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[Comparative studies on the alkylation of embryonic and matel tissues by cyclophosphamide].

作者信息

Engels K, Krowke R, Neubert D

出版信息

Naunyn Schmiedebergs Arch Exp Pathol Pharmakol. 1968;260(2):110-1.

PMID:4239150
Abstract
摘要

相似文献

1
[Comparative studies on the alkylation of embryonic and matel tissues by cyclophosphamide].[环磷酰胺对胚胎组织和成熟组织烷基化作用的比较研究]
Naunyn Schmiedebergs Arch Exp Pathol Pharmakol. 1968;260(2):110-1.
2
Effects of dosage, phenobarbital, and 2-diethylaminoethyl-2,2-diphenylvalerate on the binding of cyclophosphamide and-or its metabolites to the DNA, RNA, and protein of the embryo and liver in pregnant mice.剂量、苯巴比妥和2-二乙氨基乙基-2,2-二苯基戊酸酯对环磷酰胺及其代谢产物与妊娠小鼠胚胎和肝脏的DNA、RNA及蛋白质结合的影响。
Cancer Res. 1973 Apr;33(4):664-70.
3
Biochemical studies on the nucleic acid metabolism of embryonic tissue and the effect of drugs.
Naunyn Schmiedebergs Arch Exp Pathol Pharmakol. 1968;259(2):186-8. doi: 10.1007/BF00537777.
4
[Susceptibility to inhibition by cyclophosphamide of DNA polymerases in cell nuclei and mitochondria of liver and tumor tissue].
Naunyn Schmiedebergs Arch Exp Pathol Pharmakol. 1968;260(2):139-40.
5
[Administration of 3H-benzpyrene to pregnant mice and rats: incorporation of radioactivity into subcellular fractions of various tissues].给怀孕小鼠和大鼠注射3H-苯并芘:放射性物质掺入各种组织的亚细胞组分中
Arch Geschwulstforsch. 1973;42(2):95-106.
6
14C-cyclophosphamide alkylation of mouse embryo macromolecules.
Proc Soc Exp Biol Med. 1974 Feb;145(2):620-4. doi: 10.3181/00379727-145-37862.
7
The in vivo biosynthesis of DNA, RNA, and proteins by mouse embryos after a teratogenic dose of cyclophosphamide.致畸剂量的环磷酰胺作用后小鼠胚胎中DNA、RNA和蛋白质的体内生物合成。
Teratology. 1972 Oct;6(2):129-37. doi: 10.1002/tera.1420060203.
8
[Alkylation of nuclear DNA of various rat organs by nitrosomethyl urea in vivo].[体内亚硝基甲基脲对大鼠各器官细胞核DNA的烷基化作用]
Arch Geschwulstforsch. 1970;35(3):251-8.
9
[Changes in the protein level of nuclei and mitochondria in various stages of liver regeneration].[肝脏再生各阶段细胞核与线粒体蛋白质水平的变化]
Tsitologiia. 1974 Nov;16(11):1382-7.
10
Hepatic intracellular distribution of foreign compounds in relation to their biliary excretion.
J Pharmacol Exp Ther. 1972 Nov;183(2):411-9.

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Manifestation of carcinogenesis as a stochastic process on the basis of an altered mitochondrial genome.
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