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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., J Biol Chem. September 4, 2009; 284 (36): 24568-82.
Isolation and structure-activity of mu-conotoxin TIIIA, a potent inhibitor of tetrodotoxin-sensitive voltage-gated sodium channels. , Lewis RJ., Mol Pharmacol. March 1, 2007; 71 (3): 676-85.
Distribution and functional characterization of human Nav1.3 splice variants. , Thimmapaya R., Eur J Neurosci. July 1, 2005; 22 (1): 1-9.
Lidocaine block of neonatal Nav1.3 is differentially modulated by co-expression of beta1 and beta3 subunits. , Lenkowski PW., Eur J Pharmacol. April 25, 2003; 467 (1-3): 23-30.
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., J Neurosci. August 15, 2001; 21 (16): 5952-61.
Developmental expression of the novel voltage-gated sodium channel auxiliary subunit beta3, in rat CNS. , Shah BS., J Physiol. August 1, 2001; 534 (Pt 3): 763-76.