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Summary Anatomy Item Literature (128) Expression Attributions Wiki
XB-ANAT-208

Papers associated with spinal ganglion (and nav1)

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Isolation, synthesis and characterization of ω-TRTX-Cc1a, a novel tarantula venom peptide that selectively targets L-type Cav channels., Klint JK., Biochem Pharmacol. May 15, 2014; 89 (2): 276-86.

Functional properties and toxin pharmacology of a dorsal root ganglion sodium channel viewed through its voltage sensors., Bosmans F., J Gen Physiol. July 1, 2011; 138 (1): 59-72.                  

Phyla- and Subtype-Selectivity of CgNa, a Na Channel Toxin from the Venom of the Giant Caribbean Sea Anemone Condylactis Gigantea., Billen B., Front Pharmacol. November 23, 2010; 1 133.        

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.

State-dependent block of rat Nav1.4 sodium channels expressed in xenopus oocytes by pyrazoline-type insecticides., Silver K., Neurotoxicology. June 1, 2005; 26 (3): 397-406.

Role of auxiliary beta1-, beta2-, and beta3-subunits and their interaction with Na(v)1.8 voltage-gated sodium channel., Vijayaragavan K., Biochem Biophys Res Commun. June 25, 2004; 319 (2): 531-40.

Differential modulation of Nav1.7 and Nav1.8 peripheral nerve sodium channels by the local anesthetic lidocaine., Chevrier P., Br J Pharmacol. June 1, 2004; 142 (3): 576-84.

Molecular cloning and functional expression of the human sodium channel beta1B subunit, a novel splicing variant of the beta1 subunit., Qin N., Eur J Biochem. December 1, 2003; 270 (23): 4762-70.

Gating properties of Na(v)1.7 and Na(v)1.8 peripheral nerve sodium channels., Vijayaragavan K., J Neurosci. October 15, 2001; 21 (20): 7909-18.

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.

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