Lysosomes and mucopolysaccharidoses.
作者信息
Hers H G, van Hoof F
出版信息
Biochem J. 1969 Dec;115(5):34P-36P. doi: 10.1042/bj1150034p.
Abstract
摘要
相似文献
1
Lysosomes and mucopolysaccharidoses.溶酶体与黏多糖贮积症
Biochem J. 1969 Dec;115(5):34P-36P. doi: 10.1042/bj1150034p.
2
Deficiency of lysosomal enzymes in storage diseases.贮积病中溶酶体酶的缺乏。
Biochem Med. 1973 Jun;7(3):441-51. doi: 10.1016/0006-2944(73)90065-3.
3
Lysosomal enzymes in cultured cells from mucopolysaccharidoses.黏多糖贮积症培养细胞中的溶酶体酶
Lab Invest. 1972 Dec;27(6):600-5.
4
Mucopolysaccharide storage diseases and lysosomal hydrolases in cultured fibroblasts.培养成纤维细胞中的黏多糖贮积病和溶酶体水解酶
Pathol Eur. 1973;8(1):3-11.
5
Hurler's syndrome, an -L-iduronidase deficiency.胡勒综合征，一种α-L-艾杜糖醛酸酶缺乏症。
Biochem Biophys Res Commun. 1972 May 26;47(4):959-64. doi: 10.1016/0006-291x(72)90586-4.
6
Enzyme patterns in tissues and body fluids in mucopolysaccharidoses.黏多糖贮积症中组织和体液的酶谱。
Clin Chim Acta. 1969 Jul;25(1):97-102. doi: 10.1016/0009-8981(69)90233-2.
7
Arylsulfatase B deficiency in Maroteaux-Lamy syndrome cultured fibroblasts.马罗-拉米综合征培养成纤维细胞中的芳基硫酸酯酶B缺乏症
Biochem Biophys Res Commun. 1974 Jul 24;59(2):455-61. doi: 10.1016/s0006-291x(74)80001-x.
8
Multiple lysosomal enzyme deficiency due to enzyme leakage?酶泄漏导致多种溶酶体酶缺乏？
N Engl J Med. 1971 Jan 14;284(2):109-10. doi: 10.1056/NEJM197101142840221.
9
The abnormalities of lysosomal enzymes in mucopolysacc- haridoses.黏多糖贮积症中溶酶体酶的异常。
Eur J Biochem. 1968 Dec;7(1):34-44. doi: 10.1111/j.1432-1033.1968.tb19570.x.
10
Abnormal distribution patterns of lysosomal isoenzymes in mucopolysaccharidosis.黏多糖贮积症中溶酶体同工酶的异常分布模式。
N Engl J Med. 1971 Dec 30;285(27):1537-8. doi: 10.1056/NEJM197112302852715.
引用本文的文献
1
Hunter syndrome in an 11-year old girl on enzyme replacement therapy with idursulfase: brain magnetic resonance imaging features and evolution.伊杜硫酸酶治疗 11 岁亨特综合征女孩：脑磁共振成像特征与演变。
J Inherit Metab Dis. 2010 Dec;33 Suppl 3:S67-72. doi: 10.1007/s10545-009-9023-8. Epub 2010 Jan 6.
本文引用的文献
1
Mutant enzymatic and cytological phenotypes in cultured human fibroblasts.培养的人成纤维细胞中的突变酶学和细胞学表型。
Science. 1967 Aug 18;157(3790):804-6. doi: 10.1126/science.157.3790.804.
2
ELECTRON MICROSCOPY OF TWO CEREBRAL BIOPSIES IN GARGOYLISM.黏多糖贮积症Ⅱ型患者两份脑活检组织的电子显微镜检查
J Neuropathol Exp Neurol. 1965 Apr;24:304-17. doi: 10.1097/00005072-196504000-00010.
3
Separation and properties of beta-galactosidase, beta-glucosidase, beta-glucuronidase and N-acetyl-beta-glucosaminidase from rat kidney.大鼠肾脏中β-半乳糖苷酶、β-葡萄糖苷酶、β-葡萄糖醛酸酶和N-乙酰-β-葡萄糖胺酶的分离及性质
Biochem J. 1967 Feb;102(2):525-32. doi: 10.1042/bj1020525.
4
GM1-ganglioside accumulation and beta-galactosidase deficiency in a case of GM1-gangliosidosis (Landing disease).GM1神经节苷脂贮积症（兰丁病）一例中的GM1神经节苷脂蓄积及β-半乳糖苷酶缺乏
Clin Chim Acta. 1968 Sep;21(3):421-5. doi: 10.1016/0009-8981(68)90071-5.
5
Generalized gangliosidosis: beta-galactosidase deficiency.全身性神经节苷脂沉积症：β-半乳糖苷酶缺乏症。
Science. 1968 May 31;160(3831):1002-4. doi: 10.1126/science.160.3831.1002.
6
Functions of lysosomes.溶酶体的功能。
Annu Rev Physiol. 1966;28:435-92. doi: 10.1146/annurev.ph.28.030166.002251.
7
Hurler's syndrome: deficiency of a specific beta galactosidase isoenzyme.胡勒氏综合征：一种特定β-半乳糖苷酶同工酶缺乏症。
Science. 1969 Aug 8;165(3893):611-3. doi: 10.1126/science.165.3893.611.
8
Fractionation of j-methylumbelliferyl-beta-galactosidase activities in liver in gargoylism.黏多糖贮积症中肝脏β-半乳糖苷酶活性的分级分离。
Scand J Clin Lab Invest. 1968;22(3):199-202. doi: 10.3109/00365516809166488.
9
Clinical, biochemical and ultrastructural studies of an atypical form of mucopolysaccharidosis.一种非典型黏多糖贮积症的临床、生化及超微结构研究
Acta Paediatr Scand. 1969 May;58(3):220-8. doi: 10.1111/j.1651-2227.1969.tb04710.x.
10
The abnormalities of lysosomal enzymes in mucopolysacc- haridoses.黏多糖贮积症中溶酶体酶的异常。
Eur J Biochem. 1968 Dec;7(1):34-44. doi: 10.1111/j.1432-1033.1968.tb19570.x.
Zotero 插件