MOLPARK

Molecular mechanisms of neuronal restoration: novel approaches for Parkinson's Disease

 Coordinatore CARDIFF UNIVERSITY 

 Organization address address: Newport Road 30-36
city: CARDIFF
postcode: CF24 ODE

contact info
Titolo: Mr.
Nome: Nick
Cognome: Bodycombe
Email: send email
Telefono: 442921000000
Fax: 442921000000

 Nazionalità Coordinatore United Kingdom [UK]
 Sito del progetto http://www.molpark.co.uk
 Totale costo 4˙590˙740 €
 EC contributo 3˙472˙653 €
 Programma FP7-HEALTH
Specific Programme "Cooperation": Health
 Code Call FP7-HEALTH-2007-B
 Funding Scheme CP-FP
 Anno di inizio 2009
 Periodo (anno-mese-giorno) 2009-04-01   -   2012-09-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    CARDIFF UNIVERSITY

 Organization address address: Newport Road 30-36
city: CARDIFF
postcode: CF24 ODE

contact info
Titolo: Mr.
Nome: Nick
Cognome: Bodycombe
Email: send email
Telefono: 442921000000
Fax: 442921000000

UK (CARDIFF) coordinator 636˙163.00
2    KAROLINSKA INSTITUTET

 Organization address address: Nobels Vag 5
city: STOCKHOLM
postcode: 17177

contact info
Titolo: Ms.
Nome: Eva
Cognome: Tegelberg
Email: send email
Telefono: 46852487855
Fax: 468333864

SE (STOCKHOLM) participant 1˙035˙517.00
3    UNIVERSITY COLLEGE LONDON

 Organization address address: GOWER STREET
city: LONDON
postcode: WC1E 6BT

contact info
Titolo: Mr.
Nome: Kent
Cognome: Lee
Email: send email
Telefono: 442077000000
Fax: 442077000000

UK (LONDON) participant 517˙760.00
4    HELSINGIN YLIOPISTO

 Organization address address: YLIOPISTONKATU 4
city: HELSINGIN YLIOPISTO
postcode: 14

contact info
Titolo: Dr.
Nome: Sanna-Maija
Cognome: Miettinen
Email: send email
Telefono: 358919000000
Fax: 358919000000

FI (HELSINGIN YLIOPISTO) participant 388˙162.00
5    MAX PLANCK GESELLSCHAFT ZUR FOERDERUNG DER WISSENSCHAFTEN E.V.

 Organization address address: Hofgartenstrasse 8
city: MUENCHEN
postcode: 80539

contact info
Titolo: Ms.
Nome: Angelika
Cognome: Haefeker
Email: send email
Telefono: 498986000000
Fax: 498986000000

DE (MUENCHEN) participant 388˙162.00
6    CEREBRICON OY

 Organization address address: MICROKATU 1
city: KUOPIO
postcode: 70210

contact info
Titolo: Ms.
Nome: Kirsi
Cognome: Pohjolainen
Email: send email
Telefono: 358174000000
Fax: 358174000000

FI (KUOPIO) participant 253˙445.00
7    KDEV EXPLORATORY AB

 Organization address address: NOBELS VAEG 3
city: STOCKHOLM
postcode: 171 77

contact info
Titolo: Ms.
Nome: Eva
Cognome: Montgomerie
Email: send email
Telefono: 46852484801
Fax: 46852484800

SE (STOCKHOLM) participant 253˙444.00

Mappa


 Word cloud

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

stem    connections    molpark    survival    disease    cell    renewal    restoring    dopaminergic    mechanisms    self    strategies    pd    neurons    nigrostriatal    differentiation    therapeutic   

 Obiettivo del progetto (Objective)

'MOLPARK aims to define the basic cellular and molecular mechanisms underlying the generation, differentiation, survival and connectivity of nigrostriatal dopaminergic neurons and translate this knowledge into radically new therapeutic strategies for Parkinson's disease (PD). MOLPARK brings together two industrial partners and 6 world-renowned academic groups with a uniquely advantageous knowledge platform based on complementary state-of-the-art technologies and recent relevant discoveries in their laboratories. These include, unique approaches for stem cell renewal control based on novel insights into the function of GABA receptors and intracellular signaling components such as Bex1, novel neurotrophic factors for dopaminergic neurons such as CDNF and MANF, novel approaches to harness the power of GDNF and Wnt proteins for stimulating the growth of dopaminergic terminals and novel ways to enhance synaptogenesis, MOLPARK’s strategy is based on four major interrelated objectives. I). Define the mechanisms of stem cell self-renewal, differentiation and integration and exploit these mechanisms to induce or boost existing self-repair processes with the aim of replenishing neurons in PD. 2). Define the mechanisms for sustaining dopaminergic neuron survival in health and disease with the aim of developing new, effective growth factor-based therapies aimed at protecting neurons in PD. 3). Define the mechanisms that promote the growth of DA nigrostriatal axons and dendrites with the aim of identifying therapeutic strategies based on restoring neural processes in PD. 4). Define the mechanisms that promote and sustain the synaptic connections of dopaminergic neurons with the aim of restoring connections in PD.'

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