IndraLab

Statements


1 1 | 1 3

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"The concentration dependence of the lidocaine block of hH1 Na current was consistent with a binding stoichiometry of 1:1."

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"In contrast, lidocaine markedly reduced hH1 I Na after a prepulse to -100 mV."

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"Further investigations indicated that blocking NaV1.5 by lidocaine or sodium ion channel blocker decreased the ovarian malignancy through inactivation of FAK / Paxillin signaling pathway ( Figure 7 ) ."

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No evidence text available

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"When expressed in Xenopus oocytes, lidocaine block of hH1 (human cardiac) Na current greatly exceeded that of mu1 (rat skeletal muscle) at membrane potentials near V (rest), whereas hyperpolarization to -140 mV equalized block of the two isoforms."