Detalhe da pesquisa
1.
Epigenetic Changes Governing Scn5a Expression in Denervated Skeletal Muscle.
Int J Mol Sci
; 22(5)2021 Mar 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33803193
2.
Experimental Models of Brugada syndrome.
Int J Mol Sci
; 20(9)2019 Apr 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-31032819
3.
Sodium channel current loss of function in induced pluripotent stem cell-derived cardiomyocytes from a Brugada syndrome patient.
J Mol Cell Cardiol
; 114: 10-19, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29024690
4.
Loss of sodium current caused by a Brugada syndrome-associated variant is determined by patient-specific genetic background.
Heart Rhythm
; 21(3): 331-339, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38008367
5.
A missense mutation in the sodium channel ß2 subunit reveals SCN2B as a new candidate gene for Brugada syndrome.
Hum Mutat
; 34(7): 961-6, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23559163
6.
Large-conductance calcium-activated potassium current modulates excitability in isolated canine intracardiac neurons.
Am J Physiol Cell Physiol
; 304(3): C280-6, 2013 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23195072
7.
DiBAC4(3) hits a "sweet spot" for the activation of arterial large-conductance Ca²âº-activated potassium channels independently of the ß1-subunit.
Am J Physiol Heart Circ Physiol
; 304(11): H1471-82, 2013 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23542916
8.
Generation of the induced pluripotent stem cell line ESi108-A from a familial atrial fibrillation patient.
Stem Cell Res
; 73: 103239, 2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37922745
9.
Generation of four induced pluripotent stem cell lines from a family harboring a single nucleotide variant in SCN5A.
Stem Cell Res
; 63: 102847, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35772296
10.
Generation of an induced pluripotent stem cell line from a healthy Caucasian male.
Stem Cell Res
; 60: 102717, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35231795
11.
An SCN1B Variant Affects Both Cardiac-Type (NaV1.5) and Brain-Type (NaV1.1) Sodium Currents and Contributes to Complex Concomitant Brain and Cardiac Disorders.
Front Cell Dev Biol
; 8: 528742, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33134290
12.
Sudden infant death as the most severe phenotype caused by genetic modulation in a family with atrial fibrillation.
Forensic Sci Int Genet
; 43: 102159, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31522018
13.
Extra Virgin Olive Oil Contains a Phenolic Inhibitor of the Histone Demethylase LSD1/KDM1A.
Nutrients
; 11(7)2019 Jul 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-31331073
14.
Functional expression of "cardiac-type" Nav1.5 sodium channel in canine intracardiac ganglia.
Heart Rhythm
; 3(7): 842-50, 2006 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-16818219
15.
Ionic and cellular basis for the predominance of the Brugada syndrome phenotype in males.
Circulation
; 106(15): 2004-11, 2002 Oct 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-12370227
16.
Clinical and molecular characterization of a cardiac ryanodine receptor founder mutation causing catecholaminergic polymorphic ventricular tachycardia.
Heart Rhythm
; 12(7): 1636-43, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25814417
17.
Genetic analysis, in silico prediction, and family segregation in long QT syndrome.
Eur J Hum Genet
; 23(1): 79-85, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24667783
18.
The smooth muscle-type ß1 subunit potentiates activation by DiBAC4(3) in recombinant BK channels.
Channels (Austin)
; 8(1): 95-102, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24299688
19.
A missense mutation in the sodium channel ß1b subunit reveals SCN1B as a susceptibility gene underlying long QT syndrome.
Heart Rhythm
; 11(7): 1202-9, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24662403
20.
Molecular heterogeneity of large-conductance calcium-activated potassium channels in canine intracardiac ganglia.
Channels (Austin)
; 7(4): 322-8, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23807090