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Dynamical modulation of hypersynchronous seizure onset with transcranial magneto-acoustic stimulation in a hippocampal computational model

Chaos (Woodbury, N.Y.), 2024-04, Vol.34 (4)

2024

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Inhibition of long non-coding RNA XIST upregulates microRNA-149-3p to repress ovarian cancer cell progression

Cell death & disease, 2021-02, Vol.12 (2), p.145-145, Article 145

2021

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Prediction of Urban Taxi Travel Demand by Using Hybrid Dynamic Graph Convolutional Network Model

Sensors (Basel, Switzerland), 2022-08, Vol.22 (16), p.5982

2022

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Economic evaluation of first-line treatments for metastatic renal cell carcinoma: a cost-effectiveness analysis in a health resource-limited setting

PloS one, 2012-03, Vol.7 (3), p.e32530-e32530

2012

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Identification of diagnostic model in heart failure with myocardial fibrosis and conduction block by integrated gene co-expression network analysis

BMC medical genomics, 2024-02, Vol.17 (1), p.52-52

2024

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Variants in a cis-regulatory element of TBX1 in conotruncal heart defect patients impair GATA6-mediated transactivation

Orphanet journal of rare diseases, 2021-07, Vol.16 (1), p.334-334, Article 334

2021

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Predisposition to atrioventricular septal defects may be caused by SOX7 variants that impair interaction with GATA4

Molecular genetics and genomics : MGG, 2022-05, Vol.297 (3), p.671-687

2022

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Rare copy number variation analysis identifies disease-related variants in atrioventricular septal defect patients

Frontiers in genetics, 2023-02, Vol.14, p.1075349-1075349

2023

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Rare copy number variants analysis identifies novel candidate genes in heterotaxy syndrome patients with congenital heart defects

Genome medicine, 2018-05, Vol.10 (1), p.40-13, Article 40

2018

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Mutation Screening of Gata4 Gene in CTD Patients Within Chinese Han Population

Pediatric cardiology, 2017-03, Vol.38 (3), p.506-512

2017

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MiRNA-26a Contributes to the Acquisition of Malignant Behaviors of Doctaxel-Resistant Lung Adenocarcinoma Cells through Targeting EZH2

Cellular physiology and biochemistry, 2017-05, Vol.41 (2), p.583-597

2017

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Cost-Effectiveness and Budget Impact Analysis of Apatinib for Advanced Metastatic Gastric Cancer from the Perspective of Health Insurance System

Gastroenterology research and practice, 2017-01, Vol.2017, p.2816737-7

2017

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CTL Attenuation Regulated by PS1 in Cancer-Associated Fibroblast

Frontiers in immunology, 2020-06, Vol.11, p.999-999

2020

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Novel mutations of the SRF gene in Chinese sporadic conotruncal heart defect patients

BMC medical genetics, 2020-05, Vol.21 (1), p.95-95, Article 95

2020

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Investigating the Multiscale Impact of Environmental Factors on the Integrated Use of Dockless Bike-Sharing and Urban Rail Transit

Promet, 2023-01, Vol.35 (6), p.886-903

2023

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Efficacy and Safety of SPN-812 (Extended-Release Viloxazine) in Children and Adolescents with Attention-Deficit/Hyperactivity Disorder: A Systematic Review and Meta-Analysis

Brain sciences, 2023-11, Vol.13 (12), p.1627

2023

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Rare Copy Number Variants Identify Novel Genes in Sporadic Total Anomalous Pulmonary Vein Connection

Frontiers in genetics, 2018-11, Vol.9, p.559-559

2018

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A potential relationship among beta-defensins haplotype, SOX7 duplication and cardiac defects

PloS one, 2013-08, Vol.8 (8), p.e72515

2013

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Two genetic variants in NEXN and ABCC6 genes found in a patient with right coronary artery to right ventricle fistula combined with giant coronary aneurysm and patent ductus arteriosus

Frontiers in cardiovascular medicine, 2022-11, Vol.9, p.1048795-1048795

2022

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A 3 base pair deletion in TBX1 leads to reduced protein expression and transcriptional activity

