https://www.selleckchem.com/pr....oducts/Beta-Sitoster
expression of some genes which were up-regulated by ZEB1. Exogenous miR-194 administration in vivo effectively suppressed PVR in the rat model, both functionally and structurally. Conclusions Our findings demonstrate for the first time that miR-194 suppresses RPE cell EMT by functionally targeting ZEB1. The clinical application of miR-194 in patients with PVR merits further investigation. 2019 Annals of Translational Medicine. All rights reserved.Background Beta-adrenergic receptor antagonists have been the first-line treatment