犬α-L-艾杜糖醛酸酶缺乏症。黏多糖贮积症I型的一种模型。 - Suppr

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超能文献

Canine alpha-L-iduronidase deficiency. A model of mucopolysaccharidosis I.

作者信息

Shull R M, Munger R J, Spellacy E, Hall C W, Constantopoulos G, Neufeld E F

出版信息

Am J Pathol. 1982 Nov;109(2):244-8.

PMID:6215865

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1916101/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9da4/1916101/684199d84239/amjpathol00200-0118-a.jpg

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Canine alpha-L-iduronidase deficiency. A model of mucopolysaccharidosis I.犬α-L-艾杜糖醛酸酶缺乏症。黏多糖贮积症I型的一种模型。

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本文引用的文献

[ULTRASTRUCTURE OF THE HEPATIC CELLS IN HURLER'S DISEASE (GARGOYLISM)].[黏多糖贮积症Ⅰ型（承霤病）肝细胞的超微结构]

C R Hebd Seances Acad Sci. 1964 Aug 3;259:1281-3.

Animal model of human disease: Mucopolysaccharidosis VI Maroteaux-Lamy syndrome, Arylsulfatase B-deficient mucopolysaccharidosis in the Siamese cat.人类疾病的动物模型：黏多糖贮积症VI型马罗-拉米综合征，暹罗猫中芳基硫酸酯酶B缺乏型黏多糖贮积症

Am J Pathol. 1981 Nov;105(2):191-3.

The pathology of the feline model of mucopolysaccharidosis VI.猫黏多糖贮积症VI型模型的病理学

Am J Pathol. 1980 Dec;101(3):657-74.

Reversal of clinical features of Hurler's disease and biochemical improvement after treatment by bone-marrow transplantation.骨髓移植治疗后，黏多糖贮积症I型临床特征的逆转及生化指标的改善。

Lancet. 1981 Oct 3;2(8249):709-12. doi: 10.1016/s0140-6736(81)91046-1.

Keratoplasty and electron microscopy of the cornea in systemic mucopolysaccharidosis (Hurler's disease).

Can J Ophthalmol. 1968 Jul;3(3):218-30.

The defect in the Hurler and Scheie syndromes: deficiency of -L-iduronidase.黏多糖贮积症Ⅰ型（Hurler综合征）和黏多糖贮积症Ⅴ型（Scheie综合征）的缺陷：α-L-艾杜糖醛酸酶缺乏。

Proc Natl Acad Sci U S A. 1972 Aug;69(8):2048-51. doi: 10.1073/pnas.69.8.2048.

The Hurler corrective factor. Purification and some properties.赫尔勒校正因子。纯化及某些性质。

J Biol Chem. 1971 Dec 25;246(24):7773-9.

The ultrastructure of the skin in patients with mucopolysaccharidoses.黏多糖贮积症患者皮肤的超微结构

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The mucopolysaccharidoses (a review).黏多糖贮积症（综述）

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Two species of lysosomal organelles in cultured human fibroblasts.

Cell. 1979 May;17(1):143-53. doi: 10.1016/0092-8674(79)90302-7.

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