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Finanziato da un ente associato a IRDiRC =

Progetti di ricerca

BELGIO

OOST-VLAANDEREN
GENT

BELGIO

OOST-VLAANDEREN
GENT

Belgian Medical Genomics Initiative (BeMGI)
Center for Medical Genetics Ghent

BELGIO

VLAAMS BRABANT
LEUVEN

Genetic testing in Europe - Network for the further development, harmonization, validation and standardization of services
University Hospitals Leuven - Gasthuisberg
Laboratory for Molecular Diagnostics

CANADA

Ontario
TORONTO

Finanziato da un ente associato a IRDiRCGRIP: Global Research in Paediatrics - CA
The Hospital for Sick Children
Department of Paediatrics

CANADA

Ontario
TORONTO

Finanziato da un ente associato a IRDiRCGRIP: Global Research in Paediatrics - CA
The Hospital for Sick Children
Division of Clinical Pharmacology and Toxicology, Department of Paediatrics

CANADA

Ontario
TORONTO

Finanziato da un ente associato a IRDiRCComputerized Patient Phenotyping to Connect Canadian Clinical Genetics Clinics
University of Toronto
Department of Computer Science

FRANCIA

ALSACE
STRASBOURG

Retinis Pigmentosa: validation of the molecular diagnostic using next generation sequencing
CHU de Strasbourg - Hôpital Civil
Laboratoire de diagnostic génétique

FRANCIA

ILE-DE-FRANCE
PARIS

FRANCIA

ILE-DE-FRANCE
PARIS

Epidemiological study in hereditary dystrophies of retina
Institut de la Vision
Recherche Clinique

FRANCIA

LANGUEDOC-ROUSSILLON
MONTPELLIER

Genetics of autosomal recessive retinitis pigmentosa and of macular dystrophies
Hôpital Saint Eloi - Bâtiment INM
Equipe "Génétique et thérapie des cécités rétiniennes et du nerf optique"

FRANCIA

LANGUEDOC-ROUSSILLON
MONTPELLIER

Dominant autosomic retinitis pigmentosa: prevalence of known genes and identification of new ones
Hôpital Saint Eloi - Bâtiment INM
Equipe "Génétique et thérapie des cécités rétiniennes et du nerf optique"

FRANCIA

LANGUEDOC-ROUSSILLON
MONTPELLIER

Gene therapy of retinal dystrophy on human models: differentiation of patients iPS cells to retinal cells
Hôpital Saint Eloi - Bâtiment INM
Equipe "Génétique et thérapie des cécités rétiniennes et du nerf optique"

FRANCIA

PAYS DE LA LOIRE
NANTES

Evaluation of the immune response in Briards dogs RPE65 -/- treated with gene therapy
CHU de Nantes - Hôtel Dieu
Vecteurs viraux et transfert de genes in vivo

FRANCIA

RHONE-ALPES
LYON

GERMANIA

Bayern
REGENSBURG

Functional analysis of FAM161A proteine and investigation of FAM161A associated retinal degeneration
Universitätsklinikum Regensburg
Zentrum und Institut für Humangenetik Regensburg

GERMANIA

Hessen
GIEßEN

Diagnosis and therapy of hereditary retinal diseases
Augenklinik des UKGM am Standort Gießen
Klinik und Poliklinik für Augenheilkunde

GERMANIA

Nordrhein-Westfalen
KÖLN

ITALIA

CAMPANIA
NAPOLI

ITALIA

LAZIO
ROMA

Le politiche sanitarie in Italia sulla genomica
IRCCS Ospedale Pediatrico Bambino Gesù - SEDE GIANICOLO
Servizio Clinico di Consulenza Genetica

ITALIA

LOMBARDIA
MILANO

Finanziato da un ente associato a IRDiRCMigliorando la biosicurezza del trasferimento genico con vettori lentivirali
IRCCS Ospedale San Raffaele
Centro di Genomica, Bioinformatica e Biostatistica - Unità di Genetica Umana e Molecolare

ITALIA

LOMBARDIA
MILANO

Finanziato da un ente associato a IRDiRCStrategie di terapia cellulare per induzione della tolleranza immunologica
Istituto San Raffaele Telethon per la Terapia Genica - TIGET
Istituto San Raffaele Telethon per la Terapia Genica

ITALIA

LOMBARDIA
MILANO

Finanziato da un ente associato a IRDiRCStrategie di terapia genica per l'induzione della tolleranza antigene-specifica in vivo
Istituto San Raffaele Telethon per la Terapia Genica - TIGET
Unità di Ricerca Clinica Pediatrica

