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Yuanzheng Feng

Showing results (1-10 of 5) with videos related to

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Archaea (Vancouver, B.C.)|August 8, 2020
Simulation of a Novel Tubular Microalgae Photobioreactor with Aerated Tangent Inner Tubes: Improvements in Mixing Performance and Flashing-Light EffectsXuyang Cui, Junhong Yang, Yuanzheng Feng, et al.
Sensors (Basel, Switzerland)|February 27, 2026
Experimental and Localisation Method for Non-Destructive Testing of Cable Corrosion Based on Weak Magnetic ImagingYujie Wu, Runchuan Xia, Yuanzheng Feng, et al.
Genes|October 23, 2021
Characterization of a Missense Mutation in the Catalytic Domain and a Splicing Mutation of Coagulation Factor X Compound Heterozygous in a Chinese PedigreeYuanzheng Feng, Jiewen Ma, Liang V Tang, et al.
Medcomm|October 9, 2023
Tissue-type plasminogen activator (tPA) homozygous Tyr471His mutation associates with thromboembolic diseaseYanyi Tao, Jiewen Ma, Yuanzheng Feng, et al.
Science Translational Medicine|November 30, 2022
Gene editing of human iPSCs rescues thrombophilia in hereditary antithrombin deficiency in miceLiang V Tang, Yanyi Tao, Yuanzheng Feng, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Archaea (Vancouver, B.C.)|August 8, 2020
Simulation of a Novel Tubular Microalgae Photobioreactor with Aerated Tangent Inner Tubes: Improvements in Mixing Performance and Flashing-Light EffectsXuyang Cui, Junhong Yang, Yuanzheng Feng, et al.
Sensors (Basel, Switzerland)|February 27, 2026
Experimental and Localisation Method for Non-Destructive Testing of Cable Corrosion Based on Weak Magnetic ImagingYujie Wu, Runchuan Xia, Yuanzheng Feng, et al.
Genes|October 23, 2021
Characterization of a Missense Mutation in the Catalytic Domain and a Splicing Mutation of Coagulation Factor X Compound Heterozygous in a Chinese PedigreeYuanzheng Feng, Jiewen Ma, Liang V Tang, et al.
Medcomm|October 9, 2023
Tissue-type plasminogen activator (tPA) homozygous Tyr471His mutation associates with thromboembolic diseaseYanyi Tao, Jiewen Ma, Yuanzheng Feng, et al.
Science Translational Medicine|November 30, 2022
Gene editing of human iPSCs rescues thrombophilia in hereditary antithrombin deficiency in miceLiang V Tang, Yanyi Tao, Yuanzheng Feng, et al.
Pageof 1