These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
2. Human acyl-CoA dehydrogenase-9 plays a novel role in the mitochondrial beta-oxidation of unsaturated fatty acids. Ensenauer R, He M, Willard JM, Goetzman ES, Corydon TJ, Vandahl BB, Mohsen AW, Isaya G, Vockley J. J Biol Chem; 2005 Sep 16; 280(37):32309-16. PubMed ID: 16020546 [Abstract] [Full Text] [Related]
4. Cloning and characterization of a human cDNA ACAD10 mapped to chromosome 12q24.1. Ye X, Ji C, Zhou C, Zeng L, Gu S, Ying K, Xie Y, Mao Y. Mol Biol Rep; 2004 Sep 16; 31(3):191-5. PubMed ID: 15560374 [Abstract] [Full Text] [Related]
5. Cloning and characterization of human very-long-chain acyl-CoA dehydrogenase cDNA, chromosomal assignment of the gene and identification in four patients of nine different mutations within the VLCAD gene. Andresen BS, Bross P, Vianey-Saban C, Divry P, Zabot MT, Roe CR, Nada MA, Byskov A, Kruse TA, Neve S, Kristiansen K, Knudsen I, Corydon MJ, Gregersen N. Hum Mol Genet; 1996 Apr 16; 5(4):461-72. PubMed ID: 8845838 [Abstract] [Full Text] [Related]
13. Identification of the catalytic base in long chain acyl-CoA dehydrogenase. Djordjevic S, Dong Y, Paschke R, Frerman FE, Strauss AW, Kim JJ. Biochemistry; 1994 Apr 12; 33(14):4258-64. PubMed ID: 8155643 [Abstract] [Full Text] [Related]
14. Acyl-CoA dehydrogenase 9 (ACAD 9) is the long-chain acyl-CoA dehydrogenase in human embryonic and fetal brain. Oey NA, Ruiter JP, Ijlst L, Attie-Bitach T, Vekemans M, Wanders RJ, Wijburg FA. Biochem Biophys Res Commun; 2006 Jul 21; 346(1):33-7. PubMed ID: 16750164 [Abstract] [Full Text] [Related]
17. Cloning of a cDNA for short/branched chain acyl-Coenzyme A dehydrogenase from rat and characterization of its tissue expression and substrate specificity. Willard J, Vicanek C, Battaile KP, Van Veldhoven PP, Fauq AH, Rozen R, Vockley J. Arch Biochem Biophys; 1996 Jul 01; 331(1):127-33. PubMed ID: 8660691 [Abstract] [Full Text] [Related]
18. Molecular basis of human mitochondrial very-long-chain acyl-CoA dehydrogenase deficiency causing cardiomyopathy and sudden death in childhood. Strauss AW, Powell CK, Hale DE, Anderson MM, Ahuja A, Brackett JC, Sims HF. Proc Natl Acad Sci U S A; 1995 Nov 07; 92(23):10496-500. PubMed ID: 7479827 [Abstract] [Full Text] [Related]
19. Isolation and expression of a cDNA encoding the precursor for a novel member (ACADSB) of the acyl-CoA dehydrogenase gene family. Rozen R, Vockley J, Zhou L, Milos R, Willard J, Fu K, Vicanek C, Low-Nang L, Torban E, Fournier B. Genomics; 1994 Nov 15; 24(2):280-7. PubMed ID: 7698750 [Abstract] [Full Text] [Related]