Mutant FUS proteins that cause amyotrophic lateral sclerosis incorporate into stress granules (Q34308339)

1 August 2017

title

Mutant FUS proteins that cause amyotrophic lateral sclerosis incorporate into stress granules (English)

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amyotrophic lateral sclerosis

1 August 2017

main subject

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Diane McKenna-Yasek

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Robert H Brown

object named as

Robert H Brown

1 reference

1 August 2017

Daryl A Bosco

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1 August 2017

Nathan Lemay

1 reference

1 August 2017

Hae Kyung Ko

1 reference

1 August 2017

Hongru Zhou

1 reference

1 August 2017

Chris Burke

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1 August 2017

Thomas J Kwiatkowski

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1 August 2017

Peter Sapp

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1 August 2017

Lawrence J Hayward

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1 August 2017

publication date

10 August 2010

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1 August 2017

published in

Human Molecular Genetics

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1 August 2017

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1 August 2017

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1 August 2017

page(s)

4160-4175

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describes a project that uses

1 August 2017

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2981014/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

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RNA processing pathways in amyotrophic lateral sclerosis

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6 July 2018

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6 July 2018

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6 July 2018

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Proto-oncoprotein TLS/FUS is associated to the nuclear matrix and complexed with splicing factors PTB, SRm160, and SR proteins

6 July 2018

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6 July 2018

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Male sterility and enhanced radiation sensitivity in TLS(-/-) mice

6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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TLS (FUS) binds RNA in vivo and engages in nucleo-cytoplasmic shuttling

6 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2981014

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6 July 2018

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6 July 2018

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6 July 2018

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A novel effector domain from the RNA-binding protein TLS or EWS is required for oncogenic transformation by CHOP

6 July 2018

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6 July 2018

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Fusion of the dominant negative transcription regulator CHOP with a novel gene FUS by translocation t(12;16) in malignant liposarcoma

6 July 2018

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TDP-43: an emerging new player in neurodegenerative diseases

6 July 2018

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FUS mutations in amyotrophic lateral sclerosis: clinical, pathological, neurophysiological and genetic analysis

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDQ335

The occurrence of mutations inFUSin a Belgian cohort of patients with familial ALS

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDQ335

Mammalian Staufen 1 is recruited to stress granules and impairs their assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ335

Neuromuscular synapses can form in vivo by incorporation of initially aneural postsynaptic specializations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ335

The RNA binding protein TLS is translocated to dendritic spines by mGluR5 activation and regulates spine morphology.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ335

Immunohistochemical identification of messenger RNA-related proteins in basophilic inclusions of adult-onset atypical motor neuron disease

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDQ335

Cell culture medium affects GFP photostability: a solution

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDQ335

Mutations of FUS gene in sporadic amyotrophic lateral sclerosis

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20699327

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/HMG/DDQ335

1 reference

1 August 2017

1 reference

1 August 2017

1 reference