Glycoprotein catabolism in brain tissue in the lysosomal enzyme deficiency diseases.
作者信息
Brunngraber E G, Davis L G, Javaid J I, Berra B
出版信息
Adv Exp Med Biol. 1976;68:31-48. doi: 10.1007/978-1-4684-7735-1_3.
PMID:820170
Abstract
摘要
相似文献
1
Glycoprotein catabolism in brain tissue in the lysosomal enzyme deficiency diseases.溶酶体酶缺乏疾病中脑组织的糖蛋白分解代谢
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Genetic disorders of lysosomes.溶酶体的遗传性疾病。
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Clinical and biochemical pathophysiology of ataxia in the sphingolipidoses.鞘脂贮积症中共济失调的临床与生化病理生理学
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[Hereditary diseases related to a disorder in the breakdown of carbohydrate-containing compounds].[与含碳水化合物化合物分解紊乱相关的遗传性疾病]
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Concentrations of an activator protein for sphingolipid hydrolysis in liver and brain samples from patients with lysosomal storage diseases.溶酶体贮积病患者肝脏和脑样本中鞘脂水解激活蛋白的浓度。
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Neuropathological changes in brain glycoproteins.
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Disorders of lipid metabolism.脂质代谢紊乱
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引用本文的文献
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Effects of a carbohydrate supplement upon resting brain activity.碳水化合物补充剂对静息脑活动的影响。
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Hepatic storage of oligosaccharides and glycolipids in a cat affected with GM1 gangliosidosis.一只患有GM1神经节苷脂贮积症的猫肝脏中寡糖和糖脂的储存情况。
Biochem J. 1978 Dec 1;175(3):945-53. doi: 10.1042/bj1750945.
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