SLK-mediated phosphorylation of paxillin is required for focal adhesion turnover and cell migration-Reference-Cited by-同舟云学术

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SLK-mediated phosphorylation of paxillin is required for focal adhesion turnover and cell migration

Published:2012-11-05 Issue:39 Volume:32 Page:4656-4663
ISSN:0950-9232
Container-title:Oncogene
language:en
Short-container-title:Oncogene

Author:

Quizi J L,Baron K,Al-Zahrani K N,O'Reilly P,Sriram R K,Conway J,Laurin A-A,Sabourin L A

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Genetics,Molecular Biology

Link

http://www.nature.com/articles/onc2012488.pdf

Reference36 articles.

1. Horwitz AR, Parsons JT . Cell migration—movin’ on [comment]. Science 1999; 286: 1102–1103.

2. Abou Z N, Valles AM, Boyer B . Serine phosphorylation regulates paxillin turnover during cell migration. Cell Commun Signal 2006; 4: 8.

3. Bellis SL, Perrotta JA, Curtis MS, Turner CE . Adhesion of fibroblasts to fibronectin stimulates both serine and tyrosine phosphorylation of paxillin. Biochem J 1997; 325 (Pt 2): 375–381.

4. Hoellerer MK, Noble ME, Labesse G, Campbell ID, Werner JM, Arold ST . Molecular recognition of paxillin LD motifs by the focal adhesion targeting domain. Structure 2003; 11: 1207–1217.

5. Webb DJ, Donais K, Whitmore LA, Thomas SM, Turner CE, Parsons JT et al. FAK-Src signalling through paxillin, ERK and MLCK regulates adhesion disassembly. Nat Cell Biol 2004; 6: 154–161.

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