黏脂贮积症I型患者尿液中排泄的唾液酸寡糖结构 - Suppr

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Structures of sialyl-oligosaccharides excreted in the urine of a patient with mucolipidosis I.

作者信息

Michalski J C, Strecker G, Fournet B

出版信息

FEBS Lett. 1977 Jul 1;79(1):101-4. doi: 10.1016/0014-5793(77)80359-1.

DOI:10.1016/0014-5793(77)80359-1

PMID:891917

Abstract

摘要

相似文献

Structures of sialyl-oligosaccharides excreted in the urine of a patient with mucolipidosis I.黏脂贮积症I型患者尿液中排泄的唾液酸寡糖结构

FEBS Lett. 1977 Jul 1;79(1):101-4. doi: 10.1016/0014-5793(77)80359-1.

Structure of nine sialyl-oligosaccharides accumulated in urine of eleven patients with three different types of sialidosis. Mucolipidosis II and two new types of mucolipidosis.11例患有三种不同类型唾液酸沉积症、黏脂贮积症II型和两种新型黏脂贮积症患者尿液中积累的9种唾液酸寡糖的结构。

Eur J Biochem. 1977 May 16;75(2):391-403. doi: 10.1111/j.1432-1033.1977.tb11540.x.

Hypersialyloligosacchariduria in mucolipidoses: a method for diagnosis.黏脂贮积症中的高唾液酸化寡糖尿症：一种诊断方法。

Clin Chim Acta. 1978 Jun;86(2):159-67. doi: 10.1016/0009-8981(78)90129-8.

360-MHz 1H nuclear-magnetic-resonance spectroscopy of sialyl-oligosaccharides from patients with sialidosis (mucolipidosis I and II).唾液酸贮积症（黏脂贮积症I型和II型）患者唾液酸寡糖的360兆赫1H核磁共振光谱分析

Eur J Biochem. 1978 Jun 15;87(2):323-9. doi: 10.1111/j.1432-1033.1978.tb12381.x.

Structure of a novel sialooligosaccharide from the urine of a patient with mucolipidosis.来自黏脂贮积症患者尿液的一种新型唾液酸寡糖的结构

Tohoku J Exp Med. 1978 Apr;124(4):361-6. doi: 10.1620/tjem.124.361.

Urinary excretion patterns of sialoglycoconjugates in patients with mucolipidosis.黏脂贮积症患者唾液酸糖结合物的尿排泄模式。

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The simple detection of neuraminic acid-containing urinary oligosaccharides in patients with glycoprotein storage diseases.糖蛋白贮积病患者中含神经氨酸的尿寡糖的简易检测

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Sialidosis, a new type of inborn disease.

Curr Probl Clin Biochem. 1979(9):370-82.

Sialogluciduria in lysosomal diseases: quantitative and qualitative analysis of urinary low molecular sialoglucides from patients with mucopolysaccharidosis and with mucolipidosis.溶酶体疾病中的唾液酸糖尿症：黏多糖贮积症和黏脂贮积症患者尿中低分子唾液酸糖的定量和定性分析

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Studies on the pathogenesis of mucolipidosis.

Monogr Hum Genet. 1978;10:27-31. doi: 10.1159/000401561.

引用本文的文献

Exploration of the Sialic Acid World.探索唾液酸世界。

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Structural basis for substrate specificity of mammalian neuraminidases.哺乳动物神经氨酸酶底物特异性的结构基础。

PLoS One. 2014 Sep 15;9(9):e106320. doi: 10.1371/journal.pone.0106320. eCollection 2014.

Where catabolism meets signalling: neuraminidase 1 as a modulator of cell receptors.在分解代谢与信号转导相遇的地方：神经氨酸酶 1 作为细胞受体的调节剂。

Glycoconj J. 2011 Oct;28(7):441-52. doi: 10.1007/s10719-011-9350-5. Epub 2011 Sep 20.

Urinary oligosaccharides in lysosomal and other metabolic disorders.溶酶体及其他代谢紊乱中的尿寡糖

Ital J Neurol Sci. 1982 Mar;3(1):7-13. doi: 10.1007/BF02043342.

Urinary oligosaccharide excretion in disorders of glycolipid, glycoprotein and glycogen metabolism. A review of screening for differential diagnosis.糖脂、糖蛋白和糖原代谢紊乱时的尿低聚糖排泄。鉴别诊断筛查综述。

Eur J Pediatr. 1980 Sep;134(3):183-94. doi: 10.1007/BF00441471.

Purification and characterization of sialic acid containing materials accumulated in cultured skin fibroblasts from a patient with type II sialidosis.

J Inherit Metab Dis. 1987;10(1):33-47. doi: 10.1007/BF01799486.

Glycoprotein metabolism in normal and beta-mannosidase-deficient cultured goat skin fibroblasts.正常和β-甘露糖苷酶缺陷型培养山羊皮肤成纤维细胞中的糖蛋白代谢

Biochem J. 1986 Feb 15;234(1):175-83. doi: 10.1042/bj2340175.

A case of neuraminidase deficiency associated with a partial beta-galactosidase defect. Clinical, biochemical and radiological studies.一例与部分β-半乳糖苷酶缺陷相关的神经氨酸酶缺乏症。临床、生化及放射学研究。

Eur J Pediatr. 1979 Apr 3;130(4):239-49. doi: 10.1007/BF00441360.

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