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Current Medicinal Chemistry|December 6, 2013
Interlinking of hypoxia and estrogen in thyroid cancer progressionS Rajoria, E Hanly, A Nicolini, et al.Neurology|January 5, 2002
Partial and generalized epilepsy with febrile seizures plus and a novel SCN1A mutationB Abou-Khalil, Q Ge, R Desai, et al.The Journal of Physiology|August 1, 1994
K(+)-aggravated myotonia: destabilization of the inactivated state of the human muscle Na+ channel by the V1589M mutationN Mitrović, A L George, R Heine, et al.The Journal of Physiology|October 1, 1993
Human sodium channel myotonia: slowed channel inactivation due to substitutions for a glycine within the III-IV linkerH Lerche, R Heine, U Pika, et al.Cell|December 9, 1991
Identification of a mutation in the gene causing hyperkalemic periodic paralysisL J Ptácek, A L George, R C Griggs, et al.Anesthesiology|May 1, 1995
Masseter muscle rigidity associated with glycine1306-to-alanine mutation in the adult muscle sodium channel alpha-subunit geneG M Vita, A Olckers, A E Jedlicka, et al.Current Biology : CB|March 7, 2001
CLH-3, a ClC-2 anion channel ortholog activated during meiotic maturation in C. elegans oocytesE Rutledge, L Bianchi, M Christensen, et al.Cytogenetics and Cell Genetics|January 1, 1995
Assignment of the human heart tetrodotoxin-resistant voltage-gated Na+ channel alpha-subunit gene (SCN5A) to band 3p21A L George, T A Varkony, H A Drabkin, et al.Annals of Neurology|March 1, 1993
Sodium channel mutations in paramyotonia congenita and hyperkalemic periodic paralysisL J Ptacek, L Gouw, H Kwieciński, et al.The Pharmacogenomics Journal|May 16, 2012
Novel rare variants in congenital cardiac arrhythmia genes are frequent in drug-induced torsades de pointesA H Ramirez, C M Shaffer, J T Delaney, et al.Pageof 12