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左??(Zuo, Wei-gang),?毅(Zhang, Yi) 한국중어중문학회 2020 中語中文學 Vol.- No.80
The Chen Chunsheng was an important Christian writer in the late Qing Dynasty and early Republic of China. His work of Eastern Aesop’s fable was a parody of Aesop’s Fables, which was very popular among readers in the late Qing Dynasty and early Republic of China. In terms of content, it is mostly a story of Christian preaching, trying to establish an ideal Christian order, while at the same time seeking the moral improvement of the people, exposing social defects, caring about the destiny of the country, and full of enlightenment. Compared with the early translation and imitation of Aesop’s fables, Eastern Aesop’s fable presents two distinct features. First, it was completed by the Chinese writer instead of the preacher;Second, the content is entirely based on Chinese classics, not the western countries. From the perspective of religious communication, this is the result of a “cultural adaptation” policy, and from the literary point of view, in the early 20th century, Western literature was incorporated into China in a large amount, and in the context of “looking at the west,” Eastern Aesop’s fable turned to tradition, showing the reasonable landing of the world literature "text travel”.
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Apoptin Induces Apoptosis in Human Bladder Cancer EJ and BIU-87 Cells
Zhan, Hui,Wang, Jian-Song,Wang, Hai-Feng,Zuo, Yi-Gang,Wang, Chun-Hui,Ding, Ming-Xia Asian Pacific Journal of Cancer Prevention 2012 Asian Pacific journal of cancer prevention Vol.13 No.1
Objective: To investigate whether apoptin is a apoptosis-inducing protein with a potential for bladder cancer therapy. Methods: We constructed a PCDNA3/Apoptin eukaryotic expression vector, and transfected this vector into bladder cancer cell lines BIU-87 and EJ, then observed the results by RT-PCR, transmission electron microscopy, MTT assay and the flow cytometry (TUNEL method). Results: PCDNA3/Apoptin successfully induced a high level apoptosis in both bladder cancer cell lines, compared with the controls (p<0.05). Conclusions: Apoptin can induce high level apoptosis in human bladder cancer EJ and BIU-87 cells, which suggests a potential for human bladder cancer therapy.
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ppGalNAc T1 as a Potential Novel Marker for Human Bladder Cancer
Ding, Ming-Xia,Wang, Hai-Feng,Wang, Jian-Song,Zhan, Hui,Zuo, Yi-Gang,Yang, De-Lin,Liu, Jing-Yu,Wang, Wei,Ke, Chang-Xing,Yan, Ru-Ping Asian Pacific Journal of Cancer Prevention 2012 Asian Pacific journal of cancer prevention Vol.13 No.11
Objectives: To investigate the effect of glycopeptide-preferring polypeptide GalNAc transferase 1 (ppGalNAc T1 ) targeted RNA interference (RNAi) on the growth and migration of human bladder carcinoma EJ cells in vitro and in vivo. Methods: DNA microarray assays were performed to determine ppGalNAc Ts(ppGalNAc T1-9) expression in human bladder cancer and normal bladder tissues. We transfected the EJ bladder cancer cell line with well-designed ppGalNAc T1 siRNA. Boyden chamber and Wound healing assays were used to investigate changes of shppGalNAc T1-EJ cell migration. Proliferation of shppGalNAc T1-EJ cells in vitro was assessed using [3H]-thymidine incorporation assay and soft agar colony formation assays. Subcutaneous bladder tumors in BALB/c nude mice were induced by inoculation of shppGalNAc T1-EJ cells and after inoculation diameters of tumors were measured every 5 days to determine gross tumor volumes. Results: ppGalNAc T1 mRNA in bladder cancer tissues was 11.2-fold higher than in normal bladder tissues. When ppGalNAc T1 expression in EJ cells was knocked down through transfection by pSUPER-shppGalNAc T1 vector, markedly reduced incorporation of [3H]-thymidine into DNA of EJ cells was observed at all time points compared with the empty vector transfected control cells. However, ppGalNAc T1 knockdown did not significantly inhibited cell migration (only 12.3%). Silenced ppGalNAc T1 expression significantly inhibited subcutaneous tumor growth compared with the control groups injected with empty vector transfected control cells. At the end of observation course (40 days), the inhibitory rate of cancerous growth for ppGalNAc T1 knockdown was 52.5%. Conclusion: ppGalNAc T1 might be a potential novel marker for human bladder cancer. Although ppGalNAc T1 knockdown caused no remarkable change in cell migration, silenced expression significantly inhibited proliferation and tumor growth of the bladder cancer EJ cell line.
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