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Proyectos de investigación
ALEMANIA
Baden-Württemberg
ULM
REPETOMICS: Genomic Instability of Expanded Repeats in HD and ALS/FTD -DE
Universitäts- und Rehabilitationskliniken Ulm (RKU)
Klinik für Neurologie
ALEMANIA
Bayern
NEUHERBERG
PolyQure: Causal treatment of polyglutamine diseases by inhibition of TRMT2A : High-throughput and structural biological methods
Helmholtz Zentrum München
Institut für Strukturbiologie - AG Niessing
ALEMANIA
Nordrhein-Westfalen
BOCHUM
TreatPolyQ: Allele-specific lowering of mutant polyQ proteins as treatment for Huntington disease, spinocerebellar ataxia type 3 and spinocerebellar ataxia type 7 -DE
Ruhr-Universität Bochum
Humangenetik Bochum
BELGICA
HAINAUT
GOSSELIES
Enroll-HD: A Prospective Registry Study in a Global Huntington's Disease Cohort - BE
Institut de Pathologie et de Génétique
Département de Génétique Clinique - Institut de Pathologie et de Génétique (IPG)
BELGICA
VLAAMS BRABANT
LEUVEN
Longitudinal Measurement of Synaptic Density to Monitor Progression of Huntington's Disease
UZ Leuven - Campus Gasthuisberg
Huntington Clinic
BELGICA
VLAAMS BRABANT
LEUVEN
Direct Quantitative Comparison Between [11C]UCB-J and [18F]SynVest-1 PET as Markers for Synaptic Density in Premanifest and Manifest Huntington's Disease
UZ Leuven - Campus Gasthuisberg
Huntington Clinic
CANADA
Alberta
EDMONTON
Therapeutic role of ganglioside GM1 in Huntington's disease
University of Alberta
Department of Pharmacology
CANADA
Colombie-Britannique
VANCOUVER
Novel approaches to modulate key targets in the pathogenesis of Huntington Disease
Centre for Molecular Medicine and Therapeutics
CANADA
Colombie-Britannique
VANCOUVER
Altered balance of synaptic/extrasynaptic NMDA receptor signaling in Huntington disease
University of British Columbia
Centre for Huntington Disease- UBC Hospital
CANADA
Ontario
HAMILTON
Elucidating the Protective Mechanism of Phospho-N17 Huntingtin in Huntington's disease
McMaster University
Biochemistry and Biomedical Sciences
CANADA
Ontario
HAMILTON
Defective DNA Damage Repair and Aberrant PARylation as a Mechanism of Mutant Huntingtin in Huntington's Disease
McMaster University
Biochemistry and Biomedical Sciences
CANADA
Ontario
TORONTO
DNA repair proteins as modifiers of CAG repeat instability in Huntington's disease
The Hospital for Sick Children
Genetics and Genome Biology
CANADA
Québec
QUÉBEC
Preventing pathological protein spread in Huntington's disease: relevance to pathology and treatment
CHUQ - (CHUL) Centre hospitalier de l'Université Laval
Axe Neuosciences, CHUL
ESPAÑA
Cataluña
BARCELONA
Desarrollo y validación de instrumentos específicos de evaluación cognitiva basados en la biologia de la enfermedad de Huntington
IIB Sant Pau - Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
ESPAÑA
Cataluña
BARCELONA
Gliotransmisores y receptores de cannabinoides en el origen de los déficits cognitivos y de plasticidad sináptica en la enfermedad de Huntington
Universitat de Barcelona. Campus de Medicina - Clínic August Pi i Sunyer
Departamento de Biología Celular, Inmunología y Neurociencias
ESPAÑA
Comunidad Valenciana
VALENCIA
Modulación de la actividad de genes que controlan el metabolismo de las grasas como estrategia terapéutica en la enfermedad de Huntington
Hospital Universitario y Politécnico La Fe
Fundación para la Investigación del Hospital Universitari La Fe
ESPAÑA
Madrid
MADRID
Gliotransmisores y receptores de cannabinoides en el origen de los déficits cognitivos y de plasticidad sináptica en la enfermedad de Huntington
Instituto Cajal (CSIC)
Laboratorio de redes neuro-gliales
ESPAÑA
Madrid
MADRID
Gliotransmisores y receptores de cannabinoides en el origen de los déficits cognitivos y de plasticidad sináptica en la enfermedad de Huntington
Universidad Complutense de Madrid. Facultad de Medicina
Departamento de Bioquímica y Biología Molecular (Medicina)
ESTADOS UNIDOS
Maryland
BETHESDA
Developing inhibitors for PIP4Kgamma for Huntington's disease
National Center for Advancing Translational Sciences (NCATS-NIH)
Chemistry Technologies
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Investigating cd47-sirpa as novel protective signals during cns synaptic pruning
