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    • CANADA
    • Ontario
    • TORONTO
    • Inherited bone marrow failure syndromes: from genomic discoveries to biology
    • Hospital for Sick Children, Research Institute
    • More details
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Blackfan-Diamond anemia: genotyping of the French cohort of patients and genotype/phenotype correlation study
    • CHU Paris - Hôpital Robert Debré
    • Service d'hématologie biologique
    • More details
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Constitutive hematologic diseases: clinical and therapeutic research, molecular biology
    • CHU Paris-GH St-Louis Lariboisière F.Widal - Hôpital Saint-Louis
    • Service d'hématologie pédiatrique
    • More details
    • FRANCE
    • MIDI-PYRENEES
    • TOULOUSE
    • RIBODBA: Blackfan-Diamond anemia: molecular mechanisms of a ribosomal disease
    • Université Paul Sabatier
    • Laboratoire de biologie moléculaire eucaryote
    • More details
    • FRANCE
    • MIDI-PYRENEES
    • TOULOUSE
    • RiboCrash: the Diamond-Blackfan anemia, a model of ribosomal disease
    • Université Paul Sabatier
    • Laboratoire de biologie moléculaire eucaryote
    • More details
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Prospective multicenter study for pediatric and adult patients with Blackfan-Diamond disease
    • Universitätsklinikum Freiburg
    • Klinik für Pädiatrische Hämatologie und Onkologie
    • More details
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Mutation analysis of candidate genes in Congenital Hypoplastic Anemia (Blackfan-Diamond disease)
    • Universitätsklinikum Freiburg
    • Klinik für Pädiatrische Hämatologie und Onkologie
    • More details
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Generation and characterisation of expanding hematopoietic stem cell cultures to investigate genetic and development specific aspects of Congenital Bone Marrow Failure Syndromes
    • LMU Klinikum der Universität München - Campus Innenstadt
    • Kinderklinik und Kinderpoliklinik im Dr. von Haunerschen Kinderspital
    • More details
    • GERMANY
    • Niedersachsen
    • HANNOVER
    • Platform for high-resolution genetic characterization of secondary myelodysplastic syndromes/leukemia and identification of new disease causing gene mutations in patients with bone marrow failure syndromes
    • Medizinische Hochschule Hannover
    • Molekulare Hämatopoese
    • More details
    • GERMANY
    • Saarland
    • HOMBURG
    • CoMMiTMenT: Combined Molecular Microscopy for Therapy and Personalized Medication in Rare Anaemias Treatments (coordination)
    • Universitätsklinikum des Saarlandes
    • Forschungsstelle für Molekulares Imaging und Screening
    • More details
    • ITALY
    • PIEMONTE
    • NOVARA
    • Analysis of the role of ribosomal protein RPS19 in erythropoiesis
    • Università degli Studi del Piemonte Orientale
    • Laboratorio di Patologia Genetica
    • More details
    • ITALY
    • PIEMONTE
    • NOVARA
    • Molecular basis of Diamond-Blackfan Anemia
    • Università degli Studi del Piemonte Orientale
    • Laboratorio di Patologia Genetica
    • More details
    • KOREA, REPUBLIC OF
    • KOREA, REPUBLIC OF
    • SEOUL
    • Development of cell and gene therapy for blood disorders, in particularly Gaucher and Blackfan-Diamond diseases
    • Seoul National University Hospital
    • Molecular Diagnostics Laboratory
    • More details
    • PORTUGAL
    • NORTE
    • PORTO
    • Integrated Micro-Nano-OPTO Fluidic systems for high-content diagnosis and studies of rare cancer cells
    • Instituto de Patologia e Imunologia Molecular da Universidade do Porto
    • Genética de Tumores
    • More details
    • SPAIN
    • Madrid
    • MADRID
    • Genomic, Epigenetic and Transcriptional Study of Tumours in Polymalformative Genetic Syndromes
    • Hospital Infantil Universitario la Paz
    • Unidad de Hemato-Oncologia y trasplante de Médula Ósea Pediátrica
    • More details
    • SPAIN
    • Madrid
    • MADRID
    • Genomic, Epigenetic and Transcriptional Study of Tumours in Polymalformative Genetic Syndromes
    • Hospital Universitario La Paz
    • Instituto de Genética Médica y Molecular
    • More details
    • UNITED KINGDOM
    • Cambridgeshire
    • CAMBRIDGE
    • NIHR BioResource - Rare Disease: MPMT - Multiple primary malignant tumours
    • Addenbrooke's Hospital
    • Academic Department of Medical Genetics
    • 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