Lista de obras -

A propensity score-based case-control study of renin-angiotensin system gene polymorphisms and diastolic heart failure

artículo científico publicado en 2008

ATP-binding cassette transporter A1 gene I823M polymorphism affects plasma high-density lipoprotein cholesterol level and modifies the effect of low high-density lipoprotein cholesterol on the risk of coronary artery disease

scientific article published on 30 January 2007

Acute effects of biventricular pacing in heart failure patients with a normal ejection fraction and mechanical dyssynchrony

artículo científico publicado en 2015

Additive effect of the metabolic syndrome score to the conventional CHADS₂ score for the thromboembolic risk stratification of patients with atrial fibrillation

artículo científico publicado en 2013

Angiotensin II activates signal transducer and activators of transcription 3 via Rac1 in atrial myocytes and fibroblasts: implication for the therapeutic effect of statin in atrial structural remodeling

artículo científico publicado en 2008

Angiotensin II does not influence expression of sarcoplasmic reticulum Ca2 + ATPase in atrial myocytes.

artículo científico publicado en 2009

Angiotensin II increases expression of alpha1C subunit of L-type calcium channel through a reactive oxygen species and cAMP response element-binding protein-dependent pathway in HL-1 myocytes

artículo científico publicado en 2007

Angiotensin II induces complex fractionated electrogram in a cultured atrial myocyte monolayer mediated by calcium and sodium-calcium exchanger.

artículo científico publicado en 2010

Anti-anxiety drugs use and cardiovascular outcomes in patients with myocardial infarction: a national wide assessment

artículo científico publicado en 2014

Arrhythmogenic right ventricular dysplasia: clinical characteristics and identification of novel desmosome gene mutations

artículo científico publicado en 2008

Association of the human minK gene 38G allele with atrial fibrillation: evidence of possible genetic control on the pathogenesis of atrial fibrillation

artículo científico publicado en 2002

Atorvastatin prevents atrial fibrillation in patients with bradyarrhythmias and implantation of an atrial-based or dual-chamber pacemaker: a prospective randomized trial

artículo científico publicado en 2008

Atrial flutter/fibrillation in patients receiving transcatheter closure of atrial septal defect.

artículo científico publicado en 2016

Brugada-type electrocardiogram in the Taiwanese population--is it a risk factor for sudden death?

artículo científico publicado en 2011

Cardiac myosin binding protein C and MAP-kinase activating death domain-containing gene polymorphisms and diastolic heart failure

artículo científico publicado en 2012

Characteristics of Chinese patients with symptomatic Brugada syndrome in Taiwan

artículo científico publicado en 2003

Coexistence and exercise exacerbation of intraleft ventricular contractile dyssynchrony in hypertensive patients with diastolic heart failure.

artículo científico publicado en 2007

Comparisons of clinical impacts on individuals with Brugada electrocardiographic patterns defined by ISHNE criteria or EHRA/HRS/APHRS criteria: a nationwide community-based study

artículo científico publicado en 2017

Connective tissue growth factor and cardiac diastolic dysfunction: human data from the Taiwan diastolic heart failure registry and molecular basis by cellular and animal models

artículo científico publicado en 2013

Denaturing high-performance liquid chromatography screening of the long QT syndrome-related cardiac sodium and potassium channel genes and identification of novel mutations and single nucleotide polymorphisms

scientific article published on 10 September 2005

Detrended Fluctuation Analysis of Heart Rate Dynamics Is an Important Prognostic Factor in Patients with End-Stage Renal Disease Receiving Peritoneal Dialysis

artículo científico publicado en 2016

Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome

artículo científico publicado en 2014

Distinct clinical features in the recipients of the implantable cardioverter defibrillator in Taiwan: a multicenter registry study.

