Displacement of hepatic ornithine carbamoyltransferase from mitochondria to cytosol in Reye's Syndrome-Reference-Cited by-同舟云学术

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Displacement of hepatic ornithine carbamoyltransferase from mitochondria to cytosol in Reye's Syndrome

Published:1991-10 Issue:2 Volume:46 Page:255-262
ISSN:0885-4505
Container-title:Biochemical Medicine and Metabolic Biology
language:en
Short-container-title:Biochemical Medicine and Metabolic Biology

Author:

Woodfin Beulah M.,Davis Larry E.

Publisher

Elsevier BV

Subject

Biochemistry,Endocrinology, Diabetes and Metabolism

Reference36 articles.

1. ENCEPHALOPATHY AND FATTY DEGENERATION OF THE VISCERA A DISEASE ENTITY IN CHILDHOOD

2. Mitochondrial Ultrastructure in Reye's Syndrome (Encephalopathy and Fatty Degeneration of the Viscera)

3. Transiently Reduced Activity of Carbamyl Phosphate Synthetase and Ornithine Transcarbamylase in Liver of Children with Reye's Syndrome

Cited by 3 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. Aminoacidopathies and Organic Acidopathies, Mitochondrial Enzyme Defects, and Other Metabolic Errors;Textbook of Clinical Neurology;2007

2. The Liver in Systemic Illness;Zakim and Boyer's Hepatology;2006

3. Inherited and Acquired Syndromes of Hyperammonemia and Encephalopathy in Children;Seminars in Liver Disease;1994-08

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