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Dongmei Su

Showing results (11-20 of 73) with videos related to

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Molecular Medicine (Cambridge, Mass.)|February 11, 2021
Elevated MST1 leads to apoptosis via depletion of YAP1 in cardiomyocytes exposed to high glucoseDongmei Su, Yanhua Li, Lina Guan, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 3, 2026
Integrated Proteomics and Metabolomics Analysis in Hippocampus of Rats With T2DM-Associated Cognitive DeclineYing Zhang, Jiale Yu, Dongmei Su, et al.
Behavioural Brain Research|March 7, 2024
Transcriptomic analysis to identify genes associated with hypothalamus vulnerability in aging mice with cognitive declineXiaofeng Tian, Zhixing Zhao, Jing Zhao, et al.
Neuroscience|May 27, 2025
Transcriptomic analysis reveals potential targets associated with hippocampus vulnerability in spatial cognitive dysfunctionof type 2 diabetes mellitus ratsYing Zhang, Dongmei Su, Yuru Liu, et al.
Genetic Testing and Molecular Biomarkers|March 28, 2017
TCF21 rs12190287 Polymorphisms Are Associated with Ventricular Septal Defects in a Chinese PopulationLiping Yang, Xiaobo Gao, Haiyan Luo, et al.
Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire|April 30, 2014
Role of Nodal-PITX2C signaling pathway in glucose-induced cardiomyocyte hypertrophyDongmei Su, Sun Jing, Lina Guan, et al.
Molecular Vision|August 10, 2012
A nonsense mutation of CRYGC associated with autosomal dominant congenital nuclear cataracts and microcornea in a Chinese pedigreeYuanyuan Guo, Dongmei Su, Qian Li, et al.
Plos One|May 11, 2022
Genome-wide analysis of methylation in rat fetal heart under hyperglycemia by methylation-dependent restriction site-associated DNA sequencingRui Meng, Junxian Song, Lina Guan, et al.
Cell Death Discovery|January 11, 2022
Metformin protects lens epithelial cells against senescence in a naturally aged mouse modelMengmeng Chen, Yushan Fu, Xu Wang, et al.
Molecular Vision|June 6, 2012
A novel T→G splice site mutation of CRYBA1/A3 associated with autosomal dominant nuclear cataracts in a Chinese familyZhenfei Yang, Dongmei Su, Qian Li, et al.
Pageof 8

Showing results (11-20 of 73) with videos related to

Sort By:
Pageof 8
Molecular Medicine (Cambridge, Mass.)|February 11, 2021
Elevated MST1 leads to apoptosis via depletion of YAP1 in cardiomyocytes exposed to high glucoseDongmei Su, Yanhua Li, Lina Guan, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 3, 2026
Integrated Proteomics and Metabolomics Analysis in Hippocampus of Rats With T2DM-Associated Cognitive DeclineYing Zhang, Jiale Yu, Dongmei Su, et al.
Behavioural Brain Research|March 7, 2024
Transcriptomic analysis to identify genes associated with hypothalamus vulnerability in aging mice with cognitive declineXiaofeng Tian, Zhixing Zhao, Jing Zhao, et al.
Neuroscience|May 27, 2025
Transcriptomic analysis reveals potential targets associated with hippocampus vulnerability in spatial cognitive dysfunctionof type 2 diabetes mellitus ratsYing Zhang, Dongmei Su, Yuru Liu, et al.
Genetic Testing and Molecular Biomarkers|March 28, 2017
TCF21 rs12190287 Polymorphisms Are Associated with Ventricular Septal Defects in a Chinese PopulationLiping Yang, Xiaobo Gao, Haiyan Luo, et al.
Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire|April 30, 2014
Role of Nodal-PITX2C signaling pathway in glucose-induced cardiomyocyte hypertrophyDongmei Su, Sun Jing, Lina Guan, et al.
Molecular Vision|August 10, 2012
A nonsense mutation of CRYGC associated with autosomal dominant congenital nuclear cataracts and microcornea in a Chinese pedigreeYuanyuan Guo, Dongmei Su, Qian Li, et al.
Plos One|May 11, 2022
Genome-wide analysis of methylation in rat fetal heart under hyperglycemia by methylation-dependent restriction site-associated DNA sequencingRui Meng, Junxian Song, Lina Guan, et al.
Cell Death Discovery|January 11, 2022
Metformin protects lens epithelial cells against senescence in a naturally aged mouse modelMengmeng Chen, Yushan Fu, Xu Wang, et al.
Molecular Vision|June 6, 2012
A novel T→G splice site mutation of CRYBA1/A3 associated with autosomal dominant nuclear cataracts in a Chinese familyZhenfei Yang, Dongmei Su, Qian Li, et al.
Pageof 8