• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

不对称与对称染色体畸变的频率及分布研究。

Frequency and distribution studies of asymmetrical versus symmetrical chromosome aberrations.

作者信息

Savage J R, Papworth D G

出版信息

Mutat Res. 1982 Jul;95(1):7-18. doi: 10.1016/0027-5107(82)90062-8.

DOI:10.1016/0027-5107(82)90062-8
PMID:7110190
Abstract

Two aspects of the relationship between Asymmetrical (A) and Symmetrical (S) radiation-induced chromosomal aberrations are considered in this paper. (1) Are A and S truly alternative modes of lesion interactions? Relative frequencies for chromatid-type and chromosome-type are examined, and new lymphocyte data using banding is used to look at this, and also for parallelism in chromosome participation of the two forms for various aberration categories. All the tests applied suggest that A and S are alternative interaction modes. (2) The long-term survival characteristics of A and S are discussed, and the differences in expected frequencies of derived S per surviving cell from chromosome-type and chromatid-types are stressed. Since many in vivo tissues have varying mixtures of potential chromatid and chromosome aberration-bearing target cells, ultimate cell survival and derived S frequencies may differ between tissues for the same absorbed dose. An Appendix gives Relative Corrected Lengths (RCL) for chromosomes of the human karyotype which should be used when testing the various exchange aberration categories for random chromosome participation.

摘要

本文考虑了不对称(A)和对称(S)辐射诱导的染色体畸变之间关系的两个方面。(1)A和S真的是损伤相互作用的替代模式吗?检查了染色单体型和染色体型的相对频率,并使用新的带型淋巴细胞数据来研究这一点,同时也研究了两种形式在各种畸变类别中染色体参与的平行性。所应用的所有测试都表明A和S是替代的相互作用模式。(2)讨论了A和S的长期存活特征,并强调了从染色体型和染色单体型存活细胞中衍生出的S的预期频率差异。由于许多体内组织具有不同混合比例的潜在携带染色单体和染色体畸变的靶细胞,对于相同的吸收剂量,不同组织的最终细胞存活率和衍生出的S频率可能会有所不同。附录给出了人类核型染色体的相对校正长度(RCL),在测试各种交换畸变类别中染色体随机参与情况时应使用该长度。

相似文献

1
Frequency and distribution studies of asymmetrical versus symmetrical chromosome aberrations.不对称与对称染色体畸变的频率及分布研究。
Mutat Res. 1982 Jul;95(1):7-18. doi: 10.1016/0027-5107(82)90062-8.
2
Distribution of radiation-induced exchange aberrations in all human chromosomes.辐射诱导的交换畸变在所有人染色体中的分布。
Int J Radiat Biol. 2003 Jun;79(6):393-403. doi: 10.1080/0955300031000137805.
3
Radiation induced chromosome aberrations and clonogenic survival in human lymphoblastoid cell lines with different p53 status.不同p53状态的人淋巴母细胞系中辐射诱导的染色体畸变和克隆形成存活率
Strahlenther Onkol. 1999 Jun;175(6):289-92. doi: 10.1007/BF02743582.
4
Distribution of the various radiation-induced chromosomal rearrangements in relation to the dose and sampling time.各种辐射诱导的染色体重排与剂量和采样时间的关系分布。
Mutat Res. 1985 Nov-Dec;152(2-3):197-203. doi: 10.1016/0027-5107(85)90061-2.
5
Chromosomal instability in an oxygen-tolerant variant of Chinese hamster ovary cells.中国仓鼠卵巢细胞耐氧变体中的染色体不稳定性。
Mutat Res. 1989 Jan;219(1):17-28. doi: 10.1016/0921-8734(89)90037-4.
6
Rejoining and misrejoining of radiation-induced chromatin breaks. I. experiments with human lymphocytes.辐射诱导的染色质断裂的重新连接和错误重新连接。I. 对人类淋巴细胞的实验。
Radiat Res. 1996 Mar;145(3):274-80.
7
[Cytogenetic studies of human lymphocytes following blue light irradiation in vitro].[体外蓝光照射后人淋巴细胞的细胞遗传学研究]
Acta Biol Med Ger. 1980;39(2-3):229-36.
8
[Repair of chromosomal aberrations in a human peripheral blood lymphocyte system after single and split-dose x-irradiation].[单次和分次剂量X射线照射后人类外周血淋巴细胞系统中染色体畸变的修复]
Genetika. 1980;16(3):543-50.
9
Cell cycle-dependent potentiation of X-ray-induced chromosomal aberrations by 3-aminobenzamide.3-氨基苯甲酰胺对X射线诱导的染色体畸变的细胞周期依赖性增强作用。
Biochem Biophys Res Commun. 1987 Feb 27;143(1):372-6. doi: 10.1016/0006-291x(87)90675-9.
10
Increased complexity of radiation-induced chromosome aberrations consistent with a mechanism of sequential formation.辐射诱导的染色体畸变复杂性增加,这与顺序形成机制相一致。
Cytogenet Genome Res. 2006;112(1-2):35-44. doi: 10.1159/000087511.

引用本文的文献

1
Mechanisms Underlying the Suppression of Chromosome Rearrangements by Ataxia-Telangiectasia Mutated.共济失调毛细血管扩张症突变抑制染色体重排的机制。
Genes (Basel). 2021 Aug 10;12(8):1232. doi: 10.3390/genes12081232.
2
Three-Color Chromosome Painting as Seen through the Eyes of mFISH: Another Look at Radiation-Induced Exchanges and Their Conversion to Whole-Genome Equivalency.从多重荧光原位杂交视角看三色染色体描绘:再探辐射诱导交换及其向全基因组等效性的转化
Front Oncol. 2016 Mar 15;6:52. doi: 10.3389/fonc.2016.00052. eCollection 2016.
3
The production of chromosome structural changes by radiation.
辐射导致的染色体结构变化的产生。
Experientia. 1989 Jan 15;45(1):52-9. doi: 10.1007/BF01990452.