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Inhibition of fast axonal transport by pathogenic SOD1 involves activation of p38 MAP kinase

PloS one, 2013-06, Vol.8 (6), p.e65235

2013

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A yeast model of FUS/TLS-dependent cytotoxicity

PLoS biology, 2011-04, Vol.9 (4), p.e1001052-e1001052

2011

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Nuclear Localization of Huntingtin mRNA Is Specific to Cells of Neuronal Origin

Cell reports (Cambridge), 2018-09, Vol.24 (10), p.2553-2560.e5

2018

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Familial Amyotrophic Lateral Sclerosis Mutants of Copper/Zinc Superoxide Dismutase Are Susceptible to Disulfide Reduction

The Journal of biological chemistry, 2003-02, Vol.278 (8), p.5984-5992

2003

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Meeting report: the 2021 FSHD International Research Congress

Skeletal muscle, 2022-01, Vol.12 (1), p.1-1, Article 1

2022

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Interaction between Familial Amyotrophic Lateral Sclerosis (ALS)-linked SOD1 Mutants and the Dynein Complex

The Journal of biological chemistry, 2007-06, Vol.282 (22), p.16691-16699

2007

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iMyoblasts for ex vivo and in vivo investigations of human myogenesis and disease modeling

eLife, 2022-01, Vol.11

2022

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Outcome Measures in Facioscapulohumeral Muscular Dystrophy Clinical Trials

Cells (Basel, Switzerland), 2022-02, Vol.11 (4), p.687

2022

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Decreased Metallation and Activity in Subsets of Mutant Superoxide Dismutases Associated with Familial Amyotrophic Lateral Sclerosis

The Journal of biological chemistry, 2002-05, Vol.277 (18), p.15923-15931

2002

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Aberrantly Increased Hydrophobicity Shared by Mutants of Cu,Zn-Superoxide Dismutase in Familial Amyotrophic Lateral Sclerosis

The Journal of biological chemistry, 2005-08, Vol.280 (33), p.29771-29779

2005

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Sensitive and Specific Identification of Wild Type and Variant Proteins from 8 to 669 kDa Using Top-down Mass Spectrometry

Molecular & cellular proteomics, 2009-04, Vol.8 (4), p.846-856

2009

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Dimer Destabilization in Superoxide Dismutase May Result in Disease-Causing Properties: Structures of Motor Neuron Disease Mutants

Proceedings of the National Academy of Sciences - PNAS, 2004-04, Vol.101 (16), p.5976-5981

2004

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The Structure of Holo and Metal-deficient Wild-type Human Cu, Zn Superoxide Dismutase and its Relevance to Familial Amyotrophic Lateral Sclerosis

Journal of molecular biology, 2003-05, Vol.328 (4), p.877-891

2003

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Metal Deficiency Increases Aberrant Hydrophobicity of Mutant Superoxide Dismutases That Cause Amyotrophic Lateral Sclerosis

The Journal of biological chemistry, 2009-10, Vol.284 (40), p.27746-27758

2009

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Destabilization of Apoprotein Is Insufficient to Explain Cu,Zn-Superoxide Dismutase-Linked ALS Pathogenesis

Proceedings of the National Academy of Sciences - PNAS, 2005-07, Vol.102 (30), p.10516-10521

2005

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Familial Amyotrophic Lateral Sclerosis-associated Mutations Decrease the Thermal Stability of Distinctly Metallated Species of Human Copper/Zinc Superoxide Dismutase

The Journal of biological chemistry, 2002-05, Vol.277 (18), p.15932-15937

2002

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Retrograde axonal transport and motor neuron disease

Journal of neurochemistry, 2008-07, Vol.106 (2), p.495-505

2008

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Lower Ca2+ enhances the K+-induced force depression in normal and HyperKPP mouse muscles

The Journal of general physiology, 2020-07, Vol.152 (7)

2020

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Structures of the G85R Variant of SOD1 in Familial Amyotrophic Lateral Sclerosis

The Journal of biological chemistry, 2008-06, Vol.283 (23), p.16169-16177

2008

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Detergent-insoluble Aggregates Associated with Amyotrophic Lateral Sclerosis in Transgenic Mice Contain Primarily Full-length, Unmodified Superoxide Dismutase-1

