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I-cell disease: activities of lysosomal enzymes toward natural and synthetic substrates.

作者信息

Wenger D A, Sattler M, Clark C, Wharton C

出版信息

Life Sci. 1976 Aug 1;19(3):413-20. doi: 10.1016/0024-3205(76)90047-3.

DOI:10.1016/0024-3205(76)90047-3
PMID:822246
Abstract
摘要

相似文献

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I-cell disease: activities of lysosomal enzymes toward natural and synthetic substrates.I型细胞病:溶酶体酶对天然和合成底物的活性
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Lysosomal enzyme activities during ageing of adult human liver cell lines.成人肝细胞系衰老过程中的溶酶体酶活性
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[Effect of cyclic AMP on the activity of lysosomal enzymes of hamster fibroblasts].[环磷酸腺苷对仓鼠成纤维细胞溶酶体酶活性的影响]
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Increased levels of several lysosomal enzymes in sera from women using oral contraceptives.使用口服避孕药的女性血清中几种溶酶体酶水平升高。
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Isoelectric focusing pattern of acid hydrolases in cultured fibroblasts, leucocytes and cell-free amniotic fluid.培养的成纤维细胞、白细胞和无细胞羊水酸性水解酶的等电聚焦图谱。
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[Comparative studies of the acid hydrolases of human leucocytes and human and guinea pig alveolar macrophages. I. Study of the activities of glycosidases, arylsulfatase and acid phosphatase (author's transl)].人白细胞、人及豚鼠肺泡巨噬细胞酸性水解酶的比较研究。I. 糖苷酶、芳基硫酸酯酶和酸性磷酸酶活性的研究(作者译)
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Activity of some lysosomal enzymes in Hurler's syndrome (type i mucopolysaccharidosis).
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[Lysosomal glycosidases in heteropolysaccharide catabolism (author's transl)].[溶酶体糖苷酶在杂多糖分解代谢中的作用(作者译)]
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Tay-Sachs disease with atypical chronic course and limited brain storage: alpha-locus hexosaminidase genetic compound.具有非典型慢性病程和有限脑内蓄积的泰-萨克斯病:α位点己糖胺酶基因复合杂合子。
Neurochem Res. 1995 Nov;20(11):1323-8. doi: 10.1007/BF00992507.
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Evidence against involvement of the acid lysosomal sphingomyelinase in the tumor-necrosis-factor- and interleukin-1-induced sphingomyelin cycle and cell proliferation in human fibroblasts.反对酸性溶酶体鞘磷脂酶参与肿瘤坏死因子和白细胞介素-1诱导的人成纤维细胞鞘磷脂循环及细胞增殖的证据。
Biochem J. 1994 Oct 15;303 ( Pt 2)(Pt 2):341-5. doi: 10.1042/bj3030341.
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Central nervous system involvement in adult-onset Gaucher's disease.成人型戈谢病的中枢神经系统受累情况。
Acta Neuropathol. 1980;49(1):1-6. doi: 10.1007/BF00692212.
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Defective catabolism of low-density lipoprotein by fibroblasts from patients with I-cell disease.I型细胞病患者的成纤维细胞对低密度脂蛋白的分解代谢存在缺陷。
Biochem J. 1982 Jan 15;202(1):183-90. doi: 10.1042/bj2020183.
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Evidence for the deficiency of beta-glucosidase-activating factor in fibroblasts of patients with I-cell disease.I型细胞病患者成纤维细胞中β-葡萄糖苷酶激活因子缺乏的证据。
Hum Genet. 1982;62(1):66-9. doi: 10.1007/BF00295605.
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Niemann-Pick disease type B: prenatal diagnosis and enzymatic and chemical studies on fetal brain and liver.B型尼曼-匹克病:胎儿脑和肝脏的产前诊断以及酶学和化学研究
Am J Hum Genet. 1981 May;33(3):337-44.
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Juvenile GM2 gangliosidosis (AMB variant): inability to activate hexosaminidase A by activator protein.青少年GM2神经节苷脂沉积症(AMB变异型):无法通过激活蛋白激活己糖胺酶A。
Am J Hum Genet. 1983 Jul;35(4):551-64.