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I型异常红细胞生成性贫血:由于DNA-核蛋白复合物紊乱导致的无效红细胞生成

[Dyserythropoietic anemia, type I: ineffective erythropoiesis due to disorders in the DNA-nucleoprotein complex].

作者信息

Meuret G, Tschan P

出版信息

Schweiz Med Wochenschr. 1975 Nov 22;105(47):1580-1.

PMID:1209222
Abstract

The relative DNA, RNA histone and hemoglobin contents and 3H-thymidine incorporation in vitro were determined sequentially in individual erythroblasts of type I dyserythropoietic anemia. The histone/DNA ratio was increased due to a rise in histone extinction, indicating a pathological DNA-nucleoprotein complex. In addition, the erythroblasts displayed an increase in DNA content exceeding tetraploid values, a loss of DNA-synthesis activity at immature stages with low hemoglobin content, and a reduction of RNA. These variations were assumed to be caused by the preceding and primary impairment of the DNA-nucleoprotein complex.

摘要

对I型异常红细胞生成性贫血的单个成红细胞依次测定其相对DNA、RNA、组蛋白和血红蛋白含量以及体外3H-胸腺嘧啶核苷掺入情况。由于组蛋白消光增加,组蛋白/DNA比值升高,表明存在病理性DNA-核蛋白复合体。此外,成红细胞显示DNA含量增加超过四倍体值,在血红蛋白含量低的未成熟阶段DNA合成活性丧失,以及RNA减少。这些变化被认为是由DNA-核蛋白复合体先前的原发性损伤引起的。

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