Excretion of Nsovalerylglutamic acid in isovaleric acidemia
Author:
Publisher
Elsevier BV
Subject
Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine
Reference12 articles.
1. Isovaleric acidemia: A new genetic defect of leucine metabolism;Tanaka,1966
2. Identification of β-hydroxylisovaleric acid in the urine of a patient with isovaleric acidemia;Tanaka;Biochim. Biophys. Acta,1968
3. 4-Hydroxyisovaleric acid: a new metabolite in isovaleric acidemia;Lehnert;Eur. J. Pediatr.,1981
4. Inborn Errors of Metabolism;Baerlocher,1973
5. Microdetermination of methylmalonic acid and other short chain dicarboxylic acids by gas chromatography: use in prenatal diagnosis of methyl-malonic acidemia and in studies of isovaleric acidemia;Nakamura;Clin. Chim. Acta,1976
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1. The glycine N-acyltransferases, GLYAT and GLYATL1, contribute to the detoxification of isovaleryl-CoA - an in-silico and in vitro validation;Computational and Structural Biotechnology Journal;2023
2. Enzymology of Mitochondrial Amino Acid Conjugation Reactions;Reference Module in Biomedical Sciences;2023
3. Inhibition of N-acetylglutamate synthase by various monocarboxylic and dicarboxylic short-chain coenzyme A esters and the production of alternative glutamate esters;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;2014-12
4. Concurrent class analysis identifies discriminatory variables from metabolomics data on isovaleric acidemia;Metabolomics;2011-07-07
5. Abnormal tricarboxylic acid cycle metabolites in isovaleric acidaemia;Journal of Inherited Metabolic Disease;2009-04-05
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