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Macrophage MST1/2 Disruption Impairs Post-Infarction Cardiac Repair via LTB4

Circulation research, 2021-10, Vol.129 (10), p.909-926

2021

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Variants of genes encoding collagens and matrix metalloproteinase system increased the risk of aortic dissection

Science China. Life sciences, 2017, Vol.60 (1), p.57-65

2017

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Sclerosteosis caused by a novel nonsense mutation of SOST in a consanguineous family

Clinical genetics, 2016-02, Vol.89 (2), p.205-209

2016

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Updated Genetic Testing of Primary Hyperoxaluria Type 1 in a Chinese Population: Results from a Single Center Study and a Systematic Review

Current medical science, 2018-10, Vol.38 (5), p.749-757

2018

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Glucose-Sensitive Myokine/Cardiokine MG53 Regulates Systemic Insulin Response and Metabolic Homeostasis

Circulation (New York, N.Y.), 2019-02, Vol.139 (7), p.901-914

2019

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Let-7b inhibits human cancer phenotype by targeting cytochrome P450 epoxygenase 2J2

PloS one, 2012-06, Vol.7 (6), p.e39197-e39197

2012

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Genotyping on ALDH2: comparison of four different technologies

PloS one, 2015-03, Vol.10 (3), p.e0122745-e0122745

2015

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Positive Association between APOA5 rs662799 Polymorphism and Coronary Heart Disease: A Case-Control Study and Meta-Analysis

PloS one, 2015-08, Vol.10 (8), p.e0135683-e0135683

2015

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An echo score raises the suspicion of cardiac amyloidosis in Chinese with heart failure with preserved ejection fraction

ESC Heart Failure, 2022-12, Vol.9 (6), p.4280-4290

2022

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Zero-fluoroscopy catheter ablation of severe drug-resistant arrhythmia guided by Ensite NavX system during pregnancy: Two case reports and literature review

Medicine (Baltimore), 2016-08, Vol.95 (32), p.e4487

2016

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Subtypes of SERPINC1 mutations and the thrombotic phenotype of inherited antithrombin deficient individuals in Chinese Han population

Blood cells, molecules, & diseases, 2016-11, Vol.62, p.38-41

2016

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Loss of Mbd2 Protects Mice Against High-Fat Diet-Induced Obesity and Insulin Resistance by Regulating the Homeostasis of Energy Storage and Expenditure

Diabetes (New York, N.Y.), 2016-11, Vol.65 (11), p.3384-3395

2016

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A novel nonsense mutation in LMNA gene identified by Exome Sequencing in an atrial fibrillation family

European journal of medical genetics, 2016-08, Vol.59 (8), p.396-400

2016

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Partial anomalous pulmonary venous connection to superior vena cava that overrides across the intact atrial septum and has bi-atrial connection in a 75-year-old female presenting with pulmonary hypertension

BMC cardiovascular disorders, 2014-10, Vol.14 (1), p.149-149, Article 149

2014

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Arteriogenesis induced by intramyocardial recombinant adeno-associated virus vector encoding human CD151 cDNA gene transfer in swines with coronary artery occlusion

Zhōnghuá xīnxuèguănbìng zázhì, 2009-06, Vol.37 (6), p.537

2009

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Functional consequences of a novel point mutation in the CYP21A2 gene identified in a Chinese Han patient with nonclassic 21-hydroxylase deficiency

Clinical endocrinology (Oxford), 2014-06, Vol.80 (6), p.927-928

2014

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Prevalence of common mutations in the CYP17A1 gene in Chinese Han population

Clinica chimica acta, 2011-06, Vol.412 (13), p.1240-1243

2011

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Next-generation sequencing identifies novel mutations in the FBN1 gene for two Chinese families with Marfan syndrome

Molecular medicine reports, 2016-07, Vol.14 (1), p.151-158

2016

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Rosuvastatin attenuates mucus secretion in a murine model of chronic asthma by inhibiting the gamma-aminobutyric acid type A receptor

Chinese medical journal, 2012-04, Vol.125 (8), p.1457-1464

2012

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A case of arrhythmogenic right ventricular cardiomyopathy without arrhythmias

