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Loss of cyclic 3'5'-AMP dependent kinase and reduction of phosphorylase kinase in skeletal muscle of a girl with deactivated phosphorylase and glycogenosis of liver and muscle.

作者信息

Hug G, Schubert W K, Chuck G

出版信息

Biochem Biophys Res Commun. 1970 Aug 24;40(4):982-8. doi: 10.1016/0006-291x(70)91000-4.

DOI:10.1016/0006-291x(70)91000-4
PMID:4322108
Abstract
摘要

相似文献

1
Loss of cyclic 3'5'-AMP dependent kinase and reduction of phosphorylase kinase in skeletal muscle of a girl with deactivated phosphorylase and glycogenosis of liver and muscle.一名患有磷酸化酶失活及肝和肌肉糖原贮积症的女孩，其骨骼肌中依赖环3',5'-AMP的激酶缺失，磷酸化酶激酶减少。
Biochem Biophys Res Commun. 1970 Aug 24;40(4):982-8. doi: 10.1016/0006-291x(70)91000-4.
2
Hepatic glycogenosis due to phosphorylase deficiency. Limitations of enzyme studies on liver biopsy specimens.因磷酸化酶缺乏导致的肝糖原贮积症。肝活检标本酶学研究的局限性。
Am J Med. 1971 Nov;51(5):685-91. doi: 10.1016/0002-9343(71)90295-6.
3
Glycogen phosphorylase and its converter enzymes in haemolysates of normal human subjects and of patients with type VI glycogen-storage disease. A study of phosphorylase kinase deficiency.正常人及Ⅵ型糖原贮积病患者溶血产物中的糖原磷酸化酶及其转换酶。磷酸化酶激酶缺乏症的研究。
Biochem J. 1975 Apr;147(1):23-35. doi: 10.1042/bj1470023.
4
Glycogen phosphorylase kinase deficiency: a survey of enzymes in phosphorylase activating system.糖原磷酸化酶激酶缺乏症：磷酸化酶激活系统中酶的研究
Biochem Biophys Res Commun. 1973 Oct 1;54(3):833-41. doi: 10.1016/0006-291x(73)90769-9.
5
A new type of glycogen storage disease caused by deficiency of cardiac phosphorylase kinase.一种由心脏磷酸化酶激酶缺乏引起的新型糖原贮积病。
Biochem Biophys Res Commun. 1984 Mar 15;119(2):582-7. doi: 10.1016/s0006-291x(84)80288-0.
6
Type VI glycogenosis: biochemical demonstration of liver phosphorylase deficiency.
Biochem Biophys Res Commun. 1970 Dec 9;41(5):1178-84. doi: 10.1016/0006-291x(70)90210-x.
7
Developmental changes in cyclic AMP, protein kinase, phosphorylase kinase, and phosphorylase in liver, heart, and skeletal muscle of the rat.
Arch Biochem Biophys. 1972 Jun;150(2):511-8. doi: 10.1016/0003-9861(72)90069-0.
8
Hepatic glycogenosis.肝糖原沉积症
Lancet. 1971 Sep 4;2(7723):550. doi: 10.1016/s0140-6736(71)90475-2.
9
Glycogenosis due to liver and muscle phosphorylase kinase deficiency.由于肝脏和肌肉磷酸化酶激酶缺乏引起的糖原贮积病。
Pediatr Res. 1981 Apr;15(4 Pt 1):299-303. doi: 10.1203/00006450-198104000-00002.
10
Glycogen storage disease type IX: benign glycogenosis of liver and hepatic phosphorylase kinase deficiency.IX型糖原贮积病：肝脏良性糖原贮积症与肝磷酸化酶激酶缺乏症
J Pediatr. 1973 Dec;83(6):1031-4. doi: 10.1016/s0022-3476(73)80544-x.

引用本文的文献

1
Glycogen storage diseases in animals and their potential value as models of human disease.动物中的糖原贮积病及其作为人类疾病模型的潜在价值。
J Inherit Metab Dis. 1983;6(1):3-16. doi: 10.1007/BF02391186.
2
Inhibition of the glycogen phosphorylase system during ochratoxicosis in chickens.鸡赭曲霉毒素中毒期间糖原磷酸化酶系统的抑制作用。
Appl Environ Microbiol. 1980 Sep;40(3):522-5.
3
The glycogen storage diseases.糖原贮积病
J Clin Pathol Suppl (R Coll Pathol). 1974;8:106-21.
4
Hepatic phosphorylase deficiency. Its differentiation from other hepatic glycogenoses.肝磷酸化酶缺乏症。它与其他肝糖原贮积症的鉴别。
Arch Dis Child. 1974 Mar;49(3):186-91. doi: 10.1136/adc.49.3.186.
5
Glycogen storage disease, type 8.8型糖原贮积病
Arch Dis Child. 1972 Oct;47(255):830-3. doi: 10.1136/adc.47.255.830.
6
Triglyceride storage disease: a disorder of lipolysis in adipose tissue in two patients.甘油三酯贮积病：两名患者脂肪组织脂解障碍。
Br Med J. 1973 Jan 6;1(5844):25-7. doi: 10.1136/bmj.1.5844.25.
7
Acid maltase deficiency: a case study and review of the pathophysiological changes and proposed therapeutic measures.酸性麦芽糖酶缺乏症：一项病例研究及对病理生理变化和拟议治疗措施的综述。
J Neurol Neurosurg Psychiatry. 1986 Sep;49(9):1011-8. doi: 10.1136/jnnp.49.9.1011.
8
A female case of type VIII glycogenosis who developed cirrhosis of the liver and hepatocellular tumor.一名患有VIII型糖原贮积病的女性病例，该患者出现了肝硬化和肝细胞肿瘤。
Gastroenterol Jpn. 1989 Dec;24(6):711-4. doi: 10.1007/BF02774172.
9
Myopathic evolution of an exertional muscle pain syndrome with phosphorylase b kinase deficiency.伴有磷酸化酶b激酶缺乏的劳力性肌肉疼痛综合征的肌病性演变。
Acta Neuropathol. 1990;81(1):84-8. doi: 10.1007/BF00662642.
10
Phosphorylase b kinase deficiency in man: a review.人类磷酸化酶b激酶缺乏症：综述
J Inherit Metab Dis. 1990;13(4):442-51. doi: 10.1007/BF01799501.