(Q44971569)

7 December 2017

title

Decrease of Hsp25 protein expression precedes degeneration of motoneurons in ALS-SOD1 mice (English)

1 reference

amyotrophic lateral sclerosis

7 December 2017

main subject

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Arjen Maatkamp

1

1 reference

7 December 2017

Angela Vlug

2

1 reference

7 December 2017

Elize Haasdijk

3

1 reference

7 December 2017

Dirk Troost

4

1 reference

7 December 2017

Pim J French

5

1 reference

7 December 2017

Dick Jaarsma

6

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7 December 2017

language of work or name

English

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publication date

1 July 2004

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European Journal of Neuroscience

7 December 2017

published in

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7 December 2017

volume

20

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7 December 2017

issue

1

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7 December 2017

page(s)

14-28

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The neuroprotective effects of heat shock protein 27 overexpression in transgenic animals against kainate-induced seizures and hippocampal cell death

7 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2004.03430.X

Hsp27 upregulation and phosphorylation is required for injured sensory and motor neuron survival.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2004.03430.X

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/10.1111%2FJ.1460-9568.2004.03430.X

Hsp27 negatively regulates cell death by interacting with cytochrome c.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2004.03430.X

S-thiolation of HSP27 regulates its multimeric aggregate size independently of phosphorylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2004.03430.X

The dynamics of Hsp25 quaternary structure. Structure and function of different oligomeric species

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2004.03430.X

Amyloid-like filaments and water-filled nanotubes formed by SOD1 mutant proteins linked to familial ALS

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2004.03430.X

Factors controlling the uptake of yeast copper/zinc superoxide dismutase into mitochondria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2004.03430.X

Inhibition of proteasomes induces accumulation, phosphorylation, and recruitment of HSP27 and alphaB-crystallin to aggresomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2004.03430.X

Human Cu/Zn superoxide dismutase (SOD1) overexpression in mice causes mitochondrial vacuolization, axonal degeneration, and premature motoneuron death and accelerates motoneuron disease in mice expressing a familial amyotrophic lateral sclerosis mut

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2004.03430.X

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/10.1111%2FJ.1460-9568.2004.03430.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2004.03430.X

Responses of heat shock proteins hsp27, alphaB-crystallin, and hsp70 in rat brain after kainic acid-induced seizure activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2004.03430.X

Immunohistochemical localization of the low molecular weight stress protein HSP27 following focal cerebral ischemia in the rat

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2004.03430.X

Mutant Cu,Zn superoxide dismutases and familial amyotrophic lateral sclerosis: evaluation of oxidative hypotheses

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2004.03430.X

Small stress proteins as novel regulators of apoptosis. Heat shock protein 27 blocks Fas/APO-1- and staurosporine-induced cell death.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2004.03430.X

Crosstalk between p38, Hsp25 and Akt in spinal motor neurons after sciatic nerve injury

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2004.03430.X

Role of heat shock protein Hsp25 in the response of the orofacial nuclei motor system to physiological stress

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2004.03430.X

Amyotrophic lateral sclerosis: a proposed mechanism

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2004.03430.X

Expression of the 27,000 mol. wt heat shock protein following kainic acid-induced status epilepticus in the rat.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2004.03430.X

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/10.1111%2FJ.1460-9568.2004.03430.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2004.03430.X

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/10.1111%2FJ.1460-9568.2004.03430.X

Hsp70 and Hsp40 improve neurite outgrowth and suppress intracytoplasmic aggregate formation in cultured neuronal cells expressing mutant SOD1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2004.03430.X

Oligomerization properties of fragile-X mental-retardation protein (FMRP) and the fragile-X-related proteins FXR1P and FXR2P

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2004.03430.X

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/10.1111%2FJ.1460-9568.2004.03430.X

Proteasomal inhibition by misfolded mutant superoxide dismutase 1 induces selective motor neuron death in familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2004.03430.X

Misfolded CuZnSOD and amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2004.03430.X

Molecular chaperones--cellular machines for protein folding

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2004.03430.X

High molecular weight complexes of mutant superoxide dismutase 1: age-dependent and tissue-specific accumulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2004.03430.X

Down-regulation of heat shock protein 27 in neuronal cells and non-neuronal cells expressing mutant ataxin-3

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2004.03430.X

Interaction between GRIP and liprin-alpha/SYD2 is required for AMPA receptor targeting

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2004.03430.X

Upregulation of HSP27 in a Transgenic Model of ALS

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1460-9568.2004.03430.X

10.1111/J.1460-9568.2004.03430.X

21 January 2018

Identifiers

DOI

1 reference

7 December 2017

1 reference