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JOHN ZWAAGSTRA


Associate Member – Department of Medicine, Division of Experimental Medicine
 

Contact information:

Telephone: (514) 496-6384
e-mail address: john.zwaagstra@nrc.ca
website:  http://bri-irb.nrc-cnrc.gc.ca/rd/health/receptors/activities_e.html


Projects for Thesis Supervision:

1. Mechanisms of TGF-beta receptor oligomerization and internalization.

2. Design and production of TGF-beta receptor-based traps for imaging and therapeutics in cancer.


Recent Publications:

Zwaagstra, J.C., Collins, C., Langlois, M.-J. and O'Connor-McCourt, M.D.
Analysis of the contribution of receptor subdomains to the cooperative binding and internalization of TGF-
b Type I and II receptors.  Submitted to Experimental Cell Research.

De Crescenzo, G., Chao, H., Zwaagstra, J., Durocher, Y. and O'Connor-McCourt, M.D. (2007)
Engineering TGF-
b traps: Artificially dimerizaed receptor ectodomains as high affinity blockers of TGF-b action. In: "Cancer Drug Discovery and Development: Transforming Growth Factor-b in Cancer Therapy",  Vol. 2, edited by S.B. Jakowlew, Humana Press, Totowa, N.J.

Ogorelkova, M., Zwaagstra, J.C., Elahi, S.M., Dias, C., Guilbault, C., Lo, R., Collins, C., Jaramillo, M., Mullick, A., O'Connor-McCourt, M.D. and Massie, B. (2006)
Adenovirus-delivered antisense RNA and siRNA exhibit different silencing efficiencies for th eendogenous transforming growth factor-
b (TGFb) Type II receptor. Oligonucleotides 16: 2-14.