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通过甲氨蝶呤同步化和胸腺嘧啶核苷释放对血液学细胞进行高分辨率染色体显带分析。

An evaluation of high resolution chromosome banding of hematologic cells by methotrexate synchronization and thymidine release.

作者信息

Morris C M, Fitzgerald P H

出版信息

Cancer Genet Cytogenet. 1985 Jan 15;14(3-4):275-84. doi: 10.1016/0165-4608(85)90193-1.

Abstract

Methotrexate-thymidine synchronization increased mitotic yield and the numbers of cells with longer chromosomes when compared with direct and day culture (24 hr) techniques. The longer chromosomes overlapped more than shorter ones, but this adverse effect of cell synchronization was outweighed by the substantial gains from increased band number of metaphase cells. A critical feature of the synchronization technique that determines chromosome length is the period of cell culture following thymidine release. This will depend on cell cycle time. Variable results obtained with the synchronization technique probably occur because the cell cycle time of leukemic cells differs from that of normal hematologic cells and normal lymphocytes. It may also differ between patients and between acute and chronic forms of leukemia.

摘要

与直接培养和日培养(24小时)技术相比,甲氨蝶呤-胸腺嘧啶核苷同步化增加了有丝分裂产量以及具有较长染色体的细胞数量。较长的染色体比较短的染色体重叠更多,但细胞同步化的这种不利影响被中期细胞带数增加带来的显著收益所抵消。决定染色体长度的同步化技术的一个关键特征是胸腺嘧啶核苷释放后的细胞培养时间。这将取决于细胞周期时间。同步化技术获得的结果不一致,可能是因为白血病细胞的细胞周期时间与正常血液学细胞和正常淋巴细胞不同。它在患者之间以及白血病的急性和慢性形式之间也可能不同。

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