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2. The TTX metabolite 4,9-anhydro-TTX is a highly specific blocker of the Na(v1.6) voltage-dependent sodium channel. Rosker C; Lohberger B; Hofer D; Steinecker B; Quasthoff S; Schreibmayer W Am J Physiol Cell Physiol; 2007 Aug; 293(2):C783-9. PubMed ID: 17522141 [TBL] [Abstract][Full Text] [Related]
3. Resurgent-like currents in mouse vas deferens myocytes are mediated by NaV1.6 voltage-gated sodium channels. Teramoto N; Zhu HL; Yotsu-Yamashita M; Inai T; Cunnane TC Pflugers Arch; 2012 Nov; 464(5):493-502. PubMed ID: 22986623 [TBL] [Abstract][Full Text] [Related]
4. Tetrodotoxin-sensitive α-subunits of voltage-gated sodium channels are relevant for inhibition of cardiac sodium currents by local anesthetics. Stoetzer C; Doll T; Stueber T; Herzog C; Echtermeyer F; Greulich F; Rudat C; Kispert A; Wegner F; Leffler A Naunyn Schmiedebergs Arch Pharmacol; 2016 Jun; 389(6):625-36. PubMed ID: 27000037 [TBL] [Abstract][Full Text] [Related]
5. Selective blocking effects of 4,9-anhydrotetrodotoxin, purified from a crude mixture of tetrodotoxin analogues, on NaV1.6 channels and its chemical aspects. Teramoto N; Yotsu-Yamashita M Mar Drugs; 2015 Feb; 13(2):984-95. PubMed ID: 25686275 [TBL] [Abstract][Full Text] [Related]
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7. Low concentrations of tetrodotoxin interact with tetrodotoxin-resistant voltage-gated sodium channels. Farmer C; Smith K; Docherty R Br J Pharmacol; 2008 Sep; 155(1):34-43. PubMed ID: 18552876 [TBL] [Abstract][Full Text] [Related]
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