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. 2014 Mar 27;9(3):e92706. doi: 10.1371/journal.pone.0092706

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© 2014 Lee et al

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.

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K562 cells were transduced with MKRN2 cDNA subcloned into lentiviral vector (pLEF1α-IG-MKRN2). MTT assay of pLEF1α-IG-MKRN2-transduced cells showed a significantly increased proliferation in culture, compared with pLEF1α-IG (empty vector) control cells (*P = 0.05; n = 3).