RETACTIVITYIMAGING

Imaging light evoked activity at different strata of the mammalian retina

 Coordinatore Novartis Forschungsstiftung 

 Organization address address: Maulbeerstrasse 66
city: BASEL
postcode: 4058

contact info
Titolo: Dr.
Nome: Botond
Cognome: Roska
Email: send email
Telefono: 41616978575
Fax: 41616973976

 Nazionalità Coordinatore Switzerland [CH]
 Totale costo 187˙659 €
 EC contributo 187˙659 €
 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-2007-2-1-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2008
 Periodo (anno-mese-giorno) 2008-11-01   -   2010-10-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    Novartis Forschungsstiftung

 Organization address address: Maulbeerstrasse 66
city: BASEL
postcode: 4058

contact info
Titolo: Dr.
Nome: Botond
Cognome: Roska
Email: send email
Telefono: 41616978575
Fax: 41616973976

CH (BASEL) coordinator 0.00

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 Word cloud

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

mammalian    channels    ganglion    dendritic    retinal    inner    retina    cells    layer    visual    cell    plexiform    strata   

 Obiettivo del progetto (Objective)

'The mammalian visual system analyzes the world through a set of separate spatio-temporal channels. The organization of these channels begins in the retina where the precise laminations of both the axon terminals of bipolar cells and the dendritic arbors of ganglion cells form a vertical stack of neural strata at the inner plexiform layer. A major challenge is to understand how the different 'visual features' extracted by different retinal ganglion cell types are computed by each, ganglion cell type specific, circuitry at different depths in the inner plexiform layer. My specific research aim is to use in vivo electroporated, genetically encoded fluorescent activity reporters in subtypes of inner retinal cells to image in real-time the patterns of light evoked activity at the dendritic or axonal processes of the labeled cells using two-photon microscopy. My goal is to understand the 'rules' of local activities in different strata of the mammalian inner retina.'

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