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共济失调毛细血管扩张症中的一种可扩散致裂因子。

A diffusable clastogenic factor in ataxia telangiectasia.

作者信息

Shaham M, Becker Y, Cohen M M

出版信息

Cytogenet Cell Genet. 1980;27(2-3):155-61. doi: 10.1159/000131476.

DOI:10.1159/000131476
PMID:6967388
Abstract

Cocultivation of plasma and lymphocytes from ataxia telangiectasia (AT) patients with those of normal individuals resulted in a significant increase in chromosomal damage in the normal cells. Tissue culture medium used to cultivate AT skin fibroblasts also significantly increased chromosome breakage in PHA-stimulated normal lymphocytes. This clastogenic effect was maximal when the "conditioned medium" was 8-9 days old. A similar effect was not observed with medium derived from normal skin fibroblasts. These observations suggest the presence of a clastogenic factor in the plasma of AT patients which may also be produced by AT skin fibroblasts in culture.

摘要

将共济失调毛细血管扩张症(AT)患者的血浆和淋巴细胞与正常个体的血浆和淋巴细胞共同培养,导致正常细胞中的染色体损伤显著增加。用于培养AT皮肤成纤维细胞的组织培养基也显著增加了PHA刺激的正常淋巴细胞中的染色体断裂。当“条件培养基”培养8 - 9天时,这种致断裂效应最大。从正常皮肤成纤维细胞获得的培养基未观察到类似效应。这些观察结果表明,AT患者血浆中存在一种致断裂因子,培养中的AT皮肤成纤维细胞也可能产生这种因子。

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A diffusable clastogenic factor in ataxia telangiectasia.共济失调毛细血管扩张症中的一种可扩散致裂因子。
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引用本文的文献

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Human DNA repair defects.人类DNA修复缺陷。
J Inherit Metab Dis. 1986;9 Suppl 1:69-84. doi: 10.1007/BF01800860.
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Heterogeneity of chromosomal breakage levels in epithelial tissue of ataxia-telangiectasia homozygotes and heterozygotes.共济失调毛细血管扩张症纯合子和杂合子上皮组织中染色体断裂水平的异质性。
Hum Genet. 1989 Sep;83(2):133-8. doi: 10.1007/BF00286705.
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