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Research projects

FRANCE

AUVERGNE-RHONE-ALPES
ADDRESS: NOT PROVIDED - FR

FRANCE

AUVERGNE-RHONE-ALPES
ADDRESS: NOT PROVIDED - FR

Funded by an IRDiRC memberMechanosensitive ionic channels in zebrafish heart regeneration
Institution: Information not provided - FR

FRANCE

AUVERGNE-RHONE-ALPES
ADDRESS: NOT PROVIDED - FR

FRANCE

ILE-DE-FRANCE
CHÂTENAY-MALABRY

Funded by an IRDiRC memberNAD-HEART: NAD+ precursor supplementation for metabolic therapy of heart failure - FR
Faculté de Pharmacie - Université Paris-Sud
Laboratoire "Signalisation et Physiopathologie Cardiovasculaire" - INSERM UMR-S 1180

BELGIUM

VLAAMS BRABANT
LEUVEN

FRANCE

AUVERGNE-RHONE-ALPES
ADDRESS: NOT PROVIDED - FR

FRANCE

AUVERGNE-RHONE-ALPES
ADDRESS: NOT PROVIDED - FR

FRANCE

ILE-DE-FRANCE
PARIS

Identification of genes and phenotype/genotype relations in arrythmogenic right vendricular dysplasia (ARVD)
APHP.Sorbonne Université, Hôpital de la Pitié-Salpêtrière
Départements de génétique et de cardiologie - Centre de référence des maladies cardiaques héréditaires

FRANCE

ILE-DE-FRANCE
PARIS

JAPAN

JAPAN
TOKYO

Funded by an IRDiRC memberDevelopment of gene therapy for cardiac regeneration in dilated cardiomyopathy
Keio University School of Medicine
Department of Cardiology

JAPAN

JAPAN
TOKYO

Funded by an IRDiRC memberDevelopment of novel disease-causing gene based therapies for cardiomyopathies
Tokyo Medical and Dental University Medical Research Institute

SPAIN

Comunidad Valenciana
VALENCIA

Funded by an IRDiRC memberModulation of the arrhythmogenic myocardiopatia phenotype to improve the diagnosis, search for new treatments and understand its physiopathogenic mechanisms. Role of epicardic fat.
IIS La Fe - Instituto de Investigación Sanitaria La Fe
Grupo de investigación en cardiopatías familiares, muerte súbita y mecasnismos de enfermedad

SPAIN

Madrid
MADRID

Funded by an IRDiRC memberPersonalizing The Risk Of Stroke And Silent Brain Infarct In Cardiovascular Disease
Hospital General Universitario Gregorio Marañón
Servicio de Cardiología

CANADA

Colombie-Britannique
VICTORIA

Funded by an IRDiRC memberLong QT Syndrome in Northern British Columbia:Understanding the impact
University of Victoria
Community Genetics Research Program/Island Medical Program

FRANCE

AUVERGNE-RHONE-ALPES
ADDRESS: NOT PROVIDED - FR

FRANCE

AUVERGNE-RHONE-ALPES
ADDRESS: NOT PROVIDED - FR

FRANCE

AUVERGNE-RHONE-ALPES
ADDRESS: NOT PROVIDED - FR

FRANCE

HAUTS-DE-FRANCE
LILLE

Research of genes and mutations involved in ventricle disorders with sudden death risk
CHRU de Lille - Hôpital Albert Calmette
Service de cardiologie

FRANCE

ILE-DE-FRANCE
PARIS

Identification of causative genes for familial dilated cardiomyopathies and of susceptibility genes for non familial forms of the disease
APHP.Sorbonne Université, Hôpital de la Pitié-Salpêtrière
Physiopathologie, génétique et pharmacologie du remodelage cardiovasculaire

FRANCE

ILE-DE-FRANCE
PARIS

Identification of causative genes for familial dilated cardiomyopathies and of susceptibility genes for non familial forms of the disease
APHP.Sorbonne Université, Hôpital de la Pitié-Salpêtrière
Départements de génétique et de cardiologie - Centre de référence des maladies cardiaques héréditaires

