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从小鼠L1210细胞的细胞核中合成的DNA的性质。

The nature of DNA synthesized in nuclei from mouse L1210 cells.

作者信息

Müllbacher A, Ralph R K

出版信息

Eur J Biochem. 1977 May 16;75(2):347-55. doi: 10.1111/j.1432-1033.1977.tb11535.x.

DOI:10.1111/j.1432-1033.1977.tb11535.x
PMID:885134
Abstract

A DNA-synthesizing system in vitro from mouse L1210 cell nuclei is described. A high proportion of the DNA synthesized by the L1210 nuclei in vitro appeared to be covalently linked complementary DNA. DNA synthesis by L1210 nuclei was not inhibited by the anti-leukaemia compound 4'-9-acridinylamino)-methansulphon-m-anisidine, although this drug binds to isolated DNA and is active against L1210 leukaemia.

摘要

本文描述了一种从小鼠L1210细胞核体外合成DNA的系统。体外由L1210细胞核合成的DNA中,很大一部分似乎是共价连接的互补DNA。L1210细胞核的DNA合成不受抗白血病化合物4'-(9-吖啶基氨基)-甲磺基间茴香胺的抑制,尽管这种药物能与分离的DNA结合且对L1210白血病有活性。

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1
The nature of DNA synthesized in nuclei from mouse L1210 cells.从小鼠L1210细胞的细胞核中合成的DNA的性质。
Eur J Biochem. 1977 May 16;75(2):347-55. doi: 10.1111/j.1432-1033.1977.tb11535.x.
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Studies on camptothecin-induced degradation and apparent reaggregation of DNA from L1210 cells.喜树碱诱导L1210细胞DNA降解及明显再聚集的研究。
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Inhibition of macromolecular biosynthesis in cultured L1210 mouse leukemia cells by thalicarpine (NSC 68075).唐松草碱(NSC 68075)对培养的L1210小鼠白血病细胞中大分子生物合成的抑制作用。
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Topoisomerase II-mediated DNA damage produced by 4'-(9-acridinylamino)methanesulfon-m-anisidide and related acridines in L1210 cells and isolated nuclei: relation to cytotoxicity.4'-(9-吖啶基氨基)甲磺基间茴香胺及相关吖啶在L1210细胞和分离细胞核中产生的拓扑异构酶II介导的DNA损伤:与细胞毒性的关系
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