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Max Koppers

Showing results (11-20 of 27) with videos related to

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Neurobiology of Aging|November 13, 2012
Screening for rare variants in the coding region of ALS-associated genes at 9p21.2 and 19p13.3Max Koppers, Ewout J N Groen, Paul W J van Vught, et al.
Neurobiology of Aging|April 18, 2012
CGG-repeat expansion in FMR1 is not associated with amyotrophic lateral sclerosisEwout J N Groen, Wouter van Rheenen, Max Koppers, et al.
Neurobiology of Aging|August 11, 2012
VAPB and C9orf72 mutations in 1 familial amyotrophic lateral sclerosis patientMarka van Blitterswijk, Michael A van Es, Max Koppers, et al.
Developmental Cell|May 30, 2024
Axonal endoplasmic reticulum tubules control local translation via P180/RRBP1-mediated ribosome interactionsMax Koppers, Nazmiye Özkan, Ha H Nguyen, et al.
Elife|November 21, 2019
Receptor-specific interactome as a hub for rapid cue-induced selective translation in axonsMax Koppers, Roberta Cagnetta, Toshiaki Shigeoka, et al.
Annals of Neurology|June 6, 2015
C9orf72 ablation in mice does not cause motor neuron degeneration or motor deficitsMax Koppers, Anna M Blokhuis, Henk-Jan Westeneng, et al.
Neurobiology of Aging|November 29, 2011
UNC13A is a modifier of survival in amyotrophic lateral sclerosisFrank P Diekstra, Paul W J van Vught, Wouter van Rheenen, et al.
Cell Reports|December 12, 2019
On-Site Ribosome Remodeling by Locally Synthesized Ribosomal Proteins in AxonsToshiaki Shigeoka, Max Koppers, Hovy Ho-Wai Wong, et al.
Human Molecular Genetics|March 2, 2012
NIPA1 polyalanine repeat expansions are associated with amyotrophic lateral sclerosisHylke M Blauw, Wouter van Rheenen, Max Koppers, et al.
Neurobiology of Aging|November 15, 2011
VCP mutations in familial and sporadic amyotrophic lateral sclerosisMax Koppers, Marka M van Blitterswijk, Lotte Vlam, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Neurobiology of Aging|November 13, 2012
Screening for rare variants in the coding region of ALS-associated genes at 9p21.2 and 19p13.3Max Koppers, Ewout J N Groen, Paul W J van Vught, et al.
Neurobiology of Aging|April 18, 2012
CGG-repeat expansion in FMR1 is not associated with amyotrophic lateral sclerosisEwout J N Groen, Wouter van Rheenen, Max Koppers, et al.
Neurobiology of Aging|August 11, 2012
VAPB and C9orf72 mutations in 1 familial amyotrophic lateral sclerosis patientMarka van Blitterswijk, Michael A van Es, Max Koppers, et al.
Developmental Cell|May 30, 2024
Axonal endoplasmic reticulum tubules control local translation via P180/RRBP1-mediated ribosome interactionsMax Koppers, Nazmiye Özkan, Ha H Nguyen, et al.
Elife|November 21, 2019
Receptor-specific interactome as a hub for rapid cue-induced selective translation in axonsMax Koppers, Roberta Cagnetta, Toshiaki Shigeoka, et al.
Annals of Neurology|June 6, 2015
C9orf72 ablation in mice does not cause motor neuron degeneration or motor deficitsMax Koppers, Anna M Blokhuis, Henk-Jan Westeneng, et al.
Neurobiology of Aging|November 29, 2011
UNC13A is a modifier of survival in amyotrophic lateral sclerosisFrank P Diekstra, Paul W J van Vught, Wouter van Rheenen, et al.
Cell Reports|December 12, 2019
On-Site Ribosome Remodeling by Locally Synthesized Ribosomal Proteins in AxonsToshiaki Shigeoka, Max Koppers, Hovy Ho-Wai Wong, et al.
Human Molecular Genetics|March 2, 2012
NIPA1 polyalanine repeat expansions are associated with amyotrophic lateral sclerosisHylke M Blauw, Wouter van Rheenen, Max Koppers, et al.
Neurobiology of Aging|November 15, 2011
VCP mutations in familial and sporadic amyotrophic lateral sclerosisMax Koppers, Marka M van Blitterswijk, Lotte Vlam, et al.
Pageof 3