FUS and TARDBP but not SOD1 interact in genetic models of amyotrophic lateral sclerosis (Q27339258)

object named as

Alexandra Lissouba

0 references

Edna Brustein

object named as

Edna Brustein

0 references

Meijiang Liao

object named as

Meijiang Liao

0 references

author name string

Edor Kabashi

Creative Commons Attribution 4.0 International

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language of work or name

English

0 references

publication date

August 2011

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0 references

0 references

0 references

e1002214

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start time

4 August 2011

1 reference

April 2022 Public Data File from Crossref

copyrighted

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cites work

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Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43.

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Amyotrophic lateral sclerosis-associated proteins TDP-43 and FUS/TLS function in a common biochemical complex to co-regulate HDAC6 mRNA.

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

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ALS-associated mutations in TDP-43 increase its stability and promote TDP-43 complexes with FUS/TLS.

29 September 2017

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29 September 2017

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29 September 2017

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Mutations in FUS cause FALS and SALS in French and French Canadian populations

29 September 2017

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29 September 2017

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29 September 2017

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VCP mutations causing frontotemporal lobar degeneration disrupt localization of TDP-43 and induce cell death

29 September 2017

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Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degeneration

29 September 2017

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Structural determinants of the cellular localization and shuttling of TDP-43.

29 September 2017

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Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia

29 September 2017

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TDP-43 A315T mutation in familial motor neuron disease

29 September 2017

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29 September 2017

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Progranulin mediates caspase-dependent cleavage of TAR DNA binding protein-43.

29 September 2017

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29 September 2017

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29 September 2017

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29 September 2017

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Expression of human FUS/TLS in yeast leads to protein aggregation and cytotoxicity, recapitulating key features of FUS proteinopathy

29 September 2017

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Multiple system degeneration with basophilic inclusions in Japanese ALS patients with FUS mutation

2 June 2018

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FALS with FUS mutation in Japan, with early onset, rapid progress and basophilic inclusion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002214

Mutation within TARDBP leads to frontotemporal dementia without motor neuron disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002214

Genetic contribution of FUS to frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002214

Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002214

Neurodegenerative disease: pink, parkin and the brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002214

Als2 mRNA splicing variants detected in KO mice rescue severe motor dysfunction phenotype in Als2 knock-down zebrafish.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002214

Nuclear transport impairment of amyotrophic lateral sclerosis-linked mutations in FUS/TLS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002214

Increased caspase activation and decreased TDP-43 solubility in progranulin knockout cortical cultures

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002214

Overexpression of mutant superoxide dismutase 1 causes a motor axonopathy in the zebrafish

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002214

Mutational analysis reveals the FUS homolog TAF15 as a candidate gene for familial amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3150442

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

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3150442

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3150442

Erratum: Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

27 November 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002214

SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21829392

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Double in situ hybridization techniques in zebrafish

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21829392

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Mutations of FUS gene in sporadic amyotrophic lateral sclerosis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21829392

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PGEN.1002214

1 reference

release_i3krzjncmvdu7ptlwz65gn52bq

Fatcat ID

0 references

1 reference

1 reference

PubMed publication ID

21829392

1 reference