(Q37132099)

English

Fused in sarcoma (FUS) protein lacking nuclear localization signal (NLS) and major RNA binding motifs triggers proteinopathy and severe motor phenotype in transgenic mice

scientific article published on 18 July 2013

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scholarly article

1 reference

Europe PubMed Central

18 August 2017

Fused in sarcoma (FUS) protein lacking nuclear localization signal (NLS) and major RNA binding motifs triggers proteinopathy and severe motor phenotype in transgenic mice (English)

1 reference

Europe PubMed Central

18 August 2017

1 reference

based on heuristic

inferred from title

author name string

Tatyana A Shelkovnikova

1

1 reference

Europe PubMed Central

18 August 2017

Owen M Peters

2

1 reference

Europe PubMed Central

18 August 2017

Alexey V Deykin

3

1 reference

Europe PubMed Central

18 August 2017

Natalie Connor-Robson

4

1 reference

Europe PubMed Central

18 August 2017

Hannah Robinson

5

1 reference

Europe PubMed Central

18 August 2017

Alexey A Ustyugov

6

1 reference

Europe PubMed Central

18 August 2017

Sergey O Bachurin

7

1 reference

Europe PubMed Central

18 August 2017

Tatyana G Ermolkevich

8

1 reference

Europe PubMed Central

18 August 2017

Igor L Goldman

9

1 reference

Europe PubMed Central

18 August 2017

Elena R Sadchikova

10

1 reference

Europe PubMed Central

18 August 2017

Elena A Kovrazhkina

11

1 reference

Europe PubMed Central

18 August 2017

Veronica I Skvortsova

12

1 reference

Europe PubMed Central

18 August 2017

Shuo-Chien Ling

13

1 reference

Europe PubMed Central

18 August 2017

Sandrine Da Cruz

14

1 reference

Europe PubMed Central

18 August 2017

Philippe A Parone

15

1 reference

Europe PubMed Central

18 August 2017

Vladimir L Buchman

16

1 reference

Europe PubMed Central

18 August 2017

Natalia N Ninkina

17

1 reference

Europe PubMed Central

18 August 2017

language of work or name

0 references

publication date

18 July 2013

1 reference

Europe PubMed Central

18 August 2017

Journal of Biological Chemistry

1 reference

Europe PubMed Central

18 August 2017

288

1 reference

Europe PubMed Central

18 August 2017

35

1 reference

Europe PubMed Central

18 August 2017

25266-25274

1 reference

Europe PubMed Central

18 August 2017

Expression of Fused in sarcoma mutations in mice recapitulates the neuropathology of FUS proteinopathies and provides insight into disease pathogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757190

14 September 2017

Divergent roles of ALS-linked proteins FUS/TLS and TDP-43 intersect in processing long pre-mRNAs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757190

14 September 2017

Overexpression of human wild-type FUS causes progressive motor neuron degeneration in an age- and dose-dependent fashion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757190

14 September 2017

Structural and energetic basis of ALS-causing mutations in the atypical proline–tyrosine nuclear localization signal of the Fused in Sarcoma protein (FUS)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757190

14 September 2017

Selective pattern of motor system damage in gamma-synuclein transgenic mice mirrors the respective pathology in amyotrophic lateral sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757190

14 September 2017

Motor neuron apoptosis and neuromuscular junction perturbation are prominent features in a Drosophila model of Fus-mediated ALS

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757190

14 September 2017

ALS mutations in FUS cause neuronal dysfunction and death in Caenorhabditis elegans by a dominant gain-of-function mechanism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757190

14 September 2017

A comparative clinical, pathological, biochemical and genetic study of fused in sarcoma proteinopathies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757190

14 September 2017

Expression of human FUS protein in Drosophila leads to progressive neurodegeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757190

14 September 2017

FUS transgenic rats develop the phenotypes of amyotrophic lateral sclerosis and frontotemporal lobar degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757190

14 September 2017

FUS-immunoreactive inclusions are a common feature in sporadic and non-SOD1 familial amyotrophic lateral sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757190

14 September 2017

FUS pathology in basophilic inclusion body disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757190

14 September 2017

A new subtype of frontotemporal lobar degeneration with FUS pathology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757190

14 September 2017

Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757190

14 September 2017

Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757190

14 September 2017

Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757190

14 September 2017

Gamma-synucleinopathy: neurodegeneration associated with overexpression of the mouse protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757190

14 September 2017

Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757190

14 September 2017

Neurons Expressing the Highest Levels of γ-Synuclein Are Unaffected by Targeted Inactivation of the Gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757190

14 September 2017

Accelerated oligomerization by Parkinson's disease linked alpha-synuclein mutants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757190

14 September 2017

Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757190

14 September 2017

Prion-like disorders: blurring the divide between transmissibility and infectivity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757190

14 September 2017

Accumulation of insoluble forms of FUS protein correlates with toxicity in Drosophila

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3757190

3 September 2018

New neuropathological findings in Unverricht-Lundborg disease: neuronal intranuclear and cytoplasmic inclusions

1 reference

https://pubmed.ncbi.nlm.nih.gov/23867462

12 December 2020

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Identifiers

10.1074/JBC.M113.492017

1 reference

Europe PubMed Central

18 August 2017

release_orjf6glyubdjdhau26ayc5lth4

1 reference

https://api.fatcat.wiki/v0/release/orjf6glyubdjdhau26ayc5lth4

24 November 2022

based on heuristic

mapped directly with Wikidata item

1 reference

Europe PubMed Central

18 August 2017

1 reference

Europe PubMed Central

18 August 2017

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