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Progetti di ricerca

CANADA

Québec
MONTRÉAL

Finanziato da un ente associato a IRDiRCEmerging Team to identify and characterize novel and existing Hereditary Spastic Paraplegia (HSP) disease genes
CHUM Research Centre
Centre d'excellence en neuroscience de l'Université de Montréal

FINLANDIA

Finland
HELSINKI

Hereditary neuropathy and spastic paraplegia: new mechanisms, biomarkers and treatment
University of Helsinki
Stem Cells and Metabolism Research Program

FRANCIA

ILE-DE-FRANCE
PARIS

Finanziato da un ente associato a IRDiRCSPATAX-QUEST: Identification of new causative genes in spinocerebellar degenerations by combination of whole genome scan, next-generation sequencing and biological validation in vitro and in vivo
Institut du Cerveau et de la Moelle épinière (ICM) - Hôpital Pitié-Salpêtrière
Equipe "Bases moléculaires, physiopathologie et traitement des maladies neurodégénératives"

FRANCIA

ILE-DE-FRANCE
PARIS

Finanziato da un ente associato a IRDiRCNeuromics: Integrated European -omics research project for diagnosis and therapy in rare neuromuscular and neurodegenerative diseases - FR
Institut du Cerveau et de la Moelle épinière (ICM) - Hôpital Pitié-Salpêtrière
Equipe "Bases moléculaires, physiopathologie et traitement des maladies neurodégénératives"

FRANCIA

ILE-DE-FRANCE
PARIS

Finanziato da un ente associato a IRDiRCWhole genome sequencing in 5 families with hereditary spastic paraplegia
Institut du Cerveau et de la Moelle épinière (ICM) - Hôpital Pitié-Salpêtrière
Equipe "Bases moléculaires, physiopathologie et traitement des maladies neurodégénératives"

FRANCIA

PROVENCE-ALPES-COTE D'AZUR
MARSEILLE

MITOTARGET: mitochondrial apoptotic pathways in neurodegenerative diseases and assessment of the effects of new small molecules (WP4)
Parc scientifique et technologiques de Luminy
Institut de Biologie du Développement de Marseille-Luminy

FRANCIA

PROVENCE-ALPES-COTE D'AZUR
MARSEILLE

GERMANIA

Baden-Württemberg
TÜBINGEN

Finanziato da un ente associato a IRDiRCNEUROMICS: Integrated European Project on Omics Research of Rare Neuromuscular and Neurodegenerative Diseases -DE-
Institut für Medizinische Genetik und angewandte Genomik Tübingen
Institut für Medizinische Genetik und angewandte Genomik

GERMANIA

Hessen
FRANKFURT AM MAIN

MITOTARGET: mitochondrial membrane properties in the process of neurodegeneration and assessment of the effects of new small molecules (WP2)
Johann Wolfgang Goethe-Universität Frankfurt
Pharmakologisches Institut für Naturwissenschaftler

GERMANIA

Nordrhein-Westfalen
BONN

GERMANIA

Nordrhein-Westfalen
KÖLN

Finanziato da un ente associato a IRDiRCNEUROMICS: Integrated European Project on Omics Research of Rare Neuromuscular and Neurodegenerative Diseases -DE-
Institut für Humangenetik am Universitätsklinikum Köln
Institut für Humangenetik

GERMANIA

Nordrhein-Westfalen
KÖLN

Finanziato da un ente associato a IRDiRCNEUROLIPID: Lipid metabolism in the pathogenesis of hereditary spastic paraplegia: genes, biomarkers, and models for therapy (coordination) - DE
Mathematisch-Naturwissenschaftlichen Fakultät der Universität zu Köln
Zoologisches Institut - Rugarli Lab

GERMANIA

Nordrhein-Westfalen
KÖLN

ITALIA

LAZIO
ROMA

Ricerca per nuovi geni malattia nella paraplegia spastica erediatria
Fondazione EBRI
Istituto di Neurobiologia e Medicina Molecolare

ITALIA

LAZIO
ROMA

Finanziato da un ente associato a IRDiRCParaplegia spastica ereditaria: indagine sulla regolazione della proteina spastina da parte della chinasi HIPK2 in cellule proliferanti e nei neuroni
Sapienza Università di Roma - Dip. di Biologia e Biotecnologie Charles Darwin
Dipartimento di Biologia e Biotecnologie - Charles Darwin

ITALIA

LOMBARDIA
MILANO

Finanziato da un ente associato a IRDiRCNEUROMICS: progetto europeo integrato di ricerca "omica" sulle malattie neuromuscolari e neurodegenerative - IT
Università degli Studi di Milano - Scienze Farmacologiche e Biomolecolari
Laboratorio di Biologia delle Cellule Staminali

PORTOGALLO

NORTE
PORTO

SPATAX: Clinical and Genetic Analysis of Cerebellar Ataxias and Spastic Paraplegias
Instituto de Biologia Molecular e Celular
Centro de Genética Preditiva e Preventiva

