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Projets de recherche
AUTRICHE
WIEN
WIEN
Nucleocytoskeleton-mediated endothelial aging in progeria
Universität für Bodenkultur
Department für Biotechnologie
AUTRICHE
WIEN
WIEN
Molecular mechanisms of cardiovascular disease in progeria
Vienna Biocenter
Department for Medical Biochemistry of the Medical University of Vienna
ESPAGNE
Madrid
MADRID
New mechanisms for regulating the immune response for lamin A/C and progerine: implications in Hutchinson-Gilford premature ageing síndrome
CNIC - Centro Nacional de Investigaciones Cardiovasculares
Fisiopatología cardiovascular molecular y genética
ESPAGNE
Madrid
MADRID
Molecular therapy for Laminopathies
Centro Nacional de Biotecnología (CNB-CSIC)
Dianas moleculares para cáncer e inflamación, enfoque en PI3-quinasa
ROYAUME-UNI
Cambridgeshire
CAMBRIDGE
Chemical reversion of nuclear shape and other defects of Hutchinson Gilford Progeria Syndrome and Lamin A/C depleted cells
University of Cambridge
Wellcome Trust/Cancer Research UK Gurdon Institute
ROYAUME-UNI
Oxfordshire
OXFORD
Structure and function of ZMPSTE24, an integral membrane protease mutated in progeria
University of Oxford
Structural Genomics Consortium
SUEDE
Stockholms läns landsting
HUDDINGE
Genetic mechanisms in progeria
Karolinska Institutet - Huddinge
Department of Biosciences and Nutrition
SUEDE
Västra Götalandsregionen
GÖTEBORG
Targeting the CAAX protein processing enzymes in the treatment of progeria
Göteborg University
Department of Molecular and Clinical Medicine
ETATS-UNIS
South Dakota
SIOUX FALLS
Investigating the mechanisms of disease for the nuclear laminopathies
Sanford Research
Roux Lab
ITALIE
LAZIO
ROMA
GENESKIN: European network on rare genetic skin diseases (coordination)
Istituto Dermopatico dell'Immacolata - IRCCS
Laboratorio di Biologia Molecolare e Cellulare
ROYAUME-UNI
Cambridgeshire
HINXTON
The Deciphering Developmental Disorders (the DDD study)
Wellcome Trust Sanger Institute
DECIPHER
ROYAUME-UNI
Devon
EXETER
Exploring the Genetics of Renal Developmental Disease
Royal Devon and Exeter Hospital - Wonford site
Department of Urology
SUISSE
Suisse Alémanique
BASEL
Massively parallel sequencing for gene discovery in lethal fetal disorders
Universitätsspital Basel
Abteilung für Medizinische Genetik
CANADA
Ontario
OTTAWA, ONTARIO
Detection and simulation of femoroacetabular impingement
University of Ottawa
School of Electrical Engineering and Computer Science (EECS)
ITALIE
CAMPANIA
NAPOLI
Telethon Undiagnosed Disease Program - Revised Proposal
Azienda Ospedaliera Universitaria - Seconda Università degli Studi di Napoli
Laboratorio di Genetica Medica
ROYAUME-UNI
Tyne & Wear
NEWCASTLE UPON TYNE
ESDN: European Skeletal Dysplasia Network (coordination)
Newcastle upon Tyne Hospitals NHS Trust
Institute of Genetic Medicine
Projets de recherche multicentriques
- Institut de Biologie et Chimie des Protéines
- Laboratoire de Biologie Tissulaire et d'ingénierie Thérapeutique
- CHU de Marseille - Hôpital de la Timone
- Laboratoire de génétique moléculaire
- Universitätsklinikum Magdeburg A.ö.R
- MONZ - Fehlbildungsmonitoring Sachsen-Anhalt
- Vienna Biocenter
- Department for Medical Biochemistry of the Medical University of Vienna
- CHU Paris - Hôpital Necker-Enfants Malades
- Service de dermatologie
- Istituto Dermopatico dell'Immacolata - IRCCS
- Laboratorio di Biologia Molecolare e Cellulare
- University of British Columbia
- Maternal Infant Child and Youth Research Network
- IRCCS Ospedale Pediatrico Bambino Gesù - SEDE GIANICOLO
- Servizio Clinico di Consulenza Genetica
- Faculty of of Life Sciences - University of Manchester
- Wellcome Trust Centre for Cell Matrix Research - B.3016
FRANCE
AUVERGNE-RHONE-ALPES
LYON
ELAST-AGE: targeting the elastic tissues ageing to improve the quality of ageing (FINISHED)
FRANCE
PROVENCE-ALPES-COTE D'AZUR
MARSEILLE
EUROPROGERIA: réseau européen d'investigation scientifiqu sur les maladies d'Hutchinson-Gilford-Progeria et associées
ALLEMAGNE
Sachsen-Anhalt
MAGDEBURG
International Clearinghouse for Birth Defects Monitoring Systems
AUTRICHE
WIEN
WIEN
EURO-LAMINOPATHIES: nuclear envelope-linked rare human diseases: from molecular pathophysiology towards clinical applications (FINISHED)
FRANCE
ILE-DE-FRANCE
PARIS
GM: Génodermatoses et Méditerranée
ITALIE
LAZIO
ROMA
GENESKIN: European network on rare genetic skin diseases
CANADA
Colombie-Britannique
VANCOUVER
Maternal Infant Child and Youth Research Network (MICYRN)
ITALIE
LAZIO
ROMA
UnRareNet: a muticenter collaborative research network for the identification and study of rare undiagnosed patients (completed)
ROYAUME-UNI
Greater Manchester
MANCHESTER