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蹒跚者,一种患有小脑疾病的新型突变小鼠。

Stumbler, a new mutant mouse with cerebellar disease.

作者信息

Caddy K W, Sidman R L, Eicher E M

出版信息

Brain Res. 1981 Mar 9;208(1):251-5. doi: 10.1016/0006-8993(81)90643-0.

DOI:10.1016/0006-8993(81)90643-0
PMID:7470926
Abstract

A new mutant mouse named Stumbler (stu) displays clinical features suggesting a cerebellar lesion. The main light microscopic findings, based on a Golgi technique and on sections of plastic embedded material, are that Purkinje cells in the mutant cerebellum have small dendritic arborizations and exhibit immature spines on their somata. Purkinje cells also contain an increased number of mitochondrial profiles both in cell bodies and in swellings on dendrites.

摘要

一种名为“蹒跚者”(stu)的新突变小鼠表现出提示小脑病变的临床特征。基于高尔基技术和塑料包埋材料切片的主要光学显微镜观察结果是,突变小鼠小脑中的浦肯野细胞具有小的树突分支,并且其胞体上呈现未成熟的棘突。浦肯野细胞的细胞体和树突肿胀处的线粒体轮廓数量也增加。

相似文献

1
Stumbler, a new mutant mouse with cerebellar disease.蹒跚者,一种患有小脑疾病的新型突变小鼠。
Brain Res. 1981 Mar 9;208(1):251-5. doi: 10.1016/0006-8993(81)90643-0.
2
Purkinje cells and granule cells in the cerebellum of the Stumbler mutant mouse.蹒跚突变小鼠小脑中的浦肯野细胞和颗粒细胞。
Brain Res. 1981 Apr;227(2):221-36. doi: 10.1016/0165-3806(81)90110-3.
3
Heterologous synapses upon Purkinje cells in the cerebellum of the Reeler mutant mouse: an experimental light and electron microscopic study.瑞勒氏突变小鼠小脑浦肯野细胞上的异源性突触:一项光镜和电镜实验研究
Brain Res. 1981 May 25;213(1):63-82. doi: 10.1016/0006-8993(81)91248-8.
4
Cerebellar Purkinje cells from the lurcher mutant and wild-type mouse grown in vitro: a light and electron microscope study.体外培养的蹒跚突变型和野生型小鼠的小脑浦肯野细胞:光镜和电镜研究
J Comp Neurol. 1995 Jun 19;357(1):161-79. doi: 10.1002/cne.903570114.
5
Anatomical, physiological and biochemical studies of the cerebellum from mutant mice. II. Morphological study of cerebellar cortical neurons and circuits in the weaver mouse.突变小鼠小脑的解剖学、生理学和生物化学研究。II. 织工鼠小脑皮质神经元和神经回路的形态学研究。
Brain Res. 1975 Aug 22;94(1):19-44. doi: 10.1016/0006-8993(75)90874-4.
6
Quantitative study of the Purkinje cell dendritic spines in the rat cerebellum.大鼠小脑浦肯野细胞树突棘的定量研究。
J Comp Neurol. 1988 Aug 8;274(2):158-67. doi: 10.1002/cne.902740203.
7
The stumbler mutation maps to proximal mouse chromosome 2.
Mamm Genome. 1994 Nov;5(11):659-62. doi: 10.1007/BF00426071.
8
Fate of grafted embryonic Purkinje cells in the cerebellum of the adult "Purkinje cell degeneration" mutant mouse. I. Development of reciprocal graft-host interactions.成年“浦肯野细胞变性”突变小鼠小脑内移植的胚胎浦肯野细胞的命运。I. 相互移植-宿主相互作用的发展
J Comp Neurol. 1990 May 8;295(2):165-87. doi: 10.1002/cne.902950202.
9
Stunted morphologies of cerebellar Purkinje cells in lurcher and staggerer mice are cell-intrinsic effects of the mutant genes.蹒跚症和摇晃症小鼠中,小脑浦肯野细胞的发育不良形态是突变基因的细胞内在效应。
J Comp Neurol. 1995 Jun 19;357(1):65-75. doi: 10.1002/cne.903570107.
10
Correlative light and electron microscopic observations on ectopic neurons in the cerebellum of dreher mutant mouse.
J Electron Microsc (Tokyo). 1991 Feb;40(1):11-8.

引用本文的文献

1
Cerebellar nuclei cells produce distinct pathogenic spike signatures in mouse models of ataxia, dystonia, and tremor.小脑核细胞在共济失调、肌张力障碍和震颤的小鼠模型中产生独特的致病棘波特征。
Elife. 2024 Jul 29;12:RP91483. doi: 10.7554/eLife.91483.
2
Cerebellar dysfunction in rodent models with dystonia, tremor, and ataxia.患有肌张力障碍、震颤和共济失调的啮齿动物模型中的小脑功能障碍。
Dystonia. 2023;2. doi: 10.3389/dyst.2023.11515. Epub 2023 Dec 8.
3
Mutational ataxia resulting from abnormal vestibular acquisition and processing is partially compensated for.
由异常的前庭获取和处理导致的突变性共济失调得到了部分代偿。
Behav Neurosci. 2012 Apr;126(2):301-13. doi: 10.1037/a0026896. Epub 2012 Feb 6.
4
The stumbler mutation maps to proximal mouse chromosome 2.
Mamm Genome. 1994 Nov;5(11):659-62. doi: 10.1007/BF00426071.