The Journal of biological chemistry, 2008-03, Vol.283 (13), p.8340-8350

2008

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Mutant FUS proteins that cause amyotrophic lateral sclerosis incorporate into stress granules

Human molecular genetics, 2010-11, Vol.19 (21), p.4160-4175

2010

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Interaction of Amyotrophic Lateral Sclerosis (ALS)-related Mutant Copper-Zinc Superoxide Dismutase with the Dynein-Dynactin Complex Contributes to Inclusion Formation

The Journal of biological chemistry, 2008-08, Vol.283 (33), p.22795-22805

2008

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ALS mutant SOD1 interacts with G3BP1 and affects stress granule dynamics

Acta neuropathologica, 2016-10, Vol.132 (4), p.563-576

2016

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Renewal of oligodendrocyte lineage reverses dysmyelination and CNS neurodegeneration through corrected N-acetylaspartate metabolism

Progress in neurobiology, 2023-07, Vol.226, p.102460-102460, Article 102460

2023

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Safety and efficacy of losmapimod in facioscapulohumeral muscular dystrophy (ReDUX4): a randomised, double-blind, placebo-controlled phase 2b trial

Lancet neurology, 2024-05, Vol.23 (5), p.477-486

2024

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Inhibition of fast axonal transport by pathogenic SOD1 involves activation of p38 MAP kinase

A yeast model of FUS/TLS-dependent cytotoxicity

Nuclear Localization of Huntingtin mRNA Is Specific to Cells of Neuronal Origin

Familial Amyotrophic Lateral Sclerosis Mutants of Copper/Zinc Superoxide Dismutase Are Susceptible to Disulfide Reduction

Meeting report: the 2021 FSHD International Research Congress

Interaction between Familial Amyotrophic Lateral Sclerosis (ALS)-linked SOD1 Mutants and the Dynein Complex

iMyoblasts for ex vivo and in vivo investigations of human myogenesis and disease modeling

Outcome Measures in Facioscapulohumeral Muscular Dystrophy Clinical Trials

Decreased Metallation and Activity in Subsets of Mutant Superoxide Dismutases Associated with Familial Amyotrophic Lateral Sclerosis

Aberrantly Increased Hydrophobicity Shared by Mutants of Cu,Zn-Superoxide Dismutase in Familial Amyotrophic Lateral Sclerosis

Sensitive and Specific Identification of Wild Type and Variant Proteins from 8 to 669 kDa Using Top-down Mass Spectrometry

Dimer Destabilization in Superoxide Dismutase May Result in Disease-Causing Properties: Structures of Motor Neuron Disease Mutants

The Structure of Holo and Metal-deficient Wild-type Human Cu, Zn Superoxide Dismutase and its Relevance to Familial Amyotrophic Lateral Sclerosis

Metal Deficiency Increases Aberrant Hydrophobicity of Mutant Superoxide Dismutases That Cause Amyotrophic Lateral Sclerosis

Destabilization of Apoprotein Is Insufficient to Explain Cu,Zn-Superoxide Dismutase-Linked ALS Pathogenesis

Familial Amyotrophic Lateral Sclerosis-associated Mutations Decrease the Thermal Stability of Distinctly Metallated Species of Human Copper/Zinc Superoxide Dismutase

Retrograde axonal transport and motor neuron disease

Lower Ca2+ enhances the K+-induced force depression in normal and HyperKPP mouse muscles

Structures of the G85R Variant of SOD1 in Familial Amyotrophic Lateral Sclerosis

Detergent-insoluble Aggregates Associated with Amyotrophic Lateral Sclerosis in Transgenic Mice Contain Primarily Full-length, Unmodified Superoxide Dismutase-1

Mutant FUS proteins that cause amyotrophic lateral sclerosis incorporate into stress granules

Interaction of Amyotrophic Lateral Sclerosis (ALS)-related Mutant Copper-Zinc Superoxide Dismutase with the Dynein-Dynactin Complex Contributes to Inclusion Formation

ALS mutant SOD1 interacts with G3BP1 and affects stress granule dynamics

Renewal of oligodendrocyte lineage reverses dysmyelination and CNS neurodegeneration through corrected N-acetylaspartate metabolism

Safety and efficacy of losmapimod in facioscapulohumeral muscular dystrophy (ReDUX4): a randomised, double-blind, placebo-controlled phase 2b trial

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