人芳基硫酸酯酶B的尿苷二磷酸-N-乙酰半乳糖胺-4-硫酸硫酸水解酶活性及其在马罗-拉米综合征中的缺陷。 - Suppr

Suppr

超能文献

Uridine diphospho-N-acetylgalactosamine-4-sulfate sulfohydrolase activity of human arylsulfatase B and its deficiency in the Maroteaux-Lamy syndrome.

作者信息

Fluharty A L, Stevens R L, Fung D, Peak S, Kihara H

出版信息

Biochem Biophys Res Commun. 1975 Jan 2;64(3):955-62. doi: 10.1016/0006-291x(75)90140-0.

DOI:10.1016/0006-291x(75)90140-0

PMID:238522

Abstract

摘要

相似文献

Uridine diphospho-N-acetylgalactosamine-4-sulfate sulfohydrolase activity of human arylsulfatase B and its deficiency in the Maroteaux-Lamy syndrome.

Biochem Biophys Res Commun. 1975 Jan 2;64(3):955-62. doi: 10.1016/0006-291x(75)90140-0.

Arylsulfatases A and B in metachromatic leukodystrophy and Maroteaux-Lamy syndrome: studies with 4-methylumelliferyl sulfate.

Adv Exp Med Biol. 1976;68:239-51. doi: 10.1007/978-1-4684-7735-1_16.

Proceedings: The defect in Maroteaux-Lamy disease (mucopolysaccharidosis VI, subtype A): deficiency of N-acetylgalactosamine-4-sulfatase.

Hoppe Seylers Z Physiol Chem. 1974 Oct;355(10):1235.

Deficiency of chondroitin sulfate N-acetylgalactosamine 4-sulfate sulfatase in Maroteaux-Lamy syndrome.

Biochem Biophys Res Commun. 1974 Dec 23;61(4):1450-7. doi: 10.1016/s0006-291x(74)80446-8.

[The early diagnosis of Maroteaux-Lamy syndrome with confirmation of arylsulphatase deficiency].

Arch Fr Pediatr. 1977 Apr;34(4):362-70.

Arylsulphatase B (Maroteaux-Lamy factor): a part of the enzyme system responsible for sulphate release from mucopolysaccharide fragment.

FEBS Lett. 1976 May 15;65(1):63-8. doi: 10.1016/0014-5793(76)80622-9.

Arylsulfatase B deficiency in Maroteaux-Lamy syndrome: Cellular studies and carrier identification.

Pediatr Res. 1975 May;9(5):475-80. doi: 10.1203/00006450-197505000-00003.

Diagnosis of Maroteaux-Lamy syndrome by the use of radiolabelled oligosaccharides as substrates for the determination of arylsulphatase B activity.

Biochem J. 1986 Mar 15;234(3):507-14. doi: 10.1042/bj2340507.

Reduced arylsulfatase B activity of the mutant enzyme protein in Maroteaux-Lamy syndrome.

Biochem Biophys Res Commun. 1975 Jan 20;62(2):448-55. doi: 10.1016/s0006-291x(75)80159-8.

Human N-acetylgalactosamine-4-sulphatase biosynthesis and maturation in normal, Maroteaux-Lamy and multiple-sulphatase-deficient fibroblasts.

Biochem J. 1990 Jun 1;268(2):379-86. doi: 10.1042/bj2680379.

引用本文的文献

Stimulation of aryl sulfatase in rat peritoneal macrophages exposed to bone in vitro.

Calcif Tissue Int. 1981;33(2):181-4. doi: 10.1007/BF02409433.

The effect of pH on the kinetics of arylsulphatases A and B.

Biochem J. 1983 Sep 1;213(3):603-7. doi: 10.1042/bj2130603.

The slow kinetic transients of arylsulphatase A.

Biochem J. 1982 Feb 1;201(2):345-52. doi: 10.1042/bj2010345.

Tissue-specific expression of human arylsulfatase-C isozymes and steroid sulfatase.

Am J Hum Genet. 1987 Feb;40(2):102-14.

A distinct terminal structure in newly synthesized chondroitin sulphate chains.

Biochem J. 1985 Apr 1;227(1):37-48. doi: 10.1042/bj2270037.

Comparison of arylsulphatases from Eimeria tenella (parasite) and chicken caecum (host).

Biochem J. 1987 Feb 15;242(1):97-102. doi: 10.1042/bj2420097.

Arylsulphatases in the rabbit oviduct: postovulatory changes tested by histochemical and biochemical procedures.

Histochem J. 1985 Aug;17(8):883-90. doi: 10.1007/BF01004183.

The human arylsulfatase-C isoenzymes: two distinct genes that escape from X inactivation.

Am J Hum Genet. 1990 Apr;46(4):729-37.

Mucopolysaccharidosis type VI: identification of three mutations in the arylsulfatase B gene of patients with the severe and mild phenotypes provides molecular evidence for genetic heterogeneity.

Am J Hum Genet. 1992 Apr;50(4):795-800.

Arylsulphatase and glycosulphatase of Charonia lampas. Substrate specificity towards sugar sulphate derivatives.

Biochem J. 1976 Nov;159(2):445-8. doi: 10.1042/bj1590445.

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。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验