Compounds > phenylalanine

phenylalanine and ethylnitrosourea

phenylalanine has been researched along with ethylnitrosourea in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19902 (33.33)18.7374
1990's2 (33.33)18.2507
2000's2 (33.33)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bode, VC; Dove, WF; McDonald, JD; Shedlovsky, A1
Bode, VC; Guenet, JL; McDonald, JD; Simon, D1
Ebel, JP; Giege, R; Vlassov, VV1
Blain, F; Chang, TM; Heft, R; Peevers, R; Sarkissian, CN; Scriver, CR; Shao, Z; Su, H1
Bentley, L; Browne, M; Cox, RD; Goldsworthy, M; Haynes, A; Hough, T; Hugill, A; Hunter, AJ; Mijat, V; Moir, L; Quarterman, J; Spurr, N; Toye, AA1
Beutler, B; Ding, L; Du, X; Gong, X; Horwitz, J; Huang, Q; Liu, H; McDonald, HW; Wang, M; Yates, JR1

Other Studies

6 other study(ies) available for phenylalanine and ethylnitrosourea

ArticleYear
The use of N-ethyl-N-nitrosourea to produce mouse models for human phenylketonuria and hyperphenylalaninemia.
    Progress in clinical and biological research, 1990, Volume: 340C

    Topics: Amino Acid Metabolism, Inborn Errors; Animals; Crosses, Genetic; Disease Models, Animal; Ethylnitrosourea; Female; Humans; Male; Mice; Mice, Mutant Strains; Mutation; Phenotype; Phenylalanine; Phenylketonurias

1990
hph-1: a mouse mutant with hereditary hyperphenylalaninemia induced by ethylnitrosourea mutagenesis.
    Genetics, 1988, Volume: 118, Issue:2

    Topics: Amino Acid Metabolism, Inborn Errors; Animals; Chromosome Mapping; Crosses, Genetic; Ethylnitrosourea; Female; Genetic Linkage; Genotype; Male; Mice; Mice, Inbred Strains; Mice, Mutant Strains; Mutation; Pedigree; Phenotype; Phenylalanine

1988
The tertiary structure of yeast tRNAPhe in solution studied by phosphodiester bond modification with ethylnitrosourea.
    FEBS letters, 1980, Oct-20, Volume: 120, Issue:1

    Topics: Alkylation; Ethylnitrosourea; Macromolecular Substances; Molecular Weight; Nitrosourea Compounds; Nucleic Acid Conformation; Phenylalanine; RNA, Transfer; Saccharomyces cerevisiae; Solutions

1980
A different approach to treatment of phenylketonuria: phenylalanine degradation with recombinant phenylalanine ammonia lyase.
    Proceedings of the National Academy of Sciences of the United States of America, 1999, Mar-02, Volume: 96, Issue:5

    Topics: Animals; Basidiomycota; Cloning, Molecular; Disease Models, Animal; Escherichia coli; Ethylnitrosourea; Humans; Injections, Intraperitoneal; Mice; Phenylalanine; Phenylalanine Ammonia-Lyase; Phenylketonurias; Recombinant Proteins

1999
A new mouse model of type 2 diabetes, produced by N-ethyl-nitrosourea mutagenesis, is the result of a missense mutation in the glucokinase gene.
    Diabetes, 2004, Volume: 53, Issue:6

    Topics: Adenine; Amino Acid Sequence; Amino Acid Substitution; Animals; Chromosome Mapping; Diabetes Mellitus, Type 2; Disease Models, Animal; Ethylnitrosourea; Glucokinase; Glucose; Glucose Intolerance; Heterozygote; Homozygote; Isoleucine; Male; Mice; Mice, Mutant Strains; Molecular Sequence Data; Mutagens; Mutation, Missense; Phenylalanine; Phosphorylation; Thymine

2004
Crystallin {gamma}B-I4F mutant protein binds to {alpha}-crystallin and affects lens transparency.
    The Journal of biological chemistry, 2005, Jul-01, Volume: 280, Issue:26

    Topics: alpha-Crystallins; Angiography; Animals; Chromatography, Gel; Circular Dichroism; Cloning, Molecular; Crystallins; Disease Models, Animal; DNA Primers; Electrophoresis, Gel, Two-Dimensional; Ethylnitrosourea; Fluorescein; gamma-Crystallins; Genetic Linkage; Homozygote; Immunohistochemistry; Isoleucine; Lens, Crystalline; Mice; Mice, Mutant Strains; Mutagenesis; Mutagens; Mutation; Mutation, Missense; Phenotype; Phenylalanine; Protein Binding; Recombinant Proteins; Retinal Vessels; Sequence Analysis, DNA; Ultraviolet Rays

2005