FRANCE

ILE-DE-FRANCE
PARIS

Identification of genes in myocardial noncompaction
APHP.Sorbonne Université, Hôpital de la Pitié-Salpêtrière
Départements de génétique et de cardiologie - Centre de référence des maladies cardiaques héréditaires

FRANCE

ILE-DE-FRANCE
PARIS

Identification of genes in familial atrial fibrillation
APHP.Sorbonne Université, Hôpital de la Pitié-Salpêtrière
Départements de génétique et de cardiologie - Centre de référence des maladies cardiaques héréditaires

FRANCE

ILE-DE-FRANCE
PARIS

Phenotypic and genetic studies on long QT syndrome, familial
CHU Paris Nord-Val de Seine - Hôpital Xavier Bichat-Claude Bernard
Service de cardiologie - Rythmologie

FRANCE

ILE-DE-FRANCE
PARIS

Research of genes and mutations involved in ventricle disorders with sudden death risk
CHU Paris Nord-Val de Seine - Hôpital Xavier Bichat-Claude Bernard
Service de cardiologie - Rythmologie

FRANCE

ILE-DE-FRANCE
PARIS

Clinical, electrophysiological and genetic aspects of Brugada syndrome
CHU Paris Nord-Val de Seine - Hôpital Xavier Bichat-Claude Bernard
Service de cardiologie - Rythmologie

FRANCE

ILE-DE-FRANCE
PARIS

Research of genes and mutations involved in ventricle disorders with sudden death risk
Hôpital Necker-Enfants Malades
Cardiologie pédiatrique : Unité médico-chirurgicale de cardiologie congénitale et pédiatrique

FRANCE

PAYS DE LA LOIRE
NANTES

Clinical research on Brugada syndrome
Faculté de médecine de Nantes
Physiopathologie et pharmacologie cellulaire et moléculaire

FRANCE

PAYS DE LA LOIRE
NANTES

Phenotype profile of the Brugada syndrome
Faculté de médecine de Nantes
Physiopathologie et pharmacologie cellulaire et moléculaire

FRANCE

PAYS DE LA LOIRE
NANTES

Genetics of the Brugada syndrome
Faculté de médecine de Nantes
Physiopathologie et pharmacologie cellulaire et moléculaire

FRANCE

PROVENCE-ALPES-COTE D'AZUR
MARSEILLE

Funded by an IRDiRC memberCaGeD : Cardiogenic Genome Dynamics
Faculté de Médecine de la Timone
Centre d'enseignement et de recherche en génétique médicale - INSERM UMR S910

GERMANY

Bayern
MÜNCHEN

Patient-specific induced pluripotent stem cell models to elucidate the role of TRP channels in the pathogenesis of CPVT1 and of PFHBI (TRR 152: P17)
Klinikum rechts der Isar der Technischen Universität München
Klinik und Poliklinik für Innere Medizin I

GERMANY

Berlin
ADDRESS: NOT PROVIDED - DE

GERMANY

Schleswig-Holstein
LÜBECK

The GErman Italian Spanish Takotsubo (GEIST) Registry
Universitätsklinikum Schleswig-Holstein - Campus Lübeck
Medizinische Klinik II - Kardiologie, Angiologie, Intensivmedizin

ITALY

LOMBARDIA
MILANO

Funded by an IRDiRC memberContribution of lipids and their oxidized metabolites on Arrhythmogenic Cardiomyopathy pathogenesis
Centro Cardiologico Monzino
Unità di Biologia vascolare e Medicina rigenerativa

ITALY

LOMBARDIA
MILANO

Funded by an IRDiRC memberContribution of lipids and their oxidized metabolites on Arrhythmogenic Cardiomyopathy pathogenesis
Università degli Studi di Milano - Scienze Farmacologiche e Biomolecolari
Laboratorio di Farmacologia Cellulare dell'Aterosclerosi

