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Peter M Andersen

Showing results (31-40 of 241) with videos related to

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The Journal of Biological Chemistry|April 16, 2011
Proteins that bind to misfolded mutant superoxide dismutase-1 in spinal cords from transgenic amyotrophic lateral sclerosis (ALS) model micePer Zetterström, Karin S Graffmo, Peter M Andersen, et al.
JAMA Neurology|November 29, 2016
Association of Mutations in TBK1 With Sporadic and Familial Amyotrophic Lateral Sclerosis and Frontotemporal DementiaAxel Freischmidt, Kathrin Müller, Albert C Ludolph, et al.
The Journal of Biological Chemistry|May 22, 2007
Amyotrophic lateral sclerosis-associated copper/zinc superoxide dismutase mutations preferentially reduce the repulsive charge of the proteinsErik Sandelin, Anna Nordlund, Peter M Andersen, et al.
Investigative Ophthalmology & Visual Science|July 25, 2017
Impact of Amyotrophic Lateral Sclerosis on Slow Tonic Myofiber Composition in Human Extraocular MusclesAnton E Tjust, Adam Danielsson, Peter M Andersen, et al.
Neuromolecular Medicine|October 19, 2012
Composition of soluble misfolded superoxide dismutase-1 in murine models of amyotrophic lateral sclerosisPer Zetterström, Karin S Graffmo, Peter M Andersen, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|January 5, 2012
Early onset Parkinsonism associated with an intronic SOD1 mutationImen Kacem, Benoît Funalot, Frédéric Torny, et al.
Frontiers in Neuroscience|October 5, 2020
Commentary: Effects of ALS-associated TANK binding kinase 1 mutations on protein-protein interactions and kinase activityAxel Freischmidt, David Brenner, Albert C Ludolph, et al.
Plos One|November 22, 2014
Cholesterol, oxysterol, triglyceride, and coenzyme Q homeostasis in ALS. Evidence against the hypothesis that elevated 27-hydroxycholesterol is a pathogenic factorAnna Wuolikainen, Jure Acimovic, Anita Lövgren-Sandblom, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|September 18, 2018
Current knowledge and recent insights into the genetic basis of amyotrophic lateral sclerosisAlexander E Volk, Jochen H Weishaupt, Peter M Andersen, et al.
Human Molecular Genetics|June 1, 2025
Diverse effects of coexpression of human SOD1 variants on motor neuron diseaseEiichi Tokuda, Laura Leykam, Per Zetterström, et al.
Pageof 25

Showing results (31-40 of 241) with videos related to

Sort By:
Pageof 25
The Journal of Biological Chemistry|April 16, 2011
Proteins that bind to misfolded mutant superoxide dismutase-1 in spinal cords from transgenic amyotrophic lateral sclerosis (ALS) model micePer Zetterström, Karin S Graffmo, Peter M Andersen, et al.
JAMA Neurology|November 29, 2016
Association of Mutations in TBK1 With Sporadic and Familial Amyotrophic Lateral Sclerosis and Frontotemporal DementiaAxel Freischmidt, Kathrin Müller, Albert C Ludolph, et al.
The Journal of Biological Chemistry|May 22, 2007
Amyotrophic lateral sclerosis-associated copper/zinc superoxide dismutase mutations preferentially reduce the repulsive charge of the proteinsErik Sandelin, Anna Nordlund, Peter M Andersen, et al.
Investigative Ophthalmology & Visual Science|July 25, 2017
Impact of Amyotrophic Lateral Sclerosis on Slow Tonic Myofiber Composition in Human Extraocular MusclesAnton E Tjust, Adam Danielsson, Peter M Andersen, et al.
Neuromolecular Medicine|October 19, 2012
Composition of soluble misfolded superoxide dismutase-1 in murine models of amyotrophic lateral sclerosisPer Zetterström, Karin S Graffmo, Peter M Andersen, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|January 5, 2012
Early onset Parkinsonism associated with an intronic SOD1 mutationImen Kacem, Benoît Funalot, Frédéric Torny, et al.
Frontiers in Neuroscience|October 5, 2020
Commentary: Effects of ALS-associated TANK binding kinase 1 mutations on protein-protein interactions and kinase activityAxel Freischmidt, David Brenner, Albert C Ludolph, et al.
Plos One|November 22, 2014
Cholesterol, oxysterol, triglyceride, and coenzyme Q homeostasis in ALS. Evidence against the hypothesis that elevated 27-hydroxycholesterol is a pathogenic factorAnna Wuolikainen, Jure Acimovic, Anita Lövgren-Sandblom, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|September 18, 2018
Current knowledge and recent insights into the genetic basis of amyotrophic lateral sclerosisAlexander E Volk, Jochen H Weishaupt, Peter M Andersen, et al.
Human Molecular Genetics|June 1, 2025
Diverse effects of coexpression of human SOD1 variants on motor neuron diseaseEiichi Tokuda, Laura Leykam, Per Zetterström, et al.
Pageof 25