(Q36584516)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21748598%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

title

Expression of human FUS protein in Drosophila leads to progressive neurodegeneration (English)

1 reference

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7 February 2020

0 references

1 reference

3

1 reference

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7 February 2020

Xiaohong Zhou

13

1 reference

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7 February 2020

15

Marsel Mesulam

1 reference

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7 February 2020

14

Eileen H Bigio

1 reference

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7 February 2020

author name string

Yanbo Chen

1

1 reference

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7 February 2020

Mengxue Yang

2

1 reference

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7 February 2020

Xiaoping Chen

4

1 reference

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7 February 2020

Ye Ye

5

1 reference

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7 February 2020

Li Zhu

6

1 reference

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7 February 2020

Jianghong Liu

7

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7 February 2020

Haihong Ye

8

1 reference

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7 February 2020

Yan Shen

9

1 reference

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7 February 2020

Yan Li

10

1 reference

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7 February 2020

Elizabeth J Rao

11

1 reference

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7 February 2020

Kazuo Fushimi

12

1 reference

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7 February 2020

Qi Xu

16

1 reference

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7 February 2020

Jane Y Wu

17

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7 February 2020

publication date

1 June 2011

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7 February 2020

1 reference

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7 February 2020

volume

2

1 reference

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7 February 2020

issue

6

1 reference

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7 February 2020

page(s)

477-486

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https://scigraph.springernature.com/pub.10.1007/s13238-011-1065-7

7 February 2020

exact match

0 references

cites work

A Drosophila model of FUS-related neurodegeneration reveals genetic interaction between FUS and TDP-43.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3563268

Distinct pathological subtypes of FTLD-FUS.

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3563268

Juvenile ALS with basophilic inclusions is a FUS proteinopathy with FUS mutations

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3563268

ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3563268

Extensive FUS-immunoreactive pathology in juvenile amyotrophic lateral sclerosis with basophilic inclusions

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3563268

A Drosophila model for TDP-43 proteinopathy

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3563268

FUS pathology in basophilic inclusion body disease

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3563268

A new subtype of frontotemporal lobar degeneration with FUS pathology

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3563268

Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3563268

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

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3563268

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

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3563268

The neurite outgrowth inhibitor Nogo-A promotes denervation in an amyotrophic lateral sclerosis model

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3563268

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

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3563268

Delocalization of the multifunctional RNA splicing factor TLS/FUS in hippocampal neurones: exclusion from the nucleus and accumulation in dendritic granules and spine heads

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3563268

Human 75-kDa DNA-pairing protein is identical to the pro-oncoprotein TLS/FUS and is able to promote D-loop formation

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3563268

Oncoprotein TLS interacts with serine-arginine proteins involved in RNA splicing

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3563268

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

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3563268

Expression patterns of the human sarcoma-associated genes FUS and EWS and the genomic structure of FUS

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3563268

Fusion of CHOP to a novel RNA-binding protein in human myxoid liposarcoma

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3563268

Targeted gene expression as a means of altering cell fates and generating dominant phenotypes

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3563268

TLS/FUS fusion domain of TLS/FUS-erg chimeric protein resulting from the t(16;21) chromosomal translocation in human myeloid leukemia functions as a transcriptional activation domain

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3563268

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

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3563268

Stereotypic morphology of glutamatergic synapses on identified muscle cells of Drosophila larvae.

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3563268

Axonal swellings in the corticospinal tracts in amyotrophic lateral sclerosis

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3563268

A perisynaptic ménage à trois between Dlg, DLin-7, and Metro controls proper organization of Drosophila synaptic junctions.

28 June 2018

1 reference

https://api.crossref.org/works/10.1007%2FS13238-011-1065-7

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/10.1007%2FS13238-011-1065-7

Fus deficiency in mice results in defective B-lymphocyte development and activation, high levels of chromosomal instability and perinatal death.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS13238-011-1065-7

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS13238-011-1065-7

Neuronal death in Drosophila triggered by GAL4 accumulation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS13238-011-1065-7

GAL4 causes developmental defects and apoptosis when expressed in the developing eye of Drosophila melanogaster.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3563268

Homeostasis of synaptic transmission in Drosophila with genetically altered nerve terminal morphology.

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3563268

Decreased synaptophysin immunoreactivity of the anterior horns in motor neuron disease

20 September 2018

1 reference

12 December 2020

Early diagnosis of ALS: the search for signs of denervation in clinically normal muscles

1 reference

12 December 2020

FUS/TLS gene mutations are the second most frequent cause of familial ALS in the Spanish population

1 reference

12 December 2020

Numerous FUS-positive inclusions in an elderly woman with motor neuron disease

1 reference

12 December 2020

10.1007/S13238-011-1065-7

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21748598%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21748598%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

PubMed publication ID

21748598

1 reference