The Existence of Two Different h-3-Hydroxyacyl-Coenzyme A Dehydrogenases in Rat Tissues
Author:
Affiliation:
1. Department of Biochemistry, University of Nottingham Medical School, Queen's Medical Centre, Nottingham NG7 2UH, U.K.
Publisher
Portland Press Ltd.
Subject
Biochemistry
Link
https://portlandpress.com/biochemsoctrans/article-pdf/7/2/392/552796/bst0070392.pdf
Cited by 12 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. 3-Hydroxyacyl-CoA dehydrogenase;Enzyme Handbook 9;1995
2. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: A severe fatty acid oxidation disorder;European Journal of Pediatrics;1994-10
3. Fatty acid oxidation disorders: A new class of metabolic diseases;The Journal of Pediatrics;1992-07
4. Peripheral sensory-motor polyneuropathy, pigmentary retinopathy, and fatal cardiomyopathy in long-chain 3-hydroxy-acyl-CoA dehydrogenase deficiency;European Journal of Pediatrics;1992-02
5. Novel fatty acid beta-oxidation enzymes in rat liver mitochondria. II. Purification and properties of enoyl-coenzyme A (CoA) hydratase/3-hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase trifunctional protein.;Journal of Biological Chemistry;1992-01
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