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2 tion of similar behavior with another L type calcium channel agonist, and the protection afforded by
3 currents are substantially increased by the calcium channel agonist Bay K 8644 and inhibited by the
5 elevated extracellular potassium or with the calcium channel agonist Bay K 8644 protected neurons.
9 mutTARDBP results in defective NMJs and that calcium channel agonists could be novel therapeutics for
11 To further verify the mechanism, the L-type calcium channel agonist FPL 64176 was administered to pr
14 nown actions of (+/-)Bay K 8644 as an L type calcium channel agonist, the reproduction of similar beh
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