2019
Disease-associated mutations of claudin-19 disrupt retinal neurogenesis and visual function
Wang SB, Xu T, Peng S, Singh D, Ghiassi-Nejad M, Adelman RA, Rizzolo LJ. Disease-associated mutations of claudin-19 disrupt retinal neurogenesis and visual function. Communications Biology 2019, 2: 113. PMID: 30937396, PMCID: PMC6433901, DOI: 10.1038/s42003-019-0355-0.Peer-Reviewed Original ResearchConceptsRetinal pigment epitheliumClaudin-19Retinal neurogenesisP1 waveOuter nuclear layerRPE signature genesARPE19 cell lineOcular involvementKidney diseaseVisual functionFamilial hypomagnesaemiaNuclear layerBipolar cellsNewborn miceOcular diseasesPigment epitheliumRetinal isomeraseDiseaseMiceHuman induced pluripotent cellsRetinal differentiationSignature genesCell linesNeurogenesisInduced pluripotent cells
2011
Differential Expression of Claudins in Retinas during Normal Development and the Angiogenesis of Oxygen-Induced Retinopathy
Luo Y, Xiao W, Zhu X, Mao Y, Liu X, Chen X, Huang J, Tang S, Rizzolo LJ. Differential Expression of Claudins in Retinas during Normal Development and the Angiogenesis of Oxygen-Induced Retinopathy. Investigative Ophthalmology & Visual Science 2011, 52: 7556-7564. PMID: 21862644, DOI: 10.1167/iovs.11-7185.Peer-Reviewed Original ResearchMeSH KeywordsAnimalsAnimals, NewbornBlood-Retinal BarrierClaudinsDisease Models, AnimalFluorescent Antibody Technique, IndirectGene Expression Regulation, DevelopmentalHumansInfant, NewbornMembrane ProteinsMiceMice, Inbred C57BLNeovascularization, PhysiologicOccludinOxygenPlant LectinsReal-Time Polymerase Chain ReactionRetinaRetinal NeovascularizationRetinal VesselsRetinopathy of PrematurityRNA, Messenger