SINGLECELLGENOMICS

Single cell genomic profiling of renal cancer stem cells

 Coordinatore BAR ILAN UNIVERSITY 

 Organization address address: BAR ILAN UNIVERSITY CAMPUS
city: RAMAT GAN
postcode: 52900

contact info
Titolo: Mrs.
Nome: Estelle
Cognome: Waise
Email: send email
Telefono: 97235317439
Fax: 97236353277

 Nazionalità Coordinatore Israel [IL]
 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-2013-CIG
 Funding Scheme MC-CIG
 Anno di inizio 2015
 Periodo (anno-mese-giorno) 2015-07-01   -   2019-06-30

 Partecipanti

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

 Organization address address: BAR ILAN UNIVERSITY CAMPUS
city: RAMAT GAN
postcode: 52900

contact info
Titolo: Mrs.
Nome: Estelle
Cognome: Waise
Email: send email
Telefono: 97235317439
Fax: 97236353277

IL (RAMAT GAN) coordinator 100˙000.00

Mappa


 Word cloud

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

biological    cancer    stem    single    types    tissue    cell    gene    tumor    tumors    cells    individual   

 Obiettivo del progetto (Objective)

'Complex biological systems such as a developing embryo, a regenerating tissue, or a tumor are composed of heterogeneous cell types. The complex behavior of these systems is often dominated by a minority cell population such as the embryonic stem cells in a developing organism or cancer stem cells in tumors. Thus, in order to properly understand development, tissue regeneration, and cancer, a single cell approach must be taken: the biological sample must be 'dissected' into many individual cells and each single cell has to be characterized independently. In this study we will develop and apply high throughput genomic methods for measuring gene expression in hundreds of individual cells in order to characterize transcriptional heterogeneity in tissues and tumors. This approach will allow us to find unique markers to identify cancer stem cells, elucidate their interactions with other cell types in the tumor, and systematically discover key gene circuits responsible for their long-term survival, self-renewal, and proliferation. As a starting point, we will focus on Wilms’ tumor, which is a common pediatric renal malignancy.'

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