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XB-GENEPAGE-5812329
Papers associated with scn3a
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Genomic Takeover by Transposable Elements in the Strawberry Poison Frog., Rogers RL, Zhou L, Chu C, Márquez R, Corl A, Linderoth T, Freeborn L, MacManes MD, Xiong Z, Zheng J, Guo C, Xun X, Kronforst MR, Summers K, Wu Y, Yang H, Richards-Zawacki CL, Zhang G, Nielsen R., Mol Biol Evol. December 1, 2018; 35 (12): 2913-2927.  |
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The Scorpion Toxin Tf2 from Tityus fasciolatus Promotes Nav1.3 Opening., Camargos TS, Bosmans F, Rego SC, Mourão CB, Schwartz EF., PLoS One. June 5, 2015; 10 (6): e0128578.  |
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Pharmacological kinetics of BmK AS, a sodium channel site 4-specific modulator on Nav1.3., Liu ZR, Tao J, Dong BQ, Ding G, Cheng ZJ, He HQ, Ji YH., Neurosci Bull. June 1, 2012; 28 (3): 209-21. |
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Localization of receptor site on insect sodium channel for depressant β-toxin BmK IT2., He H, Liu Z, Dong B, Zhang J, Shu X, Zhou J, Ji Y., PLoS One. January 7, 2011; 6 (1): e14510.  |
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Synthesis, solution structure, and phylum selectivity of a spider delta-toxin that slows inactivation of specific voltage-gated sodium channel subtypes., Yamaji N, Little MJ, Nishio H, Billen B, Villegas E, Nishiuchi Y, Tytgat J, Nicholson GM, Corzo G., J Biol Chem. September 4, 2009; 284 (36): 24568-82. |
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Human and rat Nav1.3 voltage-gated sodium channels differ in inactivation properties and sensitivity to the pyrethroid insecticide tefluthrin., Tan J, Soderlund DM., Neurotoxicology. January 1, 2009; 30 (1): 81-9. |
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Structure/function characterization of micro-conotoxin KIIIA, an analgesic, nearly irreversible blocker of mammalian neuronal sodium channels., Zhang MM, Green BR, Catlin P, Fiedler B, Azam L, Chadwick A, Terlau H, McArthur JR, French RJ, Gulyas J, Rivier JE, Smith BJ, Norton RS, Olivera BM, Yoshikami D, Bulaj G., J Biol Chem. October 19, 2007; 282 (42): 30699-706. |
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Modulatory effect of auxiliary beta1 subunit on Nav1.3 voltage-gated sodium channel expressed in Xenopus oocyte., Wang YW, Cheng ZJ, Tan H, Xia YM, Ren RR, Ding YQ., Chin Med J (Engl). April 20, 2007; 120 (8): 721-3. |
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Isolation and structure-activity of mu-conotoxin TIIIA, a potent inhibitor of tetrodotoxin-sensitive voltage-gated sodium channels., Lewis RJ, Schroeder CI, Ekberg J, Nielsen KJ, Loughnan M, Thomas L, Adams DA, Drinkwater R, Adams DJ, Alewood PF., Mol Pharmacol. March 1, 2007; 71 (3): 676-85. |
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Potent modulation of the voltage-gated sodium channel Nav1.7 by OD1, a toxin from the scorpion Odonthobuthus doriae., Maertens C, Cuypers E, Amininasab M, Jalali A, Vatanpour H, Tytgat J., Mol Pharmacol. July 1, 2006; 70 (1): 405-14. |
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Four novel tarantula toxins as selective modulators of voltage-gated sodium channel subtypes., Bosmans F, Rash L, Zhu S, Diochot S, Lazdunski M, Escoubas P, Tytgat J., Mol Pharmacol. February 1, 2006; 69 (2): 419-29. |
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Distribution and functional characterization of human Nav1.3 splice variants., Thimmapaya R, Neelands T, Niforatos W, Davis-Taber RA, Choi W, Putman CB, Kroeger PE, Packer J, Gopalakrishnan M, Faltynek CR, Surowy CS, Scott VE., Eur J Neurosci. July 1, 2005; 22 (1): 1-9. |
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Lidocaine block of neonatal Nav1.3 is differentially modulated by co-expression of beta1 and beta3 subunits., Lenkowski PW, Shah BS, Dinn AE, Lee K, Patel MK., Eur J Pharmacol. April 25, 2003; 467 (1-3): 23-30. |
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Nav1.3 sodium channels: rapid repriming and slow closed-state inactivation display quantitative differences after expression in a mammalian cell line and in spinal sensory neurons., Cummins TR, Aglieco F, Renganathan M, Herzog RI, Dib-Hajj SD, Waxman SG., J Neurosci. August 15, 2001; 21 (16): 5952-61. |
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Developmental expression of the novel voltage-gated sodium channel auxiliary subunit beta3, in rat CNS., Shah BS, Stevens EB, Pinnock RD, Dixon AK, Lee K., J Physiol. August 1, 2001; 534 (Pt 3): 763-76. |
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