DIVIMAGE

Bridging spatial and temporal resolution gaps in the study of cell division

 Coordinatore INSTITUT FUER MOLEKULARE BIOTECHNOLOGIE GMBH 

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 Nazionalità Coordinatore Austria [AT]
 Totale costo 1˙500˙000 €
 EC contributo 1˙500˙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-2011-StG_20101109
 Funding Scheme ERC-SG
 Anno di inizio 2012
 Periodo (anno-mese-giorno) 2012-03-01   -   2017-02-28

 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 790444410
Fax: +43 1 7987153

AT (VIENNA) hostInstitution 1˙500˙000.00
2    INSTITUT FUER MOLEKULARE BIOTECHNOLOGIE GMBH

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

contact info
Titolo: Prof.
Nome: Daniel Wolfram
Cognome: Gerlich
Email: send email
Telefono: +41 79 7582328
Fax: +43 1 79044 4110

AT (VIENNA) hostInstitution 1˙500˙000.00

Mappa


 Word cloud

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computational    abscission    intercellular    resolution    correlative    split    cells    bridge    imaging    temporal    mechanism   

 Obiettivo del progetto (Objective)

'Cell division underlies the growth and development of all living organisms. Following partitioning of bulk cytoplasmic contents by cleavage furrow ingression, dividing animal cells split by a distinct process termed abscission. Whereas a number of factors required for abscission have been identified in previous studies, it is not known by which mechanism they mediate fission of the intercellular bridge between the nascent sister cells. Here, we will establish correlative workflows of time-lapse imaging, super resolution fluorescence microscopy, electron tomography, and electrophysiological assays to bridge spatial and temporal resolution gaps in the study of abscission. We will further develop computational tools for image-based RNAi screening. With this, we aim to: 1) elucidate how membrane and cytoskeletal dynamics coordinately split the intercellular bridge; 2) uncover the signaling pathways controlling abscission timing. Failure in abscission can lead to aneuploidy and cancer. Elucidating its mechanism and temporal control is therefore of general biological and medical relevance. The computational and correlative imaging methods developed in this project will further provide the research community new possibilities for mechanistic studies in intact cells.'

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