cysteine has been researched along with Lipid Metabolism, Inborn Error in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (50.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Bastin, J; Bennett, MJ; Chen, J; Doulias, PT; Ischiropoulos, H; Tenopoulou, M | 1 |
Andresen, BS; Bolund, L; Bross, P; Duran, M; Jensen, TG; Jensen, UB; Kim, JJ; Knudsen, I; Kølvraa, S; Winter, V | 1 |
2 other study(ies) available for cysteine and Lipid Metabolism, Inborn Error
Article | Year |
---|---|
Strategies for correcting very long chain acyl-CoA dehydrogenase deficiency.
Topics: Acetylcysteine; Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenase, Long-Chain; Amino Acid Sequence; Carnitine; Congenital Bone Marrow Failure Syndromes; Cysteine; Dose-Response Relationship, Drug; Fatty Acids; Fibroblasts; Genetic Therapy; Humans; Kinetics; Lipid Metabolism, Inborn Errors; Mitochondrial Diseases; Molecular Sequence Data; Muscular Diseases; Mutation; Oxidation-Reduction; Primary Cell Culture; Skin | 2015 |
A rare disease-associated mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene changes a conserved arginine, previously shown to be functionally essential in short-chain acyl-CoA dehydrogenase (SCAD).
Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenases; Arginine; Base Sequence; Cells, Cultured; Cysteine; DNA Mutational Analysis; Female; Heterozygote; Humans; Infant; Infant, Newborn; Lipid Metabolism, Inborn Errors; Male; Molecular Sequence Data; Mutagenesis, Site-Directed; Oxidation-Reduction; Pedigree; Point Mutation; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Protein Structure, Secondary; Recombinant Proteins; Structure-Activity Relationship | 1993 |