cysteine and Lipid Metabolism, Inborn Error

cysteine has been researched along with Lipid Metabolism, Inborn Error in 2 studies

Research

Studies (2)

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

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

Other Studies

2 other study(ies) available for cysteine and Lipid Metabolism, Inborn Error

Article	Year
Strategies for correcting very long chain acyl-CoA dehydrogenase deficiency. The Journal of biological chemistry, 2015, Apr-17, Volume: 290, Issue:16 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). American journal of human genetics, 1993, Volume: 53, Issue:3 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

Article

Year

Strategies for correcting very long chain acyl-CoA dehydrogenase deficiency.

The Journal of biological chemistry, 2015, Apr-17, Volume: 290, Issue:16

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).

American journal of human genetics, 1993, Volume: 53, Issue:3

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