Concerted modulation of paxillin dynamics at focal adhesions by deleted in liver cancer-1 and focal adhesion kinase during early cell spreading
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Title
Concerted modulation of paxillin dynamics at focal adhesions by deleted in liver cancer-1 and focal adhesion kinase during early cell spreading
Authors
Keywords
-
Journal
Cytoskeleton
Volume 71, Issue 12, Pages 677-694
Publisher
Wiley
Online
2014-11-29
DOI
10.1002/cm.21201
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Related references
Note: Only part of the references are listed.- Signaling networks of Rho GTPases in cell motility
- (2013) Samer Hanna et al. CELLULAR SIGNALLING
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- (2013) Frankie Chi Fat Ko et al. Nature Communications
- Inside-out, outside-in, and inside–outside-in: G protein signaling in integrin-mediated cell adhesion, spreading, and retraction
- (2012) Bo Shen et al. CURRENT OPINION IN CELL BIOLOGY
- FAK promotes recruitment of talin to nascent adhesions to control cell motility
- (2012) Christine Lawson et al. JOURNAL OF CELL BIOLOGY
- Differential regulation of the activity of deleted in liver cancer 1 (DLC1) by tensins controls cell migration and transformation
- (2012) X. Cao et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Silencing of DLC1 Upregulates PAI-1 Expression and Reduces Migration in Normal Prostate Cells
- (2011) Y.-P. Shih et al. MOLECULAR CANCER RESEARCH
- Full activity of the deleted in liver cancer 1 (DLC1) tumor suppressor depends on an LD-like motif that binds talin and focal adhesion kinase (FAK)
- (2011) G. Li et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Rho protein crosstalk: another social network?
- (2011) Christophe Guilluy et al. TRENDS IN CELL BIOLOGY
- Role of DLC-1, a tumor suppressor protein with RhoGAP activity, in regulation of the cytoskeleton and cell motility
- (2009) T. Y. Kim et al. CANCER AND METASTASIS REVIEWS
- Simultaneous loss of the DLC1 and PTEN tumor suppressors enhances breast cancer cell migration
- (2009) Johanna Heering et al. EXPERIMENTAL CELL RESEARCH
- Focal adhesion-localization of START-GAP1/DLC1 is essential for cell motility and morphology
- (2009) Katsuhisa Kawai et al. GENES TO CELLS
- A FAK-p120RasGAP-p190RhoGAP complex regulates polarity in migrating cells
- (2009) A. Tomar et al. JOURNAL OF CELL SCIENCE
- The SAM domain of the RhoGAP DLC1 binds EF1A1 to regulate cell migration
- (2009) D. Zhong et al. JOURNAL OF CELL SCIENCE
- DLC1 Activation Requires Lipid Interaction through a Polybasic Region Preceding the RhoGAP Domain
- (2009) Patrik Erlmann et al. MOLECULAR BIOLOGY OF THE CELL
- p120Ras-GAP binds the DLC1 Rho-GAP tumor suppressor protein and inhibits its RhoA GTPase and growth-suppressing activities
- (2009) X-Y Yang et al. ONCOGENE
- Investigating complexity of protein–protein interactions in focal adhesions
- (2008) Tanmay P. Lele et al. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
- Deleted in Liver Cancer 1 Controls Cell Migration through a Dia1-Dependent Signaling Pathway
- (2008) Gerlinde Holeiter et al. CANCER RESEARCH
- Rho GTPases in cancer cell biology
- (2008) Francisco M. Vega et al. FEBS LETTERS
- Effects of Structure of Rho GTPase-activating Protein DLC-1 on Cell Morphology and Migration
- (2008) Tai Young Kim et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Paxillin comes of age
- (2008) N. O. Deakin et al. JOURNAL OF CELL SCIENCE
- Deleted in liver cancer-1 (DLC-1): A tumor suppressor not just for liver
- (2007) Yi-Chun Liao et al. INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY
- DLC-1 suppresses non-small cell lung cancer growth and invasion by RhoGAP-dependent and independent mechanisms
- (2007) Kevin D. Healy et al. MOLECULAR CARCINOGENESIS
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