This is a table of type trigram and their frequencies. Use it to search & browse the list to learn more about your study carrel.
trigram | frequency |
---|---|
type i ifn | 468 |
type i interferon | 312 |
hepatitis c virus | 308 |
of type i | 280 |
i and mda | 258 |
innate immune response | 236 |
the activation of | 236 |
the innate immune | 218 |
the expression of | 212 |
been shown to | 201 |
as well as | 186 |
influenza a virus | 173 |
the induction of | 150 |
activation of the | 144 |
in response to | 140 |
innate immune responses | 137 |
the production of | 136 |
type i ifns | 133 |
the formation of | 129 |
the type i | 122 |
has been shown | 119 |
the role of | 118 |
respiratory syncytial virus | 117 |
respiratory syndrome coronavirus | 112 |
is essential for | 104 |
is required for | 103 |
of the rig | 103 |
involved in the | 103 |
interferon regulatory factor | 102 |
severe acute respiratory | 101 |
acute respiratory syndrome | 100 |
of the viral | 99 |
of innate immune | 94 |
e ubiquitin ligase | 92 |
i ifn production | 91 |
the presence of | 88 |
in addition to | 85 |
innate immune system | 85 |
tlr and tlr | 85 |
innate immune signaling | 82 |
the absence of | 80 |
ns and ns | 80 |
it has been | 79 |
have been shown | 78 |
the recognition of | 75 |
hek t cells | 74 |
and activation of | 74 |
of the ifn | 71 |
role in the | 69 |
in the cytoplasm | 69 |
was shown to | 69 |
west nile virus | 68 |
herpes simplex virus | 67 |
the interaction between | 67 |
in innate immunity | 66 |
antiviral innate immunity | 66 |
the interaction of | 65 |
of viral rna | 65 |
one of the | 64 |
the inhibition of | 64 |
pattern recognition receptors | 64 |
i ifn response | 64 |
the regulation of | 63 |
structural basis for | 63 |
antiviral innate immune | 63 |
in the cytosol | 63 |
mitochondrial antiviral signaling | 62 |
a variety of | 62 |
in order to | 61 |
production of type | 60 |
in the absence | 60 |
of the innate | 60 |
type i interferons | 60 |
has also been | 58 |
plasmacytoid dendritic cells | 57 |
a role in | 56 |
antiviral signaling protein | 56 |
shown to be | 56 |
cells infected with | 56 |
the level of | 56 |
to the nucleus | 56 |
virus ns protein | 56 |
i ifn signaling | 55 |
a number of | 55 |
induction of type | 55 |
strand rna viruses | 54 |
is involved in | 54 |
immune response to | 54 |
been found to | 53 |
regulation of the | 52 |
east respiratory syndrome | 52 |
middle east respiratory | 52 |
the activity of | 51 |
on the other | 51 |
in mammalian cells | 51 |
of hepatitis c | 51 |
i interferon production | 51 |
in the regulation | 51 |
leading to the | 51 |
porcine epidemic diarrhea | 51 |
ubiquitination of rig | 50 |
the importance of | 50 |
is associated with | 50 |
type i and | 49 |
the effect of | 49 |
in the nucleus | 49 |
innate antiviral response | 49 |
of the type | 48 |
antiviral response by | 48 |
found to be | 48 |
crystal structure of | 48 |
activation of nf | 48 |
kato et al | 48 |
in infected cells | 48 |
a virus ns | 47 |
the other hand | 47 |
induction of ifn | 47 |
members of the | 47 |
the development of | 47 |
resulting in the | 46 |
the cells were | 46 |
has been reported | 46 |
japanese encephalitis virus | 46 |
by hepatitis c | 46 |
in this review | 46 |
word w j | 46 |
epidemic diarrhea virus | 46 |
to interact with | 46 |
the ability of | 45 |
during viral infection | 45 |
of interferon regulatory | 45 |
is mediated by | 45 |
cd t cells | 45 |
such as the | 45 |
been reported to | 45 |
inducible gene i | 44 |
have also been | 44 |
an important role | 44 |
like receptors and | 44 |
stress granule formation | 44 |
host innate immune | 44 |
in contrast to | 43 |
the immune response | 43 |
is critical for | 43 |
tumor necrosis factor | 43 |
of the interferon | 43 |
structure of the | 43 |
member of the | 42 |
interacts with the | 42 |
is able to | 42 |
activation of rig | 42 |
also known as | 42 |
negative regulation of | 42 |
of the host | 42 |
are involved in | 42 |
activation of irf | 41 |
expression of the | 41 |
essential for rig | 41 |
results in the | 41 |
the number of | 41 |
by the innate | 41 |
recognition by the | 41 |
production of ifn | 41 |
acts as a | 40 |
innate and adaptive | 40 |
i ifn induction | 40 |
leads to the | 40 |
which in turn | 40 |
responsible for the | 40 |
the function of | 40 |
of influenza a | 40 |
of rna viruses | 40 |
the release of | 39 |
innate antiviral responses | 39 |
binds to the | 39 |
like receptor signaling | 39 |
of nucleic acid | 39 |
rna polymerase iii | 39 |
the rna helicase | 39 |
in the recognition | 38 |
important role in | 38 |
i interferon signaling | 38 |
interaction with the | 38 |
the meaning of | 38 |
associated molecular patterns | 38 |
the viral rna | 38 |
viral nucleic acids | 38 |
the ns protein | 38 |
have been identified | 38 |
i and iii | 38 |
the ubiquitin ligase | 38 |
in the activation | 37 |
viral replication and | 37 |
in the context | 37 |
