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Progetti di ricerca

FRANCIA

ILE-DE-FRANCE
PARIS

Finanziato da un ente associato a IRDiRCPsychosocial impact of deafblindness handicap on autonomy within the life course in people with Usher, Wolfram and Stickler Syndromes
Université Denis Diderot - Paris 7
Centre de recherches psychanalyse, médecine et société (EA3522)

GERMANIA

Rheinland-Pfalz
MAINZ

Deciphering the cellular function of proteins and protein networks related to the human Usher syndrome (USH)
Institut für Zoologie der Universität Mainz
Institut für Zoologie - Abt. I - AG Wolfrum

GERMANIA

Rheinland-Pfalz
MAINZ

Evaluation of gene based therapies for the human Usher syndrome in the retina
Institut für Zoologie der Universität Mainz
Institut für Zoologie - Abt. I - AG Wolfrum

GERMANIA

Saarland
HOMBURG

Visual impairment and blindness in multiple-handicapped children
Universitätsklinikum des Saarlandes
AG Kinder- & Neuroophthalmologie

SPAGNA

Comunidad Valenciana
VALENCIA

Finanziato da un ente associato a IRDiRC3D retinas derived from iPS cells as a tool to find effective therapies for inherited diseases of the retina
Centro de Investigación Príncipe Felipe (CIPF)
Banco de Líneas Celulares

SPAGNA

Comunidad Valenciana
VALENCIA

Finanziato da un ente associato a IRDiRCGenomics, preclinical and clinical studies for a precision medicine in hereditary retinal dystrophies: Usher syndrome
IIS La Fe - Instituto de Investigación Sanitaria La Fe
Grupo de investigación en biomedicina molecular, celular y genómica

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

Washington
ADDRESS: NOT PROVIDED - US

Finanziato da un ente associato a IRDiRCDisease mechanism and therapies for retinal degeneration
Institution: Information not provided - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

Finanziato da un ente associato a IRDiRCRetinal aging and inherited neurodegenerative diseases
Institution: Information not provided - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

Finanziato da un ente associato a IRDiRCReciprocal signaling in synaptogenesis
Institution: Information not provided - US

FRANCIA

ILE-DE-FRANCE
EVRY

Finanziato da un ente associato a IRDiRCStem cell Therapy for Retinal Epithelium replacement Assay in Monogenic retinopathies
GENOPOLE - Campus 1
I-Stem - Institut des cellules Souches pour le Traitement et l'Etude des maladies Monogéniques

FRANCIA

ILE-DE-FRANCE
PARIS

Finanziato da un ente associato a IRDiRCModeling the Usher Syndrome type I (USH1) retinopathy in pig: physiopathology and gene therapy
Institut Pasteur
Génétique et Physiologie de l'audition - Inserm U1120 Paris 6

FRANCIA

OCCITANIE
MONTPELLIER

Zebrafish to study the impact of identified variants in neurosensory pathologies
IURC - Institut Universitaire de Recherche Clinique
Laboratoire de génétique moléculaire

GERMANIA

Baden-Württemberg
TÜBINGEN

Rate of Progression in USH2A Related Retinal Degeneration
Department für Augenheilkunde Tübingen
Universitäts-Augenklinik

STATI UNITI

South Carolina
COLUMBIA

Rate of Progression in USH2A Related Retinal Degeneration
Foundation Fighting Blindness
Foundation Fighting Blindness USA

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

Finanziato da un ente associato a IRDiRCNatural history and genetic studies of usher syndrome
Institution: Information not provided - US

REGNO UNITO; GRAN BRETAGNA

Cambridgeshire
HINXTON

The Deciphering Developmental Disorders (the DDD study)
Wellcome Trust Sanger Institute
DECIPHER

BELGIO

OOST-VLAANDEREN
GENT

FRANCIA

AUVERGNE-RHONE-ALPES
LYON

Finanziato da un ente associato a IRDiRCDIVERCIL: Understanding cilia and flagella diversity - FR
Faculté de Médecine Lyon Est
Institut NeuroMyoGène (INMG) - CNRS UMR 5310 / INSERM U1217

FRANCIA

GRAND-EST
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

Epidemiological study in hereditary dystrophies of retina
Institut de la Vision
Centre d'Investigation Clinique (CIC) de l'hôpital des Quinze-Vingts

FRANCIA

ILE-DE-FRANCE
PARIS

FRANCIA

OCCITANIE
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"

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

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 Medicina Maternofetal, Genética y Reproducción

SPAGNA

Cataluña
BARCELONA

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

SPAGNA

Madrid
MADRID

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

Progetti di ricerca multicentrici