Decreased metallation and activity in subsets of mutant superoxide dismutases associated with familial amyotrophic lateral sclerosis. (Q38291855)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11854284%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

title

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

1 reference

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amyotrophic lateral sclerosis

7 December 2019

main subject

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author

Ashutosh Tiwari

4

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7 December 2019

8

Robert H Brown

1 reference

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7 December 2019

author name string

Lawrence J Hayward

1

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7 December 2019

Jorge A Rodriguez

2

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7 December 2019

Ji W Kim

3

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7 December 2019

Joy J Goto

5

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7 December 2019

Diane E Cabelli

6

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7 December 2019

Joan Selverstone Valentine

7

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7 December 2019

language of work or name

English

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publication date

19 February 2002

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Journal of Biological Chemistry

7 December 2019

number of pages

9

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based on heuristic

inferred from page(s)

published in

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7 December 2019

volume

277

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7 December 2019

issue

18

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7 December 2019

page(s)

15923-15931

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Amyotrophic lateral sclerosis: recent insights from genetics and transgenic mice

7 December 2019

cites work

1 reference

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

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Current status of SOD1 mutations in familial amyotrophic lateral sclerosis

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From Charcot to Lou Gehrig: deciphering selective motor neuron death in ALS

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

21 January 2018

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

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

21 January 2018

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

21 January 2018

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ALS-linked SOD1 mutant G85R mediates damage to astrocytes and promotes rapidly progressive disease with SOD1-containing inclusions.

21 January 2018

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Human Cu/Zn superoxide dismutase (SOD1) overexpression in mice causes mitochondrial vacuolization, axonal degeneration, and premature motoneuron death and accelerates motoneuron disease in mice expressing a familial amyotrophic lateral sclerosis mut

21 January 2018

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Aggregation and Motor Neuron Toxicity of an ALS-Linked SOD1 Mutant Independent from Wild-Type SOD1

21 January 2018

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Mutations in copper-zinc superoxide dismutase that cause amyotrophic lateral sclerosis alter the zinc binding site and the redox behavior of the protein

21 January 2018

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Loss of in vitro metal ion binding specificity in mutant copper-zinc superoxide dismutases associated with familial amyotrophic lateral sclerosis

21 January 2018

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Loss of oxidation-reduction specificity in amyotrophic lateral sclerosis-associated CuZnSOD mutants.

21 January 2018

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Efficient amplification using 'megaprimer' by asymmetric polymerase chain reaction

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Approaches to DNA mutagenesis: an overview

21 January 2018

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How to measure and predict the molar absorption coefficient of a protein

21 January 2018

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Epidemiology of mutations in superoxide dismutase in amyotrophic lateral sclerosis

21 January 2018

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Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase

21 January 2018

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Subunit asymmetry in the three-dimensional structure of a human CuZnSOD mutant found in familial amyotrophic lateral sclerosis

21 January 2018

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A structure-based mechanism for copper-zinc superoxide dismutase

21 January 2018

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Three novel mutations and two variants in the gene for Cu/Zn superoxide dismutase in familial amyotrophic lateral sclerosis.

21 January 2018

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

21 January 2018

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Tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis for the separation of proteins in the range from 1 to 100 kDa

21 January 2018

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Superoxide dismutase in familial amyotrophic lateral sclerosis: models for gain of function

21 January 2018

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Oxidation versus aggregation - how do SOD1 mutants cause ALS?

21 January 2018

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Superoxide dismutase and the death of motoneurons in ALS.

21 January 2018

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Altered reactivity of superoxide dismutase in familial amyotrophic lateral sclerosis

21 January 2018

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A gain-of-function of an amyotrophic lateral sclerosis-associated Cu,Zn-superoxide dismutase mutant: An enhancement of free radical formation due to a decrease in Km for hydrogen peroxide

21 January 2018

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Up-regulation of protein chaperones preserves viability of cells expressing toxic Cu/Zn-superoxide dismutase mutants associated with amyotrophic lateral sclerosis

21 January 2018

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

21 January 2018

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Variation in the biochemical/biophysical properties of mutant superoxide dismutase 1 enzymes and the rate of disease progression in familial amyotrophic lateral sclerosis kindreds.

21 January 2018

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Toxicity of ALS-linked SOD1 mutants

21 January 2018

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Familial amyotrophic lateral sclerosis-associated mutations decrease the thermal stability of distinctly metallated species of human copper/zinc superoxide dismutase

21 January 2018

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21 January 2018

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Atomic structures of wild-type and thermostable mutant recombinant human Cu,Zn superoxide dismutase

21 January 2018

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21 January 2018

Identifiers

DOI

10.1074/JBC.M112087200

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11854284%20AND%20SRC:MED&resulttype=core&format=json

release_i74ut34korf2lh3uols6d3pgdu

7 December 2019

Fatcat ID

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mapped directly with Wikidata item

24 November 2022

based on heuristic

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