to viral infection | 37 |
recognition of viral | 37 |
and characterization of | 37 |
activated protein kinase | 37 |
the context of | 37 |
mediated type i | 37 |
were transfected with | 37 |
rna recognition by | 37 |
category c k | 37 |
the phosphorylation of | 37 |
nucleic acid immunity | 36 |
the immune system | 36 |
mda and rig | 36 |
the recruitment of | 36 |
irf and irf | 36 |
c virus infection | 36 |
of irf and | 36 |
of innate immunity | 35 |
protein kinase pkr | 35 |
inhibits type i | 35 |
in the presence | 35 |
is responsible for | 35 |
the word w | 35 |
of the virus | 35 |
recognition of rna | 35 |
interferon production by | 35 |
the transcription of | 35 |
mediated antiviral responses | 35 |
role of the | 35 |
dependent on the | 35 |
the n protein | 35 |
the adaptor protein | 35 |
to type i | 34 |
in innate immune | 34 |
the ubiquitination of | 34 |
the category c | 34 |
of mda and | 34 |
of the rna | 34 |
the most informative | 34 |
was found to | 34 |
in the rig | 34 |
rna sensor rig | 34 |
innate immune sensor | 33 |
binding to the | 33 |
hornung et al | 33 |
of viral replication | 33 |
in type i | 33 |
vesicular stomatitis virus | 33 |
antiviral immune responses | 33 |
protein kinase r | 33 |
the binding of | 33 |
i interferon induction | 33 |
the ability to | 33 |
the replication of | 33 |
inhibition of the | 33 |
have shown that | 33 |
the use of | 33 |
are required for | 32 |
wang et al | 32 |
in cells infected | 32 |
associated with the | 32 |
well as the | 32 |
functions as a | 32 |
of the immune | 32 |
is activated by | 32 |
mhc class i | 32 |
due to the | 32 |
and degradation of | 32 |
were infected with | 32 |
play a role | 32 |
t cells were | 32 |
by the host | 32 |
is targeted by | 32 |
stranded rna and | 32 |
dexd h box | 32 |
of the antiviral | 32 |
influenza virus infection | 32 |
in this study | 32 |
ubiquitin ligase trim | 31 |
expression of type | 31 |
activation of ifn | 31 |
of viral infection | 31 |
negative regulator of | 31 |
by interacting with | 31 |
analysis of the | 31 |
into the nucleus | 31 |
ebola virus vp | 31 |
be activated by | 31 |
the degradation of | 31 |
is dependent on | 31 |
ifn production in | 31 |
words in the | 30 |
the cell surface | 30 |
reproductive and respiratory | 30 |
have been reported | 30 |
in antiviral innate | 30 |
rlr signaling pathway | 30 |
in the host | 30 |
immune responses to | 30 |
of innate antiviral | 30 |
ifn induction by | 30 |
nuclear translocation of | 30 |
linked polyubiquitination of | 30 |
the case of | 30 |
emcv and jev | 30 |
porcine reproductive and | 30 |
in the induction | 30 |
innate immune evasion | 30 |
activity of the | 30 |
the innate antiviral | 30 |
the ifn system | 30 |
identification and characterization | 29 |
viral rna sensor | 29 |
the e ubiquitin | 29 |
mediated antiviral signaling | 29 |
also been shown | 29 |
antiviral signaling by | 29 |
human immunodeficiency virus | 29 |
rna virus infection | 29 |
it is possible | 29 |
recognized by rig | 29 |
the viral genome | 29 |
the control of | 29 |
essential for the | 29 |
and respiratory syndrome | 29 |
most informative words | 28 |
the generation of | 28 |
mediated by the | 28 |
an essential function | 28 |
c virus ns | 28 |
immune response in | 28 |
immune responses in | 28 |
to inhibit the | 28 |
recognition by rig | 28 |
has not been | 28 |
degradation of the | 28 |
traf and traf | 28 |
the host innate | 28 |
based on the | 28 |
linked ubiquitination of | 28 |
components of the | 28 |
a member of | 28 |
a negative regulator | 28 |
in the case | 28 |
the ifn response | 28 |
the suppression of | 28 |
ifn production and | 27 |
the identification of | 27 |
innate immunity by | 27 |
a type i | 27 |
required for the | 27 |
i signaling by | 27 |
induced activation of | 27 |
been shown that | 27 |
respiratory syndrome virus | 27 |
appears to be | 27 |
cells were transfected | 27 |
of a word | 27 |
is possible that | 27 |
to induce ifn | 27 |
in hek t | 27 |
in the innate | 27 |
part of the | 27 |
mediated activation of | 27 |
innate immunity and | 27 |
c virus rna | 27 |
mda and lgp | 27 |
remains to be | 27 |
we found that | 27 |
addition to the | 27 |
and innate immunity | 27 |
structural basis of | 27 |
the host immune | 27 |
inhibition of rig | 27 |
to induce the | 26 |
yoneyama et al | 26 |
a critical role | 26 |
response to viral | 26 |
virus nonstructural protein | 26 |
function of the | 26 |
type lectin receptors | 26 |
immune response by | 26 |
basis for the | 26 |
of ns and | 26 |
the helicase domain | 26 |
to bind to | 26 |
some of the | 26 |
of the most | 26 |
newcastle disease virus | 26 |
required for virus | 26 |
the fact that | 26 |
hepatitis b virus | 26 |
interact with the | 26 |
be involved in | 26 |
dna and rna | 26 |
by rna viruses | 26 |
the severe acute | 26 |
has been demonstrated | 25 |
the nucleus and | 25 |
the detection of | 25 |
understanding of the | 25 |
