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    • CANADA
    • Ontario
    • OTTAWA, ONTARIO
    • Detection and simulation of femoroacetabular impingement
    • University of Ottawa
    • School of Electrical Engineering and Computer Science (EECS)
    • More details
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Cartography and genetic identification of dyschodrosteosis
    • CHU Paris - Hôpital Necker-Enfants Malades
    • Laboratoire de Génétique Moléculaire
    • More details
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Research for SHOX gene errors in dyschondorsteosis and idiopathic little size
    • CHU Paris - Hôpital Robert Debré
    • Service d'endocrinologie diabétologie pédiatrique
    • More details
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • SKELNET - Skeletal Dysplasia Network (coordination)
    • Universitätsklinikum Freiburg
    • Geschäftsstelle SKELNET e.V.
    • More details
    • GERMANY
    • Baden-Württemberg
    • HEIDELBERG
    • Characterization of SHOX functions in bone formation: Identification of target genes and interacting proteins
    • Universitätsklinikum Heidelberg
    • Abteilung Molekulare Humangenetik
    • More details
    • GERMANY
    • Baden-Württemberg
    • HEIDELBERG
    • Animal models for functional analysis of the SHOX gene implicated in Leri-Weill and Turner syndrome
    • Universitätsklinikum Heidelberg
    • Abteilung Molekulare Humangenetik
    • More details
    • GERMANY
    • Nordrhein-Westfalen
    • BONN
    • Characterization of SHOX functions in bone formation: Identification of target genes and interacting proteins
    • Deutsche Forschungsgemeinschaft
    • More details
    • GERMANY
    • Nordrhein-Westfalen
    • BONN
    • Animal models for functional analysis of the SHOX gene implicated in Leri-Weill and Turner syndrome
    • Deutsche Forschungsgemeinschaft
    • More details
    • GERMANY
    • Nordrhein-Westfalen
    • ESSEN
    • SKELNET : Chondrocyte specific genes as part of the signaling regulation of chondrocyte differentiation
    • Universität Duisburg-Essen
    • Abteilung Entwicklungsbiologie
    • 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
    • Cambridgeshire
    • HINXTON
    • The Deciphering Developmental Disorders (the DDD study)
    • Wellcome Trust Sanger Institute
    • DECIPHER
    • More details
    • UNITED KINGDOM
    • Devon
    • EXETER
    • Exploring the Genetics of Renal Developmental Disease
    • Royal Devon and Exeter Hospital - Wonford site
    • Department of Urology
    • More details
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Natural history and management in Skeletal Dysplasias
    • Great Ormond Street Hospital for Children, NHS Foundation Trust
    • Clinical Genetics
    • More details
    • UNITED KINGDOM
    • Tyne & Wear
    • NEWCASTLE UPON TYNE
    • ESDN: European Skeletal Dysplasia Network (coordination)
    • International Centre for Life
    • Institute of Genetic Medicine
    • 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