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Differences in uptake of adriamycin and daunomycin by normal BM cells and acute leukemia cell determined by flow cytometry.

作者信息

Sonneveld P, van den Engh G J

出版信息

Leuk Res. 1981;5(3):251-7. doi: 10.1016/0145-2126(81)90110-7.

DOI:10.1016/0145-2126(81)90110-7
PMID:7266019
Abstract
摘要

相似文献

1
Differences in uptake of adriamycin and daunomycin by normal BM cells and acute leukemia cell determined by flow cytometry.通过流式细胞术测定正常骨髓细胞和急性白血病细胞对阿霉素和柔红霉素摄取的差异。
Leuk Res. 1981;5(3):251-7. doi: 10.1016/0145-2126(81)90110-7.
2
In vivo cellular adriamycin concentrations related to growth inhibition of normal and leukemic human bone marrow cells.体内阿霉素浓度与正常及白血病人类骨髓细胞生长抑制的关系。
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3
Individual nuclear uptake patterns for adriamycin and daunomycin in human leukemia and lymphoma cells.阿霉素和柔红霉素在人白血病和淋巴瘤细胞中的个体核摄取模式。
Blut. 1981 Jun;42(6):355-65. doi: 10.1007/BF00996898.
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Analysis of heterogeneity in daunorubicin uptake by human leukemia cells using laser flow cytometry.利用激光流式细胞术分析柔红霉素在人白血病细胞中的摄取异质性。
Invest New Drugs. 1985;3(3):273-7. doi: 10.1007/BF00179431.
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Differences in the pharmacokinetics of daunomycin in normal and leukemic rats.
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6
Uptake of adriamycin and daunomycin in L1210 and human leukemia cells: a comparative study.
J Med. 1976;7(1):63-79.
7
[Comparative evaluation of the myelotoxic action of rubomycin, adriamycin and carminomycin by their delayed effects in an experiment].[通过实验中它们的延迟效应比较柔红霉素、阿霉素和洋红霉素的骨髓毒性作用]
Antibiot Med Biotekhnol. 1985 Apr;30(4):284-8.
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Comparative toxicity of detorubicin and doxorubicin, free and DNA-bound, for hemopoietic stem cells.
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Uptake of free and DNA-bound daunorubicin and doxorubicin into human leukemic cells.游离及与DNA结合的柔红霉素和阿霉素进入人白血病细胞的摄取情况。
Cancer Chemother Pharmacol. 1979;2(1):49-52. doi: 10.1007/BF00253105.
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Liposomal encapsulation of a synergistic molar ratio of cytarabine and daunorubicin enhances selective toxicity for acute myeloid leukemia progenitors as compared to analogous normal hematopoietic cells.脂质体包封阿糖胞苷和柔红霉素协同摩尔比增强了对急性髓系白血病祖细胞的选择性毒性,与类似的正常造血细胞相比。
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Synthesis of a dual functional anti-MDR tumor agent PH II-7 with elucidations of anti-tumor effects and mechanisms.合成具有双重功能的抗多药耐药肿瘤试剂 PH II-7,并阐明其抗肿瘤作用和机制。
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