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Nanocarriers designed to deliver nucleic acids to brain
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Epigenetic pathology and therapy in huntington's disease
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Extrinsic mechanisms governing injury-induced axon degeneration
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Identification of gpr52 antagonists as potential treatments for huntington disease
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Identification of small molecules that decrease the activity of the huntingtin gene promoter for the potential treatment of huntington disease
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Identification of small molecules that increase activity of the huntingtin antisense promoter for the potential treatment of huntington disease
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Quantitative systems pharmacology approach to identify cytoprotective agents and pathways for huntington's disease
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Using a disease-affected cell to synthesize its own drug
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Cortical pathophysiology in mouse models of huntington's disease
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Cortico-basal ganglia connectivity in a non-human primate model of huntington's disease
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Early detection of huntington's disease: longitudinal analysis of basal ganglia and cortical thickness
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Genetic correction of mutant huntingtin in vivo
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Huntington's disease: a novel developmental oligodendrogliopathy
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Identifying factors regulating medium spiny neuron differentiation or maintenance as therapeutic targets for huntington's disease using induced pluripotent stem cells
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Mechanism of dna strand-break repair deficiency in huntington's disease
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Mechanism of modulation of huntingtin exon 1 aggregation by profilin
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Rhes-sumo circuitry in huntington's disease pathogenesis
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Structure of triplet repeat mrna in neurodegenerative disease
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
The regulation of synaptic connectivity and homeostasis by huntingtin
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Crmp2; mitochondria; and huntington's disease
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Control of excitatory synapse formation by huntingtin
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Determinants of cell type-specific vulnerability in huntington's disease
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Expanding the chemical diversity of therapeutic oligonucleotides to treat neurodegenerative disorders
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Improved monitoring of premanifest and early huntingtons using 7t multimodal mri
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Mitochondrial fragmentation and neurodegeneration in huntington's disease
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Mscs engineered to produce brain-derived neurotrophic factor for the treatment of huntington's disease
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
N-terminal huntingtin and huntington disease neuropathology
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Phosphoinositide signaling: novel potential targets for huntington disease
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Rare variant whole genome analysis and ipsc validation of putative genetic modifiers of huntington disease
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Statistical disease modeling and clinimetrics to prepare for preventive trials in huntington disease
