(Q28261111)

English

The synthesis and characterisation of 2-methylacetoacetyl coenzyme A and its use in the identification of the site of the defect in 2-methylacetoacetic and 2-methyl-3-hydroxybutyric aciduria

scientific article published on March 14, 1983

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scholarly article

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The synthesis and characterisation of 2-methylacetoacetyl coenzyme A and its use in the identification of the site of the defect in 2-methylacetoacetic and 2-methyl-3-hydroxybutyric aciduria (English)

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1 reference

10.1016/0009-8981(83)90329-7

https://api.crossref.org/works/10.1016/0009-8981(83)90329-7

11 August 2023

author name string

B. Middleton

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6133656

11 August 2023

K. Bartlett

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6133656

11 August 2023

language of work or name

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publication date

14 March 1983

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full work available at URL

https://api.elsevier.com/content/article/PII:0009898183903297?httpAccept=text/xml

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10.1016/0009-8981(83)90329-7

https://api.crossref.org/works/10.1016/0009-8981(83)90329-7

11 August 2023

https://api.elsevier.com/content/article/PII:0009898183903297?httpAccept=text/plain

1 reference

10.1016/0009-8981(83)90329-7

https://api.crossref.org/works/10.1016/0009-8981(83)90329-7

11 August 2023

Clinica Chimica Acta

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128

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291-305

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2-3

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A " NEW " DISORDER OF ISOLEUCINE CATABOLISM

1

1 reference

10.1016/0009-8981(83)90329-7

https://api.crossref.org/works/10.1016/0009-8981(83)90329-7

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An inherited disorder of isoleucine catabolism causing accumulation of alpha-methylacetoacetate and alpha-methyl-beta -hydroxybutyrate, and intermittent metabolic acidosis

2

1 reference

10.1016/0009-8981(83)90329-7

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11 August 2023

A defect in l-isoleucine metabolism associated with alpha-methyl-beta-hydroxybutyric and alpha-methylacetoacetic aciduria: quantitative in vivo and in vitro studies.

5

1 reference

10.1016/0009-8981(83)90329-7

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11 August 2023

A variant form of 2-methyl-3-hydroxybutyric and 2-methylacetoacetic aciduria

6

1 reference

10.1016/0009-8981(83)90329-7

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Acetoacetyl CoA thiolase deficiency: A cause of severe ketoacidosis in infancy simulating salicylism

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A rapid, sensitive, and versatile assay for protein using Coomassie brilliant blue G250.

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A new fluorometric method for RNA and DNA determination

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Preparation of crystalline lithium acetoacetate

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Tissue sulfhydryl groups

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The kinetic mechanism of 3-hydroxy-3-methylglutaryl-coenzyme A synthase from baker's yeast

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Analysis and purification of acyl coenzyme A thioesters by reversed-phase ion-pair liquid chromatography

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The oxoacyl-coenzyme A thiolases of animal tissues

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A SOURCE OF ERROR IN THE ASSAY OF ACETYL-COENZYME A

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Peroxisomal β-ketothiolase

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The kinetic mechanism and properties of the cytoplasmic acetoacetyl-coenzyme A thiolase from rat liver

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10.1016/0009-8981(83)90329-7

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