Virus Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
The use of a human cell line expressing a debilitated RIG-I molecule, together with overexpression studies of wild type RIG-I, showed that the IFN-beta induction by virus infection or by leader RNA required RIG-I to be functional.
|
17356690 |
2007 |
Virus Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
RIG-I and MDA5 are cytoplasmic DEX(D/H) helicase proteins that can induce signaling in response to RNA ligands, including those from viral infections.
|
18411269 |
2008 |
Virus Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
IRF-3 depletion was dependent on a productive HIV-1 replication cycle and caused the specific disruption of Toll-like receptor and RIG-I-like receptor innate immune signaling that rendered cells permissive to secondary virus infection.
|
19706707 |
2009 |
Virus Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
TRAF3 appears to undergo sequential ubiquitin "immuno-editing" following virus infection that is crucial for regulation of RIG-I-dependent signaling to the antiviral response.
|
19893624 |
2009 |
Virus Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
Apart from TLRs, other PRRs such as RIG-1 and MDA-5 are also able to recognize viral infection and participate in the activation of type I interferon synthesis.
|
20533094 |
2010 |
Virus Diseases
|
0.100 |
AlteredExpression
|
group |
BEFREE |
RIG-I-like receptors (RLRs) are expressed ubiquitously at low levels, and their expression is induced by treatment with type I interferon (IFN) or a viral infection.
|
20950133 |
2011 |
Virus Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
The relative roles of the endosomal TLR3/7/8 versus the intracellular RNA helicases RIG-I and MDA5 in viral infection is much debated.
|
21079690 |
2010 |
Virus Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
Resolving influenza infection in mammals has been shown to require RIG-I; however, the apparent absence of a RIG-I homolog in chickens raises intriguing questions regarding how this species deals with influenza virus infection.
|
21444763 |
2011 |
Virus Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
The RIG-I-like receptor (RLR) family of pattern recognition receptors (PRRs) is a group of cytosolic RNA helicase proteins that can identify viral RNA as nonself via binding to pathogen associated molecular patter (PAMP) motifs within RNA ligands that accumulate during virus infection.
|
21949557 |
2011 |
Virus Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
Compared with H1N1 virus-induced mediators, H5N1 mediators markedly enhance the cytokine response to PolyIC and to both seasonal and H5N1 virus infection in a RIG-I-dependent manner.
|
22013225 |
2011 |
Virus Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
RIG-I-like receptors and Toll-like receptors (TLRs) play important roles in the recognition of viral infections.
|
22072781 |
2012 |
Virus Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
Goose RIG-I functions in innate immunity against Newcastle disease virus infections.
|
23063767 |
2013 |
Virus Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
RIG-I is a cytoplasmic viral RNA sensor that triggers the signal to induce type I interferon production in response to viral infection.
|
23950712 |
2013 |
Virus Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
RIG-I-like receptors (RLRs: RIG-I, MDA5 and LGP2) play a major role in the innate immune response against viral infections and detect patterns on viral RNA molecules that are typically absent from host RNA.
|
24743923 |
2014 |
Virus Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
This is critical for promoting the growth and survival of T lymphocytes as well as the regulation of the RIG-I helicase pathway for type I interferon production in response to viral infections.
|
24816846 |
2014 |
Virus Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
Virus infection is sensed in the cytoplasm by retinoic acid-inducible gene I (RIG-I, also known as DDX58), which requires RNA and polyubiquitin binding to induce type I interferon (IFN) and activate cellular innate immunity.
|
24931123 |
2014 |
Virus Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
RIG-I-like receptor regulation in virus infection and immunity.
|
25644461 |
2015 |
Virus Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
RIG-I-like receptors detect viral RNA in infected cells and promote oligomerization of the outer mitochondrial membrane protein MAVS to induce innate immunity to viral infection through type I interferon production.
|
26317833 |
2015 |
Virus Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
Two cytosolic RIG-like RNA helicases, RIG-I and MDA5, are key to type I interferon (IFN) induction in response to viral infection.
|
26939124 |
2016 |
Virus Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
Sumoylation of the caspase recruitment domains of MDA5 and RIG-I is also required for their dephosphorylation by PP1 and activation upon viral infection.
|
28250012 |
2017 |
Virus Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
RIG-I Activation Protects and Rescues from Lethal Influenza Virus Infection and Bacterial Superinfection.
|
28760668 |
2017 |
Virus Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
The RNA binding protein La/SS-B promotes RIG-I-mediated type I and type III IFN responses following Sendai viral infection.
|
29109527 |
2017 |
Virus Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
A recent study found that the delivery of circRNAs generated <i>in vitro</i> activates RIG-I-mediated innate immune responses and provides protection against viral infection.
|
29230098 |
2017 |
Virus Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
Defective RNA sensing by RIG-I in severe influenza virus infection.
|
29453856 |
2018 |
Virus Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
We found that intracellular poly(I·C) transfection to mimic viral infection enhances the RIG-I/MDA5 (melanoma differentiation-associated gene 5)-mediated dimerization of interferon regulatory factor 3 (IRF-3).
|
29496994 |
2018 |