Compounds > arginine

arginine and Lipid Metabolism, Inborn Error

arginine has been researched along with Lipid Metabolism, Inborn Error in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's3 (60.00)18.2507
2000's0 (0.00)29.6817
2010's2 (40.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ding, X; Han, Y; Yang, Z; Yi, Y; Yu, H2
Andresen, BS; Bolund, L; Bross, P; Duran, M; Jensen, TG; Jensen, UB; Kim, JJ; Knudsen, I; Kølvraa, S; Winter, V1
Gibson, B; Hahn, SH; Hong, CH; Jung, JW; Lee, EH; Rinaldo, P; Sims, H; Strauss, AW; Yoon, HR1
Fischer, J; Keller, C; Rauh, G; Schuster, H; Wolfram, G; Zöllner, N1

Other Studies

5 other study(ies) available for arginine and Lipid Metabolism, Inborn Error

ArticleYear
[Expression of long chain fatty acid oxidase in maternal and fetal tissues in preeclampsia-like mouse model in mid-gestation].
    Zhonghua yi xue za zhi, 2015, Jan-06, Volume: 95, Issue:1

    Topics: 3-Hydroxyacyl CoA Dehydrogenases; Animals; Arginine; Cardiomyopathies; Disease Models, Animal; Fatty Acids; Female; Fetal Development; Fetus; Humans; Lipid Metabolism, Inborn Errors; Liver; Mice; Mice, Inbred C57BL; Mitochondrial Myopathies; Mitochondrial Trifunctional Protein; Nervous System Diseases; Oxidation-Reduction; Oxidoreductases; Placenta; Pre-Eclampsia; Pregnancy; Rhabdomyolysis

2015
[Variation of long-chain 3-hydroxyacyl-CoA dehydrogenase DNA methylation in placenta of different preeclampsia-like mouse models].
    Zhonghua fu chan ke za zhi, 2015, Volume: 50, Issue:10

    Topics: 3-Hydroxyacyl CoA Dehydrogenases; 3-Hydroxyacyl-CoA Dehydrogenase; Animals; Arginine; Cardiomyopathies; Disease Models, Animal; DNA Methylation; Fatty Acids; Female; Humans; Lipid Metabolism; Lipid Metabolism, Inborn Errors; Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase; Mice; Mitochondrial Myopathies; Mitochondrial Trifunctional Protein; Nervous System Diseases; Oxidation-Reduction; Oxidative Stress; Placenta; Pre-Eclampsia; Pregnancy; Rhabdomyolysis

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
Very long chain acyl coenzyme A dehydrogenase deficiency in a 5-month-old Korean boy: identification of a novel mutation.
    The Journal of pediatrics, 1999, Volume: 135, Issue:2 Pt 1

    Topics: Acyl-CoA Dehydrogenase, Long-Chain; Arginine; Cardiomyopathies; Carnitine; Codon, Terminator; Fatal Outcome; Fatty Acid Desaturases; Genetic Heterogeneity; Humans; Infant; Korea; Lipid Metabolism, Inborn Errors; Male; Mutation

1999
Identification of a heterozygous compound individual with familial hypercholesterolemia and familial defective apolipoprotein B-100.
    Klinische Wochenschrift, 1991, May-03, Volume: 69, Issue:7

    Topics: Adolescent; Adult; Aged; Apolipoprotein B-100; Apolipoproteins B; Arginine; Base Sequence; Child; DNA, Circular; Female; Glutamine; Heterozygote; Humans; Hydroxymethylglutaryl CoA Reductases; Hyperlipoproteinemia Type II; Lipid Metabolism, Inborn Errors; Male; Middle Aged; Molecular Sequence Data; Mutation; Pedigree; Protein Binding

1991