Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Sandra, Tremblay"'
Autor:
Rachid El Fatimy, Laetitia Davidovic, Sandra Tremblay, Xavier Jaglin, Alain Dury, Claude Robert, Paul De Koninck, Edouard W Khandjian
Publikováno v:
PLoS Genetics, Vol 12, Iss 7, p e1006192 (2016)
Local translation at the synapse plays key roles in neuron development and activity-dependent synaptic plasticity. mRNAs are translocated from the neuronal soma to the distant synapses as compacted ribonucleoparticles referred to as RNA granules. The
Externí odkaz:
https://doaj.org/article/c5fbd6ced8b943a98d5ad1b967e2e301
Autor:
Angela Genge, Genevieve Matte, Sandra Tremblay, Michel Melanson, Sylvie Gosselin, Colleen O'Connell, Nancy Anoja, Amer Ghavanini, Kerri Schellenberg, Benjamin Ritsma, Nicolas Dupré, Christen Shoesmith, Amanda Fiander, Marvin Chum, Sanjay Kalra, Aaron Izenberg, Ari Breiner, Heather Williams, Wendy Johnston, Annie Dionne, Daniel Fok, Kristiana Salmon
Publikováno v:
Amyotrophic lateral sclerosisfrontotemporal degeneration. 23(3-4)
Objective: To understand current genetic testing practices at Canadian ALS clinics. Methods: An online survey and phone interviews, with clinicians practicing in 27 ALS clinics in Canada, were employed to collect data. Quantitative and qualitative an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::140f69a34a243fd08ef1d9ff8e8b4b92
https://pubmed.ncbi.nlm.nih.gov/34569363
https://pubmed.ncbi.nlm.nih.gov/34569363
Autor:
Alain Y Dury, Rachid El Fatimy, Sandra Tremblay, Timothy M Rose, Jocelyn Côté, Paul De Koninck, Edouard W Khandjian
Publikováno v:
PLoS Genetics, Vol 9, Iss 10, p e1003890 (2013)
Fragile X syndrome is caused by loss of function of a single gene encoding the Fragile X Mental Retardation Protein (FMRP). This RNA-binding protein, widely expressed in mammalian tissues, is particularly abundant in neurons and is a component of mes
Externí odkaz:
https://doaj.org/article/4b5a46fea61d4c4484eb7565507996d8
Autor:
Rachid El Fatimy, Sandra Tremblay, Alain Y Dury, Samuel Solomon, Paul De Koninck, John W Schrader, Edouard W Khandjian
Publikováno v:
PLoS ONE, Vol 7, Iss 6, p e39338 (2012)
Fragile X syndrome is caused by the absence of the Fragile X Mental Retardation Protein (FMRP), an RNA-binding protein. FMRP is associated with messenger RiboNucleoParticles (mRNPs) present in polyribosomes and its absence in neurons leads to alterat
Externí odkaz:
https://doaj.org/article/59f98efe0a234313bc0095744bc6a714
Autor:
Rachid El Fatimy, Sandra Tremblay, Alain Y. Dury, Samuel Solomon, Paul De Koninck, John W. Schrader, Edouard W. Khandjian
Publikováno v:
PLoS ONE, Vol 7, Iss 9 (2012)
Externí odkaz:
https://doaj.org/article/fbc24c20334a41cf896bb5416452d46e
Autor:
Denise Cook, Maria del Rayo Sanchez-Carbente, Claude Lachance, Danuta Radzioch, Sandra Tremblay, Edouard W Khandjian, Luc DesGroseillers, Keith K Murai
Publikováno v:
PLoS ONE, Vol 6, Iss 10, p e26120 (2011)
The formation and storage of memories in neuronal networks relies on new protein synthesis, which can occur locally at synapses using translational machinery present in dendrites and at spines. These new proteins support long-lasting changes in synap
Externí odkaz:
https://doaj.org/article/9846529771ad4966841094e98b4e7e38
Autor:
Soma Das, Jennifer A. Lee, Amy K. Johnson, Jennifer Burton, Sandra Tremblay, Ying Ying Hu, Daniela del Gaudio, Kirsten Donato, Daniel B. Magner, Zejuan Li, Sarah E. Noon, Ian D. Krantz, Rachel Laframboise, Brett Deml, Jacea Deml, George E. Hoganson, Christian P. Schaaf, Maria Helgeson, Jennifer Keller-Ramey
Publikováno v:
Journal of Human Genetics. 63:349-356
Cornelia de Lange syndrome (CdLS) is a rare neurodevelopmental syndrome for which mutations in five causative genes that encode (SMC1A, SMC3, RAD21) or regulate (NIPBL, HDAC8) the cohesin complex, account for ~70% of cases. Herein we report on four f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7987cd68c6efe8bfa8eb3f74b5d1342d
https://doi.org/10.1038/s10038-017-0387-6
https://doi.org/10.1038/s10038-017-0387-6
Autor:
Sandra Tremblay, Tamarha Pierce
Publikováno v:
Canadian Journal of Behavioural Science / Revue canadienne des sciences du comportement. 43:99-110
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7bab5bfe2c5f745a7664bdb6937be633
https://doi.org/10.1037/a0022635
https://doi.org/10.1037/a0022635
Autor:
Paul De Koninck, Alain Y. Dury, Sandra Tremblay, Rachid El Fatimy, Claude Robert, Xavier H. Jaglin, Laetitia Davidovic, Edouard W. Khandjian
Publikováno v:
PLoS Genetics
PLoS Genetics, Vol 12, Iss 7, p e1006192 (2016)
PLoS Genetics, Vol 12, Iss 7, p e1006192 (2016)
Local translation at the synapse plays key roles in neuron development and activity-dependent synaptic plasticity. mRNAs are translocated from the neuronal soma to the distant synapses as compacted ribonucleoparticles referred to as RNA granules. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31f541444ad9ce2dfba829237f456ab9
https://pubmed.ncbi.nlm.nih.gov/27462983
https://pubmed.ncbi.nlm.nih.gov/27462983
Autor:
Barbara Bardoni, Marc-Étienne Huot, Edouard W. Khandjian, Rachid Mazroui, Laetitia Davidovic, Sandra Tremblay
Publikováno v:
Proceedings of the National Academy of Sciences. 101:13357-13362
Fragile X syndrome is caused by the absence of the fragile X mental retardation protein (FMRP). This RNA-binding protein is widely expressed in human and mouse tissues, and it is particularly abundant in the brain because of its high expression in ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c002acaffe7578fc680347f959adb19d
https://doi.org/10.1073/pnas.0405398101
https://doi.org/10.1073/pnas.0405398101