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Sensitive assay of carnitine palmitoyl transferase activity in tissue homogenates with a modified spectrophotometric method for enzymatic carnitine determination.

作者信息

Deufel T, Wieland O H

出版信息

Clin Chim Acta. 1983 Dec 15;135(2):247-51. doi: 10.1016/0009-8981(83)90142-0.

DOI:10.1016/0009-8981(83)90142-0
PMID:6652930
Abstract
摘要

相似文献

1
Sensitive assay of carnitine palmitoyl transferase activity in tissue homogenates with a modified spectrophotometric method for enzymatic carnitine determination.采用改良分光光度法测定酶促肉碱,对组织匀浆中肉碱棕榈酰转移酶活性进行灵敏检测。
Clin Chim Acta. 1983 Dec 15;135(2):247-51. doi: 10.1016/0009-8981(83)90142-0.
2
Tissue carnitine in Reye syndrome.瑞氏综合征中的组织肉碱
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3
Measurements of carnitine palmitoyl-transferase I and II.肉碱棕榈酰转移酶I和II的测定
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4
Determination of overt carnitine palmitoyltransferase by reversed-phase high-performance liquid chromatography.
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5
Carnitine palmitoyltransferase I and II.肉碱棕榈酰转移酶I和II
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6
Regulatory properties of a mutant carnitine palmitoyltransferase in human skeletal muscle.人骨骼肌中一种突变型肉碱棕榈酰转移酶的调节特性
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7
Importance of albumin binding in the assay for carnitine palmitoyltransferase.白蛋白结合在肉碱棕榈酰转移酶测定中的重要性。
Biochem J. 1983 Nov 15;216(2):495-8. doi: 10.1042/bj2160495.
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Hepatic and cardiac carnitine palmitoyltransferase activity. Effects of adriamycin and galactosamine.肝脏和心脏肉碱棕榈酰转移酶活性。阿霉素和半乳糖胺的作用。
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9
Palmitate oxidation in human muscle: comparison to CPT and carnitine.人体肌肉中的棕榈酸氧化:与肉碱棕榈酰转移酶及肉碱的比较
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[Alterations of mitochondria in metabolic diseases. Carnitine deficiency, carnitine palmitoyltransferase deficiency and beta oxidation].[代谢性疾病中线粒体的改变。肉碱缺乏、肉碱棕榈酰转移酶缺乏与β氧化]
Acta Neurol (Napoli). 1989 Oct;11(5):330-4.

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Screening for carnitine palmitoyltransferase II deficiency by tandem mass spectrometry.通过串联质谱法筛查肉碱棕榈酰转移酶II缺乏症。
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Myoadenylate deaminase deficiency with severe rhabdomyolysis.伴有严重横纹肌溶解症的肌腺苷酸脱氨酶缺乏症
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Eur J Pediatr. 1993 May;152(5):433-6. doi: 10.1007/BF01955905.
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Eur J Appl Physiol Occup Physiol. 1995;70(4):281-7. doi: 10.1007/BF00865023.
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Myopathic carnitine deficiency associated with lymphocytic malignant non-Hodgkin lymphoma and monoclonal immunoglobulin G-K.与淋巴细胞性恶性非霍奇金淋巴瘤和单克隆免疫球蛋白G-K相关的肌病性肉碱缺乏症
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Type 2a fibre rhabdomyolysis in myoadenylate deaminase deficiency.
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