Multiple human hexosaminidases.
作者信息
Sandhoff K
出版信息
Birth Defects Orig Artic Ser. 1973 Mar;9(2):214-22.
PMID:4611533
Abstract
摘要
相似文献
1
Multiple human hexosaminidases.多种人类己糖胺酶。
Birth Defects Orig Artic Ser. 1973 Mar;9(2):214-22.
2
Enzyme alterations and lipid storage in three variants of Tay-Sachs disease.三种泰-萨克斯病变体中的酶改变与脂质储存
J Neurochem. 1971 Dec;18(12):2469-89. doi: 10.1111/j.1471-4159.1971.tb00204.x.
3
Hexosaminidases and ganglioside catabolism in the GM2-gangliosidoses.GM2神经节苷脂贮积症中的己糖胺酶与神经节苷脂分解代谢
Chem Phys Lipids. 1974 Dec;13(4):292-304. doi: 10.1016/0009-3084(74)90005-x.
4
Isolation and relationship of human hexosaminidases.人己糖胺酶的分离及其相互关系
J Biol Chem. 1974 Jun 10;249(11):3489-99.
5
Gm2-gangliosidosis: studies in cultured fibroblasts.
Birth Defects Orig Artic Ser. 1973 Mar;9(2):130-5.
6
The enzymology of Tay-Sachs disease and its variant forms.泰-萨克斯病及其变异型的酶学
UCLA Forum Med Sci. 1975(18):479-99. doi: 10.1016/b978-0-12-139050-1.50035-5.
7
Asialo GM-ganglioside in brain fetal Tay-Sachs disease.脑胎儿型泰-萨克斯病中的脱唾液酸GM神经节苷脂
J Neurochem. 1975 Jan;24(1):183-4. doi: 10.1111/j.1471-4159.1975.tb07646.x.
8
[Enrichment and characterization of 2 forms of human N-acetyl-beta-D-hexosaminidase].[两种形式的人N-乙酰-β-D-己糖胺酶的富集与特性分析]
Hoppe Seylers Z Physiol Chem. 1971 Aug;352(8):1119-33.
9
[Sphingolipidosis].[鞘脂贮积症]
Pol Tyg Lek. 1980 Dec 29;35(52):2067-71.
10
[A sphingolipidosis with the accumulation of neutral glycosphingolipids, AO2(GM3) and A1(GM2)-ganglioside (author's transl)].一种伴有中性糖鞘脂、AO2（GM3）和A1（GM2）神经节苷脂蓄积的鞘脂沉积症（作者译）
Z Klin Chem Klin Biochem. 1974 Nov;12(11):487-93.
引用本文的文献
1
Membrane lipids and their degradation compounds control GM2 catabolism at intralysosomal luminal vesicles.膜脂及其降解产物控制溶酶体腔内囊泡中的 GM2 分解代谢。
J Lipid Res. 2019 Jun;60(6):1099-1111. doi: 10.1194/jlr.M092551. Epub 2019 Apr 15.
2
My journey into the world of sphingolipids and sphingolipidoses.我在神经鞘脂类和神经鞘脂贮积症领域的探索之旅。
Proc Jpn Acad Ser B Phys Biol Sci. 2012;88(10):554-82. doi: 10.2183/pjab.88.554.
3
Sphingolipidoses.鞘脂贮积症
J Clin Pathol Suppl (R Coll Pathol). 1974;8:94-105.
4
[Sphingolipid storage disease as an example of a molecular neuropathology (author's transl)].以鞘脂贮积病为例的分子神经病理学（作者译）
Arch Psychiatr Nervenkr (1970). 1976 Apr 30;221(3):213-25. doi: 10.1007/BF00418481.
5
Biochemistry and genetics of gangliosidoses.神经节苷脂贮积症的生物化学与遗传学
Hum Genet. 1979;50(2):107-43. doi: 10.1007/BF00390234.
Zotero 插件