Alpha-L-fucosidase and alpha-D-mannosidase activity in the white blood cells in the disease and carrier state of fucosidosis.
作者信息
Matsuda I, Arashima S, Anakura M, Oka Y
出版信息
Clin Chim Acta. 1973 Sep 28;48(1):9-13. doi: 10.1016/0009-8981(73)90210-6.
PMID:4746732
Abstract
摘要
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Alpha-L-fucosidase and alpha-D-mannosidase activity in the white blood cells in the disease and carrier state of fucosidosis.岩藻糖贮积症患者及携带者状态下白细胞中α-L-岩藻糖苷酶和α-D-甘露糖苷酶的活性
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Deficiency of alpha-L-fucosidase.α-L-岩藻糖苷酶缺乏症
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Two different families with alpha-L-fucosidase deficiency.两个患有α-L-岩藻糖苷酶缺乏症的不同家族。
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Determination of lysosomal enzymes in saliva. Confirmation of the diagnosis of metachromatic leukodystrophy and fucosidosis by enzyme analysis.唾液中溶酶体酶的测定。通过酶分析确诊异染性脑白质营养不良和岩藻糖苷贮积症。
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Identification of mannosidosis heterozygotes--factors affecting normal plasma alpha-mannosidase levels.甘露糖苷贮积症杂合子的鉴定——影响正常血浆α-甘露糖苷酶水平的因素
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Fucosidosis: detection of the carrier state in peripheral blood leukocytes.岩藻糖苷贮积症：外周血白细胞中携带者状态的检测
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Mannosidosis: studies of the alpha-D-mannosidase isozymes in health and disease.甘露糖苷贮积症：健康与疾病状态下α-D-甘露糖苷酶同工酶的研究
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Glycosidases in normal human leukocytes and abnormalities in G M1 -gangliosidosis.
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alpha-L-fucosidase in cultured skin fibroblasts from normal subjects and fucosidosis patients.来自正常受试者和岩藻糖贮积症患者的培养皮肤成纤维细胞中的α-L-岩藻糖苷酶
Pediatr Res. 1977 Jul;11(7):862-6. doi: 10.1203/00006450-197707000-00017.
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The nature of the residual alpha-mannosidase in plasma in bovine mannosidosis.牛甘露糖苷贮积症中血浆残留α-甘露糖苷酶的性质
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