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Study on diamond vacuum brazed with Cu-based filler metal containing Cr

International journal of advanced manufacturing technology, 2017-07, Vol.91 (5-8), p.1453-1460

2017

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Influence of inorganic ions and humic acid on the removal of Pb(II) and Hg(II) in water by zero-valent iron

Huanjing kexue, 2014-08, Vol.35 (8), p.2985

2014

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Removal of Hg in wastewater by zero-valent iron

Huanjing kexue, 2013-11, Vol.34 (11), p.4304

2013

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Transcatheter coil embolization of multiple coronary artery-to-left ventricle fistulas： report of a rare case

Chinese medical journal, 2008-07, Vol.121 (14), p.1342-1344

2008

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Wall shear stress in portal vein of cirrhotic patients with portal hypertension

World journal of gastroenterology : WJG, 2017-05, Vol.23 (18), p.3279-3286

2017

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Dearomatization‐Rearomatization Reaction of Metal‐Polarized Aza‐ortho‐Quinone Methides

Angewandte Chemie International Edition, 2023-05, Vol.62 (21), p.e202301592-n/a

International ed. in English, 2023

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De Novo Construction of Chiral Aminoindolines by Cu-Catalyzed Asymmetric Cyclization and Subsequent Discovery of an Unexpected Sulfonyl Migration

Journal of the American Chemical Society, 2022-11, Vol.144 (43), p.19932-19941

2022

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In situ trace element and sulfur isotope of pyrite constrain ore genesis in the Shapoling molybdenum deposit, East Qinling Orogen, China

Ore geology reviews, 2019-02, Vol.105, p.123-136

2019

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Knockdown of LINC01087 inhibits gastric cancer malignant behavior by regulating the miR-135a-5p/CAAP1 axis

Functional & integrative genomics, 2023-09, Vol.23 (3), p.248-248, Article 248

2023

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GATA4 Loss-of-Function Mutations Underlie Familial Tetralogy of Fallot

Human mutation, 2013-12, Vol.34 (12), p.1662-1671

2013

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GATA4 Loss-of-Function Mutation and the Congenitally Bicuspid Aortic Valve

The American journal of cardiology, 2018-02, Vol.121 (4), p.469-474

2018

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MEF2C loss-of-function mutation associated with familial dilated cardiomyopathy

Clinical chemistry and laboratory medicine, 2018-02, Vol.56 (3), p.502

2018

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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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Real-time observation of soliton pulsation in net normal-dispersion dissipative soliton fiber laser

Chinese physics B, 2023-02, Vol.32 (2), p.24210-366

2023

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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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Prevalence and Spectrum of NKX2-5 Mutations Associated With Sporadic Adult-Onset Dilated Cardiomyopathy

International Heart Journal, 2017, Vol.58(4), pp.521-529

2017

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Large scale environmental drivers of biocrust distribution and development across a sandy desert in China

Catena (Giessen), 2021-05, Vol.200, p.105137, Article 105137

2021

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ZBTB17 loss-of-function mutation contributes to familial dilated cardiomyopathy

Heart and vessels, 2018-07, Vol.33 (7), p.722-732

2018

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GATA4 loss-of-function mutation underlies familial dilated cardiomyopathy

Biochemical and biophysical research communications, 2013-10, Vol.439 (4), p.591-596

2013

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A novel NKX2-5 loss-of-function mutation predisposes to familial dilated cardiomyopathy and arrhythmias

International journal of molecular medicine, 2015-02, Vol.35 (2), p.478-486

2015

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GATA6 loss-of-function mutations contribute to familial dilated cardiomyopathy

International journal of molecular medicine, 2014-11, Vol.34 (5), p.1315-1322

2014

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CASZ1 loss-of-function mutation contributes to familial dilated cardiomyopathy

Clinical chemistry and laboratory medicine, 2017, Vol.55 (9), p.1417

2017

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A novel NR2F2 loss-of-function mutation predisposes to congenital heart defect

European journal of medical genetics, 2018-04, Vol.61 (4), p.197-203

2018

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HAND2 loss-of-function mutation causes familial dilated cardiomyopathy

European journal of medical genetics, 2019-09, Vol.62 (9), p.103540-103540, Article 103540

2019

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A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis

G3 : genes - genomes - genetics, 2016-04, Vol.6 (4), p.987-992

2016

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Study on diamond vacuum brazed with Cu-based filler metal containing Cr

Influence of inorganic ions and humic acid on the removal of Pb(II) and Hg(II) in water by zero-valent iron

Removal of Hg in wastewater by zero-valent iron

Transcatheter coil embolization of multiple coronary artery-to-left ventricle fistulas： report of a rare case

Wall shear stress in portal vein of cirrhotic patients with portal hypertension

Dearomatization‐Rearomatization Reaction of Metal‐Polarized Aza‐ortho‐Quinone Methides

De Novo Construction of Chiral Aminoindolines by Cu-Catalyzed Asymmetric Cyclization and Subsequent Discovery of an Unexpected Sulfonyl Migration

In situ trace element and sulfur isotope of pyrite constrain ore genesis in the Shapoling molybdenum deposit, East Qinling Orogen, China

Knockdown of LINC01087 inhibits gastric cancer malignant behavior by regulating the miR-135a-5p/CAAP1 axis

GATA4 Loss-of-Function Mutations Underlie Familial Tetralogy of Fallot

GATA4 Loss-of-Function Mutation and the Congenitally Bicuspid Aortic Valve

MEF2C loss-of-function mutation associated with familial dilated cardiomyopathy

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

Real-time observation of soliton pulsation in net normal-dispersion dissipative soliton fiber laser

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

Prevalence and Spectrum of NKX2-5 Mutations Associated With Sporadic Adult-Onset Dilated Cardiomyopathy

Large scale environmental drivers of biocrust distribution and development across a sandy desert in China

ZBTB17 loss-of-function mutation contributes to familial dilated cardiomyopathy

GATA4 loss-of-function mutation underlies familial dilated cardiomyopathy

A novel NKX2-5 loss-of-function mutation predisposes to familial dilated cardiomyopathy and arrhythmias

GATA6 loss-of-function mutations contribute to familial dilated cardiomyopathy

CASZ1 loss-of-function mutation contributes to familial dilated cardiomyopathy

A novel NR2F2 loss-of-function mutation predisposes to congenital heart defect

HAND2 loss-of-function mutation causes familial dilated cardiomyopathy

A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis

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