Disrupted structure and aberrant function of CHIP mediates the loss of motor and cognitive function in preclinical models of SCAR16 (Q58730541)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30222779%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

title

Disrupted structure and aberrant function of CHIP mediates the loss of motor and cognitive function in preclinical models of SCAR16 (English)

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22 April 2020

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Rebekah Sanchez-Hodge

4

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22 April 2020

Richard C Page

9

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22 April 2020

Walter J Chazin

10

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22 April 2020

Monte Willis

13

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22 April 2020

Donté A Stevens

16

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22 April 2020

Pan Du

18

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22 April 2020

Jonathan Schisler

22

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22 April 2020

author name string

Chang-He Shi

1

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22 April 2020

Carrie Rubel

2

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22 April 2020

Sarah E Soss

3

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22 April 2020

Shuo Zhang

5

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22 April 2020

Sabrina C Madrigal

6

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22 April 2020

Saranya Ravi

7

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22 April 2020

Holly McDonough

8

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22 April 2020

Cam Patterson

11

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22 April 2020

Cheng-Yuan Mao

12

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22 April 2020

Hai-Yang Luo

14

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22 April 2020

Yu-Sheng Li

15

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22 April 2020

Mi-Bo Tang

17

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22 April 2020

Yao-He Wang

19

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22 April 2020

Zheng-Wei Hu

20

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22 April 2020

Yu-Ming Xu

21

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22 April 2020

language of work or name

English

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publication date

17 September 2018

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22 April 2020

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22 April 2020

volume

14

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22 April 2020

issue

9

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22 April 2020

page(s)

e1007664

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Creative Commons Attribution 4.0 International

22 April 2020

copyright license

start time

17 September 2018

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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30 November 2018

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Deletion of the ubiquitin ligase CHIP leads to the accumulation, but not the aggregation, of both endogenous phospho- and caspase-3-cleaved tau species.

30 November 2018

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30 November 2018

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CHIP-mediated stress recovery by sequential ubiquitination of substrates and Hsp70

30 November 2018

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Regulation of the cytoplasmic quality control protein degradation pathway by BAG2

30 November 2018

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The co-chaperone carboxyl terminus of Hsp70-interacting protein (CHIP) mediates alpha-synuclein degradation decisions between proteasomal and lysosomal pathways

30 November 2018

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Purkinje cell loss affects differentially the execution, acquisition and prepulse inhibition of skeletal and facial motor responses in Lurcher mice.

30 November 2018

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Disorders of the Cerebellum: Ataxia, Dysmetria of Thought, and the Cerebellar Cognitive Affective Syndrome

30 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6160236

Normalization of real-time quantitative reverse transcription-PCR data: a model-based variance estimation approach to identify genes suited for normalization, applied to bladder and colon cancer data sets

30 November 2018

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Dimerization of the human E3 ligase CHIP via a coiled-coil domain is essential for its activity.

30 November 2018

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CHIP activates HSF1 and confers protection against apoptosis and cellular stress

30 November 2018

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Overexpression of the cochaperone CHIP enhances Hsp70-dependent folding activity in mammalian cells.

30 November 2018

1 reference

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CHIP is a U-box-dependent E3 ubiquitin ligase: identification of Hsc70 as a target for ubiquitylation

30 November 2018

1 reference

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Identification of CHIP, a novel tetratricopeptide repeat-containing protein that interacts with heat shock proteins and negatively regulates chaperone functions

30 November 2018

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The cerebellar cognitive affective syndrome

30 November 2018

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NMRPipe: a multidimensional spectral processing system based on UNIX pipes

30 November 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6160236

Autosomal recessive cerebellar ataxia of adult onset due to STUB1 mutations

30 November 2018

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12 December 2020

Cerebellar ataxia and functional genomics: Identifying the routes to cerebellar neurodegeneration

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12 December 2020

Ataxia plus myoclonus in a 23-year-old patient due to STUB1 mutations

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12 December 2020

Clinical and Neuropathological Features of Spastic Ataxia in a Spanish Family with Novel Compound Heterozygous Mutations in STUB1

1 reference

12 December 2020

10.1371/JOURNAL.PGEN.1007664

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22 April 2020

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22 April 2020

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