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用BrdU-33258 Hoechst法分析具有额外或结构异常X染色体的人淋巴细胞中的DNA复制情况。

BrdU-33258 Hoechst analysis of DNA replication in human lymphocytes with supernumerary or structurally abnormal X chromosomes.

作者信息

Latt S A, Willard H F, Gerald P S

出版信息

Chromosoma. 1976 Aug 17;57(2):135-53. doi: 10.1007/BF00292912.

Abstract

BrdU-33258 Hoechst techniques have been used to characterize DNA replication patterns in lymphocytes from hunam females with supernumerary or structurally abnormal X chromosomes. Fluorescence analysis permits identification of late replicating X chromosomes in a very high proportion of cells and affords a high resolution method for determining the interchange points of X-X and X-autosome translocations. Asynchrony among terminal replication patterns of multiple late replicating X chromosomes within an individual cell can occasionally be demonstrated. The arms of isochromosomes usually exhibit symmetrical fluorescence patterns, with replication terminating in bands Xq21 and Xq23 (predominant pattern) or in bands Xq25 and Xq27 (alternative pattern) in both arms. In the vast majority of lymphocytes containing a balanced X-13 or X-19 translocation, the normal X is late replicating. However, DNA synthesis in the translocation products occasionally appears somewhat delayed relative to that expected for an early replicating X, consistent with possible position effects on replication kinetics.

摘要

BrdU - 33258 Hoechst技术已被用于表征具有额外或结构异常X染色体的人类女性淋巴细胞中的DNA复制模式。荧光分析能够在很高比例的细胞中识别晚期复制的X染色体,并提供一种高分辨率方法来确定X - X和X - 常染色体易位的交换点。偶尔可以证明单个细胞内多个晚期复制X染色体的末端复制模式之间存在异步性。等臂染色体的臂通常呈现对称的荧光模式,两条臂的复制均在Xq21和Xq23带(主要模式)或Xq25和Xq27带(替代模式)终止。在绝大多数含有平衡的X - 13或X - 19易位的淋巴细胞中,正常X染色体是晚期复制的。然而,易位产物中的DNA合成偶尔相对于早期复制X染色体预期的情况似乎有所延迟,这与复制动力学可能受到的位置效应一致。

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