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Developmental mechanism for changes in cerebellum of "staggerer" mouse, a neurological mutant of genetic origin.

作者信息

Yoon C H

出版信息

Neurology. 1972 Jul;22(7):743-54. doi: 10.1212/wnl.22.7.743.

DOI:10.1212/wnl.22.7.743
PMID:4673255
Abstract
摘要

相似文献

1
Developmental mechanism for changes in cerebellum of "staggerer" mouse, a neurological mutant of genetic origin.
Neurology. 1972 Jul;22(7):743-54. doi: 10.1212/wnl.22.7.743.
2
Abnormal rate of granule cell migration in the cerebellum of "Weaver" mutant mice.“Weaver”突变小鼠小脑颗粒细胞迁移速率异常。
Dev Biol. 1972 Sep;29(1):17-26. doi: 10.1016/0012-1606(72)90039-5.
3
Cribriform degeneration (cri): a new recessive neurological mutation in the mouse.
Science. 1972 May 19;176(4036):800-3. doi: 10.1126/science.176.4036.800.
4
Pleiotropic effect of the staggerer gene.蹒跚基因的多效性效应。
Brain Res. 1976 Jun 4;109(1):206-15. doi: 10.1016/0006-8993(76)90395-4.
5
A new rat mutant with defective overhairs and spongy degeneration of the central nervous system: clinical and pathologic studies.
Lab Anim Sci. 1982 Feb;32(1):70-3.
6
[3H-thymidine autoradiographic studies on the neurogenesis of the mouse cerebellum].
Kaibogaku Zasshi. 1971 Oct;46(5):289-311.
7
Multiple increase of DNA content in Purkinje cells in the ontogeny of the rat.大鼠个体发育过程中小脑浦肯野细胞DNA含量的多次增加。
Sov J Dev Biol. 1971 Jan-Feb;2(1):23-5.
8
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.
9
Staggerer, a new mutation in the mouse affecting the cerebellum.蹒跚者，一种影响小鼠小脑的新突变。
Science. 1962 Aug 24;137(3530):610-2. doi: 10.1126/science.137.3530.610.
10
Fine structure of the cerebellum of "staggerer-reeler", a double mutant of mice affected by staggerer and reeler conditions. II. Purkinje cell anomalies.“蹒跚 - 摇晃”小鼠（一种受蹒跚和摇晃病症影响的双突变小鼠）小脑的精细结构。II. 浦肯野细胞异常。
J Neuropathol Exp Neurol. 1977 May;36(3):427-39. doi: 10.1097/00005072-197705000-00002.

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显性 RORA 突变的双重分子效应导致伴有自闭症或小脑共济失调的两种综合征性智力障碍变异体。
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An innate immune response and altered nuclear receptor activation defines the spinal cord transcriptome during alpha-tocopherol deficiency in Ttpa-null mice.在 Ttpa 基因敲除小鼠的α-生育酚缺乏症期间，固有免疫反应和核受体激活的改变定义了脊髓转录组。
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Abnormal cerebellar cytoarchitecture and impaired inhibitory signaling in adult mice lacking TR4 orphan nuclear receptor.缺乏TR4孤儿核受体的成年小鼠中，小脑细胞结构异常且抑制性信号传导受损。
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RORalpha coordinates reciprocal signaling in cerebellar development through sonic hedgehog and calcium-dependent pathways.RORα通过音猬因子和钙依赖途径在小脑发育过程中协调相互信号传导。
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In vitro and in vivo evidence for orphan nuclear receptor RORalpha function in bone metabolism.孤儿核受体RORα在骨代谢中作用的体外和体内证据
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Cerebellar alterations in the weaver mouse.韦弗小鼠的小脑改变
J Cell Biol. 1973 Feb;56(2):478-86. doi: 10.1083/jcb.56.2.478.
10
Staggerer-specific protein SP47: a unique species among age- and genotype-dependent cerebellar proteins.蹒跚突变小鼠特异性蛋白SP47：年龄和基因型依赖性小脑蛋白中的独特物种。
Neurochem Res. 1987 Jan;12(1):53-60. doi: 10.1007/BF00971364.