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Roxanne Lariviere, Ph.D. - Publications

Affiliations: 
2004 McGill University, Montreal, QC, Canada 
Area:
Neuroscience Biology
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10 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Choquet K, Pinard M, Yang S, Moir RD, Poitras C, Dicaire MJ, Sgarioto N, Larivière R, Kleinman CL, Willis IM, Gauthier MS, Coulombe B, Brais B. The leukodystrophy mutation Polr3b R103H causes homozygote mouse embryonic lethality and impairs RNA polymerase III biogenesis. Molecular Brain. 12: 59. PMID 31221184 DOI: 10.1186/S13041-019-0479-7  0.388
2019 Larivière R, Sgarioto N, Márquez BT, Gaudet R, Choquet K, McKinney RA, Watt AJ, Brais B. Sacs R272C missense homozygous mice develop an ataxia phenotype. Molecular Brain. 12: 19. PMID 30866998 DOI: 10.1186/S13041-019-0438-3  0.438
2018 Walker CL, Uchida A, Li Y, Trivedi N, Fenn JD, Monsma PC, Lariviére RC, Julien JP, Jung P, Brown A. Local acceleration of neurofilament transport at nodes of Ranvier. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 30541916 DOI: 10.1523/Jneurosci.2272-18.2018  0.44
2018 Gentil BJ, Lai GT, Menade M, Larivière R, Minotti S, Gehring K, Chapple JP, Brais B, Durham HD. Sacsin, mutated in the ataxia ARSACS, regulates intermediate filament assembly and dynamics. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. fj201801556R. PMID 30332300 DOI: 10.1096/Fj.201801556R  0.361
2017 Duncan EJ, Larivière R, Bradshaw TY, Longo F, Sgarioto N, Hayes MJ, Romano LEL, Nethisinghe S, Giunti P, Bruntraeger MB, Durham HD, Brais B, Maltecca F, Gentil BJ, Paul Chapple J. Altered organisation of the intermediate filament cytoskeleton and relocalisation of proteostasis modulators in cells lacking the ataxia protein sacsin. Human Molecular Genetics. PMID 28535259 DOI: 10.1093/Hmg/Ddx197  0.376
2017 Choquet K, Yang S, Moir RD, Forget D, Larivière R, Bouchard A, Poitras C, Sgarioto N, Dicaire MJ, Noohi F, Kennedy TE, Rochford J, Bernard G, Teichmann M, Coulombe B, et al. Absence of neurological abnormalities in mice homozygous for the Polr3a G672E hypomyelinating leukodystrophy mutation. Molecular Brain. 10: 13. PMID 28407788 DOI: 10.1186/S13041-017-0294-Y  0.42
2015 Larroquette F, Seto L, Gaub PL, Kamal B, Wallis D, Larivière R, Vallée J, Robitaille R, Tsuda H. Vapb/Amyotrophic lateral sclerosis 8 knock-in mice display slowly progressive motor behavior defects accompanying ER stress and autophagic response. Human Molecular Genetics. 24: 6515-29. PMID 26362257 DOI: 10.1093/Hmg/Ddv360  0.464
2015 Larivière R, Gaudet R, Gentil BJ, Girard M, Conte TC, Minotti S, Leclerc-Desaulniers K, Gehring K, McKinney RA, Shoubridge EA, McPherson PS, Durham HD, Brais B. Sacs knockout mice present pathophysiological defects underlying autosomal recessive spastic ataxia of Charlevoix-Saguenay. Human Molecular Genetics. 24: 727-39. PMID 25260547 DOI: 10.1093/Hmg/Ddu491  0.472
2006 Millecamps S, Robertson J, Lariviere R, Mallet J, Julien JP. Defective axonal transport of neurofilament proteins in neurons overexpressing peripherin. Journal of Neurochemistry. 98: 926-38. PMID 16787413 DOI: 10.1111/J.1471-4159.2006.03932.X  0.525
2004 Lariviere RC, Julien JP. Functions of intermediate filaments in neuronal development and disease. Journal of Neurobiology. 58: 131-48. PMID 14598376 DOI: 10.1002/Neu.10270  0.552
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