• 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

关于小鼠早期胚胎致死性多指(趾)畸形(Os)的体内和体外研究。

In vivo and in vitro studies on the early embryonic lethal oligosyndactylism (Os) in the mouse.

作者信息

Paterson H F

出版信息

J Embryol Exp Morphol. 1979 Aug;52:115-25.

PMID:230280
Abstract

The development of mouse embryos homozygous for oligosyndactylism (Os) is arrested during implantation. Histological investigations confirm a previous report that cells become blocked in mitosis, and air-dried spreads of the mutant embryos reveal that large numbers of cells accumulate in metaphase. Trophoblastic giant cells appear unaffected by the action of the mutant gene both in utero and during culture over the lethal phase. It is proposed that the form of endoreduplication undergone by giant cells renders them refractory to the metaphase block.

摘要

纯合少指(趾)畸形(Os)小鼠胚胎在着床期间发育停滞。组织学研究证实了之前的一份报告,即细胞在有丝分裂中受阻,突变胚胎的空气干燥涂片显示大量细胞积聚在中期。滋养层巨细胞在子宫内以及在致死期的培养过程中似乎不受突变基因作用的影响。有人提出,巨细胞经历的核内复制形式使它们对中期阻断具有抗性。

相似文献

1
In vivo and in vitro studies on the early embryonic lethal oligosyndactylism (Os) in the mouse.关于小鼠早期胚胎致死性多指(趾)畸形(Os)的体内和体外研究。
J Embryol Exp Morphol. 1979 Aug;52:115-25.
2
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.
3
In vivo and in vitro development of mouse embryos homozygous for the embryonic lethal velvet coat (Ve) mutation.胚胎致死性天鹅绒被毛(Ve)突变纯合小鼠胚胎的体内和体外发育
J Embryol Exp Morphol. 1981 Dec;66:43-55.
4
Enhanced susceptibility of mouse embryos heterozygous for oligosyndactyly (Os/+) to mitomycin C-induced skeletal abnormalities.少指(趾)畸形杂合子(Os/+)小鼠胚胎对丝裂霉素C诱导的骨骼异常的易感性增强。
Teratology. 1987 Apr;35(2):261-5. doi: 10.1002/tera.1420350213.
5
Arp3 is required during preimplantation development of the mouse embryo.Arp3在小鼠胚胎植入前发育过程中是必需的。
FEBS Lett. 2007 Dec 11;581(29):5691-7. doi: 10.1016/j.febslet.2007.11.031. Epub 2007 Nov 21.
6
Development of mouse embryos in hanging drop culture.
Anat Rec. 1985 Jan;211(1):48-56. doi: 10.1002/ar.1092110109.
7
Ginkgolides induce apoptosis and decrease cell numbers in mouse blastocysts.银杏内酯可诱导小鼠囊胚细胞凋亡并减少细胞数量。
Biochem Biophys Res Commun. 2005 Dec 16;338(2):1263-7. doi: 10.1016/j.bbrc.2005.10.085. Epub 2005 Oct 24.
8
Mouse half embryos: viability and allocation of cells in the blastocyst.
Dev Dyn. 1995 Aug;203(4):393-8. doi: 10.1002/aja.1002030402.
9
Oligosyndactyly: a lethal mutation in the mouse that results in mitotic arrest very early in development.少指(趾)并指(趾)畸形:小鼠中的一种致死性突变,导致发育早期的有丝分裂停滞。
Cell. 1984 Oct;38(3):823-33. doi: 10.1016/0092-8674(84)90277-0.
10
Time of commitment of inside cells isolated from preimplantation mouse embryos.从植入前小鼠胚胎中分离出的内细胞的确定时间。
J Embryol Exp Morphol. 1978 Jun;45:37-53.

引用本文的文献

1
Phenotyping by magnetic resonance imaging nondestructively measures glomerular number and volume distribution in mice with and without nephron reduction.通过磁共振成像进行表型分析可无损测量有或没有肾单位减少的小鼠的肾小球数量和体积分布。
Kidney Int. 2016 Feb;89(2):498-505. doi: 10.1038/ki.2015.316.
2
Oligosyndactylism mice have an inversion of chromosome 8.少趾畸形小鼠存在8号染色体倒位。
Genetics. 2004 Dec;168(4):2099-112. doi: 10.1534/genetics.104.031914.
3
A transgene-induced mitotic arrest mutation in the mouse allelic with Oligosyndactylism.
一种与少指(趾)畸形等位的转基因诱导的小鼠有丝分裂停滞突变。
Genetics. 1996 Dec;144(4):1747-56. doi: 10.1093/genetics/144.4.1747.
4
Developmental genetics.发育遗传学
Experientia. 1986 Oct 15;42(10):1117-28. doi: 10.1007/BF01941286.