MIRNAVASC

Role of microRNAs in vascular diseases

 Coordinatore CHARITE - UNIVERSITAETSMEDIZIN BERLIN 

 Organization address address: Chariteplatz 1
city: BERLIN
postcode: 10117

contact info
Nome: Eveline
Cognome: Fräßdorf
Email: send email
Telefono: +49 30450576024
Fax: +49 30450576954

 Nazionalità Coordinatore Germany [DE]
 Totale costo 162˙661 €
 EC contributo 162˙661 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-2009-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2010
 Periodo (anno-mese-giorno) 2010-10-01   -   2013-11-19

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    CHARITE - UNIVERSITAETSMEDIZIN BERLIN

 Organization address address: Chariteplatz 1
city: BERLIN
postcode: 10117

contact info
Nome: Eveline
Cognome: Fräßdorf
Email: send email
Telefono: +49 30450576024
Fax: +49 30450576954

DE (BERLIN) coordinator 162˙661.00

Mappa


 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

acute    dysregulation    atherothrombosis    event    modulate    risk    mirna    cardiovascular    atherotrombosis    mirnas    rupture   

 Obiettivo del progetto (Objective)

'Atherothrombosis still represents the major cause of death in developed countries. All forms of atheroma are characterized by a risk of arterial wall rupture leading to clinical complications. This involves medial and adventitial ruptures in abdominal aortic aneurysm (AAA) and intimal cap rupture in vulnerable atherosclerotic plaques. In both cases the rupture may result in the occlusion of an artery by the formation of a thrombus causing an acute event. Being able to predict who is at risk of an acute cardiovascular event is at present one of the major challenges of cardiovascular medicine. MicroRNAs (miRNAs) are small (typically 22 nt in size) regulatory RNA molecules that function to modulate the activity of specific mRNA targets and play important roles in a wide range of physiologic and pathologic processes. Recent studies have revealed that miRNAs are able to modulate different pathological process involved in atherotrombosis. Our working hypothesis is that the development of atherothrombosis is a chronic process that is associated with miRNA dysregulation, that is, altered miRNA expression profiles may be the cause of many of the abnormalities related to atherotrombosis. The aim of this project is to link miRNA dysregulation to pathophysiology of atherothrombosis, with the aim of characterizing novel biomarkers which could be used in the diagnostic, prognostic and therapeutic setting.'

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