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Yanling Yang

Showing results (221-230 of 376) with videos related to

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Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|August 28, 2015
[Seven patients of argininemia with spastic tetraplegia as the first and major symptom and prenatal diagnosis of two fetuses with high risk]Tongfei Wu, Xiyuan Li, Yuan Ding, et al.
Annals of the Academy of Medicine, Singapore|November 12, 2009
Outcome of organic acidurias in ChinaYanling Yang, Zhang Yao, Jinqing Song, et al.
Langmuir : the ACS Journal of Surfaces and Colloids|December 12, 2025
Flexible Piezoresistive Sensors Based on PPy Particles Encapsulating Natural Flat Silkworm CocoonsShengnan Wang, Yujia Wang, Yanling Yang, et al.
Journal of Environmental Sciences (China)|May 29, 2019
Optimized coagulation pretreatment alleviates ultrafiltration membrane fouling: The role of floc properties and slow-mixing speed on mechanisms of chitosan-assisted coagulationPeng Du, Xing Li, Yanling Yang, et al.
Plos Pathogens|January 10, 2025
SLC35A2 gene product modulates paramyxovirus fusion events during infectionYanling Yang, Yuchen Wang, Danielle E Campbell, et al.
Bioresource Technology|November 18, 2024
Impact of carbon/nitrogen ratio on sequencing batch biofilm reactors initiated with different seed sludges for treating actual mariculture effluentsXiao-Yan Fan, Shi-Long Zhou, Yanling Yang, et al.
Angewandte Chemie (International Ed. in English)|December 6, 2023
Cascade In Situ Self-Assembly and Bioorthogonal Reaction Enable the Enrichment of Photosensitizers and Carbonic Anhydrase Inhibitors for Pretargeted Cancer TheranosticsXidan Wen, Wenhui Zeng, Junya Zhang, et al.
Scientific Reports|October 24, 2017
Molecular spectrum of excision repair cross-complementation group 8 gene defects in Chinese patients with Cockayne syndrome type AXiaozhu Wang, Yu Huang, Ming Yan, et al.
Gene|June 23, 2018
SURF1 mutations in Chinese patients with Leigh syndrome: Novel mutations, mutation spectrum, and the functional consequencesYuanyuan Li, Shumeng Wen, Dongxiao Li, et al.
Gene|July 30, 2015
Succinic semialdehyde dehydrogenase deficiency of four Chinese patients and prenatal diagnosis for three fetusesXiyuan Li, Yuan Ding, Yupeng Liu, et al.
Pageof 38

Showing results (221-230 of 376) with videos related to

Sort By:
Pageof 38
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|August 28, 2015
[Seven patients of argininemia with spastic tetraplegia as the first and major symptom and prenatal diagnosis of two fetuses with high risk]Tongfei Wu, Xiyuan Li, Yuan Ding, et al.
Annals of the Academy of Medicine, Singapore|November 12, 2009
Outcome of organic acidurias in ChinaYanling Yang, Zhang Yao, Jinqing Song, et al.
Langmuir : the ACS Journal of Surfaces and Colloids|December 12, 2025
Flexible Piezoresistive Sensors Based on PPy Particles Encapsulating Natural Flat Silkworm CocoonsShengnan Wang, Yujia Wang, Yanling Yang, et al.
Journal of Environmental Sciences (China)|May 29, 2019
Optimized coagulation pretreatment alleviates ultrafiltration membrane fouling: The role of floc properties and slow-mixing speed on mechanisms of chitosan-assisted coagulationPeng Du, Xing Li, Yanling Yang, et al.
Plos Pathogens|January 10, 2025
SLC35A2 gene product modulates paramyxovirus fusion events during infectionYanling Yang, Yuchen Wang, Danielle E Campbell, et al.
Bioresource Technology|November 18, 2024
Impact of carbon/nitrogen ratio on sequencing batch biofilm reactors initiated with different seed sludges for treating actual mariculture effluentsXiao-Yan Fan, Shi-Long Zhou, Yanling Yang, et al.
Angewandte Chemie (International Ed. in English)|December 6, 2023
Cascade In Situ Self-Assembly and Bioorthogonal Reaction Enable the Enrichment of Photosensitizers and Carbonic Anhydrase Inhibitors for Pretargeted Cancer TheranosticsXidan Wen, Wenhui Zeng, Junya Zhang, et al.
Scientific Reports|October 24, 2017
Molecular spectrum of excision repair cross-complementation group 8 gene defects in Chinese patients with Cockayne syndrome type AXiaozhu Wang, Yu Huang, Ming Yan, et al.
Gene|June 23, 2018
SURF1 mutations in Chinese patients with Leigh syndrome: Novel mutations, mutation spectrum, and the functional consequencesYuanyuan Li, Shumeng Wen, Dongxiao Li, et al.
Gene|July 30, 2015
Succinic semialdehyde dehydrogenase deficiency of four Chinese patients and prenatal diagnosis for three fetusesXiyuan Li, Yuan Ding, Yupeng Liu, et al.
Pageof 38