glycine has been researched along with Hyperlipoproteinemia Type I in 2 studies
Hyperlipoproteinemia Type I: An inherited condition due to a deficiency of either LIPOPROTEIN LIPASE or APOLIPOPROTEIN C-II (a lipase-activating protein). The lack of lipase activities results in inability to remove CHYLOMICRONS and TRIGLYCERIDES from the blood which has a creamy top layer after standing.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (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 |
|---|---|
| Sprecher, DL | 1 |
| Harris, BV | 1 |
| Stein, EA | 1 |
| Bellet, PS | 1 |
| Keilson, LM | 1 |
| Simbartl, LA | 1 |
| Faustinella, F | 1 |
| Chang, A | 1 |
| Van Biervliet, JP | 1 |
| Rosseneu, M | 1 |
| Vinaimont, N | 1 |
| Smith, LC | 1 |
| Chen, SH | 1 |
| Chan, L | 1 |
2 other studies available for glycine 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 | 1996 |
Catalytic triad residue mutation (Asp156----Gly) causing familial lipoprotein lipase deficiency. Co-inheritance with a nonsense mutation (Ser447----Ter) in a Turkish family.
Topics: Adipose Tissue; Alleles; Aspartic Acid; Base Sequence; Catalysis; DNA; Glycine; Humans; Hyperlipopro | 1991 |