Novel mutations that enhance or repress the aggregation potential of SOD1. (Q40296867)

19 September 2017

title

Novel mutations that enhance or repress the aggregation potential of SOD1. (English)

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19 September 2017

Uma Krishnan

1

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19 September 2017

Marjatta Son

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2

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19 September 2017

Bhagya Rajendran

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3

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19 September 2017

Jeffrey L Elliott

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4

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19 September 2017

publication date

1 April 2006

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Molecular and Cellular Biochemistry

19 September 2017

published in

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19 September 2017

volume

287

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19 September 2017

issue

1-2

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19 September 2017

page(s)

201-211

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Aggregate formation in Cu,Zn superoxide dismutase-related proteins

19 September 2017

cites work

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12 December 2020

Proteasomal inhibition causes the formation of protein aggregates containing a wide range of proteins, including nitrated proteins

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12 December 2020

Induction of nitric oxide-dependent apoptosis in motor neurons by zinc-deficient superoxide dismutase

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12 December 2020

Current status of SOD1 mutations in familial amyotrophic lateral sclerosis

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12 December 2020

Copper-binding-site-null SOD1 causes ALS in transgenic mice: aggregates of non-native SOD1 delineate a common feature

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12 December 2020

Dorfin ubiquitylates mutant SOD1 and prevents mutant SOD1-mediated neurotoxicity

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12 December 2020

Transgenic mice expressing an altered murine superoxide dismutase gene provide an animal model of amyotrophic lateral sclerosis

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12 December 2020

Mutant SOD1 causes motor neuron disease independent of copper chaperone-mediated copper loading

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12 December 2020

Intense superoxide dismutase-1 immunoreactivity in intracytoplasmic hyaline inclusions of familial amyotrophic lateral sclerosis with posterior column involvement

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12 December 2020

An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria

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12 December 2020

Decreased metallation and activity in subsets of mutant superoxide dismutases associated with familial amyotrophic lateral sclerosis.

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12 December 2020

Decreased zinc affinity of amyotrophic lateral sclerosis-associated superoxide dismutase mutants leads to enhanced catalysis of tyrosine nitration by peroxynitrite

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12 December 2020

Fibrillar inclusions and motor neuron degeneration in transgenic mice expressing superoxide dismutase 1 with a disrupted copper-binding site

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12 December 2020

Oxidation-induced misfolding and aggregation of superoxide dismutase and its implications for amyotrophic lateral sclerosis

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12 December 2020

Serine 776 of ataxin-1 is critical for polyglutamine-induced disease in SCA1 transgenic mice

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12 December 2020

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

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12 December 2020

Interaction of Akt-phosphorylated ataxin-1 with 14-3-3 mediates neurodegeneration in spinocerebellar ataxia type 1.

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12 December 2020

Oligomeric and polymeric aggregates formed by proteins containing expanded polyglutamine

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12 December 2020

Impairment of the ubiquitin-proteasome system by protein aggregation

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12 December 2020

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

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12 December 2020

Histological evidence of protein aggregation in mutant SOD1 transgenic mice and in amyotrophic lateral sclerosis neural tissues

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12 December 2020

Misfolded CuZnSOD and amyotrophic lateral sclerosis

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12 December 2020

High molecular weight complexes of mutant superoxide dismutase 1: age-dependent and tissue-specific accumulation

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12 December 2020

Superoxide dismutase 1 with mutations linked to familial amyotrophic lateral sclerosis possesses significant activity

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12 December 2020

Zinc and copper in the pathogenesis of amyotrophic lateral sclerosis

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12 December 2020

Common denominator of Cu/Zn superoxide dismutase mutants associated with amyotrophic lateral sclerosis: decreased stability of the apo state

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12 December 2020

Mutation of the E6-AP ubiquitin ligase reduces nuclear inclusion frequency while accelerating polyglutamine-induced pathology in SCA1 mice.

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12 December 2020

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

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12 December 2020

Formation of high molecular weight complexes of mutant Cu, Zn-superoxide dismutase in a mouse model for familial amyotrophic lateral sclerosis.

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12 December 2020

Parkin protects against the toxicity associated with mutant alpha-synuclein: proteasome dysfunction selectively affects catecholaminergic neurons

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12 December 2020

The copper chaperone for superoxide dismutase

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12 December 2020

Disease progression in a transgenic model of familial amyotrophic lateral sclerosis is dependent on both neuronal and non-neuronal zinc binding proteins

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12 December 2020

NEDL1, a novel ubiquitin-protein isopeptide ligase for dishevelled-1, targets mutant superoxide dismutase-1.

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12 December 2020

Motor neurons in Cu/Zn superoxide dismutase-deficient mice develop normally but exhibit enhanced cell death after axonal injury

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12 December 2020

Ataxin-1 nuclear localization and aggregation: role in polyglutamine-induced disease in SCA1 transgenic mice

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12 December 2020

10.1007/S11010-005-9112-4

Identifiers

DOI

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19 September 2017

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