(Q21202841)

17 August 2022

2

Rebecca Schüle

Rebecca

Schüle

1 reference

17 August 2022

10

Stephan Züchner

Stephan

Züchner

1 reference

17 August 2022

Ingeborg Krägeloh-Mann

7

object named as

Ingeborg Krägeloh-Mann

Ingeborg

Krägeloh-Mann

1 reference

17 August 2022

1

Matthis Synofzik

Matthis

Synofzik

1 reference

17 August 2022

Martin Schulze

3

Martin

Schulze

1 reference

17 August 2022

Janina Gburek-Augustat

4

Janina

Gburek-Augustat

1 reference

17 August 2022

Roland Schweizer

5

Roland

Schweizer

1 reference

17 August 2022

Anja Schirmacher

6

Anja

Schirmacher

1 reference

17 August 2022

Michael Gonzalez

8

Michael

Gonzalez

1 reference

17 August 2022

Peter Young

9

Peter

Young

1 reference

17 August 2022

Peter Bauer

12

Peter

Bauer

1 reference

Orphanet Journal of Rare Diseases

17 August 2022

language of work or name

English

0 references

publication date

2014

0 references

published in

0 references

volume

9

0 references

issue

1

0 references

page(s)

57

0 references

exact match

https://scigraph.springernature.com/pub.10.1186/1750-1172-9-57

0 references

cites work

Endoplasmic reticulum protein quality control is determined by cooperative interactions between Hsp/c70 protein and the CHIP E3 ligase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4021831

CHIP protects from the neurotoxicity of expanded and wild-type ataxin-1 and promotes their ubiquitination and degradation

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4021831

Identification of CHIP as a novel causative gene for autosomal recessive cerebellar ataxia

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4021831

PNPLA6 mutations cause Boucher-Neuhauser and Gordon Holmes syndromes as part of a broad neurodegenerative spectrum

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4021831

Ataxia and hypogonadism caused by the loss of ubiquitin ligase activity of the U box protein CHIP

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4021831

Electrophysiological characterisation of motor and sensory tracts in patients with hereditary spastic paraplegia (HSP).

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4021831

Reviewing the genetic causes of spastic-ataxias

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4021831

The autosomal recessive cerebellar ataxias

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4021831

In vivo suppression of polyglutamine neurotoxicity by C-terminus of Hsp70-interacting protein (CHIP) supports an aggregation model of pathogenesis.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4021831

A critical role for CHIP in the aggresome pathway

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4021831

Dorfin-CHIP chimeric proteins potently ubiquitylate and degrade familial ALS-related mutant SOD1 proteins and reduce their cellular toxicity

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4021831

Scale for the assessment and rating of ataxia: development of a new clinical scale

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4021831

The small heat shock protein B8 (HspB8) promotes autophagic removal of misfolded proteins involved in amyotrophic lateral sclerosis (ALS).

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4021831

Co-chaperone CHIP associates with expanded polyglutamine protein and promotes their degradation by proteasomes.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4021831

GEnomes Management Application (GEM.app): a new software tool for large-scale collaborative genome analysis

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4021831

The Spastic Paraplegia Rating Scale (SPRS): a reliable and valid measure of disease severity.

30 May 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2F1750-1172-9-57

CHIP promotes proteasomal degradation of familial ALS-linked mutant SOD1 by ubiquitinating Hsp/Hsc70.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2F1750-1172-9-57

21 January 2018

Identifiers

DOI

10.1186/1750-1172-9-57

0 references