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RECOLOR SIGNED

Regulation and consequences of LRRK2 phosphorylation,a path to Parkinson’s disease therapy and diagnostics

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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 RECOLOR project word cloud

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

mechanisms    disease    host    excellence    experimental    parkinson    player    strategically    pathogenesis    lille    neurodegenerative    france    tau    collaborating    profile    repeat    internationally    transcriptome    coordinated    performed    diagnostic    adding    mixed    verify    reposition    elucidate    international    papers    signalling    phosphatases    expertise    neurobiologist    health    understand    network    hospital    clinical    training    inserm    diseases    fertile    reveal    chosen    samples    follow    modifying    leverage    biology    lrrk2    center    movement    leucine    phosphorylation    incurable    dimension    fellowship    downstream    kinase    models    24    biosample    visibility    phenotypes    regulation    community    biomarkers    jpa    extensive    neurodegeneration    therapy    pd    builds    profiling    cellular    exploited    shown    therapeutic    functions    ground    protein    groups    university    locally    molecular    translation    disorder    biosamples    pursuing   

Project "RECOLOR" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITE DE LILLE II - DROIT ET SANTE 

Organization address
address: RUE PAUL DUEZ 42
city: Lille
postcode: 59800
website: www.univ-lille2.fr

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 France [FR]
 Project website http://www.lrrk2.info
 Total cost 185˙076 €
 EC max contribution 185˙076 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2014
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2015
 Duration (year-month-day) from 2015-06-01   to  2017-05-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITE DE LILLE II - DROIT ET SANTE FR (Lille) coordinator 185˙076.00

Map

Leaflet | Map data © OpenStreetMap contributors, CC-BY-SA, Imagery © Mapbox

 Project objective

Parkinson’s disease (PD) is the most common neurodegenerative movement disorder, currently incurable. Studies in the PD field show that leucine-rich repeat kinase 2 (LRRK2) is both a major player in PD pathogenesis and a promising PD therapeutic target. LRRK2 functions in health and disease are not defined; however the applicant and others have shown that LRRK2 phosphorylation is the key to understanding LRRK2 biology. This project’s goal is therefore to understand the role of LRRK2 phosphorylation in PD by pursuing 3 specific aims: 1) elucidate the regulation of LRRK2 phosphorylation by phosphatases, 2) determine LRRK2 phosphorylation downstream phenotypes in cellular models through transcriptome profiling, protein translation profiling and protein tau related phenotypes, and 3) verify these findings from experimental models in PD biosamples. The project builds on the applicant’s extensive expertise in the field of LRRK2 biology (24 papers in 8 years) required for aim 1 and will leverage expertise on PD biosample analysis of the host institution (training for aims 2 and 3). The research program will be performed at the JPA research center (a mixed Inserm-Lille 2 University-Lille University Hospital center for excellence research, Lille, France), with a network of strategically chosen collaborating research groups locally and internationally, coordinated by the applicant. The study of LRRK2 phosphorylation in experimental models and translation of experimental results to clinical samples will reveal the most relevant molecular mechanisms of LRRK2 in PD which can be exploited in follow up work as diagnostic biomarkers and targeted for disease-modifying therapy. Given the importance of PD and neurodegeneration in Europe, this project is fertile ground for a high visibility fellowship and will reposition the applicant in the international neurodegenerative diseases research community by adding a clinical translation dimension to his signalling neurobiologist profile.

 Publications

year authors and title journal last update
List of publications.
2017 Kushal Sejwal, Mohamed Chami, Hervé Rémigy, Renée Vancraenenbroeck, William Sibran, Rosmarie Sütterlin, Paul Baumgartner, Robert McLeod, Marie-Christine Chartier-Harlin, Veerle Baekelandt, Henning Stahlberg, Jean-Marc Taymans
Cryo-EM analysis of homodimeric full-length LRRK2 and LRRK1 protein complexes
published pages: 8667, ISSN: 2045-2322, DOI: 10.1038/s41598-017-09126-z
Scientific Reports 7/1 2019-06-17
2016 Jean-Marc Taymans, Elisa Greggio
LRRK2 Kinase Inhibition as a Therapeutic Strategy for Parkinson\'s Disease, Where Do We Stand?
published pages: 214-225, ISSN: 1570-159X, DOI: 10.2174/1570159X13666151030102847
Current Neuropharmacology 14/3 2019-06-17
2017 Jean-Marc Taymans, Eugénie Mutez, Matthieu Drouyer, William Sibran, Marie-Christine Chartier-Harlin
LRRK2 detection in human biofluids: potential use as a Parkinson\'s disease biomarker?
published pages: 207-212, ISSN: 0300-5127, DOI: 10.1042/BST20160334
Biochemical Society Transactions 45/1 2019-06-17

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

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