Vockley J - Search Results

1

Misfolding, degradation, and aggregation of variant proteins. The molecular pathogenesis of short chain acyl-CoA dehydrogenase (SCAD) deficiency.

Pedersen CB, Bross P, Winter VS, Corydon TJ, Bolund L, Bartlett K, Vockley J, Gregersen N. Pedersen CB, et al. Among authors: vockley j. J Biol Chem. 2003 Nov 28;278(48):47449-58. doi: 10.1074/jbc.M309514200. Epub 2003 Sep 23. J Biol Chem. 2003. PMID: 14506246 Free article.

2

Impaired tetramer assembly of variant medium-chain acyl-coenzyme A dehydrogenase with a glutamate or aspartate substitution for lysine 304 causing instability of the protein.

Yokota I, Saijo T, Vockley J, Tanaka K. Yokota I, et al. Among authors: vockley j. J Biol Chem. 1992 Dec 25;267(36):26004-10. J Biol Chem. 1992. PMID: 1361190 Free article.

3

Molecular cloning and nucleotide sequence of cDNAs encoding the precursors of rat long chain acyl-coenzyme A, short chain acyl-coenzyme A, and isovaleryl-coenzyme A dehydrogenases. Sequence homology of four enzymes of the acyl-CoA dehydrogenase family.

Matsubara Y, Indo Y, Naito E, Ozasa H, Glassberg R, Vockley J, Ikeda Y, Kraus J, Tanaka K. Matsubara Y, et al. Among authors: vockley j. J Biol Chem. 1989 Sep 25;264(27):16321-31. J Biol Chem. 1989. PMID: 2777793 Free article.

4

Mitochondrial import and processing of wild type and type III mutant isovaleryl-CoA dehydrogenase.

Volchenboum SL, Vockley J. Volchenboum SL, et al. Among authors: vockley j. J Biol Chem. 2000 Mar 17;275(11):7958-63. doi: 10.1074/jbc.275.11.7958. J Biol Chem. 2000. PMID: 10713113 Free article.

5

Role of common gene variations in the molecular pathogenesis of short-chain acyl-CoA dehydrogenase deficiency.

Corydon MJ, Vockley J, Rinaldo P, Rhead WJ, Kjeldsen M, Winter V, Riggs C, Babovic-Vuksanovic D, Smeitink J, De Jong J, Levy H, Sewell AC, Roe C, Matern D, Dasouki M, Gregersen N. Corydon MJ, et al. Among authors: vockley j. Pediatr Res. 2001 Jan;49(1):18-23. doi: 10.1203/00006450-200101000-00008. Pediatr Res. 2001. PMID: 11134486

6

Acute fatty liver of pregnancy associated with short-chain acyl-coenzyme A dehydrogenase deficiency.

Matern D, Hart P, Murtha AP, Vockley J, Gregersen N, Millington DS, Treem WR. Matern D, et al. Among authors: vockley j. J Pediatr. 2001 Apr;138(4):585-8. doi: 10.1067/mpd.2001.111814. J Pediatr. 2001. PMID: 11295727

7

Crystal structure of rat short chain acyl-CoA dehydrogenase complexed with acetoacetyl-CoA: comparison with other acyl-CoA dehydrogenases.

Battaile KP, Molin-Case J, Paschke R, Wang M, Bennett D, Vockley J, Kim JJ. Battaile KP, et al. Among authors: vockley j. J Biol Chem. 2002 Apr 5;277(14):12200-7. doi: 10.1074/jbc.M111296200. Epub 2002 Jan 25. J Biol Chem. 2002. PMID: 11812788 Free article.

8

Purification and characterization of two polymorphic variants of short chain acyl-CoA dehydrogenase reveal reduction of catalytic activity and stability of the Gly185Ser enzyme.

Nguyen TV, Riggs C, Babovic-Vuksanovic D, Kim YS, Carpenter JF, Burghardt TP, Gregersen N, Vockley J. Nguyen TV, et al. Among authors: vockley j. Biochemistry. 2002 Sep 17;41(37):11126-33. doi: 10.1021/bi026030r. Biochemistry. 2002. PMID: 12220177

9

Identification of isobutyryl-CoA dehydrogenase and its deficiency in humans.

Nguyen TV, Andresen BS, Corydon TJ, Ghisla S, Abd-El Razik N, Mohsen AW, Cederbaum SD, Roe DS, Roe CR, Lench NJ, Vockley J. Nguyen TV, et al. Among authors: vockley j. Mol Genet Metab. 2002 Sep-Oct;77(1-2):68-79. doi: 10.1016/s1096-7192(02)00152-x. Mol Genet Metab. 2002. PMID: 12359132

10

Rare disorders of metabolism with elevated butyryl- and isobutyryl-carnitine detected by tandem mass spectrometry newborn screening.

Koeberl DD, Young SP, Gregersen NS, Vockley J, Smith WE, Benjamin DK Jr, An Y, Weavil SD, Chaing SH, Bali D, McDonald MT, Kishnani PS, Chen YT, Millington DS. Koeberl DD, et al. Among authors: vockley j. Pediatr Res. 2003 Aug;54(2):219-23. doi: 10.1203/01.PDR.0000074972.36356.89. Epub 2003 May 7. Pediatr Res. 2003. PMID: 12736383

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