Compounds > aspartic acid
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aspartic acid and CBS Deficiency

aspartic acid has been researched along with CBS Deficiency in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19901 (33.33)18.7374
1990's1 (33.33)18.2507
2000's1 (33.33)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Blom, HJ; Boulanger, Y; Debray, FG; Decarie, JC; Jakobs, C; Khiat, A; Lambert, M; Levy, E; Lortie, A; Mitchell, GA; Orquin, J; Ramos, F; Roy, MS; Struys, E; Verhoeven, NM1
Blom, HJ; Boers, GH; Kluijtmans, LA; Kraus, JP; Renier, WO; Stevens, EM; Trijbels, FJ; van den Heuvel, LP1
Barkin, E; Levy, HL1

Other Studies

3 other study(ies) available for aspartic acid and CBS Deficiency

ArticleYear
Reduced brain choline in homocystinuria due to remethylation defects.
    Neurology, 2008, Jul-01, Volume: 71, Issue:1

    Topics: Adolescent; Adult; Aspartic Acid; Brain; Brain Chemistry; Child; Child, Preschool; Choline; Choline Deficiency; Creatine; Female; Homocysteine S-Methyltransferase; Homocystinuria; Humans; Magnetic Resonance Spectroscopy; Male; Methylation; S-Adenosylmethionine

2008
Defective cystathionine beta-synthase regulation by S-adenosylmethionine in a partially pyridoxine responsive homocystinuria patient.
    The Journal of clinical investigation, 1996, Jul-15, Volume: 98, Issue:2

    Topics: Adult; Amino Acid Sequence; Asparagine; Aspartic Acid; Base Sequence; Cystathionine beta-Synthase; DNA; DNA Primers; Female; Gene Expression Regulation, Enzymologic; Heterozygote; Homocystinuria; Homozygote; Humans; Male; Molecular Sequence Data; Pedigree; Point Mutation; Polymerase Chain Reaction; Pyridoxine; Reference Values; S-Adenosylmethionine

1996
Comparison of amino acid concentrations between plasma and erythrocytes. Studies in normal human subjects and those with metabolic disorders.
    The Journal of laboratory and clinical medicine, 1971, Volume: 78, Issue:4

    Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Arginine; Aspartic Acid; Biological Transport; Child; Chromatography, Ion Exchange; Cystine; Erythrocytes; Glutamates; Glutathione; Glycine; Histidine; Homocystine; Homocystinuria; Humans; Infant; Maple Syrup Urine Disease; Methionine; Ornithine; Phenylketonurias; Plasma; Renal Tubular Transport, Inborn Errors; Serine; Spectrophotometry; Threonine; Tyrosine

1971