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Finanziato da un ente associato a IRDiRC =

Progetti di ricerca

BELGIO

OOST-VLAANDEREN
GENT

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 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

IRLANDA

County Dublin
DUBLIN 4

Finanziato da un ente associato a IRDiRCSYSCILIA: A systems biology approach to dissect cilia function and its disruption in human genetic disease - IE
University College Dublin
School of Biomolecular and Biomedical Science

ITALIA

CAMPANIA
NAPOLI

ITALIA

EMILIA ROMAGNA
MODENA

Finanziato da un ente associato a IRDiRCIl PEDF come agente terapeutico per la retinite pigmentosa
Università degli Studi di Modena e Reggio Emilia
Laboratorio Eye Diseases

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

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

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

REGNO UNITO; GRAN BRETAGNA

Greater London
LONDON

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

SPAGNA

Andalucía
SEVILLA

Finanziato da un ente associato a IRDiRCGenomic approaches for rare conditions: Inherited Retinal Dystrophies as a model
Hospital Universitario Virgen del Rocío
Unidad de Gestión Clínica Medicina Maternofetal, Genética y Reproducción

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
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

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