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Meimei Dongye

Showing results (1-10 of 22) with videos related to

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Genes|November 11, 2022
Anterior Umbilication of Lens in a Family with Congenital Cataracts Associated with a Missense Mutation of <i>MIP</i> GeneZhixing Cheng, Xun Wang, Qiwei Wang, et al.
Drug Delivery|March 22, 2019
Development and effects of tacrolimus-loaded nanoparticles on the inhibition of corneal allograft rejectionQianni Wu, Dong Liu, Xulin Zhang, et al.
Annals of Translational Medicine|March 12, 2021
Elongated axial length and myopia-related fundus changes associated with the Arg130Cys mutation in the <i>LIM2</i> gene in four Chinese families with congenital cataractsXun Wang, Yanli Qin, Aierxiding Abudoukeremuahong, et al.
Frontiers in Cell and Developmental Biology|January 25, 2021
The Metabolic Reprogramming of <i>Frem2</i> Mutant Mice Embryos in Cryptophthalmos DevelopmentXiayin Zhang, Ruixin Wang, Ting Wang, et al.
Npj Aging|May 20, 2026
Discordance between measured and perceived vision in older adults: the need for objective screening despite health consciousnessXueer Tu, Xun Wang, Lanqin Zhao, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 28, 2025
The synergistic effect of c-Myb hyperactivation and Pu.1 deficiency induces Pelger-Huët anomaly and promotes sAMLSong'en Xu, Jiaxin Hong, Meimei Dongye, et al.
Communications Biology|June 1, 2026
CBX4 enhances acute monocytic leukemia development via HDAC-mediated suppression of Runx1Yin Ye, Yueying Zhang, Tingting Wang, et al.
Experimental Cell Research|November 22, 2020
Extracellular vesicles promote epithelial-to-mesenchymal transition of lens epithelial cells under oxidative stressRuixin Wang, Jianbing Li, Xiayin Zhang, et al.
NPJ Digital Medicine|November 4, 2020
Deep learning from "passive feeding" to "selective eating" of real-world dataZhongwen Li, Chong Guo, Danyao Nie, et al.
Frontiers in Medicine|November 1, 2021
Broadening the Mutation Spectrum in <i>GJA8</i> and <i>CHMP4B</i>: Novel Missense Variants and the Associated Phenotypes in Six Chinese Han Congenital Cataracts FamiliesXun Wang, Dongni Wang, Qiwei Wang, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Genes|November 11, 2022
Anterior Umbilication of Lens in a Family with Congenital Cataracts Associated with a Missense Mutation of <i>MIP</i> GeneZhixing Cheng, Xun Wang, Qiwei Wang, et al.
Drug Delivery|March 22, 2019
Development and effects of tacrolimus-loaded nanoparticles on the inhibition of corneal allograft rejectionQianni Wu, Dong Liu, Xulin Zhang, et al.
Annals of Translational Medicine|March 12, 2021
Elongated axial length and myopia-related fundus changes associated with the Arg130Cys mutation in the <i>LIM2</i> gene in four Chinese families with congenital cataractsXun Wang, Yanli Qin, Aierxiding Abudoukeremuahong, et al.
Frontiers in Cell and Developmental Biology|January 25, 2021
The Metabolic Reprogramming of <i>Frem2</i> Mutant Mice Embryos in Cryptophthalmos DevelopmentXiayin Zhang, Ruixin Wang, Ting Wang, et al.
Npj Aging|May 20, 2026
Discordance between measured and perceived vision in older adults: the need for objective screening despite health consciousnessXueer Tu, Xun Wang, Lanqin Zhao, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 28, 2025
The synergistic effect of c-Myb hyperactivation and Pu.1 deficiency induces Pelger-Huët anomaly and promotes sAMLSong'en Xu, Jiaxin Hong, Meimei Dongye, et al.
Communications Biology|June 1, 2026
CBX4 enhances acute monocytic leukemia development via HDAC-mediated suppression of Runx1Yin Ye, Yueying Zhang, Tingting Wang, et al.
Experimental Cell Research|November 22, 2020
Extracellular vesicles promote epithelial-to-mesenchymal transition of lens epithelial cells under oxidative stressRuixin Wang, Jianbing Li, Xiayin Zhang, et al.
NPJ Digital Medicine|November 4, 2020
Deep learning from "passive feeding" to "selective eating" of real-world dataZhongwen Li, Chong Guo, Danyao Nie, et al.
Frontiers in Medicine|November 1, 2021
Broadening the Mutation Spectrum in <i>GJA8</i> and <i>CHMP4B</i>: Novel Missense Variants and the Associated Phenotypes in Six Chinese Han Congenital Cataracts FamiliesXun Wang, Dongni Wang, Qiwei Wang, et al.
Pageof 3