Inhibition of the Electron Transport Chain and Creatine Kinase Activity by Ethylmalonic Acid in Human Skeletal Muscle-Reference-Cited by-同舟云学术

Inhibition of the Electron Transport Chain and Creatine Kinase Activity by Ethylmalonic Acid in Human Skeletal Muscle

Published:2006-03 Issue:1 Volume:21 Page:11-19
ISSN:0885-7490
Container-title:Metabolic Brain Disease
language:en
Short-container-title:Metab Brain Dis

Author:

Barschak Alethea G.,Ferreira Gustavo da C.,André Karina R.,Schuck Patrícia F.,Viegas Carolina M.,Tonin Anelise,Filho Carlos S. Dutra,Wyse Angela T. S.,Wannmacher Clóvis M. D.,Vargas Carmen R.,Wajner Moacir

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Clinical Neurology,Biochemistry

Link

http://link.springer.com/content/pdf/10.1007/s11011-006-9000-y.pdf

Reference45 articles.

1. Amendt BA, Greene C, Sweetman L, Cloherty J, Shih V, Moon A, Teel L, Rhead WJ (1987) Short-chain acyl-coenzyme A dehydrogenase deficiency clinical and biochemical studies in two patients. J Clin Invest 79:1303–1309

2. Aoyama T, Uchida Y, Kelley RI, Marble M, Hofman K, Tonsgard JH, Rhead WJ, Hashimoto T (1993) A novel disease with deficiency of mitochondrial very-long-chain acyl-CoA dehydrogenase. Biochem Biophys Res Commun 191:1369–1372

3. Bär PRD (2000) Chronic mitochondrial inhibition induces selective motoneuron death in vitro. J Neurochem 74:1158–1165

4. Bennett MJ, Weinberger MJ, Kobori JA, Rinaldo P, Burlina AB (1996) Mitochondrial short-chain L-3-hydroxyacyl-coenzyme A dehydrogenase deficiency: A new defect of fatty acid oxidation. Pediatr Res 39:185–188

5. Bertrand C, Largilliere C, Zabot MT, Mathieu M, Vianey-Saban C (1993) Very-long-chain acyl-CoA dehydrogenase deficiency: Identification of a new inborn error of mitochondrial fatty acid oxidation in fibroblasts. Biochim Biophys Acta 1180:327–329

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