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范可尼贫血患者及其杂合子父母中的自发性6-硫鸟嘌呤抗性淋巴细胞。

Spontaneous 6-thioguanine-resistant lymphocytes in Fanconi anemia patients and their heterozygous parents.

作者信息

Wunder E, Schroeder T M

出版信息

Hum Genet. 1985;70(3):264-70. doi: 10.1007/BF00273454.

Abstract

The incidence of spontaneous 6-thioguanine-resistant (TGr) lymphocytes was studied in the peripheral blood collected from seven Fanconi anemia (FA) patients and five of their heterozygous parents using an autoradiographic or a lymphocyte cloning method. Five of the seven patients showed a significantly elevated incidence of TGr lymphocytes as compared to age- and sex-matched healthy controls. There was, however, no difference between FA heterozygotes and controls. These results suggest some variability among the patients similar to those reported in clinical and cytogenetic investigations. The basis for the increase in TGr cells in the patients is not known, but the inherent genomic instability reflected as increased frequencies of chromosomal aberrations is one possible explanation.

摘要

采用放射自显影或淋巴细胞克隆方法,对7例范科尼贫血(FA)患者及其5名杂合子父母外周血中自发6-硫鸟嘌呤抗性(TGr)淋巴细胞的发生率进行了研究。与年龄和性别匹配的健康对照相比,7例患者中有5例TGr淋巴细胞的发生率显著升高。然而,FA杂合子与对照之间没有差异。这些结果表明患者之间存在一些变异性,类似于临床和细胞遗传学研究中报道的情况。患者中TGr细胞增加的原因尚不清楚,但作为染色体畸变频率增加所反映的内在基因组不稳定性是一种可能的解释。

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