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SOX17 Loss-of-Function Mutation Underlying Familial Pulmonary Arterial Hypertension

International Heart Journal, 2021/05/29, Vol.62(3), pp.566-574

2021

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A New TBX5 Loss-of-Function Mutation Contributes to Congenital Heart Defect and Atrioventricular Block

International Heart Journal, 2020/07/30, Vol.61(4), pp.761-768

2020

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PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome

PloS one, 2015-04, Vol.10 (4), p.e0124409-e0124409

2015

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A Novel NKX2.5 Loss-of-Function Mutation Associated With Congenital Bicuspid Aortic Valve

The American journal of cardiology, 2014-12, Vol.114 (12), p.1891-1895

2014

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Detection and functional characterization of a novel MEF2A variation responsible for familial dilated cardiomyopathy

Clinical chemistry and laboratory medicine, 2021-04, Vol.59 (5), p.955

2021

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A New ISL1 Loss-of-Function Mutation Predisposes to Congenital Double Outlet Right Ventricle

International Heart Journal, 2019/09/27, Vol.60(5), pp.1113-1122

2019

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TBX5 loss-of-function mutation contributes to familial dilated cardiomyopathy

Biochemical and biophysical research communications, 2015-03, Vol.459 (1), p.166-171

2015

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Identification and functional characterization of KLF5 as a novel disease gene responsible for familial dilated cardiomyopathy

European journal of medical genetics, 2020-04, Vol.63 (4), p.103827-103827, Article 103827

2020

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A novel TBX5 mutation predisposes to familial cardiac septal defects and atrial fibrillation as well as bicuspid aortic valve

Genetics and molecular biology, 2020-01, Vol.43 (4), p.e20200142-e20200142

2020

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The Resonance Suppression for Parallel Photovoltaic Grid-connected Inverters in Weak Grid

International journal of automation and computing, 2018-12, Vol.15 (6), p.716-727

2018

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TBX20 loss-of-function mutation contributes to double outlet right ventricle

International journal of molecular medicine, 2015-04, Vol.35 (4), p.1058-1066

2015

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miR-218 Involvement in Cardiomyocyte Hypertrophy Is Likely through Targeting REST

International journal of molecular sciences, 2016-06, Vol.17 (6), p.848-848

2016

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GATA5 loss-of-function mutation in familial dilated cardiomyopathy

International journal of molecular medicine, 2015-03, Vol.35 (3), p.763-770

2015

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Methylglyoxal accumulation contributes to accelerated brain aging in spontaneously hypertensive rats

Free radical biology & medicine, 2024-01, Vol.210, p.108-119

2024

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Effects of antiarrhythmic peptide 10 on acute ventricular arrhythmia

Asian Pacific journal of tropical medicine, 2015-03, Vol.8 (3), p.229-233

2015

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Research progress of cathode catalyst for field-assisted Li-O2/CO2 battery

Journal of energy storage, 2024-05, Vol.86, p.111252, Article 111252

2024

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A novel HAND2 loss-of-function mutation responsible for tetralogy of Fallot

International journal of molecular medicine, 2016-02, Vol.37 (2), p.445-451

2016

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From Amorphous Carbon to Carbon Nanobelts and Vertically Oriented Graphene Nanosheets Synthesized by Plasma-enhanced Chemical Vapor Deposition

Chemical research in Chinese universities, 2013-08, Vol.29 (4), p.755-758

2013

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MnOx/Ni(OH)2 Nanocomposite Materials for High-Performance Electrochemical Capacitor Application

Journal of nano research, 2012-12, Vol.20, p.53-60

2012

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Multi-objective economic dispatch of power system with wind farm considering flexible load response

IET generation, transmission & distribution, 2018-05

2018

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Effects of antiarrhythmic peptide 10 on acute ventricular arrhythmia

亚太热带医药杂志（英文版）, 2015, Vol.8 (3), p.229-233

2015

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Expression of the CXCL12/CXCR4 and CXCL16/CXCR6 axes in cervical intraepithelial neoplasia and cervical cancer

Ai zheng, 2013-05, Vol.32 (5), p.289-296

2013

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PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome: e0124409

PloS one, 2015-04, Vol.10 (4)

2015

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The study on screening of subsidiary heterogeneity of enterprise group

Zhao, Mei Cui

2011

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High Saturation Magnetization Fe-Co-N Thin Film Deposited by Facing-Target Direct Current Magnetron Sputtering

Advanced materials research, 2012, Vol.415-417, p.1949-1952

2012

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SOX17 Loss-of-Function Mutation Underlying Familial Pulmonary Arterial Hypertension

A New TBX5 Loss-of-Function Mutation Contributes to Congenital Heart Defect and Atrioventricular Block

PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome

A Novel NKX2.5 Loss-of-Function Mutation Associated With Congenital Bicuspid Aortic Valve

Detection and functional characterization of a novel MEF2A variation responsible for familial dilated cardiomyopathy

A New ISL1 Loss-of-Function Mutation Predisposes to Congenital Double Outlet Right Ventricle

TBX5 loss-of-function mutation contributes to familial dilated cardiomyopathy

Identification and functional characterization of KLF5 as a novel disease gene responsible for familial dilated cardiomyopathy

A novel TBX5 mutation predisposes to familial cardiac septal defects and atrial fibrillation as well as bicuspid aortic valve

The Resonance Suppression for Parallel Photovoltaic Grid-connected Inverters in Weak Grid

TBX20 loss-of-function mutation contributes to double outlet right ventricle

miR-218 Involvement in Cardiomyocyte Hypertrophy Is Likely through Targeting REST

GATA5 loss-of-function mutation in familial dilated cardiomyopathy

Methylglyoxal accumulation contributes to accelerated brain aging in spontaneously hypertensive rats

Effects of antiarrhythmic peptide 10 on acute ventricular arrhythmia

Research progress of cathode catalyst for field-assisted Li-O2/CO2 battery

A novel HAND2 loss-of-function mutation responsible for tetralogy of Fallot

From Amorphous Carbon to Carbon Nanobelts and Vertically Oriented Graphene Nanosheets Synthesized by Plasma-enhanced Chemical Vapor Deposition

MnOx/Ni(OH)2 Nanocomposite Materials for High-Performance Electrochemical Capacitor Application

Multi-objective economic dispatch of power system with wind farm considering flexible load response

Effects of antiarrhythmic peptide 10 on acute ventricular arrhythmia

Expression of the CXCL12/CXCR4 and CXCL16/CXCR6 axes in cervical intraepithelial neoplasia and cervical cancer

PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome: e0124409

The study on screening of subsidiary heterogeneity of enterprise group

High Saturation Magnetization Fe-Co-N Thin Film Deposited by Facing-Target Direct Current Magnetron Sputtering

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