Year |
Citation |
Score |
2019 |
Bai X, Melesse M, Sorensen Turpin CG, Sloan D, Chen CY, Wang WC, Lee PY, Simmons JR, Nebenfuehr B, Mitchell D, Klebanow LR, Mattson N, Betzig E, Chen BC, Cheerambathur D, et al. Aurora B functions at the apical surface after specialized cytokinesis during morphogenesis in . Development (Cambridge, England). PMID 31806662 DOI: 10.1242/Dev.181099 |
0.613 |
|
2019 |
Chen CY, Liu YT, Lu CH, Lee PY, Tsai YC, Wu JS, Chen P, Chen BC. The Applications of Lattice Light-sheet Microscopy for Functional Volumetric Imaging of Hippocampal Neurons in a Three-Dimensional Culture System. Micromachines. 10. PMID 31514427 DOI: 10.3390/Mi10090599 |
0.596 |
|
2019 |
Lu CH, Tang WC, Liu YT, Chang SW, Wu FCM, Chen CY, Tsai YC, Yang SM, Kuo CW, Okada Y, Hwu YK, Chen P, Chen BC. Lightsheet localization microscopy enables fast, large-scale, and three-dimensional super-resolution imaging. Communications Biology. 2: 177. PMID 31098410 DOI: 10.1038/s42003-019-0403-9 |
0.551 |
|
2016 |
Chen CY, Chen YT, Wang JY, Huang YS, Tai CY. Postsynaptic Y654 dephosphorylation of β-catenin modulates presynaptic vesicle turnover through increased N-cadherin-mediated transsynaptic signaling. Developmental Neurobiology. PMID 27328456 DOI: 10.1002/Dneu.22411 |
0.614 |
|
2016 |
Liu YT, Nian FS, Chou WJ, Tai CY, Kwan SY, Chen C, Kuo PW, Lin PH, Chen CY, Huang CW, Lee YC, Soong BW, Tsai JW. PRRT2 mutations lead to neuronal dysfunction and neurodevelopmental defects. Oncotarget. PMID 27172900 DOI: 10.18632/oncotarget.9258 |
0.638 |
|
2012 |
Chen HF, Chen CY, Lin TH, Huang ZW, Chi TH, Ma YS, Wu SB, Wei YH, Hsieh M. The protective roles of phosphorylated heat shock protein 27 in human cells harboring myoclonus epilepsy with ragged-red fibers A8344G mtDNA mutation. The Febs Journal. 279: 2987-3001. PMID 22742457 DOI: 10.1111/J.1742-4658.2012.08678.X |
0.578 |
|
2011 |
Chen CY, Chen HF, Gi SJ, Chi TH, Cheng CK, Hsu CF, Ma YS, Wei YH, Liu CS, Hsieh M. Decreased heat shock protein 27 expression and altered autophagy in human cells harboring A8344G mitochondrial DNA mutation. Mitochondrion. 11: 739-49. PMID 21679777 DOI: 10.1016/J.Mito.2011.05.014 |
0.587 |
|
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