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Endogenous regulation of huntingtin expression as a therapeutic target for huntington's disease
Institution: Information not provided - US
ESTADOS UNIDOS
Washington
ADDRESS: NOT PROVIDED - US
Validation of Novel Pathogenic Post-Translational Modifications of Huntingtin, and of Modifying Enzymes as Therapeutic Targets for Huntington's Disease
Institution: Information not provided - US
FRANCIA
AUVERGNE-RHONE-ALPES
LA TRONCHE
Axonal transport and neuronal maturation: consequences for synaptic function and neuronal connections in normal situation and in Huntington's disease
Grenoble-Institut des Neurosciences (GIN)
Grenoble-Institut des Neurosciences
FRANCIA
AUVERGNE-RHONE-ALPES
SAINT-MARTIN-D'HÈRES
FUELING-TRANSPORT: Untangling the role of the huntingtin protein in health and in Huntington's disease
Université Grenoble Alpes
FRANCIA
HAUTS-DE-FRANCE
ADDRESS: NOT PROVIDED - FR
Neuroprotective role of CYP46A1 in Huntington’s disease using gene transfer therapy in brain
Institution: Information not provided - FR
FRANCIA
HAUTS-DE-FRANCE
VILLENEUVE D'ASCQ
Dyadic dynamics of couples in Huntington disease
Université Lille 3
Equipe Dynamique Emotionnelle et Pathologies
FRANCIA
ILE-DE-FRANCE
FONTENAY-AUX-ROSES
Innovative Imaging and BIO Cognitive Markers to Predict the Progression of Huntington's Disease
CEA - Commissariat à l'Energie Atomique
Laboratoire des Maladies Neurodégénératives
FRANCIA
ILE-DE-FRANCE
PARIS
Efficient Gene and Sterol regulations by gene transfer for striatal protection in Huntington's Disease
AP-HP.Sorbonne Université - Hôpital de la Pitié-Salpêtrière
APHP.Sorbonne Université, Hôpital de la Pitié-Salpêtrière
FRANCIA
ILE-DE-FRANCE
PARIS
Development of therapeutic strategies for human degenerative diseases
Centre Paul Broca
Biologie et pathologie du neurone
FRANCIA
ILE-DE-FRANCE
PARIS
Cell-Type-Specific Gene and Sterol Profiling following CYP46A1 gene therapy in Huntington disease
Université Pierre et Marie Curie - Paris 6 - UPMC
Neuroscience Paris Seine (CNRS UMR8246/Inserm U1130/UMPC UMCR18)
FRANCIA
ILE-DE-FRANCE
PARIS
Brain response to Huntington's disease: role of small vesicles
Université Pierre et Marie Curie - Paris 6 - UPMC
Adaptation Biologique et Vieillissement
FRANCIA
PROVENCE-ALPES-COTE D'AZUR
MARSEILLE
REPETOMICS: Genomic Instability of Expanded Repeats in HD and ALS/FTD - FR
Institut de Neurosciences de la Timone
UMR7289
ITALIA
EMILIA ROMAGNA
ADDRESS: NOT PROVIDED - IT
Role of the Coiled-coil structure of the Huntingtin protein in the intercellular propagation of polyQ aggregates and in the progression of the disease
Institution: Information not provided - IT
ITALIA
EMILIA ROMAGNA
BOLOGNA
Enroll-HD - A Prospective Registry Study in a Global HD Cohort - IT
Università di Bologna - Istituto di Clinica Neurologica
Laboratorio di Neurogenetica
ITALIA
LAZIO
ROMA
Alteration in cortical parvalbuminergic System in murine model of Huntington's disease: pharmacological effect of phosphodiesterase type 4 (PDE4) inhibition
Fondazione EBRI
Istituto di Neurobiologia e Medicina Molecolare
ITALIA
LAZIO
ROMA
Analysis of apoptosis in neurodegenerative diseases by apaf1 conditional mutagenesis (terminated)
Università degli Studi di Roma Tor Vergata
Laboratorio di Genetica delle Popolazioni
ITALIA
LOMBARDIA
MILANO
Innovative Therapeutic Strategy Targeting Neurons With Cholesterol in Huntington Disease: From Preclinical Studies to Clinical Trial Readiness
Fondazione IRCCS Istituto Neurologico "Carlo Besta"
U.O.C. Genetica Medica e Neurogenetica
ITALIA
LOMBARDIA
MILANO
Targeting neurons with cholesterol. How can it change the future of Huntington Disease patients
Università degli Studi di Milano - Scienze Biomolecolari e Biotecnologiche
Dipartimento di Bioscienze
PAISES BAJOS (LOS)
Zuid-Holland
LEIDEN
Investigating cell-specific pathology in Huntington's disease and spinocerebellar ataxia iPSC-derived brain assembloids before and after treatment with targeted antisense oligonucleotides
LUMC - Leids Universitair Medisch Centrum
PORTUGAL
CENTRO
COIMBRA
Analysis of transcription deregulation in brain and peripheral Huntington disease models - influence of modulating histone deacetylases.