Scientific reports, 2017-03, Vol.7 (1), p.44165-44165, Article 44165

2017

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Subgroup economic analysis for glioblastoma in a health resource-limited setting

PloS one, 2012-04, Vol.7 (4), p.e34588

2012

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A loss-of-function mutation p.T52S in RIPPLY3 is a potential predisposing genetic risk factor for Chinese Han conotruncal heart defect patients without the 22q11.2 deletion/duplication

Journal of translational medicine, 2018-09, Vol.16 (1), p.260-260, Article 260

2018

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Gene-guided gefitinib switch maintenance therapy for patients with advanced EGFR mutation-positive non-small cell lung cancer: an economic analysis

BMC cancer, 2013-01, Vol.13 (1), p.39-39, Article 39

2013

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miR-21 Is a Promising Novel Biomarker for Lymph Node Metastasis in Patients with Gastric Cancer

Gastroenterology research and practice, 2012-01, Vol.2012, p.640168-5

2012

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Patients Carrying 9q31.1-q32 Deletion Share Common Features with Cornelia de Lange Syndrome

Cellular physiology and biochemistry, 2015-01, Vol.35 (1), p.270-280

2015

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Dynamical modulation of hypersynchronous seizure onset with transcranial magneto-acoustic stimulation in a hippocampal computational model

Inhibition of long non-coding RNA XIST upregulates microRNA-149-3p to repress ovarian cancer cell progression

Prediction of Urban Taxi Travel Demand by Using Hybrid Dynamic Graph Convolutional Network Model

Economic evaluation of first-line treatments for metastatic renal cell carcinoma: a cost-effectiveness analysis in a health resource-limited setting

Identification of diagnostic model in heart failure with myocardial fibrosis and conduction block by integrated gene co-expression network analysis

Variants in a cis-regulatory element of TBX1 in conotruncal heart defect patients impair GATA6-mediated transactivation

Predisposition to atrioventricular septal defects may be caused by SOX7 variants that impair interaction with GATA4

Rare copy number variation analysis identifies disease-related variants in atrioventricular septal defect patients

Rare copy number variants analysis identifies novel candidate genes in heterotaxy syndrome patients with congenital heart defects

Mutation Screening of Gata4 Gene in CTD Patients Within Chinese Han Population

MiRNA-26a Contributes to the Acquisition of Malignant Behaviors of Doctaxel-Resistant Lung Adenocarcinoma Cells through Targeting EZH2

Cost-Effectiveness and Budget Impact Analysis of Apatinib for Advanced Metastatic Gastric Cancer from the Perspective of Health Insurance System

CTL Attenuation Regulated by PS1 in Cancer-Associated Fibroblast

Novel mutations of the SRF gene in Chinese sporadic conotruncal heart defect patients

Investigating the Multiscale Impact of Environmental Factors on the Integrated Use of Dockless Bike-Sharing and Urban Rail Transit

Efficacy and Safety of SPN-812 (Extended-Release Viloxazine) in Children and Adolescents with Attention-Deficit/Hyperactivity Disorder: A Systematic Review and Meta-Analysis

Rare Copy Number Variants Identify Novel Genes in Sporadic Total Anomalous Pulmonary Vein Connection

A potential relationship among beta-defensins haplotype, SOX7 duplication and cardiac defects

Two genetic variants in NEXN and ABCC6 genes found in a patient with right coronary artery to right ventricle fistula combined with giant coronary aneurysm and patent ductus arteriosus

A 3 base pair deletion in TBX1 leads to reduced protein expression and transcriptional activity

Subgroup economic analysis for glioblastoma in a health resource-limited setting

A loss-of-function mutation p.T52S in RIPPLY3 is a potential predisposing genetic risk factor for Chinese Han conotruncal heart defect patients without the 22q11.2 deletion/duplication

Gene-guided gefitinib switch maintenance therapy for patients with advanced EGFR mutation-positive non-small cell lung cancer: an economic analysis

miR-21 Is a Promising Novel Biomarker for Lymph Node Metastasis in Patients with Gastric Cancer

Patients Carrying 9q31.1-q32 Deletion Share Common Features with Cornelia de Lange Syndrome

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