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Al-Walid Mohsen
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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
1832010
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
1822013
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
1562014
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
1282005
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
1281997
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
1192008
Acyl-CoA dehydrogenases: dynamic history of protein family evolution
Z Swigoňová, AW Mohsen, J Vockley
Journal of molecular evolution 69, 176-193, 2009
1162009
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
1052011
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
852016
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
822002
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
821998
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
662015
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
652021
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
612018
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
611995
Identification of the active site catalytic residue in human isovaleryl-CoA dehydrogenase
AWA Mohsen, J Vockley
Biochemistry 34 (32), 10146-10152, 1995
591995
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
582013
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
522019
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
512007
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
422010
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