(Q28264387)

4

object named as

Catriona A McLean

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author name string

Manal A Farg

2

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Chris R Bye

3

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Malcolm K Horne

5

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Julie D Atkin

The human PDI family: versatility packed into a single fold.

6

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language of work or name

English

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publication date

January 2010

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published in

Brain

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volume

133

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issue

Pt 1

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page(s)

105-16

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cites work

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

Endoplasmic reticulum stress and induction of the unfolded protein response in human sporadic amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

Unraveling the mechanisms involved in motor neuron degeneration in ALS

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

Initiation and elongation in fibrillation of ALS-linked superoxide dismutase

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

Protein S-nitrosylation: a physiological signal for neuronal nitric oxide

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

Degradation of Amyotrophic Lateral Sclerosis-linked Mutant Cu,Zn-Superoxide Dismutase Proteins by Macroautophagy and the Proteasome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

Catalysis of Protein Folding by Protein Disulfide Isomerase and Small-Molecule Mimics

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

Deletion of the BH3-only protein puma protects motoneurons from ER stress-induced apoptosis and delays motoneuron loss in ALS mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

Spinal cord endoplasmic reticulum stress associated with a microsomal accumulation of mutant superoxide dismutase-1 in an ALS model

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

Structural properties and neuronal toxicity of amyotrophic lateral sclerosis-associated Cu/Zn superoxide dismutase 1 aggregates.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

ALS-linked mutant SOD1 induces ER stress- and ASK1-dependent motor neuron death by targeting Derlin-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

Disulfide bond mediates aggregation, toxicity, and ubiquitylation of familial amyotrophic lateral sclerosis-linked mutant SOD1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

A new mathematical model for relative quantification in real-time RT-PCR

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

Mechanism of transfer of NO from extracellular S-nitrosothiols into the cytosol by cell-surface protein disulfide isomerase

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

Endoplasmic reticulum-associated degradation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

Current hypotheses for the underlying biology of amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

A role for motoneuron subtype-selective ER stress in disease manifestations of FALS mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

Endoplasmic reticulum protein quality control in neurodegenerative disease: the good, the bad and the therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

Endoplasmic reticulum stress responses

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

Copper-zinc superoxide dismutase and amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

Endoplasmic reticulum stress inhibition protects against excitotoxic neuronal injury in the rat brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

Recruitment of mitochondria into apoptotic signaling correlates with the presence of inclusions formed by amyotrophic lateral sclerosis-associated SOD1 mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

Vaticanol B, a resveratrol tetramer, regulates endoplasmic reticulum stress and inflammation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

Accumulation of misfolded protein through nitrosative stress linked to neurodegenerative disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

S-nitrosylated protein-disulphide isomerase links protein misfolding to neurodegeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

The endoplasmic reticulum-Golgi pathway is a target for translocation and aggregation of mutant superoxide dismutase linked to ALS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

Protein disulfide isomerase

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

A small-molecule catalyst of protein folding in vitro and in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

An in vitro model for Lewy body-like hyaline inclusion/astrocytic hyaline inclusion: induction by ER stress with an ALS-linked SOD1 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP267