rs104894251
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The HPS phenotype in man can be explained by the lower expression of functional channels by the Kir1.1a[N124K] mutant.
|
9727001 |
1998 |
rs11614913
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The MIR196A2 rs11614913 C > T polymorphism may contribute to an increased risk of HPS in liver cirrhosis patients.
|
27509319 |
2017 |
rs119471022
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The two patients with HPS were homozygous for nonsense mutation (T/T) for the c.541C>T (rs119471022) in the HPS4 gene, which is mapped to human chromosome 22q12.1.
|
23563589 |
2013 |
rs119471022
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The two patients with HPS were homozygous for nonsense mutation (T/T) for the c.541C>T (rs119471022) in the HPS4 gene, which is mapped to human chromosome 22q12.1.
|
23563589 |
2013 |
rs145036301
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We added thalidomide to the conventional dexamethasone-containing therapy regimen for two patients with HPS who expressed ECSIT-V140A, and we observed reversal of their HPS and disease-free survival for longer than 3 years.
|
29291352 |
2018 |
rs1799983
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Endothelial Nitric Oxide Synthase G894T Polymorphism Associates with Disease Severity in Puumala Hantavirus Infection.
|
26561052 |
2015 |
rs243865
|
|
|
0.010 |
GeneticVariation |
BEFREE |
CC/CT genotype and C allele of MMP-2 rs243865</span> polymorphism as well as CC/TT genotype and T allele of MMP-9 rs3918242 polymorphism increased the risk of HPS in cirrhotic patients.
|
30392570 |
2018 |
rs3918242
|
|
|
0.010 |
GeneticVariation |
BEFREE |
CC/CT genotype and C allele of MMP-2 rs243865 polymorphism as well as CC/TT genotype and T allele of MMP-9 rs3918242 polymorphism increased the risk of HPS in cirrhotic patients.
|
30392570 |
2018 |
rs62106244
|
|
|
0.010 |
GeneticVariation |
BEFREE |
However, the T allele of rs62106244 (intron 10 of DNMT1 gene) was over-represented in cases with HPS (p<0.01) compared with population controls.
|
21347319 |
2011 |
rs752317734
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We added thalidomide to the conventional dexamethasone-containing therapy regimen for two patients with HPS who expressed ECSIT-V140A, and we observed reversal of their HPS and disease-free survival for longer than 3 years.
|
29291352 |
2018 |
rs769446880
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The two patients with HPS were homozygous for nonsense mutation (T/T) for the c.541C>T (rs119471022) in the HPS4 gene, which is mapped to human chromosome 22q12.1.
|
23563589 |
2013 |