APPI

ANTAGONISTS OF PROTEIN-PROTEIN INTERACTIONS

 Coordinatore HELMHOLTZ-ZENTRUM FUER INFEKTIONSFORSCHUNG GMBH 

 Organization address address: Inhoffenstrasse 7
city: BRAUNSCHWEIG
postcode: 38124

contact info
Titolo: Dr.
Nome: Michael
Cognome: Strätz
Email: send email
Telefono: +49 531 6181 2020
Fax: +49 531 6181 2299

 Nazionalità Coordinatore Germany [DE]
 Totale costo 318˙727 €
 EC contributo 318˙727 €
 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-2007-4-1-IOF
 Funding Scheme MC-IOF
 Anno di inizio 2008
 Periodo (anno-mese-giorno) 2008-03-15   -   2011-03-14

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    HELMHOLTZ-ZENTRUM FUER INFEKTIONSFORSCHUNG GMBH

 Organization address address: Inhoffenstrasse 7
city: BRAUNSCHWEIG
postcode: 38124

contact info
Titolo: Dr.
Nome: Michael
Cognome: Strätz
Email: send email
Telefono: +49 531 6181 2020
Fax: +49 531 6181 2299

DE (BRAUNSCHWEIG) coordinator 0.00

Mappa


 Word cloud

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

genetic    genomic    cytokine    effort    infection    interactions    tools    platform    inflammation    genomics    hzi    genetics    models    molecular    diseases    gene    biology    researcher    expression    disease    protein    translational    enabled    tgen    genes   

 Obiettivo del progetto (Objective)

'Dysregulation of cytokine gene expression and cytokine regulated gene expression is the root cause of many diseases including viral and bacterial infections and chronic inflammation. In recent years, a variety of molecular biology and biochemistry research tools enabled the study of direct protein-protein interactions among various cytokine receptors and transcription factors which establish, maintain, and coordinate transcriptional regulation of cytokine genes. Currently, novel technologies and emerging statistical tools have enabled the use of translational genomics which involves the study of large sets of genes and proteins, with the goal of understanding systems, not simply components. An excellent complement to state of the art will be to apply translational genomic tools and molecular biology techniques to establish novel experimental models leading to a functional understanding of disease and the development of systems-based medical solutions. The aim of this proposal is to enable the researcher to acquire substantiated state of knowledge in translational genetics in the partner organisation 'Translational Genomics Research Institute' (TGen) which provides the data and tools necessary to identify the genes that play a role in hereditable diseases and understand the genetic changes contributing to disease progression. The researcher will assemble its own genomic research platform in order to translate genetic information of infection and inflammation diseases at TGen. She will build up a new independent platform in The Helmholtz Centre for Infection Research (HZI) which utilizes translational genetics research to establish infection and inflammation relevant cell-based models and uses chemical biology and competent compound collections in HZI to identify and create new bioactive small molecules for targeting disease relevant protein-protein interactions. This forward-looking project will significantly contribute to HZI competitiveness.'

Introduzione (Teaser)

A European effort addressed a key issue of inflammatory-related diseases in an effort to determine how protein interactions affect cytokine expression in type I diabetes and gastric cancer.

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