suggesting that the | 25 |
to be a | 25 |
to the activation | 25 |
ligand for rig | 25 |
cov and mers | 25 |
the association of | 25 |
component of the | 25 |
a recent study | 25 |
of viral proteins | 25 |
is important for | 25 |
proteins have been | 25 |
infected with the | 25 |
insights into the | 25 |
viruses such as | 25 |
the host cell | 25 |
essential function in | 25 |
single nucleotide polymorphisms | 25 |
indicating that the | 25 |
regulation of rig | 25 |
its interaction with | 25 |
as shown in | 25 |
our understanding of | 24 |
has an essential | 24 |
t cells and | 24 |
mediated antiviral activity | 24 |
as a result | 24 |
krug et al | 24 |
an antiviral state | 24 |
activation of innate | 24 |
the antiviral response | 24 |
the synthesis of | 24 |
of stress granules | 24 |
induced innate antiviral | 24 |
binding of the | 24 |
to the category | 24 |
antiviral immune response | 24 |
human respiratory syncytial | 24 |
i has an | 24 |
by the viral | 24 |
expression of ifn | 24 |
for scientific texts | 24 |
activator of transcription | 24 |
interferon antiviral response | 24 |
rna helicase rig | 24 |
i ifn responses | 24 |
with the indicated | 24 |
for the activation | 24 |
the accumulation of | 24 |
the lack of | 24 |
regulation of innate | 24 |
spry domain of | 24 |
belongs to the | 24 |
and function of | 24 |
by binding to | 24 |
a series of | 24 |
allele of rs | 24 |
li et al | 24 |
signal transducer and | 24 |
is a novel | 24 |
host innate immunity | 24 |
methylation of the | 23 |
end of the | 23 |
functions of the | 23 |
its ability to | 23 |
seems to be | 23 |
irf and nf | 23 |
transducer and activator | 23 |
pichlmair et al | 23 |
identified as a | 23 |
are responsible for | 23 |
according to the | 23 |
the meaning space | 23 |
the influenza a | 23 |
of influenza virus | 23 |
have been described | 23 |
antiviral responses to | 23 |
in patients with | 23 |
virus infection and | 23 |
of the signaling | 23 |
and activator of | 23 |
is one of | 23 |
response by targeting | 23 |
protein in the | 23 |
virus replication and | 23 |
stat and stat | 23 |
domain of trim | 23 |
showed that the | 22 |
laboratory of genetics | 22 |
by retinoic acid | 22 |
the mechanism of | 22 |
the nucleus to | 22 |
linked polyubiquitin chains | 22 |
the pathogenesis of | 22 |
an adaptor protein | 22 |
been identified as | 22 |
has been found | 22 |
to be the | 22 |
formation of the | 22 |
in vitro and | 22 |
viral rna replication | 22 |
of the first | 22 |
dependent innate immune | 22 |
antiviral activity of | 22 |
svv c pro | 22 |
it is also | 22 |
can be found | 22 |
strand rna virus | 22 |
repressor domain in | 22 |
i ifns and | 22 |
saito et al | 22 |
of genetics and | 22 |
genetics and physiology | 22 |
viral rna species | 22 |
cytokines and chemokines | 22 |
the majority of | 22 |
rna in the | 22 |
are associated with | 22 |
the crystal structure | 22 |
induce type i | 22 |
present in the | 22 |
are recognized by | 22 |
is an essential | 22 |
by interfering with | 22 |
as a negative | 22 |
the involvement of | 21 |
adaptive immune response | 21 |
and the activation | 21 |
interferon signaling by | 21 |
by type i | 21 |
mediated inhibition of | 21 |
can also be | 21 |
is important to | 21 |
translation initiation factor | 21 |
the loss of | 21 |
ubiquitin ligase is | 21 |
has been identified | 21 |
and mda signaling | 21 |
innate immune receptor | 21 |
regulator of rig | 21 |
k and k | 21 |
ifn production by | 21 |
mouth disease virus | 21 |
induces type i | 21 |
ligase is essential | 21 |
critical role in | 21 |
i interferon response | 21 |
be found in | 21 |
a positive regulator | 21 |
and nuclear translocation | 21 |
helicases in the | 21 |
space of meaning | 21 |
i ifn and | 21 |
and innate immune | 21 |
its role in | 21 |
in the ifn | 21 |
sensing of viral | 21 |
ifn regulatory factor | 21 |
but not in | 21 |
viruses have evolved | 21 |
of the ubiquitin | 21 |
the e ligase | 21 |
is crucial for | 21 |
differential roles of | 21 |
interaction between rig | 21 |
to note that | 21 |
mediated innate immune | 21 |
are essential for | 21 |
upon binding to | 20 |
plays a role | 20 |
in the antiviral | 20 |
of tlr and | 20 |
immune signaling by | 20 |
of words in | 20 |
mediated degradation of | 20 |
type iii ifn | 20 |
vitro and in | 20 |
for innate immune | 20 |
these results indicate | 20 |
the nlrp inflammasome | 20 |
self and non | 20 |
increase in the | 20 |
roles of mda | 20 |
i helicases in | 20 |
ring finger protein | 20 |
category rig matrix | 20 |
and is targeted | 20 |
bat cell lines | 20 |
ns protein of | 20 |
contribute to the | 20 |
oshiumi et al | 20 |
the cytosol of | 20 |
mediated recognition of | 20 |
which leads to | 20 |
was identified as | 20 |
structural and functional | 20 |
in which the | 20 |
activation and recruitment | 20 |
studies suggest that | 20 |
cells were lysed | 20 |
their ability to | 20 |
the ligand for | 20 |