JAPAN

JAPAN
HIROSHIMA

Funded by an IRDiRC memberRisk stratification of sudden cardiac death in Brugada syndrome and construction of predictive model for clinical application
Hiroshima University Graduate School of Biomedical and Health Sciences
Department of Cardiovascular Medicine

JAPAN

JAPAN
KYOTO

Funded by an IRDiRC memberDrug discovery targeted to alternative splicing variants in congenital long-QT syndrome
Kyoto University Graduate School of Medicine
Department of Cardiovascular Medicine

SPAIN

Comunidad Valenciana
VALENCIA

Molecular mechanisms in the development of scoliosis in limb-girdle muscular dystrophies
Universitat de València. Facultat de Medicina i Odontologia
Departamento de Bioquímica y Biología Molecular

SPAIN

Murcia
EL PALMAR

Funded by an IRDiRC memberCharacterization of arrhythmogenic cardiomyopathy from zebrafish models and development of gene therapy
IMIB - Instituto Murciano de Investigación Biosanitaria Virgen de la Arrixaca
Grupo de investigación en Cardiología Clínica y Experimental

SWEDEN

Region Västerbotten
UMEÅ

SWITZERLAND

Suisse Alémanique
BERN

Co-regulation of cardiac ion channels: focus on the sodium channel Nav1.5
Universität Bern
Institute of Biochemistry and Molecular Medicine (IBMM)

UNITED KINGDOM

Aberdeen
ABERDEEN

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberModeling a rare autonomic disease
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

FRANCE

ILE-DE-FRANCE
PARIS

Funded by an IRDiRC memberGenomic editing by CRISPR / Cas9 to treat cardiomyopathies linked to mutations in the LMNA gene
Institut de Myologie - Hôpital Pitié-Salpêtrière
Centre de Recherche en Myologie

GERMANY

Baden-Württemberg
HEIDELBERG

Funded by an IRDiRC memberReDox: Repurposing doxycycline in the treatment of AL amyloidosis - DE
Zentrum für Innere Medizin (Krehl-Klinik)
Abteilung Innere Medizin V - Hämatologie, Onkologie und Rheumatologie

GERMANY

Schleswig-Holstein
KIEL

Role of microRNA-582 in cardiac signal transduction, hypertrophy and heart failure
Universitätsklinikum Schleswig-Holstein - Campus Kiel
Klinik für Innere Medizin III - Kardiologie, Angiologie und internistische Intensivmedizin

JAPAN

JAPAN
OSAKA

Funded by an IRDiRC memberThe combination of clinical and basic research about peripartum cardiomyopathy to develop the novel biomarkers and treatment
National Cerebral and Cardiovascular Center
Division of Obstetrics and Gynecology

JAPAN

JAPAN
OSAKA

Funded by an IRDiRC memberInvestigation of clinical index for stratifying phenotypes of cardiomyopathy with newly developed nuclear chromatin assessment
Osaka University Graduate School of Medicine
Department of Cardiovascular Medicine

JAPAN

JAPAN
SHIGA

Funded by an IRDiRC memberNovel therapeutic effect of l-cis-Diltiazem on ventricular fibrillation in congenital long-QT syndrome
Shiga University of Medical Science
Department of Cardiovascular Medicine

SWITZERLAND

Suisse Alémanique
BERN

ATTR Amyloidosis in Elderly Patients With Aortic Stenosis
University Hospital Inselspital
Universitätsklinik für Kardiologie

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberDiabetic pregnancies and gastrulation
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Funded by an IRDiRC memberEpigenetic mechanisms in diabetic embryopathy
Institution: Information not provided - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

AUSTRIA

TIROL
INNSBRUCK

Funded by an IRDiRC memberTTRACK: Prevalence and Characteristics of Transthyretin Amyloidosis in Patients With Left Ventricular Hypertrophy of Unknown Etiology - AT
Medizinische Universität Innsbruck
Universitätsklinik für Innere Medizin III - Kardiologie und Angiologie

