Synthesis and characterisation of acyl glycines their measurement in single blood spots by gas chromatography-mass spectrometry to diagnose inborn errors of metabolism
Author:
Publisher
Elsevier BV
Subject
General Chemistry
Reference12 articles.
1. Medium-Chain Acyl-CoA Dehydrogenase Deficiency
2. Measurement of urinary medium chain acyl glycines by gas chromatography—negative ion chemical ionization mass spectrometry
3. Population Screening for Medium-Chain Acyl-CoA Dehydrogenase Deficiency: Analysis of Medium-Chain Fatty Acids and Acylglyeines in Blood Spots
4. ACETYLGLYCINE
5. Formation of Propionyl-, Butyryl-, and other Acylglycines by Enzymes of Clostridium Kluyveri
Cited by 7 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Identification of glycineN‐acyltransferase‐like 2 (GLYATL2) as a transferase that producesN‐acyl glycines in humans;The FASEB Journal;2010-03-19
2. Solid phase synthesis of acylglycine human metabolites;Bioorganic & Medicinal Chemistry Letters;2009-12
3. Use of reversed phase HP liquid chromatography to assay conversion of N-acylglycines to primary fatty acid amides by peptidylglycine-α-amidating monooxygenase;Journal of Chromatography B;2004-09
4. The Human Bile Acid-CoA:Amino Acid N-Acyltransferase Functions in the Conjugation of Fatty Acids to Glycine;Journal of Biological Chemistry;2003-09
5. Evaluation of Urinary Acylglycines by Electrospray Tandem Mass Spectrometry in Mitochondrial Energy Metabolism Defects and Organic Acidurias;Molecular Genetics and Metabolism;2000-04
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