urea has been researched along with Nephritis, Hereditary 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.
Nephritis, Hereditary: A group of inherited conditions characterized initially by HEMATURIA and slowly progressing to RENAL INSUFFICIENCY. The most common form is the Alport syndrome (hereditary nephritis with HEARING LOSS) which is caused by mutations in genes for TYPE IV COLLAGEN and defective GLOMERULAR BASEMENT MEMBRANE.
| 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 Nephritis, Hereditary
| 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 Nephritis, Hereditary
| 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 |