the transcription factors | 20 |
positive regulator of | 20 |
to virus infection | 20 |
essential role of | 20 |
type iii ifns | 20 |
induced by rig | 20 |
of rnase l | 20 |
expression levels of | 20 |
the card domain | 20 |
located in the | 20 |
to play a | 20 |
by viral rna | 20 |
critical for the | 20 |
the endoplasmic reticulum | 20 |
the interferon antiviral | 20 |
interfere with the | 20 |
signaling pathway in | 20 |
of protein synthesis | 19 |
polyubiquitination of the | 19 |
immune sensing of | 19 |
of proinflammatory cytokines | 19 |
is necessary for | 19 |
recognition of double | 19 |
in the production | 19 |
adaptive immune responses | 19 |
viral infection and | 19 |
at the end | 19 |
is the ligand | 19 |
to be involved | 19 |
regulation of interferon | 19 |
alpha beta interferon | 19 |
the levels of | 19 |
and in vivo | 19 |
by the proteasome | 19 |
of viral nucleic | 19 |
induced type i | 19 |
virus ns targets | 19 |
antiviral responses by | 19 |
degradation of irf | 19 |
leads to a | 19 |
of the transcription | 19 |
host antiviral response | 19 |
in plasmacytoid dendritic | 19 |
signaling by the | 19 |
rna is the | 19 |
h box rna | 19 |
of tlr in | 19 |
of the trim | 19 |
triphosphate rna is | 19 |
the host antiviral | 19 |
of meaning for | 19 |
viral nucleic acid | 19 |
proteasomal degradation of | 19 |
the possibility that | 19 |
function in double | 19 |
known to be | 19 |
to the cytoplasm | 19 |
virus vp protein | 19 |
play an important | 19 |
targeted by hepatitis | 19 |
cells were infected | 19 |
the dexd h | 19 |
are able to | 19 |
mechanisms by which | 19 |
studies have shown | 19 |
of the rlr | 19 |
domain of the | 19 |
effect of ns | 19 |
the end of | 19 |
with or without | 19 |
i or mda | 19 |
distinction of self | 19 |
caspase activation and | 19 |
related to the | 19 |
innate antiviral immunity | 19 |
domain of rig | 19 |
inhibition of ifn | 19 |
and adaptive immunity | 19 |
yoneyama and fujita | 19 |
and type i | 19 |
by targeting rig | 19 |
cells transfected with | 18 |
phosphorylation of irf | 18 |
evade recognition by | 18 |
the ns a | 18 |
been demonstrated to | 18 |
protein that activates | 18 |
act as a | 18 |
a mitochondrial antiviral | 18 |
most of the | 18 |
activation of pkr | 18 |
acting as a | 18 |
characterization of mavs | 18 |
lead to the | 18 |
been reported that | 18 |
in the text | 18 |
rna recognition and | 18 |
phosphorylation of the | 18 |
of traf and | 18 |
meaning of a | 18 |
for the development | 18 |
has been described | 18 |
the influenza virus | 18 |
results showed that | 18 |
line of defense | 18 |
c virus replication | 18 |
activation of type | 18 |
been implicated in | 18 |
in a cells | 18 |
cellular antiviral response | 18 |
negatively regulates the | 18 |
stranded rna bearing | 18 |
antiviral signal activation | 18 |
of ube l | 18 |
schlee et al | 18 |
responses to single | 18 |
signaling protein that | 18 |
degradation by the | 18 |
host immune response | 18 |
for viral replication | 18 |
a novel mechanism | 18 |
on the cell | 18 |
o methylation of | 18 |
need to be | 18 |
irie et al | 18 |
a role for | 18 |
rna viruses in | 18 |
to evade recognition | 18 |
is a negative | 18 |
innate immunity the | 18 |
of the n | 18 |
activation of interferon | 18 |
to activate rig | 18 |
of rlr signaling | 18 |
it is important | 18 |
results indicate that | 18 |
that activates nf | 18 |
mechanism by which | 18 |
in the formation | 18 |
recognition of single | 18 |
different types of | 18 |
antiviral response through | 18 |
cells were seeded | 18 |
is an adaptor | 18 |
of isg and | 18 |
plays an important | 18 |
by western blotting | 18 |
cell lysates were | 18 |
e ligase activity | 18 |
for the induction | 18 |
virus ns a | 18 |
the rna sensor | 17 |
meaning for scientific | 17 |
first line of | 17 |
molecular mechanism of | 17 |
of cytokine signaling | 17 |
inhibition of interferon | 17 |
the course of | 17 |
mediated cleavage of | 17 |
h n virus | 17 |
cd t cell | 17 |
the spry domain | 17 |
the inhibitory effect | 17 |
the distinction of | 17 |
of the human | 17 |
of the nf | 17 |
of protein kinase | 17 |
data suggest that | 17 |
of the two | 17 |
kappab and irf | 17 |
informational space of | 17 |
signal activation by | 17 |
implicated in the | 17 |
of beta interferon | 17 |
infected with iav | 17 |
and melanoma differentiation | 17 |
belong to the | 17 |
the cleavage of | 17 |
cellular and viral | 17 |
in t cells | 17 |
conflict of interest | 17 |
the authors declare | 17 |
ubiquitination and degradation | 17 |
the cytoplasm of | 17 |
to interfere with | 17 |
the interferon response | 17 |
a family of | 17 |
as described above | 17 |
to the c | 17 |
i and lgp | 17 |
box rna helicase | 17 |
structural insights into | 17 |
mediated induction of | 17 |
virus replication by | 17 |
immune response and | 17 |
the structure of | 17 |
proteins involved in | 17 |
consistent with the | 17 |
