Compounds > tryptophan

tryptophan and Deficiency Disease, Ornithine Carbamoyltransferase

tryptophan has been researched along with Deficiency Disease, Ornithine Carbamoyltransferase in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19901 (25.00)18.7374
1990's3 (75.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bachmann, C; Colombo, JP1
Endo, F; Hoshide, R; Ishikawa, K; Kato, I; Kiwaki, K; Koike, E; Komaki, S; Matsuura, T; Oyanagi, K; Suzuki, Y1
Batshaw, ML; Heyes, MP; Hopkins, K; McLaughlin, BA; Oster-Granite, ML; Robinson, MB1
Akaboshi, I; Hata, A; Matsuda, I; Matsuura, T; Setoyama, C; Shimada, K; Yokoi, T1

Other Studies

4 other study(ies) available for tryptophan and Deficiency Disease, Ornithine Carbamoyltransferase

ArticleYear
Increase of tryptophan and 5-hydroxyindole acetic acid in the brain of ornithine carbamoyltransferase deficient sparse-fur mice.
    Pediatric research, 1984, Volume: 18, Issue:4

    Topics: Animals; Brain Chemistry; Carbamoyl-Phosphate Synthase (Ammonia); Female; Hydroxyindoleacetic Acid; Male; Mice; Mice, Inbred Strains; Ornithine Carbamoyltransferase Deficiency Disease; Serotonin; Tryptophan

1984
Four newly identified ornithine transcarbamylase (OTC) mutations (D126G, R129H, I172M and W332X) in Japanese male patients with early-onset OTC deficiency.
    Human mutation, 1994, Volume: 3, Issue:4

    Topics: Amino Acid Metabolism, Inborn Errors; Arginine; Aspartic Acid; Base Sequence; DNA Mutational Analysis; DNA Primers; DNA, Single-Stranded; Glycine; Histidine; Humans; Infant; Infant, Newborn; Isoleucine; Male; Methionine; Molecular Epidemiology; Molecular Sequence Data; Nucleic Acid Conformation; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Pedigree; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; Tryptophan; X Chromosome

1994
Evidence of excitotoxicity in the brain of the ornithine carbamoyltransferase deficient sparse fur mouse.
    Brain research. Developmental brain research, 1995, Dec-21, Volume: 90, Issue:1-2

    Topics: Ammonia; Animals; Brain Damage, Chronic; Disease Models, Animal; Glutamine; Hair; Metabolism, Inborn Errors; Mice; Mice, Inbred Strains; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Quinolinic Acid; Tryptophan

1995
A novel missense mutation in exon 8 of the ornithine transcarbamylase gene in two unrelated male patients with mild ornithine transcarbamylase deficiency.
    Human genetics, 1991, Volume: 87, Issue:1

    Topics: Alleles; Amino Acid Sequence; Arginine; Base Sequence; Exons; Genotype; Heterozygote; Humans; Infant; Male; Molecular Sequence Data; Mutation; Nucleic Acid Hybridization; Oligonucleotide Probes; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Orotic Acid; Pedigree; Tryptophan

1991