正常人组织及伴有多种硫酸酯酶缺乏的异染性脑白质营养不良中硫酸酯酶的酶学研究：芳基硫酸酯酶A、B和C、脑苷脂硫酸酯酶、鞘氨醇半乳糖苷硫酸酯酶及类固醇硫酸酯酶。 - Suppr

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超能文献

Enzymic studies of sulphatases in tissues of the normal human and in metachromatic leukodystrophy with multiple sulphatase deficiencies: arylsulphatases A, B and C, cerebroside sulphatase, psychosine sulphatase and steroid sulphatases.

作者信息

Eto Y, Rampini S, Wiesmann U, Herschkowitz N N

出版信息

J Neurochem. 1974 Dec;23(6):1161-70. doi: 10.1111/j.1471-4159.1974.tb12213.x.

DOI:10.1111/j.1471-4159.1974.tb12213.x

PMID:4281441

Abstract

摘要

相似文献

Enzymic studies of sulphatases in tissues of the normal human and in metachromatic leukodystrophy with multiple sulphatase deficiencies: arylsulphatases A, B and C, cerebroside sulphatase, psychosine sulphatase and steroid sulphatases.正常人组织及伴有多种硫酸酯酶缺乏的异染性脑白质营养不良中硫酸酯酶的酶学研究：芳基硫酸酯酶A、B和C、脑苷脂硫酸酯酶、鞘氨醇半乳糖苷硫酸酯酶及类固醇硫酸酯酶。

J Neurochem. 1974 Dec;23(6):1161-70. doi: 10.1111/j.1471-4159.1974.tb12213.x.

The patterns of arylsulphatases A and B in human normal and metachromatic leucodystrophy tissues and their relationship to the cerebroside sulphatase activity.人正常组织和异染性脑白质营养不良组织中芳基硫酸酯酶A和B的模式及其与脑苷脂硫酸酯酶活性的关系。

J Neurochem. 1973 Feb;20(2):279-87. doi: 10.1111/j.1471-4159.1973.tb12127.x.

Multiple sulfatase deficiencies in cultured skin fibroblasts. Occurrence in patients with a variant form of metachromatic leukodystrophy.培养的皮肤成纤维细胞中的多种硫酸酯酶缺乏症。在异染性脑白质营养不良变异型患者中的发生情况。

Arch Neurol. 1974 Feb;30(2):153-6. doi: 10.1001/archneur.1974.00490320041005.

Cerebroside-sulphatase and arylsulphatase A deficiency in metachromatic leukodystrophy (ML).异染性脑白质营养不良（ML）中的脑苷脂硫酸酯酶和芳基硫酸酯酶A缺乏症。

J Neurochem. 1969 Jan;16(1):19-28. doi: 10.1111/j.1471-4159.1969.tb10339.x.

An activator of cerebroside sulphatase in human normal liver and in cases of congenital metachromatic leukodystrophy.人类正常肝脏及先天性异染性脑白质营养不良病例中脑苷脂硫酸酯酶的一种激活剂。

FEBS Lett. 1973 May 15;32(1):129-31. doi: 10.1016/0014-5793(73)80754-9.

Comparison of properties of the enzymes involved in metachromatic leukodystrophy and in Tay-Sachs disease.异染性脑白质营养不良和泰-萨克斯病相关酶的特性比较。

Biochem Soc Symp. 1972(35):141-50.

Sulfogalactosylsphingosine sulfatase. Characteristics of the enzyme and its deficiency in metachromatic leukodystrophy in human cultured skin fibroblasts.

J Biol Chem. 1974 Aug 10;249(15):4955-60.

Steroid sulfatase in brain: comparison of sulfohydrolase activities for various steroid sulfates in normal and pathological brains, including the various forms of metachromatic leukodystrophy.脑中的类固醇硫酸酯酶：正常和病理脑（包括各种形式的异染性脑白质营养不良）中各种类固醇硫酸盐的硫酸酯酶活性比较。

J Neurochem. 1976 Dec;27(6):1389-95. doi: 10.1111/j.1471-4159.1976.tb02620.x.

