Compounds > 3-hydroxy-3-methylglutaryl-coenzyme a

3-hydroxy-3-methylglutaryl-coenzyme a and Metabolism, Inborn Errors

3-hydroxy-3-methylglutaryl-coenzyme a has been researched along with Metabolism, Inborn Errors in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Mitchell, GA; Miziorko, HM; Roberts, JR1
Kikuchi, M; Narisawa, K; Sweetman, L; Tada, K1

Other Studies

2 other study(ies) available for 3-hydroxy-3-methylglutaryl-coenzyme a and Metabolism, Inborn Errors

ArticleYear
Modeling of a mutation responsible for human 3-hydroxy-3-methylglutaryl-CoA lyase deficiency implicates histidine 233 as an active site residue.
    The Journal of biological chemistry, 1996, Oct-04, Volume: 271, Issue:40

    Topics: Acyl Coenzyme A; Binding Sites; Diethyl Pyrocarbonate; Enzyme Inhibitors; Histidine; Humans; Hydrolysis; Metabolism, Inborn Errors; Oxo-Acid-Lyases; Point Mutation

1996
Enzymatic diagnosis of 3-hydroxy-3-methylglutaryl-CoA lyase deficiency with high-performance liquid chromatography.
    Clinica chimica acta; international journal of clinical chemistry, 1990, Aug-31, Volume: 189, Issue:3

    Topics: Acetyl Coenzyme A; Acyl Coenzyme A; Child, Preschool; Chromatography, High Pressure Liquid; Humans; Infant; Kinetics; Metabolism, Inborn Errors; Oxo-Acid-Lyases

1990