|
rs1800471
|
|
|
0.010 |
GeneticVariation |
BEFREE |
To investigate whether the genetic polymorphisms of rs1800470 (codon 10 T/C), rs1800471 (codon 25 C/G) from the TGF-β, and rs2430561 (+874 T/A) from IFN-γ may be a risk factor for ICU patients to the development of AKI and/or death.
|
25147823 |
2014 |
|
rs2430561
|
|
|
0.010 |
GeneticVariation |
BEFREE |
To investigate whether the genetic polymorphisms of rs1800470 (codon 10 T/C), rs1800471 (codon 25 C/G) from the TGF-β, and rs2430561 (+874 T/A) from IFN-γ may be a risk factor for ICU patients to the development of AKI and/or death.
|
25147823 |
2014 |
|
rs767816037
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Apolipoprotein E genotype, TNF-α 308G/A and risk for cardiac surgery associated-acute kidney injury in Caucasians.
|
24059882 |
2014 |
|
rs775020499
|
|
|
0.010 |
GeneticVariation |
BEFREE |
COMT-Val158Met-polymorphism is not a risk factor for acute kidney injury after cardiac surgery.
|
24167357 |
2013 |
|
rs12457893
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Two of these were in the BCL2 gene and both were associated with a decreased risk of acute kidney injury (rs8094315: odds ratio 0.61, p = .0002; rs12457893: odds ratio 0.67, p = .0002, both for combined data).
|
22710204 |
2012 |
|
rs1444669684
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Both tumors develop in mice upon conditional deletion in melanocytes of Ink4a/Arf tumor suppressor genes with concomitant expression of oncogene H-Ras(G12V) and a known tumor antigen.
|
23173060 |
2012 |
|
rs561633150
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Our findings suggest that homozygous and/or compound heterozygous loss-of-function mutations p.G216R and p.N333S cause renal hypouricaemia via loss of uric acid absorption and do lead to acute kidney injury.
|
22527535 |
2012 |
|
rs753482595
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Our findings suggest that homozygous and/or compound heterozygous loss-of-function mutations p.G216R and p.N333S cause renal hypouricaemia via loss of uric acid absorption and do lead to acute kidney injury.
|
22527535 |
2012 |
|
rs8094315
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Two of these were in the BCL2 gene and both were associated with a decreased risk of acute kidney injury (rs8094315: odds ratio 0.61, p = .0002; rs12457893: odds ratio 0.67, p = .0002, both for combined data).
|
22710204 |
2012 |
|
rs1451506414
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We here described a 25-yr-old man showing idiopathic renal hypouricemia with G774A mutation in SCL22A12 who presented exercise-induced acute renal failure.
|
21935282 |
2011 |
|
rs121907896
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The patient had compound heterozygous mutations in the hURAT1 gene (R90H and W258X), but showed no clinical manifestations such as urolithiasis or exercise-induced acute renal failure.
|
17362586 |
2007 |
|
rs782818582
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Novel compound heterozygote mutations (H234Q/R1206X) of the ADAMTS13 gene in an adult patient with Upshaw-Schulman syndrome showing predominant episodes of repeated acute renal failure.
|
16449289 |
2006 |