丙二酸尿症与心肌病 - Suppr

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超能文献

Malonic aciduria and cardiomyopathy.

作者信息

Matalon R, Michaels K, Kaul R, Whitman V, Rodriguez-Novo J, Goodman S, Thorburn D

机构信息

Division of Genetics, Miami Children's Hospital, Florida, USA.

出版信息

J Inherit Metab Dis. 1993;16(3):571-3. doi: 10.1007/BF00711684.

DOI:10.1007/BF00711684

PMID:7609455

Abstract

摘要

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本文引用的文献

Diagnosis of organic acidemias by gas chromatography--mass spectrometry.通过气相色谱-质谱联用技术诊断有机酸血症。

Lab Res Methods Biol Med. 1981;6:1-158.

Malonyl coenzyme A decarboxylase deficiency.丙二酰辅酶A脱羧酶缺乏症

J Inherit Metab Dis. 1984;7(1):21-6. doi: 10.1007/BF01805615.

Properties of malonyl-CoA decarboxylase and its relation with malonyl-CoA incorporation into fatty acids by rat liver mitochondria.丙二酰辅酶A脱羧酶的特性及其与大鼠肝脏线粒体将丙二酰辅酶A掺入脂肪酸的关系。

Eur J Biochem. 1971 Apr 30;19(4):573-80. doi: 10.1111/j.1432-1033.1971.tb01351.x.

Hurler's syndrome: biosynthesis of acid mucopolysaccharides in tissue culture.胡勒氏综合征：组织培养中酸性粘多糖的生物合成。

Proc Natl Acad Sci U S A. 1966 Oct;56(4):1310-6. doi: 10.1073/pnas.56.4.1310.

Malonate metabolism in rat brain mitochondria.大鼠脑线粒体中的丙二酸代谢

Biochemistry. 1974 Aug 13;13(17):3589-95. doi: 10.1021/bi00714a029.

Malonyl coenzyme A decarboxylase deficiency. Clinical and biochemical findings in a second child with a more severe enzyme defect.丙二酰辅酶A脱羧酶缺乏症。对第二例酶缺陷更严重患儿的临床及生化检查结果

Eur J Pediatr. 1986 Apr;144(6):567-70. doi: 10.1007/BF00496037.

The source of malonyl-CoA in rat heart. The calcium paradox releases acetyl-CoA carboxylase and not propionyl-CoA carboxylase.大鼠心脏中丙二酰辅酶A的来源。钙反常释放的是乙酰辅酶A羧化酶而非丙酰辅酶A羧化酶。

FEBS Lett. 1986 Mar 17;198(1):47-50. doi: 10.1016/0014-5793(86)81182-6.

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