Search research articles
Contact Us
Filters
Showing results (571-580 of 651) with videos related to
Page
of 66
Sort By:
Cell Reports
|
July 19, 2018
Molecular Dissection of FUS Points at Synergistic Effect of Low-Complexity Domains in Toxicity
Elke Bogaert, Steven Boeynaems, Masato Kato, et al.
Neurology
|
September 30, 2010
Mutations in SACS cause atypical and late-onset forms of ARSACS
J 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 factor
A 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 mechanism
Bart 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 meeting
Albert C Ludolph, Caterina Bendotti, Eran Blaugrund, et al.
The Journal of Biological Chemistry
|
May 21, 2017
Identification and characterization of Nanobodies targeting the EphA4 receptor
Lies 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 degeneration
Thomas 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 sclerosis
Frank 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 ALS
Ilse Gijselinck, Kristel Sleegers, Sebastiaan Engelborghs, et al.
Human Molecular Genetics
|
March 2, 2012
NIPA1 polyalanine repeat expansions are associated with amyotrophic lateral sclerosis
Hylke M Blauw, Wouter van Rheenen, Max Koppers, et al.
Page
of 66
Search research articles
Search
Showing results (571-580 of 651) with videos related to
Sort By:
Page
of 66
Cell Reports
|
July 19, 2018
Molecular Dissection of FUS Points at Synergistic Effect of Low-Complexity Domains in Toxicity
Elke Bogaert, Steven Boeynaems, Masato Kato, et al.
Neurology
|
September 30, 2010
Mutations in SACS cause atypical and late-onset forms of ARSACS
J 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 factor
A 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 mechanism
Bart 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 meeting
Albert C Ludolph, Caterina Bendotti, Eran Blaugrund, et al.
The Journal of Biological Chemistry
|
May 21, 2017
Identification and characterization of Nanobodies targeting the EphA4 receptor
Lies 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 degeneration
Thomas 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 sclerosis
Frank 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 ALS
Ilse Gijselinck, Kristel Sleegers, Sebastiaan Engelborghs, et al.
Human Molecular Genetics
|
March 2, 2012
NIPA1 polyalanine repeat expansions are associated with amyotrophic lateral sclerosis
Hylke M Blauw, Wouter van Rheenen, Max Koppers, et al.
Page
of 66