threonine has been researched along with Albuminuria in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (33.33) | 2.80 |
| Authors | Studies |
|---|---|
| Haase, R; Hoch, H; Königshausen, E; Meyer-Schwesinger, C; Potthoff, SA; Quack, I; Rump, LC; Sellin, L; Stegbauer, J; Wiech, T; Woznowski, MP | 1 |
| Beck, SR; Bowden, DW; Burdon, KP; Freedman, BI; Langefeld, CD; Liu, Y; Rich, SS; Wagenknecht, LE | 1 |
| Cambien, F; Hansen, BV; Nielsen, FS; Parving, HH; Poirier, O; Ricard, S; Rossing, P; Tarnow, L | 1 |
3 other study(ies) available for threonine and Albuminuria
| Article | Year |
|---|---|
Inhibition of p38 MAPK decreases hyperglycemia-induced nephrin endocytosis and attenuates albuminuria.
Topics: Albuminuria; Endocytosis; Humans; Hyperglycemia; Membrane Proteins; p38 Mitogen-Activated Protein Kinases; Podocytes; Protein Kinase C-alpha; Serine; Threonine | 2022 |
T-786C polymorphism of the endothelial nitric oxide synthase gene is associated with albuminuria in the diabetes heart study.
Topics: Aged; Albuminuria; Aspartic Acid; Creatinine; Cysteine; Diabetes Mellitus, Type 1; Diabetes Mellitus, Type 2; Exons; Female; Genetic Predisposition to Disease; Genotype; Glutamic Acid; Homozygote; Humans; Linkage Disequilibrium; Male; Middle Aged; Nitric Oxide Synthase; Nitric Oxide Synthase Type III; Odds Ratio; Polymorphism, Genetic; Promoter Regions, Genetic; Threonine | 2005 |
Angiotensinogen gene polymorphisms in IDDM patients with diabetic nephropathy.
Topics: Adult; Albuminuria; Angiotensinogen; Blood Pressure; Diabetes Mellitus, Type 1; Diabetic Nephropathies; Female; Genotype; Humans; Male; Methionine; Middle Aged; Polymorphism, Genetic; Risk Factors; Threonine | 1996 |