Opendata, web and dolomites

EnDeCAD SIGNED

Enhancers Decoding the Mechanisms Underlying CAD Risk

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 EnDeCAD project word cloud

Explore the words cloud of the EnDeCAD project. It provides you a very rough idea of what is the project "EnDeCAD" about.

gene    regions    genetic    identification    lying    correlative    interaction    discoveries    physical    vast    ultimately    data    obtain    hepatocytes    parallel    loci    strives    array    vessel    relationships    single    hope    fundamental    portion    candidate    complete    picture    cad    enhancer    events    search    date    smooth    gwas    eqtl    collection    discovered    polymorphisms    muscle    nucleotide    genes    combination    association    pioneering    molecular    causal    artery    functional    heritability    hundreds    basis    prediction    disease    driving    explained    link    characterization    endothelial    biological    mechanisms    function    trait    types    linking    cardiovascular    understand    breakthrough    roles    snps    linked    macrophages    genome    establishment    stimuli    biomarker    deep    treatment    adipocytes    majority    coronary    enhancers    significantly    metabolomics    provides    noncoding    cells    variants    phenotypic    clinical    progression    additionally    regulatory    snp    translatable    wall    risk    cell    small    expression    massively   

Project "EnDeCAD" data sheet

The following table provides information about the project.

Coordinator
ITA-SUOMEN YLIOPISTO 

Organization address
address: YLIOPISTONRANTA 1 E
city: KUOPIO
postcode: 70211
website: www.uef.fi

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Finland [FI]
 Total cost 1˙498˙647 €
 EC max contribution 1˙498˙647 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2018-STG
 Funding Scheme ERC-STG
 Starting year 2019
 Duration (year-month-day) from 2019-01-01   to  2023-12-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    ITA-SUOMEN YLIOPISTO FI (KUOPIO) coordinator 1˙498˙647.00

Map

 Project objective

In recent years, genome-wide association studies (GWAS) have discovered hundreds of single nucleotide polymorphisms (SNPs) which are significantly associated with coronary artery disease (CAD). However, the SNPs identified by GWAS explain typically only small portion of the trait heritability and vast majority of variants do not have known biological roles. This is explained by variants lying within noncoding regions such as in cell type specific enhancers and additionally ‘the lead SNP’ identified in GWAS may not be the ‘the causal SNP’ but only linked with a trait associated SNP. Therefore, a major priority for understanding disease mechanisms is to understand at the molecular level the function of each CAD loci. In this study we aim to bring the functional characterization of SNPs associated with CAD risk to date by focusing our search for causal SNPs to enhancers of disease relevant cell types, namely endothelial cells, macrophages and smooth muscle cells of the vessel wall, hepatocytes and adipocytes. By combination of massively parallel enhancer activity measurements, collection of novel eQTL data throughout cell types under disease relevant stimuli, identification of the target genes in physical interaction with the candidate enhancers and establishment of correlative relationships between enhancer activity and gene expression we hope to identify causal enhancer variants and link them with target genes to obtain a more complete picture of the gene regulatory events driving disease progression and the genetic basis of CAD. Linking these findings with our deep phenotypic data for cardiovascular risk factors, gene expression and metabolomics has the potential to improve risk prediction, biomarker identification and treatment selection in clinical practice. Ultimately, this research strives for fundamental discoveries and breakthrough that advance our knowledge of CAD and provides pioneering steps towards taking the growing array of GWAS for translatable results.

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "ENDECAD" project.

For instance: the website url (it has not provided by EU-opendata yet), the logo, a more detailed description of the project (in plain text as a rtf file or a word file), some pictures (as picture files, not embedded into any word file), twitter account, linkedin page, etc.

Send me an  email (fabio@fabiodisconzi.com) and I put them in your project's page as son as possible.

Thanks. And then put a link of this page into your project's website.

The information about "ENDECAD" are provided by the European Opendata Portal: CORDIS opendata.

More projects from the same programme (H2020-EU.1.1.)

CITISENSE (2019)

Evolving communication systems in response to altered sensory environments

Read More  

TORYD (2020)

TOpological many-body states with ultracold RYDberg atoms

Read More  

Mu-MASS (2019)

Muonium Laser Spectroscopy

Read More