Sialidase deficiency in adult-type neuronal storage disease.
作者信息
Miyatake T, Yamada T, Suzuki M, Pallmann B, Sandhoff K, Ariga T, Atsumi T
出版信息
FEBS Lett. 1979 Jan 15;97(2):257-9. doi: 10.1016/0014-5793(79)80097-6.
PMID:761631
Abstract
摘要
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Sialidase deficiency in adult-type neuronal storage disease.成人型神经元贮积病中的唾液酸酶缺乏症
FEBS Lett. 1979 Jan 15;97(2):257-9. doi: 10.1016/0014-5793(79)80097-6.
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The identification of lysosomal ganglioside sialidase in human cells.人类细胞中溶酶体神经节苷脂唾液酸酶的鉴定。
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Molecular mechanism of lysosomal sialidase deficiency in galactosialidosis involves its rapid degradation.半乳糖唾液酸贮积症中溶酶体唾液酸酶缺乏的分子机制涉及其快速降解。
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[Adult type of neuronal storage disease with insufficient beta-galactosidase activity (author's transl)].成人型β-半乳糖苷酶活性不足的神经元贮积病（作者译）
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Sialidosis and galactosialidosis: chromosomal assignment of two genes associated with neuraminidase-deficiency disorders.唾液酸沉积症和半乳糖唾液酸沉积症：与神经氨酸酶缺乏症相关的两个基因的染色体定位
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