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328 related items for PubMed ID: 8740377
1. Functional consequences of lidocaine binding to slow-inactivated sodium channels. Balser JR, Nuss HB, Romashko DN, Marban E, Tomaselli GF. J Gen Physiol; 1996 May; 107(5):643-58. PubMed ID: 8740377 [Abstract] [Full Text] [Related]
4. Cardiac sodium channels (hH1) are intrinsically more sensitive to block by lidocaine than are skeletal muscle (mu 1) channels. Nuss HB, Tomaselli GF, Marbán E. J Gen Physiol; 1995 Dec; 106(6):1193-209. PubMed ID: 8786356 [Abstract] [Full Text] [Related]
5. External pore residue mediates slow inactivation in mu 1 rat skeletal muscle sodium channels. Balser JR, Nuss HB, Chiamvimonvat N, Pérez-García MT, Marban E, Tomaselli GF. J Physiol; 1996 Jul 15; 494 ( Pt 2)(Pt 2):431-42. PubMed ID: 8842002 [Abstract] [Full Text] [Related]
6. Intrinsic lidocaine affinity for Na channels expressed in Xenopus oocytes depends on alpha (hH1 vs. rSkM1) and beta 1 subunits. Makielski JC, Limberis J, Fan Z, Kyle JW. Cardiovasc Res; 1999 May 15; 42(2):503-9. PubMed ID: 10533585 [Abstract] [Full Text] [Related]
8. An improved model for the binding of lidocaine and structurally related local anaesthetics to fast-inactivated voltage-operated sodium channels, showing evidence of cooperativity. Leuwer M, Haeseler G, Hecker H, Bufler J, Dengler R, Aronson JK. Br J Pharmacol; 2004 Jan 15; 141(1):47-54. PubMed ID: 14662728 [Abstract] [Full Text] [Related]
10. Local anesthetics as effectors of allosteric gating. Lidocaine effects on inactivation-deficient rat skeletal muscle Na channels. Balser JR, Nuss HB, Orias DW, Johns DC, Marban E, Tomaselli GF, Lawrence JH. J Clin Invest; 1996 Dec 15; 98(12):2874-86. PubMed ID: 8981936 [Abstract] [Full Text] [Related]
11. Lidocaine induces a slow inactivated state in rat skeletal muscle sodium channels. Chen Z, Ong BH, Kambouris NG, Marbán E, Tomaselli GF, Balser JR. J Physiol; 2000 Apr 01; 524 Pt 1(Pt 1):37-49. PubMed ID: 10747182 [Abstract] [Full Text] [Related]
13. Two human paramyotonia congenita mutations have opposite effects on lidocaine block of Na+ channels expressed in a mammalian cell line. Fan Z, George AL, Kyle JW, Makielski JC. J Physiol; 1996 Oct 01; 496 ( Pt 1)(Pt 1):275-86. PubMed ID: 8910215 [Abstract] [Full Text] [Related]
17. Coupling between fast and slow inactivation revealed by analysis of a point mutation (F1304Q) in mu 1 rat skeletal muscle sodium channels. Nuss HB, Balser JR, Orias DW, Lawrence JH, Tomaselli GF, Marban E. J Physiol; 1996 Jul 15; 494 ( Pt 2)(Pt 2):411-29. PubMed ID: 8842001 [Abstract] [Full Text] [Related]
18. Cocaine binds to a common site on open and inactivated human heart (Na(v)1.5) sodium channels. O'Leary ME, Chahine M. J Physiol; 2002 Jun 15; 541(Pt 3):701-16. PubMed ID: 12068034 [Abstract] [Full Text] [Related]
19. Coexpression of beta 1 with cardiac sodium channel alpha subunits in oocytes decreases lidocaine block. Makielski JC, Limberis JT, Chang SY, Fan Z, Kyle JW. Mol Pharmacol; 1996 Jan 15; 49(1):30-9. PubMed ID: 8569709 [Abstract] [Full Text] [Related]