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To minimize the effect of RNase on the
stability of miRNAs, all glassware and centrifuge tubes were
autoclaved, all solutions were treated with diethylpyrocarbon-
ate, and all surfaces were decontaminated with RNaseZap
(Ambion, TX). RNase-free ultrapure water was used
throughout. Reference values of miRNA expression levels in
the samples were obtained by using a commercial miRNA qRT-
PCR kit from Agilent Technologies (Santa Clara, U.S.).

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