Disorders of mitochondrial long-chain fatty acid oxidation and the carnitine shuttle-Reference-Cited by-同舟云学术

Disorders of mitochondrial long-chain fatty acid oxidation and the carnitine shuttle

Published:2018-03 Issue:1 Volume:19 Page:93-106
ISSN:1389-9155
Container-title:Reviews in Endocrine and Metabolic Disorders
language:en
Short-container-title:Rev Endocr Metab Disord

Author:

Knottnerus Suzan J. G.,Bleeker Jeannette C.,Wüst Rob C. I.,Ferdinandusse Sacha,IJlst Lodewijk,Wijburg Frits A.,Wanders Ronald J. A.,Visser Gepke,Houtkooper Riekelt H.^ORCID

Funder

Academic Medical Center

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

http://link.springer.com/article/10.1007/s11154-018-9448-1/fulltext.html

Reference175 articles.

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2. Bartlett K, Eaton S. Mitochondrial β-oxidation. Eur J Biochem. 2004;271(3):462–9.

3. Grevengoed TJ, Klett EL, Coleman RA. Acyl-CoA metabolism and partitioning. Annu Rev Nutr. 2014;34:1–30.

4. Swigonova Z, Mohsen AW, Vockley J. Acyl-CoA dehydrogenases: dynamic history of protein family evolution. J Mol Evol. 2009;69(2):176–93.

5. Wanders RJ, et al. The enzymology of mitochondrial fatty acid beta-oxidation and its application to follow-up analysis of positive neonatal screening results. J Inherit Metab Dis. 2010;33(5):479–94.

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