Edor Kabashi
Edor Kabashi
ICM - Institut du Cerveau et de la Moelle épiničre
Verified email at icm-institute.org - Homepage
Cited by
Cited by
TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
E Kabashi, PN Valdmanis, P Dion, D Spiegelman, BJ McConkey, ...
Nature genetics 40 (5), 572, 2008
Gain and loss of function of ALS-related mutations of TARDBP (TDP-43) cause motor deficits in vivo
E Kabashi, L Lin, ML Tradewell, PA Dion, V Bercier, P Bourgouin, ...
Human molecular genetics 19 (4), 671-683, 2010
Loss of function of C9orf72 causes motor deficits in a zebrafish model of amyotrophic lateral sclerosis
S Ciura, S Lattante, I Le Ber, M Latouche, H Tostivint, A Brice, E Kabashi
Annals of neurology 74 (2), 180-187, 2013
Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis
H Daoud, PN Valdmanis, E Kabashi, P Dion, N Dupre, W Camu, ...
Journal of medical genetics 46 (2), 112-114, 2009
Loss of C9ORF72 impairs autophagy and synergizes with polyQ Ataxin‐2 to induce motor neuron dysfunction and cell death
C Sellier, ML Campanari, CJ Corbier, A Gaucherot, I Kolb‐Cheynel, ...
The EMBO journal 35 (12), 1276-1297, 2016
TARDBP and FUS Mutations Associated with Amyotrophic Lateral Sclerosis: Summary and Update
S Lattante, GA Rouleau, E Kabashi
Human mutation 34 (6), 812-826, 2013
FUS and TARDBP but not SOD1 interact in genetic models of amyotrophic lateral sclerosis
E Kabashi, V Bercier, A Lissouba, M Liao, E Brustein, GA Rouleau, ...
PLoS genetics 7 (8), 2011
Focal dysfunction of the proteasome: a pathogenic factor in a mouse model of amyotrophic lateral sclerosis
E Kabashi, JN Agar, DM Taylor, S Minotti, HD Durham
Journal of neurochemistry 89 (6), 1325-1335, 2004
Loss of VPS13C function in autosomal-recessive Parkinsonism causes mitochondrial dysfunction and increases PINK1/Parkin-dependent mitophagy
S Lesage, V Drouet, E Majounie, V Deramecourt, M Jacoupy, A Nicolas, ...
The American Journal of Human Genetics 98 (3), 500-513, 2016
Oxidized/misfolded superoxide dismutase‐1: the cause of all amyotrophic lateral sclerosis?
E Kabashi, PN Valdmanis, P Dion, GA Rouleau
Annals of Neurology: Official Journal of the American Neurological …, 2007
Loss of function of glucocerebrosidase GBA2 is responsible for motor neuron defects in hereditary spastic paraplegia
E Martin, R Schüle, K Smets, A Rastetter, A Boukhris, JL Loureiro, ...
The American Journal of Human Genetics 92 (2), 238-244, 2013
Mutations in FUS cause FALS and SALS in French and French Canadian populations
VV Belzil, PN Valdmanis, PA Dion, H Daoud, E Kabashi, A Noreau, ...
Neurology 73 (15), 1176-1179, 2009
SQSTM1 mutations in French patients with frontotemporal dementia or frontotemporal dementia with amyotrophic lateral sclerosis
I Le Ber, A Camuzat, R Guerreiro, K Bouya-Ahmed, J Bras, G Nicolas, ...
JAMA neurology 70 (11), 1403-1410, 2013
Zebrafish models for the functional genomics of neurogenetic disorders
E Kabashi, E Brustein, N Champagne, P Drapeau
Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1812 (3), 335-345, 2011
Failure of protein quality control in amyotrophic lateral sclerosis
E Kabashi, HD Durham
Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1762 (11-12 …, 2006
Defining the genetic connection linking amyotrophic lateral sclerosis (ALS) with frontotemporal dementia (FTD)
S Lattante, S Ciura, GA Rouleau, E Kabashi
Trends in Genetics 31 (5), 263-273, 2015
Pharmacological reduction of ER stress protects against TDP-43 neuronal toxicity in vivo
A Vaccaro, SA Patten, D Aggad, C Julien, C Maios, E Kabashi, P Drapeau, ...
Neurobiology of disease 55, 64-75, 2013
Methylene blue protects against TDP-43 and FUS neuronal toxicity in C. elegans and D. rerio
A Vaccaro, SA Patten, S Ciura, C Maios, M Therrien, P Drapeau, ...
PLoS One 7 (7), 2012
Tryptophan 32 potentiates aggregation and cytotoxicity of a copper/zinc superoxide dismutase mutant associated with familial amyotrophic lateral sclerosis
DM Taylor, BF Gibbs, E Kabashi, S Minotti, HD Durham, JN Agar
Journal of Biological Chemistry 282 (22), 16329-16335, 2007
Homozygous TREM2 mutation in a family with atypical frontotemporal dementia
I Le Ber, A De Septenville, R Guerreiro, J Bras, A Camuzat, P Caroppo, ...
Neurobiology of aging 35 (10), 2419. e23-2419. e25, 2014
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