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Background
In this study, we aimed to explore whether COL1A2 and miR‐1297 participated in the progression of diabetic nephropathy (DN) in vitro and classified the underlying mechanisms.
Methods
d‐Glucose (30 mM; high glucose, HG)‐stimulated HK‐2 cells were used to mimic DN condition. RNA and non‐coding RNA profiles were from Gene Expression Omnibus (GEO) database. The interaction between miR‐1297...
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