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PMID |
Sentence |
1 |
18449425
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We found that DV up-regulates Protease Activated receptor type-1 (inflammation) and TF (coagulation) receptors, via the phosphorylation of p38 and ERK1/2 MAPKs, which favor the activation of NF-kappaB transcription factor.
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2 |
18449425
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This induces pro-inflammatory (IL-8) or pro-adhesive (VCAM-1) gene expression which may lead to EVC activation.
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3 |
24533461
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Low genetic diversity and functional constraint in loci encoding Plasmodium vivax P12 and P38 proteins in the Colombian population.
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4 |
25826372
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MicroRNA-22 impairs anti-tumor ability of dendritic cells by targeting p38.
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5 |
25826372
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In this study, we identified microRNA-22 (miR-22) as a microRNA inhibiting p38 protein expression by directly binding to the 3' untranslated region (3'UTR) of its mRNA.
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6 |
25826372
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The p38 down-regulation further interfered with the synthesis of DC-derived IL-6 and the differentiation of DC-driven Th17 cells.
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7 |
25826372
|
MicroRNA-22 impairs anti-tumor ability of dendritic cells by targeting p38.
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8 |
25826372
|
In this study, we identified microRNA-22 (miR-22) as a microRNA inhibiting p38 protein expression by directly binding to the 3' untranslated region (3'UTR) of its mRNA.
|
9 |
25826372
|
The p38 down-regulation further interfered with the synthesis of DC-derived IL-6 and the differentiation of DC-driven Th17 cells.
|
10 |
25826372
|
MicroRNA-22 impairs anti-tumor ability of dendritic cells by targeting p38.
|
11 |
25826372
|
In this study, we identified microRNA-22 (miR-22) as a microRNA inhibiting p38 protein expression by directly binding to the 3' untranslated region (3'UTR) of its mRNA.
|
12 |
25826372
|
The p38 down-regulation further interfered with the synthesis of DC-derived IL-6 and the differentiation of DC-driven Th17 cells.
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13 |
25879277
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Antigens accumulated to high levels in BdT38 and BdT19 transgenic cell lines co-expressing silencing suppressor protein P38 or P19.
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14 |
16428781
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Rabbit antibodies elicited by the heterologously produced MSP-1 processing products p83, p30, p38, and p42, derived from strain 3D7, were analyzed for the potential to inhibit in vitro erythrocyte invasion by the parasite and parasite growth.
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