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抗肿瘤药的神经毒性 被引量:5

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作者 张仲苗
出处 《国外医药(合成药.生化药.制剂分册)》 1995年第4期230-234,共5页 World Pharmacy
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同被引文献53

  • 1张彦,陈燕忠.生物碱类抗肿瘤药物及其新剂型的研究进展[J].药品评价,2006,3(4):264-266. 被引量:9
  • 2国家食品药品监督管理局安全监管司,国家药品不良反应监测中心.药品不良反应报告和监测工作手册[S] ,2005,9:55-75.
  • 3张之南.血液病学[M].北京:人民卫生出版社,2003.1101-1106.
  • 4叶金朝.抗肿瘤药物的神经毒性研究进展[J].药物流行病学杂志,1997,6(1):29-31. 被引量:7
  • 5叶金朝 李定国.顺铂的神经毒性[J].武汉医药情报通讯,1992,8(2):47-47.
  • 6J. M. A. Gerven,A. Hovestadt,J. W. B. Moll,C. J. Rodenburg,T. A. W. Splinter,A. T. Oosterom,L. Keizer,T. E. Drogendijk,C. M. Groenhout,Ch. J. Vecht,J. P. Neijt. The effects of an ACTH (4–9) analogue on development of cisplatin neuropathy in testicular cancer: A randomized trial[J] 1994,Journal of Neurology(7):432~435
  • 7Wall ME, Wani MC, Cook CE, et al. Plant antitumor agent. I. The isolation and structure of camptothecin, a novel alkaloidal leukemia and tumor inhibitor from Camptotheca acuminate[J]. J Am ChemSoc, 1966,88(16): 3888-3890.
  • 8Hsiang YH, Hertzberg R, Heeht S, et al. Camptotheein induces protein-linked DNA breaks via mammalian DNA topoisomerase I[J]. J Biol Chem,1985,(260):14873-14878.
  • 9Srewart L, Ireton GC,Parker LH,et al.Biochemical and biophysical analyses of recombinant forms of human topoisomerase I[J]. J Biol Chem,1996, 271(13) : 7593.
  • 10Laco GS, Co llins JR, Luke BT, et al. Human topoi- som erase I inhibition:docking camptothecin and deriva- tives in to a structure-based active site model[J]. Biochem- istry, 2002,41 (5) : 28.

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