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

par Zheng, Zhenzhu, Hu, Juan, He, Zhaodong
Publié dans Sensors (Basel) (2014)

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

par Zheng, Zhenzhu, Han, Jing, Pang, Wensheng, Hu, Juan
Publié 2013

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

par Lin, Yiming, Zheng, Zhenzhu, Sun, Wenjia, Fu, Qingliu
Publié dans 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...

par Zheng, Zhenzhu, Lei, Ying, Wang, Yinna, Lin, Chunli, Lin, Jiansheng
Publié dans Infect Drug Resist (2021)

Hypoglycemic effect of polysaccharides with different molecular weight of Pseudostellaria heterophylla

par Hu, Juan, Pang, Wensheng, chen, Jinlong, Bai, Shaowei, Zheng, Zhenzhu, Wu, Xiaohua
Publié 2013

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

par Lin, Yiming, Lin, Chunmei, Lin, Weihua, Zheng, Zhenzhu, Han, Mingya, Fu, Qingliu
Publié dans BMC Med Genet (2018)

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

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

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

par Lin, Yiming, Lin, Weihua, Chen, Yanru, Lin, Chunmei, Zheng, Zhenzhu, Zhuang, Jianlong, Fu, Qingliu
Publié dans BMC Pediatr (2020)

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

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

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

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