Analysis of the role of heat shock protein (Hsp) molecular chaperones in polyglutamine disease (Q73212216)

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2 November 2019

title

Analysis of the role of heat shock protein (Hsp) molecular chaperones in polyglutamine disease (English)

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2 November 2019

author name string

Y Chai

1

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2 November 2019

S L Koppenhafer

2

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2 November 2019

N M Bonini

3

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2 November 2019

H L Paulson

4

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2 November 2019

publication date

1 December 1999

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2 November 2019

published in

Journal of Neuroscience

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2 November 2019

volume

19

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2 November 2019

issue

23

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2 November 2019

page(s)

10338-10347

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Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias

2 November 2019

cites work

1 reference

12 December 2020

The Hsp70 and Hsp60 chaperone machines

1 reference

12 December 2020

Glutamine repeats and neurodegenerative diseases: molecular aspects

1 reference

12 December 2020

Recruitment and the role of nuclear localization in polyglutamine-mediated aggregation

1 reference

12 December 2020

Mutant huntingtin expression in clonal striatal cells: dissociation of inclusion formation and neuronal survival by caspase inhibition.

1 reference

12 December 2020

Huntingtin acts in the nucleus to induce apoptosis but death does not correlate with the formation of intranuclear inclusions.

1 reference

12 December 2020

Inhibition of caspase-1 slows disease progression in a mouse model of Huntington's disease

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12 December 2020

Machado-Joseph disease gene product is a cytoplasmic protein widely expressed in brain

1 reference

12 December 2020

Nuclear inclusions in glutamine repeat disorders: are they pernicious, coincidental, or beneficial?

1 reference

12 December 2020

Expanded polyglutamine protein forms nuclear inclusions and causes neural degeneration in Drosophila.

1 reference

12 December 2020

Evidence for proteasome involvement in polyglutamine disease: localization to nuclear inclusions in SCA3/MJD and suppression of polyglutamine aggregation in vitro

1 reference

12 December 2020

A system for characterizing cellular and molecular events in programmed neuronal cell death.

1 reference

12 December 2020

Molecular chaperones in cellular protein folding

1 reference

12 December 2020

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

1 reference

12 December 2020

Protein precipitation: a common etiology in neurodegenerative disorders?

1 reference

12 December 2020

Protein quality control: triage by chaperones and proteases

1 reference

12 December 2020

Nuclear and neuropil aggregates in Huntington's disease: relationship to neuropathology.

1 reference

12 December 2020

Protein fate in neurodegenerative proteinopathies: polyglutamine diseases join the (mis)fold

1 reference

12 December 2020

High level expression of expanded full-length ataxin-3 in vitro causes cell death and formation of intranuclear inclusions in neuronal cells

1 reference

12 December 2020

Length of huntingtin and its polyglutamine tract influences localization and frequency of intracellular aggregates

1 reference

12 December 2020

Intranuclear inclusions of expanded polyglutamine protein in spinocerebellar ataxia type 3.

1 reference

12 December 2020

Hsp104, Hsp70, and Hsp40: a novel chaperone system that rescues previously aggregated proteins

1 reference

12 December 2020

1 reference

12 December 2020

An isoform of ataxin-3 accumulates in the nucleus of neuronal cells in affected brain regions of SCA3 patients.

1 reference

12 December 2020

The CAG/polyglutamine tract diseases: gene products and molecular pathogenesis

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12 December 2020

Cellular defects and altered gene expression in PC12 cells stably expressing mutant huntingtin

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12 December 2020

Opposing effects of ERK and JNK-p38 MAP kinases on apoptosis

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12 December 2020

Expanded polyglutamine in the Machado-Joseph disease protein induces cell death in vitro and in vivo

1 reference

12 December 2020

Oligomerization of expanded-polyglutamine domain fluorescent fusion proteins in cultured mammalian cells

1 reference

12 December 2020

Truncated N-terminal fragments of huntingtin with expanded glutamine repeats form nuclear and cytoplasmic aggregates in cell culture.

1 reference

12 December 2020

The fatal attraction of polyglutamine-containing proteins.

1 reference

12 December 2020

Regulation of the heat shock transcriptional response: cross talk between a family of heat shock factors, molecular chaperones, and negative regulators

1 reference

12 December 2020

Huntingtin-encoded polyglutamine expansions form amyloid-like protein aggregates in vitro and in vivo

1 reference

12 December 2020

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

1 reference

12 December 2020

Ataxin-1 nuclear localization and aggregation: role in polyglutamine-induced disease in SCA1 transgenic mice.

1 reference

12 December 2020

Caspase-8 is required for cell death induced by expanded polyglutamine repeats.

1 reference

12 December 2020

Heat shock response and protein degradation: regulation of HSF2 by the ubiquitin-proteasome pathway

1 reference

12 December 2020

DnaJ-like proteins: molecular chaperones and specific regulators of Hsp70.

1 reference

12 December 2020

Roles of molecular chaperones in protein degradation

1 reference

12 December 2020

Generation of neuronal intranuclear inclusions by polyglutamine-GFP: analysis of inclusion clearance and toxicity as a function of polyglutamine length.

1 reference

12 December 2020

Neuronal intranuclear inclusions in polyglutamine diseases: nuclear weapons or nuclear fallout?

1 reference

12 December 2020

10.1523/JNEUROSCI.19-23-10338.1999

Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10575031%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

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2 November 2019

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