ets1 associates with KMT5A to participate in high glucose-mediated EndMT via upregulation of PFN2 expression in diabetic nephropathy - Lu, Lihong; Zhong, Ziwen; Gu, Jiahui; Nan, Ke; Zhu, Minmin; Miao, Changhong (Molecular medicine (Cambridge, Mass.), 2021)
Keywords: Aged; Animals; Binding Sites; Biomarkers; Diabetic Nephropathies - etiology; Diabetic Nephropathies - metabolism; Diabetic Nephropathies - pathology; Diabetic nephropathy; Disease Models, Animal; Disease Susceptibility; EndMT; Epithelial-Mesenchymal Transition - genetics; ets1; Female; Gene Expression; Gene Expression Profiling; Glucose - metabolism; Histone-Lysine N-Methyltransferase - genetics; Histone-Lysine N-Methyltransferase - metabolism; Human Umbilical Vein Endothelial Cells; Humans; Immunohistochemistry; KMT5A; Male; Middle Aged; Models, Biological; PFN2; Profilins - genetics; Profilins - metabolism; Protein Binding; Proto-Oncogene Protein c-ets-1 - genetics; Proto-Oncogene Protein c-ets-1 - metabolism; Rats; Diabetic nephropathy; ets1; KMT5A; EndMT; PFN2