(Q44491457)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21438137%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21438137%20AND%20SRC:MED&resulttype=core&format=json

amyotrophic lateral sclerosis

26 January 2020

main subject

0 references

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21438137%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

Caroline Vance

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21438137%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

Vincenzo Silani

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21438137%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

Christopher Shaw

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21438137%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

12

J E Landers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21438137%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

author name string

A L Leclerc

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21438137%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

P Keagle

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21438137%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

J D Glass

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21438137%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

D McKenna-Yasek

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21438137%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

P C Sapp

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21438137%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

D A Bosco

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21438137%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

R H Brown

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21438137%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

publication date

13 January 2011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21438137%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

26 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21438137%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

volume

156B

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21438137%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

page(s)

285-290

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21438137%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21438137%20AND%20SRC:MED&resulttype=core&format=json

The multifunctional FUS, EWS and TAF15 proto-oncoproteins show cell type-specific expression patterns and involvement in cell spreading and stress response

26 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31158

Beyond Mendel: an evolving view of human genetic disease transmission

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31158

Conserved structures and diversity of functions of RNA-binding proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31158

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31158

Progranulin mutations in ubiquitin-positive frontotemporal dementia linked to chromosome 17q21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31158

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31158

Copper/zinc superoxide dismutase 1 and sporadic amyotrophic lateral sclerosis: analysis of 155 cases and identification of a novel insertion mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31158

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31158

Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31158

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31158

Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31158

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31158

Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31158

Cloning and mapping of a human RBP56 gene encoding a putative RNA binding protein similar to FUS/TLS and EWS proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31158

Genomic structure of the human RBP56/hTAFII68 and FUS/TLS genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31158

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31158

Genome-wide association studies in neurological disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31158

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31158

Oligogenic basis of isolated gonadotropin-releasing hormone deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31158

Paraoxonase gene mutations in amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31158

Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohort

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31158

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31158

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31158

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31158

Identification and characterization of the nuclear localization/retention signal in the EWS proto-oncoprotein

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31158

21 January 2018

Identifiers

DOI

10.1002/AJMG.B.31158

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21438137%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

1 reference