(Q28236805)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19251628%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19251628%20AND%20SRC:MED&resulttype=core&format=json

amyotrophic lateral sclerosis

22 January 2020

main subject

0 references

amyotrophic lateral sclerosis type 6

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19251628%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

Boris Rogelj

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19251628%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

Kurt J De Vos

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19251628%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

Agnes Lumi Nishimura

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19251628%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

Bradley N. Smith

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19251628%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

Paul Wright

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19251628%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

Kelly L Williams

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19251628%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

Ammar Al-Chalabi

15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19251628%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

Ian P Blair

17

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19251628%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

Jean-Marc Gallo

20

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19251628%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

Christopher C. Miller

21

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19251628%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

Christopher Shaw

22

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19251628%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

13

Vineeta Tripathi

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19251628%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

9

Deborah Ruddy

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19251628%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

11

Jeban Ganesalingam

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19251628%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

author name string

Tibor Hortobágyi

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19251628%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

Jemeen Sreedharan

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19251628%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

Xun Hu

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19251628%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

Safa Al-Saraj

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19251628%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

Garth Nicholson

18

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19251628%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

Jackie de Belleroche

19

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19251628%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

P Nigel Leigh

16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19251628%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

language of work or name

English

0 references

publication date

1 February 2009

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19251628%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19251628%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

volume

323

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19251628%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

issue

5918

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19251628%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

page(s)

1208-1211

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19251628%20AND%20SRC:MED&resulttype=core&format=json

Role of axonal transport in neurodegenerative diseases

22 January 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4516382

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4516382

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

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4516382

TLS, EWS and TAF15: a model for transcriptional integration of gene expression

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4516382

Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4516382

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4516382

Onset and progression in inherited ALS determined by motor neurons and microglia

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4516382

Kinesin transports RNA: isolation and characterization of an RNA-transporting granule

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4516382

TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4516382

TDP-43 A315T mutation in familial motor neuron disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4516382

Identification of two novel loci for dominantly inherited familial amyotrophic lateral sclerosis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4516382

Two families with familial amyotrophic lateral sclerosis are linked to a novel locus on chromosome 16q.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4516382

Progress in the pathogenesis of amyotrophic lateral sclerosis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4516382

A novel locus for familial amyotrophic lateral sclerosis, on chromosome 18q

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4516382

Familial amyotrophic lateral sclerosis. Molecular pathology of a patient with a SOD1 mutation

29 September 2017

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1165942

ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1165942

High molecular weight complexes of mutant superoxide dismutase 1: age-dependent and tissue-specific accumulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1165942

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/10.1126%2FSCIENCE.1165942

Three families with amyotrophic lateral sclerosis and frontotemporal dementia with evidence of linkage to chromosome 9p.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1165942

Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2-21.3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1165942

Myosin-Va facilitates the accumulation of mRNA/protein complex in dendritic spines.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1165942

Mutations in all five exons ofSOD-1 may cause ALS

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1165942

A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1165942

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

21 January 2018

1 reference

12 December 2020

A novel Angiogenin gene mutation in a sporadic patient with amyotrophic lateral sclerosis from southern Italy

1 reference

12 December 2020

Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22

1 reference

12 December 2020

Mutations of the ANG gene in French patients with sporadic amyotrophic lateral sclerosis

1 reference

12 December 2020

Identifiers

DOI

10.1126/SCIENCE.1165942

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19251628%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

1 reference

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19251628%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

PubMed publication ID

19251628

2 references