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An Improved Flower Pollination Optimizer Algorithm for Multilevel Image Thresholding

IEEE access, 2019, Vol.7, p.165571-165582

2019

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Detection and localization of citrus fruit based on improved You Only Look Once v5s and binocular vision in the orchard

Frontiers in plant science, 2022-07, Vol.13, p.972445-972445

2022

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Global Survey of Phosphotyrosine Signaling Identifies Oncogenic Kinases in Lung Cancer

Cell, 2007-12, Vol.131 (6), p.1190-1203

2007

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An adaptive gravitational search algorithm for multilevel image thresholding

The Journal of supercomputing, 2021-09, Vol.77 (9), p.10590-10607

2021

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Comprehensive analysis of lncRNA biomarkers in kidney renal clear cell carcinoma by lncRNA-mediated ceRNA network

PloS one, 2021-06, Vol.16 (6), p.e0252452-e0252452

2021

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Identification of circRNA-miRNA-mRNA regulatory network and its role in cardiac hypertrophy

PloS one, 2023-03, Vol.18 (3), p.e0279638-e0279638

2023

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Deep color calibration for UAV imagery in crop monitoring using semantic style transfer with local to global attention

International journal of applied earth observation and geoinformation, 2021-12, Vol.104, p.102590, Article 102590

2021

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Identification of circRNA-miRNA-mRNA regulatory network and its role in cardiac hypertrophy

PloS one, 2023-03, Vol.18 (3)

2023

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Survey of tyrosine kinase signaling reveals ROS kinase fusions in human cholangiocarcinoma

PloS one, 2011-01, Vol.6 (1), p.e15640-e15640

2011

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Differential evolution with mixed mutation strategy based on deep reinforcement learning

Applied soft computing, 2021-11, Vol.111, p.107678, Article 107678

2021

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Whole-exome sequencing identified a novel heterozygous mutation of SALL1 and a new homozygous mutation of PTPRQ in a Chinese family with Townes-Brocks syndrome and hearing loss

BMC medical genomics, 2021-01, Vol.14 (1), p.24-7, Article 24

2021

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Identification and Integrate Analysis of Key Biomarkers for Diagnosis and Prognosis of Non-Small Cell Lung Cancer Based on Bioinformatics Analysis

Technology in cancer research & treatment, 2021, Vol.20, p.15330338211060202

2021

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Whole-exome sequencing identifies a novel CCDC151 mutation, c.325G>T (p.E109X), in a patient with primary ciliary dyskinesia and situs inversus

Journal of human genetics, 2019-03, Vol.64 (3), p.249-252

2019

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The M310T mutation in the GATA4 gene is a novel pathogenic target of the familial atrial septal defect

BMC cardiovascular disorders, 2021-01, Vol.21 (1), p.12-12, Article 12

2021

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Whole-Exome Sequencing Identified CFTR Variants in Two Consanguineous Families in China

Frontiers in genetics, 2021-07, Vol.12, p.631221-631221

2021

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Case report: A new de novo mutation of the Troponin T2 gene in a Chinese patient with dilated cardiomyopathy

Frontiers in cardiovascular medicine, 2023-11, Vol.10

2023

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An Improved Integrated Prediction Method of Cyber Security Situation Based on Spatial-time Analysis

Wangji Wanglu Jishu Xuekan = Journal of Internet Technology, 2018-11, Vol.19 (6), p.1789-1800

2018

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A novel mutation of glycogen synthase kinase-3β leads to a reduced level of GSK3β protein in a patient with dilated cardiomyopathy

Genes & diseases, 2024-01, Vol.11 (1), p.84-86

2024

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Differential evolution with adaptive mutation strategy based on fitness landscape analysis

Information sciences, 2021-03, Vol.549, p.142-163

2021

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A novel mutation in the tropomyosin 1 gene in a Chinese patient with hypertrophic cardiomyopathy

All life (Online), 2022-12, Vol.15 (1), p.1264-1272

2022

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Establishment of a Dihydrofolate Reductase Gene Knock-In Zebrafish Strain to Aid Preliminary Analysis of Congenital Heart Disease Mechanisms

