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Site of pcd gene action and Purkinje cell mosaicism in cerebella of chimaeric mice.

作者信息

Mullen R J

出版信息

Nature. 1977 Nov 17;270(5634):245-7. doi: 10.1038/270245a0.

DOI:10.1038/270245a0
PMID:593342
Abstract
摘要

相似文献

1
Site of pcd gene action and Purkinje cell mosaicism in cerebella of chimaeric mice.嵌合小鼠小脑浦肯野细胞基因作用位点及浦肯野细胞镶嵌现象
Nature. 1977 Nov 17;270(5634):245-7. doi: 10.1038/270245a0.
2
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.
3
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.
4
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.
5
A new neurological mutant rat with symmetrical calcification of Purkinje cells in cerebellum.
Proc Soc Exp Biol Med. 1999 Sep;221(4):361-8. doi: 10.1046/j.1525-1373.1999.d01-93.x.
6
Genetic ablation of PLA2G6 in mice leads to cerebellar atrophy characterized by Purkinje cell loss and glial cell activation.在小鼠中基因敲除 PLA2G6 会导致小脑萎缩，其特征是浦肯野细胞丢失和神经胶质细胞激活。
PLoS One. 2011;6(10):e26991. doi: 10.1371/journal.pone.0026991. Epub 2011 Oct 28.
7
Staggerer chimeras: intrinsic nature of Purkinje cell defects and implications for normal cerebellar development.蹒跚突变嵌合体：浦肯野细胞缺陷的内在本质及其对正常小脑发育的影响。
Brain Res. 1979 Dec 14;178(2-3):443-57. doi: 10.1016/0006-8993(79)90705-4.
8
Hereditary disease of the cerebellar parenchyma.
Birth Defects Orig Artic Ser. 1971 Feb;7(1):192-6.
9
Tottering mouse motor dysfunction is abolished on the Purkinje cell degeneration (pcd) mutant background.蹒跚小鼠的运动功能障碍在浦肯野细胞变性（pcd）突变背景下消失。
Exp Neurol. 1999 Nov;160(1):268-78. doi: 10.1006/exnr.1999.7171.
10
Cerebellar abiotrophy in a family of Border Collie dogs.
Vet Pathol. 2002 Nov;39(6):736-8. doi: 10.1354/vp.39-6-736.

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1
Mutation of NEKL-4/NEK10 and TTLL genes suppress neuronal ciliary degeneration caused by loss of CCPP-1 deglutamylase function.NEKL-4/NEK10 和 TTLL 基因突变可抑制由 CCPP-1 脱谷氨酰胺酶功能丧失引起的神经元纤毛退化。
PLoS Genet. 2020 Oct 16;16(10):e1009052. doi: 10.1371/journal.pgen.1009052. eCollection 2020 Oct.
2
Cerebellar Pathways in Mouse Model of Purkinje Cell Degeneration Detected by High-Angular Resolution Diffusion Imaging Tractography.通过高角分辨率扩散成像纤维束成像检测浦肯野细胞变性小鼠模型中的小脑通路。
Cerebellum. 2017 Jun;16(3):648-655. doi: 10.1007/s12311-016-0842-5.
3
Evaluation of methods for one-dimensional spatial analysis of two-dimensional patterns in mouse chimaeras.
评估用于分析小鼠嵌合体二维模式的一维空间分析方法。
J Anat. 2011 Sep;219(3):418-37. doi: 10.1111/j.1469-7580.2011.01395.x. Epub 2011 May 27.
4
Nna1 mediates Purkinje cell dendritic development via lysyl oxidase propeptide and NF-κB signaling.Nna1 通过赖氨酰氧化酶前肽和 NF-κB 信号传导介导浦肯野细胞树突发育。
Neuron. 2010 Oct 6;68(1):45-60. doi: 10.1016/j.neuron.2010.08.013.
5
Quantitative analysis of patch patterns in mosaic tissues with ClonalTools software.使用 ClonalTools 软件对镶嵌组织中的嵌合体模式进行定量分析。
J Anat. 2009 Dec;215(6):698-704. doi: 10.1111/j.1469-7580.2009.01150.x. Epub 2009 Oct 13.
6
Autophagy activation and enhanced mitophagy characterize the Purkinje cells of pcd mice prior to neuronal death.自噬激活和增强的线粒体自噬是 pcd 小鼠浦肯野细胞在神经元死亡前的特征。
Mol Brain. 2009 Jul 29;2:24. doi: 10.1186/1756-6606-2-24.
7
Neocortical cell migration: GABAergic neurons and cells in layers I and VI move in a cyclin-dependent kinase 5-independent manner.新皮质细胞迁移：I层和VI层中的γ-氨基丁酸能神经元及细胞以不依赖细胞周期蛋白依赖性激酶5的方式移动。
J Neurosci. 2001 Dec 15;21(24):9690-700. doi: 10.1523/JNEUROSCI.21-24-09690.2001.
8
Pattern deformities and cell loss in Engrailed-2 mutant mice suggest two separate patterning events during cerebellar development.Engrailed-2突变小鼠中的模式畸形和细胞丢失表明在小脑发育过程中有两个独立的模式形成事件。
J Neurosci. 1997 Oct 15;17(20):7881-9. doi: 10.1523/JNEUROSCI.17-20-07881.1997.
9
Localization of the dopamine transporter gene, Dat1, on mouse chromosome 13.
Mamm Genome. 1994 Feb;5(2):117-8. doi: 10.1007/BF00292340.
10
Evidence for a genetically encoded map of functional development in the cerebellum.
Histochemistry. 1994 Aug;102(1):1-14. doi: 10.1007/BF00271044.