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Published Erratum
. 2015 Aug 3;14(15):2537.
doi: 10.1080/15384101.2015.1066140.

Corrigendum

Johanna G Miquet, Thomas Freund, Carolina S Martinez, Lorena Gonzalez, Maria E Diaz, Giannina P Micucci, Elsa Zotta, Ravneet K Boparai, Andrzej Bartke, Daniel Turyn, Ana I Sotelo
Published Erratum

Corrigendum

Johanna G Miquet et al. Cell Cycle. .
No abstract available

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Figures

Figure 3.
Figure 3.
Expression and phosphorylation of STAT5, STAT3, Akt, mTOR and EGFR in the liver of GH-overexpressing transgenic mice and normal controls. Liver extracts from young adult normal female (NF), normal male (NM), GH-transgenic female (TF) and GH-transgenic male (TM) mice were analyzed by immunoblotting to determine the phosphorylation and protein content, or by reverse-transcriptase quantitative PCR (qRT-PCR) to assess mRNA levels. (A) Representative results of immunoblots are shown. (B) sTAT5 phosphorylation at Tyr694/696 (pSTAT5), protein content and phos-phorylation/protein content ratio. STAT5 was also used as a control for equal loading. (C) STAT3 phosphorylation at Tyr705 (pSTAT3), protein content and phosphorylation/protein content ratio. (D) Akt phosphorylation at ser473 (pAkt), Akt2 protein content, phosphorylation/protein content ratio and mRNA levels. (E) mTOR phosphorylation at ser2448 (pmTOR), protein content, phosphorylation/protein content ratio and mRNA levels. (F) EGFR phosphorylation at Tyr845 (pEGFR), protein content, phosphorylation/protein content ratio and mRNA levels. Results are expressed as % of the mean values in normal female mice. Data are the mean ±SEM of 9 sets of different individuals per group (n). Different letters denote significant difference at p < 0.05. NS, not significant.
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