Universidade de Coimbra - Centro de Neurociências e Biologia Celular
Grupo de Disfunção Mitocondrial e Morte Celular
REINO UNIDO (EL)
Avon
BRISTOL
Enroll-HD: A Prospective Registry Study in a Global Huntington's Disease Cohort - UK
Southmead Hospital
North Bristol NHS Trust
REINO UNIDO (EL)
Gwent
CARDIFF
Enroll-HD: A Prospective Registry Study in a Global Huntington's Disease Cohort - UK
Cardiff School of Biosciences
REPUBLICA CHECA (LA)
Capital City Prague
PRAHA 2
Markers of mitochondrial dysfunction in presymptomatic and early stages of Huntington's disease
Vseobecna fakultni nemocnice a 1. lekarska fakulta UK
Neurologicka klinika
SUECIA
Region Skåne
LUND
BAGADILICO: Hypothalamic changes and biomarkers in Huntington's disease
Lunds Universitet
Department of Experimental Medical Science
SUECIA
Region Skåne
LUND
Immune response in Huntington's disease and delineation of its importance for disease pathogenesis and biomarkers
Lunds Universitet
Department of Experimental Medical Science
SUECIA
Region Stockholm
SOLNA
The functional organisation of the brain
Karolinska Institutet
Department of Clinical Neuroscience (CNS)
SUIZA
Suisse Alémanique
ZÜRICH
Multinational research projects on Health and Social Care for Neurodegenerative Diseases DOMINO-HD (HESOCARE-329-017)
Universitätsspital Zürich
Klinik für Neurologie
SUIZA
Suisse Romande
LAUSANNE
Toward gene repair for Huntington's disease
Centre Hospitalier Universitaire Vaudois CHUV
Laboratoire des neurothérapies et neuromodulation
ESPAÑA
Asturias
OVIEDO
El papel patogénico emergente de los alelos intermedios en el gen HTT: desde las evidencias neuropatológicas a las moleculares
Fundación para la Investigación Biosanitaria del Principado de Asturias
FINBA: Fundación para la Investigación Biosanitaria del Principado de Asturias
ESPAÑA
Cataluña
BARCELONA
Genómica avanzada y lipidómica para la identificación de nuevas causas genéticas de trastornos de movimiento hereditarios
Instituto de Química Avanzada de Cataluña
Unidad de Investigación en Moléculas Bioactivas
ESPAÑA
Cataluña
L'HOSPITALET DE LLOBREGAT
Genómica avanzada y lipidómica para la identificación de nuevas causas genéticas de trastornos de movimiento hereditarios
IDIBELL - Instituto de Investigación Biomédica de Bellvitge
Laboratorio de Enfermedades Neurometabólicas
ESPAÑA
País Vasco
SAN SEBASTIÁN
Genómica avanzada y lipidómica para la identificación de nuevas causas genéticas de trastornos de movimiento hereditarios
Instituto de Investigación Sanitaria Biodonostia
Área de Neurociencias
FINLANDIA
Finland
OULU
FINCA mouse as a tool to study mechanisms behind severe fibrosis and neurodegeneration
University of Oulu
Biocenter Oulu
ESPAÑA
Cataluña
BARCELONA
iGenCO: análisis genómico exhaustivo y análisis cross-ómico para enfermedades minoritarias no diagnosticadas en una plataforma colaborativa amigable
Centro de Regulación Genómica
Centro Nacional de Análisis Genómico
ESPAÑA
Cataluña
BARCELONA
iGenCO: análisis genómico exhaustivo y análisis cross-ómico para enfermedades minoritarias no diagnosticadas en una plataforma colaborativa amigable
ISGlobal - Instituto de Salud Global de Barcelona
Programa de investigación en Enfermedades no transmisibles y medio ambiente
FRANCIA
ILE-DE-FRANCE
PARIS
Neuroglobin gene overexpression: a promising tool for treating a large spectrum of neurological disorders thanks to its ability to safely and sustainably preserve mitochondrial integrity
Institut National de la Santé et de la Recherche Médicale
ITALIA
LAZIO
ROMA
Diverse rare diseases caused by functional dysregulation of Rho GTPase-related proteins
