• 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

C57BL/KsJ小鼠的自发性肾盂积水

Spontaneous hydronephrosis in C57BL/KsJ mice.

作者信息

Wright J R, Lacy P E

机构信息

Department of Pathology, Washington University School of Medicine, St Louis, MO 63110.

出版信息

J Comp Pathol. 1988 Nov;99(4):449-54. doi: 10.1016/0021-9975(88)90063-1.

DOI:10.1016/0021-9975(88)90063-1
PMID:3204174
Abstract

Spontaneous hydronephrosis was observed in 15 of 33 necropsied C57BL/KsJ mice. The gross and histological appearances of these lesions are described. Spontaneous hydronephrosis is rare in mice and has not been previously described in this strain. At least four different mutations are reported to cause hydronephrosis in the mouse; each is associated with a high incidence of severe skeletal defects. Because no skeletal malformations were observed in the present study, it is likely that either a multigenic trait which has been present for a long time but is expressed variably, or a mutation other than those previously described may be responsible for hydronephrosis in C57BL/KsJ mice.

摘要

在33只接受尸检的C57BL/KsJ小鼠中,有15只观察到自发性肾积水。本文描述了这些病变的大体和组织学表现。自发性肾积水在小鼠中较为罕见,此前在该品系中尚未有过相关报道。据报道,至少有四种不同的突变可导致小鼠肾积水;每种突变都与严重骨骼缺陷的高发生率相关。由于在本研究中未观察到骨骼畸形,因此C57BL/KsJ小鼠的肾积水可能是由长期存在但表达可变的多基因性状,或者是先前未描述过的突变引起的。

相似文献

1
Spontaneous hydronephrosis in C57BL/KsJ mice.C57BL/KsJ小鼠的自发性肾盂积水
J Comp Pathol. 1988 Nov;99(4):449-54. doi: 10.1016/0021-9975(88)90063-1.
2
Unilateral perinephric pseudocyst secondary to hydronephrosis in a C57BL/6J mouse.一只C57BL/6J小鼠因肾积水继发单侧肾周假性囊肿。
Vet Pathol. 2005 Jul;42(4):496-8. doi: 10.1354/vp.42-4-496.
3
[Predisposition to hydronephrosis in C57BL/KsJ mice].
Z Versuchstierkd. 1981;23(6):327-32.
4
Hydronephrosis in inbred strains of mice with particular reference to the BRVR strain.近交系小鼠中的肾积水,特别提及BRVR品系。
Lab Anim. 1973 Sep;7(3):229-36. doi: 10.1258/002367773780944067.
5
Spontaneous heritable hydronephrosis in inbred mice. 1. Description, incidence, and distribution of lesions.
Lab Anim Sci. 1972 Jun;22(3):333-8.
6
Congenital progressive hydronephrosis in mice: a new recessive mutation.
J Urol. 1988 Nov;140(5 Pt 2):1310-5. doi: 10.1016/s0022-5347(17)42033-7.
7
Heritable hydronephrosis in a mutant strain of brown Norway rats.
Lab Anim Care. 1970 Jun;20(3):489-93.
8
Inheritance of hydronephrosis in the inbred mouse strain DDD.近交系小鼠DDD中肾盂积水的遗传
Lab Anim. 1984 Jan;18(1):22-5. doi: 10.1258/002367784780864893.
9
Microvasculature of hydronephrotic kidneys in KK-A(Y) mice.
J Vet Med Sci. 2000 Oct;62(10):1093-8. doi: 10.1292/jvms.62.1093.
10
Obstructive uropathy and hydronephrosis in male KK-Ay mice: a report of cases.雄性 KK-Ay 小鼠的梗阻性尿路病和肾积水:病例报告
J Vet Med Sci. 1999 Jan;61(1):53-7. doi: 10.1292/jvms.61.53.

引用本文的文献

1
Eosinophilic inflammation that begins in the juvenile stage causes hydronephrosis and urothelial cancer in mutant mice.始于幼年阶段的嗜酸性粒细胞炎症会在突变小鼠中引发肾积水和尿路上皮癌。
Sci Rep. 2024 Dec 4;14(1):30217. doi: 10.1038/s41598-024-81013-w.
2
Implications of Genetic Factors Underlying Mouse Hydronephrosis: Cautionary Considerations on Phenotypic Interpretation in Genetically Engineered Mice.遗传因素对小鼠肾盂积水的影响:对遗传工程小鼠表型解释的警示性考虑。
Int J Mol Sci. 2024 Jun 29;25(13):7203. doi: 10.3390/ijms25137203.
3
Investigation and identification of etiologies involved in the development of acquired hydronephrosis in aged laboratory mice with the use of high-frequency ultrasound imaging.
利用高频超声成像技术对老年实验小鼠获得性肾积水发病过程中涉及的病因进行调查与鉴定。
Pathobiol Aging Age Relat Dis. 2014 Aug 1;4. doi: 10.3402/pba.v4.24932. eCollection 2014.
4
Transgenic overexpression of p23 induces spontaneous hydronephrosis in mice.转基因过表达 p23 可诱导小鼠自发性肾盂积水。
Int J Exp Pathol. 2011 Aug;92(4):251-9. doi: 10.1111/j.1365-2613.2011.00762.x. Epub 2011 Feb 16.