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Gene Therapy|May 20, 2000
Telomerase allows the immortalization of T antigen-positive DMD myoblasts: a new source of cells for gene transfer applicationS Seigneurin-Venin, V Bernard, J P TremblayBrain Research|December 1, 1983
Is the MEPP due to the release of one vesicle or to the simultaneous release of several vesicles at one active zone?J P Tremblay, R E Laurie, M ColonnierExperimental Neurology|April 1, 1988
Scanning electron microscopic study of the neuromuscular junction of dystrophic miceC Labrecque, J P Tremblay, M A FahimCanadian Journal of Biochemistry and Cell Biology = Revue Canadienne De Biochimie Et Biologie Cellulaire|June 1, 1985
A monoclonal antibody to beta-tubulin distinguishes a subset of neurons and axons in the chick ciliary ganglionJ P Tremblay, C Gravel, R B HawkesBiochemical and Biophysical Research Communications|October 1, 1998
Normal myoblast implantation in MDX mice prevents muscle damage by exerciseV Brussee, F Merly, F Tardif, et al.Muscle & Nerve|May 1, 1987
Repeated stimulation of the dystrophic mouse neuromuscular junctionsJ P Tremblay, L Grégoire, R Sasseville, et al.The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|October 1, 1993
Use of fluorescent latex microspheres (FLMs) to follow the fate of transplanted myoblastsA Satoh, J Huard, C Labrecque, et al.Experimental Brain Research|January 1, 1986
Non monotonic morphometric changes produced at mouse neuromuscular junctions following in vivo stimulation at various frequenciesJ P Tremblay, C Belhumeur, R Sasseville, et al.Transplantation|March 27, 1997
Role of non-major histocompatibility complex antigens in the rejection of transplanted myoblastsA Boulanger, I Asselin, R Roy, et al.Gene Therapy|February 4, 1999
Expression of human dystrophin following the transplantation of genetically modified mdx myoblastsP A Moisset, Y Gagnon, G Karpati, et al.Pageof 12