• 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

[The characteristics of the localization of induced ruptures in human chromosomes].

作者信息

Druzhinin V G

出版信息

Tsitologiia. 1990;32(8):847-51.

PMID:2125763
Abstract

Levels of spontaneous and of C-mitomycine and cyclophosphane-induced chromosome aberrations are determined among the persons not subject to professionally industrial hazards. It has been revealed that in all the experimental series the aberration rate in those, who carried extreme polymorphic variants, was much higher compared to those without these variants in their karyotypes. Among the persons with the above extreme versions, the impact of chromosome ruptures is stronger in the vicinity of the structural heterochromatin. Possible causes of the discovered phenomenon are discussed.

摘要

相似文献

1
[The characteristics of the localization of induced ruptures in human chromosomes].
Tsitologiia. 1990;32(8):847-51.
2
[Mitomycin C induced structural changes in heterochromatic regions of human chromosomes 1, 9, 16 and Y].[丝裂霉素C诱导人类1号、9号、16号染色体及Y染色体异染色质区域的结构变化]
Tsitologiia. 1988 Nov;30(11):1350-4.
3
[Heterochromatic regions and the nondisjunction of human chromosome 21. I. Polymorphism of the C-bands of chromosomes 1, 9 and 16 in children with Down's syndrome].[异染色质区与人类21号染色体不分离。I. 唐氏综合征患儿1、9和16号染色体C带的多态性]
Tsitologiia. 1987 Jun;29(6):711-4.
4
[Polymorphism of the C-band segments of chromosomes 1, 9 and 16 in the peripheral blood lymphocytes of patients with endometrial cancer].[子宫内膜癌患者外周血淋巴细胞中1、9和16号染色体C带区段的多态性]
Tsitol Genet. 1993 Jul-Aug;27(4):66-71.
5
[Heterochromatic regions and chromosome 21 nondisjunction in man. II. A comparative analysis of the polymorphism of the C bands of chromosomes 1, 9 and 16 in the fathers and mothers of Down's disease children].[人类异染色质区与21号染色体不分离。II. 唐氏综合征患儿父母中1、9和16号染色体C带多态性的比较分析]
Tsitologiia. 1987 Jul;29(7):848-50.
6
[The C heterochromatin of chromosomes 1, 9, 16 and Y in patients with Noonan's syndrome].[努南综合征患者1、9、16号染色体及Y染色体的C异染色质]
Tsitol Genet. 1994 May-Jun;28(3):85-8.
7
Analysis of centromere size in human chromosomes 1, 9, 15, and 16 by electron microscopy.通过电子显微镜分析人类1号、9号、15号和16号染色体的着丝粒大小。
Genome. 1991 Oct;34(5):710-3. doi: 10.1139/g91-109.
8
Analysis of chromosomes in paternity cases.亲子鉴定中的染色体分析。
Acta Med Leg Soc (Liege). 1989;39(2):485-98.
9
[Analysis of the inheritance of heterochromatic regions in human chromosomes 1, 9, 16 and Y].[人类1号、9号、16号染色体及Y染色体异染色质区域的遗传分析]
Tsitol Genet. 1987 Sep-Oct;21(5):339-43.
10
[Comparative study of methods for the quantitative assessment of the C-segment size of human chromosomes].[人类染色体C区段大小定量评估方法的比较研究]
Biull Eksp Biol Med. 1987 Mar;103(3):348-9.