The aim of this call was to enable scientists in different countries to build effective collaborations on common interdisciplinary research projects on rare diseases, based on complementarities and sharing of expertise.
Ten countries: France, Germany, Israel, Spain, Turkey, The Netherlands, Italy, Portugal, Austria and Greece participated in this 2nd E-Rare Transnational Call.
More information on the Aims, the Topics, and the Application and Evaluation procedures can be found in the Call documents (see the "Downlaod documents" section).
To see the list and more information about financed projects click on the button FUNDED PROJECTS.
If you need more information please contact the 2nd Joint Call Secretariat:
Dr. Ralph Schuster
e-mail: ralph.schuster@dlr.de
Tel: +49 228 382 12 33 or +49 228 3821 775
The Call text of JTC 2009 is available in the Download documents section of this call.
| Year | Acronym | Project Coordinator | Title |
|---|---|---|---|
2009 | Understanding and treating neurodegeneration caused by mucopolysaccharidoses | ||
2009 | Targeting Rho-signalling, a new therapeutic avenue in fragile X syndrome | ||
2009 | Identification of revertant mosaicism in epidermolysis bullosa and subsequently using the revertant keratinocytes in a pre-clinical mouse model suitable to test revertant cell therapy | ||
2009 | Congenital neutropenia with ELA-2 mutations (ELA2-CN): Identification of (epi)genetic co-factors and molecular pathways underlying clinical heterogeneity | ||
2009 | European Multidisciplinary Initiative on Neuroacanthocytosis | ||
2009 | European pulmonary alveolar proteinosis network : molecular determinants of causes, variability and outcome | ||
2009 | Genetics and pathogenesis of chronic granulomatous disease and development of new gene transfer therapeutic approaches | ||
2009 | European network on genetics, pathophysiology and translational research into rare pancreatic beta-cell insufficiency diseases | ||
2009 | Improvements of vector technology and safety for the gene therapy of thalassemia | ||
2009 | Towards improved diagnosis and treatment of rare inherited microcytic hypochromic anemias related to iron metabolism | ||
2009 | Megalencephalic leukoencephalopathy with subcortical cysts: from molecular basis to search for therapy | ||
2009 | Functional characterization of nemaline myopathy in a murine model with nebulin mutation: moving from basic understanding towards therapeutic interventions | ||
2009 | Inherited inhibition of inborn immunity – an integrated molecular genetic approach to discover novel human gene defects | ||
2009 | European network on noonan syndrome and related disorders | ||
2009 | Comprehensive analysis of rod-cone photoreceptor degeneration associated with rhodopsin gene mutations |
If you need more information please contact the 2nd Joint Call Secretariat:
Dr. Ralph Schuster
e-mail: ralph.schuster@dlr.de
Tel: +49 228 382 12 33 or +49 228 3821 775
To find all national contact points for this call please refer to the Call text document that is available in the Download documents section of this call.
Looking for collaborations | Contact | Interactive FAQ |
For more information ABOUT E-Rare please contact:
E-Rare Coordinator
Daria JULKOWSKA
Tel.: +33(0) 1 78 09 80 78
daria.julkowska@agencerecherche.fr
Agence Nationale de la Recherche - ANR
Health & Biology Department
50 Avenue Daumesnil
75012 Paris, France
E-Rare 2012 - Created by Toussaint Biger
