about
Identification and characterization of new long chain acyl-CoA dehydrogenasesStructural basis for substrate fatty acyl chain specificity: crystal structure of human very-long-chain acyl-CoA dehydrogenaseThermal unfolding of medium-chain acyl-CoA dehydrogenase and iso(3)valeryl-CoA dehydrogenase: study of the effect of genetic defects on enzyme stabilityCharacterization of new ACADSB gene sequence mutations and clinical implications in patients with 2-methylbutyrylglycinuria identified by newborn screeningHuman acyl-CoA dehydrogenase-9 plays a novel role in the mitochondrial beta-oxidation of unsaturated fatty acids.Complex changes in the liver mitochondrial proteome of short chain acyl-CoA dehydrogenase deficient mice.Kinetic and spectral properties of isovaleryl-CoA dehydrogenase and interaction with ligandsRole of isovaleryl-CoA dehydrogenase and short branched-chain acyl-CoA dehydrogenase in the metabolism of valproic acid: implications for the branched-chain amino acid oxidation pathway.Flavoenzyme catalysed oxidation of amines: roles for flavin and protein-based radicals.Molecular and cellular pathology of very-long-chain acyl-CoA dehydrogenase deficiencySirtuin 3 (SIRT3) protein regulates long-chain acyl-CoA dehydrogenase by deacetylating conserved lysines near the active site.Low expression of long-chain acyl-CoA dehydrogenase in human skeletal muscleComplex I assembly function and fatty acid oxidation enzyme activity of ACAD9 both contribute to disease severity in ACAD9 deficiency.Fasting induces prominent proteomic changes in liver in very long chain Acyl-CoA dehydrogenase deficient mice.Expression and characterization of mutations in human very long-chain acyl-CoA dehydrogenase using a prokaryotic system.Outcomes and genotype-phenotype correlations in 52 individuals with VLCAD deficiency diagnosed by NBS and enrolled in the IBEM-IS databaseCloning of genomic and cDNA for mouse isovaleryl-CoA dehydrogenase (IVD) and evolutionary comparison to other known IVDs.Arginine 387 of human isovaleryl-CoA dehydrogenase plays a crucial role in substrate/product binding.Investigating the link of ACAD10 deficiency to type 2 diabetes mellitus.Evaluation of mitochondrial bioenergetics, dynamics, endoplasmic reticulum-mitochondria crosstalk, and reactive oxygen species in fibroblasts from patients with complex I deficiency.Mitochondrial respiratory chain disorders in the Old Order Amish population.High-level expression of an altered cDNA encoding human isovaleryl-CoA dehydrogenase in Escherichia coliMechanism-based inhibitor discrimination in the acyl-CoA dehydrogenasesNovel mutation in MYH7 gene associated with distal myopathy and cardiomyopathyReticular Dysgenesis and Mitochondriopathy Induced by Adenylate Kinase 2 Deficiency with Atypical PresentationAn acyl-CoA dehydrogenase microplate activity assay using recombinant porcine electron transfer flavoproteinETHE1 and MOCS1 deficiencies: Disruption of mitochondrial bioenergetics, dynamics, redox homeostasis and endoplasmic reticulum-mitochondria crosstalk in patient fibroblastsMitochondrial energetics is impaired in very long-chain acyl-CoA dehydrogenase deficiency and can be rescued by treatment with mitochondria-targeted electron scavengers
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description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Al-Walid Mohsen
@ast
Al-Walid Mohsen
@en
Al-Walid Mohsen
@es
Al-Walid Mohsen
@nl
Al-Walid Mohsen
@sl
type
label
Al-Walid Mohsen
@ast
Al-Walid Mohsen
@en
Al-Walid Mohsen
@es
Al-Walid Mohsen
@nl
Al-Walid Mohsen
@sl
prefLabel
Al-Walid Mohsen
@ast
Al-Walid Mohsen
@en
Al-Walid Mohsen
@es
Al-Walid Mohsen
@nl
Al-Walid Mohsen
@sl
P106
P1153
8279900100
P31
P496
0000-0002-0096-5959