(Q46931165)

26 December 2017

title

A mutation in CHN-1/CHIP suppresses muscle degeneration in Caenorhabditis elegans (English)

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26 December 2017

main subject

Caenorhabditis elegans

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author

Davide Faggionato

2

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26 December 2017

author name string

Oyunbileg Nyamsuren

1

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26 December 2017

Wiebke Loch

3

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26 December 2017

Ekkehard Schulze

4

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26 December 2017

Ralf Baumeister

5

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26 December 2017

language of work or name

English

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publication date

24 October 2007

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26 December 2017

number of pages

10

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based on heuristic

inferred from page(s)

published in

Developmental Biology

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26 December 2017

volume

312

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26 December 2017

issue

1

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26 December 2017

page(s)

193-202

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26 December 2017

CHIP overexpression reduces mutant androgen receptor protein and ameliorates phenotypes of the spinal and bulbar muscular atrophy transgenic mouse model.

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1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2007.09.033

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

7 January 2021

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Mutations in the Caenorhabditis elegans dystrophin-like gene dys-1 lead to hyperactivity and suggest a link with cholinergic transmission

7 January 2021

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Proteasome inhibitor (MG-132) treatment of mdx mice rescues the expression and membrane localization of dystrophin and dystrophin-associated proteins

7 January 2021

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X chromosome-linked muscular dystrophy (mdx) in the mouse

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Three-dimensional high-resolution second-harmonic generation imaging of endogenous structural proteins in biological tissues

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CHIP activates HSF1 and confers protection against apoptosis and cellular stress

7 January 2021

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Membrane organization of the dystrophin-glycoprotein complex

7 January 2021

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A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin.

7 January 2021

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Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans

7 January 2021

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Prednisone reduces muscle degeneration in dystrophin-deficient Caenorhabditis elegans

7 January 2021

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Genetic suppression of phenotypes arising from mutations in dystrophin-related genes in Caenorhabditis elegans.

7 January 2021

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Genetic evidence for a dystrophin-glycoprotein complex (DGC) in Caenorhabditis elegans

7 January 2021

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Stochastic and genetic factors influence tissue-specific decline in ageing C. elegans

7 January 2021

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Regulation of the myosin-directed chaperone UNC-45 by a novel E3/E4-multiubiquitylation complex in C. elegans

7 January 2021

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CHIP is associated with Parkin, a gene responsible for familial Parkinson's disease, and enhances its ubiquitin ligase activity

7 January 2021

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The ubiquitin-selective chaperone CDC-48/p97 links myosin assembly to human myopathy

7 January 2021

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Small-caliber skeletal muscle fibers do not suffer necrosis in mdx mouse dystrophy.

7 January 2021

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A novel ubiquitination factor, E4, is involved in multiubiquitin chain assembly.

7 January 2021

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Muscle protein breakdown and the critical role of the ubiquitin-proteasome pathway in normal and disease states

7 January 2021

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Dystrophin-dependent muscle degeneration requires a fully functional contractile machinery to occur in C. elegans

7 January 2021

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Gene expression profiling of cells, tissues, and developmental stages of the nematode C. elegans

7 January 2021

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Severe cardiomyopathy in mice lacking dystrophin and MyoD

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7 January 2021

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Chaperone functions of the E3 ubiquitin ligase CHIP.

7 January 2021

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A Caenorhabditis elegans Parkin mutant with altered solubility couples alpha-synuclein aggregation to proteotoxic stress

7 January 2021

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Death by necrosis. Uncontrollable catastrophe, or is there order behind the chaos?

7 January 2021

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Dominant mutations affecting muscle structure in Caenorhabditis elegans that map near the actin gene cluster

7 January 2021

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A nitric oxide synthase transgene ameliorates muscular dystrophy in mdx mice

7 January 2021

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7 January 2021

Identifiers

DOI

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26 December 2017

1 reference

26 December 2017