x

Cerca un progetto di ricerca

* (*) campo obbligatorio

78 Risultato/i

Ordinato per

Finanziato da un ente associato a IRDiRC =

Progetti di ricerca

FRANCIA

ILE-DE-FRANCE
PARIS

BIOSCA:Biomarkers in Autosomal Dominant Cerebellar Ataxia
CHU Paris-GH La Pitié Salpêtrière-Charles Foix - Hôpital Pitié-Salpêtrière
UF de Neurogénétique Moléculaire et Cellulaire

GERMANIA

Baden-Württemberg
TÜBINGEN

Finanziato da un ente associato a IRDiRCSCA-CYP: Gene Therapy for Cerebellar Ataxias: restoring cholesterol metabolism by targeting brain cholesterol 24 hydroxylase (CYP46A1) (partner No 3)
Institut für Medizinische Genetik und angewandte Genomik Tübingen
Institut für Medizinische Genetik und angewandte Genomik

GERMANIA

Bayern
MARTINSRIED

Cellular Toxicity of Polyglutamine Proteins in Neurodegenerative Disease
Max-Planck-Institut für Biochemie
Abteilung zelluläre Biochemie

GERMANIA

Nordrhein-Westfalen
BONN

GERMANIA

Nordrhein-Westfalen
BONN

Finanziato da un ente associato a IRDiRCESMI: European Spinocerebellar Ataxia Type 3/Machado-Joseph Disease Initiative (Koordination)
Universitätsklinikum Bonn
Klinik und Poliklinik für Neurologie

PAESI BASSI

Gelderland
NIJMEGEN

Understanding and manipulating neural compensatory mechanisms in patients with SCA3
Radboudumc - Radboud universitair medisch centrum
Afdeling Neurologie

PAESI BASSI

Gelderland
NIJMEGEN

Cerebellar dysfunction and its compensation in presymptomatic carriers of the SCA3 mutation
Radboudumc - Radboud universitair medisch centrum
Afdeling Neurologie

PAESI BASSI

Zuid-Holland
LEIDEN

Finanziato da un ente associato a IRDiRCAntisense therapy for several major rare diseases
LUMC - Leids Universitair Medisch Centrum
Afdeling Humane Genetica

PORTOGALLO

CENTRO
ADDRESS: NOT PROVIDED - PT

PORTOGALLO

CENTRO
ADDRESS: NOT PROVIDED - PT

PORTOGALLO

CENTRO
BRAGA

PORTOGALLO

CENTRO
COIMBRA

The role of calpain-mediated proteolysis of ataxin-3 in Machado-Joseph disease: a molecular therapy approach with viral vectors.
Centro de Neurociências da Universidade de Coimbra
Departmento de vectores e terapia génica

PORTOGALLO

CENTRO
COIMBRA

Regulation by phosphorylation of ataxin-3, the mutated protein in Machado Joseph Disease
Centro de Neurociências da Universidade de Coimbra
Glutamatergic Synapses: Formation and regulation of synapses

PORTOGALLO

CENTRO
COIMBRA

Finanziato da un ente associato a IRDiRCSYNSPREAD: Role and mechanism of alpha-synuclein and ataxin-3 spreading in Parkinson and Machado-Joseph diseases
Centro de Neurociências da Universidade de Coimbra
Center for Neuroscience and Cell Biology

PORTOGALLO

NORTE
PORTO

A peptide aptamer-based approach to neurodegenerative disorders.
Instituto de Biologia Molecular e Celular
Protein Crystallography Group

PORTOGALLO

NORTE
PORTO

Search for disease modifiers in spinocerebellar ataxias: human and animal-based approaches.
Instituto de Biologia Molecular e Celular
Unidade de Investigação Genética e Epidemiológica em Doenças Neurológicas

REGNO UNITO; GRAN BRETAGNA

Greater London
LONDON

Finanziato da un ente associato a IRDiRCJPND European Spinocerebellar Ataxia Type 3/Machado-Joseph Disease Initiative
University College London - UCL Darwin Building
University College London

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

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"

GERMANIA

Schleswig-Holstein
LÜBECK

Phenotypic spectrum and molecular characterization of Movement disorders
Universität Lübeck
Institut für Neurogenetik

ITALIA

LAZIO
ROMA

SPATAX: Network europeo per le atassie e paraplegie spastiche ereditarie
Fondazione EBRI
Istituto di Neurobiologia e Medicina Molecolare

ITALIA

PIEMONTE
TORINO

Identificazione del gene responsabile di una nuova forma di atassia autosomica dominante
A.O. Città della Salute e della Scienza di Torino - Ospedale Molinette
Genetica Medica

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

Clinical implications of genetic factors causing neurodegenerative diseases characterized by movement or cognitive dysfunction.
Instituto de Biologia Molecular e Celular
Unidade de Investigação Genética e Epidemiológica em Doenças Neurológicas

PORTOGALLO

NORTE
PORTO

Mapping and identification of new disease genes in autosomal dominant spinocerebellar ataxias
Instituto de Biologia Molecular e Celular
Unidade de Investigação Genética e Epidemiológica em Doenças Neurológicas

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

Greater London
LONDON

Endogenous Cerebellar Human Stem Cells and their Potential Neuroregenerative Role in Inherited Ataxias
Barts and The London School of Medicine and Dentistry
Centre for Neuroscience and Trauma

REGNO UNITO; GRAN BRETAGNA

Lothian
EDINBURGH

Developing non-invasive therapeutic technology to improve motor coordination in cerebellar ataxias
PMARC - The University of Edinburgh
Perception-Movement-Action Research Consortium

REGNO UNITO; GRAN BRETAGNA

Lothian
EDINBURGH

Developing non-invasive therapeutic technology to improve motor coordination in cerebellar ataxias
School of Informatics, The University of Edinburgh
Human Communication Research Centre

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"

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

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

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

REGNO UNITO; GRAN BRETAGNA

Greater Manchester
ADDRESS: NOT PROVIDED - UK

STATI UNITI

Arizona
PHOENIX

Finanziato da un ente associato a IRDiRCThe etiology of inherited neurological diseases
Phoenix Children's Hospital
Barrow Neurological Institute

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

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

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

GERMANIA

Bayern
MÜNCHEN

Finanziato da un ente associato a IRDiRCRHAPSODY - Research to Assess Policies and Strategies for Dementia in the Young
Klinikum rechts der Isar der Technischen Universität München
Klinik und Poliklinik für Psychiatrie und Psychotherapie

Progetti di ricerca multicentrici