Sialidase deficiency in adult-type neuronal storage disease. - Suppr | 超能文献

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.

DOI:10.1016/0014-5793(79)80097-6

Abstract

摘要

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

文档翻译

学术文献翻译模型，支持多种主流文档格式。

相似文献

1

Sialidase deficiency in adult-type neuronal storage disease.

FEBS Lett. 1979 Jan 15;97(2):257-9. doi: 10.1016/0014-5793(79)80097-6.

2

Adult type neuronal storage disease with neuraminidase deficiency.成人型神经氨酸酶缺乏性神经元贮积病。

Ann Neurol. 1979 Sep;6(3):232-44. doi: 10.1002/ana.410060310.

3

Mucolipidosis type IV: ganglioside sialidase deficiency.

Biochem Biophys Res Commun. 1979 Oct 29;90(4):1341-7. doi: 10.1016/0006-291x(79)91183-5.

4

Neuraminidase studies in sialidosis.唾液酸贮积症中的神经氨酸酶研究。

Adv Exp Med Biol. 1980;125:415-30. doi: 10.1007/978-1-4684-7844-0_38.

5

Oligosaccharide and ganglioside neuraminidase activities of mucolipidosis I (sialidosis) and mucolipidosis II (I-cell disease) fibroblasts.黏脂贮积症I型（唾液酸沉积症）和黏脂贮积症II型（I-细胞病）成纤维细胞的寡糖和神经节苷脂神经氨酸酶活性

Eur J Biochem. 1979 Jun;97(1):113-8. doi: 10.1111/j.1432-1033.1979.tb13091.x.

6

Mucolipidosis IV, a sialolipidosis due to ganglioside sialidase deficiency.IV型黏脂贮积症，一种由于神经节苷脂唾液酸酶缺乏引起的唾液酸脂沉积症。

J Inherit Metab Dis. 1982;5(4):218-24. doi: 10.1007/BF02179146.

7

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。

Eur J Biochem. 1989 Aug 1;183(2):455-8. doi: 10.1111/j.1432-1033.1989.tb14949.x.

8

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。

Biochem J. 1998 Mar 1;330 ( Pt 2)(Pt 2):641-50. doi: 10.1042/bj3300641.

9

[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）

Rinsho Shinkeigaku. 1978 Dec;18(12):771-2.

10

Beta-galactosidase-neuraminidase deficiency: restoration of beta-galactosidase activity by protease inhibitors.β-半乳糖苷酶-神经氨酸酶缺乏症：蛋白酶抑制剂恢复β-半乳糖苷酶活性

J Biochem. 1981 Jul;90(1):271-3. doi: 10.1093/oxfordjournals.jbchem.a133462.

引用本文的文献

1

Cherry-red spot myoclonus syndrome and alpha-neuraminidase deficiency: neurophysiological, pharmacological and biochemical study in an adult.

J Neurol Neurosurg Psychiatry. 1980 Oct;43(10):934-40. doi: 10.1136/jnnp.43.10.934.

2

Ganglioside GM1 metabolism in living human fibroblasts with beta-galactosidase deficiency.β-半乳糖苷酶缺乏的人活体成纤维细胞中神经节苷脂GM1的代谢

Hum Genet. 1986 May;73(1):35-8. doi: 10.1007/BF00292661.

3

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

Proc Natl Acad Sci U S A. 1986 Mar;83(6):1817-21. doi: 10.1073/pnas.83.6.1817.