Upregulation of HSP27 in a Transgenic Model of ALS (Q57244970)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12430713%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

title

Upregulation of HSP27 in a transgenic model of ALS (English)

1 reference

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amyotrophic lateral sclerosis

14 December 2019

main subject

1 reference

2

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14 December 2019

Ludo Van Den Bosch

5

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14 December 2019

author name string

Vicky Vleminckx

1

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14 December 2019

Karolien Goffin

3

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14 December 2019

Hans Delye

4

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14 December 2019

Wim Robberecht

6

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14 December 2019

publication date

1 November 2002

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Journal of Neuropathology & Experimental Neurology

14 December 2019

published in

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14 December 2019

volume

61

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14 December 2019

issue

11

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14 December 2019

page(s)

968-974

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

14 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.11.968

From Charcot to SOD1: mechanisms of selective motor neuron death in ALS.

21 January 2018

1 reference

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Cellular defenses against unfolded proteins: a cell biologist thinks about neurodegenerative diseases

21 January 2018

1 reference

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.11.968

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.11.968

Expression of small heat-shock protein hsp 27 in reactive gliosis in Alzheimer disease and other types of dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.11.968

Dementia, gliosis and expression of the small heat shock proteins hsp27 and alpha B-crystallin in Parkinson's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.11.968

Heat shock proteins, molecular chaperones and the prion encephalopathies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.11.968

Dynamic changes in the structure and intracellular locale of the mammalian low-molecular-weight heat shock protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.11.968

Tumor necrosis factor-alpha induces changes in the phosphorylation, cellular localization, and oligomerization of human hsp27, a stress protein that confers cellular resistance to this cytokine.

21 January 2018

1 reference

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Large unphosphorylated aggregates as the active form of hsp27 which controls intracellular reactive oxygen species and glutathione levels and generates a protection against TNFalpha in NIH-3T3-ras cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.11.968

Hsp27 negatively regulates cell death by interacting with cytochrome c.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.11.968

Chaperone suppression of aggregation and altered subcellular proteasome localization imply protein misfolding in SCA1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.11.968

Polyglutamine length-dependent interaction of Hsp40 and Hsp70 family chaperones with truncated N-terminal huntingtin: their role in suppression of aggregation and cellular toxicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.11.968

Polyglutamine-expanded androgen receptors form aggregates that sequester heat shock proteins, proteasome components and SRC-1, and are suppressed by the HDJ-2 chaperone

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.11.968

From Charcot to Lou Gehrig: deciphering selective motor neuron death in ALS

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.11.968

Regulation of Hsp27 oligomerization, chaperone function, and protective activity against oxidative stress/tumor necrosis factor alpha by phosphorylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.11.968

A small heat shock protein stably binds heat-denatured model substrates and can maintain a substrate in a folding-competent state

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.11.968

Binding of non-native protein to Hsp25 during heat shock creates a reservoir of folding intermediates for reactivation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.11.968

The Hsp70 and Hsp60 chaperone machines

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.11.968

Mechanisms of chaperone suppression of polyglutamine disease: selectivity, synergy and modulation of protein solubility in Drosophila.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.11.968

Aggregation of huntingtin in yeast varies with the length of the polyglutamine expansion and the expression of chaperone proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.11.968

Suppression of polyglutamine-mediated neurodegeneration in Drosophila by the molecular chaperone HSP70.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.11.968

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.11.968

21 January 2018

Identifiers

DOI

10.1093/JNEN/61.11.968

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12430713%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

1 reference