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摇摆小鼠展神经核中的运动神经元损失。

Motoneuron loss in the abducens nucleus of wobbler mice.

作者信息

LaVail J H, Koo E H, Dekker N P

出版信息

Brain Res. 1987 Feb 24;404(1-2):127-32. doi: 10.1016/0006-8993(87)91363-1.

DOI:10.1016/0006-8993(87)91363-1
PMID:3567560
Abstract

The 'wobbler' mutant mouse can be recognized at about 4 weeks of age by its tremor and atrophy of forelimb muscles. In addition to degeneration of spinal motoneurons, especially in cervical spinal cord, selected bulbar motoneurons have also been reported to degenerate in the mutant. We examined a cranial motor nucleus and found a 31% loss of abducens motoneurons in 4-5-week-old wobbler mice as compared to age-matched control mice.

摘要

“摇摆症”突变小鼠在约4周龄时,可通过其震颤和前肢肌肉萎缩被识别出来。除了脊髓运动神经元退化,尤其是颈脊髓中的运动神经元,据报道该突变体中特定的延髓运动神经元也会退化。我们检查了一个颅神经运动核,发现与年龄匹配的对照小鼠相比,4-5周龄的摇摆症小鼠展神经运动神经元损失了31%。

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1
Motoneuron loss in the abducens nucleus of wobbler mice.摇摆小鼠展神经核中的运动神经元损失。
Brain Res. 1987 Feb 24;404(1-2):127-32. doi: 10.1016/0006-8993(87)91363-1.
2
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Loss of motor neurons from the median nerve motor nucleus of the mutant mouse 'wobbler'.突变小鼠“摇摆者”正中神经运动核运动神经元的丧失。
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Alteration in the levels of thyrotropin releasing hormone, substance P and enkephalins in the spinal cord, brainstem, hypothalamus and midbrain of the Wobbler mouse at different stages of the motoneuron disease.运动神经元病不同阶段的摇摆小鼠脊髓、脑干、下丘脑和中脑促甲状腺激素释放激素、P物质和脑啡肽水平的变化
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Quantitative light and electron microscopic studies on the ventral roots of the wobbler mutant mouse.对摆动小鼠腹根的定量光镜和电镜研究。
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Rodent models of tremor.震颤的啮齿动物模型。
Cerebellum. 2007;6(1):66-72. doi: 10.1080/14734220601016080.
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Turning heads: development of vertebrate branchiomotor neurons.引人注目:脊椎动物鳃运动神经元的发育
Dev Dyn. 2004 Jan;229(1):143-61. doi: 10.1002/dvdy.10444.
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The wobbler mouse: a neurodegeneration jigsaw puzzle.摇摆小鼠:一幅神经退行性变的拼图。
Mol Neurobiol. 2003 Aug;28(1):65-106. doi: 10.1385/MN:28:1:65.
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Neuron volume in the ventral horn in Wobbler mouse motoneuron disease: a light microscope stereological study.摇摆小鼠运动神经元疾病腹角神经元体积:光镜体视学研究
J Anat. 1997 Jul;191 ( Pt 1)(Pt 1):89-98. doi: 10.1046/j.1469-7580.1997.19110089.x.
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Bcl-2 sensitivity differentiates two pathways for motoneuronal death in the wobbler mutant mouse.Bcl-2敏感性区分了摇摆小鼠运动神经元死亡的两条途径。
J Neurosci. 1996 Oct 1;16(19):5897-904. doi: 10.1523/JNEUROSCI.16-19-05897.1996.
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Exclusion of two candidate genes, Spnb-2 and Dcd, for the wobbler spinal muscular atrophy gene on proximal mouse chromosome 11.
Mamm Genome. 1994 Mar;5(3):163-6. doi: 10.1007/BF00352348.