ISS - Istituto Superiore di Sanità
Centro Nazionale Malattie Rare
CANADA
Colombie-Britannique
VICTORIA
Silent Genomes: Reducing health care disparities and improving diagnostic success for children with genetic diseases from Indigenous populations
University of Victoria
Community Genetics Research Program/Island Medical Program
CANADA
Ontario
TORONTO
Beyond the Genome: Transcriptome Based Diagnostics for Rare Diseases and Cancer
Hospital for Sick Children, Research Institute
ESPAÑA
Andalucía
SEVILLA
Desarrollo de herramientas bioinformáticas para el manejo automático de hallazgos secundarios y su uso en el asesoramiento genético y farmacogenético
Fundación Progreso y Salud
Área de bioinformática clínica
ESPAÑA
Cataluña
BARCELONA
Red interhospitalaria catalana de variantes genéticas para mejorar el diagnóstico genético en enfermedades raras
Centro de Regulación Genómica
Archivo europeo de genomas y fenomas del CRG
ESPAÑA
Cataluña
BARCELONA
Red interhospitalaria catalana de variantes genéticas para mejorar el diagnóstico genético en enfermedades raras
Hospital Clínic de Barcelona
Servicio de Inmunologia
ESPAÑA
Cataluña
BARCELONA
Red interhospitalaria catalana de variantes genéticas para mejorar el diagnóstico genético en enfermedades raras
Hospital Universitari Vall d'Hebron
Laboratorio de Genética
ESPAÑA
Cataluña
BARCELONA
Red interhospitalaria catalana de variantes genéticas para mejorar el diagnóstico genético en enfermedades raras
Hospital de la Santa Creu i Sant Pau
Servicio de Genética
ESPAÑA
Cataluña
ESPLUGUES DE LLOBREGAT
Red federada de genómica funcional de enfermedades no diagnosticadas y enfermedades raras, RareFunction
Fundació Sant Joan de Déu - Institut de Recerca Sant Joan de Déu
Grupo de investigación en Neurogenética y Medicina Molecular
ESPAÑA
Cataluña
ESPLUGUES DE LLOBREGAT
Red interhospitalaria catalana de variantes genéticas para mejorar el diagnóstico genético en enfermedades raras
Hospital Sant Joan de Déu Barcelona
Servicio de Laboratorio
ESPAÑA
Cataluña
L'HOSPITALET DE LLOBREGAT
Red interhospitalaria catalana de variantes genéticas para mejorar el diagnóstico genético en enfermedades raras
Hospital Universitari de Bellvitge
Unidad de Genética Molecular
ESPAÑA
Comunidad Valenciana
VALENCIA
Estudios clínicos, bases genéticas y biomarcadores pronóstico en enfermedades raras neurodegenerativas
Centro de Investigación Príncipe Felipe (CIPF)
CIPF: Centro de Investigación Príncipe Felipe
ESPAÑA
Madrid
MADRID
Identificación de nuevos genes causantes de enfermedades raras en pacientes pediátricos, identificación de dianas farmacológicas, y descubrimiento de fármacos, los pasos para una medicina personalizada
Instituto de Investigación Hospital 12 de Octubre
Grupo de investigación en enfermedades raras, mitocondriales y neuromusculares
FINLANDIA
Finland
OULU
Novel Diagnostics and Treatment Strategies for Developmental Disorders, Childhood Epilepsies and Movement Disorders
University of Oulu
Biocenter Oulu
Proyectos de investigación multicéntricos
- Institut für Medizinische Genetik und angewandte Genomik Tübingen
- Institut für Medizinische Genetik und angewandte Genomik
- Institut für Medizinische Genetik und angewandte Genomik Tübingen
- Institut für Medizinische Genetik und angewandte Genomik
- Institut für Medizinische Genetik und angewandte Genomik Tübingen
- Institut für Medizinische Genetik und angewandte Genomik
- Institut für Medizinische Genetik und angewandte Genomik Tübingen
- Institut für Medizinische Genetik und angewandte Genomik
