(Q35063529)

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Proteins that bind to misfolded mutant superoxide dismutase-1 in spinal cords from transgenic amyotrophic lateral sclerosis (ALS) model mice

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Proteins that bind to misfolded mutant superoxide dismutase-1 in spinal cords from transgenic amyotrophic lateral sclerosis (ALS) model mice (English)

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

amyotrophic lateral sclerosis

0 references

Peter M Andersen

3

object named as

Peter M Andersen

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

author name string

Per Zetterström

1

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Karin S Graffmo

2

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Thomas Brännström

4

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Stefan L Marklund

5

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

language of work or name

0 references

publication date

14 April 2011

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Journal of Biological Chemistry

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

286

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

23

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

20130-20136

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Novel antibodies reveal inclusions containing non-native SOD1 in sporadic ALS patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121531

8 July 2018

Non-cell autonomous toxicity in neurodegenerative disorders: ALS and beyond

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121531

8 July 2018

Arimoclomol: a potential therapy under development for ALS.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121531

8 July 2018

Amyotrophic lateral sclerosis: Protein chaperone dysfunction revealed by proteomic studies of animal models

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121531

8 July 2018

Role of mutant SOD1 disulfide oxidation and aggregation in the pathogenesis of familial ALS

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121531

8 July 2018

Changes in the spinal cord proteome of an amyotrophic lateral sclerosis murine model determined by differential in-gel electrophoresis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121531

8 July 2018

Progressive aggregation despite chaperone associations of a mutant SOD1-YFP in transgenic mice that develop ALS.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121531

8 July 2018

Adherent monomer-misfolded SOD1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121531

8 July 2018

Soluble misfolded subfractions of mutant superoxide dismutase-1s are enriched in spinal cords throughout life in murine ALS models

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121531

8 July 2018

Neuronal expression of constitutive heat shock proteins: implications for neurodegenerative diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121531

8 July 2018

Elevation of the Hsp70 chaperone does not effect toxicity in mouse models of 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=3121531

8 July 2018

Co-chaperone CHIP associates with mutant Cu/Zn-superoxide dismutase proteins linked to familial amyotrophic lateral sclerosis and promotes their degradation by proteasomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121531

8 July 2018

Treatment with arimoclomol, a coinducer of heat shock proteins, delays disease progression in ALS mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121531

8 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121531

8 July 2018

Amyotrophic lateral sclerosis: a proposed mechanism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121531

8 July 2018

Heterodimeric structure of superoxide dismutase in complex with its metallochaperone

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121531

8 July 2018

The copper chaperone CCS directly interacts with copper/zinc superoxide dismutase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121531

8 July 2018

Tissue-specific differences in heat shock protein hsc70 and hsp70 in the control and hyperthermic rabbit

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3121531

8 July 2018

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=3121531

8 July 2018

Natural history of amyotrophic lateral sclerosis in a database population Validation of a scoring system and a model for survival prediction

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111.218842

21 January 2018

Minute quantities of misfolded mutant superoxide dismutase-1 cause amyotrophic lateral sclerosis.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111.218842

21 January 2018

Coexpression of yeast copper chaperone (yCCS) and CuZn-superoxide dismutases in Escherichia coli yields protein with high copper contents.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111.218842

21 January 2018

Superoxide dismutase-1 and other proteins in inclusions from transgenic amyotrophic lateral sclerosis model mice.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111.218842

21 January 2018

Overexpression of mutated Cu,Zn-SOD in neuroblastoma cells results in cytoskeletal change.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111.218842

21 January 2018

Mutant Cu/Zn-superoxide dismutase proteins have altered solubility and interact with heat shock/stress proteins in models of amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111.218842

21 January 2018

CHIP promotes proteasomal degradation of familial ALS-linked mutant SOD1 by ubiquitinating Hsp/Hsc70.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111.218842

21 January 2018

ALSOD: The Amyotrophic Lateral Sclerosis Online Database

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111.218842

21 January 2018

Familial amyotrophic lateral sclerosis-linked mutant SOD1 aberrantly interacts with tubulin

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M111.218842

21 January 2018

Disulphide-reduced superoxide dismutase-1 in CNS of transgenic amyotrophic lateral sclerosis models

1 reference

https://pubmed.ncbi.nlm.nih.gov/21493711

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Amyotrophic lateral sclerosis associated with homozygosity for an Asp90Ala mutation in CuZn-superoxide dismutase

1 reference

https://pubmed.ncbi.nlm.nih.gov/21493711

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Motor neuron disease in mice expressing the wild type-like D90A mutant superoxide dismutase-1

1 reference

https://pubmed.ncbi.nlm.nih.gov/21493711

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Wild-type superoxide dismutase acquires binding and toxic properties of ALS-linked mutant forms through oxidation

1 reference

https://pubmed.ncbi.nlm.nih.gov/21493711

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rats expressing human cytosolic copper-zinc superoxide dismutase transgenes with amyotrophic lateral sclerosis: associated mutations develop motor neuron disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/21493711

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1074/JBC.M111.218842

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

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