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. 2017 Jul 26;8(35):59345–59358. doi: 10.18632/oncotarget.19581

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Copyright: © 2017 Liu et al.

This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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(A) Bar graph summary of average % inhibition of Kv2.1 channel in HEK293 cells (open bar) or after σ1-R knockout (black bar) in HEK 293 cells in presence of various σ1- and σ2-R ligands. Data is mean ± SEM (n = 4 at least) and *P < 0.05. Concentrations of the ligands are presented in the parentheses under the bar graph. (B) σ1-R and σ2-R binding affinities, functions, and chemical structures of σ1-R ligands.

(A) Bar graph summary of average % inhibition of Kv2.1 channel in HEK293 cells (open bar) or after σ1-R knockout (black bar) in HEK 293 cells in presence of various σ1- and σ2-R ligands. Data is mean ± SEM (n = 4 at least) and *P < 0.05. Concentrations of the ligands are presented in the parentheses under the bar graph. (B) σ1-R and σ2-R binding affinities, functions, and chemical structures of σ1-R ligands.