the assembly of | 17 |
rna viruses to | 17 |
foreign nucleic acids | 17 |
and iii ifns | 17 |
the hepatitis c | 17 |
to determine the | 17 |
pathway and is | 17 |
of transcription factors | 17 |
in the c | 17 |
semliki forest virus | 17 |
rna viruses and | 17 |
is induced by | 17 |
an essential role | 17 |
are known to | 17 |
ligase trim to | 17 |
inhibitory effect of | 17 |
the roles of | 17 |
and dendritic cells | 17 |
in vitro transcription | 17 |
the antiviral activity | 17 |
found that the | 17 |
i like receptors | 17 |
it is not | 17 |
by blocking the | 16 |
by innate immune | 16 |
unanchored polyubiquitin chains | 16 |
an adaptor triggering | 16 |
the discovery of | 16 |
polymorphisms of genes | 16 |
and the host | 16 |
viral mrna cap | 16 |
upon viral infection | 16 |
an innate immune | 16 |
and adaptive immune | 16 |
immune receptor rig | 16 |
has been proposed | 16 |
immune signaling pathways | 16 |
similar to the | 16 |
important roles in | 16 |
replication and spread | 16 |
i activation by | 16 |
will be discussed | 16 |
the viral mrna | 16 |
the card domains | 16 |
of the cellular | 16 |
in line with | 16 |
cardif is an | 16 |
of ifn production | 16 |
viral and cellular | 16 |
results in a | 16 |
in the cell | 16 |
found in the | 16 |
induction of an | 16 |
mouse hepatitis virus | 16 |
of the irf | 16 |
contributes to the | 16 |
in a dose | 16 |
induced by the | 16 |
antiviral pathway and | 16 |
of a novel | 16 |
in the pathogenesis | 16 |
also involved in | 16 |
at h p | 16 |
rna helicase lgp | 16 |
the host viral | 16 |
trim to evade | 16 |
the transcription factor | 16 |
of trim in | 16 |
i interferon and | 16 |
appear to be | 16 |
isg and its | 16 |
to suppress the | 16 |
in the immune | 16 |
recruitment of the | 16 |
also been found | 16 |
of genes encoding | 16 |
adaptor protein in | 16 |
early phase of | 16 |
thought to be | 16 |
acid inducible gene | 16 |
serves as a | 16 |
phosphorylation of stat | 16 |
innate immune recognition | 16 |
immune response against | 16 |
suppression of rig | 16 |
i antiviral pathway | 16 |
the signaling cascade | 16 |
targets the ubiquitin | 16 |
of retinoic acid | 16 |
ns targets the | 16 |
adaptor triggering rig | 16 |
the rna sensors | 16 |
is also a | 16 |
of the word | 16 |
of trims in | 16 |
in the human | 16 |
suppressor of cytokine | 16 |
host viral rna | 16 |
expression level of | 16 |
to negatively regulate | 16 |
in vitro transcribed | 16 |
characterization of the | 16 |
of the toll | 16 |
of the cards | 16 |
feedback regulation of | 16 |
is the first | 16 |
bind to the | 16 |
proteins that are | 16 |
recognized by the | 16 |
were found to | 16 |
in viral replication | 16 |
modulation of the | 16 |
influenza b virus | 16 |
pathogen recognition and | 16 |
encoded by the | 16 |
versus the iav | 16 |
terminal domain of | 15 |
of nucleic acids | 15 |
of positive selection | 15 |
and a c | 15 |
led to the | 15 |
expression of rig | 15 |
mavs signaling pathway | 15 |
it is likely | 15 |
associated with a | 15 |
has recently been | 15 |
of porcine epidemic | 15 |
activity of trim | 15 |
ubiquitin ligase rnf | 15 |
suggests that the | 15 |
is recognized by | 15 |
the downstream signaling | 15 |
be explained by | 15 |
induction by the | 15 |
antiviral immunity in | 15 |
regulation of antiviral | 15 |
finger e ubiquitin | 15 |
eukaryotic translation initiation | 15 |
not required for | 15 |
tbk and ikk | 15 |
lu et al | 15 |
shown that the | 15 |
formation of a | 15 |
words in categories | 15 |
as described previously | 15 |
innate immune sensors | 15 |
downstream of the | 15 |
is the most | 15 |
an e ubiquitin | 15 |
replication and transcription | 15 |
and or ns | 15 |
as found in | 15 |
is an important | 15 |
viral replication by | 15 |
depending on the | 15 |
myeloid dendritic cells | 15 |
the response to | 15 |
and dna viruses | 15 |
the site of | 15 |
chronic hepatitis c | 15 |
informative words in | 15 |
structure and function | 15 |
the mitochondrial membrane | 15 |
reviewed in ref | 15 |
by the ubiquitin | 15 |
to activate the | 15 |
viral genomic rna | 15 |
of gene expression | 15 |
for activation of | 15 |
assembly of the | 15 |
activation of tbk | 15 |
and inhibition of | 15 |
the protein kinase | 15 |
mediated signaling by | 15 |
shown to inhibit | 15 |
response to infection | 15 |
virus rna replication | 15 |
ablasser et al | 15 |
sitosterol on the | 15 |
as an antiviral | 15 |
stranded rna viruses | 15 |
of isg in | 15 |
of viral dsrna | 15 |
a conformational change | 15 |
was reported to | 15 |
to that of | 15 |
innate antiviral immune | 15 |
as a novel | 15 |
and tlr are | 15 |
recognition receptors and | 15 |
translocate to the | 15 |
due to its | 15 |
i and mavs | 15 |
and cell death | 15 |
a virus infection | 15 |
effector functions of | 15 |
in the past | 15 |
the phosphorylation and | 15 |
yet to be | 15 |
interaction of the | 15 |
expression of isgs | 15 |