ITALIA

TOSCANA
PISA

Come trasformare cellule staminali embrionali in cellule retiniche: ruolo di geni specifici dell'occhio
Azienda Ospedaliero Universitaria Pisana - Ospedale S. Chiara
Dipartimento di Biologia

ITALIA

TOSCANA
PISA

Istopatologia della retina in modelli animali di Retinite Pigmentosa. Approcci terapeutici per i fotorecettori.
Fondazione "Gabriele Monasterio" - Consiglio Nazionale delle Ricerche CNR
Area della Ricerca

PAESI BASSI

Gelderland
NIJMEGEN

PAESI BASSI

Gelderland
NIJMEGEN

Identification of the genetic causes of inherited retinal dystrophies
Radboudumc - Radboud universitair medisch centrum
Afdeling Genetica

PAESI BASSI

Gelderland
NIJMEGEN

Identification of the genetic causes of inherited retinal dystrophies
Radboudumc - Radboud universitair medisch centrum
Afdeling Oogheelkunde

PAESI BASSI

Noord-Holland
AMSTERDAM

Finanziato da un ente associato a IRDiRCGRiP: Global Research in Paediatrics - NL
AMC - Academisch Medisch Centrum
Afdeling Klinische Epidemiologie in de Kindergeneeskunde

PAESI BASSI

Utrecht
SOEST

Finanziato da un ente associato a IRDiRCGRiP: Global Research in Paediatrics - NL
VSOP
Vereniging Samenwerkende Ouder- en Patiëntenorganisaties

PAESI BASSI

Utrecht
UTRECHT

Finanziato da un ente associato a IRDiRCSYSCILIA: A systems biology approach to dissect cilia function and its disruption in human genetic disease - NL (Terminated)
UMC Utrecht - Universitair Medisch Centrum Utrecht
Afdeling Nefrologie en Hypertensie

PAESI BASSI

Zuid-Holland
ROTTERDAM

Finanziato da un ente associato a IRDiRCGRiP: Global Research in Paediatrics - NL
Erasmus MC - Erasmus Medisch Centrum
Vakgroep Medische Informatica

POLONIA

Warszawa
WARSAW

Finanziato da un ente associato a IRDiRCGRIP: Global Research in Paediatrics
Instytut "Pomnik-Centrum Zdrowia Dziecka"
Klinika Anestezjologii i Intensywnej Terapii

REGNO UNITO; GRAN BRETAGNA

Cambridgeshire
CAMBRIDGE

REGNO UNITO; GRAN BRETAGNA

Cambridgeshire
CAMBRIDGE

Finanziato da un ente associato a IRDiRCActive BRIDGE Studies - Specialist Pathology: Evaluating Exomes in Diagnostics (SPEED)
Wellcome Trust/MRC Building
Cambridge Institute for Medical Research

REGNO UNITO; GRAN BRETAGNA

Greater London
LONDON

GRIP: Global Research in Paediatrics
St George's Hospital University of London
Institute of Infection and immunity

REGNO UNITO; GRAN BRETAGNA

Greater London
LONDON

SYSCILIA: A systems biology approach to dissect cilia function and its disruption in human genetic disease - UK
UCL Institute of Child Health, University College London
Molecular Medicine Unit

REGNO UNITO; GRAN BRETAGNA

Greater London
LONDON

REGNO UNITO; GRAN BRETAGNA

Greater London
LONDON

AAVEYE: gene replacement therapy in Pde6B and Aipl1 murine mutants (WP2)
UCL Institute of Ophthalmology
Molecular Therapy

REGNO UNITO; GRAN BRETAGNA

Greater London
LONDON

GRIP: Global Research in Paediatrics
University College London
School of Pharmacy

REGNO UNITO; GRAN BRETAGNA

Merseyside
LIVERPOOL

GRIP: Global Research in Paediatrics
Liverpool Women's NHS Foundation Trust
Department of Women's and Children's Health

REGNO UNITO; GRAN BRETAGNA

West Midlands
BIRMINGHAM

REGNO UNITO; GRAN BRETAGNA

West Yorkshire
LEEDS

SYSCILIA: A systems biology approach to dissect cilia function and its disruption in human genetic disease - UK
St. James University Hospital
Leeds Institute of Biomedical and Clinical Sciences

