Papers associated with blastomere V1 (and nav1)

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	Electrophysiological characterization of a large set of novel variants in the SCN5A-gene: identification of novel LQTS3 and BrS mutations., Ortiz-Bonnin B., Pflugers Arch. August 1, 2016; 468 (8): 1375-87.
	Binary architecture of the Nav1.2-β2 signaling complex., Das S., Elife. January 28, 2016; 5
	The endocannabinoid anandamide inhibits voltage-gated sodium channels Nav1.2, Nav1.6, Nav1.7, and Nav1.8 in Xenopus oocytes., Okura D., Anesth Analg. March 1, 2014; 118 (3): 554-62.
	Tuning voltage-gated channel activity and cellular excitability with a sphingomyelinase., Combs DJ., J Gen Physiol. October 1, 2013; 142 (4): 367-80.
	Domain IV voltage-sensor movement is both sufficient and rate limiting for fast inactivation in sodium channels., Capes DL., J Gen Physiol. August 1, 2013; 142 (2): 101-12.
	Molecular mechanism of voltage sensing in voltage-gated proton channels., Gonzalez C., J Gen Physiol. March 1, 2013; 141 (3): 275-85.
	Multiple pore conformations driven by asynchronous movements of voltage sensors in a eukaryotic sodium channel., Goldschen-Ohm MP., Nat Commun. January 1, 2013; 4 1350.
	A proton leak current through the cardiac sodium channel is linked to mixed arrhythmia and the dilated cardiomyopathy phenotype., Gosselin-Badaroudine P., PLoS One. January 1, 2012; 7 (5): e38331.
	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.
	Correlations between clinical and physiological consequences of the novel mutation R878C in a highly conserved pore residue in the cardiac Na+ channel., Zhang Y., Acta Physiol (Oxf). December 1, 2008; 194 (4): 311-23.

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