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范科尼贫血患者的成纤维细胞在切除胸腺嘧啶二聚体方面并不缺乏。

Fibroblasts from patients with Fanconi's anemia are not deficient in excision of thymine dimer.

作者信息

Klocker H, Burtscher H J, Auer B, Hirsch-Kauffmann M, Schweiger M

出版信息

Eur J Cell Biol. 1985 May;37:240-2.

PMID:4029168
Abstract

Fibroblasts from a patient with Fanconi's anemia were reported to show a defective excision of pyrimidine dimer [15]. We developed a sensitive radioimmuno assay which is specific for thymine dimer, the main ultraviolet photoproduct, and reinvestigated the thymine dimer excision in fibroblasts from patients with Fanconi's anemia. The analysis of 7 Fanconi's anemia cell lines did not agree with the claim mentioned above that was derived from only one Fanconi's anemia cell line. All cell lines we studied, including the cell line used previously [15], excised thymine dimer from their DNA with excision rates similar to those of normal fibroblasts. Additionally, in two Fanconi's anemia and in two normal fibroblast cell lines the repair capacity was examined.

摘要

据报道,一名范可尼贫血患者的成纤维细胞显示出嘧啶二聚体切除缺陷[15]。我们开发了一种对主要紫外线光产物胸腺嘧啶二聚体具有特异性的灵敏放射免疫测定法,并重新研究了范可尼贫血患者成纤维细胞中胸腺嘧啶二聚体的切除情况。对7个范可尼贫血细胞系的分析与上述仅来自一个范可尼贫血细胞系的说法不一致。我们研究的所有细胞系,包括先前使用的细胞系[15],都能从其DNA中切除胸腺嘧啶二聚体,切除率与正常成纤维细胞相似。此外,还检测了两个范可尼贫血细胞系和两个正常成纤维细胞系的修复能力。

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