Modulation of mutant superoxide dismutase 1 aggregation by co-expression of wild-type enzyme (Q33570225)

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English	Modulation of mutant superoxide dismutase 1 aggregation by co-expression of wild-type enzyme	scientific article

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instance of

scholarly article

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Europe PubMed Central

PubMed publication ID

19077113

retrieved

28 July 2017

title

Modulation of mutant superoxide dismutase 1 aggregation by co-expression of wild-type enzyme (English)

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stated in

Europe PubMed Central

PubMed publication ID

19077113

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28 July 2017

author

Mercedes Prudencio

object named as

Mercedes Prudencio

series ordinal

1

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Julian P Whitelegge

series ordinal

3

object named as

Julian P Whitelegge

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stated in

Europe PubMed Central

PubMed publication ID

19077113

retrieved

28 July 2017

author name string

Armando Durazo

series ordinal

2

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Europe PubMed Central

PubMed publication ID

19077113

retrieved

28 July 2017

David R Borchelt

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19077113

retrieved

28 July 2017

language of work or name

English

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publication date

11 December 2008

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Europe PubMed Central

PubMed publication ID

19077113

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28 July 2017

number of pages

10

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published in

Journal of Neurochemistry

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Europe PubMed Central

PubMed publication ID

19077113

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28 July 2017

volume

108

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Europe PubMed Central

PubMed publication ID

19077113

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28 July 2017

issue

4

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Europe PubMed Central

PubMed publication ID

19077113

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28 July 2017

page(s)

1009-1018

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stated in

Europe PubMed Central

PubMed publication ID

19077113

retrieved

28 July 2017

cites work

A limited role for disulfide cross-linking in the aggregation of mutant SOD1 linked to familial amyotrophic lateral sclerosis.

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Detergent-insoluble aggregates associated with amyotrophic lateral sclerosis in transgenic mice contain primarily full-length, unmodified superoxide dismutase-1.

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Cysteine 111 affects aggregation and cytotoxicity of mutant Cu,Zn-superoxide dismutase associated with familial amyotrophic lateral sclerosis

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Overexpression of CCS in G93A-SOD1 mice leads to accelerated neurological deficits with severe mitochondrial pathology

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Conversion to the amyotrophic lateral sclerosis phenotype is associated with intermolecular linked insoluble aggregates of SOD1 in mitochondria

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Mapping superoxide dismutase 1 domains of non-native interaction: roles of intra- and intermolecular disulfide bonding in aggregation

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Intersheet rearrangement of polypeptides during nucleation of {beta}-sheet aggregates

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Copper-zinc superoxide dismutase and amyotrophic lateral sclerosis

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Prions as adaptive conduits of memory and inheritance

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Correlations among morphology, beta-sheet stability, and molecular structure in prion peptide aggregates

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Complex genetics of amyotrophic lateral sclerosis

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Unraveling the mechanisms involved in motor neuron degeneration in ALS

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Amyotrophic lateral sclerosis: a proposed mechanism

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

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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.

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Recent advances in research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1 gene mutations: neuronal Lewy body-like hyaline inclusions and astrocytic hyaline inclusions

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Familial amyotrophic lateral sclerosis with widespread vacuolation and hyaline inclusions

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21 June 2018

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

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

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PubMed Central

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21 June 2018

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

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PubMed Central

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21 June 2018

Transgenic mice carrying a human mutant superoxide dismutase transgene develop neuronal cytoskeletal pathology resembling human amyotrophic lateral sclerosis lesions

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PubMed Central

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21 June 2018

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

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PubMed Central

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21 June 2018

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

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PubMed Central

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21 June 2018

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

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PubMed Central

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21 June 2018

Serial transmission in rodents of neurodegeneration from transgenic mice expressing mutant prion protein

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PubMed Central

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21 June 2018

Superoxide dismutase is an abundant component in cell bodies, dendrites, and axons of motor neurons and in a subset of other neurons

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PubMed Central

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21 June 2018

Neuropathological changes in two lines of mice carrying a transgene for mutant human Cu,Zn SOD, and in mice overexpressing wild type human SOD: a model of familial amyotrophic lateral sclerosis (FALS).

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2801375

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21 June 2018

pEF-BOS, a powerful mammalian expression vector

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PubMed Central

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21 June 2018

Amyloid fibril formation requires a chemically discriminating nucleation event: studies of an amyloidogenic sequence from the bacterial protein OsmB

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21 June 2018

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

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PubMed Central

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31 October 2018

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

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2801375

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31 October 2018

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

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2801375

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31 October 2018

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

1 reference

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2801375

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31 October 2018

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

1 reference

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2801375

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31 October 2018

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

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PubMed Central

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31 October 2018

Accumulation of neurofilaments and SOD1-immunoreactive products in a patient with familial amyotrophic lateral sclerosis with I113T SOD1 mutation

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https://pubmed.ncbi.nlm.nih.gov/19077113

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12 December 2020

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

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/19077113

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12 December 2020

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Sporadic amyotrophic lateral sclerosis with dementia and Cu/Zn superoxide dismutase-positive Lewy body-like inclusions

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/19077113

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12 December 2020

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Astrocytic hyaline inclusions contain advanced glycation endproducts in familial amyotrophic lateral sclerosis with superoxide dismutase 1 gene mutation: immunohistochemical and immunoelectron microscopical analyses

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19077113

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12 December 2020

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Ultrastructural study of aggregates in the spinal cord of transgenic mice with a G93A mutant SOD1 gene

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19077113

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12 December 2020

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Somatodendritic accumulation of misfolded SOD1-L126Z in motor neurons mediates degeneration: alphaB-crystallin modulates aggregation

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19077113

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12 December 2020

based on heuristic

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Coincident thresholds of mutant protein for paralytic disease and protein aggregation caused by restrictively expressed superoxide dismutase cDNA

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19077113

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12 December 2020

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Motor neuron disease in transgenic mice with an H46R mutant SOD1 gene

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19077113

retrieved

12 December 2020

based on heuristic

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Aggregates of mutant protein appear progressively in dendrites, in periaxonal processes of oligodendrocytes, and in neuronal and astrocytic perikarya of mice expressing the SOD1(G93A) mutation of familial amyotrophic lateral sclerosis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19077113

retrieved

12 December 2020

based on heuristic

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Identifiers

DOI

10.1111/J.1471-4159.2008.05839.X

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19077113

retrieved

28 July 2017

PMC publication ID

2801375

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19077113

retrieved

28 July 2017

PubMed publication ID

19077113

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19077113

retrieved

28 July 2017

ResearchGate publication ID

23657983

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