• 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

A detailed genetic map of the long arm of chromosome 11.

作者信息

Julier C, Nakamura Y, Lathrop M, O'Connell P, Leppert M, Litt M, Mohandas T, Lalouel J M, White R

机构信息

Howard Hughes Medical Institute, University of Utah School of Medicine, Salt Lake City 84132.

出版信息

Genomics. 1990 Jul;7(3):335-45. doi: 10.1016/0888-7543(90)90167-s.

DOI:10.1016/0888-7543(90)90167-s
PMID:1973139
Abstract

We describe 14 new restriction fragment length polymorphisms, corresponding to 13 loci on the long arm of chromosome 11. A detailed genetic map of chromosome 11q has been constructed from these and other loci (a total of 31 loci) typed in 59 reference families. The 23 most informative markers were selected to establish a map with a strongly supported order; regional localizations are provided for eight other markers. The loci span 88 cM in males and 148 cM in females and form a dense continuum on 11q. These ordered polymorphic markers will be of help in studying the genes responsible for several diseases that have been localized to this region, including genes responsible for multiple endocrine neoplasia type I (MEN1), ataxia telangiectasia (AT), tuberous sclerosis (TSC), and some forms of asthma and rhinitis.

摘要

相似文献

1
A detailed genetic map of the long arm of chromosome 11.
Genomics. 1990 Jul;7(3):335-45. doi: 10.1016/0888-7543(90)90167-s.
2
A genetic linkage map of 32 loci on human chromosome 10.人类10号染色体上32个基因座的遗传连锁图谱。
Genomics. 1989 Nov;5(4):718-26. doi: 10.1016/0888-7543(89)90113-4.
3
A genetic linkage map of 17 markers on human chromosome 21.人类21号染色体上17个标记的遗传连锁图谱。
Genomics. 1989 May;4(4):579-91. doi: 10.1016/0888-7543(89)90282-6.
4
A genetic linkage map of 41 restriction fragment length polymorphism markers for human chromosome 3.人类3号染色体41个限制性片段长度多态性标记的遗传连锁图谱。
Genomics. 1991 Nov;11(3):565-72. doi: 10.1016/0888-7543(91)90063-k.
5
A genetic linkage map of human chromosome 5 with 60 RFLP loci.一张含有60个限制性片段长度多态性(RFLP)位点的人类5号染色体遗传连锁图谱。
Genomics. 1991 May;10(1):173-85. doi: 10.1016/0888-7543(91)90498-4.
6
A primary genetic linkage map of 14 polymorphic loci for the short arm of human chromosome 8.人类8号染色体短臂14个多态性位点的初步遗传连锁图谱。
Genomics. 1993 Mar;15(3):530-4. doi: 10.1006/geno.1993.1105.
7
A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination rates.一份详细的人类4号染色体多点图谱为连锁异质性和位置特异性重组率提供了证据。
Am J Hum Genet. 1991 May;48(5):911-25.
8
Detailed physical map of human chromosomal region 11q12-13 shows high meiotic recombination rate around the MEN1 locus.人类染色体区域11q12 - 13的详细物理图谱显示,在MEN1基因座周围减数分裂重组率很高。
Proc Natl Acad Sci U S A. 1991 Dec 1;88(23):10609-13. doi: 10.1073/pnas.88.23.10609.
9
An extended genetic linkage map of markers for human chromosome 10.人类10号染色体标记的扩展遗传连锁图谱。
Genomics. 1988 Nov;3(4):389-92. doi: 10.1016/0888-7543(88)90133-4.
10
A primary genetic linkage map for human chromosome 12.人类12号染色体的初级遗传连锁图谱。
Genomics. 1987 Sep;1(1):93-102. doi: 10.1016/0888-7543(87)90110-8.

引用本文的文献

1
Molecular mapping of four ovule lethal mutants in soybean.大豆中四个胚珠致死突变体的分子图谱分析
Theor Appl Genet. 2004 Feb;108(4):577-85. doi: 10.1007/s00122-003-1482-y. Epub 2003 Nov 11.
2
Genetic mapping of hph2, a mutation affecting amino acid transport in the mouse.hph2的基因定位,hph2是一种影响小鼠氨基酸转运的突变。
Mamm Genome. 1997 Feb;8(2):98-101. doi: 10.1007/s003359900366.
3
Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p13-11q13, and exclusion of mu-calpain as the multiple endocrine neoplasia type 1 gene.
对11号染色体p13 - 11q13区域的40个基因座和23个黏粒进行基因定位研究,并排除μ - 钙蛋白酶作为1型多发性内分泌肿瘤基因。
Hum Genet. 1996 Jun;97(6):732-41. doi: 10.1007/BF02346182.
4
Comparative mapping of the barley genome with male and female recombination-derived, doubled haploid populations.利用雄性和雌性重组衍生的双单倍体群体对大麦基因组进行比较作图。
Mol Gen Genet. 1995 Dec 20;249(6):600-8. doi: 10.1007/BF00418029.
5
Human chromosome 11 complements ataxia-telangiectasia cells but does not complement the defect in AT-like Chinese hamster cell mutants.人类11号染色体可互补共济失调毛细血管扩张症细胞,但不能互补类共济失调毛细血管扩张症的中国仓鼠细胞突变体中的缺陷。
Hum Genet. 1993 Oct 1;92(3):259-64. doi: 10.1007/BF00244469.
6
Schizophrenia-associated chromosome 11q21 translocation: identification of flanking markers and development of chromosome 11q fragment hybrids as cloning and mapping resources.精神分裂症相关的11号染色体q21易位:侧翼标记的鉴定以及11号染色体q片段杂种的构建作为克隆和定位资源
Am J Hum Genet. 1993 Mar;52(3):478-90.
7
Evidence for involvement of a second genetic locus on chromosome 11q in porphyrin metabolism.
Hum Genet. 1993 Jul;91(6):576-8. doi: 10.1007/BF00205083.
8
Ordering markers in the region of the ataxia-telangiectasia gene (11q22-q23) by fluorescence in situ hybridization (FISH) to interphase nuclei.通过荧光原位杂交(FISH)技术对间期细胞核进行检测,以确定共济失调毛细血管扩张症基因(11q22-q23)区域的标记物。
Hum Genet. 1994 Jan;93(1):1-6. doi: 10.1007/BF00218903.
9
Mapping the gene for hereditary hyperparathyroidism and prolactinoma (MEN1Burin) to chromosome 11q: evidence for a founder effect in patients from Newfoundland.将遗传性甲状旁腺功能亢进症和泌乳素瘤基因(MEN1Burin)定位到11号染色体q臂:来自纽芬兰患者存在奠基者效应的证据
Am J Hum Genet. 1994 Jun;54(6):1060-6.
10
Homozygotes for the autosomal dominant neoplasia syndrome (MEN1).常染色体显性肿瘤综合征(MEN1)的纯合子。
Am J Hum Genet. 1993 Dec;53(6):1167-72.