BRAINPLASTICITY

In vivo imaging of functional plasticity in the mammalian brain

 Coordinatore THE HEBREW UNIVERSITY OF JERUSALEM. 

Spiacenti, non ci sono informazioni su questo coordinatore. Contattare Fabio per maggiori infomrazioni, grazie.

 Nazionalità Coordinatore Israel [IL]
 Totale costo 1˙750˙000 €
 EC contributo 1˙750˙000 €
 Programma FP7-IDEAS-ERC
Specific programme: "Ideas" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call ERC-2007-StG
 Funding Scheme ERC-SG
 Anno di inizio 2008
 Periodo (anno-mese-giorno) 2008-08-01   -   2013-07-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    THE HEBREW UNIVERSITY OF JERUSALEM.

 Organization address address: GIVAT RAM CAMPUS
city: JERUSALEM
postcode: 91904

contact info
Titolo: Dr.
Nome: Adi
Cognome: Mizrahi
Email: send email
Telefono: 972-2-6586460
Fax: 972-2-6584703

IL (JERUSALEM) hostInstitution 0.00
2    THE HEBREW UNIVERSITY OF JERUSALEM.

 Organization address address: GIVAT RAM CAMPUS
city: JERUSALEM
postcode: 91904

contact info
Titolo: Ms.
Nome: Irit
Cognome: Harat
Email: send email
Telefono: +972 2 6586679
Fax: +972 7 22447007

IL (JERUSALEM) hostInstitution 0.00

Mappa


 Word cloud

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vivo    reveal    mammalian    neuronal    scales    adult    time    physiological    plasticity    tools    single    optical    disparate    neurons    born    brain   

 Obiettivo del progetto (Objective)

'The dynamic nature of the brain operates at disparate time scales ranging from milliseconds to months. How do single neurons change over such long time scales? This question remains stubborn to answer in the field of brain plasticity mainly because of limited tools to study the physiology of single neurons over time in the complex environment of the brain. The research aim of this proposal is to reveal the physiological changes of single neurons in the mammalian brain over disparate time scales using time-lapse optical imaging. Specifically, we aim to establish a new team that will develop genetic and optical tools to probe the physiological activity of single neurons, in vivo. As a model system, we will study a unique neuronal population in the mammalian brain; the adult-born local neurons in the olfactory bulb. These neurons have tremendous potential to reveal how neurons develop and maintain in the intact brain because they are accessible both genetically and optically. By following the behavior of adult-born neurons in vivo we will discover how neurons mature and maintain over days and weeks. If our objectives will be met, this study has the potential to significantly 'raise the bar' on how neuronal plasticity is studied and reveal some basic secrets of the ever changing mammalian brain.'

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