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Clinical, Genetic and Histopathological Characteristics of CRX-associated Retinal DystrophiesComparative gene expression study and pathway analysis of the human iris- and the retinal pigment epitheliumLONG-TERM FOLLOW-UP OF PATIENTS WITH RETINITIS PIGMENTOSA TYPE 12 CAUSED BY CRB1 MUTATIONSThe Spectrum of Structural and Functional Abnormalities in Female Carriers of Pathogenic Variants in the RPGR GeneDietary magnesium, not calcium, prevents vascular calcification in a mouse model for pseudoxanthoma elasticum.LONG-TERM FOLLOW-UP OF PATIENTS WITH CHOROIDEREMIA WITH SCLERAL PITS AND TUNNELS AS A NOVEL OBSERVATIONThe circadian clock regulates RPE-mediated lactate transport via SLC16A1 (MCT1)Long-Term Follow-Up of Retinal Degenerations Associated With LRAT Mutations and Their Comparability to Phenotypes Associated With RPE65 MutationsClinical characteristics and natural history of rho-associated retinitis pigmentosa.Course of visual decline in relation to the Best1 genotype in vitelliform macular dystrophy.Gene expression and functional annotation of the human and mouse choroid plexus epithelium.CLINICAL AND GENETIC CHARACTERISTICS OF MALE PATIENTS WITH RPGR-ASSOCIATED RETINAL DYSTROPHIESStem Cell Derived Retinal Pigment EpitheliumUltrasrtuctural localization and expression of Trpm1 in the human retina.Comparison of Mouse and Human Retinal Pigment Epithelium Gene Expression ProfilesGene expression-based comparison of the human secretory neuroepithelia of the brain choroid plexus and the ocular ciliary bodyCore-clock genes Period 1 and 2 regulate visual cascade and cell cycle components during mouse eye developmentCore circadian clock genes Per1 and Per2 regulate the rhythm in photoreceptor outer segment phagocytosisGene expression and functional annotation of the human ciliary body epithelia.Multicenter cohort association study of SLC2A1 single nucleotide polymorphisms and age-related macular degeneration.A gene for X-linked optic atrophy is closely linked to Xp11.4-Xp11.2 region of the X-chromosomeThe ERCC6 gene and age-related macular degeneration.CRB1-associated retinal dystrophiesX-linked RetinoschisisThe Natural History of Leber Congenital Amaurosis and Cone-Rod Dystrophy Associated with Variants in the GUCY2D GeneA new strategy to identify and annotate human RPE-specific gene expression.The Lrat-/- RatGenotypic and Phenotypic Characteristics of CRB1-Associated Retinal DystrophiesComplement component C3 and risk of age-related macular degeneration.An alternative approach to produce versatile retinal organoids with accelerated ganglion cell developmentGenome-wide CNV investigation suggests a role for cadherin, Wnt, and p53 pathways in primary open-angle glaucomaGene expression and functional annotation of human choroid plexus epithelium failure in Alzheimer's diseaseDefining inclusion criteria and endpoints for clinical trials
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J.B. ten Brink
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Public - No restriction
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Publiek - Geen beperking
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ing.
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