artículo científico publicado en 2003

Distinct functional defect of three novel Brugada syndrome related cardiac sodium channel mutations

artículo científico publicado en 2009

Effect of physical activity on the prevalence of metabolic syndrome and left ventricular hypertrophy in apparently healthy adults

artículo científico publicado en 2010

Effects of Additional Intra-aortic Balloon Counter-Pulsation Therapy to Cardiogenic Shock Patients Supported by Extra-corporeal Membranous Oxygenation

artículo científico publicado en 2016

Effects of angiotensin converting enzyme inhibition or angiotensin receptor blockade in dialysis patients: a nationwide data survey and propensity analysis

artículo científico publicado en 2015

Evolution of left atrial systolic and diastolic functions in different stages of hypertension: distinct effects of blood pressure control

scientific article published on 06 August 2007

Galectin-3 level and the severity of cardiac diastolic dysfunction using cellular and animal models and clinical indices

artículo científico publicado en 2015

Genetic polymorphisms of the angiotensin II type 1 receptor gene and diastolic heart failure.

artículo científico publicado en 2009

Genome-wide screening identifies a KCNIP1 copy number variant as a genetic predictor for atrial fibrillation

artículo científico publicado en 2016

Impact of ventricular dyssynchrony on postexercise accommodation of systolic myocardial motion in hypertensive patients with heart failure and a normal ejection fraction: a tissue-Doppler echocardiography study

scientific article published on 22 December 2011

Impacts of mitral E/e' on myocardial contractile motion and synchronicity in heart failure patients with reduced ejection fraction: An exercise-echocardiography study

scientific article published on 13 May 2013

In-vitro recording of adult zebrafish heart electrocardiogram - a platform for pharmacological testing

artículo científico publicado en 2011

Increased expression of mineralocorticoid receptor in human atrial fibrillation and a cellular model of atrial fibrillation

artículo científico publicado en 2010

Interaction of gender, hypertension, and the angiotensinogen gene haplotypes on the risk of coronary artery disease in a large angiographic cohort

artículo científico publicado en 2008

Interventricular mechanical dyssynchrony determines abnormal heightening of plasma N-terminal probrain natriuretic peptide level in symptomatic bradyarrhythmia patients with chronic dual-chamber vs. single-chamber atrial pacing

artículo científico publicado en 2007

Joint effects of N-terminal pro-B-type-natriuretic peptide and C-reactive protein vs angiographic severity in predicting major adverse cardiovascular events and clinical restenosis after coronary angioplasty in patients with stable coronary artery d

artículo científico publicado en 2008

KCNN2 polymorphisms and cardiac tachyarrhythmias

artículo científico publicado en 2016

Left ventricular diastolic dysfunction in peritoneal dialysis: a forgotten risk factor

artículo científico publicado en 2015

Mechanical stretch of atrial myocyte monolayer decreases sarcoplasmic reticulum calcium adenosine triphosphatase expression and increases susceptibility to repolarization alternans

artículo científico publicado en 2011

Membrane translocation of small GTPase Rac1 and activation of STAT1 and STAT3 in pacing-induced sustained atrial fibrillation

scientific article published on 16 May 2008

Molecular genetics of atrial fibrillation

artículo científico publicado en 2008

Morphologic and topologic characteristics of coronary venous system delineated by noninvasive multidetector computed tomography in chronic systolic heart failure patients

artículo científico publicado en 2007

Myocardial Regional Interstitial Fibrosis is Associated With Left Intra-Ventricular Dyssynchrony in Patients With Heart Failure: A Cardiovascular Magnetic Resonance Study

artículo científico publicado en 2016

Next-generation sequencing of nine atrial fibrillation candidate genes identified novel de novo mutations in patients with extreme trait of atrial fibrillation.

artículo científico publicado en 2014

Plasma levels of tumor necrosis factor-α and interleukin-6 are associated with diastolic heart failure through downregulation of sarcoplasmic reticulum Ca2+ ATPase

artículo científico publicado en 2011

Polygenetic regression model of renin-angiotensin system genes and the risk of coronary artery disease in a large angiographic population

artículo científico publicado en 2010

Prevalence and prognosis of Brugada electrocardiogram patterns in an elderly Han Chinese population: a nation-wide community-based study (HALST cohort).

