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43 Result(s)

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    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular characterization of uncommon splice-mutations in neurofibromatosis type 1
    • Medizinische Universität Wien
    • Klinisches Institut für Medizinische und Chemische Labordiagnostik
    • More details
    • AUSTRIA
    • WIEN
    • WIEN
    • Role of the NF1 gene as a tumor suppressor gene in NF1-associated tumors and other NF1 symptoms
    • Medizinische Universität Wien
    • Klinisches Institut für Medizinische und Chemische Labordiagnostik
    • More details
    • BELGIUM
    • OOST-VLAANDEREN
    • GENT
    • Study of the genotype / phenotype correlation in genetic brain diseases
    • Ghent University Hospital - UZGent
    • Center for Medical Genetics
    • More details
    • BELGIUM
    • VLAAMS BRABANT
    • LEUVEN
    • Characterization of large NF1 gene deletions.
    • University Hospitals Leuven - Gasthuisberg
    • Clinical Genetics Unit
    • More details
    • BELGIUM
    • VLAAMS BRABANT
    • LEUVEN
    • The impact of NF1 microdeletions and tumor development in NF1.
    • University Hospitals Leuven - Gasthuisberg
    • Clinical Genetics Unit
    • More details
    • BELGIUM
    • VLAAMS BRABANT
    • LEUVEN
    • Identification and characterisation of new tumor suppressor genes involved in the formation of neurofibromas an MPNSTs in patients with neurofibromatosis type I.
    • University Hospitals Leuven - Gasthuisberg
    • Clinical Genetics Unit
    • More details
    • BELGIUM
    • VLAAMS BRABANT
    • LEUVEN
    • Molecular pathogenesis of tumors in neurofibromatosis type 1.
    • University Hospitals Leuven - Gasthuisberg
    • Clinical Genetics Unit
    • More details
    • FINLAND
    • Länsi-Suomen lääni
    • TURKU
    • Clinical research study on neurofibromatosis type 1 in Finland
    • Central Hospital University of Turku
    • Department of Cell Biology and Anatomy
    • More details
    • FRANCE
    • CENTRE
    • TOURS
    • Morpho-functional characterization of cerebral hamartomas in type 1 neurofibromatosis: study of the correlations with scholar training troubles
    • CHRU de Clocheville
    • Service de neuropédiatrie
    • More details
    • FRANCE
    • CENTRE
    • TOURS
    • Clinical research on type 1 neurofibromatosis
    • CHU Hôpital Trousseau
    • Service de dermatologie
    • More details
    • FRANCE
    • ILE DE FRANCE
    • CLICHY
    • Genotype-phenotype analysis: study of expressivity of type 1 and type 2 neurofibromatoses
    • Hôpital Beaujon
    • Service de neurochirurgie
    • More details
    • FRANCE
    • ILE DE FRANCE
    • CRETEIL
    • NF-France: patients at risk for evolutivity during Neurofibromatosis I study phenotypicgenotypic and proteomic comparising in a cohort
    • CHU Hôpital Henri Mondor
    • Centre d'Investigation Clinique
    • More details
    • FRANCE
    • ILE DE FRANCE
    • CRETEIL
    • NF-France: study of neurofibromatosis type 1 expressivity and genotype/phenotype correlation
    • CHU Hôpital Henri Mondor
    • Service de dermatologie
    • More details
    • FRANCE
    • ILE DE FRANCE
    • PARIS
    • Genetic diversity and phenotypic monotonicity of non-atheromatous arterial aneurysms
    • CHU Hôpital Xavier Bichat - Claude Bernard
    • Service de cardiologie
    • More details
    • FRANCE
    • ILE DE FRANCE
    • PARIS
    • Child neurofibromatosis: french study group on neurofibromatosis
    • Hopital Necker - Enfants Malades
    • Service de dermatologie
    • More details
    • FRANCE
    • ILE DE FRANCE
    • PARIS
    • Neurofibromatosis type 1: physiopathology of neurofibromes and their transformation into neursarcomes
    • Université Paris 5 - Faculté des sciences pharmaceutiques et biologiques
    • Génétique et Biothérapies des maladies dégénératives et prolifératives du système nerveux
    • More details
    • FRANCE
    • ILE DE FRANCE
    • PARIS
