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Suppression of long non‐coding RNA TNRC6C‐AS1 protects against thyroid carcinoma through DNA demethylation of STK4 via the Hippo signalling pathway

Cell proliferation, 2019-05, Vol.52 (3), p.e12564-n/a

2019

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Treatment of lidocaine on subacute thyroiditis via restraining inflammatory factor expression and inhibiting pyroptosis pathway

Journal of cellular biochemistry, 2019-07, Vol.120 (7), p.10964-10971

2019

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Construction of core-shell heterojunction regulating α-Fe2O3 layer on CeO2 nanotube arrays enables highly efficient Z-scheme photoelectrocatalysis

Applied catalysis. B, Environmental, 2020-11, Vol.276, p.119138, Article 119138

2020

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Compound Heterozygous Mutations in the DUOX2/DUOXA2 Genes Cause Congenital Hypothyroidism

Yonsei Medical Journal, 2017, 58(4), , pp.888-890

2017

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Enhanced photoelectrocatalytic activity of direct Z-scheme porous amorphous carbon nitride/manganese dioxide nanorod arrays

Journal of colloid and interface science, 2019-12, Vol.557, p.644-654

2019

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Coexistence of resistance to thyroid hormone and ectopic thyroid: ten-year follow-up

Archives of Endocrinology and Metabolism, 2016-12, Vol.60 (6), p.601-604

2016

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Idebenone-Activating Autophagic Degradation of α-Synuclein via Inhibition of AKT-mTOR Pathway in a SH-SY5Y-A53T Model of Parkinson’s Disease: A Network Pharmacological Approach

Evidence-based complementary and alternative medicine, 2021, Vol.2021, p.8548380-14

2021

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Improvement of therapeutic effects of mesenchymal stem cells in myocardial infarction through genetic suppression of microRNA-142

Oncotarget, 2017-10, Vol.8 (49), p.85549-85558

2017

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A Novel c.554+5C>T Mutation in the DUOXA2 Gene Combined with p.R885Q Mutation in the DUOX2 Gene Causing Congenital Hypothyroidism

Journal of clinical research in pediatric endocrinology, 2016-06, Vol.8 (2), p.224-227

2016

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Compound heterozygous mutations (p.T561M and c.2422delT) in the TPO gene associated with congenital hypothyroidism

Journal of pediatric endocrinology & metabolism : JPEM, 2016-05, Vol.29 (5), p.567

2016

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The relationship between different feeding paterns on the colonization of s.mutans in the infants and early childhood and correlation analysis of s.mutans' genotype of the mother-children

Guo, Man Li

2011

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Incidence of Pleural Effusion in Patients with Pulmonary Embolism

Chinese medical journal, 2015-04, Vol.128 (8), p.1032-1036

2015

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Compound Heterozygous Mutations in the DUOX2/DUOXA2 Genes Cause Congenital Hypothyroidism

Yonsei medical journal, 2017-07, p.888-890

2017

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Ginsenoside Rd inhibits apoptosis following spinal cord ischemia/reperfusion injury

Neural regeneration research, 2014-09, Vol.9 (18), p.1678-1687

2014

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A Novel c.554+5CT Mutation in the DUOXA2 Gene Combined with p.R885Q Mutation in the DUOX2 Gene Causing Congenital Hypothyroidism

Journal of clinical research in pediatric endocrinology, 2016-06, Vol.8 (2), p.224

2016

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Value of 18F-FDG PET-CT in surveillance of postoperative colorectal cancer patients with various carcinoembryonic antigen concentrations

World journal of gastroenterology : WJG, 2014-06, Vol.20 (21), p.6608-6614

2014

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Protein sequence analysis based on hydropathy profile of amino acids

Journal of Zhejiang University. B. Science, 2012-02, Vol.13 (2), p.152-158

2012

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Feasibility and simulation model of a pilot scale membrane bioreactor for wastewater treatment and reuse from Chinese traditional medicine

Journal of environmental sciences (China), 2007-01, Vol.19 (2), p.129-134

2007

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Efficacy of Mild Hypothermia for the Treatment of Patients with Cardiac Arrest

Chinese medical journal, 2015-06, Vol.128 (11), p.1536-1542

2015

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Consensus by Chinese Expert Panel on Chlamydia trachomatis-Resistant and Chlamydia trachomatis-Persistent Infection

