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252 Resultado(s)

Ordenados por

Financiado por um membro do IRDiRC = Membro de uma ERN =

Projetos de investigação

ALEMANHA

Nordrhein-Westfalen
ESSEN

Retinoblastoma-Registry: A clinical registry for prospective data on retinoblastoma epidemiology and clinical course
Universitätsklinikum Essen
Klinik für Kinderheilkunde III - Abteilung für pädiatrische Hämatologie und Onkologie

ALEMANHA

Nordrhein-Westfalen
ESSEN

Financiado por um membro do IRDiRCERA-NET TRANSCAN: NIRBTEST - Development of a new blood-based test for the early detection of tumors with hereditary predisposition to retinoblastoma
Universitätsklinikum Essen
Klinik für Kinderheilkunde III - Abteilung für pädiatrische Hämatologie und Onkologie

ESPANHA

Cataluña
ESPLUGUES DE LLOBREGAT

Financiado por um membro do IRDiRCCombination of oncolytic adenovirus and chemotherapy in retinoblastoma
Fundació Sant Joan de Déu - Institut de Recerca Sant Joan de Déu
Grupo de investigación del Tratamiento del cáncer pediátrico

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

FRANCA

ILE-DE-FRANCE
ORSAY

Stem cells and transdifferentiation of the retina: the retinoblastoma as a model study
Institut Curie
Mécanismes moléculaires et oncogenèse

ALEMANHA

Baden-Württemberg
TÜBINGEN

Genetics and pathophysiology of autosomal recessive achromatopsia
Department für Augenheilkunde Tübingen
Molekulargenetisches Labor

ALEMANHA

Baden-Württemberg
TÜBINGEN

ALEMANHA

Baden-Württemberg
TÜBINGEN

ESPANHA

Andalucía
SEVILLA

Financiado por um membro do IRDiRCBiomedical research and clinical innovation in hereditary retinal dystrophies: towards personalized medicine in rare diseases
Hospital Universitario Virgen del Rocío
Unidad de Medicina Maternofetal, Genética y Reproducción

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCDeveloping classification criteria for the uveitides
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCDiagnosis and treatment of ocular inflammatory disease (uveitis)
Institution: Information not provided - US

ALEMANHA

Saarland
HOMBURG

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

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

FRANCA

NOUVELLE AQUITAINE
BORDEAUX

Research for one gene involved in Goldenhar syndrome
CHU de Bordeaux-GH Pellegrin
Laboratoire Maladies Rares : Génétique et Métabolisme (MRGM)

IRLANDA

County Dublin
DUBLIN

Exploration of theraputic strategies for ocular disorders
Trinity College Dublin
Smurfit Institute of Genetics

ITALIA

LOMBARDIA
MILANO

ALEMANHA

Niedersachsen
GÖTTINGEN

KFO 303: Pemphigoid Diseases - Molecular Pathways and their Therapeutic Potential
Institut für Humangenetik der Universität Göttingen
Institut für Humangenetik

ALEMANHA

Nordrhein-Westfalen
BONN

ALEMANHA

Saarland
HOMBURG

Description of clinical variability of ocular and cutaneous phenotypes in albinism
Universitätsklinikum des Saarlandes
AG Kinder- & Neuroophthalmologie

ALEMANHA

Schleswig-Holstein
LÜBECK

KFO 303: Pemphigoid Diseases - Molecular Pathways and their Therapeutic Potential
Universitätsklinikum Schleswig-Holstein - Campus Lübeck
Klinik für Dermatologie, Allergologie und Venerologie

ALEMANHA

Schleswig-Holstein
LÜBECK

KFO 303: Pemphigoid Diseases - Molecular Pathways and their Therapeutic Potential
Universitätsklinikum Schleswig-Holstein - Campus Lübeck
Lübecker Institut für Experimentelle Dermatologie

ESPANHA

Castilla - La Mancha
ALBACETE

Financiado por um membro do IRDiRCAnalysis of the genetic and molecular bases of congenital and juvenile glaucoma: Diagnostic and therapeutic implications
Universidad de Castilla-La Mancha. Campus de Albacete. Facultad de Medicina
Departamento de Genética

