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Targeting the PDGF/PDGFR signaling pathway for cancer therapy: A review

International journal of biological macromolecules, 2022-03, Vol.202, p.539-557

2022

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Access to colorectal cancer screening in populations in China, 2020: A coverage‐focused synthesis analysis

International journal of cancer, 2024-08, Vol.155 (3), p.558-568

2024

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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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Connexin45 (GJC1) loss-of-function mutation contributes to familial atrial fibrillation and conduction disease

Heart rhythm, 2021-05, Vol.18 (5), p.684-693

2021

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An update on the molecular diagnosis of congenital heart disease: focus on loss-of-function mutations

Expert review of molecular diagnostics, 2017-04, Vol.17 (4), p.393-401

2017

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Estimating disability-adjusted life years for breast cancer and the impact of screening in female populations in China, 2015-2030: an exploratory prevalence-based analysis applying local weights

Population health metrics, 2022-10, Vol.20 (1), p.19-11, Article 19

2022

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Advanced interatrial block predicts clinical recurrence of atrial fibrillation after catheter ablation

Journal of cardiology, 2016-10, Vol.68 (4), p.352-356

2016

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Proteomic identification of malignant transformation-related proteins in esophageal squamous cell carcinoma

Journal of cellular biochemistry, 2008-08, Vol.104 (5), p.1625-1635

2008

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Effect of catheter ablation on clinical outcomes in patients with atrial fibrillation and significant functional mitral regurgitation

BMC cardiovascular disorders, 2021-12, Vol.21 (1), p.587-587, Article 587

2021

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Oncogenic PAX6 elicits CDK4/6 inhibitor resistance by epigenetically inactivating the LATS2‐Hippo signaling pathway

Clinical and translational medicine, 2021-08, Vol.11 (8), p.e503-n/a

2021

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HAND1 loss-of-function mutation contributes to congenital double outlet right ventricle

International journal of molecular medicine, 2017-03, Vol.39 (3), p.711-718

2017

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HAND1 Loss-of-Function Mutation Causes Tetralogy of Fallot

Pediatric cardiology, 2017-03, Vol.38 (3), p.547-557

2017

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Stent implantation for severe pulmonary vein stenosis or occlusion secondary to atrial fibrillation ablation

International journal of cardiology, 2020-02, Vol.301, p.85-89

2020

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Impact of prior permanent pacemaker on long‐term clinical outcomes of patients undergoing percutaneous coronary intervention

Clinical cardiology (Mahwah, N.J.), 2017-04, Vol.40 (4), p.205-209

2017

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MESP1 loss-of-function mutation contributes to double outlet right ventricle

Molecular medicine reports, 2017-09, Vol.16 (3), p.2747-2754

2017

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Dairy products consumption and metabolic syndrome in adults: systematic review and meta-analysis of observational studies

Scientific reports, 2015-09, Vol.5 (1), p.14606-14606, Article 14606

2015

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CASZ1 loss-of-function mutation associated with congenital heart disease

Gene, 2016-12, Vol.595 (1), p.62-68

2016

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CYP1A1, GSTs and mEH polymorphisms and susceptibility to esophageal carcinoma: study of population from a high- incidence area in north China

World journal of gastroenterology : WJG, 2003-07, Vol.9 (7), p.1394

2003

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Effect of Monascus aged vinegar on isoflavone conversion in soy germ by soaking treatment

Food chemistry, 2015-11, Vol.186, p.256-264

2015

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TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus

International journal of medical sciences, 2017-01, Vol.14 (4), p.323-332

2017

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Expression of Versican and Its Related Molecules in Patient with Multiple Myeloma and Its Clinical Significance

Zhongguo shi yan xue ye xue za zhi, 2020-08, Vol.28 (4), p.1228

2020

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Efficacy of intermittent pneumatic compression for venous thromboembolism prophylaxis in patients undergoing gynecologic surgery: A systematic review and meta-analysis

Oncotarget, 2017-03, Vol.8 (12), p.20371-20379

2017

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An Orthodontic Technique for Minimally Invasive Extraction of Impacted Lower Third Molar

Journal of oral and maxillofacial surgery, 2013-08, Vol.71 (8), p.1309-1317

2013

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Oocyte-expressed yes-associated protein is a key activator of the early zygotic genome in mouse

Cell research, 2016-03, Vol.26 (3), p.275-287

2016

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Expression of MUC1 in esophageal squamous-cell carcinoma and its relationship with prognosis of patients from Linzhou city, a high incidence area of northern China

World journal of gastroenterology : WJG, 2003-03, Vol.9 (3), p.404

2003

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Targeting the PDGF/PDGFR signaling pathway for cancer therapy: A review

Access to colorectal cancer screening in populations in China, 2020: A coverage‐focused synthesis analysis

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

Connexin45 (GJC1) loss-of-function mutation contributes to familial atrial fibrillation and conduction disease

An update on the molecular diagnosis of congenital heart disease: focus on loss-of-function mutations

Estimating disability-adjusted life years for breast cancer and the impact of screening in female populations in China, 2015-2030: an exploratory prevalence-based analysis applying local weights

Advanced interatrial block predicts clinical recurrence of atrial fibrillation after catheter ablation

Proteomic identification of malignant transformation-related proteins in esophageal squamous cell carcinoma

Effect of catheter ablation on clinical outcomes in patients with atrial fibrillation and significant functional mitral regurgitation

Oncogenic PAX6 elicits CDK4/6 inhibitor resistance by epigenetically inactivating the LATS2‐Hippo signaling pathway

HAND1 loss-of-function mutation contributes to congenital double outlet right ventricle

HAND1 Loss-of-Function Mutation Causes Tetralogy of Fallot

Stent implantation for severe pulmonary vein stenosis or occlusion secondary to atrial fibrillation ablation

Impact of prior permanent pacemaker on long‐term clinical outcomes of patients undergoing percutaneous coronary intervention

MESP1 loss-of-function mutation contributes to double outlet right ventricle

Dairy products consumption and metabolic syndrome in adults: systematic review and meta-analysis of observational studies

CASZ1 loss-of-function mutation associated with congenital heart disease

CYP1A1, GSTs and mEH polymorphisms and susceptibility to esophageal carcinoma: study of population from a high- incidence area in north China

Effect of Monascus aged vinegar on isoflavone conversion in soy germ by soaking treatment

TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus

Expression of Versican and Its Related Molecules in Patient with Multiple Myeloma and Its Clinical Significance

Efficacy of intermittent pneumatic compression for venous thromboembolism prophylaxis in patients undergoing gynecologic surgery: A systematic review and meta-analysis

An Orthodontic Technique for Minimally Invasive Extraction of Impacted Lower Third Molar

Oocyte-expressed yes-associated protein is a key activator of the early zygotic genome in mouse

Expression of MUC1 in esophageal squamous-cell carcinoma and its relationship with prognosis of patients from Linzhou city, a high incidence area of northern China

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