SPAGNA

Aragón
ZARAGOZA

Finanziato da un ente associato a IRDiRCFunctional and anatomical preservation of Melatonin and Epigallocatechin Gallate on retinal neurodegenerative models
Hospital Clínico Universitario "Lozano Blesa" de Zaragoza
Servicio de Oftalmología

SPAGNA

Cataluña
BARCELONA

Design of a genetic diagnostic chip for retinal dystrophies
Universitat de Barcelona. Facultat de Biologia
Departamento de Genética

SPAGNA

Comunidad Valenciana
VALENCIA

SPAGNA

País Vasco
BARAKALDO

Finanziato da un ente associato a IRDiRCGRiP: Global Research in Paediatrics - ES
Hospital Universitario Cruces - Osakidetza
Unidad Neonatal

SPAGNA

País Vasco
SAN SEBASTIÁN

Finanziato da un ente associato a IRDiRCAnalysis of microRNAs in patients and in murine models of retinitis pigmentosa: novel therapeuthic targets
Instituto de Investigación Sanitaria Biodonostia
Área de Neurociencias: Grupo de neurodegeneración sensorial

STATI UNITI

California
BERKELEY

Finanziato da un ente associato a IRDiRCTherapeutic approaches for abca4-associated disorders
University Of California Berkeley
Ophthalmology

STATI UNITI

California
BERKELEY

Finanziato da un ente associato a IRDiRCCompleting genetic analysis of the abca4 locus
University Of California Berkeley
Ophthalmology

STATI UNITI

California
BERKELEY

Finanziato da un ente associato a IRDiRCRole of impaired protein degradation in photoreceptor degeneration
University Of California Berkeley
Ophthalmology

STATI UNITI

California
BERKELEY

Finanziato da un ente associato a IRDiRCHdac4-mediated photoreceptor protection in retinal degeneration
University Of California Berkeley
Ophthalmology

STATI UNITI

California
BERKELEY

STATI UNITI

California
BERKELEY

STATI UNITI

California
BERKELEY

Finanziato da un ente associato a IRDiRCSerotonin receptor modulation of neurotrophic factors in the retina
University Of California Berkeley
Ophthalmology

STATI UNITI

California
BERKELEY

Finanziato da un ente associato a IRDiRCDelaying cone death in retinitis pigmentosa
University Of California Berkeley
Ophthalmology

STATI UNITI

California
BERKELEY

STATI UNITI

Massachusetts
BOSTON

Finanziato da un ente associato a IRDiRCThe pathogenesis of rna splicing factor rp
Massachusetts Eye And Ear Infirmary

STATI UNITI

Missouri
SAINT LOUIS

STATI UNITI

Missouri
SAINT LOUIS

Finanziato da un ente associato a IRDiRCMolecular mechanisms of human retinal disease
Washington University
Pathology

STATI UNITI

North Carolina
DURHAM

STATI UNITI

Ohio
CLEVELAND

Finanziato da un ente associato a IRDiRCIlluminating the process of rod outer segment morphogenesis
Case Western Reserve University
Pharmacology

STATI UNITI

Ohio
CLEVELAND

Finanziato da un ente associato a IRDiRCPharmacological treatment of retinal diseases
Case Western Reserve University
Pharmacology

STATI UNITI

Ohio
CLEVELAND

Finanziato da un ente associato a IRDiRCCarotinoids in vision
Case Western Reserve University
Pharmacology

STATI UNITI

Texas
DALLAS

STATI UNITI

Texas
HOUSTON

STATI UNITI

Texas
HOUSTON

Finanziato da un ente associato a IRDiRCMolecular basis of human visual system disorders
Baylor College Of Medicine
Genetics

SVEZIA

Skane
LUND

SVEZIA

Stockholms läns landsting
STOCKHOLM

Genetic and molecular mechanisms in familial visual impairment
Karolinska Institutet - Solna
Department of molecular medicine and surgery

SVIZZERA

Suisse Italienne
BELLINZONA

Investigating cellular mechanisms regulating protein folding and quality control to intervene in conformational diseases
Istituto di Ricerca in Biomedicina
Protein Folding and Quality Control - Institute for Research in Biomedicine

SVIZZERA

Suisse Romande
LAUSANNE

AAVEYE: combined therapies to restore vision in Pde6B and Aipl1 murine mutants (WP3)
Hopital Ophtalmique Jules Gonin - Fondation Asile des aveugles
Unit of Gene Therapy & Stem Cell Biology - Hôpital Ophtalmique Jules Gonin

Progetti di ricerca multicentrici