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在不同严谨条件下通过原位杂交快速鉴定标记染色体。

Rapid identification of marker chromosomes by in situ hybridization under different stringency conditions.

作者信息

Vorsanova S G, Yurov Y B, Soloviev I V, Demidova I A, Malet P

机构信息

Institute of Pediatrics and Childrens Surgery, MH RF, Moscow, Russia.

出版信息

Anal Cell Pathol. 1994 Oct;7(3):251-8.

PMID:7848878
Abstract

Six metacentric non-satellite chromosome markers and 4 satellite markers of unknown origin were discovered by routine cytogenetic analysis. These markers were then investigated by isotopic and nonisotopic (FISH) in situ hybridization. In order to determine the origin of small marker chromosomes, a special protocol involving sequential application of defined alphoid and 'classical' satellite DNA probes with chromosome specificity was used. In situ hybridization under low stringency conditions has been performed with DNA probes specific for 4 groups of chromosomes. After preliminary analysis and determination of the possible origin of these marker chromosomes, DNA probes with high chromosome specificity were used under high stringency conditions. Marker chromosomes were found to be derivatives of chromosomes 7, 9 (3 cases), 13, 14 or 22, 21 (2 cases), X and Y.

摘要

通过常规细胞遗传学分析发现了6个中着丝粒非卫星染色体标记和4个来源不明的卫星标记。然后通过同位素和非同位素(荧光原位杂交)原位杂交对这些标记进行了研究。为了确定小标记染色体的来源,采用了一种特殊方案,该方案涉及顺序应用具有染色体特异性的特定α卫星和“经典”卫星DNA探针。使用针对4组染色体的DNA探针在低严谨度条件下进行原位杂交。在对这些标记染色体的可能来源进行初步分析和确定后,在高严谨度条件下使用了具有高染色体特异性的DNA探针。发现标记染色体是7号、9号(3例)、13号、14号或22号、21号(2例)、X和Y染色体的衍生物。

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