Nuclear localization of human SOD1 and mutant SOD1-specific disruption of survival motor neuron protein complex in transgenic amyotrophic lateral sclerosis mice (Q36205839)

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English	Nuclear localization of human SOD1 and mutant SOD1-specific disruption of survival motor neuron protein complex in transgenic amyotrophic lateral sclerosis mice	scientific article

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scholarly article

1 reference

Europe PubMed Central

12 August 2017

Nuclear localization of human SOD1 and mutant SOD1-specific disruption of survival motor neuron protein complex in transgenic amyotrophic lateral sclerosis mice (English)

1 reference

Europe PubMed Central

12 August 2017

amyotrophic lateral sclerosis

0 references

author name string

Barry Gertz

1

1 reference

Europe PubMed Central

12 August 2017

Margaret Wong

2

1 reference

Europe PubMed Central

12 August 2017

Lee J Martin

3

1 reference

Europe PubMed Central

12 August 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

1 February 2012

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Europe PubMed Central

12 August 2017

Journal of Neuropathology & Experimental Neurology

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Europe PubMed Central

12 August 2017

71

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Europe PubMed Central

12 August 2017

2

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Europe PubMed Central

12 August 2017

162-177

1 reference

Europe PubMed Central

12 August 2017

Glial nuclear aggregates of superoxide dismutase-1 are regularly present in patients with amyotrophic lateral sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432922

1 October 2017

Mitochondrial and Cell Death Mechanisms in Neurodegenerative Diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432922

1 October 2017

ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432922

1 October 2017

RNA processing pathways in amyotrophic lateral sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432922

1 October 2017

Skeletal muscle-restricted expression of human SOD1 causes motor neuron degeneration in transgenic mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432922

1 October 2017

Inducible nitric oxide synthase is present in motor neuron mitochondria and Schwann cells and contributes to disease mechanisms in ALS mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432922

1 October 2017

Survival motor neuron deficiency enhances progression in an amyotrophic lateral sclerosis mouse model.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432922

1 October 2017

The mitochondrial permeability transition pore in motor neurons: involvement in the pathobiology of ALS mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432922

1 October 2017

Isolation of neuronal chromatin from brain tissue

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1 October 2017

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

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1 October 2017

Transgenics, toxicity and therapeutics in rodent models of mutant SOD1-mediated familial ALS.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432922

1 October 2017

SMN protects cells against mutant SOD1 toxicity by increasing chaperone activity

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432922

1 October 2017

Molecular functions of the SMN complex

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1 October 2017

Mitochondriopathy in Parkinson disease and amyotrophic lateral sclerosis

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432922

1 October 2017

Lessons from models of SOD1-linked familial ALS.

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1 October 2017

Superoxide dismutase and the death of motoneurons in ALS.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432922

1 October 2017

Amyotrophic lateral sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432922

1 October 2017

Neuronal cell death in nervous system development, disease, and injury (Review).

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1 October 2017

Amyotrophic lateral sclerosis. unfolding the toxicity of the misfolded

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1 October 2017

Neuronal death in amyotrophic lateral sclerosis is apoptosis: possible contribution of a programmed cell death mechanism

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432922

1 October 2017

CRM1-mediated recycling of snurportin 1 to the cytoplasm

1 reference

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1 October 2017

The spinal muscular atrophy disease gene product, SMN, and its associated protein SIP1 are in a complex with spliceosomal snRNP proteins

1 reference

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1 October 2017

A novel nuclear structure containing the survival of motor neurons protein

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1 October 2017

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

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432922

1 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432922

1 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432922

1 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432922

1 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432922

1 October 2017

Identification and characterization of a spinal muscular atrophy-determining gene

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1 October 2017

Superoxide dismutase. An enzymic function for erythrocuprein (hemocuprein)

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1 October 2017

Molecular immunocytochemistry of the CuZn superoxide dismutase in rat hepatocytes

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1 October 2017

Endogenous oxidative DNA damage, aging, and cancer

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1 October 2017

Copper,zinc superoxide dismutase is primarily a cytosolic protein in human cells

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1 October 2017

SOD1 Is Essential for the Viability of DT40 Cells and Nuclear SOD1 Functions as a Guardian of Genomic DNA

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29 June 2018

Sensitive enzyme immunoassay for human Cu/Zn superoxide dismutase.

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29 June 2018

Nuclear transport impairment of amyotrophic lateral sclerosis-linked mutations in FUS/TLS.

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22 September 2018

Increased SOD1 association with chromatin, DNA damage, p53 activation, and apoptosis in a cellular model of SOD1-linked ALS.

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22 September 2018

Motor neuron degeneration in amyotrophic lateral sclerosis mutant superoxide dismutase-1 transgenic mice: mechanisms of mitochondriopathy and cell death.

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22 September 2018

Increased oxidative damage to DNA in an animal model of amyotrophic lateral sclerosis

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22 September 2018

Amyotrophic lateral sclerosis with neuronal intranuclear protein inclusions

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22 September 2018

Motoneuron death triggered by a specific pathway downstream of Fas. potentiation by ALS-linked SOD1 mutations.

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22 September 2018

DNA base-excision repair enzyme apurinic/apyrimidinic endonuclease/redox factor-1 is increased and competent in the brain and spinal cord of individuals with amyotrophic lateral sclerosis.

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22 September 2018

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22 September 2018

Early vacuolization and mitochondrial damage in motor neurons of FALS mice are not associated with apoptosis or with changes in cytochrome oxidase histochemical reactivity.

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22 September 2018

Age-dependent penetrance of disease in a transgenic mouse model of familial amyotrophic lateral sclerosis

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22 September 2018

ALS, SOD and peroxynitrite

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21 January 2018

SMN1 gene, but not SMN2, is a risk factor for sporadic ALS

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5 December 2018

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

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12 December 2020

based on heuristic

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DNA damage profiling in motor neurons: a single-cell analysis by comet assay

1 reference

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12 December 2020

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Swelling and vacuolisation of mitochondria in transgenic SOD1-ALS mice: a consequence of supranormal SOD1 expression?

1 reference

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12 December 2020

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Altered distributions of nucleocytoplasmic transport-related proteins in the spinal cord of a mouse model of amyotrophic lateral sclerosis

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https://pubmed.ncbi.nlm.nih.gov/22249462

12 December 2020

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Evidence for DNA damage in amyotrophic lateral sclerosis

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https://pubmed.ncbi.nlm.nih.gov/22249462

12 December 2020

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inferred from PubMed ID database lookup

Nuclear contour irregularity and abnormal transporter protein distribution in anterior horn cells in amyotrophic lateral sclerosis

1 reference

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12 December 2020

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Selective loss of alpha motoneurons innervating the medial gastrocnemius muscle in a mouse model of amyotrophic lateral sclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/22249462

12 December 2020

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Identifiers

10.1097/NEN.0B013E318244B635

1 reference

Europe PubMed Central

12 August 2017

1 reference

Europe PubMed Central

12 August 2017

1 reference

Europe PubMed Central

12 August 2017

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