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Mathieu Lachance
Mathieu Lachance
CHU Sainte-Justine
Verified email at umontreal.ca
Title
Cited by
Cited by
Year
Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia
DL Guernsey, H Jiang, DR Campagna, SC Evans, M Ferguson, ...
Nature genetics 41 (6), 651-653, 2009
2572009
The genetic landscape of infantile spasms
JL Michaud, M Lachance, FF Hamdan, L Carmant, A Lortie, P Diadori, ...
Human molecular genetics 23 (18), 4846-4858, 2014
1982014
Involvement of cortical fast-spiking parvalbumin-positive basket cells in epilepsy
X Jiang, M Lachance, E Rossignol
Progress in brain research 226, 81-126, 2016
1022016
Gβγ subunit combinations differentially modulate receptor and effector coupling in vivo
L Robillard, N Ethier, M Lachance, TE Hébert
Cellular signalling 12 (9-10), 673-682, 2000
832000
Both gain‐of‐function and loss‐of‐function de novo CACNA1A mutations cause severe developmental epileptic encephalopathies in the spectrum of Lennox …
X Jiang, PK Raju, N D'Avanzo, M Lachance, J Pepin, F Dubeau, ...
Epilepsia 60 (9), 1881-1894, 2019
742019
Stable association of G proteins with β2AR is independent of the state of receptor activation
M Lachance, N Ethier, G Wolbring, PPM Schnetkamp, TE Hébert
Cellular signalling 11 (7), 523-533, 1999
561999
A mutation in the RNF170 gene causes autosomal dominant sensory ataxia
PN Valdmanis, N Dupre, M Lachance, SJ Stochmanski, VV Belzil, ...
Brain 134 (2), 602-607, 2011
402011
Touch responsiveness in zebrafish requires voltage-gated calcium channel 2.1 b
SE Low, IG Woods, M Lachance, J Ryan, AF Schier, L Saint-Amant
Journal of neurophysiology 108 (1), 148-159, 2012
352012
Remodeled cortical inhibition prevents motor seizures in generalized epilepsy
X Jiang, A Lupien‐Meilleur, S Tazerart, M Lachance, E Samarova, ...
Annals of Neurology 84 (3), 436-451, 2018
202018
Reversing frontal disinhibition rescues behavioural deficits in models of CACNA1A-associated neurodevelopment disorders
A Lupien-Meilleur, X Jiang, M Lachance, V Taschereau-Dumouchel, ...
Molecular Psychiatry 26 (12), 7225-7246, 2021
182021
Ex utero electroporation and organotypic slice cultures of embryonic mouse brains for live-imaging of migrating GABAergic interneurons
L Eid, M Lachance, G Hickson, E Rossignol
JoVE (Journal of Visualized Experiments), e57526, 2018
72018
Novel Mutation in ATP6V1A Gene with Infantile Spasms in an Indian Boy
RA Kadwa
Neuropediatrics 51 (04), 292-294, 2020
32020
Outcome of west syndrome: A critical review
S Adhikari, D Gautam
Journal of Pediatric Epilepsy 9 (01), 001-006, 2020
12020
Both GEF domains of the autism and epilepsy-associated Trio protein are required for proper tangential migration of GABAergic interneurons
E Rossignol, L Eid, PK Raju, L Lokmane, SBT Tadoum, X Jiang, ...
2023
Both GEF domains of the autism and epilepsy-associated Trio protein are required for proper tangential migration of GABAergic interneurons
L Eid, L Lokmane, PK Raju, SBT Tadoum, X Jiang, K Toulouse, ...
bioRxiv, 2022.12. 31.522400, 2023
2023
Touch responsiveness in zebrafish requires
L Saint-Amant, SE Low, IG Woods, M Lachance, J Ryan, AF Schier
J. Neurosci 33 (17), 7384-7392, 2013
2013
Touch responsiveness in zebrafish requires voltage-gated calcium channel 2.1 b 1 2 Abbreviated title: fakir is caused by a mutation in CaV2. 1b 3 4
SE Low, IG Woods, M Lachance, J Ryan, AF Schier, L Saint-Amant, ...
2012
Stable association of G proteins with the beta (2)-adrenergic receptor complex
M Lachance, N Ethier, TE Hebert
BIOPHYSICAL JOURNAL 78 (1), 42A-42A, 2000
2000
Specificity of G beta gamma in the beta 2-adrenergic receptor complex.
M Lachance, N Ethier, TE Hebert
BIOPHYSICAL JOURNAL 76 (1), A429-A429, 1999
1999
Reconstitution of beta (2)-adrenergic signalling in SF9 cells.
M Lachance, N Ethier, G Wolbring, TE Hebert
BIOPHYSICAL JOURNAL 74 (2), A390-A390, 1998
1998
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