be responsible for | 15 |
viral rna to | 15 |
is represented by | 15 |
can be activated | 15 |
the evolution of | 15 |
is independent of | 15 |
induce the expression | 15 |
of the influenza | 15 |
an immune response | 15 |
the observation that | 15 |
stranded rna in | 15 |
kim et al | 15 |
dependent recognition of | 15 |
gack et al | 15 |
roles in the | 15 |
immune responses and | 15 |
of severe acute | 15 |
is regulated by | 15 |
of the text | 15 |
shown to bind | 15 |
of the protein | 15 |
identified as an | 15 |
and recruitment domains | 15 |
dependent protein kinase | 15 |
which is a | 15 |
recognition receptors in | 15 |
to determine whether | 15 |
innate immune pattern | 15 |
antiviral defenses through | 15 |
a word is | 15 |
a vector of | 14 |
to rna virus | 14 |
signaling role of | 14 |
function as a | 14 |
host and viral | 14 |
of the ctd | 14 |
rna and dna | 14 |
interaction between trim | 14 |
cytosolic dna and | 14 |
and the c | 14 |
the sensing of | 14 |
the word in | 14 |
to induce type | 14 |
and stress granule | 14 |
nucleic acid sensors | 14 |
iav control group | 14 |
which can be | 14 |
stranded rna as | 14 |
for each word | 14 |
can act as | 14 |
production and signaling | 14 |
or infected with | 14 |
to activate ifn | 14 |
functions as an | 14 |
not yet been | 14 |
beta interferon production | 14 |
by the ns | 14 |
during virus infection | 14 |
in this section | 14 |
rna sensor mda | 14 |
trim interacts with | 14 |
text belongs to | 14 |
or absence of | 14 |
interaction with mavs | 14 |
human dendritic cells | 14 |
activation of stat | 14 |
dependent innate immunity | 14 |
were treated with | 14 |
ubiquitination of the | 14 |
identified as the | 14 |
the adaptive immune | 14 |
of cytosolic dna | 14 |
production induced by | 14 |
binding oligomerization domain | 14 |
results suggest that | 14 |
positive and negative | 14 |
recognition of the | 14 |
is a positive | 14 |
but not the | 14 |
inflammatory cytokines and | 14 |
absence of the | 14 |
takahasi et al | 14 |
a cells were | 14 |
of the mammalian | 14 |
to inhibit ifn | 14 |
resulting in a | 14 |
retinoic acid inducible | 14 |
syncytial virus nonstructural | 14 |
by the influenza | 14 |
there is no | 14 |
to the production | 14 |
supported by the | 14 |
are capable of | 14 |
of an antiviral | 14 |
rna sensors rig | 14 |
a set of | 14 |
demonstrated that the | 14 |
and proinflammatory cytokines | 14 |
is sufficient to | 14 |
are targeted by | 14 |
ectopic expression of | 14 |
between trim and | 14 |
the viral replication | 14 |
a ring finger | 14 |
cys and his | 14 |
of the ns | 14 |
shown to play | 14 |
are important for | 14 |
by viruses to | 14 |
of the cell | 14 |
ns and or | 14 |
the amount of | 14 |
to activate and | 14 |
gitlin et al | 14 |
followed by the | 14 |
more susceptible to | 14 |
i interferon pathway | 14 |
tbk and irf | 14 |
is inhibited by | 14 |
of the three | 14 |
the early phase | 14 |
in human cells | 14 |
and it is | 14 |
finger antiviral protein | 14 |
can be used | 14 |
h n influenza | 14 |
an increase in | 14 |
region of the | 14 |
and laboratory of | 14 |
an overview of | 14 |
of self and | 14 |
ifit and ifit | 14 |
yang et al | 14 |
to evade innate | 14 |
to be determined | 14 |
innate antiviral defenses | 14 |
in complex with | 14 |
were shown to | 14 |
supplementary figure s | 14 |
explained by the | 14 |
on the rna | 14 |
protein interacts with | 14 |
protein has been | 14 |
dependent rna polymerase | 14 |
helicase domain and | 14 |
induction of isg | 14 |
it was shown | 14 |
the first line | 14 |
regulatory factor activation | 14 |
interfering with trim | 14 |
regulator of the | 14 |
like receptor and | 14 |
of hundreds of | 14 |
shown to induce | 14 |
in dendritic cells | 14 |
diebold et al | 14 |
binding to dsrna | 14 |
unfolded protein response | 14 |
expression of trim | 14 |
suggest that the | 14 |
ifn response in | 14 |
critical role of | 14 |
expression of ns | 14 |
is capable of | 13 |
involvement of rig | 13 |
the rlr pathway | 13 |
crucial role in | 13 |
rna as contained | 13 |
is a key | 13 |
role of tlr | 13 |
the ifn signaling | 13 |
presence or absence | 13 |
these data suggest | 13 |
of cd t | 13 |
in the word | 13 |
and regulation of | 13 |
interaction between the | 13 |
requires short blunt | 13 |
specific recognition of | 13 |
influenza a viruses | 13 |
defenses through a | 13 |
of defense against | 13 |
proteins in the | 13 |
protein is a | 13 |
in a cell | 13 |
and activates the | 13 |
to the n | 13 |
these results suggest | 13 |
in each category | 13 |
activation in the | 13 |
a shared repressor | 13 |
domain in rig | 13 |
the ns proteins | 13 |
interferon induction and | 13 |
localized in the | 13 |
innate immune signalling | 13 |
simplex virus type | 13 |
triphosphate by rig | 13 |
new insights into | 13 |
to suppress rig | 13 |
into the cytoplasm | 13 |
of the adaptor | 13 |
rnase l in | 13 |
may also be | 13 |
