INDUVIR

Improved gene transfer system to iPS cells in mouse

 Coordinatore BIOTALENTUM TUDASFEJLESZTO KFT 

 Organization address address: AULICH LAJOS UTCA 26
city: GOEDOELLO
postcode: 2100

contact info
Titolo: Prof.
Nome: Andras
Cognome: Dinnyes
Email: send email
Telefono: +36 20 510 9632
Fax: +36 28 526 151

 Nazionalità Coordinatore Hungary [HU]
 Totale costo 100˙000 €
 EC contributo 100˙000 €
 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-RG
 Funding Scheme MC-IRG
 Anno di inizio 2009
 Periodo (anno-mese-giorno) 2009-10-01   -   2013-09-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    BIOTALENTUM TUDASFEJLESZTO KFT

 Organization address address: AULICH LAJOS UTCA 26
city: GOEDOELLO
postcode: 2100

contact info
Titolo: Prof.
Nome: Andras
Cognome: Dinnyes
Email: send email
Telefono: +36 20 510 9632
Fax: +36 28 526 151

HU (GOEDOELLO) coordinator 100˙000.00

Mappa


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cells    therapy    ips    stem    cardiac    induvir    differentiation    cell   

 Obiettivo del progetto (Objective)

'The scientific aim of InduVir is to produce novel comparative information on the generation, maintenance and characteristics of iPS cells in mouse and on their differentiation towards different, especially cardiac lineages. In InduVir we are aiming to develop a novel system, by using removable transposons and polycistronic, deletable lentiviruses and therefore significantly reduce the risk of malignant transformations associated with conventional iPS technologies. Technical focus will be developing a novel and potentially patentable technology in Europe for reprogramming somatic cells to an embryonic state, which have a excellent potential for future cell based therapy. InduVir will also develop methods for targeted differentiation of the iPS cells to cardiac cells. We expect to get novel information on pathways and transcriptional networks that regulate differentiation and lineage specification. The differentiated cardiac tissues would provide superior tools for pharmacological studies or high-throughput screening. IPS technology has the great potential to generate patient and disease specific stem cells and derivates, yet it lacks many of the technical, ethical and legal issues associated with human ES cell research including therapeutic cloning.The information generated by these studies will contribute to stem cell therapy and modern regenerative medicine.'

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