Complementation analysis of carnitine palmitoyltransferase I and II defects.

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Characterization of carnitine and fatty acid metabolism in the long-chain acyl-CoA dehydrogenase-deficient mouse.

P2860

Q42134737-1CC0A20F-0FE8-4A10-BFF4-AD96FD0B8103

P2860

Complementation analysis of carnitine palmitoyltransferase I and II defects.

Item

http://www.wikidata.org/entity/Q41162540

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1996 nî lūn-bûn

@nan

1996年の論文

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1996年論文

@yue

1996年論文

@zh-hant

1996年論文

@zh-hk

1996年論文

@zh-mo

1996年論文

@zh-tw

1996年论文

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1996年论文

@zh

1996年论文

@zh-cn

name

Complementation analysis of carnitine palmitoyltransferase I and II defects.

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type

Item

label

Complementation analysis of carnitine palmitoyltransferase I and II defects.

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prefLabel

Complementation analysis of carnitine palmitoyltransferase I and II defects.

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P1476

Complementation analysis of carnitine palmitoyltransferase I and II defects.

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P2093

Boutron A

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Brivet M

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Demaugre F

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Legrand A

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Saudubray JM

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Slama A

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P2860

cDNA cloning, sequence analysis, and chromosomal localization of the gene for human carnitine palmitoyltransferase

Human liver mitochondrial carnitine palmitoyltransferase I: characterization of its cDNA and chromosomal localization and partial analysis of the gene

Observations on the affinity for carnitine, and malonyl-CoA sensitivity, of carnitine palmitoyltransferase I in animal and human tissues. Demonstration of the presence of malonyl-CoA in non-hepatic tissues of the rat

Molecular characterization of inherited carnitine palmitoyltransferase II deficiency

Purification of human very-long-chain acyl-coenzyme A dehydrogenase and characterization of its deficiency in seven patients

Carnitine palmitoyltransferase II deficiency: structure of the gene and characterization of two novel disease-causing mutations

Muscle carnitine palmityltransferase deficiency and myoglobinuria

Identification of a common mutation in the carnitine palmitoyltransferase II gene in familial recurrent myoglobinuria patients

Carnitine-acylcarnitine translocase deficiency with severe hypoglycemia and auriculo ventricular block. Translocase assay in permeabilized fibroblasts.

Complementation analysis of fatty acid oxidation disorders.

P2888

00006450-199610000-00005

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scholarly article

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10.1203/00006450-199610000-00005

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English

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1996-10-01T00:00:00Z

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Complementation analysis of carnitine palmitoyltransferase I and II defects.

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P2860

P2860

Complementation analysis of carnitine palmitoyltransferase I and II defects.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P407

P433

P478

P577

P5875

P6179

P698

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P407

P433

P478

P577

P5875

P6179

P698