首页> 外文期刊>The Tohoku Journal of Experimental Medicine >Scanning electron microscopy of fragmentary marker chromosomes observed by light microscopy.
【24h】

Scanning electron microscopy of fragmentary marker chromosomes observed by light microscopy.

机译:扫描光学显微镜观察的碎片标记染色体的电子显微镜。

获取原文
获取原文并翻译 | 示例
           

摘要

To study the fine structure of fragmentary marker chromosomes, we performed scanning electron microscopy (SEM) on samples isolated from two carriers (Case 1: 46, XY/47, XY, +mar/48, XY, +mar, +mar; Case 2: 47, XY, +mar). In both cases, light microscopic observation revealed that marker chromosomes lacked a centromere and were fragmented in appearance. However, SEM observation of the metaphasic cells in both cases showed three variations. One variation was a structure that seemed to be metacentric, another was a structure that seemed to be submetacentric, and the remaining one was essentially fragmentary. However, neither the usual chromatid nor centromere formations were observed in the metacentric-like and submetacentric-like structures, even when both cases were observed by SEM. Moreover, the marker chromosomes of the boy of Case I, who suffered from various clinical troubles, included a greater population of metacentric-like or submetacentric-like structures than of essentially fragmentary structures. The marker chromosomes of the fetus of Case 2, who suffered from no clinical problems, included a much greater population of essentially fragmentary structures than metacentric-like or submetacentric like structures. Therefore, SEM observation of fragmentary marker chromosomes that are visible on light microscopy might be used to define specific structures. Moreover, SEM observation might provide clinical criteria relating to the pathogenesis of fragmentary marker chromosomes found on light microscopy.
机译:为了研究碎片中染色体的细结构,我们在两个载体中分离的样品上进行了扫描电子显微镜(SEM)(案例1:46,XY / 47,XY,+ Mar / 48,XY,+ Mar,+ Mar;案例2:47,XY,+ MAR)。在这两种情况下,光学显微镜观察表明,标记染色体缺少了符号并在外观上裂片。然而,在两种情况下,SEM观察两种情况下的变异。一种变化是似乎是偏心的结构,另一个是似乎是潜在的结构,其余的结构基本上是零碎的。然而,即使通过SEM观察到这两种情况,也没有在核心样和逐渐相似的结构中观察到通常的染色体和焦粒组。此外,患者I的男孩的标记染色体包括各种临床问题,包括比基本局部结构的更大的偏心或逐渐相似的结构。患者2的胎儿的标记染色体,患者患有没有临床问题的患者,包括比Metecration样或诸如结构的基本碎片结构的更大群体。因此,可以使用在光学显微镜上可见的碎片中标志物染色体的SEM观察来定义特定结构。此外,SEM观察可以提供与在光学显微镜显微镜检查中发现的碎片标记染色体的发病机制有关的临床标准。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号