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. Author manuscript; available in PMC: 2014 Jun 15.
Published in final edited form as: Toxicol Appl Pharmacol. 2013 Apr 6;269(3):290–296. doi: 10.1016/j.taap.2013.02.017

Fig. 9.

Fig. 9

Suppression of KRT1, KRT10 and FOXN1 expression by DUSP knockdown. Confluent SIK cultures expressing DUSP2 or DUSP14 shRNAs or the control empty vector (EV) were treated for 3 days with BMP6. The indicated mRNAs, measured by real time PCR, are shown normalized to cells treated with the empty vector, set at 1 (dashed line). Results are the means and SD of 3 independent experiments with a single DUSP2 shRNA or one experiment using 2 different DUSP14 shRNAs. Amounts of DUSP mRNA in shRNA expressing cells were 40 ± 16 % (DUSP2) and 55 ± 5 % (DUSP14) of control. Asterisks indicate values significantly different from 1.