• 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

Three syndromes produced by two mutant genes in the mouse. Clinical, pathological, and ultrastructural bases of tottering, leaner, and heterozygous mice.

作者信息

Meier H, MacPike A D

出版信息

J Hered. 1971 Sep-Oct;62(5):297-302. doi: 10.1093/oxfordjournals.jhered.a108176.

DOI:10.1093/oxfordjournals.jhered.a108176
PMID:4941467
Abstract
摘要

相似文献

1
Three syndromes produced by two mutant genes in the mouse. Clinical, pathological, and ultrastructural bases of tottering, leaner, and heterozygous mice.
J Hered. 1971 Sep-Oct;62(5):297-302. doi: 10.1093/oxfordjournals.jhered.a108176.
2
[Genetic relationship of two mutant genes which producing three different syndromes in the mouse (author's transl)].在小鼠中产生三种不同综合征的两个突变基因的遗传关系(作者译)
Jikken Dobutsu. 1975 Jul;24(3):111-8. doi: 10.1538/expanim1957.24.3_111.
3
Rocker is a new variant of the voltage-dependent calcium channel gene Cacna1a.Rocker是电压依赖性钙通道基因Cacna1a的一种新变体。
J Neurosci. 2001 Feb 15;21(4):1169-78. doi: 10.1523/JNEUROSCI.21-04-01169.2001.
4
An ultrastructural study of granule cell/Purkinje cell synapses in tottering (tg/tg), leaner (tg(la)/tg(la)) and compound heterozygous tottering/leaner (tg/tg(la)) mice.对蹒跚小鼠(tg/tg)、倾斜小鼠(tg(la)/tg(la))和复合杂合蹒跚/倾斜小鼠(tg/tg(la))颗粒细胞/浦肯野细胞突触的超微结构研究。
Neuroscience. 1999 Mar;90(3):717-28. doi: 10.1016/s0306-4522(98)00518-1.
5
The Purkinje cell dendritic tree in mutant mouse cerebellum. A quantitative Golgi study of Weaver and Staggerer mice.
Brain Res. 1978 Feb 17;142(1):135-41. doi: 10.1016/0006-8993(78)90182-8.
6
Progressive atrophy of cerebellar Purkinje cell dendrites during aging of the heterozygous staggerer mouse (Rora(+/sg)).杂合子蹒跚小鼠(Rora(+/sg))衰老过程中小脑浦肯野细胞树突的进行性萎缩。
Brain Res Dev Brain Res. 2001 Feb 28;126(2):201-9. doi: 10.1016/s0165-3806(01)00095-5.
7
Organization of cerebellar cortex secondary to deficit of granule cells in weaver mutant mice.韦弗突变小鼠颗粒细胞缺陷继发的小脑皮质组织学变化
J Comp Neurol. 1973 Nov 15;152(2):133-61. doi: 10.1002/cne.901520203.
8
The development and degeneration of Purkinje cells in pcd mutant mice.
J Comp Neurol. 1978 Jan 1;177(1):125-43. doi: 10.1002/cne.901770109.
9
Development of the paramedian lobule of the cerebellum in wild-type and tottering mice.
Dev Neurosci. 1992;14(5-6):386-93. doi: 10.1159/000111687.
10
Sequence of developmental abnormalities leading to granule cell deficit in cerebellar cortex of weaver mutant mice.导致韦弗突变小鼠小脑皮质颗粒细胞缺失的发育异常序列。
J Comp Neurol. 1973 Nov 15;152(2):103-32. doi: 10.1002/cne.901520202.

引用本文的文献

1
Altered brain state during episodic dystonia in tottering mice decouples primary motor cortex from limb kinematics.蹒跚小鼠发作性肌张力障碍期间的脑状态改变使初级运动皮层与肢体运动学解耦。
Dystonia. 2023;2. doi: 10.3389/dyst.2023.10974. Epub 2023 Feb 2.
2
Disrupted Calcium Signaling in Animal Models of Human Spinocerebellar Ataxia (SCA).人类脊髓小脑共济失调症动物模型中的钙信号紊乱。
Int J Mol Sci. 2019 Dec 27;21(1):216. doi: 10.3390/ijms21010216.
3
Using the shared genetics of dystonia and ataxia to unravel their pathogenesis.利用肌张力障碍和共济失调的共同遗传学来揭示它们的发病机制。
Neurosci Biobehav Rev. 2017 Apr;75:22-39. doi: 10.1016/j.neubiorev.2017.01.033. Epub 2017 Jan 28.
4
Linking Essential Tremor to the Cerebellum-Animal Model Evidence.将特发性震颤与小脑联系起来——动物模型证据
Cerebellum. 2016 Jun;15(3):285-98. doi: 10.1007/s12311-015-0750-0.
5
Abnormal excitability and episodic low-frequency oscillations in the cerebral cortex of the tottering mouse.蹒跚小鼠大脑皮层的异常兴奋性和阵发性低频振荡。
J Neurosci. 2015 Apr 8;35(14):5664-79. doi: 10.1523/JNEUROSCI.3107-14.2015.
6
Dystonia and cerebellar degeneration in the leaner mouse mutant.瘦型小鼠突变体中的肌张力障碍和小脑变性。
Brain Res. 2015 Jun 22;1611:56-64. doi: 10.1016/j.brainres.2015.03.011. Epub 2015 Mar 16.
7
Flocculus Purkinje cell signals in mouse Cacna1a calcium channel mutants of escalating severity: an investigation of the role of firing irregularity in ataxia.小鼠中严重程度不断升级的Cacna1a钙通道突变体的小脑绒球浦肯野细胞信号:对放电不规则性在共济失调中作用的研究
J Neurophysiol. 2014 Nov 15;112(10):2647-63. doi: 10.1152/jn.00129.2014. Epub 2014 Aug 20.
8
The first knockin mouse model of episodic ataxia type 2.发作性共济失调2型的首个基因敲入小鼠模型。
Exp Neurol. 2014 Nov;261:553-62. doi: 10.1016/j.expneurol.2014.08.001. Epub 2014 Aug 8.
9
STD-dependent and independent encoding of input irregularity as spike rate in a computational model of a cerebellar nucleus neuron.在小脑核神经元的计算模型中,输入不规则性的 STD 依赖和独立编码为尖峰率。
Cerebellum. 2011 Dec;10(4):667-82. doi: 10.1007/s12311-011-0295-9.
10
The ataxic Syrian hamster: an animal model homologous to the pcd mutant mouse?共济失调型叙利亚仓鼠:一种与pcd突变小鼠同源的动物模型?
Cerebellum. 2009 Sep;8(3):202-10. doi: 10.1007/s12311-009-0113-9. Epub 2009 May 22.