(Q41087321)

26 September 2017

title

Aberrant association of misfolded SOD1 with Na(+)/K(+)ATPase-α3 impairs its activity and contributes to motor neuron vulnerability in ALS. (English)

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amyotrophic lateral sclerosis

26 September 2017

main subject

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9

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26 September 2017

Céline Ruegsegger

1

1 reference

26 September 2017

Niran Maharjan

2

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26 September 2017

Anand Goswami

3

1 reference

26 September 2017

Audrey Filézac de L'Etang

4

1 reference

26 September 2017

Joachim Weis

5

1 reference

26 September 2017

Dirk Troost

6

1 reference

26 September 2017

Manfred Heller

7

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26 September 2017

Heinz Gut

8

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26 September 2017

publication date

30 November 2015

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26 September 2017

published in

Acta Neuropathologica

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26 September 2017

volume

131

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26 September 2017

issue

3

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26 September 2017

page(s)

427-451

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Cause or effect of arteriogenesis: compositional alterations of microparticles from CAD patients undergoing external counterpulsation therapy

26 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Endoplasmic reticulum stress and induction of the unfolded protein response in human sporadic amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

A specific and essential role for Na,K-ATPase α3 in neurons co-expressing α1 and α3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Structural and kinetic analysis of protein-aggregate strains in vivo using binary epitope mapping

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

The precise engineering of expression vectors using high-throughput In-Fusion PCR cloning.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Comparison of the enzymic properties of the Na,K-ATPase .alpha.3.beta.1 and .alpha.3.beta.2 isoenzymes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Wild-type and mutant SOD1 share an aberrant conformation and a common pathogenic pathway in ALS

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Glycinergic innervation of motoneurons is deficient in amyotrophic lateral sclerosis mice: a quantitative confocal analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Automatic and quantitative measurement of protein-protein colocalization in live cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Mutations in the Na+/K+ -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Human iPSC-derived motoneurons harbouring TARDBP or C9ORF72 ALS mutations are dysfunctional despite maintaining viability

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Intracerebroventricular injection of adeno-associated virus 6 and 9 vectors for cell type-specific transgene expression in the spinal cord

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Neuronal function and alpha3 isoform of the Na/K-ATPase.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Identification of novel spinal cholinergic genetic subtypes disclose Chodl and Pitx2 as markers for fast motor neurons and partition cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Mutant SOD1-expressing astrocytes release toxic factors that trigger motoneuron death by inducing hyperexcitability

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Current status of SOD1 mutations in familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Hyperpolarizing current of the Na/K ATPase contributes to the membrane polarization of the Purkinje cell in rat cerebellum

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

An over-oxidized form of superoxide dismutase found in sporadic amyotrophic lateral sclerosis with bulbar onset shares a toxic mechanism with mutant SOD1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Proteome remodelling during development from blood to insect-form Trypanosoma brucei quantified by SILAC and mass spectrometry

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Differential distribution of (Na, K)-ATPase? isoforms in the central nervous system

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Alterations on Na⁺,K⁺-ATPase and acetylcholinesterase activities induced by amyloid-β peptide in rat brain and GM1 ganglioside neuroprotective action

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

A computational model of motor neuron degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Early intrinsic hyperexcitability does not contribute to motoneuron degeneration in amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Changes in Na+,K(+)-ATPase, Ca2(+)-ATPase and some soluble enzymes related to energy metabolism in brains of patients with Alzheimer's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

The physiological significance of the cardiotonic steroid/ouabain-binding site of the Na,K-ATPase

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Toxicity of familial ALS-linked SOD1 mutants from selective recruitment to spinal mitochondria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Incidence of amyotrophic lateral sclerosis in Europe

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Survival of patients with amyotrophic lateral sclerosis in a population-based registry

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

ALS-linked mutant SOD1 induces ER stress- and ASK1-dependent motor neuron death by targeting Derlin-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Early excitability changes in lumbar motoneurons of transgenic SOD1G85R and SOD1G(93A-Low) mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Enhanced sensitivity of DJ-1-deficient dopaminergic neurons to energy metabolism impairment: role of Na+/K+ ATPase

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Aggregate formation in the spinal cord of mutant SOD1 transgenic mice is reversible and mediated by proteasomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Monomeric Cu,Zn-superoxide dismutase is a common misfolding intermediate in the oxidation models of sporadic and familial amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

An immunological epitope selective for pathological monomer-misfolded SOD1 in ALS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Lentiviral-mediated silencing of SOD1 through RNA interference retards disease onset and progression in a mouse model of ALS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

An emerging role for misfolded wild-type SOD1 in sporadic ALS pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

A role for motoneuron subtype-selective ER stress in disease manifestations of FALS mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Selective neuronal vulnerability in neurodegenerative diseases: from stressor thresholds to degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Neuroprotection through excitability and mTOR required in ALS motoneurons to delay disease and extend survival

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Imbalanced excitatory to inhibitory synaptic input precedes motor neuron degeneration in an animal model of amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Crystal structure of the sodium-potassium pump at 2.4 A resolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Glutamate AMPA receptors change in motor neurons of SOD1G93A transgenic mice and their inhibition by a noncompetitive antagonist ameliorates the progression of amytrophic lateral sclerosis-like disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Therapeutic effects of immunization with mutant superoxide dismutase in mice models of amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Homeostatic dysregulation in membrane properties of masticatory motoneurons compared with oculomotor neurons in a mouse model for amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Upregulation of persistent sodium conductances in familial ALS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Cortical hyperexcitability may precede the onset of familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Intrinsic membrane hyperexcitability of amyotrophic lateral sclerosis patient-derived motor neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

Na,K-ATPase activity regulates AMPA receptor turnover through proteasome-mediated proteolysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

ALSOD: The Amyotrophic Lateral Sclerosis Online Database

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-015-1510-4

10.1007/S00401-015-1510-4

21 January 2018

Identifiers

DOI

1 reference

26 September 2017

1 reference