Neoplasms
|
0.010 |
AlteredExpression
|
group |
BEFREE |
The mean mRNA levels increased with NPI scores (0.0816 for NPI 1, 0.1186 for NPI 2 and 0.68 for NPI 3), however this failed to reach statistical significance (P-values= 0.33 for NPI 1 vs. 2, 0.27for NPI2 vs. 3 and 0.24 for NPI 1 vs. 3). hTERT levels also increased with increasing tumour's grade (mean= 0.0459 for grade 1, 0.111for grade 2, and 0.27 for grade 3) but this trend did not reach a statistical significance.
|
17214359 |
2007 |
Rheumatoid Arthritis
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
We confirmed the validity of our findings by analyzing independent sets of most significant disease-linked SNPs and demonstrating statistically significant KPNA1-gene expression phenotypes associated with human genotypes of CD, BD, T2D and RA populations.
|
18719369 |
2008 |
Crohn Disease
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
We confirmed the validity of our findings by analyzing independent sets of most significant disease-linked SNPs and demonstrating statistically significant KPNA1-gene expression phenotypes associated with human genotypes of CD, BD, T2D and RA populations.
|
18719369 |
2008 |
Diabetes Mellitus, Non-Insulin-Dependent
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
We confirmed the validity of our findings by analyzing independent sets of most significant disease-linked SNPs and demonstrating statistically significant KPNA1-gene expression phenotypes associated with human genotypes of CD, BD, T2D and RA populations.
|
18719369 |
2008 |
Rheumatoid Arthritis
|
0.020 |
GeneticVariation
|
disease |
LHGDN |
SNP-guided microRNA maps (MirMaps) of 16 common human disorders identify a clinically accessible therapy reversing transcriptional aberrations of nuclear import and inflammasome pathways.
|
19001869 |
2008 |
Rheumatoid Arthritis
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
Analysis of expression profiling experiments of peripheral blood mononuclear cells (PBMC) demonstrates statistically significant KPNA1-, NLRP1- and NLRP3-gene expression phenotypes associated with human genotypes of Crohn's disease (CD), Huntington's disease (HD) and rheumatoid arthritis (RA) populations.
|
19001869 |
2008 |
Crohn Disease
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
Analysis of expression profiling experiments of peripheral blood mononuclear cells (PBMC) demonstrates statistically significant KPNA1-, NLRP1- and NLRP3-gene expression phenotypes associated with human genotypes of Crohn's disease (CD), Huntington's disease (HD) and rheumatoid arthritis (RA) populations.
|
19001869 |
2008 |
Crohn Disease
|
0.020 |
GeneticVariation
|
disease |
LHGDN |
Analysis of expression profiling experiments of peripheral blood mononuclear cells (PBMC) demonstrates statistically significant KPNA1-, NLRP1- and NLRP3-gene expression phenotypes associated with human genotypes of Crohn's disease (CD), Huntington's disease (HD) and rheumatoid arthritis (RA) populations.
|
19001869 |
2008 |
Huntington Disease
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Analysis of expression profiling experiments of peripheral blood mononuclear cells (PBMC) demonstrates statistically significant KPNA1-, NLRP1- and NLRP3-gene expression phenotypes associated with human genotypes of Crohn's disease (CD), Huntington's disease (HD) and rheumatoid arthritis (RA) populations.
|
19001869 |
2008 |
Huntington Disease
|
0.010 |
GeneticVariation
|
disease |
LHGDN |
Analysis of expression profiling experiments of peripheral blood mononuclear cells (PBMC) demonstrates statistically significant KPNA1-, NLRP1- and NLRP3-gene expression phenotypes associated with human genotypes of Crohn's disease (CD), Huntington's disease (HD) and rheumatoid arthritis (RA) populations.
|
19001869 |
2008 |
Calcium measurement
|
0.100 |
GeneticVariation
|
phenotype |
GWASDB |
Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels.
|
20705733 |
2010 |
Calcium level result
|
0.100 |
GeneticVariation
|
phenotype |
GWASDB |
Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels.
|
20705733 |
2010 |
Schizophrenia
|
0.300 |
Biomarker
|
disease |
CTD_human |
Increased exonic de novo mutation rate in individuals with schizophrenia.
|
21743468 |
2011 |
Influenza
|
0.010 |
Biomarker
|
disease |
BEFREE |
Although NP binds to importin α isoforms Rch1, Qip1 and NPI-1, the role of each individual isoform during the nuclear transport of NP and replication of the influenza virus remains unknown.
|
23383277 |
2013 |
Hepatitis C
|
0.010 |
Biomarker
|
disease |
BEFREE |
The first group binds IPOA5 and inhibits infection during the replication stage of HCV life cycle.
|
25485706 |
2014 |
Hemorrhagic Fever, Ebola
|
0.010 |
Biomarker
|
disease |
BEFREE |
Combined with this prediction of the microRNA target, we identified importin-α5, which is a key regulator of interferon signaling following Ebola virus infection, as one putative target.
|
27094387 |
2016 |
Leukemia, Myelocytic, Acute
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.
|
27903959 |
2017 |
Low density lipoprotein cholesterol measurement
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels.
|
28334899 |
2017 |
Enterovirus Infections
|
0.010 |
AlteredExpression
|
group |
BEFREE |
Our study demonstrates a novel mechanism by which antiviral signaling is suppressed through degradation of KPNA1 by activated caspase-3 induced in an enteroviral infection.
|
28455446 |
2017 |
Septicemia
|
0.010 |
Biomarker
|
disease |
BEFREE |
We studied the impact of simultaneously targeting two of these shuttles, importin alpha 5 (Imp α5) and importin beta 1 (Imp β1), with a cell-penetrating Nuclear Transport Modifier (NTM) in a mouse model of polymicrobial sepsis.
|
28628637 |
2017 |
Sepsis
|
0.010 |
Biomarker
|
disease |
BEFREE |
We studied the impact of simultaneously targeting two of these shuttles, importin alpha 5 (Imp α5) and importin beta 1 (Imp β1), with a cell-penetrating Nuclear Transport Modifier (NTM) in a mouse model of polymicrobial sepsis.
|
28628637 |
2017 |
Malignant neoplasm of prostate
|
0.010 |
Biomarker
|
disease |
BEFREE |
Using in vitro and in vivo binding assays we identified that HIF-1α interacts with importin-α5 and importin-α7 in prostate cancer cells but only importin-α7 interacts with SEPT9_i1.
|
29742803 |
2019 |
Prostate carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Using in vitro and in vivo binding assays we identified that HIF-1α interacts with importin-α5 and importin-α7 in prostate cancer cells but only importin-α7 interacts with SEPT9_i1.
|
29742803 |
2019 |
mathematical ability
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.
|
30038396 |
2018 |
Low density lipoprotein cholesterol measurement
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program.
|
30275531 |
2018 |