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NEMoCuRe SIGNED

Role of S-Nitrosylation of epigenetic modifiers in vascular regeneration

Total Cost €

0

EC-Contrib. €

0

Partnership

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 NEMoCuRe project word cloud

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

proteins    proteomic    nitrosylation    activation    mutagenesis    provocative    biologist    candidate    excellent    spec    mentor    decipher    site    data    investigator    morpholinos    advantage    transition    foundations    talented    knocked    refine    toward    cardiology    consist    lines    disease    denvir    laser    extracts    strategies    career    supportive    independent    transgenic    tissues    describes    prepare    injury    dorsal    pharmacologically    mentorship    innate    coursework    vascular    msca    crispr    tlr3    builds    mutated    reader    tissue    matrone    nfkb    aorta    dr    interesting    confirm    formal    epigenetic    immune    centre    modulate    rerio    preliminary    modifiers    genetically    mechanisms    regeneration    humans    cardiovascular    skills    mass    injured    extensive    lay    inos    he    track    situ    trigger    structured    zebrafish    edinburgh    danio    sciences    nuclear    insights    cas9    martin    showing    background    university    plan   

Project "NEMoCuRe" data sheet

The following table provides information about the project.

Coordinator
THE UNIVERSITY OF EDINBURGH 

Organization address
address: OLD COLLEGE, SOUTH BRIDGE
city: EDINBURGH
postcode: EH8 9YL
website: www.ed.ac.uk

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 United Kingdom [UK]
 Total cost 195˙454 €
 EC max contribution 195˙454 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2017
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2018
 Duration (year-month-day) from 2018-09-01   to  2020-08-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    THE UNIVERSITY OF EDINBURGH UK (EDINBURGH) coordinator 195˙454.00

Map

 Project objective

This MSCA-IF describes a career development plan to prepare Dr. Matrone to become an independent investigator. This program builds on Dr. Matrone’s background as a talented biologist in cardiovascular regeneration and will provide him with the skills to decipher the mechanisms of S-Nitrosylation of epigenetic modifiers during tissue regeneration in zebrafish (Danio rerio). These studies will lay the foundations for future studies that will be carried out by Dr. Matrone as an independent investigator. The project will be carried out at the Centre for Cardiovascular Sciences at the University of Edinburgh. Dr. Matrone’s mentor is Dr. Martin Denvir, Reader in Cardiology. Dr. Denvir is an excellent mentor with extensive experience in cardiovascular disease. The MSCA-IF will consist of structured mentorship, formal coursework, a provocative research project and a program of career transition. Dr. Matrone’s research proposal is based on supportive preliminary data. Changes in S-nitrosylation of epigenetic modifiers in response to injury will be assessed in nuclear proteins extracts from injured tissues and identified by mass spec-proteomic analyses. The most interesting and novel epigenetic modifiers will be further studied in vascular development and regeneration following laser injury in the dorsal aorta. Candidate proteins will be knocked out by CRISPR/Cas9 or knocked down by morpholinos and will be mutated by site-specific mutagenesis. Furthermore, Dr. Matrone will assess the role of the innate immune system and iNOS in S-nitrosylation of nuclear proteins (e.g. epigenetic modifiers). He will confirm and refine his preliminary data showing that the innate immune system and iNOS trigger tissue regeneration. He will pharmacologically and genetically modulate TLR3, NFkB and iNOS and will take advantage of transgenic lines to track changes in the immune system activation in situ. These studies may provide insights toward novel strategies for tissue regeneration in humans.

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