FRANCE

ILE-DE-FRANCE
PARIS

Analysis of cardiac phenotype and underlying genotype in glycogen storage disease type 2B
APHP.Sorbonne Université, Hôpital de la Pitié-Salpêtrière
Départements de génétique et de cardiologie - Centre de référence des maladies cardiaques héréditaires

GERMANY

Baden-Württemberg
ULM

Funded by an IRDiRC memberGeNeRARe: German Network for RASopathies
Institute of Comparative Molecular Endocrinology der Universität Ulm
Cirstea Lab

GERMANY

Hamburg
HAMBURG

Funded by an IRDiRC memberGeNeRARe: German Network for RASopathies
UKE - Universitätsklinikum Hamburg-Eppendorf
Institut für Humangenetik

GERMANY

Niedersachsen
GÖTTINGEN

Funded by an IRDiRC memberGeNeRARe: German Network for RASopathies
Universitätsmedizin Göttingen
Klinik für Thorax-, Herz- und Gefäßchirurgie

GERMANY

Nordrhein-Westfalen
DÜSSELDORF

Funded by an IRDiRC memberGeNeRARe: German Network for RASopathies
Heinrich-Heine-Universität Düsseldorf
Institut für Biochemie und Molekularbiologie II

GERMANY

Sachsen-Anhalt
MAGDEBURG

Funded by an IRDiRC memberGeNeRARe: German Network for RASopathies
Otto-von-Guericke-Universität Magdeburg
Abteilung Genetik & Molekulare Neurobiologie

ITALY

CAMPANIA
CASERTA

ITALY

LAZIO
ROMA

Clinical and molecular characterization of genetic syndromes with congenital heart disease
IRCCS Ospedale Pediatrico Bambino Gesù - SEDE SAN PAOLO
U.O.C. Laboratorio di Genetica Medica

JAPAN

JAPAN
MIYAGI

Funded by an IRDiRC memberPathogenesis and novel therapeutic approarches in RASoapthies
Tohoku University School of Medicine
Department of Medical Genetics

PORTUGAL

NORTE
PORTO

Dissecting nerve regeneration and the neuritogenic activity of TTR
Instituto de Biologia Molecular e Celular
Nerve Regeneration Group

PORTUGAL

NORTE
PORTO

Phenotypic variability and modifier genes in Familial Amyloid Polyneuropathy (FAP ATTRV30M)
Instituto de Biologia Molecular e Celular
Unidade de Investigação Genética e Epidemiológica em Doenças Neurológicas

PORTUGAL

NORTE
PORTO

Therapies in familial amyloidotic polyneuropathy
Instituto de Biologia Molecular e Celular
Unidade de Neurobiologia Molecular

PORTUGAL

NORTE
PORTO

Molecular basis of nervous system dysfunction on amyloid neuropathies
Instituto de Biologia Molecular e Celular
Unidade de Neurobiologia Molecular

PORTUGAL

SUL
LISBOA

TTR amyloid fibril formation in vivo - Looking beyond genetic factors
Faculdade de Ciências da Universidade de Lisboa
Laboratório de Enzimologia

SPAIN

Comunidad Valenciana
VALENCIA

Funded by an IRDiRC memberComprehensive genomic characterization of hereditary myeloid syndromes
IIS La Fe - Instituto de Investigación Sanitaria La Fe
Grupo de investigación en hematología y hemoterapia

SPAIN

Madrid
MAJADAHONDA

Funded by an IRDiRC memberCharacterization and early detection of atrial arrhythmias and conduction disorders in transthyretin cardiac amyloidosis
Hospital Universitario Puerta de Hierro - Majadahonda
Servicio de Cardiopatías Familiares

SWEDEN

Region Västerbotten
UMEÅ

Mechanistic and structural elucidation of amyloid and its cytotoxic propensity
Umeå University
Department of medical biochemistry and biophysics

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

UNITED STATES

Washington
ADDRESS: NOT PROVIDED - US

Multicentric Research projects