“CNE”造句，怎麼用CNE造句

5、NNAV對腫瘤細胞株CNE－1和CNE－2的細胞毒作用呈明顯時效關係。

7、Method:Microcolony formation assay was used in testing sensitivity of CNE 2Z to DDP.

9、Objective To investigate the inhibitory effect of SQ on CNE cells in vitro.

11、CONCLUSIONS: Radix Astragali injection can inhibit the proliferation of human nasopharyngeal carcinoma CNE-2 cell line and induce its apoptosis.

13、OBJECTIVE: to study the inhibitory action of Radix Astragali injection on human nasopharyngeal carcinoma CNE-2 cell line in vitro.

15、Objective To observe the impact of sulfated chitin on cell proliferation and cell cycle in nasopharyngeal cell line CNE-2Z.

17、The invasion of CNE cell is also inhibited after photodynamic therapy. There is a relationship between the change of invasion and 5-ALA concentration & energy density of lasers.

19、Objective to further confirm that the human NPC cell line CNE-2Z indeed has radiosensitivity heterogeneity and to discuss its related mechanism.

21、結論：CNE-2Z細胞的遷移能力與其所在的生長週期密切相關，*通道在各期CNE-2Z細胞的遷移過程中起著重要作用。

23、結果奧沙利鉑對CNE - 2細胞的生長抑制率隨*物濃度和作用時間的增加而增大。

25、目的研究口蝦蛄提取物對人鼻咽癌細胞（CNE-2Z）明膠酶分泌及活*的抑制作用。

2、The ability to metabolize MTT of CNE 2z cells decreased.

4、CONCLUSIONS: The migratory ability is associated with the cell cycle in CNE-2Z cells. Chloride channels play an important role in cell migration of CNE-2Z cells.

8、但是CNE有三項要求都不很合理。

12、ResultsThe growth of CNE-2 cells was significantly inhibited by Oxaliplatin in a dose-dependent and time-dependent fashion.

16、Methods Nasopharyngeal human squamous cells (CNE-2Z) were cultured and divided into the normoxia culture group (20% O2) and the hypoxia culture group (1% O2).

20、We have obtained foci of transformed NIH3T3 cells through transfection of human DNA from CNE-2 (an undifferentiated epithelial cell line of nasopharyngeal carcinoma).

24、光動力作用後，CNE細胞的侵襲能力也是被抑制的，與5-ALA濃度及鐳射的能量密度相關。

3、The Effect of Radiosensitization Induced by Bufalin on CNE-1;

10、Radiosensitization effect of resveratrol on nasopharyngeal carcinorma CNE-1 cell in vitro

18、AIM: To clarify the migration capability of nasopharyngeal carcinoma cells (CNE-2Z) at different stages of the cell cycle and the roles of chloride channels in cell migration.

1、CNE Coded with no exceptions data type.

14、To investigate the impact of vincristine (VCR) on the cell proliferation and cycle in nasopharyngeal carcinoma cell line CNE-2Z.

6、MTT was used to detect the proliferation of CNE cells infected with vAd-BZGM.

22、Conclusion The vector pcDNA3.1 (-) CMV·Egr -1CDglyTK may convert nonpoisonous prodrug into toxic matter which can kill CNE - 2 cells, so it can be applied in gene therapy of nasopharyngeal carcinoma.