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Wenjun Xia

Showing results (61-70 of 83) with videos related to

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Journal of Agricultural and Food Chemistry|December 22, 2022
Transcriptome Dynamics of Common Bean Roots Exposed to Various Heavy Metals Reveal Valuable Target Genes and Promoters for Genetic EngineeringPingping Fang, Yannan Hu, Wenjun Xia, et al.
Medical Physics|October 8, 2025
A hybrid training database and evaluation benchmark for assessing metal artifact reduction methods for X-ray CT imagingNils Peters, Eri Haneda, Jiayong Zhang, et al.
Human Molecular Genetics|December 26, 2016
SLC44A4 mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing lossZhaoxin Ma, Wenjun Xia, Fei Liu, et al.
IEEE Transactions on Neural Networks and Learning Systems|October 4, 2023
SOUL-Net: A Sparse and Low-Rank Unrolling Network for Spectral CT Image ReconstructionXiang Chen, Wenjun Xia, Ziyuan Yang, et al.
Inflammation|December 20, 2024
CircIRAK3 Promotes Neutrophil Extracellular Trap Formation by Improving the Stability of ELANE mRNA in SepsisYao Lu, Huang Wu, Yuanyuan Luo, et al.
BMC Public Health|February 9, 2022
Construction of Xinjiang metabolic syndrome risk prediction model based on interpretable modelsYan Zhang, Jaina Razbek, Deyang Li, et al.
FEBS Letters|June 15, 2019
Mutations in TOP2B cause autosomal-dominant hereditary hearing loss via inhibition of the PI3K-Akt signalling pathwayWenjun Xia, Jiongjiong Hu, Jing Ma, et al.
Human Molecular Genetics|September 2, 2017
SLC44A4 mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing lossZhaoxin Ma, Wenjun Xia, Fei Liu, et al.
The International Journal of Developmental Biology|October 28, 2015
Down-regulation of msrb3 and destruction of normal auditory system development through hair cell apoptosis in zebrafishXiaofang Shen, Fei Liu, Yingzhi Wang, et al.
Iscience|January 4, 2024
Promoting fast MR imaging pipeline by full-stack AIZhiwen Wang, Bowen Li, Hui Yu, et al.
Pageof 9

Showing results (61-70 of 83) with videos related to

Sort By:
Pageof 9
Journal of Agricultural and Food Chemistry|December 22, 2022
Transcriptome Dynamics of Common Bean Roots Exposed to Various Heavy Metals Reveal Valuable Target Genes and Promoters for Genetic EngineeringPingping Fang, Yannan Hu, Wenjun Xia, et al.
Medical Physics|October 8, 2025
A hybrid training database and evaluation benchmark for assessing metal artifact reduction methods for X-ray CT imagingNils Peters, Eri Haneda, Jiayong Zhang, et al.
Human Molecular Genetics|December 26, 2016
SLC44A4 mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing lossZhaoxin Ma, Wenjun Xia, Fei Liu, et al.
IEEE Transactions on Neural Networks and Learning Systems|October 4, 2023
SOUL-Net: A Sparse and Low-Rank Unrolling Network for Spectral CT Image ReconstructionXiang Chen, Wenjun Xia, Ziyuan Yang, et al.
Inflammation|December 20, 2024
CircIRAK3 Promotes Neutrophil Extracellular Trap Formation by Improving the Stability of ELANE mRNA in SepsisYao Lu, Huang Wu, Yuanyuan Luo, et al.
BMC Public Health|February 9, 2022
Construction of Xinjiang metabolic syndrome risk prediction model based on interpretable modelsYan Zhang, Jaina Razbek, Deyang Li, et al.
FEBS Letters|June 15, 2019
Mutations in TOP2B cause autosomal-dominant hereditary hearing loss via inhibition of the PI3K-Akt signalling pathwayWenjun Xia, Jiongjiong Hu, Jing Ma, et al.
Human Molecular Genetics|September 2, 2017
SLC44A4 mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing lossZhaoxin Ma, Wenjun Xia, Fei Liu, et al.
The International Journal of Developmental Biology|October 28, 2015
Down-regulation of msrb3 and destruction of normal auditory system development through hair cell apoptosis in zebrafishXiaofang Shen, Fei Liu, Yingzhi Wang, et al.
Iscience|January 4, 2024
Promoting fast MR imaging pipeline by full-stack AIZhiwen Wang, Bowen Li, Hui Yu, et al.
Pageof 9