RNA Details
                    Disease Name
                    
                    pulmonary hypertension
                    
                    Tissue
                    
                    lung
                    
                    RNA Symbol
                    
                    miR-124-3p
                    
                RNA ID
                    
                    
                    
                RNA Type
                    
                    miRNA
                    
                Alteration Pattern
                    
                    down regulation
                    
                Species
                    
                    rattus norvegicus
                    
                Detection Methods
                    
                    qRT-PCR;  Immunohistochemistry etc.
                    
                Target
                    
                    NA
                    
                Pathway
                    
                    NA
                    
                PubMed ID
                    
                    
                    
                    
                    
                Title
                    
                    "MicroRNA-124 controls the proliferative, migratory, and inflammatory phenotype of pulmonary vascular fibroblasts"
                    
                Year
                    
                     2014
                    
                Function
                    
                    "MiR-124 expression is decreased in hypertensive fibroblasts. Overexpression of miR-124 significantly attenuated proliferation, migration, and monocyte chemotactic protein-1 expression of hypertensive fibroblasts by targeting polypyrimidine tract-binding protein 1 and subsequent regulation of Notch1/phosphatase and tensin homolog/FOXO3/p21Cip1 and p27Kip1 signaling.  MiR-124 expression is suppressed by histone deacetylases and that treatment of hypertensive fibroblasts with histone deacetylase inhibitors increased miR-124 expression and decreased proliferation and monocyte chemotactic protein-1 production."