ESPANHA

Cataluña
BARCELONA

Financiado por um membro do IRDiRCInduced pluripotent cells and cell reprogramming in cell-based therapy approaches for corneal regeneration
IIB Sant Pau - Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Grupo de investigación en medicina regenerativa y bioingeniería de tejidos

ESPANHA

Madrid
MADRID

Financiado por um membro do IRDiRCAnalysis of the genetic and molecular bases of congenital and juvenile glaucoma: Diagnostic and therapeutic implications
Universidad Complutense de Madrid. Facultad de Óptica y Optometría
Facultad de Óptica y Optometría

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCAnimal models of ocular disease
Institution: Information not provided - US

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

NOUVELLE AQUITAINE
BORDEAUX

Molecular analysis of patients affected by oculo-cutaneous albinism
CHU de Bordeaux-GH Pellegrin
Laboratoire Maladies Rares : Génétique et Métabolisme (MRGM)

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"

FRANCA

OCCITANIE
MONTPELLIER

Financiado por um membro do IRDiRCDeveloping and studying the effects of innovative therapies for rare inherited retinal disease using human retinal models derived from patient iPS cells
Hôpital Saint Eloi - Bâtiment INM
Equipe "Génétique et thérapie des cécités rétiniennes et du nerf optique"

IRLANDA

County Dublin
DUBLIN

Target 5000: A study of Inherited Retinal Degeneration
Mater Misericordiae Hospital
Department of Ophthalmology

IRLANDA

County Dublin
DUBLIN

Target 5000: A study of Inherited Retinal Degeneration
Royal Victoria Eye and Ear Hospital
Ophthalmology Research Department

IRLANDA

County Dublin
DUBLIN

Target 5000: A study of Inherited Retinal Degeneration
Trinity College Dublin
Smurfit Institute of Genetics

ALEMANHA

Baden-Württemberg
TÜBINGEN

Financiado por um membro do IRDiRCTargetRD: PKG and CNGC as targets for mutation-independent therapy for inherited retinal degeneration.
Department für Augenheilkunde Tübingen
Forschungsinstitut für Augenheilkunde

ALEMANHA

Bayern
MÜNCHEN

Financiado por um membro do IRDiRCENISNIP: European Network on Inherited Sensory Neuropathies and Insensitivity to Pain (partner DE)
Friedrich-Baur-Institut
Friedrich-Baur-Institut an der Neurologischen Klinik und Poliklinik

ALEMANHA

Bremen
BREMEN

Financiado por um membro do IRDiRCTargetRD: PKG and CNGC as targets for mutation-independent therapy for inherited retinal degeneration.
Biolog Life Science Institute GmbH & Co. KG
Biolog Life Science Institute

ALEMANHA

Hamburg
HAMBURG

Molecular and functional investigation on microphthalmia with linear skin defects (MLS) - syndrome
UKE - Universitätsklinikum Hamburg-Eppendorf
Institut für Humangenetik

ALEMANHA

Nordrhein-Westfalen
AACHEN

ALEMANHA

Rheinland-Pfalz
MAINZ

TIC-PEA: Telemedical Interdisciplinary Care for Patients with Esophageal Atresia
Universitätsmedizin Mainz
Klinik und Poliklinik für Kinderchirurgie

ALEMANHA

Schleswig-Holstein
LÜBECK

The role of complement in mucous membrane pemphigoid
Universitätsklinikum Schleswig-Holstein - Campus Lübeck
Klinik für Dermatologie, Allergologie und Venerologie

ALEMANHA

Schleswig-Holstein
LÜBECK

The role of complement in mucous membrane pemphigoid
Universitätsklinikum Schleswig-Holstein - Campus Lübeck
Lübecker Institut für Experimentelle Dermatologie

BELGICA

ARRONDISSEMENT BRUSSELS-CAPITAL
BRUSSELS

Financiado por um membro do IRDiRCENISNIP: European Network on Inherited Sensory Neuropathies and Insensitivity to Pain (coordinator)
European Commission
DG Research - Directorate General for Research

BELGICA

ARRONDISSEMENT BRUSSELS-CAPITAL
BRUSSELS

Financiado por um membro do IRDiRCENISNIP: European Network on Inherited Sensory Neuropathies and Insensitivity to Pain (partner DE)
European Commission
DG Research - Directorate General for Research

