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Chenghan Wang

Showing results (1-10 of 11) with videos related to

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Frontiers in Neurology|November 8, 2024
Efficacy and safety of thrombectomy with or without intravenous thrombolysis in the treatment of acute basilar artery occlusion ischemic stroke: an updated systematic review and meta-analysisShuyi Tian, Mengqing Zou, Dan Li, et al.
Frontiers in Genetics|September 25, 2023
Non-syndromic enlarged vestibular aqueduct caused by novel compound mutations of the <i>SLC26A4</i> gene: a case report and literature reviewYunhua Huang, Linlin Li, Liqiu Pan, et al.
RSC Advances|January 6, 2023
The multifunctional Prussian blue/graphitic carbon nitride nanocomposites for fluorescence imaging-guided photothermal and photodynamic combination therapyXinxu Wang, Chenghan Wang, Yichen Xu, et al.
Diagnostic Microbiology and Infectious Disease|July 3, 2025
Assessment of hospital environmental and personal protective equipment contamination with influenza A and B viruses by ultrasensitive droplet digital PCRNingneng Zhai, Rongheng Tang, Ziyu Huang, et al.
Medicine|May 17, 2024
A novel discriminant algorithm for differential diagnosis of mild to moderate thalassemia and iron deficiency anemiaLiqiu Pan, Linlin Li, Yuling Qiu, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 3, 2023
Third-generation sequencing for genetic diseaseXiaoting Ling, Chenghan Wang, Linlin Li, et al.
Frontiers in Immunology|February 17, 2025
Case report: Novel multi-exon homozygous deletion of <i>ZBTB24</i> causes immunodeficiency, centromeric instability, and facial anomalies syndrome 2Yan Long, Chenghan Wang, Jie Xiao, et al.
Gene|July 15, 2024
A novel duplication mutation of SLC2A1 gene causing glucose transporter 1 deficiency syndromeChaoyu Huang, Yunhua Huang, Liqiu Pan, et al.
Gene|August 30, 2024
Corrigendum to "A novel duplication mutation of SLC2A1 gene causing glucose transporter 1 deficiency syndrome" [Gene 928 (2024) 148762]Chaoyu Huang, Yunhua Huang, Liqiu Pan, et al.
ACS Sensors|August 5, 2025
Ultrasensitive Single-Molecule Immunoassays Built on Digital Techniques for Low Amounts of Biomarker DetectionNingneng Zhai, Xiaoting Ling, Yunhua Huang, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Frontiers in Neurology|November 8, 2024
Efficacy and safety of thrombectomy with or without intravenous thrombolysis in the treatment of acute basilar artery occlusion ischemic stroke: an updated systematic review and meta-analysisShuyi Tian, Mengqing Zou, Dan Li, et al.
Frontiers in Genetics|September 25, 2023
Non-syndromic enlarged vestibular aqueduct caused by novel compound mutations of the <i>SLC26A4</i> gene: a case report and literature reviewYunhua Huang, Linlin Li, Liqiu Pan, et al.
RSC Advances|January 6, 2023
The multifunctional Prussian blue/graphitic carbon nitride nanocomposites for fluorescence imaging-guided photothermal and photodynamic combination therapyXinxu Wang, Chenghan Wang, Yichen Xu, et al.
Diagnostic Microbiology and Infectious Disease|July 3, 2025
Assessment of hospital environmental and personal protective equipment contamination with influenza A and B viruses by ultrasensitive droplet digital PCRNingneng Zhai, Rongheng Tang, Ziyu Huang, et al.
Medicine|May 17, 2024
A novel discriminant algorithm for differential diagnosis of mild to moderate thalassemia and iron deficiency anemiaLiqiu Pan, Linlin Li, Yuling Qiu, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 3, 2023
Third-generation sequencing for genetic diseaseXiaoting Ling, Chenghan Wang, Linlin Li, et al.
Frontiers in Immunology|February 17, 2025
Case report: Novel multi-exon homozygous deletion of <i>ZBTB24</i> causes immunodeficiency, centromeric instability, and facial anomalies syndrome 2Yan Long, Chenghan Wang, Jie Xiao, et al.
Gene|July 15, 2024
A novel duplication mutation of SLC2A1 gene causing glucose transporter 1 deficiency syndromeChaoyu Huang, Yunhua Huang, Liqiu Pan, et al.
Gene|August 30, 2024
Corrigendum to "A novel duplication mutation of SLC2A1 gene causing glucose transporter 1 deficiency syndrome" [Gene 928 (2024) 148762]Chaoyu Huang, Yunhua Huang, Liqiu Pan, et al.
ACS Sensors|August 5, 2025
Ultrasensitive Single-Molecule Immunoassays Built on Digital Techniques for Low Amounts of Biomarker DetectionNingneng Zhai, Xiaoting Ling, Yunhua Huang, et al.
Pageof 2