(Q37090072)

18 August 2017

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

1 reference

Elongator acetyltransferase complex subunit 3

18 August 2017

1 reference

Elongator complex protein 3 Dmel_CG15433

GOA release 2020-03-11

0 references

Claire L Simpson

1

0 references

Patrik Verstreken

Patrik Verstreken

27

0 references

Petroula Proitsi

Petroula Proitsi

18

0 references

Ludo Van Den Bosch

Ludo Van Den Bosch

9

0 references

Ammar Al-Chalabi

Ammar Al-Chalabi

30

0 references

Jo Knight

Joanne Knight

10

0 references

Martin R. Turner

Martin R Turner

12

0 references

Christopher Shaw

Christopher E Shaw

23

0 references

Peter Carmeliet

20

Peter Carmeliet

1 reference

18 August 2017

Leonard H van den Berg

24

Leonard H van den Berg

1 reference

18 August 2017

29

Wim Robberecht

1 reference

18 August 2017

13

Jan H Veldink

1 reference

18 August 2017

22

P Nigel Leigh

1 reference

18 August 2017

21

H Robert Horvitz

1 reference

18 August 2017

11

Benjamin M Neale

1 reference

18 August 2017

7

John E Landers

1 reference

18 August 2017

15

Vineeta B Tripathi

1 reference

18 August 2017

8

Peter Sapp

1 reference

18 August 2017

6

Paul W J van Vught

1 reference

18 August 2017

14

Roel A Ophoff

1 reference

18 August 2017

2

Robin Lemmens

1 reference

Katarzyna A Miśkiewicz-Orczyk

18 August 2017

3

Katarzyna Miskiewicz

1 reference

18 August 2017

19

Annelies Van Hoecke

1 reference

18 August 2017

28

Robert H Brown

1 reference

18 August 2017

Wendy J Broom

4

1 reference

18 August 2017

Valerie K Hansen

5

1 reference

18 August 2017

Ana Beleza

16

1 reference

18 August 2017

Meera N Shah

17

1 reference

18 August 2017

Pak C Sham

25

1 reference

18 August 2017

John F Powell

26

1 reference

18 August 2017

7 November 2008

1 reference

18 August 2017

Human Molecular Genetics

1 reference

18 August 2017

18

1 reference

18 August 2017

472-481

1 reference

18 August 2017

3

1 reference

describes a project that uses

18 August 2017

ImageQuant

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2638803/fullTextXML

inferred from PubMed Central ID database lookup

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2638803/fullTextXML

inferred from PubMed Central ID database lookup

cites work

Linkage disequilibrium between STRPs and SNPs across the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638803

TARDBP mutations in individuals with sporadic and 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=2638803

TDP-43 mutations in familial and sporadic 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=2638803

Genetic variation in DPP6 is associated with susceptibility to 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=2638803

ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638803

PLINK: a tool set for whole-genome association and population-based linkage analyses

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638803

Whole-genome analysis of sporadic 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=2638803

Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638803

Amyotrophic lateral sclerosis as a complex genetic 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=2638803

Molecular biology of amyotrophic lateral sclerosis: insights from genetics

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638803

Synaptic mitochondria are critical for mobilization of reserve pool vesicles at Drosophila neuromuscular junctions

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638803

Microsatellite instability generates diversity in brain and sociobehavioral traits

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638803

An early step in wobble uridine tRNA modification requires the Elongator complex

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638803

A central resource for accurate allele frequency estimation from pooled DNA genotyped on DNA microarrays

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638803

An aspartic acid repeat polymorphism in asporin inhibits chondrogenesis and increases susceptibility to osteoarthritis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638803

Haploview: analysis and visualization of LD and haplotype maps

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638803

Ataxin-7 is a subunit of GCN5 histone acetyltransferase-containing complexes

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638803

DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4)

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638803

Mapping Drosophila mutations with molecularly defined P element insertions

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638803

DNA Pooling: a tool for large-scale association studies

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638803

Making connections in the fly visual system

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638803

Elongator is a histone H3 and H4 acetyltransferase important for normal histone acetylation levels in vivo

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638803

RNA polymerase II elongator holoenzyme is composed of two discrete subcomplexes

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638803

Familial dysautonomia is caused by mutations of the IKAP gene

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638803

Inference of population structure using multilocus genotype data

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638803

High threshold for induction of the stress response in motor neurons is associated with failure to activate HSF1.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638803

A genome-wide association study of sporadic ALS in a homogenous Irish population.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638803

Exogenous delivery of heat shock protein 70 increases lifespan in a mouse model of amyotrophic lateral sclerosis.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638803

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

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638803

The GTPase dMiro is required for axonal transport of mitochondria to Drosophila synapses.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638803

Dap160/intersectin acts as a stabilizing scaffold required for synaptic development and vesicle endocytosis.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638803

A microsatellite polymorphism in intron 2 of human Toll-like receptor 2 gene: functional implications and racial differences

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638803

Analysis of Drosophila photoreceptor axon guidance in eye-specific mosaics.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638803

Genetic variability in the SNCA gene influences α-synuclein levels in the blood and brain

3 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FHMG%2FDDN375

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

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FHMG%2FDDN375

Monte Carlo tests for associations between disease and alleles at highly polymorphic loci

21 January 2018

1 reference

12 December 2020

MaGIC: a program to generate targeted marker sets for genome-wide association studies

1 reference

12 December 2020

Design and Analysis of Association Studies using Pooled DNA from Large Twin Samples

1 reference

12 December 2020

Gcn5- and Elp3-induced histone H3 acetylation regulates hsp70 gene transcription in yeast

1 reference

12 December 2020

Identifiers

DOI

10.1093/HMG/DDN375

1 reference

18 August 2017

1 reference

18 August 2017

1 reference