artículo científico publicado en 2015

Primary prevention of atrial fibrillation with angiotensin-converting enzyme inhibitors and angiotensin receptor blockers in patients with end-stage renal disease undergoing dialysis

artículo científico publicado en 2015

Primary prevention of atrial fibrillation with beta-blockers in patients with end-stage renal disease undergoing dialysis

artículo científico publicado en 2015

Provocation of masked left ventricular mechanical dyssynchrony by treadmill exercise in patients with systolic heart failure and narrow QRS complex

artículo científico publicado en 2008

Renal Denervation Decreases Susceptibility to Arrhythmogenic Cardiac Alternans and Ventricular Arrhythmia in a Rat Model of Post-Myocardial Infarction Heart Failure

artículo científico publicado en 2017

Renin-angiotensin system component expression in the HL-1 atrial cell line and in a pig model of atrial fibrillation

artículo científico publicado en 2008

Renin-angiotensin system gene polymorphisms and atrial fibrillation

artículo científico publicado en 2004

Renin-angiotensin system gene polymorphisms and atrial fibrillation: a regression approach for the detection of gene-gene interactions in a large hospitalized population

artículo científico publicado en 2008

Renin-angiotensin system gene polymorphisms predict the risk of stroke in patients with atrial fibrillation: a 10-year prospective follow-up study

artículo científico publicado en 2014

Renin–angiotensin system gene polymorphisms and coronary artery disease in a large angiographic cohort: Detection of high order gene–gene interaction

article

Repolarization Alternans and Ventricular Arrhythmia in a Repaired Tetralogy of Fallot Animal Model.

artículo científico publicado en 2015

Risk factors and incidence of ischemic stroke in Taiwanese with nonvalvular atrial fibrillation—A nation wide database analysis

artículo científico publicado en 2011

Serum bilirubin is inversely associated with insulin resistance and metabolic syndrome among children and adolescents

scientific article published on 26 July 2008

Significant association of rs13376333 in KCNN3 on chromosome 1q21 with atrial fibrillation in a Taiwanese population

artículo científico publicado en 2011

Spironolactone is associated with reduced risk of new-onset atrial fibrillation in patients receiving renal replacement therapy

artículo científico publicado en 2015

Statin therapy lowers the risk of new-onset atrial fibrillation in patients with end-stage renal disease

artículo científico publicado en 2015

TNF-α down-regulates sarcoplasmic reticulum Ca²⁺ ATPase expression and leads to left ventricular diastolic dysfunction through binding of NF-κB to promoter response element

artículo científico publicado en 2015

Tachycardia of atrial myocytes induces collagen expression in atrial fibroblasts through transforming growth factor β1.

artículo científico publicado en 2010

The Effects of Metabolic SyndromeVersusInfectious Burden on Inflammation, Severity of Coronary Atherosclerosis, and Major Adverse Cardiovascular Events

artículo científico publicado en 2007

The association of human connexin 40 genetic polymorphisms with atrial fibrillation

artículo científico publicado en 2006

Three single-nucleotide polymorphisms of the angiotensinogen gene and susceptibility to hypertension: single locus genotype vs. haplotype analysis

artículo científico publicado en 2004

Unique clinical characteristics and SCN5A mutations in patients with Brugada syndrome in Taiwan

artículo científico publicado en 2013

Utilizing multiple in silico analyses to identify putative causal SCN5A variants in Brugada syndrome

artículo científico publicado en 2014

Lista de obras de

A propensity score-based case-control study of renin-angiotensin system gene polymorphisms and diastolic heart failure

ATP-binding cassette transporter A1 gene I823M polymorphism affects plasma high-density lipoprotein cholesterol level and modifies the effect of low high-density lipoprotein cholesterol on the risk of coronary artery disease

Acute effects of biventricular pacing in heart failure patients with a normal ejection fraction and mechanical dyssynchrony

Additive effect of the metabolic syndrome score to the conventional CHADS₂ score for the thromboembolic risk stratification of patients with atrial fibrillation

Angiotensin II activates signal transducer and activators of transcription 3 via Rac1 in atrial myocytes and fibroblasts: implication for the therapeutic effect of statin in atrial structural remodeling

Angiotensin II does not influence expression of sarcoplasmic reticulum Ca2 + ATPase in atrial myocytes.