Diagnostic pathology, 2012-06, Vol.7 (1), p.67-67, Article 67

2012

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Influences of recombinant adeno-associated virus-mediated Decorin gene transfection on cell cycle and apoptosis of SiHa cells

Ai zheng = Aizheng = Chinese journal of cancer, 2005-01, Vol.24 (1), p.28

2005

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Phenotype analysis of mononuclear cells in endomyocardial biopsy specimens from patients with viral myocarditis and dilated cardiomyopathy

Journal of Tongji Medical University, 1994-12, Vol.14 (4), p.213-215

1994

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Potassium intake modulates the thiazide-sensitive sodium-chloride cotransporter (NCC) activity via the Kir4.1 potassium channel

Kidney international, 2018-04, Vol.93 (4), p.893-902

2018

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Involvement of oxytocin and GABA in consolation behavior elicited by socially defeated individuals in mandarin voles

Psychoneuroendocrinology, 2019-05, Vol.103, p.14-24

2019

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Deletion of Kir5.1 Impairs Renal Ability to Excrete Potassium during Increased Dietary Potassium Intake

Journal of the American Society of Nephrology, 2019-08, Vol.30 (8), p.1425-1438

2019

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Macrophage MST1/2 Disruption Impairs Post-Infarction Cardiac Repair via LTB4

Variants of genes encoding collagens and matrix metalloproteinase system increased the risk of aortic dissection

Sclerosteosis caused by a novel nonsense mutation of SOST in a consanguineous family

Updated Genetic Testing of Primary Hyperoxaluria Type 1 in a Chinese Population: Results from a Single Center Study and a Systematic Review

Glucose-Sensitive Myokine/Cardiokine MG53 Regulates Systemic Insulin Response and Metabolic Homeostasis

Let-7b inhibits human cancer phenotype by targeting cytochrome P450 epoxygenase 2J2

Genotyping on ALDH2: comparison of four different technologies

Positive Association between APOA5 rs662799 Polymorphism and Coronary Heart Disease: A Case-Control Study and Meta-Analysis

An echo score raises the suspicion of cardiac amyloidosis in Chinese with heart failure with preserved ejection fraction

Zero-fluoroscopy catheter ablation of severe drug-resistant arrhythmia guided by Ensite NavX system during pregnancy: Two case reports and literature review

Subtypes of SERPINC1 mutations and the thrombotic phenotype of inherited antithrombin deficient individuals in Chinese Han population

Loss of Mbd2 Protects Mice Against High-Fat Diet-Induced Obesity and Insulin Resistance by Regulating the Homeostasis of Energy Storage and Expenditure

A novel nonsense mutation in LMNA gene identified by Exome Sequencing in an atrial fibrillation family

Partial anomalous pulmonary venous connection to superior vena cava that overrides across the intact atrial septum and has bi-atrial connection in a 75-year-old female presenting with pulmonary hypertension

Arteriogenesis induced by intramyocardial recombinant adeno-associated virus vector encoding human CD151 cDNA gene transfer in swines with coronary artery occlusion

Functional consequences of a novel point mutation in the CYP21A2 gene identified in a Chinese Han patient with nonclassic 21-hydroxylase deficiency

Prevalence of common mutations in the CYP17A1 gene in Chinese Han population

Next-generation sequencing identifies novel mutations in the FBN1 gene for two Chinese families with Marfan syndrome

Rosuvastatin attenuates mucus secretion in a murine model of chronic asthma by inhibiting the gamma-aminobutyric acid type A receptor

A case of arrhythmogenic right ventricular cardiomyopathy without arrhythmias

Influences of recombinant adeno-associated virus-mediated Decorin gene transfection on cell cycle and apoptosis of SiHa cells

Phenotype analysis of mononuclear cells in endomyocardial biopsy specimens from patients with viral myocarditis and dilated cardiomyopathy

Potassium intake modulates the thiazide-sensitive sodium-chloride cotransporter (NCC) activity via the Kir4.1 potassium channel

Involvement of oxytocin and GABA in consolation behavior elicited by socially defeated individuals in mandarin voles

Deletion of Kir5.1 Impairs Renal Ability to Excrete Potassium during Increased Dietary Potassium Intake

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