CANADA

Alberta
EDMONTON

ESPANHA

Andalucía
SEVILLA

Mathematical models of disease mechanisms to reformulate drugs for rare diseases
Fundación Progreso y Salud
Área de bioinformática clínica

ESPANHA

Cataluña
BARCELONA

ESPANHA

Madrid
MADRID

Genetic bases of bilateral congenital cataract
INGEMM - Instituto de Genética Médica y Molecular (IdiPAZ)
Sección de Oftalmogenética Molecular

ESTADOS UNIDOS

California
BERKELEY

Financiado por um membro do IRDiRCRole of nrf2 in retinal vascularization and rop
University Of California Berkeley
Ophthalmology

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCClinical and molecular studies of malformations
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCGenetic modifiers of retinal disease
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCPathogenic role of epac1 signaling in retinopathy of prematurity
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCRetinal neurovascular patterning in preterm infants
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCInherited ocular diseases
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCThe focal electro-oculogram in macular disease
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCPre-clinical studies of ntbc as a potential treatment for albinism
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCNeuro-ophthalmic mechanisms of disease
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCNeonatal translational
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCOcular nsaids/caffeine potentiation in oxygen-induced retinopathy
Institution: Information not provided - US

FINLANDIA

Finland
HELSINKI

CRMCC (cerebroretinal microangiopathy with calcifications and cysts)
HUS - Helsinki University Hospital
New Children's Hospital

FRANCA

AUVERGNE-RHONE-ALPES
ADDRESS: NOT PROVIDED - FR

FRANCA

GRAND-EST
ILLKIRCH-GRAFFENSTADEN

Financiado por um membro do IRDiRCRAinRARE: Integrated analyses of retinoic acid signaling to understand and treat rare form of progressive motor impairment - FR (Parner 1)
Institut de génétique et de biologie moléculaire et cellulaire - IGBMC
Département Biologie du développement et cellules souches

FRANCA

PAYS DE LA LOIRE
ANGERS

FRANCA

PROVENCE-ALPES-COTE D'AZUR
MARSEILLE

Understanding the molecular mechanisms underlying familial dysautonomia
Faculté de médecine de Marseille - Secteur Nord
Centre de Recherche en Neurobiologie et Neurophysiologie de Marseille

IRLANDA

County Dublin
DUBLIN

Financiado por um membro do IRDiRCBRAINMEND - Biological Resource Analysis to Identify New Mechanisms and phenotypes in Neurodegenerative Diseases - IE
Trinity College Dublin
Department of Neurology - Trinity Biomedical Sciences Institute

ITALIA

FRIULI VENEZIA GIULIA
TRIESTE

Financiado por um membro do IRDiRCDevelopment of Exon Specific U1 snRNA-based therapy for Familial Dysautonomia
International Centre For Genetic Engineering And Biotechnology - ICGEB
Human Molecular Genetics Laboratory

ITALIA

FRIULI VENEZIA GIULIA
TRIESTE

Financiado por um membro do IRDiRCA novel exon-specific U1 snRNA strategy to correct splicing in Familial Dysautonomia
International Centre For Genetic Engineering And Biotechnology - ICGEB
Human Molecular Genetics Laboratory

SUECIA

Region Stockholm
STOCKHOLM

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

SUECIA

Region Västra Götaland
GÖTEBORG

Molecular defence against retinopathy of prematurity: screening, prevention and treatment
The Queen Silvia Children's Hospital - Sahlgrenska
Department of clinical neurosciences

ALEMANHA

Baden-Württemberg
TÜBINGEN

Financiado por um membro do IRDiRCTreatOPON : Preclinical Development of Treatments for OPA1-linked Optic Neuropathies (coordinator)
Department für Augenheilkunde Tübingen
Molekulargenetisches Labor

ALEMANHA

Niedersachsen
OLDENBURG

Financiado por um membro do IRDiRCTreatOPON : Preclinical Development of Treatments for OPA1-linked Optic Neuropathies (partner no 2 )
Carl von Ossietzky Universität Oldenburg
Abteilung für Humangenetik

AUSTRIA

TIROL
INNSBRUCK

Epitope specificity of MOG antibodies
Medizinische Universität Innsbruck
Universitätsklinik für Neurologie

