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Journal Abstract Search

327 related items for PubMed ID: 27162340

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  • 7. Folding similarity of the outer pore region in prokaryotic and eukaryotic sodium channels revealed by docking of conotoxins GIIIA, PIIIA, and KIIIA in a NavAb-based model of Nav1.4.
    Korkosh VS, Zhorov BS, Tikhonov DB.
    J Gen Physiol; 2014 Sep; 144(3):231-44. PubMed ID: 25156117
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  • 8. Discovery of a selective, state-independent inhibitor of NaV1.7 by modification of guanidinium toxins.
    Pajouhesh H, Beckley JT, Delwig A, Hajare HS, Luu G, Monteleone D, Zhou X, Ligutti J, Amagasu S, Moyer BD, Yeomans DC, Du Bois J, Mulcahy JV.
    Sci Rep; 2020 Sep 09; 10(1):14791. PubMed ID: 32908170
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  • 9. Maleimide conjugates of saxitoxin as covalent inhibitors of voltage-gated sodium channels.
    Parsons WH, Du Bois J.
    J Am Chem Soc; 2013 Jul 24; 135(29):10582-5. PubMed ID: 23855513
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  • 12. Synthesis of skeletal analogues of saxitoxin derivatives and evaluation of their inhibitory activity on sodium ion channels Na(V)1.4 and Na(V)1.5.
    Shinohara R, Akimoto T, Iwamoto O, Hirokawa T, Yotsu-Yamashita M, Yamaoka K, Nagasawa K.
    Chemistry; 2011 Oct 17; 17(43):12144-52. PubMed ID: 21922571
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  • 13. Precise spatiotemporal control of voltage-gated sodium channels by photocaged saxitoxin.
    Elleman AV, Devienne G, Makinson CD, Haynes AL, Huguenard JR, Du Bois J.
    Nat Commun; 2021 Jul 07; 12(1):4171. PubMed ID: 34234116
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  • 14. Tonic and phasic guanidinium toxin-block of skeletal muscle Na channels expressed in Mammalian cells.
    Moran O, Picollo A, Conti F.
    Biophys J; 2003 May 07; 84(5):2999-3006. PubMed ID: 12719231
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  • 16. Phosphorylation of a chronic pain mutation in the voltage-gated sodium channel Nav1.7 increases voltage sensitivity.
    Kerth CM, Hautvast P, Körner J, Lampert A, Meents JE.
    J Biol Chem; 2021 May 07; 296():100227. PubMed ID: 33361158
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  • 17. A disubstituted succinamide is a potent sodium channel blocker with efficacy in a rat pain model.
    Priest BT, Garcia ML, Middleton RE, Brochu RM, Clark S, Dai G, Dick IE, Felix JP, Liu CJ, Reiseter BS, Schmalhofer WA, Shao PP, Tang YS, Chou MZ, Kohler MG, Smith MM, Warren VA, Williams BS, Cohen CJ, Martin WJ, Meinke PT, Parsons WH, Wafford KA, Kaczorowski GJ.
    Biochemistry; 2004 Aug 03; 43(30):9866-76. PubMed ID: 15274641
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  • 18. Direct evidence for high affinity blockade of NaV1.6 channel subtype by huwentoxin-IV spider peptide, using multiscale functional approaches.
    Gonçalves TC, Boukaiba R, Molgó J, Amar M, Partiseti M, Servent D, Benoit E.
    Neuropharmacology; 2018 May 01; 133():404-414. PubMed ID: 29474819
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