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2018
S. Pozzi, Thammisetty, S. Sampath, and J-P Julien, Chronic Administration of Pimozide Fails to Attenuate Motor and Pathological Deficits in Two Mouse Models of Amyotrophic Lateral Sclerosis., Neurotherapeutics, vol. 15, no. 3, pp. 715-727, 2018.
B. Paré, Lehmann, M., Beaudin, M., Nordström, U., Saikali, S., J-P Julien, Gilthorpe, J. D., Marklund, S. L., Cashman, N. R., Andersen, P. M., Forsberg, K., Dupré, N., Gould, P., Brännström, T., and Gros-Louis, F., Misfolded SOD1 pathology in sporadic Amyotrophic Lateral Sclerosis., Sci Rep, vol. 8, no. 1, p. 14223, 2018.
A. Yuan, Sershen, H., Basavarajappa, B. S., Smiley, J. F., Hashim, A., Bleiwas, C., Berg, M., Guifoyle, D. N., Subbanna, S., Darji, S., Kumar, A., Rao, M. V., Wilson, D. A., J-P Julien, Javitt, D. C., and Nixon, R. A., Neurofilament light interaction with GluN1 modulates neurotransmission and schizophrenia-associated behaviors., Transl Psychiatry, vol. 8, no. 1, p. 167, 2018.
V. Picher-Martel, Renaud, L., Bareil, C., and J-P Julien, Neuronal Expression of UBQLN2 Exacerbates TDP-43 Pathology in TDP-43 Mice through Interaction with Ubiquitin., Mol Neurobiol, 2018.
K. Komatsu, Imamura, K., Yamashita, H., J-P Julien, Takahashi, R., and Inoue, H., Overexpressed wild-type superoxide dismutase 1 exhibits amyotrophic lateral sclerosis-related misfolded conformation in induced pluripotent stem cell-derived spinal motor neurons., Neuroreport, vol. 29, no. 1, pp. 25-29, 2018.
K. Dutta, Patel, P., and J-P Julien, Protective effects of Withania somnifera extract in SOD1 mouse model of amyotrophic lateral sclerosis., Exp Neurol, vol. 309, pp. 193-204, 2018.
2016
Y. Iguchi, Eid, L., Parent, M., Soucy, G., Bareil, C., Riku, Y., Kawai, K., Takagi, S., Yoshida, M., Katsuno, M., Sobue, G., and J-P Julien, Exosome secretion is a key pathway for clearance of pathological TDP-43., Brain, vol. 139, no. Pt 12, pp. 3187-3201, 2016.
V. Picher-Martel, Valdmanis, P. N., Gould, P. V., J-P Julien, and Dupré, N., From animal models to human disease: a genetic approach for personalized medicine in ALS., Acta Neuropathol Commun, vol. 4, no. 1, p. 70, 2016.
E. Israeli, Dryanovski, D. I., Schumacker, P. T., Chandel, N. S., Singer, J. D., J-P Julien, Goldman, R. D., and Opal, P., Intermediate filament aggregates cause mitochondrial dysmotility and increase energy demands in giant axonal neuropathy., Hum Mol Genet, 2016.
L. MacNair, Xiao, S., Miletic, D., Ghani, M., J-P Julien, Keith, J., Zinman, L., Rogaeva, E., and Robertson, J., MTHFSD and DDX58 are novel RNA-binding proteins abnormally regulated in amyotrophic lateral sclerosis., Brain, vol. 139, no. Pt 1, pp. 86-100, 2016.
P. Yadav, Selvaraj, B. T., Bender, F. L. P., Behringer, M., Moradi, M., Sivadasan, R., Dombert, B., Blum, R., Asan, E., Sauer, M., J-P Julien, and Sendtner, M., Neurofilament depletion improves microtubule dynamics via modulation of Stat3/stathmin signaling., Acta Neuropathol, vol. 132, no. 1, pp. 93-110, 2016.
Y. Ohta, Soucy, G., Phaneuf, D., Audet, J. - N., Gros-Louis, F., Rouleau, G. A., Blasco, H., Corcia, P., Andersen, P. M., Nordin, F., Yamashita, T., Abe, K., and J-P Julien, Sex-dependent effects of chromogranin B P413L allelic variant as disease modifier in amyotrophic lateral sclerosis., Hum Mol Genet, 2016.
Y. Ohta, Soucy, G., Phaneuf, D., Audet, J. - N., Gros-Louis, F., Rouleau, G. A., Blasco, H., Corcia, P., Andersen, P. M., Nordin, F., Yamashita, T., Abe, K., and J-P Julien, Sex-dependent effects of chromogranin B P413L allelic variant as disease modifier in amyotrophic lateral sclerosis., Hum Mol Genet, vol. 25, no. 21, pp. 4771-4786, 2016.

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