urea has been researched along with Alport Syndrome in 4 studies
pseudourea: clinical use; structure
isourea : A carboximidic acid that is the imidic acid tautomer of urea, H2NC(=NH)OH, and its hydrocarbyl derivatives.
| Excerpt | Relevance | Reference |
|---|---|---|
| " Double-knockouts lived 47% longer, mice with 50% DDR1 lived 29% longer and showed improved renal function (reduction in proteinuria and blood urea nitrogen) compared to animals with 100% DDR1 expression." | 3.76 | Loss of collagen-receptor DDR1 delays renal fibrosis in hereditary type IV collagen disease. ( Beirowski, B; Busse, AC; Girgert, R; Gross, O; Kang, HG; Kretzler, M; Kruegel, J; Miosge, N; Müller, GA; Segerer, S; Vogel, WF; Weber, M, 2010) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (75.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Gross, O | 1 |
| Girgert, R | 1 |
| Beirowski, B | 1 |
| Kretzler, M | 1 |
| Kang, HG | 1 |
| Kruegel, J | 1 |
| Miosge, N | 1 |
| Busse, AC | 1 |
| Segerer, S | 1 |
| Vogel, WF | 1 |
| Müller, GA | 1 |
| Weber, M | 1 |
| CROSS, HD | 1 |
| el Matri, A | 1 |
| Kechrid, C | 1 |
| Ben Abdallah, T | 1 |
| Ben Moussa, F | 1 |
| Khder, A | 1 |
| Ben Maiz, H | 1 |
| Ben Ayed, H | 1 |
| Lyon, MF | 1 |
| Hulse, EV | 1 |
1 review available for urea and Alport Syndrome
| Article | Year |
|---|---|
[Alport's syndrome: apropos of 8 Tunisian families].
Topics: Adolescent; Adult; Female; Hematuria; Humans; Kidney; Male; Nephritis, Hereditary; Pedigree; Protein | 1988 |
3 other studies available for urea and Alport Syndrome
| Article | Year |
|---|---|
Loss of collagen-receptor DDR1 delays renal fibrosis in hereditary type IV collagen disease.
Topics: Animals; CD3 Complex; Collagen Type IV; Connective Tissue Growth Factor; Discoidin Domain Receptor 1 | 2010 |
Hereditary nephritis with unusual urea clearance--case report.
Topics: Humans; Nephritis; Nephritis, Hereditary; Urea | 1961 |
An inherited kidney disease of mice resembling human nephronophthisis.
Topics: Animals; Disease Models, Animal; Female; Genes, Recessive; Genetic Linkage; Humans; Kidney Diseases; | 1971 |