AUSTRIA

WIEN
WIEN

ESPANHA

Cataluña
ESPLUGUES DE LLOBREGAT

ESPANHA

Galicia
VIGO

Financiado por um membro do IRDiRCMolecular mechanisms in ciliopathies
Universidade de Vigo
Grupo de Enfermedades raras

ESPANHA

Madrid
MADRID

Financiado por um membro do IRDiRCDeciphering the genetic complexity of congenital hypopituitarism
INGEMM - Instituto de Genética Médica y Molecular (IdiPAZ)
Sección de Endocrinología Molecular

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCWnt signaling-mediated control of blood-retinal barrier
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCColor vision in inherited retinal degenerations
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCOcular gene therapy
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: 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

JAPAO

JAPAN
OSAKA

Financiado por um membro do IRDiRCDevelopment of an anti-RGM humanized monoclonal antibody for the treatment of multiple sclerosis
Osaka University Graduate School of Medicine
Department of Molecular Neuroscience

JAPAO

JAPAN
TOKYO

Financiado por um membro do IRDiRCResearch for the development of precision medicine for autoimmune diseases
National Center of Neurology and Psychiatry
Department of Demyelinating Disease and Aging

REINO UNIDO

West Midlands
BIRMINGHAM

EURO-WABB: EURO-Rare Diabetes Project (coordination)
Birmingham Children's Hospital NHS Foundation Trust
Diabetes Unit

SUECIA

Region Stockholm
STOCKHOLM

Understanding Genetic Mechanisms in Disorders and Development of Diagostic Methods
Karolinska Institutet - Solna
Department of Molecular Medicine and Surgery

ALEMANHA

Baden-Württemberg
TÜBINGEN

ALEMANHA

Baden-Württemberg
TÜBINGEN

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

ALEMANHA

Berlin
BERLIN

Identification of molecular mechanisms acting at the jObes1 locus in the Berlin Fat Mouse with effect on juvenile fat deposition
Humboldt-Universität zu Berlin
Fachbereich Züchtungsbiologie und molekulare Genetik

ALEMANHA

Hessen
GIEßEN

Natural History Study of CEP290-Related Retinal Degeneration
Augenklinik des UKGM am Standort Gießen
Klinik und Poliklinik für Augenheilkunde

ALEMANHA

Rheinland-Pfalz
MAINZ

Characterization of the retinal phenotype and pre-clinical evaluation of AAV mediated gene augmentation in the transgenic USH1C pig
Institut für Zoologie der Universität Mainz
Institut für Zoologie - Abt. I - AG Wolfrum

ALEMANHA

Rheinland-Pfalz
MAINZ

VLGR1 signaling at focal adhesions and ICD release as a non-canonical signaling pathway of aGPCRs
Institut für Zoologie der Universität Mainz
Institut für Zoologie - Abt. I - AG Wolfrum

ALEMANHA

Sachsen
DRESDEN

EXOSC2 zebrafish model and exosom : analysis of EXOSC2 in the development of HK syndrome
Universitätsklinikum Carl Gustav Carus an der TU Dresden
Institut für Klinische Genetik

AUSTRIA

TIROL
INNSBRUCK

Mobility_APP - Mobility in Atypical Parkinsonism: a Randomized Trial of Physiotherapy - AT
Medizinische Universität Innsbruck
Universitätsklinik für Neurologie

AUSTRIA

TIROL
INNSBRUCK

Pharmacotherapeutic potential Cav1.4 calcium channels
Universität Innsbruck
Institut für Pharmazie

BELGICA

ARRONDISSEMENT BRUSSELS-CAPITAL
BRUSSELS

ODAK - Orphan Drug for Acanthamoeba Keratitis
European Commission
DG Research - Directorate General for Research

CANADA

Ontario
TORONTO

COREIA DO SUL

KOREA, REPUBLIC OF
KOREA

COREIA DO SUL

KOREA, REPUBLIC OF
SEOUL

ESPANHA

Cataluña
BARCELONA

Mitochondrial and metabolic dynamics in a retinitis pigmentosa model. A new therapeutic approach?
Universitat de Barcelona. Facultat de Biologia
Departamento de Genética, Biología y Estadística

