Showing results (1-10 of 32) with videos related to
Sort By:
Pageof 4
Sensors (Basel, Switzerland)|December 6, 2014
A split G-quadruplex and graphene oxide-based low-background platform for fluorescence authentication of Pseudostellaria heterophyllaZhenzhu Zheng, Juan Hu, Zhaodong HeOptics Letters|May 5, 2012
Saliency model for object detection: searching for novel items in the sceneZhenzhu Zheng, Tianxu Zhang, Luxin YanBMC Medical Genetics|January 7, 2018
A novel compound heterozygous variant identified in GLDC gene in a Chinese family with non-ketotic hyperglycinemiaYiming Lin, Zhenzhu Zheng, Wenjia Sun, et al.Molecular Genetics & Genomic Medicine|September 9, 2024
Incorporating Next-Generation Sequencing as a Second-Tier Test for Primary Carnitine DeficiencyYiming Lin, Zhenzhu Zheng, Weihua Lin, et al.Sensors (Basel, Switzerland)|January 18, 2013
G-quadruplex DNAzyme molecular beacon for amplified colorimetric biosensing of Pseudostellaria heterophyllaZhenzhu Zheng, Jing Han, Wensheng Pang, et al.Infection and Drug Resistance|August 5, 2021
Occurrence of <i>mcr</i> Positive Strains and Molecular Characteristics of Two <i>mcr-1</i> Positive <i>Salmonella typhimurium</i> and <i>Escherichia coli</i> from a Chinese Women's and Children's HospitalZhenzhu Zheng, Ying Lei, Yinna Wang, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|December 30, 2023
Newborn screening for primary carnitine deficiency using a second-tier genetic testYiming Lin, Chunmei Lin, Zhenzhu Zheng, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|October 27, 2023
Clinical and genetic analysis of 26 Chinese patients with neonatal intrahepatic cholestasis due to citrin deficiencyJiansheng Lin, Weihua Lin, Yiming Lin, et al.Orphanet Journal of Rare Diseases|October 1, 2025
Clinical and genetic analysis of four Chinese patients with holocarboxylase synthetase deficiency and metabolic acidosisZhenzhu Zheng, Weilin Peng, Yiming Lin, et al.Molecular Genetics and Metabolism Reports|August 27, 2024
Newborn screening and genetic diagnosis of 3-methylcrotonyl-CoA carboxylase deficiency in Quanzhou,ChinaWeihua Lin, Kunyi Wang, Yanru Chen, et al.Pageof 4