Long-chain Acyl-CoA Dehydrogenase Deficiency as a Cause of Pulmonary Surfactant Dysfunction-Reference-Cited by-同舟云学术

Long-chain Acyl-CoA Dehydrogenase Deficiency as a Cause of Pulmonary Surfactant Dysfunction

Published:2014-04 Issue:15 Volume:289 Page:10668-10679
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Goetzman Eric S.,Alcorn John F.,Bharathi Sivakama S.,Uppala Radha,McHugh Kevin J.,Kosmider Beata,Chen Rimei,Zuo Yi Y.,Beck Megan E.,McKinney Richard W.,Skilling Helen,Suhrie Kristen R.,Karunanidhi Anuradha,Yeasted Renita,Otsubo Chikara,Ellis Bryon,Tyurina Yulia Y.,Kagan Valerian E.,Mallampalli Rama K.,Vockley Jerry

Funder

National Institutes of Health

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference69 articles.

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4. A new genetic disorder in mitochondrial fatty acid β-oxidation: ACAD9 deficiency;He;Am. J. Hum. Genet.,2007

5. 2,6-Dimethylheptanoyl-CoA is a specific substrate for long-chain acyl-CoA dehydrogenase (LCAD): Evidence for a major role of LCAD in branched-chain fatty acid oxidation;Wanders;Biochim. Biophys. Acta.,1998

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