| scholarly article | Q13442814 |
| P2093 | author name string | Ilaria Rivolta | |
| Lian-Yu Lin | |||
| Chih-Chieh Yu | |||
| Shyh-Jye Lee | |||
| Charles Antzelevitch | |||
| Ling-Ping Lai | |||
| Juey-Jen Hwang | |||
| Wen-Jone Chen | |||
| Hui-Chun Huang | |||
| Eric Y Chuang | |||
| Liang-Chuan Lai | |||
| Yen-Bin Liu | |||
| Jyh-Ming Jimmy Juang | |||
| Tzu-Pin Lu | |||
| Shih-Fan Sherri Yeh | |||
| Ching-Yu Julius Chen | |||
| Li-Ting Ho | |||
| Anna Binda | |||
| P2860 | cites work | Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method | Q25938999 |
| Genetics of Brugada syndrome | Q28074918 | ||
| Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death | Q28294931 | ||
| Genome-wide association studies for common diseases and complex traits | Q29615822 | ||
| A perfect message: RNA surveillance and nonsense-mediated decay | Q29616125 | ||
| A novel SCN5A mutation associated with long QT-3: altered inactivation kinetics and channel dysfunction. | Q33148068 | ||
| Characteristics of Chinese patients with symptomatic Brugada syndrome in Taiwan | Q33149124 | ||
| Brugada-type electrocardiogram in the Taiwanese population--is it a risk factor for sudden death? | Q33160000 | ||
| A study of the SCN5A gene in a cohort of 76 patients with Brugada syndrome. | Q33161757 | ||
| Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome | Q33164900 | ||
| Unique clinical characteristics and SCN5A mutations in patients with Brugada syndrome in Taiwan | Q33165990 | ||
| Selective gamma-ketoaldehyde scavengers protect Nav1.5 from oxidant-induced inactivation | Q33638480 | ||
| Glutathione and glutathione-dependent enzymes represent a co-ordinately regulated defence against oxidative stress. | Q33750086 | ||
| Voltage-gated sodium channels are required for heart development in zebrafish | Q33849089 | ||
| Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology | Q34465792 | ||
| J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge | Q34534329 | ||
| Using extreme phenotype sampling to identify the rare causal variants of quantitative traits in association studies | Q34546292 | ||
| Dynamic investigation of interaction of biocompatible iron oxide nanoparticles with epithelial cells for biomedical applications. | Q34974833 | ||
| Metabolic stress, reactive oxygen species, and arrhythmia. | Q35690954 | ||
| CNVkit: Genome-Wide Copy Number Detection and Visualization from Targeted DNA Sequencing. | Q35995950 | ||
| Large Genomic Imbalances in Brugada Syndrome. | Q36148081 | ||
| The Tpeak - Tend interval as an electrocardiographic risk marker of arrhythmic and mortality outcomes: A systematic review and meta-analysis. | Q36383747 | ||
| Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease | Q36439318 | ||
| Copy number variation in the human genome and its implications for cardiovascular disease | Q36852391 | ||
| Mitochondria oxidative stress, connexin43 remodeling, and sudden arrhythmic death | Q37026992 | ||
| Analysis of the human tissue-specific expression by genome-wide integration of transcriptomics and antibody-based proteomics | Q37563863 | ||
| HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: document endorsed by HRS, EHRA, and APHRS in May 2013 and by ACCF, AHA, PACES, and AEPC in June 2013. | Q38134931 | ||
| SCN4A mutation as modifying factor of myotonic dystrophy type 2 phenotype | Q38912053 | ||
| Traditional and novel electrocardiographic conduction and repolarization markers of sudden cardiac death | Q38972230 | ||
| Global Disparities of Hypertension Prevalence and Control: A Systematic Analysis of Population-Based Studies From 90 Countries. | Q39252137 | ||
| Prevalence and prognosis of Brugada electrocardiogram patterns in an elderly Han Chinese population: a nation-wide community-based study (HALST cohort). | Q40027033 | ||
| Oxidative mediated lipid peroxidation recapitulates proarrhythmic effects on cardiac sodium channels | Q40352026 | ||
| The pathophysiological mechanism underlying Brugada syndrome: depolarization versus repolarization | Q41772555 | ||
| A comparison of genomic copy number calls by Partek Genomics Suite, Genotyping Console and Birdsuite algorithms to quantitative PCR | Q42038979 | ||
| Detecting rare variant effects using extreme phenotype sampling in sequencing association studies | Q42109315 | ||
| Functional characterization of zebrafish K2P18.1 (TRESK) two-pore-domain K+ channels. | Q42631828 | ||
| Oxidative stress alters specific membrane currents in isolated cardiac myocytes | Q43604718 | ||
| Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes | Q45027885 | ||
| Copy Number Variations of SCN5A in Brugada Syndrome. SCN5A CNVs in BrS. | Q51735488 | ||
| J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge. | Q55059903 | ||
| Brugada Syndrome | Q56140211 | ||
| T-T, T-T/QT ratio and T-T dispersion for risk stratification in Brugada Syndrome: A systematic review and meta-analysis | Q62667633 | ||
| The Taiwan Heart Registries: Its Influence on Cardiovascular Patient Care | Q64046064 | ||
| Genomic organization of the human SCN5A gene encoding the cardiac sodium channel | Q71139469 | ||
| Effects of membrane lipid peroxidation by tert butyl hydroperoxide on the sodium current in isolated feline ventricular myocytes | Q72391650 | ||
| Slowly inactivating sodium currents are reduced by exposure to oxidative stress | Q74088115 | ||
| Effects of flecainide and quinidine on arrhythmogenic properties of Scn5a+/- murine hearts modelling the Brugada syndrome | Q79782343 | ||
| Exclusion of multiple candidate genes and large genomic rearrangements in SCN5A in a Dutch Brugada syndrome cohort | Q80446672 | ||
| Brugada syndrome caused by a large deletion in SCN5A only detected by multiplex ligation-dependent probe amplification | Q83353831 | ||
| J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge | Q87886309 | ||
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| ImageQuant | Q112270642 | ||
| P921 | main subject | Brugada syndrome | Q599683 |
| P304 | page(s) | 102843 | |
| P577 | publication date | 2020-07-06 | |
| P1433 | published in | EBioMedicine | Q24912341 |
| P1476 | title | GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death | |
| P478 | volume | 57 |
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