ROSETTE NSC SCREEN

Mechanisms of Neurogenesis from Drosophila to Human

 Coordinatore INSTITUT FUER MOLEKULARE BIOTECHNOLOGIE GMBH 

 Organization address address: Dr Bohrgasse 3
city: VIENNA
postcode: 1030

contact info
Titolo: Ms.
Nome: Tanja
Cognome: Winkler
Email: send email
Telefono: +43 1 79044 4410

 Nazionalità Coordinatore Austria [AT]
 Totale costo 187˙888 €
 EC contributo 187˙888 €
 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-2011-IIF
 Funding Scheme MC-IIF
 Anno di inizio 2013
 Periodo (anno-mese-giorno) 2013-03-01   -   2015-06-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    INSTITUT FUER MOLEKULARE BIOTECHNOLOGIE GMBH

 Organization address address: Dr Bohrgasse 3
city: VIENNA
postcode: 1030

contact info
Titolo: Ms.
Nome: Tanja
Cognome: Winkler
Email: send email
Telefono: +43 1 79044 4410

AT (VIENNA) coordinator 187˙888.20

Mappa


 Word cloud

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

regulators    mammalian    cortical    asymmetric    human    rosettes    neural    division    differentiation    screen    renewal    functional    mechanisms    candidates    self    cell    perform    drosophila   

 Obiettivo del progetto (Objective)

'Neurogenesis in the mammalian neocortex depends upon asymmetric cell divisions to maintain a balance between self-renewal and neuronal differentiation. This process is likely a key element governing the expansion of the human cerebral cortex, and its disruption can lead to severe developmental disorders such as microcephaly and lissencephaly. However, mechanisms of asymmetric cell division in mammalian brain development are largely unclear, and its potential role in human cortical development has not been examined. Substantial headway has been made in understanding mechanisms of asymmetric cell division in the Drosophila central nervous system. Our lab has recently published a genome-wide RNAi screen, which has identified several novel regulators of asymmetric cell division in Drosophila. To test whether these newly identified factors have conserved roles in mammals, I will use mouse neural rosettes to screen and perform functional assessments of the promising candidates. I will then perform functional studies of human neural rosettes to test our candidates, as well as previously identified regulators of asymmetric cell division. In this way, I will utilize the neural rosettes system to screen for new regulators of self-renewal and differentiation and examine the role of asymmetric cell division in human cortical development.'

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