threonine has been researched along with Hyperlipoproteinemia Type I in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 3 (100.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bellet, PS; Harris, BV; Keilson, LM; Simbartl, LA; Sprecher, DL; Stein, EA | 1 |
| Bijvoet, SM; Bruin, T; Erkelens, DW; Hayden, MR; Henderson, HE; Kastelein, JJ; Mannens, MA | 1 |
| Basdevant, A; Emi, M; Gambert, P; Hata, A; Iverius, PH; Lalouel, JM; Luc, G | 1 |
3 other study(ies) available for threonine and Hyperlipoproteinemia Type I
| Article | Year |
|---|---|
Higher triglycerides, lower high-density lipoprotein cholesterol, and higher systolic blood pressure in lipoprotein lipase-deficient heterozygotes. A preliminary report.
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 |
Ile225Thr loop mutation in the lipoprotein lipase (LPL) gene is a de novo event.
Topics: Adult; Aged; Amino Acid Substitution; Apolipoproteins E; Dinucleotide Repeats; Exons; Genotype; Haplotypes; Humans; Hyperlipoproteinemia Type I; Isoleucine; Lipids; Lipoprotein Lipase; Male; Mutation; Pedigree; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Threonine | 1998 |
Compound heterozygote for lipoprotein lipase deficiency: Ser----Thr244 and transition in 3' splice site of intron 2 (AG----AA) in the lipoprotein lipase gene.
Topics: Amino Acid Sequence; Apolipoproteins; Base Sequence; Child; Cloning, Molecular; DNA; DNA Mutational Analysis; Female; Heterozygote; Humans; Hyperlipoproteinemia Type I; Introns; Lipids; Lipoprotein Lipase; Male; Molecular Sequence Data; Mutation; Pedigree; Plasmids; Serine; Threonine | 1990 |