共济失调-毛细血管扩张的互补分析。

Kroc Foundation series Pub Date : 1985-01-01
N G Jaspers, R B Painter, M C Paterson, C Kidson, T Inoue
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引用次数: 0

摘要

在许多实验室中,通过研究融合体细胞或来自不同患者的无细胞提取物混合物中AT表型的表达,对共济失调毛细血管扩张症(AT)进行了遗传分析。考虑到AT中辐射敏感性的四个不同参数,经常观察到对电离辐射的缺陷响应的互补。来自17个不相关家族的培养成纤维细胞或淋巴母细胞样细胞的综合研究结果显示,存在至少4个,可能9个互补群。这些发现表明AT存在广泛的遗传异质性。需要更广泛的研究来整合这些数据,并为未来AT遗传缺陷的研究提供一套遗传特征的细胞株。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Complementation analysis of ataxia-telangiectasia.

In a number of laboratories genetic analysis of ataxia-telangiectasia (AT) has been performed by studying the expression of the AT phenotype in fused somatic cells or mixtures of cell-free extracts from different patients. Complementation of the defective response to ionizing radiation was observed frequently, considering four different parameters for radiosensitivity in AT. The combined results from studies on cultured fibroblasts or lymphoblastoid cells from 17 unrelated families revealed the presence of at least four and possibly nine complementation groups. These findings suggest that there is an extensive genetic heterogeneity in AT. More extensive studies are needed for an integration of these data and to provide a set of genetically characterized cell strains for future research of the AT genetic defect.

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