tryptophan and Genetic Diseases

tryptophan has been researched along with Genetic Diseases in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (50.00)29.6817
2010's0 (0.00)24.3611
2020's1 (50.00)2.80

Authors

AuthorsStudies
Avitabile, T; Choragiewicz, T; Fiedorowicz, M; Grieb, P; Kamińska, A; Kocki, T; Nowakowska, D; Rejdak, R; Toro, MD; Turski, WA; Wertejuk, K; Wełniak-Kaminska, M; Zweifel, S1
Caldovic, L; Cheng, SF; Morizono, H; Packman, S; Panglao, MG; Tuchman, M1

Other Studies

2 other study(ies) available for tryptophan and Genetic Diseases

ArticleYear
Tryptophan Pathway Abnormalities in a Murine Model of Hereditary Glaucoma.
    International journal of molecular sciences, 2021, Jan-21, Volume: 22, Issue:3

    Topics: Animals; Biomarkers; Disease Models, Animal; Disease Susceptibility; Genetic Diseases, Inborn; Glaucoma; Kynurenic Acid; Kynurenine; Magnetic Resonance Imaging; Metabolic Networks and Pathways; Mice; Retina; Species Specificity; Tryptophan

2021
Null mutations in the N-acetylglutamate synthase gene associated with acute neonatal disease and hyperammonemia.
    Human genetics, 2003, Volume: 112, Issue:4

    Topics: Acetyltransferases; Adenine; Amino-Acid N-Acetyltransferase; Base Sequence; Denmark; Female; Genetic Diseases, Inborn; Guanine; Hispanic or Latino; Homozygote; Humans; Hyperammonemia; Infant; Infant, Newborn; Male; Molecular Sequence Data; Mutation; Polymorphism, Restriction Fragment Length; Sequence Analysis, DNA; Tryptophan; White People

2003