Detalhe da pesquisa
1.
Calmodulin mutations associated with recurrent cardiac arrest in infants.
Circulation
; 127(9): 1009-17, 2013 Mar 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-23388215
2.
Long QT syndrome-associated mutations in intrauterine fetal death.
JAMA
; 309(14): 1473-82, 2013 Apr 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-23571586
3.
Activation of protein kinase C alters the intracellular distribution and mobility of cardiac Na+ channels.
Am J Physiol Heart Circ Physiol
; 302(3): H782-9, 2012 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22101522
4.
SCN5A allelic expression imbalance in African-Americans heterozygous for the common variant p.Ser1103Tyr.
BMC Med Genet
; 11: 74, 2010 May 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-20470418
5.
Intracellular calcium attenuates late current conducted by mutant human cardiac sodium channels.
Circ Arrhythm Electrophysiol
; 8(4): 933-41, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26022185
6.
Novel SCN1A frameshift mutation with absence of truncated Nav1.1 protein in severe myoclonic epilepsy of infancy.
Am J Med Genet A
; 146A(18): 2421-3, 2008 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-18680191
7.
Mechanism of sodium channel NaV1.9 potentiation by G-protein signaling.
J Gen Physiol
; 141(2): 193-202, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23359282
8.
Developmentally regulated SCN5A splice variant potentiates dysfunction of a novel mutation associated with severe fetal arrhythmia.
Heart Rhythm
; 9(4): 590-7, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22064211