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Jean-Claude Lacaille
Jean-Claude Lacaille
Dept Neurosciences, Université de Montréal
在 umontreal.ca 的电子邮件经过验证
标题
引用次数
引用次数
年份
Astrocytes are endogenous regulators of basal transmission at central synapses
A Panatier, J Vallée, M Haber, KK Murai, JC Lacaille, R Robitaille
Cell 146 (5), 785-798, 2011
6982011
Autism-related deficits via dysregulated eIF4E-dependent translational control
CG Gkogkas, A Khoutorsky, I Ran, E Rampakakis, T Nevarko, ...
Nature 493 (7432), 371-377, 2013
5722013
eIF2α phosphorylation bidirectionally regulates the switch from short-to long-term synaptic plasticity and memory
M Costa-Mattioli, D Gobert, E Stern, K Gamache, R Colina, C Cuello, ...
Cell 129 (1), 195-206, 2007
5682007
Local circuit interactions between oriens/alveus interneurons and CA1 pyramidal cells in hippocampal slices: electrophysiology and morphology
JC Lacaille, AL Mueller, DD Kunkel, PA Schwartzkroin
Journal of Neuroscience 7 (7), 1979-1993, 1987
4741987
Translational control of hippocampal synaptic plasticity and memory by the eIF2α kinase GCN2
M Costa-Mattioli, D Gobert, H Harding, B Herdy, M Azzi, M Bruno, ...
Nature 436 (7054), 1166-1170, 2005
4712005
GABAergic network activation of glial cells underlies hippocampal heterosynaptic depression
A Serrano, N Haddjeri, JC Lacaille, R Robitaille
Journal of Neuroscience 26 (20), 5370-5382, 2006
4672006
Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability
FF Hamdan, J Gauthier, Y Araki, DT Lin, Y Yoshizawa, K Higashi, AR Park, ...
The American Journal of Human Genetics 88 (3), 306-316, 2011
4112011
Mutations in SYNGAP1 in Autosomal Nonsyndromic Mental Retardation
FF Hamdan, J Gauthier, D Spiegelman, A Noreau, Y Yang, S Pellerin, ...
New England Journal of Medicine 360 (6), 599-605, 2009
3822009
Characterization of an RNA granule from developing brain
G Elvira, S Wasiak, V Blandford, XK Tong, A Serrano, X Fan, ...
Molecular & cellular proteomics 5 (4), 635-651, 2006
3332006
Stratum lacunosum-moleculare interneurons of hippocampal CA1 region. I. Intracellular response characteristics, synaptic responses, and morphology
JC Lacaille, PA Schwartzkroin
Journal of Neuroscience 8 (4), 1400-1410, 1988
3091988
Stratum lacunosum-moleculare interneurons of hippocampal CA1 region. II. Intrasomatic and intradendritic recordings of local circuit synaptic interactions
JC Lacaille, PA Schwartzkroin
Journal of Neuroscience 8 (4), 1411-1424, 1988
2981988
De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment
FF Hamdan, H Daoud, D Rochefort, A Piton, J Gauthier, M Langlois, ...
The American Journal of Human Genetics 87 (5), 671-678, 2010
2652010
Interneuron diversity series: hippocampal interneuron classifications–making things as simple as possible, not simpler
G Maccaferri, JC Lacaille
Trends in neurosciences 26 (10), 564-571, 2003
2642003
Mutations in SYNGAP1 Cause Intellectual Disability, Autism, and a Specific Form of Epilepsy by Inducing Haploinsufficiency
MH Berryer, FF Hamdan, LL Klitten, RS Møller, L Carmant, ...
Human mutation 34 (2), 385-394, 2013
2612013
A hebbian form of long-term potentiation dependent on mGluR1a in hippocampal inhibitory interneurons
Y Perez, F Morin, JC Lacaille
Proceedings of the National Academy of Sciences 98 (16), 9401-9406, 2001
2342001
De novo SYNGAP1 mutations in nonsyndromic intellectual disability and autism
FF Hamdan, H Daoud, A Piton, J Gauthier, S Dobrzeniecka, MO Krebs, ...
Biological psychiatry 69 (9), 898-901, 2011
2252011
Metformin ameliorates core deficits in a mouse model of fragile X syndrome
I Gantois, A Khoutorsky, J Popic, A Aguilar-Valles, E Freemantle, R Cao, ...
Nature medicine 23 (6), 674-677, 2017
2092017
Pharmacogenetic inhibition of eIF4E-dependent Mmp9 mRNA translation reverses fragile X syndrome-like phenotypes
CG Gkogkas, A Khoutorsky, R Cao, SM Jafarnejad, M Prager-Khoutorsky, ...
Cell reports 9 (5), 1742-1755, 2014
2022014
Axonal sprouting of CA1 pyramidal cells in hyperexcitable hippocampal slices of kainate‐treated rats
Y Perez, F Morin, C Beaulieu, JC Lacaille
European Journal of Neuroscience 8 (4), 736-748, 1996
2001996
De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy
FF Hamdan, A Piton, J Gauthier, A Lortie, F Dubeau, S Dobrzeniecka, ...
Annals of Neurology: Official Journal of the American Neurological …, 2009
1912009
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