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对患有毛发硫营养不良且紫外线光敏性正常或增强的患者细胞进行的互补研究。

Complementation studies in cells from patients affected by trichothiodystrophy with normal or enhanced UV photosensitivity.

作者信息

Stefanini M, Lagomarsini P, Giorgi R, Nuzzo F

出版信息

Mutat Res. 1987 Jun;191(2):117-9. doi: 10.1016/0165-7992(87)90139-4.

Abstract

A normal level of UV-induced DNA-repair synthesis (UDS) was observed in fibroblasts from a patient affected by trichothiodystrophy (TTD) without photosensitivity. This finding indicates that the hypersensitivity to UV light and the reduced UDS due to the presence of xeroderma pigmentosum complementation group D mutation (XP-D), described in photosensitive TTD patients, are not constantly associated with TTD. Complementation analysis in heterokaryons, obtained by fusion of repair-proficient with repair-deficient TTD cells, demonstrates that cells from the patient showing normal photosensitivity are able to restore UDS in UV-hypersensitive TTD cells.

摘要

在一名患有非光敏性毛发硫营养不良(TTD)的患者的成纤维细胞中观察到正常水平的紫外线诱导的DNA修复合成(UDS)。这一发现表明,光敏性TTD患者中所描述的由于存在着色性干皮病互补组D突变(XP-D)而导致的对紫外线的超敏反应和UDS降低,并非总是与TTD相关联。通过将修复能力正常的TTD细胞与修复缺陷的TTD细胞融合获得的异核体中的互补分析表明,来自该具有正常光敏性患者的细胞能够在紫外线超敏的TTD细胞中恢复UDS。

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