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        Nc2Eye

           A curated ncRNAomics knowledgebase for bridging basic and clinical research in eye diseases.

Detail of retinopathy of prematurity (ROP)
ncRNA name hsa-miR-106a
ncRNA Category miRNA
Disease name retinopathy of prematurity (ROP)
Species Homo sapiens
Tissues/Cell_line human RB cell line Y79
Methods qPCR, luciferase reporter assay, transfection
Expression pattern down-regulated
Functional description We evaluated the in vivo expression profile of the miR-17 family in the murine retinopathy of prematurity (ROP) model, whereby Vegfa expression is highly enhanced at the early stage of retinal neovascularization, and we found simultaneous reduction of all miR-17 family members at this stage. We observed binding of these miRs to specific sites in the 3' UTRs of Hif1a and Vegfa.
PubMed ID 25775553
Year 2015
Title Synchronous down-modulation of miR-17 family members is an early causative event in the retinal angiogenic switch.
Drug-related ncRNA NO

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