Angiotensin II increases expression of alpha1C subunit of L-type calcium channel through a reactive oxygen species and cAMP response element-binding protein-dependent pathway in HL-1 myocytes

Angiotensin II induces complex fractionated electrogram in a cultured atrial myocyte monolayer mediated by calcium and sodium-calcium exchanger.

Anti-anxiety drugs use and cardiovascular outcomes in patients with myocardial infarction: a national wide assessment

Arrhythmogenic right ventricular dysplasia: clinical characteristics and identification of novel desmosome gene mutations

Association of the human minK gene 38G allele with atrial fibrillation: evidence of possible genetic control on the pathogenesis of atrial fibrillation

Atorvastatin prevents atrial fibrillation in patients with bradyarrhythmias and implantation of an atrial-based or dual-chamber pacemaker: a prospective randomized trial

Atrial flutter/fibrillation in patients receiving transcatheter closure of atrial septal defect.

Brugada-type electrocardiogram in the Taiwanese population--is it a risk factor for sudden death?

Cardiac myosin binding protein C and MAP-kinase activating death domain-containing gene polymorphisms and diastolic heart failure

Characteristics of Chinese patients with symptomatic Brugada syndrome in Taiwan

Coexistence and exercise exacerbation of intraleft ventricular contractile dyssynchrony in hypertensive patients with diastolic heart failure.

Comparisons of clinical impacts on individuals with Brugada electrocardiographic patterns defined by ISHNE criteria or EHRA/HRS/APHRS criteria: a nationwide community-based study

Connective tissue growth factor and cardiac diastolic dysfunction: human data from the Taiwan diastolic heart failure registry and molecular basis by cellular and animal models

Denaturing high-performance liquid chromatography screening of the long QT syndrome-related cardiac sodium and potassium channel genes and identification of novel mutations and single nucleotide polymorphisms

Detrended Fluctuation Analysis of Heart Rate Dynamics Is an Important Prognostic Factor in Patients with End-Stage Renal Disease Receiving Peritoneal Dialysis

Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome

Distinct clinical features in the recipients of the implantable cardioverter defibrillator in Taiwan: a multicenter registry study.

Distinct functional defect of three novel Brugada syndrome related cardiac sodium channel mutations

Effect of physical activity on the prevalence of metabolic syndrome and left ventricular hypertrophy in apparently healthy adults

Effects of Additional Intra-aortic Balloon Counter-Pulsation Therapy to Cardiogenic Shock Patients Supported by Extra-corporeal Membranous Oxygenation

Effects of angiotensin converting enzyme inhibition or angiotensin receptor blockade in dialysis patients: a nationwide data survey and propensity analysis

Evolution of left atrial systolic and diastolic functions in different stages of hypertension: distinct effects of blood pressure control

Galectin-3 level and the severity of cardiac diastolic dysfunction using cellular and animal models and clinical indices

Genetic polymorphisms of the angiotensin II type 1 receptor gene and diastolic heart failure.

Genome-wide screening identifies a KCNIP1 copy number variant as a genetic predictor for atrial fibrillation

Impact of ventricular dyssynchrony on postexercise accommodation of systolic myocardial motion in hypertensive patients with heart failure and a normal ejection fraction: a tissue-Doppler echocardiography study

Impacts of mitral E/e' on myocardial contractile motion and synchronicity in heart failure patients with reduced ejection fraction: An exercise-echocardiography study

In-vitro recording of adult zebrafish heart electrocardiogram - a platform for pharmacological testing

Increased expression of mineralocorticoid receptor in human atrial fibrillation and a cellular model of atrial fibrillation

Interaction of gender, hypertension, and the angiotensinogen gene haplotypes on the risk of coronary artery disease in a large angiographic cohort

Interventricular mechanical dyssynchrony determines abnormal heightening of plasma N-terminal probrain natriuretic peptide level in symptomatic bradyarrhythmia patients with chronic dual-chamber vs. single-chamber atrial pacing

Joint effects of N-terminal pro-B-type-natriuretic peptide and C-reactive protein vs angiographic severity in predicting major adverse cardiovascular events and clinical restenosis after coronary angioplasty in patients with stable coronary artery d

