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Immunohistochemical demonstration of acid alpha-glucosidase in muscle in Pompe's disease.

作者信息

Ninomiya N, Matsuda I, Fukuda S, Iwamasa T, Osame M

出版信息

Histochem J. 1983 Jun;15(6):601-4. doi: 10.1007/BF01954150.

DOI:10.1007/BF01954150
PMID:6347982
Abstract
摘要

相似文献

1
Immunohistochemical demonstration of acid alpha-glucosidase in muscle in Pompe's disease.庞贝病中肌肉酸性α-葡萄糖苷酶的免疫组织化学显示
Histochem J. 1983 Jun;15(6):601-4. doi: 10.1007/BF01954150.
2
Study of alpha-D-glucosidase activity in patients with Pompe's disease.庞贝病患者α-D-葡萄糖苷酶活性的研究。
Taiwan Yi Xue Hui Za Zhi. 1986 Aug;85(8):766-70.
3
Diagnosis of Pompe's disease using pyridylamino-maltooligosaccharides as substrates of alpha-1,4-glucosidase.以吡啶基氨基麦芽寡糖作为α-1,4-葡萄糖苷酶的底物诊断庞贝氏病。
Clin Chim Acta. 1985 Apr 15;147(2):97-102. doi: 10.1016/0009-8981(85)90069-5.
4
Immunochemical studies of human acid alpha-1,4-glucosidase in type II glycogenosis.II型糖原贮积病中人类酸性α-1,4-葡糖苷酶的免疫化学研究。
Enzyme. 1981;26(4):182-90. doi: 10.1159/000459173.
5
Demonstration of acid maltase protein in Pompe disease by use of immunohistochemical and enzyme immunoassay methods.运用免疫组织化学和酶免疫测定方法对庞贝病中酸性麦芽糖酶蛋白进行检测。
J Inherit Metab Dis. 1983;6(3):131-2. doi: 10.1007/BF01800747.
6
Glycogen storage disease type II (Pompe's disease): the first biochemical evidence in Thailand.糖原贮积病II型（庞贝氏病）：泰国的首例生化证据。
J Med Assoc Thai. 1987 Sep;70(9):536-42.
7
Immunocytochemical analysis of normal and acid maltase-deficient muscle cultures.正常和酸性麦芽糖酶缺乏的肌肉培养物的免疫细胞化学分析。
Arch Neurol. 1985 Apr;42(4):371-3. doi: 10.1001/archneur.1985.04060040081017.
8
Biosynthesis of acid alpha-glucosidase in late-onset forms of glycogenosis type II (Pompe's disease).II型糖原贮积病（庞贝氏病）迟发型中酸性α-葡萄糖苷酶的生物合成
FEBS Lett. 1982 Dec 13;150(1):69-76. doi: 10.1016/0014-5793(82)81306-9.
9
Pompe's disease in Chinese and prenatal diagnosis by determination of alpha-glucosidase activity.中文的庞贝氏病及通过测定α-葡萄糖苷酶活性进行产前诊断
J Inherit Metab Dis. 1987;10(1):11-7. doi: 10.1007/BF01799482.
10
Use of immobilized antibodies in investigating acid alpha-glucosidase in urine in relation to Pompe's disease.固定化抗体在研究尿液中酸性α-葡萄糖苷酶与庞贝病关系中的应用。
Biochim Biophys Acta. 1979 Apr 12;567(2):370-83. doi: 10.1016/0005-2744(79)90123-2.

引用本文的文献

1
Demonstration of acid maltase protein in Pompe disease by use of immunohistochemical and enzyme immunoassay methods.运用免疫组织化学和酶免疫测定方法对庞贝病中酸性麦芽糖酶蛋白进行检测。
J Inherit Metab Dis. 1983;6(3):131-2. doi: 10.1007/BF01800747.
2
Subcellular distribution of acid alpha-glucosidase in fibroblasts and of antigenically cross-reactive material in Pompe's disease fibroblasts.成纤维细胞中酸性α-葡萄糖苷酶的亚细胞分布以及庞贝病成纤维细胞中抗原交叉反应物质的亚细胞分布。
Histochem J. 1986 Nov-Dec;18(11-12):613-24. doi: 10.1007/BF01675297.

本文引用的文献

1
AN ELECTRON MICROSCOPIC AND BIOCHEMICAL STUDY OF TYPE II GLYCOGENOSIS.II型糖原贮积病的电子显微镜及生化研究
Lab Invest. 1964 Sep;13:1139-52.
2
alpha-Glucosidase deficiency in generalized glycogenstorage disease (Pompe's disease).全身性糖原贮积病（庞贝氏病）中的α-葡萄糖苷酶缺乏症。
Biochem J. 1963 Jan;86(1):11-6. doi: 10.1042/bj0860011.
3
Immunohistochemical localization of acid alpha-glucosidase in rat liver.
J Histochem Cytochem. 1982 Apr;30(4):378-84. doi: 10.1177/30.4.7037944.
4
[Muscle type acid maltase deficiency. An intermediate case between childhood type and adult type (author's transl)].[肌肉型酸性麦芽糖酶缺乏症。儿童型和成人型之间的一个中间病例（作者译）]
Rinsho Shinkeigaku. 1982 Jan;22(1):57-65.
5
Acid alpha-D-glucosidase glucohydrolase from cattle liver.来自牛肝脏的酸性α-D-葡萄糖苷酶葡萄糖水解酶。
J Biol Chem. 1969 Sep 10;244(17):4735-42.
6
Comparative study of acid maltase deficiency. Biochemical differences between infantile, childhood, and adult types.酸性麦芽糖酶缺乏症的比较研究。婴儿型、儿童型和成人型之间的生化差异。
Arch Neurol. 1972 Apr;26(4):344-9. doi: 10.1001/archneur.1972.00490100074007.
7
Rodent and human acid -glucosidase. Purification, properties and inhibition by antibodies. Investigation in type II glycogenosis.啮齿动物和人类的酸性葡萄糖苷酶。纯化、特性及抗体抑制作用。II型糖原贮积病的研究。
Eur J Biochem. 1972 Nov 21;31(1):156-65. doi: 10.1111/j.1432-1033.1972.tb02514.x.
8
Type II glycogenosis. Biochemical and electron microscopic study.
Am J Med. 1968 Feb;44(2):289-300. doi: 10.1016/0002-9343(68)90160-5.
9
The unlabeled antibody enzyme method of immunohistochemistry: preparation and properties of soluble antigen-antibody complex (horseradish peroxidase-antihorseradish peroxidase) and its use in identification of spirochetes.免疫组织化学的未标记抗体酶法：可溶性抗原-抗体复合物（辣根过氧化物酶-抗辣根过氧化物酶）的制备、性质及其在螺旋体鉴定中的应用
J Histochem Cytochem. 1970 May;18(5):315-33. doi: 10.1177/18.5.315.
10
Characterization of the molecular defect in infantile and adult acid alpha-glucosidase deficiency fibroblasts.婴儿和成人酸性α-葡萄糖苷酶缺乏症成纤维细胞分子缺陷的特征分析。
J Clin Invest. 1978 Dec;62(6):1264-74. doi: 10.1172/JCI109247.