Tatiana C. Silveira Corrêa and Renato Ramos Massaro contributed equally to this work.
RECK-mediated inhibition of glioma migration and invasion
Version of Record online: 1 FEB 2010
Copyright © 2010 Wiley-Liss, Inc.
Journal of Cellular Biochemistry
Volume 110, Issue 1, pages 52–61, 1 May 2010
How to Cite
Silveira Corrêa, T. C., Massaro, R. R., Brohem, C. A., Taboga, S. R., Lamers, M. L., Santos, M. F. and Maria-Engler, S. S. (2010), RECK-mediated inhibition of glioma migration and invasion. J. Cell. Biochem., 110: 52–61. doi: 10.1002/jcb.22472
- Issue online: 16 APR 2010
- Version of Record online: 1 FEB 2010
- Manuscript Accepted: 25 NOV 2009
- Manuscript Received: 15 SEP 2009
- FAPESP. Grant Numbers: 06/50915-1, 05/51194-3
Additional Supporting Information may be found in the online version of this article.
|JCB_22472_sm_SupplFig1.tif||314K||Supplementry Figure 1. Validation of RECK Clones. (A) Eleven G418-resistent cell colonies were screened for the expression of RECK by real time PCR. (B) Immunohistochemistry showing the RECK expression in RECK+ cells overexpressing RECK.|
|JCB_22472_sm_SupplFig2.tif||649K||Supplementry Figure 2. Senescence-associated β-galactosidase assay, BrdU and cell cycle progression were performed in order to characterize cell proliferation cells overexpressing RECK. No alteration of proliferation rates was observed in RECK+ cells compared to the controls:T98G and Mock.|
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