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Interactions of monovalent cations with sodium channels in squid axon. II. Modification of pharmacological inactivation gating

The time-, frequency-, and voltage-dependent blocking actions of several cationic drug molecules on open Na channels were investigated in voltage-clamped, internally perfused squid giant axons. The relative potencies and time courses of block by the agents (pancuronium [PC], octylguanidinium [C8G],...

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書目詳細資料
格式: Artigo
語言:Inglês
出版: The Rockefeller University Press 1985
主題:
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC2215806/
https://ncbi.nlm.nih.gov/pubmed/2409221
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