PORTOGALLO

NORTE
PORTO

SPATAX: Clinical and Genetic Analysis of Cerebellar Ataxias and Spastic Paraplegias
Instituto de Biologia Molecular e Celular
Unidade de Investigação Genética e Epidemiológica em Doenças Neurológicas

PORTOGALLO

NORTE
SANTA MARIA DA FEIRA

REGNO UNITO; GRAN BRETAGNA

Cambridgeshire
CAMBRIDGE

Modeling spastic paraplegia gene molecular function and pathology in Drosophila
Department of Genetics - University of Cambridge
Department of Genetics

GERMANIA

Nordrhein-Westfalen
KÖLN

Dissecting the role of two spastin isoforms with different subcellular localization in Hereditary Spastic Paraplegia
Mathematisch-Naturwissenschaftlichen Fakultät der Universität zu Köln
Zoologisches Institut - Rugarli Lab

GERMANIA

Nordrhein-Westfalen
KÖLN

Understanding the pathogenesis of hereditary spastic paraplegia due to paraplegin deficiency
Mathematisch-Naturwissenschaftlichen Fakultät der Universität zu Köln
Zoologisches Institut - Rugarli Lab

REGNO UNITO; GRAN BRETAGNA

Greater Manchester
ADDRESS: NOT PROVIDED - UK

FRANCIA

ILE-DE-FRANCE
PARIS

Finanziato da un ente associato a IRDiRCSTaHR : Stimulation of Targeted Homologous Recombination for Gene Therapy - FR
Muséum National d'Histoire Naturelle
Laboratoire Structure et Instabilité des Génomes - INSERM U1154 - CNRS 7196

FRANCIA

NOUVELLE AQUITAINE
BORDEAUX

Zebrafish models for human motor neuron diseases and organophosphorus-induced delayed neuropathy
CHU de Bordeaux-GH Pellegrin
Laboratoire Maladies Rares : Génétique et Métabolisme (MRGM)

FRANCIA

PAYS DE LA LOIRE
NANTES

Finanziato da un ente associato a IRDiRCFROGH : FRench Regional Origins in Genetics for Health - FR
Institut de Recherche en Santé - Université de Nantes
L'Institut du thorax - Inserm UMR 1087 / CNRS UMR 6291

GERMANIA

Bayern
ERLANGEN

Analysis of the axonal pathology of motoneurons generated from iPS cells from patients with SPG4 or SPG11
Universitätsklinikum Erlangen - Kopfkliniken
Abteilung für Molekulare Neurologie

GERMANIA

Berlin
BERLIN

SPP 1629: THYROID TRANS ACT - Development of T3-peptide ligands to treat MCT8 deficiency via a Trojan horse like mechanism
Charité - Universitätsmedizin Berlin (CVK)
Institut für Experimentelle Pädiatrische Endokrinologie

GERMANIA

Berlin
BERLIN

SPP 1629: THYROID TRANS ACT - Cell type-specific inactivation of Mct8 in brain cells: Gene expression, metabolism, morphology
Charité - Universitätsmedizin Berlin (CVK)
Institut für experimentelle Endokrinologie

GERMANIA

Nordrhein-Westfalen
BONN

SPP 1629: THYROID TRANS ACT - Structure and function of the thyroid hormone transporter MCT8
Medizinische Fakultät der Universität Bonn
Institut für Biochemie und Molekularbiologie

GERMANIA

Nordrhein-Westfalen
ESSEN

Finanziato da un ente associato a IRDiRCTHYRONERVE: Allan-Herndon-Dudley Syndrome: Mechanisms of disease and therapeutic approaches in model organism (coordination) - DE
Universitätsklinikum Essen
Klinik für Endokrinologie und Stoffwechselerkrankungen

GERMANIA

Thüringen
JENA

Pathophysiology of adaptor protein 5 complex related hereditary spastic paraplegia
Institut für Humangenetik am Universitätsklinikum Jena
Institut für Humangenetik

GERMANIA

Thüringen
JENA

REEP1 as disease gene in hereditary spastic paraplegia - Characterizing of physiological function and pathogenic outcome
Universitätsklinikum Jena
Institut für Klinische Chemie und Laboratoriumsdiagnostik

GIAPPONE

JAPAN
ADDRESS : NOT PROVIDED - JP

GIAPPONE

JAPAN
ADDRESS : NOT PROVIDED - JP

ITALIA

CAMPANIA
NAPOLI

Finanziato da un ente associato a IRDiRCProgramma Telethon per le malattie senza diagnosi
TIGEM - Telethon Institute of Genetics and Medicine
Genomic Medicine - Telethon Institute of Genetics and Medicine

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

Finanziato da un ente associato a IRDiRCRole of Tenascin-C in muscle stem cell function
Institution: Information not provided - US

Progetti di ricerca multicentrici