ESPANHA

Comunidad Valenciana
VALENCIA

Financiado por um membro do IRDiRCDevelopment of anti-inflammatory nanotherapies for retinitis pigmentosa
IIS La Fe - Instituto de Investigación Sanitaria La Fe
Grupo de investigación en biomedicina molecular, celular y genómica

ESPANHA

Comunidad Valenciana
VALENCIA

Financiado por um membro do IRDiRCRetinal Dystrophies. Usher syndrome: genomic, cellular, functional and bioinformatic approaches to accelerate their diagnosis and treatment and to measure their impact
IIS La Fe - Instituto de Investigación Sanitaria La Fe
Grupo de investigación en biomedicina molecular, celular y genómica

ESPANHA

Madrid
MADRID

Lost heritability in sRP and LCA cases. Search for CNVs and new variants
Fundación Jiménez Díaz
Área de Genética y Genómica

ESPANHA

Madrid
MADRID

ESTADOS UNIDOS

California
BERKELEY

ESTADOS UNIDOS

California
SAN FRANCISCO

Financiado por um membro do IRDiRCCortical structure and function in blindness and following restored vision
University Of California, San Francisco
Neurology

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

Financiado por um membro do IRDiRCPreclinical innovation
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCDrug repurposing screening for rare and neglected diseases
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCGenetic epidemiology of complex diseases
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCThe role of complement in recessive stargardt disease
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCLarge animal therapy studies
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCCilium-associated structures in rod cells
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCCone rescue in retinitis pigmentosa
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCHeparanase in herpetic keratitis
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCMechanism of death of bystander retinal cells during mcmv infection
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCFunction of c8orf37 in photoreceptors
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCImaging the functional biomarker of photoreceptors
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCModulation of lipid bisretinoids clearance with beta-cyclodextrins
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCNoninvasive assessment of pathophysiology in retinitis pigmentosa
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCRole of microglia in retinitis pigementosa
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCThe role of arap1 in retinal photoreceptor homeostasis
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

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 IRDiRCHuman rhodopsin-adrp studies
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCInterventional approaches for restoring vision
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCLarge animal (dog) experimental support module
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCMechanisms of retinal degeneration in inherited diseases
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCMolecular genetics of early eye development
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCRetinal gene therapy
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCPreclinical safety studies
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 IRDiRCNeuroendocrine regulation of metabolism and neurocognition
Institution: Information not provided - US

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCPhysiology; psychology; and genetics of obesity
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

FINLANDIA

Finland
JYVÄSKYLÄ

Psychological well-being in families having a child with a Usher syndrome
University of Jyväskylä
Department of Psychology

FRANCA

AUVERGNE-RHONE-ALPES
ADDRESS: NOT PROVIDED - FR

FRANCA

AUVERGNE-RHONE-ALPES
ADDRESS: NOT PROVIDED - FR

FRANCA

GRAND-EST
STRASBOURG

Bardet-Biedl syndrome: new genes identification and biological characterization of a new gene BBS10
Faculté de médecine de Strasbourg - Louis Pasteur
Laboratoire de génétique médicale - Unité Inserm U1112

FRANCA

ILE-DE-FRANCE
EVRY

Financiado por um membro do IRDiRCRetinal tissue engineering from human pluripotent stem cells for the treatment of retinal dystrophies
GENOPOLE - Campus 1
I-Stem - Institut des cellules Souches pour le Traitement et l'Etude des maladies Monogéniques

FRANCA

ILE-DE-FRANCE
PARIS

Animal model creation of Stargardt disease by interfering RNA
Hôpital Necker-Enfants Malades
Génétique et épigénétique des maladies métaboliques, neurosensorielles et du développement

FRANCA

ILE-DE-FRANCE
PARIS

Decoding the genetic of Leber congenital amaurosis and progression of the therapeutic approach by exon skipping of the major mutation of the CEP290 gene
Hôpital Necker-Enfants Malades
Génétique et épigénétique des maladies métaboliques, neurosensorielles et du développement

FRANCA

ILE-DE-FRANCE
PARIS

Hereditary dystrophies of retina: physiopathologic and clinic research
Institut de la Vision
Centre d'Investigation Clinique (CIC) de l'hôpital des Quinze-Vingts

