December 2010
Volume 51, Issue 12
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Erratum  |   December 2010
Erratum
Investigative Ophthalmology & Visual Science December 2010, Vol.51, 6912. doi:10.1167/iovs.09-3511a
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      Erratum. Invest. Ophthalmol. Vis. Sci. 2010;51(12):6912. doi: 10.1167/iovs.09-3511a.

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Erratum in: “Inhibition of JAK2/STAT3-Mediated VEGF Upregulation under High Glucose Conditions by PEDF through a Mitochondrial ROS Pathway In Vitro” by Zhi Zheng, Haibing Chen, Hui Zhao, Kun Liu, Dawei Luo, Yongdong Chen, Yihui Chen, Xiaolu Yang, Qing Gu, and Xun Xu (Invest Ophthalmol Vis Sci. 2010;51:64–71) doi:10.1167/iovs.09-3511  
A corrected Figure 7 appears below. 
Figure 7.
 
Determination of VEGF mRNA and protein levels in BRECs. VEGF mRNA in BRECs cultured in six-well plates with serum-free DMEM containing NG, NG+PEDF, NG+H2O2, HG, or HG in the presence of AG490, PEDF, JAK2 sense, JAK2 antisense oligonucleotides, STAT3 sense, or STAT3 antisense oligonucleotides for 48 hours. ELISA was used to determine accumulations of VEGF in the media in the 10 groups. Data represent the mean ± SD from nine cells per group, and the experiments were repeated independently at least three times (real-time RT-PCR) or two times (ELISA) with similar results (**P < 0.01 vs. NG; ## P < 0.01 vs. HG).
Figure 7.
 
Determination of VEGF mRNA and protein levels in BRECs. VEGF mRNA in BRECs cultured in six-well plates with serum-free DMEM containing NG, NG+PEDF, NG+H2O2, HG, or HG in the presence of AG490, PEDF, JAK2 sense, JAK2 antisense oligonucleotides, STAT3 sense, or STAT3 antisense oligonucleotides for 48 hours. ELISA was used to determine accumulations of VEGF in the media in the 10 groups. Data represent the mean ± SD from nine cells per group, and the experiments were repeated independently at least three times (real-time RT-PCR) or two times (ELISA) with similar results (**P < 0.01 vs. NG; ## P < 0.01 vs. HG).
Citation: Zheng Z, Chen H, Zhao H, Liu K, Luo D, Chen Y, Chen Y, Yang X, Gu Q, Xu X. Erratum in: Inhibition of JAK2/STAT3-mediated VEGF upregulation under high glucose conditions by PEDF through a mitochondrial ROS pathway in vitro. Invest Ophthalmol Vis Sci. 2010;51:64–71. DOI:10.1167/iovs.09-3511a 
Figure 7.
 
Determination of VEGF mRNA and protein levels in BRECs. VEGF mRNA in BRECs cultured in six-well plates with serum-free DMEM containing NG, NG+PEDF, NG+H2O2, HG, or HG in the presence of AG490, PEDF, JAK2 sense, JAK2 antisense oligonucleotides, STAT3 sense, or STAT3 antisense oligonucleotides for 48 hours. ELISA was used to determine accumulations of VEGF in the media in the 10 groups. Data represent the mean ± SD from nine cells per group, and the experiments were repeated independently at least three times (real-time RT-PCR) or two times (ELISA) with similar results (**P < 0.01 vs. NG; ## P < 0.01 vs. HG).
Figure 7.
 
Determination of VEGF mRNA and protein levels in BRECs. VEGF mRNA in BRECs cultured in six-well plates with serum-free DMEM containing NG, NG+PEDF, NG+H2O2, HG, or HG in the presence of AG490, PEDF, JAK2 sense, JAK2 antisense oligonucleotides, STAT3 sense, or STAT3 antisense oligonucleotides for 48 hours. ELISA was used to determine accumulations of VEGF in the media in the 10 groups. Data represent the mean ± SD from nine cells per group, and the experiments were repeated independently at least three times (real-time RT-PCR) or two times (ELISA) with similar results (**P < 0.01 vs. NG; ## P < 0.01 vs. HG).
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