Frontiers in cardiovascular medicine, 2021-12, Vol.8, p.763851-763851

2021

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Chemical characterization of Auricularia auricula polysaccharides and its pharmacological effect on heart antioxidant enzyme activities and left ventricular function in aged mice

International journal of biological macromolecules, 2010-04, Vol.46 (3), p.284-288

2010

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Whole-Exome Sequencing Identifies a Novel Variant (c.1538T > C) of TNNI3K in Arrhythmogenic Right Ventricular Cardiomyopathy

Frontiers in cardiovascular medicine, 2022-02, Vol.9, p.843837-843837

2022

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Whole‐exome sequencing identified a novel homozygous ASPH frameshift variant causing Traboulsi syndrome in a Chinese family

Molecular genetics & genomic medicine, 2021-01, Vol.9 (1), p.e1553-n/a

2021

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Interleukin-6, tumor necrosis factor-alpha and receptor activator of nuclear factor kappa ligand are elevated in hypertrophic gastric mucosa of pachydermoperiostosis

Scientific reports, 2017-08, Vol.7 (1), p.9686-9, Article 9686

2017

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An Improved Flower Pollination Optimizer Algorithm for Multilevel Image Thresholding

Detection and localization of citrus fruit based on improved You Only Look Once v5s and binocular vision in the orchard

Global Survey of Phosphotyrosine Signaling Identifies Oncogenic Kinases in Lung Cancer

An adaptive gravitational search algorithm for multilevel image thresholding

Comprehensive analysis of lncRNA biomarkers in kidney renal clear cell carcinoma by lncRNA-mediated ceRNA network

Identification of circRNA-miRNA-mRNA regulatory network and its role in cardiac hypertrophy

Deep color calibration for UAV imagery in crop monitoring using semantic style transfer with local to global attention

Identification of circRNA-miRNA-mRNA regulatory network and its role in cardiac hypertrophy

Survey of tyrosine kinase signaling reveals ROS kinase fusions in human cholangiocarcinoma

Differential evolution with mixed mutation strategy based on deep reinforcement learning

Whole-exome sequencing identified a novel heterozygous mutation of SALL1 and a new homozygous mutation of PTPRQ in a Chinese family with Townes-Brocks syndrome and hearing loss

Identification and Integrate Analysis of Key Biomarkers for Diagnosis and Prognosis of Non-Small Cell Lung Cancer Based on Bioinformatics Analysis

Whole-exome sequencing identifies a novel CCDC151 mutation, c.325G>T (p.E109X), in a patient with primary ciliary dyskinesia and situs inversus

The M310T mutation in the GATA4 gene is a novel pathogenic target of the familial atrial septal defect

Whole-Exome Sequencing Identified CFTR Variants in Two Consanguineous Families in China

Case report: A new de novo mutation of the Troponin T2 gene in a Chinese patient with dilated cardiomyopathy

An Improved Integrated Prediction Method of Cyber Security Situation Based on Spatial-time Analysis

A novel mutation of glycogen synthase kinase-3β leads to a reduced level of GSK3β protein in a patient with dilated cardiomyopathy

Differential evolution with adaptive mutation strategy based on fitness landscape analysis

A novel mutation in the tropomyosin 1 gene in a Chinese patient with hypertrophic cardiomyopathy

Establishment of a Dihydrofolate Reductase Gene Knock-In Zebrafish Strain to Aid Preliminary Analysis of Congenital Heart Disease Mechanisms

Chemical characterization of Auricularia auricula polysaccharides and its pharmacological effect on heart antioxidant enzyme activities and left ventricular function in aged mice

Whole-Exome Sequencing Identifies a Novel Variant (c.1538T > C) of TNNI3K in Arrhythmogenic Right Ventricular Cardiomyopathy

Whole‐exome sequencing identified a novel homozygous ASPH frameshift variant causing Traboulsi syndrome in a Chinese family

Interleukin-6, tumor necrosis factor-alpha and receptor activator of nuclear factor kappa ligand are elevated in hypertrophic gastric mucosa of pachydermoperiostosis

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