• 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

[小鼠中or基因对Bld基因隐性上位作用的表型发生分析]

[Phenogenetic analysis of recessive epistasis of the or gene over the Bld gene in mice].

作者信息

Nonchev S G, Koniukhov B V

出版信息

Genetika. 1981;17(10):1798-804.

PMID:7198074
Abstract

Results concerning interaction between the genes blind (Bld) and ocular retardation (or) during mouse embryogenesis are presented. It was established that in Bld/+ or/or mice the Bld gene effects are not expressed, as a result of the pronounced eye reduction caused by the or gene action. In Bld/+ or/or embryos the phenocritic stage of the Bld gene action is deplaced to more early embryogenesis period than that in the Bld/+ +/+ embryos. This leads to the recessive epistasis of the or gene over the Bld gene. The analysis of gene interaction has also indicated that the lid mesodermal component growth is the primary target process affected by the Bld/+ constitution.

摘要

本文展示了关于小鼠胚胎发育过程中盲眼(Bld)基因与眼发育迟缓(or)基因之间相互作用的研究结果。已证实,在Bld/+ or/or小鼠中,由于or基因作用导致明显的眼睛发育不全,Bld基因的效应未得到表达。在Bld/+ or/or胚胎中,Bld基因作用的表型临界期比Bld/+ +/+胚胎的相应时期提前至更早的胚胎发育阶段。这导致or基因对Bld基因为隐性上位作用。基因相互作用分析还表明,眼睑中胚层成分的生长是受Bld/+基因型影响的主要靶标过程。

相似文献

1
[Phenogenetic analysis of recessive epistasis of the or gene over the Bld gene in mice].[小鼠中or基因对Bld基因隐性上位作用的表型发生分析]
Genetika. 1981;17(10):1798-804.
2
[Interaction of the mutant aphakia, fidget and ocular retardation genes in mice].[小鼠中突变性无晶状体、坐立不安和眼部发育迟缓基因的相互作用]
Genetika. 1982 Jul;18(7):1107-14.
3
Developmental studies of the lethal gene Bld in the mouse. I. Post-implantation development of the lethal homozygote.
J Embryol Exp Morphol. 1979 Jan;49:1-12.
4
[Interaction of mutant genes fi, or and mi in the morphogenesis of the mouse eye].[突变基因fi、or和mi在小鼠眼睛形态发生中的相互作用]
Izv Akad Nauk SSSR Biol. 1983 Jan-Feb(1):100-10.
5
Vestibular dysfunction in the epistatic circler mouse is caused by phenotypic interaction of one recessive gene and three modifier genes.上位性环行小鼠的前庭功能障碍是由一个隐性基因和三个修饰基因的表型相互作用引起的。
Genome Res. 2002 Apr;12(4):613-7. doi: 10.1101/gr.218402.
6
Mouse coat colour mutations: a molecular genetic resource which spans the centuries.
Bioessays. 1991 Sep;13(9):439-46. doi: 10.1002/bies.950130903.
7
Effects of diapause on lethal yellow (Ay/Ay) mouse embryos.
J Exp Zool. 1992 Sep 1;263(3):309-15. doi: 10.1002/jez.1402630310.
8
Morula decompaction (mdn), a preimplantation recessive lethal defect in a transgenic mouse line.桑椹胚致密化减退(mdn),一种转基因小鼠品系中的植入前隐性致死缺陷。
Dev Biol. 1993 Mar;156(1):265-77. doi: 10.1006/dbio.1993.1075.
9
Developmental analysis of the Hba(th-J) mouse mutation: effects on mouse peri-implantation development and identification of two candidate genes.Hba(th-J)小鼠突变的发育分析:对小鼠植入前发育的影响及两个候选基因的鉴定
Dev Biol. 1995 Nov;172(1):253-63. doi: 10.1006/dbio.1995.0020.
10
[Coat pigmentation and effect of the ocular retardation gene in the eye of chimeras between or/or and AKR mice].
Biull Eksp Biol Med. 1982 Mar;93(3):84-6.