Medium chain 3-ketoacyl-coenzyme A thiolase deficiency: a new disorder of mitochondrial fatty acid beta-oxidation (Q42546758)

2 November 2017

title

Medium chain 3-ketoacyl-coenzyme A thiolase deficiency: a new disorder of mitochondrial fatty acid beta-oxidation (English)

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2 November 2017

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Kamijo T

1

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2 November 2017

Indo Y

2

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2 November 2017

Souri M

3

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2 November 2017

Aoyama T

4

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2 November 2017

Hara T

5

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2 November 2017

Yamamoto S

6

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2 November 2017

Ushikubo S

7

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2 November 2017

Rinaldo P

8

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2 November 2017

Matsuda I

9

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2 November 2017

Komiyama A

10

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2 November 2017

Hashimoto T

11

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2 November 2017

language of work or name

English

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publication date

1 November 1997

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2 November 2017

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2 November 2017

volume

42

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2 November 2017

issue

5

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2 November 2017

page(s)

569-576

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Cytosolic acetoacetyl-CoA thiolase from chicken liver

2 November 2017

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21 January 2018

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Biochemical investigations on a patient with a defect in cytosolic acetoacetyl‐CoA thiolase, associated with mental retardation

21 January 2018

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Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency

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Combined enzyme defect of mitochondrial fatty acid oxidation

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Mitochondrial trifunctional protein deficiency. Catalytic heterogeneity of the mutant enzyme in two patients

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Ethylmalonic/adipic aciduria: effects of oral medium-chain triglycerides, carnitine, and glycine on urinary excretion of organic acids, acylcarnitines, and acylglycines

21 January 2018

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Stable isotope dilution analysis of n-hexanoylglycine, 3-phenylpropionylglycine and suberylglycine in human urine using chemical ionization gas chromatography/mass spectrometry selected ion monitoring

21 January 2018

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Properties of Peroxisomal 3-Ketoacyl-CoA Thiolase from Rat Liver1

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A modification of the Lowry procedure to simplify protein determination in membrane and lipoprotein samples

21 January 2018

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Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

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Effects of sodium 2-[5-(4-chlorophenyl)pentyl]-oxirane-2-carboxylate (POCA) on fatty acid oxidation in fibroblasts from patients with peroxisomal diseases

21 January 2018

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Peroxisomal beta-oxidation of palmitoyl-CoA in human liver homogenates and its deficiency in the cerebro-hepato-renal (Zellweger) syndrome

21 January 2018

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Muscle Carnitine Palmityltransferase Deficiency and Myoglobinuria

21 January 2018

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Long-chain acyl coenzyme A dehydrogenase deficiency: an inherited cause of nonketotic hypoglycemia.

21 January 2018

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Fatal infantile form of muscle phosphorylase deficiency

21 January 2018

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Defect in biosynthesis of mitochondrial acetoacetyl-coenzyme A thiolase in cultured fibroblasts from a boy with 3-ketothiolase deficiency

21 January 2018

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Human liver long-chain 3-hydroxyacyl-coenzyme A dehydrogenase is a multifunctional membrane-bound beta-oxidation enzyme of mitochondria

21 January 2018

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Molecular cloning and nucleotide sequence of cDNA encoding the entire precursor of rat mitochondrial acetoacetyl-CoA thiolase

21 January 2018

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Mitochondrial short-chain L-3-hydroxyacyl-coenzyme A dehydrogenase deficiency: a new defect of fatty acid oxidation.

21 January 2018

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Human trifunctional protein deficiency: A new disorder of mitochondrial fatty acid β-oridation

21 January 2018

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Muscle Phosphofructokinase Deficiency

21 January 2018

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10.1203/00006450-199711000-00002

21 January 2018

Identifiers

DOI

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Dimensions Publication ID

2 November 2017

1064211388

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