Hawkinsinuria — identification of quinolacetic acid and pyroglutamic acid during an acidotic phase
Author:
Publisher
Elsevier BV
Subject
General Chemistry
Reference8 articles.
1. A new sulfur amino acid, named hawkinsin, identified in a baby with transient tyrosinemia and her mother
2. Excretion of cis- and trans-4-hydroxycyclohexylacetic acid in addition to hawkinsin in a family with a postulated defect of 4-hydroxyphenylpyruvate dioxygenase
3. New tyrosine metabolites in humans: Hawkinsin and cis- and trans-4-hydroxycyclohexylacetic acids
4. Hawkinsinuria
5. �ber eine modifizierte Form der Reformatski-Reaktion
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2. A sportomics soccer investigation unveils an exercise-induced shift in tyrosine metabolism leading to hawkinsinuria;Frontiers in Nutrition;2023-06-13
3. Recent examples of α-ketoglutarate-dependent mononuclear non-haem iron enzymes in natural product biosyntheses;Natural Product Reports;2018
4. Expanding the phenotype of hawkinsinuria: new insights from response to N-acetyl-L-cysteine;Journal of Inherited Metabolic Disease;2016-08-03
5. The Fe(II)/α-ketoglutarate-dependent taurine dioxygenases from Pseudomonas putida and Escherichia coli are tetramers;FEBS Journal;2012-01-24
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