Compounds > tryptophan

tryptophan and Apolipoprotein C-II Deficiency

tryptophan has been researched along with Apolipoprotein C-II Deficiency in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's3 (75.00)18.2507
2000's1 (25.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bellet, PS; Harris, BV; Keilson, LM; Simbartl, LA; Sprecher, DL; Stein, EA1
Häring, HU; Hoffmann, MM; Jacob, S; Luft, D; März, W; Matthaei, S; Rett, K; Schmülling, RM1
Ameis, D; Bellet, PS; Black, DM; Goldberg, IJ; Harris, BV; Kobayashi, J; Rymaszewski, M; Sprecher, DL; Stein, EA; Yunker, RL1
Chan, L; Faustinella, F; Ishimura-Oka, K; Kihara, S; Oka, K; Smith, LC1

Other Studies

4 other study(ies) available for tryptophan and Apolipoprotein C-II Deficiency

ArticleYear
Higher triglycerides, lower high-density lipoprotein cholesterol, and higher systolic blood pressure in lipoprotein lipase-deficient heterozygotes. A preliminary report.
    Circulation, 1996, Dec-15, Volume: 94, Issue:12

    Topics: Adult; Blood Pressure; Body Mass Index; Cholesterol, LDL; Exons; Genetic Carrier Screening; Glutamic Acid; Glycine; Humans; Hyperlipoproteinemia Type I; Isoleucine; Lipoprotein Lipase; Point Mutation; Systole; Threonine; Triglycerides; Tryptophan

1996
Type I hyperlipoproteinemia due to a novel loss of function mutation of lipoprotein lipase, Cys(239)-->Trp, associated with recurrent severe pancreatitis.
    The Journal of clinical endocrinology and metabolism, 2000, Volume: 85, Issue:12

    Topics: Amino Acid Substitution; Anticoagulants; Apolipoproteins; Cysteine; Electrophoresis, Polyacrylamide Gel; Female; Genotype; Heparin; Humans; Hyperlipoproteinemia Type I; Lipid Metabolism; Lipoprotein Lipase; Middle Aged; Mutation; Pancreatitis; Recurrence; Triglycerides; Tryptophan

2000
Trp64----nonsense mutation in the lipoprotein lipase gene.
    Journal of lipid research, 1992, Volume: 33, Issue:6

    Topics: Amino Acid Sequence; Base Sequence; Female; Heparin; Humans; Hyperlipoproteinemia Type I; Lipoprotein Lipase; Male; Molecular Sequence Data; Mutation; Pedigree; Terminator Regions, Genetic; Tryptophan

1992
A missense mutation (Trp86----Arg) in exon 3 of the lipoprotein lipase gene: a cause of familial chylomicronemia.
    American journal of human genetics, 1992, Volume: 50, Issue:6

    Topics: Amino Acid Sequence; Arginine; Base Sequence; Chylomicrons; Cloning, Molecular; Codon; DNA; Exons; Female; Humans; Hyperlipoproteinemia Type I; Introns; Lipoprotein Lipase; Male; Molecular Sequence Data; Mutation; Pedigree; Restriction Mapping; Tryptophan

1992