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    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Genetic and cellular study of insulino resistance in human
    • Faculté de Médecine Pierre et Marie Curie - Hôpital Saint-Antoine
    • Pathologies du tissu adipeux et conséquences hépatiques
    • More details
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Genetic, cellular and clinical study of lipodystrophies in human
    • Faculté de Médecine Pierre et Marie Curie - Hôpital Saint-Antoine
    • Pathologies du tissu adipeux et conséquences hépatiques
    • More details
    • GERMANY
    • Hessen
    • MARBURG
    • Structure and function of potassium channels of the K2P family in the cardiovascular system (FOR1086)
    • Philipps-Universität Marburg
    • AG Zellphysiologie (Prof. Dr. Dr. Daut)
    • More details
    • GERMANY
    • Nordrhein-Westfalen
    • MÜNSTER
    • Genetic variants in K2P channel genes and monogenetic cardial conduction defects (FOR1086)
    • Universitätsklinikum Münster
    • Institut für Genetik von Herzerkrankungen
    • More details
    • ITALY
    • CALABRIA
    • CATANZARO
    • Genetic syndromes of extreme insulin resistance and diabetes mellitus due to defects in insulin receptor gene transcription
    • Azienda Ospedaliera Universitaria "Mater Domini"
    • Dipartimento di Medicina Sperimentale e Clinica ''G. Salvatore'' - Cattedra di Endocrinologia
    • More details
    • ITALY
    • LAZIO
    • ROMA
    • Genotype-phenotype correlations and therapeutic approaches in extreme insulin resistance syndromes due to mutation of the insulin receptor
    • Azienda Ospedaliera Universitaria Policlinico di Tor Vergata
    • Laboratorio di Endocrinologia e Metabolismo Molecolare
    • More details
    • LEBANON
    • Beyrouth
    • BEIRUT
    • Genetic causes of congenital heart diseases in the Lebanese population: screening for mutations in transcription factors implicated in heart development and cardiac function
    • American University of Beirut
    • Département de biochimie
    • More details
    • UNITED KINGDOM
    • Cambridgeshire
    • CAMBRIDGE
    • NIHR BioResource - Rare Disease: SPEED - Specialist Pathology: Evaluating Exomes in Diagnostics
    • Wellcome Trust/MRC Building
    • Cambridge Institute for Medical Research
    • More details
    • UNITED KINGDOM
    • West Midlands
    • BIRMINGHAM
    • NIPSIGEN - Clinical translation of non-invasive prenatal diagnosis (NIPD) for single gene disorders (Health Innovation Challenge Fund)
    • Birmingham Women's NHS Foundation Trust
    • Regional Genetics Unit
    • More details