(Q40254780)

English

Induction of the unfolded protein response in familial amyotrophic lateral sclerosis and association of protein-disulfide isomerase with superoxide dismutase 1.

scientific article published on 17 July 2006

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scholarly article

1 reference

Europe PubMed Central

18 September 2017

retracted paper

2 references

Dataset for "Continued use of retracted papers: Temporal trends in citations and (lack of) awareness of retractions shown in citation contexts in biomedicine"

Continued use of retracted papers: Temporal trends in citations and (lack of) awareness of retractions shown in citation contexts in biomedicine

Induction of the unfolded protein response in familial amyotrophic lateral sclerosis and association of protein-disulfide isomerase with superoxide dismutase 1. (English)

1 reference

Europe PubMed Central

18 September 2017

amyotrophic lateral sclerosis

0 references

author name string

Julie D Atkin

1

1 reference

Europe PubMed Central

18 September 2017

Manal A Farg

2

1 reference

Europe PubMed Central

18 September 2017

Bradley J Turner

3

1 reference

Europe PubMed Central

18 September 2017

Doris Tomas

4

1 reference

Europe PubMed Central

18 September 2017

Judith A Lysaght

5

1 reference

Europe PubMed Central

18 September 2017

Janelle Nunan

6

1 reference

Europe PubMed Central

18 September 2017

Alan Rembach

7

1 reference

Europe PubMed Central

18 September 2017

Phillip Nagley

8

1 reference

Europe PubMed Central

18 September 2017

Philip M Beart

9

1 reference

Europe PubMed Central

18 September 2017

Surindar S Cheema

10

1 reference

Europe PubMed Central

18 September 2017

Malcolm K Horne

11

1 reference

Europe PubMed Central

18 September 2017

language of work or name

0 references

publication date

17 July 2006

1 reference

Europe PubMed Central

18 September 2017

number of pages

14

1 reference

based on heuristic

inferred from page(s)

Journal of Biological Chemistry

1 reference

Europe PubMed Central

18 September 2017

281

1 reference

Europe PubMed Central

18 September 2017

40

1 reference

Europe PubMed Central

18 September 2017

30152-30165

1 reference

Europe PubMed Central

18 September 2017

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Focal loss of the glutamate transporter EAAT2 in a transgenic rat model of SOD1 mutant-mediated amyotrophic lateral sclerosis (ALS).

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Lessons from models of SOD1-linked familial ALS.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Familial amyotrophic lateral sclerosis mutants of copper/zinc superoxide dismutase are susceptible to disulfide reduction

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Dissociation of human copper-zinc superoxide dismutase dimers using chaotrope and reductant. Insights into the molecular basis for dimer stability

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Amyotrophic lateral sclerosis mutations have the greatest destabilizing effect on the apo- and reduced form of SOD1, leading to unfolding and oxidative aggregation.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Stress signaling from the lumen of the endoplasmic reticulum: coordination of gene transcriptional and translational controls

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Proteins of the PDI family: unpredicted non-ER locations and functions

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Caspase-12 mediates endoplasmic-reticulum-specific apoptosis and cytotoxicity by amyloid-beta

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Roles of CHOP/GADD153 in endoplasmic reticulum stress

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

A trip to the ER: coping with stress

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

ER stress and UPR in familial amyotrophic lateral sclerosis.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Mutant SOD1 linked to familial amyotrophic lateral sclerosis, but not wild-type SOD1, induces ER stress in COS7 cells and transgenic mice.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Caspase-12 cleavage and increased oxidative stress during motoneuron degeneration in transgenic mouse model of ALS.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Expression of an endoplasmic reticulum-resident chaperone, glucose-regulated stress protein 78, in the spinal cord of a mouse model of amyotrophic lateral sclerosis.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Characterization of the caspase cascade in a cell culture model of SOD1-related familial amyotrophic lateral sclerosis: expression, activation and therapeutic effects of inhibition.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Impaired extracellular secretion of mutant superoxide dismutase 1 associates with neurotoxicity in familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Chromogranin-mediated secretion of mutant superoxide dismutase proteins linked to amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Golgi-disturbing agents.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

The Cu,Zn superoxide dismutase in neuroblastoma SK-N-BE cells is exported by a microvesicles dependent pathway

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Fragmentation of the Golgi apparatus of motor neurons in amyotrophic lateral sclerosis revealed by organelle-specific antibodies

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

The Golgi apparatus of spinal cord motor neurons in transgenic mice expressing mutant Cu,Zn superoxide dismutase becomes fragmented in early, preclinical stages of the disease

