Leidsin 16 projekti. otsingusõna [ UNIVERZITA KARLOVA ]

Programmid
Partner-riigid (projektides osaluse arv)
projekti nr akronüüm ja pealkiri kestus
H2020 - 951724 B1MG - Beyond 1M Genomes 2020-2023
H2020 - 825303 Bergamot - Browser-based Multilingual Translation -
H2020 - 777389 c4c - conect4children (COllaborative Network for European Clinical Trials For Children) 2018-2024
H2020 - 765224 FATIGUE - Delayed Transformational Fatigue in Central and Eastern Europe 2018-2021
H2020 - 874864 HEDIMED - Human Exposomic Determinants of Immune Mediated Diseases 2020-2024
H2020 - 871106 ISABEL - Improving the sustainability of the European Magnetic Field Laboratory 2020-2024
H2020 - 822682 POPREBEL - Populist rebellion against modernity in 21st-century Eastern Europe: neo-traditionalism and neo-feudalism 2019-2021
FP7 - 242204 AAA-PREVENT - Effective Environmental Strategies for the Prevention of Alcohol Abuse among Adolescents in Europe 2010-2012
FP7 - 223692 CHERISH - Improving Diagnoses of Mental Retardation in Children in Central Eastern Europe and Central Asia through Genetic Characterisation and Bioinformatics/-Statistics, 2009-2012
FP7 - 212230 CLARIN - Common Language Resources and Technology Infrastructure 2008-2011
FP7 - 602453 CloSed - Clonidine for Sedation of Paediatric Patients in the Paediatric Intensive Care Unit 2013-2018
FP7 - 244749 ESTABLISH - European Science and Technology in Action Building Links with Industry, Schools and Home 2010-2013
FP7 - 262549 IATS - Development of an innovative, completely automated antifouling test system for professional examinations of marine coatings 2011-2013
FP7 - 201230 RAREDISEASEPLATFORM - A European Platform of Integrated Information Services for Researchers in the Field of Rare Diseases and Orphan Drugs Supporting Team and Project Building. 2008-2011
FP7 - 226852 SCALES - Securing the Conservation of biodiversity across Administrative Levels and spatial, temporal, and Ecological Scales 2009-2014
FP7 - 223143 TECHGENE - High throughput molecular diagnostics in individual patients for genetic diseases with heterogeneous clinical presentation 2009-2012