be due to | 13 |
and viral rna | 13 |
word in the | 13 |
i and melanoma | 13 |
is supported by | 13 |
to antagonize ifn | 13 |
interacting with the | 13 |
seneca valley virus | 13 |
the contribution of | 13 |
virus c protein | 13 |
as a viral | 13 |
linked to the | 13 |
reported to be | 13 |
innate immune receptors | 13 |
and type iii | 13 |
i ubiquitination and | 13 |
of sendai virus | 13 |
were seeded in | 13 |
induction of the | 13 |
and mda are | 13 |
s j and | 13 |
is expressed in | 13 |
trim in the | 13 |
cytosolic dna sensor | 13 |
ifit family members | 13 |
used by viruses | 13 |
and in the | 13 |
is known to | 13 |
as a strategy | 13 |
host gene expression | 13 |
level of isg | 13 |
for type i | 13 |
induces the expression | 13 |
the impact of | 13 |
important for the | 13 |
of rna recognition | 13 |
the expression levels | 13 |
dependent activation of | 13 |
of pattern recognition | 13 |
ubiquitin e ligase | 13 |
serve as a | 13 |
c k w | 13 |
that can be | 13 |
of antiviral innate | 13 |
study showed that | 13 |
arms race between | 13 |
viral rna by | 13 |
identification of the | 13 |
observed in the | 13 |
genes in the | 13 |
contained in panhandle | 13 |
during viral replication | 13 |
i ifn in | 13 |
activated by the | 13 |
of virus replication | 13 |
and cellular antiviral | 13 |
shared repressor domain | 13 |
during the early | 13 |
interferon regulatory factors | 13 |
as contained in | 13 |
i helicase requires | 13 |
with tetratricopeptide repeats | 13 |
through a shared | 13 |
with the card | 13 |
has been recently | 13 |
the stability of | 13 |
at the level | 13 |
panhandle of negative | 13 |
hemmi et al | 13 |
molecular mechanisms of | 13 |
translocation of irf | 13 |
c protease cleaves | 13 |
activation of antiviral | 13 |
interacts with rig | 13 |
viruses have been | 13 |
evade innate immunity | 13 |
helicase requires short | 13 |
a and b | 13 |
were incubated with | 13 |
virus kato et | 13 |
a crucial role | 13 |
lgp is a | 13 |
at the n | 13 |
ifn responses to | 13 |
of the dexd | 13 |
been identified in | 13 |
a decrease in | 13 |
but not rig | 13 |
are activated by | 13 |
i is the | 13 |
have not been | 13 |
overview of the | 13 |
for the distinction | 13 |
for inhibition of | 13 |
can bind to | 13 |
was supported by | 13 |
polyubiquitin chains in | 13 |
to counteract the | 13 |
signaling pathway by | 13 |
translation of viral | 13 |
viral rna and | 13 |
was the first | 13 |
in terms of | 13 |
and lgp in | 13 |
induction of interferon | 13 |
yellow fever virus | 13 |
innate immune sensing | 13 |
reactive oxygen species | 13 |
viral rna recognition | 13 |
of an rna | 13 |
activation of mda | 13 |
production in response | 13 |
direct interaction of | 13 |
in panhandle of | 13 |
syndrome coronavirus papain | 12 |
have demonstrated that | 12 |
i by viral | 12 |
wide range of | 12 |
transcription factors irf | 12 |
a wide range | 12 |
of isg conjugates | 12 |
evasion of the | 12 |
and induces type | 12 |
inhibition of translation | 12 |
of patients with | 12 |
is likely that | 12 |
in host defense | 12 |
rigs in categories | 12 |
lectin receptors and | 12 |
shown to interact | 12 |
in the expression | 12 |
findings suggest that | 12 |
to form the | 12 |
of these viruses | 12 |
and the monolayer | 12 |
to the host | 12 |
oas rnase l | 12 |
infected with drv | 12 |
model of rig | 12 |
by influenza virus | 12 |
that ns and | 12 |
pedv n protein | 12 |
in this case | 12 |
in myeloid dendritic | 12 |
coronavirus nonstructural protein | 12 |
the existence of | 12 |
dependent signaling pathway | 12 |
visa is an | 12 |
trim negatively regulates | 12 |
adapter protein required | 12 |
necrosis factor receptor | 12 |
an rsv infection | 12 |
unique functions of | 12 |
which has been | 12 |
ns a and | 12 |
the antiviral immune | 12 |
monolayer cells were | 12 |
consistent with this | 12 |
detection by rig | 12 |
antiviral signal transduction | 12 |
receptors and rig | 12 |
shared and unique | 12 |
that binds to | 12 |
by ifit family | 12 |
is thought to | 12 |
as previously described | 12 |
mda and mavs | 12 |
myeloid differentiation primary | 12 |
the translation of | 12 |
it was found | 12 |
be essential for | 12 |
dna in the | 12 |
viral replication in | 12 |
by the e | 12 |
the mechanisms by | 12 |
and rna viruses | 12 |
directly interacts with | 12 |
to form a | 12 |
mediated antiviral response | 12 |
rna with a | 12 |
different cell types | 12 |
domains of rig | 12 |
i activation and | 12 |
is that the | 12 |
ns a protease | 12 |
and the viral | 12 |
only in the | 12 |
an inhibitor of | 12 |
and his residues | 12 |
gao et al | 12 |
levels of ifn | 12 |
role of unanchored | 12 |
the functions of | 12 |
gene expression by | 12 |
n protein inhibits | 12 |
chen et al | 12 |
trim is a | 12 |
revealed that the | 12 |
eif a phosphorylation | 12 |
rna virus replication | 12 |
jak stat pathway | 12 |
of infected cells | 12 |