KCNN2 polymorphisms and cardiac tachyarrhythmias

Left ventricular diastolic dysfunction in peritoneal dialysis: a forgotten risk factor

Mechanical stretch of atrial myocyte monolayer decreases sarcoplasmic reticulum calcium adenosine triphosphatase expression and increases susceptibility to repolarization alternans

Membrane translocation of small GTPase Rac1 and activation of STAT1 and STAT3 in pacing-induced sustained atrial fibrillation

Molecular genetics of atrial fibrillation

Morphologic and topologic characteristics of coronary venous system delineated by noninvasive multidetector computed tomography in chronic systolic heart failure patients

Myocardial Regional Interstitial Fibrosis is Associated With Left Intra-Ventricular Dyssynchrony in Patients With Heart Failure: A Cardiovascular Magnetic Resonance Study

Next-generation sequencing of nine atrial fibrillation candidate genes identified novel de novo mutations in patients with extreme trait of atrial fibrillation.

Plasma levels of tumor necrosis factor-α and interleukin-6 are associated with diastolic heart failure through downregulation of sarcoplasmic reticulum Ca2+ ATPase

Polygenetic regression model of renin-angiotensin system genes and the risk of coronary artery disease in a large angiographic population

Prevalence and prognosis of Brugada electrocardiogram patterns in an elderly Han Chinese population: a nation-wide community-based study (HALST cohort).

Primary prevention of atrial fibrillation with angiotensin-converting enzyme inhibitors and angiotensin receptor blockers in patients with end-stage renal disease undergoing dialysis

Primary prevention of atrial fibrillation with beta-blockers in patients with end-stage renal disease undergoing dialysis

Provocation of masked left ventricular mechanical dyssynchrony by treadmill exercise in patients with systolic heart failure and narrow QRS complex

Renal Denervation Decreases Susceptibility to Arrhythmogenic Cardiac Alternans and Ventricular Arrhythmia in a Rat Model of Post-Myocardial Infarction Heart Failure

Renin-angiotensin system component expression in the HL-1 atrial cell line and in a pig model of atrial fibrillation

Renin-angiotensin system gene polymorphisms and atrial fibrillation

Renin-angiotensin system gene polymorphisms and atrial fibrillation: a regression approach for the detection of gene-gene interactions in a large hospitalized population

Renin-angiotensin system gene polymorphisms predict the risk of stroke in patients with atrial fibrillation: a 10-year prospective follow-up study

Renin–angiotensin system gene polymorphisms and coronary artery disease in a large angiographic cohort: Detection of high order gene–gene interaction

Repolarization Alternans and Ventricular Arrhythmia in a Repaired Tetralogy of Fallot Animal Model.

Risk factors and incidence of ischemic stroke in Taiwanese with nonvalvular atrial fibrillation—A nation wide database analysis

Serum bilirubin is inversely associated with insulin resistance and metabolic syndrome among children and adolescents

Significant association of rs13376333 in KCNN3 on chromosome 1q21 with atrial fibrillation in a Taiwanese population

Spironolactone is associated with reduced risk of new-onset atrial fibrillation in patients receiving renal replacement therapy

Statin therapy lowers the risk of new-onset atrial fibrillation in patients with end-stage renal disease

TNF-α down-regulates sarcoplasmic reticulum Ca²⁺ ATPase expression and leads to left ventricular diastolic dysfunction through binding of NF-κB to promoter response element

Tachycardia of atrial myocytes induces collagen expression in atrial fibroblasts through transforming growth factor β1.

The Effects of Metabolic SyndromeVersusInfectious Burden on Inflammation, Severity of Coronary Atherosclerosis, and Major Adverse Cardiovascular Events

The association of human connexin 40 genetic polymorphisms with atrial fibrillation

Three single-nucleotide polymorphisms of the angiotensinogen gene and susceptibility to hypertension: single locus genotype vs. haplotype analysis

Unique clinical characteristics and SCN5A mutations in patients with Brugada syndrome in Taiwan

Utilizing multiple in silico analyses to identify putative causal SCN5A variants in Brugada syndrome