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Recently, a group of noncoding microRNAs (miRNAs) binding to the 3′ untranslated region (UTR) of target mRNAs (which results in degradation of the target mRNAs or translational repression of the encoded proteins 23 ) was shown to have a critical role in controlling NK cell homoeostasis, activation and effector function, in addition to regulating diverse aspects of NK cell biology 24,25,26,27,28,29
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