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Alterations of astrocytic organelles in various lipidoses and allied diseases.

作者信息

Adachi M, Torii J, Karvounis P C, Volk B W

出版信息

Acta Neuropathol. 1971;18(1):74-83. doi: 10.1007/BF00684476.

DOI:10.1007/BF00684476
PMID:4325446
Abstract
摘要

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Acta Neuropathol. 1971;18(1):74-83. doi: 10.1007/BF00684476.
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Enzyme replacement treatment for Tay-Sachs disease brain cells in culture utilizing concanavalin A-mediated hexosaminidase A uptake: biochemical and morphological evidence of GM2 mobilization.利用伴刀豆球蛋白A介导的己糖胺酶A摄取对培养的泰-萨克斯病脑细胞进行酶替代治疗：GM2 转运的生化和形态学证据
Acta Neuropathol. 1980;50(1):9-17. doi: 10.1007/BF00688529.
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Acta Neuropathol. 1980;52(3):189-202. doi: 10.1007/BF00705807.
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Early central nervous system lesions in experimental hypercholesterolemia in normal and subdiabetic rabbits.

本文引用的文献

1
The enzymic and morphologic organization of the mitochondria.线粒体的酶学和形态学结构
Pediatrics. 1960 Sep;26:466-75.
2
Electron microscopy and the functional significance of a new cellular structure in plasmocytes: a review.浆细胞中一种新细胞结构的电子显微镜观察及其功能意义：综述
Blood. 1955 Jun;10(6):650-4.
3
ULTRASTRUCTURAL AND BIOCHEMICAL OBSERVATIONS ON A CASE OF SYSTEMIC LATE INFANTILE LIPIDOSIS AND ITS RELATIONSHIP TO TAY-SACHS DISEASE AND GARGOYLISM.一例全身性晚发性婴儿脂质沉积症的超微结构及生化观察及其与泰-萨克斯病和黏多糖贮积症的关系
正常及亚糖尿病兔实验性高胆固醇血症早期中枢神经系统病变
Acta Neuropathol. 1972;22(1):58-67. doi: 10.1007/BF00687550.
4
GM2-gangliosidosis, AB variant: clinico-pathological study of a case.GM2神经节苷脂贮积症，AB变异型：一例临床病理研究
Acta Neuropathol. 1975 Dec 19;33(3):207-26. doi: 10.1007/BF00688395.
5
Progress in investigations of sphingolipidoses.鞘脂类贮积病的研究进展
Acta Neuropathol. 1978 Aug 7;43(1-2):1-18. doi: 10.1007/BF00684994.
J Neuropathol Exp Neurol. 1965 Apr;24:318-40. doi: 10.1097/00005072-196504000-00011.
4
GENERALIZED GANGLIOSIDOSIS: ANOTHER INBORN ERROR OF GANGLIOSIDE METABOLISM?全身性神经节苷脂沉积症：另一种神经节苷脂代谢的先天性缺陷？
Am J Dis Child. 1965 Apr;109:338-46.
5
FAMILIAL NEUROVISCERAL LIPIDOSIS. AN ANALYSIS OF EIGHT CASES OF A SYNDROME PREVIOUSLY REPORTED AS "HURLER-VARIANT," "PSEUDO-HURLER," AND "TAY-SACHS DISEASE WITH VISCERAL INVOLVEMENT".家族性神经内脏脂质沉积症。对先前报告为“胡尔勒变异型”、“假性胡尔勒”和“伴有内脏受累的泰-萨克斯病”的一种综合征的8例病例分析。
Am J Dis Child. 1964 Nov;108:503-22.
6
FINE STRUCTURE OF THE LIPID BODIES IN JUVENILE AMAUROTIC IDIOCY.少年型黑蒙性白痴中脂质小体的精细结构
Acta Neuropathol. 1963 Nov 5;3:144-9. doi: 10.1007/BF00687063.
7
ON THE NATURE OF THE "STORED" LIPID SUBSTANCES IN JUVENILE AMAUROTIC IDIOCY (BATTEN-SPIELMEYER-VOGT).关于青少年黑蒙性白痴（巴滕 - 施皮尔迈尔 - 沃格特病）中“储存”脂质物质的性质
Ann Histochim. 1963 Jul-Sep;8:255-7.
8
Studies in Tay-Sachs disease. II. Ultrastructure of the cerebrum.泰-萨克斯病的研究。II. 大脑的超微结构。
J Neuropathol Exp Neurol. 1963 Jan;22:18-55. doi: 10.1097/00005072-196301000-00003.
9
How cells transform energy.
Sci Am. 1961 Sep;205:62-73. doi: 10.1038/scientificamerican0961-62.
10
Mitochondrial localization of oxidative enzymes: staining results with two tetrazolium salts.氧化酶的线粒体定位：两种四唑盐的染色结果
J Biophys Biochem Cytol. 1961 Jan;9(1):47-61. doi: 10.1083/jcb.9.1.47.