• 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

Four new DNA markers are assigned to the WAGR region of 11p13: isolation and regional assignment of 112 chromosome 11 anonymous DNA segments.

作者信息

Davis L M, Byers M G, Fukushima Y, Qin S Z, Nowak N J, Scoggin C, Shows T B

机构信息

Department of Human Genetics, Roswell Park Memorial Institute, Buffalo, New York 14263.

出版信息

Genomics. 1988 Oct;3(3):264-71. doi: 10.1016/0888-7543(88)90087-0.

DOI:10.1016/0888-7543(88)90087-0
PMID:2852164
Abstract

One hundred eighty-three human single copy clones were isolated from the Livermore Laboratory chromosome 11 library (ID code LL11NSO1) and 112 of them were mapped to chromosome 11. Using a panel of somatic cell hybrids segregating chromosome 11 translocations and short arm deletions, 54 of the clones were assigned to one of nine segments on the short arm of chromosome 11; the remainder were assigned to the long arm. Nine of these clones map to 11p13, and four of the nine [57(D11S89), 530(D11S90), 706(D11S93), and 1104(D11S95)] are confined to the same segment within p13 that contains catalase (CAT), the beta subunit of follicle stimulating hormone (FSHB), and the Wilms' tumor-aniridia (WAGR) gene complex.

摘要

相似文献

1
Four new DNA markers are assigned to the WAGR region of 11p13: isolation and regional assignment of 112 chromosome 11 anonymous DNA segments.
Genomics. 1988 Oct;3(3):264-71. doi: 10.1016/0888-7543(88)90087-0.
2
The beta-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus.患有无虹膜和威尔姆斯瘤的患者中,促卵泡激素的β亚基缺失,这有助于进一步明确WAGR基因座。
Nature. 1986;321(6073):882-7. doi: 10.1038/321882a0.
3
Two anonymous DNA segments distinguish the Wilms' tumor and aniridia loci.两个匿名DNA片段区分了威尔姆斯瘤和无虹膜基因座。
Science. 1988 Aug 12;241(4867):840-2. doi: 10.1126/science.2841760.
4
The T-ALL specific t(11;14)(p13;q11) translocation breakpoint cluster region is located near to the Wilms' tumour predisposition locus.T 细胞急性淋巴细胞白血病特异性 t(11;14)(p13;q11)易位断点簇区域位于威尔姆斯瘤易感基因座附近。
Oncogene. 1988 Dec;3(6):691-5.
5
Aniridia, Wilms' tumor and human chromosome 11.
Ophthalmic Paediatr Genet. 1989 Dec;10(4):229-48. doi: 10.3109/13816818909009878.
6
The aniridia-Wilms' tumour association: molecular and genetic analysis of chromosome deletions on the short arm of chromosome 11.无虹膜-威尔姆斯瘤综合征:11号染色体短臂染色体缺失的分子与遗传学分析
Hum Genet. 1989 May;82(2):123-6. doi: 10.1007/BF00284042.
7
Regional assignment of catalase (CAT) gene to band 11p13. Association with the aniridia-Wilms' tumor-Gonadoblastoma (WAGR) complex.过氧化氢酶(CAT)基因定位于11p13带。与无虹膜-威尔姆斯瘤-性腺母细胞瘤(WAGR)综合征相关。
Ann Genet. 1980;23(3):165-8.
8
Complete physical map of the WAGR region of 11p13 localizes a candidate Wilms' tumor gene.
Cell. 1990 Feb 9;60(3):495-508. doi: 10.1016/0092-8674(90)90600-j.
9
The gene for catalase is assigned between the antigen loci MIC4 and MIC11.过氧化氢酶基因定位于抗原基因座MIC4和MIC11之间。
Genomics. 1989 Jan;4(1):7-11. doi: 10.1016/0888-7543(89)90307-8.
10
Regional localization of DNA probes on the short arm of chromosome 11 using aniridia-Wilms' tumor-associated deletions.利用无虹膜-威尔姆斯瘤相关缺失对11号染色体短臂上的DNA探针进行区域定位。
Hum Genet. 1987 Feb;75(2):180-7. doi: 10.1007/BF00591083.

引用本文的文献

1
Mapping small DNA sequences by fluorescence in situ hybridization directly on banded metaphase chromosomes.通过荧光原位杂交直接在显带中期染色体上对小DNA序列进行定位。
Proc Natl Acad Sci U S A. 1990 Aug;87(16):6223-7. doi: 10.1073/pnas.87.16.6223.
2
Somatic cell hybrid and long-range physical mapping of 11p13 microdissected genomic clones.
Proc Natl Acad Sci U S A. 1990 Sep;87(18):7005-9. doi: 10.1073/pnas.87.18.7005.
3
Comparative map for mice and humans.小鼠与人类的比较图谱。
Mamm Genome. 1992;3(9):480-536. doi: 10.1007/BF00778825.