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An ultra-broadband terahertz metamaterial coherent absorber using multilayer electric ring resonator structures based on anti-reflection coating

Nanoscale, 2020-05, Vol.12 (17), p.9769-9775

2020

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Characteristic analysis of epileptic brain network based on attention mechanism

Scientific reports, 2023-07, Vol.13 (1), p.10742-10742, Article 10742

2023

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Comparative efficacy and tolerability of three treatments in old people with osteoporotic vertebral compression fracture: a network meta-analysis and systematic review

PloS one, 2015-04, Vol.10 (4), p.e0123153

2015

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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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Albumin-based smart nanoplatform for ultrasound-mediated enhanced chemo‐sonodynamic combination therapy

Materials & design, 2023-03, Vol.227, p.111794, Article 111794

2023

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Dual-responsive nanomotors for deep tumor penetration and subcellular arrangement

Materials & design, 2022-10, Vol.222, p.111039, Article 111039

2022

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LECT2 protects mice against bacterial sepsis by activating macrophages via the CD209a receptor

The Journal of experimental medicine, 2013-01, Vol.210 (1), p.5-13

2013

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Nafamostat mesilate attenuates inflammation and apoptosis and promotes locomotor recovery after spinal cord injury

CNS neuroscience & therapeutics, 2018-05, Vol.24 (5), p.429-438

2018

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Characterization of P2X7R and its function in the macrophages of ayu, Plecoglossus altivelis

PloS one, 2013-02, Vol.8 (2), p.e57505

2013

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Clinical presentation and outcome of pediatric patients with hemophagocytic lymphohistiocytosis in China: A retrospective multicenter study

Pediatric blood & cancer, 2017-04, Vol.64 (4), p.np-n/a

2017

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miR-496/MMP10 Is Involved in the Proliferation of IL-1β-Induced Fibroblast-Like Synoviocytes Via Mediating the NF-κB Signaling Pathway

Inflammation, 2021-08, Vol.44 (4), p.1359-1369

2021

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Centella asiatica alleviates psoriasis through JAK/STAT3-mediated inflammation: An in vitro and in vivo study

Journal of ethnopharmacology, 2023-12, Vol.317, p.116746-116746, Article 116746

2023

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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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LECT2 drives haematopoietic stem cell expansion and mobilization via regulating the macrophages and osteolineage cells

Nature communications, 2016-09, Vol.7 (1), p.12719-12719, Article 12719

2016

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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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Broad‐band angle insensitive frequency‐selective surface with multiple resonant modes

Microwave and optical technology letters, 2018-11, Vol.60 (11), p.2660-2664

2018

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Identification of SOX18 as a New Gene Predisposing to Congenital Heart Disease

Diagnostics (Basel), 2022-08, Vol.12 (8), p.1917

2022

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Consequences of the μ − τ reflection symmetry for leptogenesis in a seesaw model with diagonal Dirac neutrino mass matrix

Physical review. D, 2024-05, Vol.109 (9), Article 095047

2024

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MicroRNA changes of bone marrow-derived mesenchymal stem cells differentiated into neuronal-like cells by Schwann cell-conditioned medium

Neural regeneration research, 2019-08, Vol.14 (8), p.1462-1469

2019

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Long-Term Prognostic Factors in Patients With Antineutrophil Cytoplasmic Antibody-Associated Vasculitis: A 15-Year Multicenter Retrospective Study

Frontiers in immunology, 2022-06, Vol.13, p.913667

2022

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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.502-511

2018

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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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KLF15 Loss-of-Function Mutation Underlying Atrial Fibrillation as well as Ventricular Arrhythmias and Cardiomyopathy

Genes, 2021-03, Vol.12 (3), p.408

2021

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Characterization and immunologic functions of the macrophage migration inhibitory factor from Japanese sea bass, Lateolabrax japonicus

Fish & shellfish immunology, 2019-03, Vol.86, p.947-955

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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An ultra-broadband terahertz metamaterial coherent absorber using multilayer electric ring resonator structures based on anti-reflection coating

Characteristic analysis of epileptic brain network based on attention mechanism

Comparative efficacy and tolerability of three treatments in old people with osteoporotic vertebral compression fracture: a network meta-analysis and systematic review

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

Albumin-based smart nanoplatform for ultrasound-mediated enhanced chemo‐sonodynamic combination therapy

Dual-responsive nanomotors for deep tumor penetration and subcellular arrangement

LECT2 protects mice against bacterial sepsis by activating macrophages via the CD209a receptor

Nafamostat mesilate attenuates inflammation and apoptosis and promotes locomotor recovery after spinal cord injury

Characterization of P2X7R and its function in the macrophages of ayu, Plecoglossus altivelis

Clinical presentation and outcome of pediatric patients with hemophagocytic lymphohistiocytosis in China: A retrospective multicenter study

miR-496/MMP10 Is Involved in the Proliferation of IL-1β-Induced Fibroblast-Like Synoviocytes Via Mediating the NF-κB Signaling Pathway

Centella asiatica alleviates psoriasis through JAK/STAT3-mediated inflammation: An in vitro and in vivo study

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

LECT2 drives haematopoietic stem cell expansion and mobilization via regulating the macrophages and osteolineage cells

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

Broad‐band angle insensitive frequency‐selective surface with multiple resonant modes

Identification of SOX18 as a New Gene Predisposing to Congenital Heart Disease

Consequences of the μ − τ reflection symmetry for leptogenesis in a seesaw model with diagonal Dirac neutrino mass matrix

MicroRNA changes of bone marrow-derived mesenchymal stem cells differentiated into neuronal-like cells by Schwann cell-conditioned medium

Long-Term Prognostic Factors in Patients With Antineutrophil Cytoplasmic Antibody-Associated Vasculitis: A 15-Year Multicenter Retrospective Study

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

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

KLF15 Loss-of-Function Mutation Underlying Atrial Fibrillation as well as Ventricular Arrhythmias and Cardiomyopathy

Characterization and immunologic functions of the macrophage migration inhibitory factor from Japanese sea bass, Lateolabrax japonicus

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

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