A Split G-Quadruplex and Graphene Oxide-Based Low-Background Platform for Fluorescence Authentication of Pseudostellaria heterophylla

Tekijä Zheng, Zhenzhu, Hu, Juan, He, Zhaodong
Julkaisussa Sensors (Basel) (2014)

G-Quadruplex DNAzyme Molecular Beacon for Amplified Colorimetric Biosensing of Pseudostellaria heterophylla

Tekijä Zheng, Zhenzhu, Han, Jing, Pang, Wensheng, Hu, Juan
Julkaistu 2013

A novel compound heterozygous variant identified in GLDC gene in a Chinese family with non-ketotic hyperglycinemia

Tekijä Lin, Yiming, Zheng, Zhenzhu, Sun, Wenjia, Fu, Qingliu
Julkaisussa BMC Med Genet (2018)

Occurrence of mcr Positive Strains and Molecular Characteristics of Two mcr-1 Positive Salmonella typhimurium and Escherichia coli from a Chinese Women’s and Children’s Hospital...

Tekijä Zheng, Zhenzhu, Lei, Ying, Wang, Yinna, Lin, Chunli, Lin, Jiansheng
Julkaisussa Infect Drug Resist (2021)

Hypoglycemic effect of polysaccharides with different molecular weight of Pseudostellaria heterophylla

Tekijä Hu, Juan, Pang, Wensheng, chen, Jinlong, Bai, Shaowei, Zheng, Zhenzhu, Wu, Xiaohua
Julkaistu 2013

Mild clinical features of isolated methylmalonic acidemia associated with a novel variant in the MMAA gene in two Chinese siblings

Tekijä Lin, Yiming, Lin, Chunmei, Lin, Weihua, Zheng, Zhenzhu, Han, Mingya, Fu, Qingliu
Julkaisussa BMC Med Genet (2018)

Clinical and genetic analysis of five Chinese patients with urea cycle disorders

Tekijä Zheng, Zhenzhu, Lin, Yiming, Lin, Weihua, Zhu, Lin, Jiang, Mengyi, Wang, Wenjun, Fu, Qingliu
Julkaisussa Mol Genet Genomic Med (2020)

Combined primary carnitine deficiency with neonatal intrahepatic cholestasis caused by citrin deficiency in a Chinese newborn

Tekijä Lin, Yiming, Lin, Weihua, Chen, Yanru, Lin, Chunmei, Zheng, Zhenzhu, Zhuang, Jianlong, Fu, Qingliu
Julkaisussa BMC Pediatr (2020)

Clinical, biochemical, and genetic analysis of a Chinese Han pedigree with holocarboxylase synthetase deficiency: a case report

Tekijä Zheng, Zhenzhu, Yuan, Gaopin, Zheng, Minyan, Lin, Yiming, Zheng, Faming, Jiang, Mengyi, Zhu, Lin, Fu, Qingliu
Julkaisussa BMC Med Genet (2020)

Biochemical, Clinical, and Genetic Characteristics of Short/Branched Chain Acyl-CoA Dehydrogenase Deficiency in Chinese Patients by Newborn Screening

Tekijä Lin, Yiming, Gao, Hongzhi, Lin, Chunmei, Chen, Yanru, Zhou, Shuang, Lin, Weihua, Zheng, Zhenzhu, Li, Xiaoqing, Li, Min, Fu, Qingliu
Julkaisussa Front Genet (2019)