- Institut für Medizinische Genetik und angewandte Genomik Tübingen
- Institut für Medizinische Genetik und angewandte Genomik
- Universitäts- und Rehabilitationskliniken Ulm (RKU)
- Zentrale Koordination des Europäischen HD Netzwerks
- Zentrum für Seltene Erkrankungen am Universitätsklinikum Ulm
- Zentrum für Seltene Erkrankungen (ZSE) ULM
- Ruhr-Universität Bochum
- Humangenetik Bochum
- Centre de Recherche en Cancérologie de Marseille
- Télomères et Chromatine
- Parc scientifique et technologiques de Luminy
- Trophos SA
- Università degli Studi di Milano - Scienze Farmacologiche e Biomolecolari
- Laboratorio di Biologia delle Cellule Staminali
- SIENA BIOTECH SPA
- SIENA BIOTECH SPA
- Unità di Neurobiologia
- John van Geest Centre for Brain Repair
- NeuroNE
- Cardiff School of Biosciences
- Alzheimer Europe Office
- Max-Planck-Institut für Multidisziplinäre Naturwissenschaften
- Abteilung Molekulare Neurobiologie
- Azienda Ospedaliera di Padova
- Clinica Pediatrica
ALEMANIA
Baden-Württemberg
TÜBINGEN
RATSTREAM: European project on the characterisation of transgenic rat models for neurodegenerative and psychiatric diseases: Automated home cage analyses, live imaging and treatment (FINISHED)
ALEMANIA
Baden-Württemberg
TÜBINGEN
NEUROMODEL: Academic-Industrial Initial Training Network (ITN) on Innovative Treatment Approaches of Huntingtons and Parkinsons Disease
ALEMANIA
Baden-Württemberg
TÜBINGEN
TreatPolyQ: Industrial Academic Initial Training Network (Itn) Towards Treatment Of Polyglutamine Diseases -terminated-
ALEMANIA
Baden-Württemberg
TÜBINGEN
PhenoRat: European Industrial Doctorate on the generation, characterisation and validation of transgenic rat models of two neurodegenerative diseases: Huntington's disease and spinocerebellar ataxia type 17
ALEMANIA
Baden-Württemberg
TÜBINGEN
Neuromics: Integrated European -omics research project for diagnosis and therapy in rare neuromuscular and neurodegenerative diseases
ALEMANIA
Baden-Württemberg
ULM
EHDN: European Huntington's Disease Network
ALEMANIA
Baden-Württemberg
ULM
Enroll-HD: A Prospective Registry Study in a Global Huntington's Disease Cohort
ALEMANIA
Nordrhein-Westfalen
BOCHUM
TreatPolyQ: Allele-specific lowering of mutant polyQ proteins as treatment for Huntington disease, spinocerebellar ataxia type 3 and spinocerebellar ataxia type 7
FRANCIA
PROVENCE-ALPES-COTE D'AZUR
MARSEILLE
REPETOMICS: Genomic Instability of Expanded Repeats in HD and ALS/FTD
FRANCIA
PROVENCE-ALPES-COTE D'AZUR
MARSEILLE
MITOTARGET: mitochondrial dysfunction in neurodegenerative diseases: towards new therapeutics
ITALIA
LOMBARDIA
MILANO
NEuroStemCell: European Consortium for Stem Cell Therapy for Neurodegenerative Diseases (TERMINATED)
ITALIA
TOSCANA
SIENA
PADDINGTON: pharmacodynamic approaches to demonstration of disease-modification in Huntington's disease by SEN0014196 (TERMINATED)
ITALIA
TOSCANA
SIENA
TAMAHUD: identification of early disease markers, novel pharmacologically tractable targets and small molecule phenotypic modulators in Huntington's Disease
REINO UNIDO (EL)
Cambridgeshire
CAMBRIDGE
EUNEURONE: European Consortium for Research in Neurodegenerative Diseases
REINO UNIDO (EL)
Gwent
CARDIFF
REPAIR-HD: Human pluripotent stem cell differentiation, safety and preparation for therapeutic transplantation in Huntington's disease
LUXEMBURGO
LUXEMBOURG
LUXEMBOURG
Alzheimer Europe: European database on rare forms of dementia
ALEMANIA
Niedersachsen
GÖTTINGEN
EUROSPIN: European consortium on synaptic protein networks in Neurological and Psychiatric diseases
ITALIA
VENETO
PADOVA