Loss of ASAP3 destabilizes cytoskeletal protein ACTG1 to suppress cancer cell migration
Published 2013 View Full Article
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Title
Loss of ASAP3 destabilizes cytoskeletal protein ACTG1 to suppress cancer cell migration
Authors
Keywords
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Journal
Molecular Medicine Reports
Volume 9, Issue 2, Pages 387-394
Publisher
Spandidos Publications
Online
2013-11-27
DOI
10.3892/mmr.2013.1831
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- De novo mutations in the actin genes ACTB and ACTG1 cause Baraitser-Winter syndrome
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- (2010) Shehab A. Ismail et al. CELL
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- β-Actin and γ-Actin Are Each Dispensable for Auditory Hair Cell Development But Required for Stereocilia Maintenance
- (2010) Benjamin J. Perrin et al. PLoS Genetics
- In vivo and in vitro effects of two novel gamma-actin (ACTG1) mutations that cause DFNA20/26 hearing impairment
- (2009) Matías Morín et al. HUMAN MOLECULAR GENETICS
- -Actin is required for cytoskeletal maintenance but not development
- (2009) I. A. Belyantseva et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Aldose Reductase Regulates Hepatic Peroxisome Proliferator-activated Receptor α Phosphorylation and Activity to Impact Lipid Homeostasis
- (2008) Longxin Qiu et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- ASAP3 Is a Focal Adhesion-associated Arf GAP That Functions in Cell Migration and Invasion
- (2008) Vi Luan Ha et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Novel ACTG1 mutation causing autosomal dominant non-syndromic hearing impairment in a Chinese family
- (2008) Ping Liu et al. Journal of Genetics and Genomics
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