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Pyroptosis: A New Frontier in Kidney Diseases

Oxidative medicine and cellular longevity, 2021, Vol.2021 (1), p.6686617-6686617

2021

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Melatonin Alleviates Contrast-Induced Acute Kidney Injury by Activation of Sirt3

Oxidative medicine and cellular longevity, 2021, Vol.2021 (1), p.6668887-6668887

2021

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MCC950, the NLRP3 Inhibitor, Protects against Cartilage Degradation in a Mouse Model of Osteoarthritis

Oxidative medicine and cellular longevity, 2021, Vol.2021 (1), p.4139048-4139048

2021

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Physiological Effects of Ferroptosis on Organ Fibrosis

Oxidative medicine and cellular longevity, 2022-09, Vol.2022, p.1-17

2022

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A Novel α-Galactosidase A Splicing Mutation Predisposes to Fabry Disease

Frontiers in genetics, 2019-02, Vol.10, p.60-60

2019

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M1 Bone Marrow-Derived Macrophage-Derived Extracellular Vesicles Inhibit Angiogenesis and Myocardial Regeneration Following Myocardial Infarction via the MALAT1/MicroRNA-25-3p/CDC42 Axis

Oxidative medicine and cellular longevity, 2021, Vol.2021 (1), p.9959746-9959746

2021

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Biogenic Selenium Nanoparticles Alleviate Intestinal Epithelial Barrier Damage through Regulating Endoplasmic Reticulum Stress-Mediated Mitophagy

Oxidative medicine and cellular longevity, 2022, Vol.2022, p.3982613-19

2022

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Genetic and functional analyses detect an EXT1 splicing pathogenic variant in a Chinese hereditary multiple exostosis (HME) family

Molecular genetics & genomic medicine, 2022-03, Vol.10 (3), p.e1878-n/a

2022

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P2X7R Mediates the Synergistic Effect of ATP and MSU Crystals to Induce Acute Gouty Arthritis

Oxidative medicine and cellular longevity, 2023, Vol.2023, p.3317307-12

2023

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A novel splicing pathogenic variant in COL1A1 causing osteogenesis imperfecta (OI) type I in a Chinese family

Molecular genetics & genomic medicine, 2020-09, Vol.8 (9), p.e1366-n/a

2020

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TNF-α Induces Neutrophil Apoptosis Delay and Promotes Intestinal Ischemia-Reperfusion-Induced Lung Injury through Activating JNK/FoxO3a Pathway

Oxidative medicine and cellular longevity, 2021, Vol.2021 (1), p.8302831-8302831

2021

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Investigating the Mechanisms of Jieduquyuziyin Prescription Improves Lupus Nephritis and Fibrosis via FXR in MRL/lpr Mice

Oxidative medicine and cellular longevity, 2022-07, Vol.2022, p.1-17

2022

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High ABCG4 Expression Is Associated with Poor Prognosis in Non-Small-Cell Lung Cancer Patients Treated with Cisplatin-Based Chemotherapy

PloS one, 2015-08, Vol.10 (8), p.e0135576-e0135576

2015

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Metabolism-Related Gene TXNRD1 Regulates Inflammation and Oxidative Stress Induced by Cigarette Smoke through the Nrf2/HO-1 Pathway in the Small Airway Epithelium

Oxidative medicine and cellular longevity, 2022-12, Vol.2022, p.7067623-16

2022

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HSPA12A Stimulates p38/ERK-AP-1 Signaling to Promote Angiogenesis and Is Required for Functional Recovery Postmyocardial Infarction

Oxidative medicine and cellular longevity, 2022-06, Vol.2022, p.1-16

2022

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Nur77 Deficiency Exacerbates Macrophage NLRP3 Inflammasome-Mediated Inflammation and Accelerates Atherosclerosis

Oxidative medicine and cellular longevity, 2022, Vol.2022, p.2017815-14

2022

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GJB2 c.235delC variant associated with autosomal recessive nonsyndromic hearing loss and auditory neuropathy spectrum disorder

Genetics and molecular biology, 2019-01, Vol.42 (1), p.48-51

2019

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MTMR14 Alleviates Chronic Obstructive Pulmonary Disease as a Regulator in Inflammation and Emphysema

Oxidative medicine and cellular longevity, 2022, Vol.2022, p.9300269-21

2022

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HO-1/CO Maintains Intestinal Barrier Integrity through NF-κB/MLCK Pathway in Intestinal HO-1-/- Mice

Oxidative medicine and cellular longevity, 2021, Vol.2021 (1), p.6620873-6620873

2021

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Case Report: A Missense Mutation in Dyskeratosis Congenita 1 Leads to a Benign Form of Dyskeratosis Congenita Syndrome With the Mucocutaneous Triad