FRANCA

ILE-DE-FRANCE
PARIS

Hereditary dystrophies of retina: pharmacological research and new therapeutics development (cell and gene therapies)
Institut de la Vision
Centre d'Investigation Clinique (CIC) de l'hôpital des Quinze-Vingts

FRANCA

ILE-DE-FRANCE
PARIS

Financiado por um membro do IRDiRCeyePS: Modeling and treatment of retinal dystophies with iPS cells - FR
Institut de la Vision
Centre de Recherche Institut de la Vision

FRANCA

OCCITANIE
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"

FRANCA

OCCITANIE
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"

FRANCA

PAYS DE LA LOIRE
NANTES

FRANCA

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

IRLANDA

County Dublin
DUBLIN

Inherited childhood sight loss: understanding visual cycle biology to develop treatments
University College Dublin
UCD Conway Institute of Biomolecular and Biomedical Research

ITALIA

CAMPANIA
NAPOLI

Financiado por um membro do IRDiRCDesigning therapeutic strategies to rescue epidermal defects in AEC syndrome
Biotecnologie Avanzate Srl
Ceinge Biotecnologie Avanzate SCarl

ITALIA

LAZIO
ROMA

Financiado por um membro do IRDiRCUnderstanding molecular basis for Inherited Retinal Diseases (IRDs)
ISS - Istituto Superiore di Sanità
Centro Nazionale per la Ricerca e la Valutazione preclinica e clinica dei Farmaci

ITALIA

LIGURIA
GENOVA

Financiado por um membro do IRDiRCDevelopment and application of optoneural prosthetic devices as a therapeutic approach for Retinitis pigmentosa
IRCCS Ospedale Policlinico San Martino - IST - DIMI
Dipartimento di Medicina Sperimentale

ITALIA

SICILIA
ACI S. ANTONIO

ODAK - Orphan Drug for Acanthamoeba Keratitis
Società Industria Farmaceutica Italiana S.p.A.(S.I.F.I.)

ITALIA

TOSCANA
PISA

ITALIA

VENETO
VERONA

Financiado por um membro do IRDiRCCone dystrophies and retinal degeneration from protein structures to biological networks. Toward the design of therapeutic molecules
Università degli Studi di Verona
Dipartimento di Neuroscienze, Biomedicina e Movimento

JAPAO

JAPAN
KYOTO

Financiado por um membro do IRDiRCDevelopment and standardization of molecular pathological diagnosis for bullous keratopathy
Kyoto Prefectural University of Medicine
Department of Ophthalmology

JAPAO

JAPAN
MIYAGI

Financiado por um membro do IRDiRCIntensive genetic analysis and elucidation of the pathology by genome editing aiming at gene-specific treatment for retinitis pigmentosa
Tohoku University Graduate School of Medicine
Department of Advanced Ophthalmic Medicine

PAISES BAIXOS

Gelderland
NIJMEGEN

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

PAISES BAIXOS

Gelderland
NIJMEGEN

TREATCilia: Novel Therapeutic Avenues for dynein-related Ciliopathies
Radboudumc - Radboud universitair medisch centrum
Afdeling Genetica

PAISES BAIXOS

Gelderland
NIJMEGEN

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

PAISES BAIXOS

Noord-Holland
AMSTERDAM

Financiado por um membro do IRDiRCA retinal origin of congenital nystagmus
Nederlands Herseninstituut

REINO UNIDO

Tayside
DUNDEE

SUECIA

Region Skåne
LUND

SUICA

Suisse Alémanique
BASEL

Therapeutic RNA base editing for Stargardt disease
Institute of Molecular and Clinical Ophthalmology Basel (IOB)

SUICA

Suisse Alémanique
BASEL

Single-cell genomic reconstruction of retina developmental disorders
Institute of Molecular and Clinical Ophthalmology Basel (IOB)

ALEMANHA

Bayern
REGENSBURG

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

Financiado por um membro do IRDiRCTherapeutic genome editing to treat best disease
Institution: Information 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

ESTADOS UNIDOS

Washington
ADDRESS: NOT PROVIDED - US

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

Projetos de investigação multicêntricos