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31 Ergebnis(se)
Abgeschlossene Forschungsprojekte = 
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Forschungsprojekt(e)
DEUTSCHLAND
Bayern
REGENSBURG
Entwicklung neuer aktiver Substanzen zur Korrektur von mutanter BEST1 Chloridleitfähigkeit - Etablierung einer zielgerichteten Therapie für die Bestsche vitelliforme Makuladystrophie
Universitätsklinikum Regensburg
Zentrum für Humangenetik Regensburg
DEUTSCHLAND
Schleswig-Holstein
LÜBECK
Solve-RET: Fehlende erbliche Ursachen für genetische Netzhauterkrankungen mit Hilfe von Multiomics und Gen-Editing in menschlichen Zell- und Tiermodellen
Universitätsklinikum Schleswig-Holstein - Campus Lübeck
Institut für Humangenetik
FRANKREICH
GRAND-EST
STRASBOURG
Retinis Pigmentosa: validation of the molecular diagnostic using next generation sequencing
CHU de Strasbourg - Hôpital Civil
Laboratoire de diagnostic génétique
FRANKREICH
GRAND-EST
STRASBOURG
Solving missing heritability in inherited retinal diseases using integrated omics and gene editing in human cellular and animal models
Faculté de médecine de Strasbourg - Louis Pasteur
Laboratoire de génétique médicale - Unité Inserm U1112
FRANKREICH
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
FRANKREICH
ILE-DE-FRANCE
PARIS
Research of drugs and therapeutic targets for rare retinal dystrophies using cell models from patients
Institut de la Vision
Centre de Recherche Institut de la Vision
FRANKREICH
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"
IRLAND
County Dublin
DUBLIN
Target 5000: A study of Inherited Retinal Degeneration
Mater Misericordiae Hospital
Department of Ophthalmology
IRLAND
County Dublin
DUBLIN
Target 5000: A study of Inherited Retinal Degeneration
Royal Victoria Eye and Ear Hospital
Ophthalmology Research Department
IRLAND
County Dublin
DUBLIN
Target 5000: A study of Inherited Retinal Degeneration
Trinity College Dublin
Smurfit Institute of Genetics
ITALIEN
CAMPANIA
NAPOLI
CRISPR/Cas9 microRNAs Editing as gene-independent therapeutic approach in Inherited Retinal Dystrophies (IRDs)
TIGEM - Telethon Institute of Genetics and Medicine
Genomic Medicine - Telethon Institute of Genetics and Medicine
ITALIEN
CAMPANIA
NAPOLI
SOLVE-RET: Solving missing heritability in inherited retinal diseases using integrated omics and gene editing in human cellular and animal models - IT
TIGEM - Telethon Institute of Genetics and Medicine
Laboratorio di Ricerca
SCHWEIZ
Suisse Alémanique
BASEL
SOLVE-RET: Solving missing heritability in inherited retinal diseases using integrated omics and gene editing in human cellular and animal models - CH
Institute of Molecular and Clinical Ophthalmology Basel (IOB)
SCHWEIZ
Suisse Alémanique
BASEL
Genomics of inherited retinal diseases
Institute of Molecular and Clinical Ophthalmology Basel (IOB)
SPANIEN
Andalucía
SEVILLA
SOLVE-RET: Solving missing heritability in inherited retinal diseases using integrated omics and gene editing in human cellular and animal models - ES
Centro Andaluz de Biología del Desarrollo (CABD)
Control genético de la morfogénesis epitelial en vertebrados
SPANIEN
Comunidad Valenciana
VALENCIA
The cell therapeutic strategy for hereditary retinal dystrophies in small and large animals: MERTK associated Retinitis pigmentosa
Fundación de la Comunidad Valenciana Centro de Investigación Príncipe Felipe
Fundación de la Comunidad Valenciana Centro de Investigación Príncipe Felipe (CIPF)
SPANIEN
País Vasco
SAN SEBASTIÁN
Development of diagnostic algorithms in patients with hereditary retinal dystrophies of the Basque Country, based on the sequencing of a panel of genes (targeted NGS) and whole genome (WGS)
Instituto de Investigación Sanitaria Biodonostia
DEUTSCHLAND
Nordrhein-Westfalen
BONN
IRLAND
County Dublin
DUBLIN
Exploration of theraputic strategies for ocular disorders
Trinity College Dublin
Smurfit Institute of Genetics
KANADA
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
KANADA
Ontario
TORONTO
Beyond the Genome: Transcriptome Based Diagnostics for Rare Diseases and Cancer
Hospital for Sick Children, Research Institute
SPANIEN
Cataluña
BARCELONA
Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases
Centro de Regulación Genómica
Archivo europeo de genomas y fenomas del CRG
SPANIEN
Cataluña
BARCELONA
Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases
Hospital Clínic de Barcelona
Servicio de Inmunologia
SPANIEN
Cataluña
BARCELONA
Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases
Hospital Universitari Vall d'Hebron
Laboratorio de Genética
SPANIEN
Cataluña
BARCELONA
Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases
Hospital de la Santa Creu i Sant Pau
Servicio de Genética
SPANIEN
Cataluña
L'HOSPITALET DE LLOBREGAT
Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases
Hospital Universitari de Bellvitge
Unidad de Genética Molecular
SPANIEN
Madrid
MADRID
Identification of new genes causing rare diseases in pediatric patients, searching of genetic pharmacological targets, and drugs discovery, the steps for a personalized medicine
Instituto de Investigación Hospital 12 de Octubre
Grupo de investigación en enfermedades raras, mitocondriales y neuromusculares
VEREINIGTE STAATEN
Washington
ADDRESS: NOT PROVIDED - US
A powerful web-based discovery platform for rare disease genetics
Institution: Information not provided - US
Multizentrische Forschungsprojekte
- Centrum Medische Genetica Gent - Universitair Ziekenhuis Gent
- Centrum Medische Genetica Gent / Centre for Medical Genetics Ghent
- Institut de la Vision
- Centre d'Investigation Clinique (CIC) de l'hôpital des Quinze-Vingts
- EEIG - EUROPEAN VISION INSTITUTE
- EUROPEAN VISION INSTITUTE
BELGIEN
OOST-VLAANDEREN
GENT
SOLVE-RET: Solving missing heritability in inherited retinal diseases using integrated omics and gene editing in human cellular and animal models
FRANKREICH
ILE-DE-FRANCE
PARIS
EVI-GENORET: functional genomics of the retina in health and disease (FINISHED)
BELGIEN
ARRONDISSEMENT BRUSSELS-CAPITAL
BRUXELLES