Frontiers in pediatrics, 2022-04, Vol.10, p.834268

2022

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Coenzyme Q0 Inhibits NLRP3 Inflammasome Activation through Mitophagy Induction in LPS/ATP-Stimulated Macrophages

Oxidative medicine and cellular longevity, 2022-01, Vol.2022, p.1-15

2022

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Pharmic Activation of PKG2 Alleviates Diabetes-Induced Osteoblast Dysfunction by Suppressing PLCβ1-Ca2+-Mediated Endoplasmic Reticulum Stress

Oxidative medicine and cellular longevity, 2021-01, Vol.2021, p.5552530-5552530

2021

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Functional evaluation of a novel GLA causative mutation in Fabry disease

Molecular genetics & genomic medicine, 2019-09, Vol.7 (9), p.e864-n/a

2019

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Identification of a novel compound heterozygous IDUA mutation underlies Mucopolysaccharidoses type I in a Chinese pedigree

Molecular genetics & genomic medicine, 2020-01, Vol.8 (1), p.e1058-n/a

2020

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Effect of cauterizing esophageal mucosa in “double-patch” treatment for acquired benign tracheoesophageal fistula/bronchogastric stump fistula

The Journal of surgical research, 2017-03, Vol.209, p.1-7

2017

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Pyroptosis: A New Frontier in Kidney Diseases

Melatonin Alleviates Contrast-Induced Acute Kidney Injury by Activation of Sirt3

MCC950, the NLRP3 Inhibitor, Protects against Cartilage Degradation in a Mouse Model of Osteoarthritis

Physiological Effects of Ferroptosis on Organ Fibrosis

A Novel α-Galactosidase A Splicing Mutation Predisposes to Fabry Disease

M1 Bone Marrow-Derived Macrophage-Derived Extracellular Vesicles Inhibit Angiogenesis and Myocardial Regeneration Following Myocardial Infarction via the MALAT1/MicroRNA-25-3p/CDC42 Axis

Biogenic Selenium Nanoparticles Alleviate Intestinal Epithelial Barrier Damage through Regulating Endoplasmic Reticulum Stress-Mediated Mitophagy

Genetic and functional analyses detect an EXT1 splicing pathogenic variant in a Chinese hereditary multiple exostosis (HME) family

P2X7R Mediates the Synergistic Effect of ATP and MSU Crystals to Induce Acute Gouty Arthritis

A novel splicing pathogenic variant in COL1A1 causing osteogenesis imperfecta (OI) type I in a Chinese family

TNF-α Induces Neutrophil Apoptosis Delay and Promotes Intestinal Ischemia-Reperfusion-Induced Lung Injury through Activating JNK/FoxO3a Pathway

Investigating the Mechanisms of Jieduquyuziyin Prescription Improves Lupus Nephritis and Fibrosis via FXR in MRL/lpr Mice

High ABCG4 Expression Is Associated with Poor Prognosis in Non-Small-Cell Lung Cancer Patients Treated with Cisplatin-Based Chemotherapy

Metabolism-Related Gene TXNRD1 Regulates Inflammation and Oxidative Stress Induced by Cigarette Smoke through the Nrf2/HO-1 Pathway in the Small Airway Epithelium

HSPA12A Stimulates p38/ERK-AP-1 Signaling to Promote Angiogenesis and Is Required for Functional Recovery Postmyocardial Infarction

Nur77 Deficiency Exacerbates Macrophage NLRP3 Inflammasome-Mediated Inflammation and Accelerates Atherosclerosis

GJB2 c.235delC variant associated with autosomal recessive nonsyndromic hearing loss and auditory neuropathy spectrum disorder

MTMR14 Alleviates Chronic Obstructive Pulmonary Disease as a Regulator in Inflammation and Emphysema

HO-1/CO Maintains Intestinal Barrier Integrity through NF-κB/MLCK Pathway in Intestinal HO-1-/- Mice

Case Report: A Missense Mutation in Dyskeratosis Congenita 1 Leads to a Benign Form of Dyskeratosis Congenita Syndrome With the Mucocutaneous Triad

Coenzyme Q0 Inhibits NLRP3 Inflammasome Activation through Mitophagy Induction in LPS/ATP-Stimulated Macrophages

Pharmic Activation of PKG2 Alleviates Diabetes-Induced Osteoblast Dysfunction by Suppressing PLCβ1-Ca2+-Mediated Endoplasmic Reticulum Stress

Functional evaluation of a novel GLA causative mutation in Fabry disease

Identification of a novel compound heterozygous IDUA mutation underlies Mucopolysaccharidoses type I in a Chinese pedigree

Effect of cauterizing esophageal mucosa in “double-patch” treatment for acquired benign tracheoesophageal fistula/bronchogastric stump fistula

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