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1          Treatment with Bay K8644, an L-type calcium channel agonist, also significantly increased th
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
4                    Application of the L-type calcium channel agonist Bay K 8644 or activation of NMDA
5 elevated extracellular potassium or with the calcium channel agonist Bay K 8644 protected neurons.
6                       Conversely, the L-type calcium channel agonist Bay K8644 induced stereotypic to
7                                   The L type calcium channel agonist (+/-)Bay K 8644 has been reporte
8                               Pacing and the calcium channel agonist BAYK 8644 activated c-Jun N-term
9 mutTARDBP results in defective NMJs and that calcium channel agonists could be novel therapeutics for
10                                The lack of a calcium channel agonist (e.g., BayK8644) for CaV2 channe
11  To further verify the mechanism, the L-type calcium channel agonist FPL 64176 was administered to pr
12  chronic treatment with either of the L-type calcium channel agonists FPL 64176 or Bay K 8644.
13 provoked by administration of another L type calcium channel agonist, FPL 64176.
14 nown actions of (+/-)Bay K 8644 as an L type calcium channel agonist, the reproduction of similar beh

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