x

Pesquisar um projeto de investigação

* (*) campo(s) de preenchimento obrigatório

55 Resultado(s)

Ordenados por

Financiado por um membro do IRDiRC =

Projetos de investigação

ALEMANHA

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

ALEMANHA

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

ALEMANHA

Saarland
HOMBURG

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

ESPANHA

Comunidad Valenciana
VALENCIA

Financiado por um membro do 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

ESPANHA

Comunidad Valenciana
VALENCIA

Financiado por um membro do 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

ESTADOS UNIDOS

Ohio
CLEVELAND

Financiado por um membro do IRDiRCIlluminating the process of rod outer segment morphogenesis
Case Western Reserve University
Pharmacology

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCDisease mechanism and therapies for retinal degeneration
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCRetinal aging and inherited neurodegenerative diseases
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCReciprocal signaling in synaptogenesis
Institution: Information not provided - US

FRANCA

ILE-DE-FRANCE
PARIS

Financiado por um membro do 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)

ALEMANHA

Baden-Württemberg
TÜBINGEN

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

ESTADOS UNIDOS

South Carolina
COLUMBIA

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

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCNatural history and genetic studies of usher syndrome
Institution: Information not provided - US

FRANCA

ILE-DE-FRANCE
EVRY

Financiado por um membro do 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

FRANCA

ILE-DE-FRANCE
PARIS

Financiado por um membro do 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

FRANCA

OCCITANIE
MONTPELLIER

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

REINO UNIDO

Cambridgeshire
HINXTON

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

BELGICA

OOST-VLAANDEREN
GENT

Cis-regulatory mapping of the RPE-expressed transcription factor OTX2
Center for Medical Genetics Gent
Centrum voor Medische Genetica

ESPANHA

Madrid
MADRID

FRANCA

AUVERGNE-RHONE-ALPES
LYON

Financiado por um membro do IRDiRCDIVERCIL: Understanding cilia and flagella diversity - FR
Faculté de Médecine Lyon Est
Institut NeuroMyoGène (INMG) - CNRS UMR 5310 / INSERM U1217

FRANCA

GRAND-EST
STRASBOURG

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

FRANCA

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

FRANCA

ILE-DE-FRANCE
PARIS

FRANCA

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"

REINO UNIDO

Cambridgeshire
CAMBRIDGE

Financiado por um membro do IRDiRCActive BRIDGE Studies - Specialist Pathology: Evaluating Exomes in Diagnostics (SPEED)
Wellcome Trust/MRC Building
Cambridge Institute for Medical Research

FRANCA

ILE-DE-FRANCE
PARIS

Financiado por um membro do 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

FRANCA

PAYS DE LA LOIRE
NANTES

Financiado por um membro do 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

ITALIA

CAMPANIA
NAPOLI

Financiado por um membro do IRDiRCTelethon Undiagnosed Disease Program - Revised Proposal
TIGEM - Telethon Institute of Genetics and Medicine
Genomic Medicine - Telethon Institute of Genetics and Medicine

JAPAO

JAPAN
ADDRESS : NOT PROVIDED - JP

JAPAO

JAPAN
TOKYO

Financiado por um membro do IRDiRCFormation of integrated omics analysis base of refractory diseases in children and perinatal period
National Center for Child Health and Development
Research Institute

ESPANHA

Madrid
MADRID

Projetos de investigação multicêntricos