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Enzymatic basis for the coexistence of myopathy and hemolytic disease in inherited muscle phosphofructokinase deficiency.

作者信息

Tarui S, Kono N, Nasu T, Nishikawa M

出版信息

Biochem Biophys Res Commun. 1969 Jan 6;34(1):77-83. doi: 10.1016/0006-291x(69)90531-2.

DOI:10.1016/0006-291x(69)90531-2
PMID:4236975
Abstract
摘要

相似文献

1
Enzymatic basis for the coexistence of myopathy and hemolytic disease in inherited muscle phosphofructokinase deficiency.遗传性肌肉磷酸果糖激酶缺乏症中肌病和溶血性疾病共存的酶学基础。
Biochem Biophys Res Commun. 1969 Jan 6;34(1):77-83. doi: 10.1016/0006-291x(69)90531-2.
2
Inherited phosphofructokinase deficiency associated with hemolysis and exertional myopathy.
Eur J Haematol. 1995 Oct;55(4):279-81. doi: 10.1111/j.1600-0609.1995.tb00278.x.
3
Multiple isoenzymes of human phosphofructokinase.
Biochem Biophys Res Commun. 1970 Sep 30;40(6):1259-65. doi: 10.1016/0006-291x(70)90002-1.
4
Muscle phosphofructokinase deficiency (Tarui's disease).肌肉磷酸果糖激酶缺乏症（塔瑞氏病）。
Proc Nutr Soc. 1979 Dec;38(3):110A.
5
Inherited phosphofructokinase deficiency in an American cocker spaniel.一只美国可卡犬的遗传性磷酸果糖激酶缺乏症。
J Am Vet Med Assoc. 1992 Nov 15;201(10):1569-71.
6
Glucose- and mannose-1,6-P2 as activators of phosphofructokinase in red blood cells.葡萄糖和甘露糖-1,6-二磷酸作为红细胞中磷酸果糖激酶的激活剂。
Biochem Biophys Res Commun. 1974 Aug 19;59(4):1333-40. doi: 10.1016/0006-291x(74)90460-4.
7
Physical and kinetic properties of human phosphofructokinase from skeletal muscle and erythrocytes.来自骨骼肌和红细胞的人磷酸果糖激酶的物理和动力学特性。
J Biol Chem. 1969 Jul 25;244(14):3823-31.
8
The molecular basis of muscle phosphofructokinase deficiency.
Arch Neurol. 1974 Dec;31(6):411-7. doi: 10.1001/archneur.1974.00490420077009.
9
[Mechanisms of enzymopathy acquired by the red blood cell during hemopathy].[血液病期间红细胞获得性酶病的机制]
Nouv Rev Fr Hematol Blood Cells. 1977;18(1):214-6.
10
Phosphofructokinase deficiency associated with congenital nonspherocytic hemolytic anemia and mild myopathy: biochemical and morphological studies on the muscle.与先天性非球形细胞溶血性贫血和轻度肌病相关的磷酸果糖激酶缺乏症：肌肉的生化和形态学研究
Tohoku J Exp Med. 1983 Nov;141(3):287-93. doi: 10.1620/tjem.141.287.

引用本文的文献

1
Inherited erythrocyte phosphofructokinase deficiency: molecular mechanism.遗传性红细胞磷酸果糖激酶缺乏症：分子机制
Hum Genet. 1980;55(3):383-90. doi: 10.1007/BF00290222.
2
Histochemical technique for the demonstration of phosphofructokinase activity in heart and skeletal muscles.用于显示心脏和骨骼肌中磷酸果糖激酶活性的组织化学技术。
Histochemistry. 1980;66(1):75-81. doi: 10.1007/BF00493247.
3
Isozymes of human phosphofructokinase: identification and subunit structural characterization of a new system.人磷酸果糖激酶的同工酶：一种新系统的鉴定及亚基结构特征
Proc Natl Acad Sci U S A. 1980 Jan;77(1):62-6. doi: 10.1073/pnas.77.1.62.
4
A review of animal phosphofructokinase isozymes with an emphasis on their physiological role.动物磷酸果糖激酶同工酶综述，重点在于其生理作用。
Mol Cell Biochem. 1983;52(1):75-91. doi: 10.1007/BF00230589.
5
Kinetic properties of erythrocyte phosphofructokinase in patients with type VII glycogenosis from two families--close similarity to liver type phosphofructokinase.来自两个家族的VII型糖原贮积症患者红细胞磷酸果糖激酶的动力学特性——与肝型磷酸果糖激酶极为相似
J Inherit Metab Dis. 1984;7(3):107-11. doi: 10.1007/BF01801765.
6
The hereditary haemolytic anaemias.遗传性溶血性贫血
J R Coll Physicians Lond. 1974 Apr;8(3):206-19.
7
[Pyruvate kinase deficiency of erythrocytes in a case of hereditary myopathy].[一例遗传性肌病患者的红细胞丙酮酸激酶缺乏症]
Klin Wochenschr. 1971 Feb;49(3):156-8. doi: 10.1007/BF01496810.
8
Blood cell phosphofructokinase in Down's syndrome.唐氏综合征中的血细胞磷酸果糖激酶
Humangenetik. 1970;9(2):185-90. doi: 10.1007/BF00278934.
9
Electrophoretic methods for differentiating glycolytic enzymes of mouse and human origin.用于区分小鼠和人类来源糖酵解酶的电泳方法。
In Vitro. 1971 Nov-Dec;7(3):132-9. doi: 10.1007/BF02617956.
10
Analysis of the phosphofructokinase subunits and isoenzymes in human tissues.人体组织中磷酸果糖激酶亚基和同工酶的分析。
Biochem J. 1988 May 1;251(3):677-83. doi: 10.1042/bj2510677.