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Robberecht

Showing results (571-580 of 651) with videos related to

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Cell Reports|July 19, 2018
Molecular Dissection of FUS Points at Synergistic Effect of Low-Complexity Domains in ToxicityElke Bogaert, Steven Boeynaems, Masato Kato, et al.
Neurology|September 30, 2010
Mutations in SACS cause atypical and late-onset forms of ARSACSJ Baets, T Deconinck, K Smets, et al.
Human Molecular Genetics|November 18, 1998
Recessive amyotrophic lateral sclerosis families with the D90A SOD1 mutation share a common founder: evidence for a linked protective factorA Al-Chalabi, P M Andersen, B Chioza, et al.
Acta Neuropathologica|January 6, 2018
A zebrafish model for C9orf72 ALS reveals RNA toxicity as a pathogenic mechanismBart Swinnen, Andre Bento-Abreu, Tania F Gendron, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|February 27, 2010
Guidelines for preclinical animal research in ALS/MND: A consensus meetingAlbert C Ludolph, Caterina Bendotti, Eran Blaugrund, et al.
The Journal of Biological Chemistry|May 21, 2017
Identification and characterization of Nanobodies targeting the EphA4 receptorLies Schoonaert, Laura Rué, Bart Roucourt, et al.
Journal of Neuropathology and Experimental Neurology|November 26, 2010
Microglial upregulation of progranulin as a marker of motor neuron degenerationThomas Philips, Louis De Muynck, Hoai Nguyen Thi Thu, 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.
Neurobiology of Aging|December 11, 2007
Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALSIlse Gijselinck, Kristel Sleegers, Sebastiaan Engelborghs, 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.
Pageof 66

Showing results (571-580 of 651) with videos related to

Sort By:
Pageof 66
Cell Reports|July 19, 2018
Molecular Dissection of FUS Points at Synergistic Effect of Low-Complexity Domains in ToxicityElke Bogaert, Steven Boeynaems, Masato Kato, et al.
Neurology|September 30, 2010
Mutations in SACS cause atypical and late-onset forms of ARSACSJ Baets, T Deconinck, K Smets, et al.
Human Molecular Genetics|November 18, 1998
Recessive amyotrophic lateral sclerosis families with the D90A SOD1 mutation share a common founder: evidence for a linked protective factorA Al-Chalabi, P M Andersen, B Chioza, et al.
Acta Neuropathologica|January 6, 2018
A zebrafish model for C9orf72 ALS reveals RNA toxicity as a pathogenic mechanismBart Swinnen, Andre Bento-Abreu, Tania F Gendron, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|February 27, 2010
Guidelines for preclinical animal research in ALS/MND: A consensus meetingAlbert C Ludolph, Caterina Bendotti, Eran Blaugrund, et al.
The Journal of Biological Chemistry|May 21, 2017
Identification and characterization of Nanobodies targeting the EphA4 receptorLies Schoonaert, Laura Rué, Bart Roucourt, et al.
Journal of Neuropathology and Experimental Neurology|November 26, 2010
Microglial upregulation of progranulin as a marker of motor neuron degenerationThomas Philips, Louis De Muynck, Hoai Nguyen Thi Thu, 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.
Neurobiology of Aging|December 11, 2007
Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALSIlse Gijselinck, Kristel Sleegers, Sebastiaan Engelborghs, 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.
Pageof 66