    • NF-FRANCE: modifier genes identification and role of normal and deleterious allelic variants of NF1 gene in the occurence and involvement of neurofibromatomes in the type 1 neurofibromatosis
    • Université Paris 5 - Faculté des sciences pharmaceutiques et biologiques
    • Génétique et Biothérapies des maladies dégénératives et prolifératives du système nerveux
    • More details
    • FRANCE
    • ILE DE FRANCE
    • VILLEJUIF
    • Tumor management in type 1 neurofibromatosis patients
    • Institut Gustave Roussy
    • Département de cancérologie de l'enfant et de l'adolescent
    • More details
    • FRANCE
    • ILE DE FRANCE
    • VILLEJUIF
    • Experimental therapy of neurological tumours (brain tumours and neuroblastoma)
    • Institut Gustave Roussy
    • Département de cancérologie de l'enfant et de l'adolescent
    • More details
    • FRANCE
    • PAYS DE LOIRE
    • NANTES
    • Evaluation of NF-1 children and adults learning disorders
    • CHU de Nantes - Hôtel Dieu
    • Clinique dermatologique
    • More details
    • FRANCE
    • RHONE-ALPES
    • LYON
    • Clinical and molecular study of the variation of the phenotypic expression in type1 neurofibromatosis
    • CHRU de Lyon - Hôpital Edouard Herriot
    • Service de génétique moléculaire et clinique
    • More details
    • GERMANY
    • Berlin
    • BERLIN
    • NF1 : FGF signaling in the genesis of multiple bone phenotypes in transgene (Nf1Prx1) mice
    • Max-Planck-Institut für molekulare Genetik
    • Research Group Mundlos
    • More details
    • GERMANY
    • Berlin
    • BERLIN
    • NF1 : Lovastatin treatment of transgenic (Nf1Prx1) mice
    • Max-Planck-Institut für molekulare Genetik
    • Research Group Mundlos
    • More details
    • GREECE
    • ATTIKI
    • VARI
    • AcademicsIndustrials
    • The receptor tyrosine kinase ALK as a novel target for the treatment of neurofibromatosis 1
    • Alexander Fleming - Biomedical Sciences Research Center
    • Institute of Molecular and Genetic Biology
    • More details
    • ITALY
    • CAMPANIA
    • SALERNO
    • Neurofibromatosis 1 (NF1): refine FISH characterization of microdeletion syndromes, definition of genotype-phenotyoe correlation
    • Centro Zigote S.r.L.
    • More details
    • ITALY
    • EMILIA ROMAGNA
    • BOLOGNA
    • Mesenchymal stem cells for the treatment of tibial congenital pseudarthrosis associated with type 1 Neurofibromatosis
    • Istituto Ortopedico Rizzoli
    • Laboratorio di Fisopatologia degli Impianti Ortopedici
    • More details
    • ITALY
    • LAZIO
    • ROMA
    • Mechanisms of variable expressivity in the Neurofibromatosis type1
    • Istituto CSS-Mendel
    • Laboratorio di Biologia Molecolare e Citogenetica
    • More details
    • ITALY
    • LIGURIA
    • GENOVA
    • Relationship between learning disability, with or withourt cerebral magnetic resonance T2 hyperintensities, and NF1 gene mutations
    • Istituto G. Gaslini - Ospedale Pediatrico IRCCS
    • Dipartimento di Scienze Pediatriche
    • More details
    • ITALY
    • LOMBARDIA
    • MILANO
    • Type 1 Neurofibromatosis: advanced diagnosis and characterization of malignant neurofibromas
    • Fondazione IRCCS Istituto Nazionale Neurologico "C. Besta"
    • Neuro-Oncologia Molecolare
    • More details
    • ITALY
    • PUGLIA
    • SAN GIOVANNI ROTONDO
    • Signature of the response of aggressive and metastatic tumours
    • IRCCS Ospedale Casa Sollievo della Sofferenza
    • Servizio di Patologia dell'Invecchiamento ed Oncologia
    • More details
    • ITALY
    • PUGLIA
    • SAN GIOVANNI ROTONDO
    • Signature of the response of aggressive and metastatic tumours
    • IRCCS Ospedale Casa Sollievo della Sofferenza
    • U.O. di Oncologia
    • More details
    • SPAIN
    • Cataluña
    • L'HOSPITALET DE LLOBREGAT
    • Study of Schwann cells forming neurofibromas. Description of genic expression profile in these cells and function determination of the neurofibromine in this tumoral type.
