Aldehyde Dehydrogenases
Author:
Publisher
Elsevier
Reference171 articles.
1. Mutational spectrum of the succinate semialdehyde dehydrogenase (ALDH5A1) gene and functional analysis of 27 novel disease-causing mutations in patients with SSADH deficiency
2. Aldehyde dehydrogenase (EC 1.2.1.3): Comparison of subcellular localization of the third isozyme that dehydrogenates γ-aminobutyraldehyde in rat, guinea pig and human liver
3. Metabolism of the butylcarbamoyl moiety of benomyl in rat
4. Lipid abnormalities in succinate semialdehyde dehydrogenase (Aldh5a1−/−) deficient mouse brain provide additional evidence for myelin alterations
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1. A comparative study of two aldehyde dehydrogenases from Sphingobium sp.: the substrate spectrum and catalytic mechanism;Organic & Biomolecular Chemistry;2024
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