Detection of inborn errors of metabolism. II. Defects in propionic acid metabolism. - Suppr | 超能文献

Detection of inborn errors of metabolism. II. Defects in propionic acid metabolism.

作者信息

Hill H Z, Goodman S I

出版信息

Clin Genet. 1974;6(2):73-8.

Abstract

摘要

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引用本文的文献

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Import of TAT-Conjugated Propionyl Coenzyme A Carboxylase Using Models of Propionic Acidemia.采用丙酸血症模型导入 TAT 缀合的丙酰基辅酶 A 羧化酶。

Mol Cell Biol. 2018 Feb 27;38(6). doi: 10.1128/MCB.00491-17. Print 2018 Mar 15.

2

Genetic complementation in heterokaryons of human fibroblasts defective in cobalamin metabolism.钴胺素代谢缺陷的人成纤维细胞异核体中的基因互补作用。

Proc Natl Acad Sci U S A. 1975 Aug;72(8):3181-5. doi: 10.1073/pnas.72.8.3181.

3

Rapid prenatal and postnatal detection of inborn errors of propionate, methylmalonate, and cobalamin metabolism: a sensitive assay using cultured cells.快速产前和产后检测丙酸、甲基丙二酸和钴胺素代谢的先天性代谢缺陷：一种使用培养细胞的灵敏检测方法。

Hum Genet. 1976 Dec 15;34(3):277-83. doi: 10.1007/BF00295291.

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Propionyl-CoA-carboxylase determination: study of enzyme parameters in cultured skin fibroblasts from enzyme-deficient and normal subjects.丙酰辅酶A羧化酶测定：对酶缺乏和正常受试者培养的皮肤成纤维细胞中酶参数的研究

J Inherit Metab Dis. 1978;1(1):3-7. doi: 10.1007/BF01805705.