Search for a research project
Other search option(s)
33 Result(s)
Funded by an IRDiRC member = 
Research projects
CANADA
Colombie-Britannique
VANCOUVER
Cellular Mechanisms underlying vascular dysfunction & aortic aneurysm in Marfan syndrome
University of British Columbia
CFRI - Child and Family Research Institute
FRANCE
ILE-DE-FRANCE
PARIS
Identification of new genes involved in Marfan syndrome and Familial Thoracic Aortic Aneurysm and Dissection
CHU Paris Nord-Val de Seine - Hôpital Xavier Bichat-Claude Bernard
LVTS "Laboratoire de recherche vasculaire translationnelle" - INSERM U1148
SPAIN
Cataluña
BARCELONA
Membrane Trafficking of TGF-b receptors in Marfan cell lines: a new strategy to handle the TGF-b-induced signaling
Universitat de Barcelona. Campus de Medicina - Clínic August Pi i Sunyer
Departamento de Biología Celular, Inmunología y Neurociencias
SPAIN
Madrid
MADRID
Thoracic aortic aneurysms in Marfan syndrome: identification and validation of biomarkers to predict the risk of aortic rupture
Hospital Universitario 12 de Octubre
Servicio de Cirugía Cardiovascular
SWITZERLAND
Suisse Alémanique
SCHLIEREN
Molecular basis of Marfan syndrome and related disorders: Whole-exome sequencing and targeted therapy
Center for Cardiovascular Genetics and Gene Diagnostics
UNITED KINGDOM
Greater Manchester
ADDRESS: NOT PROVIDED - UK
TGF-Beta superfamily signalling in development and cancer
Institution: Information not provided - UK
UNITED STATES
Ohio
CLEVELAND
Zonule assembly and ectopia lentis
Cleveland Clinic Lerner Com-cwru
Department of Biomedical Engineering
UNITED STATES
Washington
ADDRESS: NOT PROVIDED - US
Developmental basis of aneurysm in marfan syndrome and therapeutic implication
Institution: Information not provided - US
UNITED STATES
Washington
ADDRESS: NOT PROVIDED - US
Marfan aortic embryologic origin influences mir-29b regulators and targets
Institution: Information not provided - US
FRANCE
AUVERGNE-RHONE-ALPES
ADDRESS: NOT PROVIDED - FR
Involvement of CXCL12 and CXCL14 chemokines in connective tissue-mediated limb muscle morphogenesis.
Institution: Information not provided - FR
FRANCE
ILE-DE-FRANCE
PARIS
Non-atheromatous aortopathies: from genetics to new pathophysiological and therapeutic concepts
CHU Paris Nord-Val de Seine - Hôpital Xavier Bichat-Claude Bernard
Maladies structurelles cardiovasculaires
UNITED STATES
Washington
ADDRESS: NOT PROVIDED - US
Elucidating the role of mir-155 in the development of paralysis consecutive to spinal cord damage caused by thoracic-abdominal aortic aneurysm repair surgery
Institution: Information not provided - US
SWITZERLAND
Suisse Alémanique
BASEL
Massively parallel sequencing for gene discovery in lethal fetal disorders
Universitätsspital Basel
Abteilung für Medizinische Genetik
UNITED STATES
Washington
ADDRESS: NOT PROVIDED - US
Unraveling the mechanisms of prenatal-onset disorders affecting the skeleton
Institution: Information not provided - US
CANADA
Ontario
OTTAWA, ONTARIO
Detection and simulation of femoroacetabular impingement
University of Ottawa
School of Electrical Engineering and Computer Science (EECS)
FRANCE
ILE-DE-FRANCE
PARIS
STaHR : Stimulation of Targeted Homologous Recombination for Gene Therapy - FR
Muséum National d'Histoire Naturelle
Laboratoire Structure et Instabilité des Génomes - INSERM U1154 - CNRS 7196
FRANCE
PAYS DE LA LOIRE
NANTES
FROGH : FRench Regional Origins in Genetics for Health - FR
Institut de Recherche en Santé - Université de Nantes
L'Institut du thorax - Inserm UMR 1087 / CNRS UMR 6291
ITALY
CAMPANIA
NAPOLI
Telethon Undiagnosed Disease Program - Revised Proposal
TIGEM - Telethon Institute of Genetics and Medicine
Genomic Medicine - Telethon Institute of Genetics and Medicine
JAPAN
JAPAN
ADDRESS : NOT PROVIDED - JP
Management ofthe clinical diagnostic centre for rare intractable diseases with genome instability and development ofpotential therapeutic medicine
Institution: Information not provided - JP
JAPAN
JAPAN
ADDRESS : NOT PROVIDED - JP
Establishment of the Next-generation Muti-omics Clinical Diagnostic Centre
Institution: Information not provided - JP
JAPAN
JAPAN
ADDRESS : NOT PROVIDED - JP
Formation of integrated omics analysis base of refractory diseases in
Institution: Information not provided - JP
UNITED KINGDOM
Tyne & Wear
NEWCASTLE UPON TYNE
ESDN: European Skeletal Dysplasia Network (coordination)
Newcastle upon Tyne Hospitals NHS Trust
Institute of Genetic Medicine
UNITED KINGDOM
Cambridgeshire
HINXTON
The Deciphering Developmental Disorders (the DDD study)
Wellcome Trust Sanger Institute
DECIPHER
Multicentric Research projects
- CHU Paris IdF Ouest - HEGP Hôpital Européen Georges Pompidou
- Thérapie cellulaire en pathologie cardiovasculaire
- CHU Paris Nord-Val de Seine - Hôpital Xavier Bichat-Claude Bernard
- Service de cardiologie
- Fondazione IRCCS Policlinico San Matteo
- Laboratorio di Diagnostica Molecolare, Patologia Cardiovascolare e dei Trapianti
- University of British Columbia
- Maternal Infant Child and Youth Research Network
- CHU de Strasbourg - Hôpital de Hautepierre
- Service de Rhumatologie
- Muséum National d'Histoire Naturelle
- Laboratoire Structure et Instabilité des Génomes - INSERM U1154 - CNRS 7196
- Institut de Recherche en Santé - Université de Nantes
- L'Institut du thorax - Inserm UMR 1087 / CNRS UMR 6291
- 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
- Universitätsklinikum Magdeburg A.ö.R
- MONZ - Fehlbildungsmonitoring Sachsen-Anhalt
FRANCE
ILE-DE-FRANCE
PARIS
MITRAL
FRANCE
ILE-DE-FRANCE
PARIS
French research network on Marfan syndrome and nonsyndromic related diseases
ITALY
LOMBARDIA
PAVIA
GIMS: Interdisciplinary Team for Marfan Syndrome
CANADA
Colombie-Britannique
VANCOUVER
Maternal Infant Child and Youth Research Network (MICYRN)
FRANCE
GRAND-EST
STRASBOURG
CRI: Club Rhumatismes et Inflammation
FRANCE
ILE-DE-FRANCE
PARIS
STaHR : Stimulation of Targeted Homologous Recombination for Gene Therapy
FRANCE
PAYS DE LA LOIRE
NANTES
FROGH : FRench Regional Origins in Genetics for Health
ITALY
LAZIO
ROMA
UnRareNet: a muticenter collaborative research network for the identification and study of rare undiagnosed patients (completed)
UNITED KINGDOM
Greater Manchester
MANCHESTER
ESDN: European Skeletal Dysplasia Network
GERMANY
Sachsen-Anhalt
MAGDEBURG