(Q43916607)

English

Protein surveillance machinery in brains with spinocerebellar ataxia type 3: redistribution and differential recruitment of 26S proteasome subunits and chaperones to neuronal intranuclear inclusions

scientific article published in March 2002

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

Protein surveillance machinery in brains with spinocerebellar ataxia type 3: redistribution and differential recruitment of 26S proteasome subunits and chaperones to neuronal intranuclear inclusions (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

molecular chaperones

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spinocerebellar ataxia

1 reference

based on heuristic

inferred from title

Bernhard Landwehrmeyer

9

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

4

object named as

Ludger Schöls

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

8

object named as

Olaf Riess

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

author name string

Thorsten Schmidt

1

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

Katrin S Lindenberg

2

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

Antje Krebs

3

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

Franco Laccone

5

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

Jochen Herms

6

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

Martin Rechsteiner

7

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

publication date

1 March 2002

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

Annals of Neurology

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

51

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Europe PubMed Central

PubMed publication ID

28 November 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

302-310

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological features.

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

Relations between genotype and phenotype in German patients with the Machado-Joseph disease mutation

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

Machado-Joseph disease mutations as the genetic basis of most spinocerebellar ataxias in Germany

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

Glutamine repeats and neurodegeneration

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

Are neuronal intranuclear inclusions the common neuropathology of triplet-repeat disorders with polyglutamine-repeat expansions?

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

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

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

The proteasome: paradigm of a self-compartmentalizing protease

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

The 26S proteasome: a molecular machine designed for controlled proteolysis

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

Expanded polyglutamines induce neurodegeneration and trans-neuronal alterations in cerebellum and retina of SCA7 transgenic mice

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

The role of the hsp90-based chaperone system in signal transduction by nuclear receptors and receptors signaling via MAP kinase

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

Involvement of heat shock protein 90 in the degradation of mutant insulin receptors by the proteasome.

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

Functional importance of heat shock protein 90 associated with insulin receptor on insulin-stimulated mitogenesis

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

Protection from oxidative inactivation of the 20S proteasome by heat-shock protein 90.

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

Hsp90's secrets unfold: new insights from structural and functional studies

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

Effects of heat shock, heat shock protein 40 (HDJ-2), and proteasome inhibition on protein aggregation in cellular models of Huntington's disease

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

Hsp70 and hsp40 chaperones can inhibit self-assembly of polyglutamine proteins into amyloid-like fibrils

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

Genetic suppression of polyglutamine toxicity in Drosophila

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

Human proteasomes analysed with monoclonal antibodies

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

An algorithm for the prediction of proteasomal cleavages

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

The base of the proteasome regulatory particle exhibits chaperone-like activity

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

A model for the quaternary structure of the proteasome activator PA28.

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

Hybrid proteasomes. Induction by interferon-gamma and contribution to ATP-dependent proteolysis

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

Simultaneous binding of PA28 and PA700 activators to 20 S proteasomes

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

Impairment of the ubiquitin-proteasome system by protein aggregation

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

Altered proteasomal function due to the expression of polyglutamine-expanded truncated N-terminal huntingtin induces apoptosis by caspase activation through mitochondrial cytochrome c release

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

Transcriptional dysregulation in Huntington's disease

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

Polyglutamine expansion down-regulates specific neuronal genes before pathologic changes in SCA1.

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

Decreased expression of striatal signaling genes in a mouse model of Huntington's disease

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

Atrophin-1, the dentato-rubral and pallido-luysian atrophy gene product, interacts with ETO/MTG8 in the nuclear matrix and represses transcription

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

CREB-binding protein sequestration by expanded polyglutamine

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

Genetic classification of primary neurodegenerative disease

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

Assembly of the regulatory complex of the 26S proteasome

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

Functional analysis of the proteasome regulatory particle

1 reference

https://api.crossref.org/works/10.1002%2FANA.10101

21 January 2018

Identifiers

10.1002/ANA.10101

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 November 2017

ResearchGate publication ID

0 references

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