|
rs1057518731
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs1057518733
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs1057520529
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs1131692245
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs113993959
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs1555580263
|
|
GAGGTAGAACCTTATCTGCCATCTTC |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs74597325
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs76992529
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs879253740
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs1217371203
|
|
|
0.010 |
GeneticVariation |
BEFREE |
To clarify the mechanism underlying these observations we have developed a model of lung inflammation using adoptively transferred CD4(+) T cells expressing a Valpha11(+)Vbeta3(+) transgenic TCR specific for I-E(k) and moth cytochrome c. Treatment with Y100F-Ig inhibited the induction of lung eosinophilia in adoptively transferred mice.
|
11290768 |
2001 |
|
rs587782477
|
|
|
0.010 |
GeneticVariation |
BEFREE |
To clarify the mechanism underlying these observations we have developed a model of lung inflammation using adoptively transferred CD4(+) T cells expressing a Valpha11(+)Vbeta3(+) transgenic TCR specific for I-E(k) and moth cytochrome c. Treatment with Y100F-Ig inhibited the induction of lung eosinophilia in adoptively transferred mice.
|
11290768 |
2001 |
|
rs868435969
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Three distal myopathy patients developed rapidly progressive dementia, became bedridden and died of cachexia and pneumonia and VCP gene mutation P137L (c.410C>T) was then identified in the family.
|
21684747 |
2011 |
|
rs213950
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Caucasian and African American children with pneumonia were genotyped for the most common variants reported to affect cystic fibrosis transmembrane conductance regulator function, the p.508del mutation, the (TG)mTn variable repeat region, and the M470V polymorphism in the cystic fibrosis transmembrane conductance regulator gene.
|
22890249 |
2012 |
|
rs5743313
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The TLR3 rs5743313/CT polymorphism was found in all of the children with pneumonia and influenza infection, but in a significantly smaller number of those with A/H1N1/2009 influenza without pneumonia (<0.0001).
|
23151015 |
2012 |
|
rs4986791
|
|
|
0.020 |
GeneticVariation |
BEFREE |
This case-control study evaluated the prevalence of D299G/T399I polymorphisms in Mexican patients with IAI and/or pneumonia and in healthy controls.
|
23871732 |
2013 |
|
rs12252
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We have genotyped a possible splice-site altering single-nucleotide polymorphism (rs12252) in the IFITM3 gene in 34 patients with H1N1 influenza and severe pneumonia, and >5000 individuals comprising patients with community-acquired mild lower respiratory tract infection and matched controls of Caucasian ancestry.
|
23997235 |
2014 |
|
rs4251961
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Higher plasma IL-1ra was associated with an increased risk of infection (other than pneumonia), and the minor C allele of rs4251961 was independently associated with a decreased risk of infection (other than pneumonia).
|
24233813 |
2014 |
|
rs4957796
|
|
|
0.710 |
GeneticVariation |
GWASCAT |
Genome-wide association study of survival from sepsis due to pneumonia: an observational cohort study.
|
25533491 |
2015 |
|
rs796051877
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
c.1437G>A intron 9 substitution on acid α-glucosidase gene associated with classic infantile-onset Pompe disease phenotype.
|
26160551 |
2015 |
|
rs4986791
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Furthermore, the cosegregating TLR4 polymorphisms Asp299Gly and Thr399Ile were independent risk factors for the development of both sepsis and pneumonia (OR: 3.55; 95% CI: 1.21-10.4, P=0.021 and OR: 3.57, 95% CI: 1.3-9.86, P=0.014, respectively).
|
25427560 |
2015 |
|
rs5743708
|
|
|
0.020 |
GeneticVariation |
BEFREE |
The presence of the TLR2 Arg753Gln polymorphism was significantly associated with pneumonia in AML patients (odds ratio (OR): 10.78; 95% confidence interval (CI): 2.0-58.23; P=0.006).
|
25427560 |
2015 |
|
rs1800629
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In the present study, we aim to investigate the association of promoter-region polymorphisms IL-6 (-174G/C) rs1800795 and TNF-α (-308G/A) rs1800629 with pneumonia-induced sepsis.
|
26025100 |
2015 |
|
rs1800795
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In intensive care unit patients, the TNF-α -308A allele and the IL-6 rs1800795 allele variants were susceptibility risk factors for septic shock induced by pneumonia.
|
26025100 |
2015 |
|
rs4986790
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Furthermore, the cosegregating TLR4 polymorphisms Asp299Gly and Thr399Ile were independent risk factors for the development of both sepsis and pneumonia (OR: 3.55; 95% CI: 1.21-10.4, P=0.021 and OR: 3.57, 95% CI: 1.3-9.86, P=0.014, respectively).
|
25427560 |
2015 |
|
rs5743708
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Patients carrying the TLR2 SNP rs5743708 (R753Q, GA/AA genotype, n = 12) also revealed a significantly higher susceptibility to pneumonia including IFD.
|
26963509 |
2016 |