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Showing results (601-610 of 651) with videos related to

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Molecular Cell|March 18, 2017
Phase Separation of C9orf72 Dipeptide Repeats Perturbs Stress Granule DynamicsSteven Boeynaems, Elke Bogaert, Denes Kovacs, et al.
Nature Medicine|August 28, 2012
EPHA4 is a disease modifier of amyotrophic lateral sclerosis in animal models and in humansAnnelies Van Hoecke, Lies Schoonaert, Robin Lemmens, et al.
Brain : a Journal of Neurology|March 8, 2008
Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies: a genotype-phenotype correlation studyInes Dierick, Jonathan Baets, Joy Irobi, et al.
Nature Genetics|January 24, 2006
Disrupted function and axonal distribution of mutant tyrosyl-tRNA synthetase in dominant intermediate Charcot-Marie-Tooth neuropathyAlbena Jordanova, Joy Irobi, Florian P Thomas, et al.
Scientific Reports|April 13, 2019
Exome array analysis of rare and low frequency variants in amyotrophic lateral sclerosisAnnelot M Dekker, Frank P Diekstra, Sara L Pulit, et al.
Brain Communications|October 28, 2021
<i>SCFD1</i> expression quantitative trait loci in amyotrophic lateral sclerosis are differentially expressedAlfredo Iacoangeli, Isabella Fogh, Sashika Selvackadunco, et al.
Neurobiology of Aging|April 23, 2010
Polymorphisms in the GluR2 gene are not associated with amyotrophic lateral sclerosisElke Bogaert, An Goris, Philip Van Damme, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 2, 2011
VEGF modulates NMDA receptors activity in cerebellar granule cells through Src-family kinases before synapse formationClaire Meissirel, Carmen Ruiz de Almodovar, Ellen Knevels, et al.
Journal of Medical Genetics|April 17, 2008
Meta-analysis of vascular endothelial growth factor variations in amyotrophic lateral sclerosis: increased susceptibility in male carriers of the -2578AA genotypeD Lambrechts, K Poesen, R Fernández-Santiago, et al.
The Lancet. Neurology|September 11, 2007
ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association studyMichael A van Es, Paul W Van Vught, Hylke M Blauw, et al.
Pageof 66

Showing results (601-610 of 651) with videos related to

Sort By:
Pageof 66
Molecular Cell|March 18, 2017
Phase Separation of C9orf72 Dipeptide Repeats Perturbs Stress Granule DynamicsSteven Boeynaems, Elke Bogaert, Denes Kovacs, et al.
Nature Medicine|August 28, 2012
EPHA4 is a disease modifier of amyotrophic lateral sclerosis in animal models and in humansAnnelies Van Hoecke, Lies Schoonaert, Robin Lemmens, et al.
Brain : a Journal of Neurology|March 8, 2008
Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies: a genotype-phenotype correlation studyInes Dierick, Jonathan Baets, Joy Irobi, et al.
Nature Genetics|January 24, 2006
Disrupted function and axonal distribution of mutant tyrosyl-tRNA synthetase in dominant intermediate Charcot-Marie-Tooth neuropathyAlbena Jordanova, Joy Irobi, Florian P Thomas, et al.
Scientific Reports|April 13, 2019
Exome array analysis of rare and low frequency variants in amyotrophic lateral sclerosisAnnelot M Dekker, Frank P Diekstra, Sara L Pulit, et al.
Brain Communications|October 28, 2021
<i>SCFD1</i> expression quantitative trait loci in amyotrophic lateral sclerosis are differentially expressedAlfredo Iacoangeli, Isabella Fogh, Sashika Selvackadunco, et al.
Neurobiology of Aging|April 23, 2010
Polymorphisms in the GluR2 gene are not associated with amyotrophic lateral sclerosisElke Bogaert, An Goris, Philip Van Damme, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 2, 2011
VEGF modulates NMDA receptors activity in cerebellar granule cells through Src-family kinases before synapse formationClaire Meissirel, Carmen Ruiz de Almodovar, Ellen Knevels, et al.
Journal of Medical Genetics|April 17, 2008
Meta-analysis of vascular endothelial growth factor variations in amyotrophic lateral sclerosis: increased susceptibility in male carriers of the -2578AA genotypeD Lambrechts, K Poesen, R Fernández-Santiago, et al.
The Lancet. Neurology|September 11, 2007
ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association studyMichael A van Es, Paul W Van Vught, Hylke M Blauw, et al.
Pageof 66