Abnormal sulphatase activities in two human diseases (metachromatic leucodystrophy and gargoylism).两种人类疾病（异染性脑白质营养不良和黏多糖贮积症Ⅱ型）中的异常硫酸酯酶活性。

Biochem J. 1964 Nov;93(2):15C-17C. doi: 10.1042/bj0930015c.

Deficiency of seminolipid sulphatase activity in brain tissue of metachromatic leucodystrophy.

J Neurochem. 1975 May;24(5):1087-9. doi: 10.1111/j.1471-4159.1975.tb03683.x.

引用本文的文献

Natural disease history and characterisation of SUMF1 molecular defects in ten unrelated patients with multiple sulfatase deficiency.十例非亲缘性多发性硫酸酯酶缺乏症患者的SUMF1分子缺陷的自然疾病史及特征

Orphanet J Rare Dis. 2015 Mar 15;10:31. doi: 10.1186/s13023-015-0244-7.

Multiple sulfatase deficiency (mucosulfatidosis): impaired degradation of labeled sulfated compounds in cultured skin fibroblasts in vivo.多种硫酸酯酶缺乏症（粘脂硫酸酯贮积症）：体内培养的皮肤成纤维细胞中标记的硫酸化化合物降解受损。

Eur J Pediatr. 1980 Oct;135(1):85-9. doi: 10.1007/BF00445900.

Simultaneous azo-coupling method for an estrogen sulfatase in human tissues.人体组织中雌激素硫酸酯酶的同步偶氮偶联法

Histochemistry. 1983;78(2):241-9. doi: 10.1007/BF00489502.

Review: the mammalian sulphatases and placental sulphatase deficiency in man.综述：哺乳动物硫酸酯酶与人类胎盘硫酸酯酶缺乏症

J Inherit Metab Dis. 1982;5(3):145-52. doi: 10.1007/BF01800170.

Prenatal diagnosis of metachromatic leukodystrophy: a diagnosis with amniotic fluid by DEAE-Sepharose column chromatography and its confirmation by kidney lipid analysis.

J Inherit Metab Dis. 1982;5(2):77-8. doi: 10.1007/BF01799995.

On the identity of arylsulphatase C and steroid sulphatase.关于芳基硫酸酯酶C与类固醇硫酸酯酶的同一性

Hum Genet. 1983;65(2):189. doi: 10.1007/BF00286661.

A direct-colouring, metal precipitation method for the demonstration of arylsulphatases A and B.一种用于显示芳基硫酸酯酶A和B的直接染色金属沉淀法。

Histochem J. 1984 May;16(5):501-6. doi: 10.1007/BF01041350.

Biochemical variability of arylsulphatases -A, -B and -C in cultured fibroblasts from patients with multiple sulphatase deficiency.多种硫酸酯酶缺乏症患者培养成纤维细胞中芳基硫酸酯酶A、B和C的生化变异性

J Inherit Metab Dis. 1983;6(4):167-72. doi: 10.1007/BF02310875.

Immunofluorescence staining and immunological studies of arylsulphatase A of multiple sulphatase deficiency (MSD) and metachromatic leukodystrophy (MLD) fibroblasts.多种硫酸酯酶缺乏症（MSD）和异染性脑白质营养不良（MLD）成纤维细胞中芳基硫酸酯酶A的免疫荧光染色及免疫学研究

J Inherit Metab Dis. 1983;6(1):21-6. doi: 10.1007/BF02391188.

Complementation of arylsulfatase A in somatic hybrids of metachromatic leukodystrophy and multiple sulfatase deficiency disorder fibroblasts.异染性脑白质营养不良和多种硫酸酯酶缺乏症成纤维细胞的体细胞杂种中芳基硫酸酯酶A的互补作用。

Proc Natl Acad Sci U S A. 1980 Oct;77(10):6166-70. doi: 10.1073/pnas.77.10.6166.

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