Chunyan Peng

发表

Profiling of carbonyl compounds in serum by stable isotope labeling - Double precursor ion scan - Mass spectrometry analysis.

Bifeng Yuan, Yuqi Feng, Quan-Fei Zhu, 2017, Analytica chimica acta.

A novel truncation mutation in CRYBB1 associated with autosomal dominant congenital cataract with nystagmus

Ming Yan, Guohua Yang, Fang Zheng, 2017, Molecular vision.

Genomic 5-mC contents in peripheral blood leukocytes were independent protective factors for coronary artery disease with a specific profile in different leukocyte subtypes

Bifeng Yuan, Qianyun Deng, F. Zheng, 2018, Clinical Epigenetics.

DNA hydroxymethylation age of human blood determined by capillary hydrophilic-interaction liquid chromatography/mass spectrometry

Bifeng Yuan, Yuqi Feng, Qianyun Deng, 2015, Clinical Epigenetics.

Associations of ChREBP and Global DNA Methylation with Genetic and Environmental Factors in Chinese Healthy Adults

Xue-bin Wang, F. Zheng, Xue-ping Qiu, 2016, PloS one.

Risk-Association of DNMT1 Gene Polymorphisms with Coronary Artery Disease in Chinese Han Population

Qianyun Deng, Cong Li, F. Zheng, 2014, International journal of molecular sciences.

Facile one-pot synthesis of a aptamer-based organic-silica hybrid monolithic capillary column by "thiol-ene" click chemistry for detection of enantiomers of chemotherapeutic anthracyclines.

Bifeng Yuan, Yuqi Feng, Yu-Xiu Xiao, 2014, The Analyst.

Glutathione S-transferase M1 null genotype and hepatocellular carcinoma susceptibility in China and India: evidence from an updated meta-analysis.

Ming Yan, Fang Zheng, Jie Peng, 2014, Asian Pacific journal of cancer prevention : APJCP.

Glutathione S-transferase M 1 Null Genotype and Hepatocellular Carcinoma Susceptibility in China and India : Evidence from an Updated Meta-analysis

Ming Yan, Fang Zheng, Jie Peng, 2014 .

Two families with Leber's hereditary optic neuropathy carrying G11778A and T14502C mutations with haplogroup H2a2a1 in mitochondrial DNA.

Ming Yan, Chen Qiao, Tanwei Wei, 2015, Molecular medicine reports.

Two families with Leber ' s hereditary optic neuropathy carrying G 11778 A and T 14502 C mutations with haplogroup H 2 a 2 a 1 in mitochondrial DNA

M. Yan, Chen Qiao, Tanwei Wei, 2022 .

Genomic 5-mC contents in peripheral blood leukocytes were independent protective factors for coronary artery disease with a specific profile in different leukocyte subtypes

Bifeng Yuan, Qianyun Deng, F. Zheng, 2018, Clinical Epigenetics.

Development and Validation of a Nomogram to Assist Monitoring Nosocomial SARS-CoV-2 Infection of Hospitalized Patients

Chen Wang, Fang-fang Zheng, Xue-ping Qiu, 2022, Journal of inflammation research.