• 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

人类中期染色体排列的定量研究。VII. 罗伯逊易位携带者及其核型正常亲属中近端着丝粒染色体的联合模式。

Quantitative studies on the arrangement of human metaphase chromosomes. VII. The association pattern of acrocentric chromosomes in carriers of Robertsonian translocations and in their relatives with normal karyotypes.

作者信息

Zankl H, Zang K D

出版信息

Hum Genet. 1979 Nov 1;52(1):119-25. doi: 10.1007/BF00284605.

DOI:10.1007/BF00284605
PMID:527972
Abstract

The pattern of association of acrocentric chromosomes was examined in ten and five carriers of a 15/21 and a 13/14 Robertsonian translocation, respectively, and was compared with that of the same numbers of relatives with normal karyotypes. In the carriers of 15/21 translocation, the number of large associations (involving more than two acrocentrics) and the association frequencies for individual acrocentric chromosomes, were significantly higher than in the control group. The mean number of associations of the single homologs of the translocation chromosomes was much higher than that of the other acrocentrics. In the carriers of 13/14 translocations, only the association frequency for chromosome 13 was higher than in the normal relatives. The uninvolved chromosomes homologous to those involved in translocation showed an insignificant increase in associations in comparison with the other acrocentrics. These results suggest that some mechanism within the cells compensates for the effect of missing acrocentrics or of acrocentrics lacking NORs on the number of associations. The possible relations of this phenomenon to the activity of the nucleolus organizing regions are discussed.

摘要

分别对10名15/21罗伯逊易位携带者和5名13/14罗伯逊易位携带者的近端着丝粒染色体的联合模式进行了检查,并与相同数量的核型正常的亲属的联合模式进行了比较。在15/21易位携带者中,大联合(涉及两个以上近端着丝粒)的数量以及单个近端着丝粒染色体的联合频率均显著高于对照组。易位染色体单个同源染色体的联合平均数远高于其他近端着丝粒染色体。在13/14易位携带者中,只有13号染色体的联合频率高于正常亲属。与易位涉及的染色体同源的未受累染色体,与其他近端着丝粒染色体相比,联合增加不显著。这些结果表明,细胞内的某种机制可补偿缺失近端着丝粒或缺乏核仁组织区的近端着丝粒对联合数量的影响。本文讨论了这一现象与核仁组织区活性的可能关系。

相似文献

1
Quantitative studies on the arrangement of human metaphase chromosomes. VII. The association pattern of acrocentric chromosomes in carriers of Robertsonian translocations and in their relatives with normal karyotypes.人类中期染色体排列的定量研究。VII. 罗伯逊易位携带者及其核型正常亲属中近端着丝粒染色体的联合模式。
Hum Genet. 1979 Nov 1;52(1):119-25. doi: 10.1007/BF00284605.
2
Nucleolus organizer regions in translocations involving acrocentric chromosomes.涉及近端着丝粒染色体易位中的核仁组织区。
Cytogenet Cell Genet. 1980;26(1):14-21. doi: 10.1159/000131416.
3
NORs and satellite associations in a family with 13/14 translocation.一个患有13/14易位的家族中的核仁组织区和随体联合
Hum Genet. 1981;59(4):342-4. doi: 10.1007/BF00295468.
4
De novo 21/21 translocation Down syndrome. Studies of parental origin of the translocation and acrocentric associations in parents.
Hum Genet. 1986 Jun;73(2):127-9. doi: 10.1007/BF00291601.
5
Polymorphisms of Ag-stained nucleolar organizer regions in man.人类中经银染的核仁组织区多态性
Hum Genet. 1982;60(4):334-9. doi: 10.1007/BF00569214.
6
Comparison of acrocentric associations in male and female cells. Relationship to the active nucleolar organizers.男性和女性细胞中近端着丝粒染色体联合的比较。与活性核仁组织者的关系。
Hum Genet. 1980;54(3):349-53. doi: 10.1007/BF00291581.
7
NOR associations with heterochromatin.核仁组织区与异染色质的关联。
Cytogenet Cell Genet. 1984;38(3):165-70. doi: 10.1159/000132054.
8
[Genetic determination of the activity of nucleolar-organizing regions of human chromosomes].[人类染色体核仁组织区活性的遗传决定]
Biull Eksp Biol Med. 1981 Mar;91(3):350-3.
9
Quantitative studies on the arrangement of human metaphase chromosomes. VI. The association pattern of acrocentric chromosomes in patients with trisomy 13.人类中期染色体排列的定量研究。VI. 13三体综合征患者近端着丝粒染色体的关联模式。
Hum Genet. 1979 Jun 19;49(2):185-9. doi: 10.1007/BF00277641.
10
Preferential association of nucleolar organizing human chromosomes as revealed by silver staining technique at mitosis.有丝分裂时银染技术揭示的核仁组织区人类染色体的优先关联
Mol Gen Genet. 1983;190(2):352-4. doi: 10.1007/BF00330664.

