[2例岩藻糖苷贮积症患者尿液中排泄的9种含大量岩藻糖的寡糖和糖肽的结构] - Suppr | 超能文献

[Structures of 9 oligosaccharides and glycopeptides containing large amounts of fucose excreted in the urine of 2 patients with fucosidosis].

作者信息

Strecker G, Fournet B, Spik G, Montreuil J, Durand P, Tondeur M

出版信息

C R Acad Hebd Seances Acad Sci D. 1977 Jan 3;284(1):85-8.

Abstract

摘要

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1

[Structures of 9 oligosaccharides and glycopeptides containing large amounts of fucose excreted in the urine of 2 patients with fucosidosis].[2例岩藻糖苷贮积症患者尿液中排泄的9种含大量岩藻糖的寡糖和糖肽的结构]

C R Acad Hebd Seances Acad Sci D. 1977 Jan 3;284(1):85-8.

2

Urinary excretion of a novel hexasaccharide and glycopeptide analogue in fucosidosis.岩藻糖贮积症中一种新型六糖和糖肽类似物的尿排泄情况。

Biochem Biophys Res Commun. 1979 May 28;88(2):696-705. doi: 10.1016/0006-291x(79)92104-1.

3

Fucosidosis in Calabria: founder effect or high gene frequency.卡拉布里亚的岩藻糖苷贮积症：奠基者效应还是高基因频率？

Lancet. 1977 Feb 12;1(8007):368-9. doi: 10.1016/s0140-6736(77)91175-8.

4

Enzyme activity in fucosidosis.岩藻糖苷贮积症中的酶活性。

Lancet. 1977 Jan 29;1(8005):264. doi: 10.1016/s0140-6736(77)91070-4.

5

Silent allele as genetic basis of fucosidosis.沉默等位基因作为岩藻糖苷贮积症的遗传基础。

Nature. 1975 Oct 2;257(5525):391-2. doi: 10.1038/257391a0.

6

[Recent acquisitions on fucosidosis].[近期关于岩藻糖苷贮积症的研究进展]

Arch Fr Pediatr. 1975 Nov;32(9):769-72.

7

Fucosidosis: How many cases undetected?岩藻糖苷贮积症：有多少未被发现的病例？

Lancet. 1975 Sep 6;2(7932):462-3. doi: 10.1016/s0140-6736(75)90883-1.

8

Structure of the three major fucosyl-glycoasparagines accumulating in the urine of a patient with fucosidosis.岩藻糖贮积症患者尿液中积累的三种主要岩藻糖基化糖天冬酰胺的结构

Biochimie. 1978;60(8):725-34. doi: 10.1016/s0300-9084(78)80017-0.

9

Enzyme activity in fucosidosis.岩藻糖苷贮积症中的酶活性。

Lancet. 1976 Dec 25;2(8000):1415-6. doi: 10.1016/s0140-6736(76)91961-9.

10

High-performance liquid chromatographic analysis of oligosaccharides and glycopeptides accumulating in lysosomal storage disorders.溶酶体贮积症中积累的寡糖和糖肽的高效液相色谱分析

Anal Biochem. 1980 Feb;102(1):213-9. doi: 10.1016/0003-2697(80)90341-3.

引用本文的文献

1

A mouse model for fucosidosis recapitulates storage pathology and neurological features of the milder form of the human disease.岩藻糖苷贮积症的小鼠模型概括了人类疾病较轻形式的储存病理学和神经学特征。

Dis Model Mech. 2016 Sep 1;9(9):1015-28. doi: 10.1242/dmm.025122. Epub 2016 Aug 4.

2

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.

3

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.