Chinese medical journal, 2017-12, Vol.130 (23), p.2852-2856

2017

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Combined effects of a high-fat diet and chronic valproic acid treatment on hepatic steatosis and hepatotoxicity in rats

Acta pharmacologica Sinica, 2014-03, Vol.35 (3), p.363-372

2014

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miR-511 promotes the proliferation of human hepatoma cells by targeting the 3＇UTR of B cell translocation gene 1 （BTG1） mRNA

中国药理学报：英文版, 2017, Vol.38 (8), p.1161-1170

Shu-qin ZHANG Zhe YANG Xiao-li CAI Man ZHAO Ming-ming SUN Jiong LI Guo-xing FENG Jin-yan FENG Li-hong YE Jun-qi NIU Xiao-dong ZHANG

2017

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Effects of subdiaphragmatic cardiac compression on cardiac arrest during liver transplantation

Chinese medical journal, 2012-06, Vol.125 (12), p.2228-2230

2012

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Regulation of lovastatin on a key inflammation-related microRNA in myocardial cells

Chinese medical journal, 2014, Vol.127 (16), p.2977-2981

2014

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Generation of dopaminergic neurons directly from mouse fibroblasts and fibroblast-derived neural progenitors

Cell research, 2012-04, Vol.22 (4), p.769-772

2012

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Suppression of long non‐coding RNA TNRC6C‐AS1 protects against thyroid carcinoma through DNA demethylation of STK4 via the Hippo signalling pathway

Treatment of lidocaine on subacute thyroiditis via restraining inflammatory factor expression and inhibiting pyroptosis pathway

Construction of core-shell heterojunction regulating α-Fe2O3 layer on CeO2 nanotube arrays enables highly efficient Z-scheme photoelectrocatalysis

Compound Heterozygous Mutations in the DUOX2/DUOXA2 Genes Cause Congenital Hypothyroidism

Enhanced photoelectrocatalytic activity of direct Z-scheme porous amorphous carbon nitride/manganese dioxide nanorod arrays

Coexistence of resistance to thyroid hormone and ectopic thyroid: ten-year follow-up

Idebenone-Activating Autophagic Degradation of α-Synuclein via Inhibition of AKT-mTOR Pathway in a SH-SY5Y-A53T Model of Parkinson’s Disease: A Network Pharmacological Approach

Improvement of therapeutic effects of mesenchymal stem cells in myocardial infarction through genetic suppression of microRNA-142

A Novel c.554+5C>T Mutation in the DUOXA2 Gene Combined with p.R885Q Mutation in the DUOX2 Gene Causing Congenital Hypothyroidism

Compound heterozygous mutations (p.T561M and c.2422delT) in the TPO gene associated with congenital hypothyroidism

The relationship between different feeding paterns on the colonization of s.mutans in the infants and early childhood and correlation analysis of s.mutans' genotype of the mother-children

Incidence of Pleural Effusion in Patients with Pulmonary Embolism

Compound Heterozygous Mutations in the DUOX2/DUOXA2 Genes Cause Congenital Hypothyroidism

Ginsenoside Rd inhibits apoptosis following spinal cord ischemia/reperfusion injury

A Novel c.554+5CT Mutation in the DUOXA2 Gene Combined with p.R885Q Mutation in the DUOX2 Gene Causing Congenital Hypothyroidism

Value of 18F-FDG PET-CT in surveillance of postoperative colorectal cancer patients with various carcinoembryonic antigen concentrations

Protein sequence analysis based on hydropathy profile of amino acids

Feasibility and simulation model of a pilot scale membrane bioreactor for wastewater treatment and reuse from Chinese traditional medicine

Efficacy of Mild Hypothermia for the Treatment of Patients with Cardiac Arrest

Consensus by Chinese Expert Panel on Chlamydia trachomatis-Resistant and Chlamydia trachomatis-Persistent Infection

Combined effects of a high-fat diet and chronic valproic acid treatment on hepatic steatosis and hepatotoxicity in rats

miR-511 promotes the proliferation of human hepatoma cells by targeting the 3＇UTR of B cell translocation gene 1 （BTG1） mRNA

Effects of subdiaphragmatic cardiac compression on cardiac arrest during liver transplantation

Regulation of lovastatin on a key inflammation-related microRNA in myocardial cells

Generation of dopaminergic neurons directly from mouse fibroblasts and fibroblast-derived neural progenitors

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