ADVANCEDMODNEURO

Multiscale analysis and hybrid simulations of neuronal microdomains: from molecular dynamics to function

 Coordinatore THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD 

 Organization address address: University Offices, Wellington Square
city: OXFORD
postcode: OX1 2JD

contact info
Titolo: Ms.
Nome: Gill
Cognome: Wells
Email: send email
Telefono: +44 1865 289800
Fax: +44 1865 289801

 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 309˙235 €
 EC contributo 309˙235 €
 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-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2015
 Periodo (anno-mese-giorno) 2015-05-08   -   2017-05-07

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD

 Organization address address: University Offices, Wellington Square
city: OXFORD
postcode: OX1 2JD

contact info
Titolo: Ms.
Nome: Gill
Cognome: Wells
Email: send email
Telefono: +44 1865 289800
Fax: +44 1865 289801

UK (OXFORD) coordinator 309˙235.20

Mappa


 Word cloud

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dynamics    data    singular    spatial    molecular    synapses    microdomains    models    neuronal    asymptotic    mathematical    cellular    perturbation    scales    stochastic    modeling    simulations   

 Obiettivo del progetto (Objective)

'Critical biological processes, such as cellular physiology or neuronal transmission have very different spatial scales are due to small binding sites inside or on the cell boundary, or narrow passages between large compartments. The great disparity in spatial scales can be resolved by singular perturbation analysis of their mathematical models. Deriving the function of neuronal synapses from their molecular organization falls precisely in the class of problems associated with diffusion and it constitutes the inherent daunting hurdle of multiple scales. We propose here to construct mathematical models of neuronal microdomains, starting from the molecular to the cellular level and to develop stochastic modeling and singular perturbation methods for asymptotic analysis of the model equations, to use the analytical and numerical approximate solutions to extract properties from newly available molecular data and from Brownian dynamics simulations. A major application of the proposed molecular level modeling is the resolution of the spatiotemporal dynamics regulating neuronal microdomains and synapses. The results of this research will be methods in mathematical modeling, data analysis, asymptotic analysis, and in the designing of stochastic simulations of subcellular processes.'

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