04-93B9-CB5D0D0C06D0Q28072132-D711A476-FD17-477F-AC72-1D510F0AC6F8Q28543921-E92F5F7A-54BF-486A-B35D-5B48CECF2E07Q28550745-B8781AB1-55A5-4AC4-AF2B-11BC68C9BD96Q30252508-A3D028C5-DF29-498D-8A63-D64109D8F90DQ30357240-AC7939EF-C22E-4A70-A61C-26BB48F53E47Q30649357-7B1D2F4C-E0EE-4536-8FF0-6EC77B32F64EQ36016865-C8631048-34E5-4A64-87BB-3DFCA39875B6Q36055656-7400005B-B981-426F-97B5-ECD832F58774Q39312764-3F1A2A65-0F46-466C-9799-6B24A7AA3B42Q39391006-C2B8528D-9CA1-4FDE-AC45-D07841D1F85DQ39416065-1CB31A24-F947-4C23-8D84-0C58C3C89126Q40455074-2BA469A0-D2E9-46A9-80CB-4189D8E28356Q41230015-19AC3284-27CD-44B4-9672-CC6D1EB35972Q42292312-0503383D-1FF4-48D9-919F-6373C34617BFQ47310923-86A06500-2C0F-49B8-A55A-C33BD9035BCCQ47345062-1BDE755A-347E-42E7-B3FA-0A9ADB503145Q47632832-643892DA-66D5-49CA-BFFF-283DA893DC06Q47661582-BAF99D2A-D8E7-469B-ADD4-9539A191A551Q48002494-DEAF9A6C-AC8C-4DD5-97D7-87A75B5A0393Q48059923-4DCEA83B-E8CB-4028-93E7-A11F67BE37B1Q48221329-DAF89585-8593-487D-85ED-0D462EDF4E76Q50879305-C46343DD-FCD7-4CFA-8853-595E6C8BBB0BQ51121772-735D2AEE-FABD-4AE9-B0F6-10748068D4B0Q51631984-A350943C-2DDA-48F1-AE0F-E96F62B02E56Q52324898-C21B5DFE-E42C-4B94-8A21-92641D7EE0B1Q52715213-DADEDFBB-09E9-4929-BDDF-047B60E2966DQ57988034-3144F62C-CCCE-47F0-A423-4839C2A1C824Q58111450-E6E5F7AD-11FE-4A50-B451-EEDDDD262D1B
P2860
Stressing the limits of focal adhesion mechanosensitivity.
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
Stressing the limits of focal adhesion mechanosensitivity.
@en
type
label
Stressing the limits of focal adhesion mechanosensitivity.
@en
prefLabel
Stressing the limits of focal adhesion mechanosensitivity.
@en
P2860
P1476
Stressing the limits of focal adhesion mechanosensitivity.
@en
P2093
Margaret L Gardel
P2860
P356
10.1016/J.CEB.2014.06.003
P577
2014-07-05T00:00:00Z