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19 Wyniki
Ufundowane przez członka IRDiRC = 
Członek Europejskiej Sieci Referencyjnej (ERN) = 
Projekt badawczy
FRANCJA
OCCITANIE
TOULOUSE
MTREAT-2: Manipuler la Matriptase-2 pour traiter les pathologies associées à une dérégulation du métabolisme du fer
CHU de Toulouse - Hôpital Purpan
Institut de Recherche en Santé Digestive - INSERM IRSD U1220
PORTUGALIA
SUL
LISBOA
Hemocromatose hereditária não-clássica e outras doenças genéticas raras associadas a distúrbios na homeostase do ferro
Instituto Nacional de Saúde Dr. Ricardo Jorge - Lisboa
Departamento de Genética
SZWAJCARIA
Suisse Alémanique
ZÜRICH
The effect of cofactors and vitamins on homocysteine and methylmalonic acid metabolism in health and disease
Universitäts - Kinderspital Zürich - Eleonorenstiftung
Abteilung für Stoffwechselkrankheiten
KANADA
Ontario
TORONTO
Inherited bone marrow failure syndromes: from genomic discoveries to biology
Hospital for Sick Children, Research Institute
KANADA
Ontario
TORONTO
Beyond the Genome: Transcriptome Based Diagnostics for Rare Diseases and Cancer
Hospital for Sick Children, Research Institute
FRANCJA
ILE-DE-FRANCE
PARIS
STaHR : Stimulation de la Recombinaison Homologue pour la Thérapie Génique - FR
Muséum National d'Histoire Naturelle
Laboratoire Structure et Instabilité des Génomes - INSERM U1154 - CNRS 7196
FRANCJA
PAYS DE LA LOIRE
NANTES
FROGH : Etude Génétique de la Population Française - FR
Institut de Recherche en Santé - Université de Nantes
L'Institut du thorax - Inserm UMR 1087 / CNRS UMR 6291
JAPONIA
JAPAN
AICHI
Management ofthe clinical diagnostic centre for rare intractable diseases with genome instability and development of potential therapeutic medicine
Research Institute of Environmental Medicine, Nagoya University
JAPONIA
JAPAN
AICHI
Establishment of the Next-generation Muti-omics Clinical Diagnostic Centre for rare intractable diseases with genome instability
Research Institute of Environmental Medicine, Nagoya University
JAPONIA
JAPAN
TOKYO
Formation of integrated omics analysis base of refractory diseases in children and perinatal period
National Center for Child Health and Development
Research Institute
HISZPANIA
Madrid
MADRID
Desarrollo de algoritmos bioinformáticos basados en redes y biología de sistemas para la búsqueda de nuevos genes responsables de enfermedades raras de origen genético
Fundación Jiménez Díaz
Área de Genética y Genómica
STANY ZJEDNOCZONE AMERYKI
Washington
ADDRESS: NOT PROVIDED - US
A powerful web-based discovery platform for rare disease genetics
Institution: Information not provided - US
Wieloośrodkowy projekt badawczy
- CHU Paris Nord-Val de Seine - Hôpital Xavier Bichat-Claude Bernard
- Fer et synthèse d'hème : génétique, physiologie et pathologie
- Universitätsklinikum des Saarlandes
- Institut für Molekulare Zellbiologie
- Institution: Information not provided - ES
- University of British Columbia
- Maternal Infant Child and Youth Research Network
- 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
FRANCJA
ILE-DE-FRANCE
PARIS
HMA-IRON: towards improved diagnosis and treatment of rare inherited microcytic hypochromic anemias related to iron metabolism
NIEMCY
Saarland
HOMBURG
CoMMiTMenT: Combined Molecular Microscopy for Therapy and Personalized Medication in Rare Anaemias Treatments
HISZPANIA
Madrid
ADDRESS: NOT PROVIDED - ES
E-Enerca: New E-Health Services For The European Reference Network On Rare Anaemias
KANADA
Colombie-Britannique
VANCOUVER
Maternal Infant Child and Youth Research Network (MICYRN)
FRANCJA
ILE-DE-FRANCE
PARIS
STaHR : Stimulation de la Recombinaison Homologue pour la Thérapie Génique
FRANCJA
PAYS DE LA LOIRE
NANTES
FROGH : Etude Génétique de la Population Française
WŁOCHY
LAZIO
ROMA