    • Instituto de Investigación Biomédica de Bellvitge (IDIBELL)
    • More details
    • SPAIN
    • Cataluña
    • L'HOSPITALET DE LLOBREGAT
    • Genetic study of the variability of the expression in Neurofibromatosis type I (NF1). Search of NF1 modifier genes.
    • Instituto de Investigación Biomédica de Bellvitge (IDIBELL)
    • More details
    • SPAIN
    • Cataluña
    • L'HOSPITALET DE LLOBREGAT
    • NF1 and NF2 mutations and neurologic tumors and familial neurofibromatosis
    • Instituto de Investigación Biomédica de Bellvitge (IDIBELL)
    • More details
    • SPAIN
    • Cataluña
    • L'HOSPITALET DE LLOBREGAT
    • Identification of mutational molecular mechanisms in Neurofibromatosis type 1
    • Instituto de Investigación Biomédica de Bellvitge (IDIBELL)
    • More details
    • SPAIN
    • Cataluña
    • L'HOSPITALET DE LLOBREGAT
    • Molecular and genetic analysis of Neurofibromatosis type I
    • Instituto de Investigación Biomédica de Bellvitge (IDIBELL)
    • More details
    • SPAIN
    • Cataluña
    • L'HOSPITALET DE LLOBREGAT
    • Therapeutic targets for neurofibromas: identification by cross-species gene expression analysis.
    • Instituto de Investigación Biomédica de Bellvitge (IDIBELL)
    • More details
    • SPAIN
    • Cataluña
    • L'HOSPITALET DE LLOBREGAT
    • DNA repair genes role as modifiers on the neurofibrome number in Neurofibromatosis 1 patients
    • Instituto de Investigación Biomédica de Bellvitge (IDIBELL)
    • More details
    • SPAIN
    • Cataluña
    • L'HOSPITALET DE LLOBREGAT
    • Therapeutic approaches to the neurofibromatosis Type 1 (NF1). Design of a model for the study of the splicing modulation by different compounds
    • Instituto de Investigación Biomédica de Bellvitge (IDIBELL)
    • 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
    • Genetic basis of phenotypic variability of Neurofibromatosis type 1: regulation of mRNA processing and modifier genes for complex phenotypes
    • Hospital Universitario Ramón y Cajal
    • Unidad de Genética Molecular
    • More details
    • SPAIN
    • Madrid
    • MADRID
    • Genetic studies of Neurofibromatosis: Designing a protocol for the molecular genetic diagnosis of Neurofibromatosis type 2 and analysis of phenotypic variability of Neurofibromatosis type 1
    • Hospital Universitario Ramón y Cajal
    • Unidad de Genética Molecular
    • More details
    • SPAIN
    • Madrid
    • MADRID
    • Genomic, Epigenetic and Transcriptional Study of Tumours in Polymalformative Genetic Syndromes
    • Instituto de Genética Médica y Molecular (INGEMM). Hospital Universitario La Paz
    • Sección de Genómica Estructural y Funcional
    • More details
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