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Dysregulation of stathmin, a microtubule-destabilizing protein, and up-regulation of Hsp25, Hsp27, and the antioxidant peroxiredoxin 6 in a mouse model of familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Inhibition of a reductive function of the plasma membrane by bacitracin and antibodies against protein disulfide-isomerase

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Protein disulfide isomerase suppresses the transcriptional activity of NF-kappaB.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Redox activation of mitochondrial intermembrane space Cu,Zn-superoxide dismutase

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Stress-induced gene expression requires programmed recovery from translational repression

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Caspase-12 and endoplasmic reticulum stress mediate neurotoxicity of pathological prion protein.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Molecular immunocytochemistry of the CuZn superoxide dismutase in rat hepatocytes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Subcellular distribution of superoxide dismutases (SOD) in rat liver: Cu,Zn-SOD in mitochondria

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Cellular distribution of superoxide dismutases in the rat CNS.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Apaf1 mediates apoptosis and mitochondrial damage induced by mutant human SOD1s typical of familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 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).

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Oxygen-induced maturation of SOD1: a key role for disulfide formation by the copper chaperone CCS.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Glutathione metabolism in brain metabolic interaction between astrocytes and neurons in the defense against reactive oxygen species

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Redox environment of the cell as viewed through the redox state of the glutathione disulfide/glutathione couple

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Glutathione directly reduces an oxidoreductase in the endoplasmic reticulum of mammalian cells

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Aberrantly increased hydrophobicity shared by mutants of Cu,Zn-superoxide dismutase in familial amyotrophic lateral sclerosis.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Disulfide cross-linked protein represents a significant fraction of ALS-associated Cu, Zn-superoxide dismutase aggregates in spinal cords of model mice

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

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.M603393200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

ERp57 is a multifunctional thiol-disulfide oxidoreductase

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Erp61 is GRP58, a stress-inducible luminal endoplasmic reticulum protein, but is devoid of phosphatidylinositide-specific phospholipase C activity

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Identification of the protein disulfide isomerase family member PDIp in experimental Parkinson's disease and Lewy body pathology

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Overexpressed protein disulfide isomerase in brains of patients with sporadic Creutzfeldt-Jakob disease

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Protein disulfide isomerase in Alzheimer disease.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

The disulfide isomerase Grp58 is a protective factor against prion neurotoxicity.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603393200

21 January 2018

Altered calcium homeostasis and ultrastructure in motoneurons of mice caused by passively transferred anti-motoneuronal IgG

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1074/JBC.M603393200

Mitochondrial localization of mutant superoxide dismutase 1 triggers caspase-dependent cell death in a cellular model of familial amyotrophic lateral sclerosis

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1074/JBC.M603393200

Orchestrating the unfolded protein response in health and disease

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1074/JBC.M603393200

Evidence for secretion of cytosolic CuZn superoxide dismutase by Hep G2 cells and human fibroblasts

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1074/JBC.M603393200

Purification and characterization of yeast protein disulfide isomerase

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1074/JBC.M603393200

ATF3 expression precedes death of spinal motoneurons in amyotrophic lateral sclerosis-SOD1 transgenic mice and correlates with c-Jun phosphorylation, CHOP expression, somato-dendritic ubiquitination and Golgi fragmentation

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1074/JBC.M603393200

The unusually stable quaternary structure of human Cu,Zn-superoxide dismutase 1 is controlled by both metal occupancy and disulfide status

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1074/JBC.M603393200

Fragmentation of the Golgi apparatus of the anterior horn cells in patients with familial amyotrophic lateral sclerosis with SOD1 mutations and posterior column involvement

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1074/JBC.M603393200

Endoplasmic reticulum stress and the unfolded protein response in cellular models of Parkinson's disease.

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1074/JBC.M603393200

Stability of mutant superoxide dismutase-1 associated with familial amyotrophic lateral sclerosis determines the manner of copper release and induction of thioredoxin in erythrocytes

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1074/JBC.M603393200

Up-regulation of protein-disulfide isomerase in response to hypoxia/brain ischemia and its protective effect against apoptotic cell death

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1074/JBC.M603393200

The thiol-dependent reductase ERp57 interacts specifically with N-glycosylated integral membrane proteins

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1074/JBC.M603393200

D90A-SOD1 mediated amyotrophic lateral sclerosis: a single founder for all cases with evidence for a Cis-acting disease modifier in the recessive haplotype.

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1074/JBC.M603393200

Two distinct stress signaling pathways converge upon the CHOP promoter during the mammalian unfolded protein response

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1074/JBC.M603393200

Identifiers

10.1074/JBC.M603393200

1 reference

Europe PubMed Central

18 September 2017

1 reference

Europe PubMed Central

18 September 2017

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