Detalhe da pesquisa
1.
Neither cardiac mitochondrial DNA variation nor copy number contribute to congenital heart disease risk.
Am J Hum Genet;
109(5): 961-966, 2022 05 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35397206
2.
Familial Associations of Prevalence and Cause-Specific Mortality for Thoracic Aortic Disease and Bicuspid Aortic Valve in a Large-Population Database.
Circulation;
148(8): 637-647, 2023 08 22.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37317837
3.
Limited Relationship Between Echocardiographic Measures and Electrocardiographic Markers of Left Ventricular Size in Healthy Children.
Pediatr Cardiol;
45(5): 1055-1063, 2024 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38520508
4.
Rare genetic variation at transcription factor binding sites modulates local DNA methylation profiles.
PLoS Genet;
16(11): e1009189, 2020 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33216750
5.
Inhibition of Notch signaling rescues cardiovascular development in Kabuki Syndrome.
PLoS Biol;
17(9): e3000087, 2019 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31479440
6.
Evaluating use of changing technologies for rapid next-generation sequencing in pediatrics.
Pediatr Res;
92(5): 1364-1369, 2022 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35115709
7.
DNA methylation reprograms cardiac metabolic gene expression in end-stage human heart failure.
Am J Physiol Heart Circ Physiol;
317(4): H674-H684, 2019 10 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31298559
8.
Modeling effects of voltage dependent properties of the cardiac muscarinic receptor on human sinus node function.
PLoS Comput Biol;
14(10): e1006438, 2018 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30303952
9.
Robust identification of deletions in exome and genome sequence data based on clustering of Mendelian errors.
Hum Mutat;
39(6): 870-881, 2018 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29527824
10.
Sheet-Like Remodeling of the Transverse Tubular System in Human Heart Failure Impairs Excitation-Contraction Coupling and Functional Recovery by Mechanical Unloading.
Circulation;
135(17): 1632-1645, 2017 Apr 25.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28073805
11.
The voltage-sensitive cardiac M2 muscarinic receptor modulates the inward rectification of the G protein-coupled, ACh-gated K+ current.
Pflugers Arch;
470(12): 1765-1776, 2018 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30155776
12.
A Functional Assay for Sick Sinus Syndrome Genetic Variants.
Cell Physiol Biochem;
42(5): 2021-2029, 2017.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28803248
13.
Pharmacological Conversion of a Cardiac Inward Rectifier into an Outward Rectifier Potassium Channel.
Mol Pharmacol;
90(3): 334-40, 2016 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27247338
14.
The agonist-specific voltage dependence of M2 muscarinic receptors modulates the deactivation of the acetylcholine-gated K(+) current (I KACh).
Pflugers Arch;
468(7): 1207-1214, 2016 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27023349
15.
3-OST-7 regulates BMP-dependent cardiac contraction.
PLoS Biol;
11(12): e1001727, 2013 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24311987
16.
Exome analysis of a family with Wolff-Parkinson-White syndrome identifies a novel disease locus.
Am J Med Genet A;
167A(12): 2975-84, 2015 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26284702
17.
An in vivo cardiac assay to determine the functional consequences of putative long QT syndrome mutations.
Circ Res;
112(5): 826-30, 2013 Mar 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23303164
18.
Lethal arrhythmias in Tbx3-deficient mice reveal extreme dosage sensitivity of cardiac conduction system function and homeostasis.
Proc Natl Acad Sci U S A;
109(3): E154-63, 2012 Jan 17.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22203979
19.
Revisiting the challenges of universal screening for long QT syndrome.
J Electrocardiol;
48(6): 1053-7, 2015.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26355713
20.
The absence of insulin signaling in the heart induces changes in potassium channel expression and ventricular repolarization.
Am J Physiol Heart Circ Physiol;
306(5): H747-54, 2014 Mar 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24375641