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12 Result(s)

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    • CANADA
    • Colombie-Britannique
    • VANCOUVER
    • FORGE - Finding of Rare Disease Genes in Canada
    • University of British Columbia
    • Faculty of Medicine
    • More details
    • CANADA
    • Ontario
    • OTTAWA, ONTARIO
    • FORGE - Finding of Rare Disease Genes in Canada
    • University of Ottawa
    • Faculty of Medicine -
    • More details
    • CANADA
    • Québec
    • MONTREAL
    • FORGE - Finding of Rare Disease Genes in Canada
    • Centre hospitalier universitaire Sainte-Justine
    • Pédiatrie
    • More details
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • GENDACTYL: Dlx and Msx genes role in aetiopathogenesis analysis in ''split hand - split foot'' syndrome (SHFM), and in utero transgene correction of the disease with lentiviral vectors
    • Muséum National d'Histoire Naturelle
    • Evolution des régulations endocriniennes
    • More details
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • SKELNET - Skeletal Dysplasia Network (coordination)
    • Universitätsklinikum Freiburg
    • Geschäftsstelle SKELNET e.V.
    • 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
    • ITALY
    • LAZIO
    • ROMA
    • Function of p63 in normal skin and in ectodermal dysplasia syndromes
    • Azienda Ospedaliera Universitaria Policlinico di Tor Vergata
    • Laboratorio di Trasduzione del Segnale
    • More details
    • ITALY
    • LOMBARDIA
    • MILANO
    • Analysis of the role played by P63 and DLX genes in the pathogenesis of split hand and foot Malformation-4
    • Università degli Studi di Milano
    • Dipartimento di Scienze Biomolecolari e Biotecnologie
    • More details
    • ITALY
    • PIEMONTE
    • TORINO
    • Transcription factors of the Dlx homeogene family in the control of limb, craniofacial, and anterior brain development: in vivo functional studies
    • Università degli Studi di Torino
    • Centro di Biotecnologie Molecolari
    • More details
    • UNITED KINGDOM
    • County Antrim
    • NEWTOWNABBEY
    • Epidemiological studies on congenital anomaly prevalence, risk factors, prevention and prenatal screening
    • University of Ulster
    • EUROCAT Central Registry
    • 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
    • Greater Manchester
    • MANCHESTER
    • ESDN: European Skeletal Dysplasia Network (coordination)
    • Faculty of Life Sciences - University of Manchester
    • Wellcome Trust Centre for Cell Matrix Research
    • More details