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Titlebook: Ataxia-Telangiectasia; Richard A. Gatti,Robert B. Painter Conference proceedings 1993 Springer-Verlag Berlin Heidelberg 1993 Ataxia-Telang

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发表于 2025-3-21 19:17:43 | 显示全部楼层 |阅读模式
期刊全称Ataxia-Telangiectasia
影响因子2023Richard A. Gatti,Robert B. Painter
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学科分类Nato ASI Subseries H:
图书封面Titlebook: Ataxia-Telangiectasia;  Richard A. Gatti,Robert B. Painter Conference proceedings 1993 Springer-Verlag Berlin Heidelberg 1993 Ataxia-Telang
影响因子Ataxia-telangiectasia or A-T is a fatal progressiveneurological disease of children. The symptoms indicatedisruptions in the development of suchdiverse body parts ascerebellum, thymus and chromosomes. The patients areundulysensitive to ionizing radiation, immunodeficient, and athird of them develops cancer. All of this stems fromdefects of a singlegene.Provided here is an up-to-date review of all important workin thefield. A wide spectrum of topics is covered, namelygenetics, chromosome 11 mapping, radiobiology,complementation, heterozygote identification,clinicalvariants, biochemistry, and treatment of A-T.
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发表于 2025-3-21 22:58:24 | 显示全部楼层
Frankreichs Verfassung 1958–2008ations were the cause for the increased incidence and suggested, therefore, that mammography screening may not be beneficial for A-T heterozygotes. We emphatically disagree: mammography screening is particularly beneficial for A-T heterozygotes whose risk for breast cancer is higher than for the general population.
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Conference proceedings 1993e body parts ascerebellum, thymus and chromosomes. The patients areundulysensitive to ionizing radiation, immunodeficient, and athird of them develops cancer. All of this stems fromdefects of a singlegene.Provided here is an up-to-date review of all important workin thefield. A wide spectrum of topi
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Bildungsdiskussionen in Frankreichd A,C,D and E) have been described (Jaspers ., 1988); although the disease is clinically indistinguishable in the four groups, radiation-sensitivity is rendered normal by fusion of cells deriving from A-T patients from different groups (whereas fusion of cells from patients from the same group has no effect).
发表于 2025-3-22 19:43:24 | 显示全部楼层
https://doi.org/10.1007/978-3-531-91665-1 to a defect in rejoining of radiation-induced DNA double strand breaks. Hence, the site-specific V(D)J DNA recombination process has been linked to the repair of randomly-induced double-strand breaks.
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Cloning and Characterization of a Candidate Gene for A-T Complementation Group Dtially radioresistant when compared with the original A-T cell line. This approach was begun in this Laboratory in 1983 and resulted in the isolation of a candidate A-T gene at the end of 1990. Currently, work is in progress to characterize this candidate gene and to determine whether it is the gene for A-T complementation group D.
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Murine scid cells and human ataxia-telangiectasia cells complement each other’s radiosensitivity to a defect in rejoining of radiation-induced DNA double strand breaks. Hence, the site-specific V(D)J DNA recombination process has been linked to the repair of randomly-induced double-strand breaks.
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