Evidence for physical association of mitochondrial fatty acid oxidation and oxidative phosphorylation complexes Y Wang, AW Mohsen, SJ Mihalik, ES Goetzman, J Vockley Journal of Biological Chemistry 285 (39), 29834-29841, 2010 | 186 | 2010 |
Sirtuin 3 (SIRT3) protein regulates long-chain acyl-CoA dehydrogenase by deacetylating conserved lysines near the active site SS Bharathi, Y Zhang, AW Mohsen, R Uppala, M Balasubramani, ... Journal of Biological Chemistry 288 (47), 33837-33847, 2013 | 183 | 2013 |
Taliglucerase alfa: an enzyme replacement therapy using plant cell expression technology GA Grabowski, M Golembo, Y Shaaltiel Molecular genetics and metabolism 112 (1), 1-8, 2014 | 161 | 2014 |
Structure of Human Isovaleryl-CoA Dehydrogenase at 2.6 Å Resolution: Structural Basis for Substrate Specificity, KA Tiffany, DL Roberts, M Wang, R Paschke, AWA Mohsen, J Vockley, ... Biochemistry 36 (28), 8455-8464, 1997 | 127 | 1997 |
Human acyl-CoA dehydrogenase-9 plays a novel role in the mitochondrial β-oxidation of unsaturated fatty acids R Ensenauer, M He, JM Willard, ES Goetzman, TJ Corydon, BB Vandahl, ... Journal of biological chemistry 280 (37), 32309-32316, 2005 | 125 | 2005 |
Structural basis for substrate fatty acyl chain specificity: crystal structure of human very-long-chain acyl-CoA dehydrogenase RP McAndrew, Y Wang, AW Mohsen, M He, J Vockley, JJP Kim Journal of Biological Chemistry 283 (14), 9435-9443, 2008 | 121 | 2008 |
Acyl-CoA dehydrogenases: dynamic history of protein family evolution Z Swigoňová, AW Mohsen, J Vockley Journal of molecular evolution 69, 176-193, 2009 | 119 | 2009 |
Identification and characterization of new long chain acyl-CoA dehydrogenases M He, Z Pei, AW Mohsen, P Watkins, G Murdoch, PP Van Veldhoven, ... Molecular genetics and metabolism 102 (4), 418-429, 2011 | 109 | 2011 |
Outcomes and genotype-phenotype correlations in 52 individuals with VLCAD deficiency diagnosed by NBS and enrolled in the IBEM-IS database LDM Pena, SC van Calcar, J Hansen, MJ Edick, CW Vockley, N Leslie, ... Molecular genetics and metabolism 118 (4), 272-281, 2016 | 90 | 2016 |
Characterization of molecular defects in isovaleryl-CoA dehydrogenase in patients with isovaleric acidemia AWA Mohsen, BD Anderson, SL Volchenboum, KP Battaile, K Tiffany, ... Biochemistry 37 (28), 10325-10335, 1998 | 83 | 1998 |
Identification of isobutyryl-CoA dehydrogenase and its deficiency in humans TV Nguyen, BS Andresen, TJ Corydon, S Ghisla, N Abd-El Razik, ... Molecular genetics and metabolism 77 (1-2), 68-79, 2002 | 82 | 2002 |
Very long chain fatty acid metabolism is required in acute myeloid leukemia M Tcheng, A Roma, N Ahmed, RW Smith, P Jayanth, MD Minden, ... Blood, The Journal of the American Society of Hematology 137 (25), 3518-3532, 2021 | 71 | 2021 |
Complex I assembly function and fatty acid oxidation enzyme activity of ACAD9 both contribute to disease severity in ACAD9 deficiency M Schiff, B Haberberger, C Xia, AW Mohsen, ES Goetzman, Y Wang, ... Human molecular genetics 24 (11), 3238-3247, 2015 | 67 | 2015 |
Evaluation of mitochondrial bioenergetics, dynamics, endoplasmic reticulum-mitochondria crosstalk, and reactive oxygen species in fibroblasts from patients with complex I … G Leipnitz, AW Mohsen, A Karunanidhi, B Seminotti, VY Roginskaya, ... Scientific reports 8 (1), 1165, 2018 | 64 | 2018 |
High-level expression of an altered cDNA encoding human isovaleryl-CoA dehydrogenase in Escherichia coli AWA Mohsen, J Vockley Gene 160 (2), 263-267, 1995 | 61 | 1995 |
Identification of the active site catalytic residue in human isovaleryl-CoA dehydrogenase AWA Mohsen, J Vockley Biochemistry 34 (32), 10146-10152, 1995 | 60 | 1995 |
Molecular and cellular pathology of very-long-chain acyl-CoA dehydrogenase deficiency M Schiff, AW Mohsen, A Karunanidhi, E McCracken, R Yeasted, J Vockley Molecular genetics and metabolism 109 (1), 21-27, 2013 | 59 | 2013 |
Mitochondrial energetics is impaired in very long-chain acyl-CoA dehydrogenase deficiency and can be rescued by treatment with mitochondria-targeted electron scavengers B Seminotti, G Leipnitz, A Karunanidhi, C Kochersperger, VY Roginskaya, ... Human molecular genetics 28 (6), 928-941, 2019 | 55 | 2019 |
Expression and characterization of mutations in human very long-chain acyl-CoA dehydrogenase using a prokaryotic system ES Goetzman, Y Wang, M He, AW Mohsen, BK Ninness, J Vockley Molecular genetics and metabolism 91 (2), 138-147, 2007 | 52 | 2007 |
Characterization of new ACADSB gene sequence mutations and clinical implications in patients with 2-methylbutyrylglycinuria identified by newborn screening J Alfardan, AW Mohsen, S Copeland, J Ellison, L Keppen-Davis, ... Molecular genetics and metabolism 100 (4), 333-338, 2010 | 43 | 2010 |