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Repair pathway for PARP-1 DNA-protein crosslinks

DNA repair, 2019-01, Vol.73, p.71-77

2019

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Oxidized nucleotide insertion by pol β confounds ligation during base excision repair

Nature communications, 2017-01, Vol.8 (1), p.14045-11, Article 14045

2017

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Systematic screening for CYP3A4 genetic polymorphisms in a Han Chinese population

Pharmacogenomics, 2017-03, Vol.18 (4), p.369-379

2017

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Transcriptional mutagenesis mediated by 8-oxoG induces translational errors in mammalian cells

Proceedings of the National Academy of Sciences - PNAS, 2018-04, Vol.115 (16), p.4218-4222

2018

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The Pol β variant containing exon α is deficient in DNA polymerase but has full dRP lyase activity

Scientific reports, 2019-07, Vol.9 (1), p.9928-11, Article 9928

2019

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Assessments of CYP-inhibition-based drug-drug interaction between vonoprazan and poziotinib in vitro and in vivo

Pharmaceutical biology, 2023-12, Vol.61 (1), p.356-361

2023

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Adipose‐specific deletion of Kif5b exacerbates obesity and insulin resistance in a mouse model of diet‐induced obesity

The FASEB journal, 2017-06, Vol.31 (6), p.2533-2547

2017

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In vitro functional characterization of 37 CYP2C9 allelic isoforms found in Chinese Han population

Acta pharmacologica Sinica, 2013-11, Vol.34 (11), p.1449-1456

2013

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Identification and drug metabolic characterization of four new CYP2C9 variants CYP2C972 - 75 in the Chinese Han population

Frontiers in pharmacology, 2022-12, Vol.13, p.1007268-1007268

2022

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In Vitro Assessment of 36 CYP2C9 Allelic Isoforms Found in the Chinese Population on the Metabolism of Glimepiride

Basic & clinical pharmacology & toxicology, 2014-04, Vol.114 (4), p.305-310

2014

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In Vitro Functional Assessment of 22 Newly Identified CYP2D6 Allelic Variants in the Chinese Population

Basic & clinical pharmacology & toxicology, 2015-07, Vol.117 (1), p.39-43

2015

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Effects of 22 Novel CYP2D6 Variants Found in the Chinese Population on the Bufuralol and Dextromethorphan Metabolisms In Vitro

Basic & clinical pharmacology & toxicology, 2016-03, Vol.118 (3), p.190-199

2016

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Genetic variants, haplotype determination, and function of novel alleles of CYP2B6 in a Han Chinese population

Heliyon, 2024-04, Vol.10 (7), p.e28952-e28952, Article e28952

2024

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Naringenin has an inhibitory effect on rivaroxaban in rats both in vitro and in vivo

Pharmacology research & perspectives, 2021-05, Vol.9 (3)

2021

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Effects of CYP2C19 variants on methadone metabolism in vitro

Drug testing and analysis, 2017-04, Vol.9 (4), p.634-639

2017

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In vitro metabolism of phenytoin in 36 CYP2C9 variants found in the Chinese population

Chemico-biological interactions, 2016-06, Vol.253, p.93-99

2016

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Functional characterization of the defective CYP2C9 variant CYP2C918

Pharmacology research & perspectives, 2021-02, Vol.9 (1), p.e00718-n/a

2021

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In vitro and in vivo characterization of 13 CYP2C9 allelic variants found in Chinese Han population

Drug metabolism and disposition, 2015-04, Vol.43 (4), p.561-569

2015

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Effect of CYP2D6 genetic polymorphism on the metabolism of citalopram in vitro

Drug metabolism and pharmacokinetics, 2016-04, Vol.31 (2), p.133-138

2016

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Functional characterization of 22 novel CYP2D6 variants for the metabolism of Tamoxifen

Journal of pharmacy and pharmacology, 2016-06, Vol.68 (6), p.819-825

2016

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Characterization of a Novel CYP2C9 Mutation (1009C>A) Detected in a Warfarin-Sensitive Patient

Journal of Pharmacological Sciences, 2014/06/20, Vol.125(2), pp.150-156

2014

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Oxidative Damage to RNA and Expression Patterns of MTH1 in the Hippocampi of Senescence-Accelerated SAMP8 Mice and Alzheimer’s Disease Patients

Neurochemical research, 2011-08, Vol.36 (8), p.1558-1565

2011

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MTH1 suppression enhances the stemness of MCF7 through upregulation of STAT3

Free radical biology & medicine, 2022-08, Vol.188, p.447-458

2022

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Role of cytochrome P450 2D6 genetic polymorphism in carvedilol hydroxylation in vitro

Drug design, development and therapy, 2016-01, Vol.10 (Issue 1), p.1909-1916

2016

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Repair pathway for PARP-1 DNA-protein crosslinks

Oxidized nucleotide insertion by pol β confounds ligation during base excision repair

Systematic screening for CYP3A4 genetic polymorphisms in a Han Chinese population

Transcriptional mutagenesis mediated by 8-oxoG induces translational errors in mammalian cells

The Pol β variant containing exon α is deficient in DNA polymerase but has full dRP lyase activity

High-Resolution Analyses of Human Leukocyte Antigens Allele and Haplotype Frequencies Based on 169,995 Volunteers from the China Bone Marrow Donor Registry Program

Assessments of CYP-inhibition-based drug-drug interaction between vonoprazan and poziotinib in vitro and in vivo

Adipose‐specific deletion of Kif5b exacerbates obesity and insulin resistance in a mouse model of diet‐induced obesity

In vitro functional characterization of 37 CYP2C9 allelic isoforms found in Chinese Han population

Identification and drug metabolic characterization of four new CYP2C9 variants CYP2C972 - 75 in the Chinese Han population

In Vitro Assessment of 36 CYP2C9 Allelic Isoforms Found in the Chinese Population on the Metabolism of Glimepiride

In Vitro Functional Assessment of 22 Newly Identified CYP2D6 Allelic Variants in the Chinese Population

Effects of 22 Novel CYP2D6 Variants Found in the Chinese Population on the Bufuralol and Dextromethorphan Metabolisms In Vitro

Genetic variants, haplotype determination, and function of novel alleles of CYP2B6 in a Han Chinese population

Naringenin has an inhibitory effect on rivaroxaban in rats both in vitro and in vivo

Effects of CYP2C19 variants on methadone metabolism in vitro

In vitro metabolism of phenytoin in 36 CYP2C9 variants found in the Chinese population

Functional characterization of the defective CYP2C9 variant CYP2C918

In vitro and in vivo characterization of 13 CYP2C9 allelic variants found in Chinese Han population

Effect of CYP2D6 genetic polymorphism on the metabolism of citalopram in vitro

Functional characterization of 22 novel CYP2D6 variants for the metabolism of Tamoxifen

Characterization of a Novel CYP2C9 Mutation (1009C>A) Detected in a Warfarin-Sensitive Patient

Oxidative Damage to RNA and Expression Patterns of MTH1 in the Hippocampi of Senescence-Accelerated SAMP8 Mice and Alzheimer’s Disease Patients

MTH1 suppression enhances the stemness of MCF7 through upregulation of STAT3

Role of cytochrome P450 2D6 genetic polymorphism in carvedilol hydroxylation in vitro

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