KINSIGN

Guarding Genome Stability: Dynamic Control of Chromosome Segregation by Kinetochore Signalling Pathways

 Coordinatore UNIVERSITAIR MEDISCH CENTRUM UTRECHT 

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 Nazionalità Coordinatore Netherlands [NL]
 Totale costo 1˙572˙000 €
 EC contributo 1˙572˙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-2009-StG
 Funding Scheme ERC-SG
 Anno di inizio 2009
 Periodo (anno-mese-giorno) 2009-11-01   -   2014-10-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITAIR MEDISCH CENTRUM UTRECHT

 Organization address address: HEIDELBERGLAAN 100
city: UTRECHT
postcode: 3584 CX

contact info
Titolo: Dr.
Nome: Geert Johannes Petrus Lambertus
Cognome: Kops
Email: send email
Telefono: -7555220
Fax: -7568158

NL (UTRECHT) hostInstitution 1˙572˙000.00
2    UNIVERSITAIR MEDISCH CENTRUM UTRECHT

 Organization address address: HEIDELBERGLAAN 100
city: UTRECHT
postcode: 3584 CX

contact info
Titolo: Mr.
Nome: Erik
Cognome: Van Den Broek
Email: send email
Telefono: +31 88 7568172
Fax: +31 88 7553660

NL (UTRECHT) hostInstitution 1˙572˙000.00

Mappa


 Word cloud

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

division    segregation    enzymes    prevent    chromosome    chromosomes    biochemical    cell   

 Obiettivo del progetto (Objective)

'Equal segregation of chromosomes during cell division is vital to all life. Using a unique combination of cell biological and biochemical techniques, I will show how an essential set of enzymes promotes error-free chromosome segregation. During each cell division, genetically identical daughter cells are generated by accurate partitioning of the duplicated chromosomes. This relies on proper spatio-temporal execution of various highly dynamic processes. The activity of a small group of enzymes is crucial for at least two of these processes: correct chromosome positioning on the cell's equator prior to cell division and the ability to prevent cell division until every chromosome is thus positioned. The molecular fundamentals of signalling to and from these enzymes will be uncovered by chemical genetics, quantitative (phospho)proteomics, rapid affinity purifications and live-cell deconvolution microscopy. The resulting insights will open research avenues that will ultimately contribute to comprehensive models of how biochemical networks manage to prevent chromosome mis-segregation.'

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