引用本文的文献

1
NORs and satellite associations in a family with 13/14 translocation.一个患有13/14易位的家族中的核仁组织区和随体联合
Hum Genet. 1981;59(4):342-4. doi: 10.1007/BF00295468.
2
Activity of rRNA genes in cells of a patient with Down syndrome mosaic.唐氏综合征嵌合体患者细胞中rRNA基因的活性。
Hum Genet. 1980;55(2):227-9. doi: 10.1007/BF00291771.
3
Satellite associations and NOR staining in mitoses of trisomy 21 mosaicism.21三体嵌合体有丝分裂中的卫星联合及核仁组织区染色

本文引用的文献

1
Nucleolus-organisers in the causation of chromosomal anomalies in man.人类染色体异常病因中的核仁组织者
Lancet. 1961 Jul 15;2(7194):123-6. doi: 10.1016/s0140-6736(61)92647-2.
2
Quantitative studies on the arrangement of human metaphase chromosomes. I. Individual features in the association pattern of the acrocentric chromosomes of normal males and females.人类中期染色体排列的定量研究。I. 正常男性和女性近端着丝粒染色体联合模式的个体特征。
Cytogenetics. 1968;7(6):455-70.
3
Satellite association. A possible cause of chromosome aberrations.
Hum Genet. 1980;55(1):115-7. doi: 10.1007/BF00329136.
4
Association frequency and silver staining of nucleolus organizing regions in hyperthyroid patients.甲状腺功能亢进患者核仁组织区的联合频率及银染
Hum Genet. 1980;54(1):111-4. doi: 10.1007/BF00279059.
卫星联合。染色体畸变的一个可能原因。
Humangenetik. 1972;16(1):147-50. doi: 10.1007/BF00394001.
4
[Satellite associations in autosomal and gonosomal chromosome abnormalities and in hypothyreosis].[常染色体和性染色体异常以及甲状腺功能减退中的卫星关联]
Humangenetik. 1969;8(1):53-61.
5
[The significance of association of satellited chromosomes].[随体染色体联合的意义]
Humangenetik. 1969;7(1):9-21. doi: 10.1007/BF00278688.
6
Expression of human and suppression of mouse nucleolus organizer activity in mouse-human somatic cell hybrids.人核仁组织区活性在小鼠 - 人类体细胞杂种中的表达及小鼠核仁组织区活性的抑制
Proc Natl Acad Sci U S A. 1976 Dec;73(12):4531-5. doi: 10.1073/pnas.73.12.4531.
7
Quantitative studies on the arrangement of human metaphase chromosomes. V. The association pattern of acrocentric chromosomes in human meningiomas after the loss of G and D chromosomes.人类中期染色体排列的定量研究。V. G组和D组染色体缺失后人脑膜瘤中近端着丝粒染色体的联合模式
Hum Genet. 1978 Jan 19;40(2):149-55. doi: 10.1007/BF00272295.
8
Quantitative studies on the arrangement of human metaphase chromosomes. VI. The association pattern of acrocentric chromosomes in patients with trisomy 13.人类中期染色体排列的定量研究。VI. 13三体综合征患者近端着丝粒染色体的关联模式。
Hum Genet. 1979 Jun 19;49(2):185-9. doi: 10.1007/BF00277641.
9
Compensatory mechanisms in the satellite association patterns of individuals with Robertsonian translocations.
Hereditas. 1975;81(1):101-12. doi: 10.1111/j.1601-5223.1975.tb01022.x.
10
Ag staining of the nucleolus organizer (NO) and its relationship to satellite association.核仁组织者(NO)的银染及其与随体联合的关系。
Hum Genet. 1978 Oct 19;44(1):71-77. doi: 10.1007/BF00283576.