Detalhe da pesquisa
1.
Multiple genetic variations in sodium channel subunits in a case of sudden infant death syndrome.
Pacing Clin Electrophysiol
; 41(6): 620-626, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29572929
2.
Live Imaging of Kv7.2/7.3 Cell Surface Dynamics at the Axon Initial Segment: High Steady-State Stability and Calpain-Dependent Excitotoxic Downregulation Revealed.
J Neurosci
; 36(7): 2261-6, 2016 Feb 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-26888935
3.
Whole-Exome Sequencing Implicates Neuronal Calcium Channel with Familial Atrial Fibrillation.
Front Genet
; 13: 806429, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35154276
4.
Functional consequences of genetic variation in sodium channel modifiers in early onset lone atrial fibrillation.
Per Med
; 15(2): 93-102, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29714131
5.
A novel Ca²âº-mediated cross-talk between endoplasmic reticulum and acidic organelles: implications for NAADP-dependent Ca²âº signalling.
Cell Calcium
; 57(2): 89-100, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25655285
6.
Homozygosity for SCN4A Arg1142Gln causes congenital myopathy with variable disease expression.
Neurol Genet
; 4(5): e267, 2018 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-30283817