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. 2015 Apr 20;10(4):e0123583. doi: 10.1371/journal.pone.0123583

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© 2015 Tóth 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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Fig 6 — Internal Ca²⁺ stores of cells were depleted by the application of 10 μM CPA in Ca²⁺-free Tyrode’s, which caused an increase in [Ca²⁺]_i.both (A) in scrambled shRNA transfected and (B) cloneC1 cells. (C) Mean values of the integral of CPA induced calcium transients. Numbers in parentheses indicate the number of cells measured. Asterisks (*) mark significant (P<0.05) differences.