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Angiolnc SIGNED

Endothelial long non-coding RNAs

Total Cost €

0

EC-Contrib. €

0

Partnership

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 Angiolnc project word cloud

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

cell    angiolnc1    cancer    central    metabolites    named    comprise    models    generation    ncrnas    examples    endothelial    largely    coding    contributes    genome    play    functions    dissect    200    molecules    unknown    explore    therapeutic    myocardial    circular    mechanisms    rna    retinopathy    cellular    begin    regulated    levels    stroke    metabolic    vasculature    angiogenesis    syndromes    encodes    angiolnc    back    inner    human    explored    molecular    tools    rnas    expression    atherosclerosis    understand    heterogenic    delivers    infarction    functionally    roles    angiolnc2    enriched    cells    cardiovascular    tissue    hypoxia    gt    oxygen    sponges    diseases    cover    suggests    regulate    active    tumor    pathophysiological    act    nucleotides    endothelium    prototypical    specimens    cytoplasm    length    lncrnas    pathological    und    diabetic    dysfunction    epigenetic    aging    class    mouse    occurs    splicing    whereas    diagnostic    regulation    sequencing    discovery    circrnas    function    portion   

Project "Angiolnc" data sheet

The following table provides information about the project.

Coordinator
JOHANN WOLFGANG GOETHE-UNIVERSITATFRANKFURT AM MAIN 

Organization address
address: THEODOR W ADORNO PLATZ 1
city: FRANKFURT AM MAIN
postcode: 60323
website: www.uni-frankfurt.de

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 Germany [DE]
 Total cost 2˙497˙398 €
 EC max contribution 2˙497˙398 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2014-ADG
 Funding Scheme ERC-ADG
 Starting year 2016
 Duration (year-month-day) from 2016-01-01   to  2020-12-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    JOHANN WOLFGANG GOETHE-UNIVERSITATFRANKFURT AM MAIN DE (FRANKFURT AM MAIN) coordinator 2˙497˙398.00

Map

 Project objective

Endothelial cells comprise the inner cellular cover of the vasculature, which delivers metabolites and oxygen to the tissue. Dysfunction of endothelial cells as it occurs during aging or metabolic syndromes can result in atherosclerosis, which can lead to myocardial infarction or stroke, whereas pathological angiogenesis contributes to tumor growth and diabetic retinopathy. Thus, endothelial cells play central roles in pathophysiological processes of many diseases including cardiovascular diseases and cancer. Many studies explored the regulation of endothelial cell functions by growth factors, but the impact of epigenetic mechanisms and particularly the role of novel non-coding RNAs is largely unknown. More than 70 % of the human genome encodes for non-coding RNAs (ncRNAs) and increasing evidence suggests that a significant portion of these ncRNAs are functionally active as RNA molecules. Angiolnc aims to explore the function of long ncRNAs (lncRNAs) and particular circular RNAs (circRNAs) in the endothelium. LncRNAs comprise a heterogenic class of RNAs with a length of > 200 nucleotides and circRNAs are generated by back splicing. Angiolnc is based on the discovery of novel endothelial hypoxia-regulated lncRNAs and circRNAs by next generation sequencing. To begin to understand the potential functions of lncRNAs in the endothelium, we will study two lncRNAs, named Angiolnc1 und Angiolnc2, as prototypical examples of endothelial cell-enriched lncRNAs that are regulated by oxygen levels. We will further dissect the epigenetic mechanisms, by which these lncRNAs regulate endothelial cell function. In the second part of the application, we will determine the regulation and function of circRNAs, which may act as molecular sponges in the cytoplasm. Finally, we will study the function of identified lncRNAs and circRNAs in mouse models and measure their expression in human specimens in order to determine their role as therapeutic targets or diagnostic tools.

 Publications

year authors and title journal last update
List of publications.
2017 Florian C. Bischoff, Astrid Werner, David John, Jes-Niels Boeckel, Maria-Theodora Melissari, Phillip Grote, Simone F. Glaser, Shemsi Demolli, Shizuka Uchida, Katharina M. Michalik, Benjamin Meder, Hugo A. Katus, Jan Haas, Wei Chen, Soni S. Pullamsetti, Werner Seeger, Andreas M. Zeiher, Stefanie Dimmeler, Christoph M. Zehendner
Identification and Functional Characterization of Hypoxia-Induced Endoplasmic Reticulum Stress Regulating lncRNA (HypERlnc) in PericytesNovelty and Significance
published pages: 368-375, ISSN: 0009-7330, DOI: 10.1161/CIRCRESAHA.116.310531
Circulation Research 121/4 2019-07-02

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