k w j | 12 |
in activation of | 12 |
receptors and their | 12 |
of herpes simplex | 12 |
the present study | 12 |
heil et al | 12 |
cells in the | 12 |
in influenza virus | 12 |
inhibition of hiv | 12 |
of antiviral immune | 12 |
stimulator of interferon | 12 |
an adapter protein | 12 |
as part of | 12 |
and unique functions | 12 |
production and antiviral | 12 |
of viral infections | 12 |
i and type | 12 |
bound to the | 12 |
cells treated with | 12 |
sars coronavirus papain | 12 |
lgp in antiviral | 12 |
are present in | 12 |
in hepatitis c | 12 |
the mitochondrial antiviral | 12 |
kawai et al | 12 |
as a potential | 12 |
plays a critical | 12 |
is a major | 12 |
mechanism of trim | 12 |
isg e ligase | 12 |
pathway reveals a | 12 |
ubiquitination of traf | 12 |
be discussed in | 12 |
the interferon regulatory | 12 |
small interfering rna | 12 |
intestinal epithelial cells | 12 |
cleavage of the | 12 |
and inflammatory cytokines | 12 |
immune evasion strategies | 12 |
recent studies have | 12 |
tlr is expressed | 12 |
protein of influenza | 12 |
of cellular mrnas | 12 |
the infected cells | 12 |
contribution of the | 12 |
natural killer cells | 12 |
mechanism of rig | 12 |
immune responses by | 12 |
i pathway reveals | 12 |
innate immunity to | 12 |
the treatment of | 12 |
seem to be | 12 |
protein required for | 12 |
reported that the | 12 |
negative feedback regulation | 12 |
in antiviral immunity | 12 |
it will be | 12 |
specific inhibition of | 12 |
rna and activation | 12 |
to be essential | 12 |
the host response | 12 |
of unanchored polyubiquitin | 12 |
ifn induction in | 12 |
ns a protein | 12 |
that the ns | 12 |
has been implicated | 12 |
pattern recognition receptor | 12 |
activation of tlr | 12 |
were analyzed by | 12 |
in the same | 12 |
to act as | 12 |
open reading frame | 12 |
ifn response to | 12 |
antiviral effect of | 12 |
host immune system | 12 |
ubiquitin ligase and | 12 |
to target proteins | 12 |
targeted by the | 12 |
with the n | 12 |
and that the | 12 |
to activation of | 12 |
and mda have | 12 |
virus infection in | 12 |
syncytial virus infection | 12 |
box helicases rig | 12 |
reconstitution of the | 12 |
evolution of the | 12 |
paramyxovirus v proteins | 12 |
protein synthesis by | 12 |
been described to | 12 |
was shown that | 12 |
borne encephalitis virus | 12 |
airway epithelial cells | 12 |
in antiviral response | 12 |
the list of | 12 |
for h at | 12 |
with the ifn | 12 |
in the control | 12 |
genes encoding c | 12 |
single nucleotide polymorphism | 12 |
the mechanism by | 12 |
for the antiviral | 12 |
i interferons and | 12 |
is characterized by | 12 |
the viral capsid | 12 |
it does not | 12 |
is an adapter | 12 |
between self and | 12 |
acute promyelocytic leukemia | 12 |
the monolayer cells | 12 |
i interferon in | 12 |
chains in innate | 12 |
viral rna synthesis | 12 |
this work was | 12 |
protein kinase c | 12 |
signaling cascade that | 11 |
ifn signaling by | 11 |
is the probability | 11 |
large tegument protein | 11 |
regulated by the | 11 |
autocrine and paracrine | 11 |
in a manner | 11 |
marques et al | 11 |
for dsrna recognition | 11 |
in the level | 11 |
the exception of | 11 |
protease ns a | 11 |
irf transcription factor | 11 |
as compared to | 11 |
account for the | 11 |
and analyzed by | 11 |
lung epithelial cells | 11 |
the tlr signaling | 11 |
as in the | 11 |
is a cytosolic | 11 |
the molecular mechanisms | 11 |
antiviral stress granule | 11 |
focus on the | 11 |
the cytoplasm and | 11 |
i in antiviral | 11 |
antiviral state in | 11 |
changes in the | 11 |
host innate antiviral | 11 |
role of isg | 11 |
degradation of rig | 11 |
i ifn expression | 11 |
weber et al | 11 |
on the ifn | 11 |
adaptor protein mita | 11 |
the antiviral effect | 11 |
is not required | 11 |
signaling by targeting | 11 |
the understanding of | 11 |
in the category | 11 |
between ns and | 11 |
aggregates to activate | 11 |
to have a | 11 |
upon binding of | 11 |
hepatitis a virus | 11 |
of the genome | 11 |
signaling pathway through | 11 |
able to bind | 11 |
for virus replication | 11 |
expression of a | 11 |
host restriction by | 11 |
these findings suggest | 11 |
their interaction with | 11 |
forms functional prion | 11 |
formation of stress | 11 |
like receptors the | 11 |
in the inhibition | 11 |
expression of proinflammatory | 11 |
phase of viral | 11 |
of antiviral responses | 11 |
of the chicken | 11 |
entry into the | 11 |
immune response is | 11 |
ribonucleic acids by | 11 |
on the contrary | 11 |
at the same | 11 |
to activate antiviral | 11 |
of infectious virus | 11 |
of dengue virus | 11 |
short blunt double | 11 |
and iii ifn | 11 |
by targeting the | 11 |
words in each | 11 |
detection of viral | 11 |
interferon response to | 11 |
as an e | 11 |
to prevent the | 11 |
to the expression | 11 |
in the infected | 11 |
card domains of | 11 |
cytosolic dna sensing | 11 |
from the word | 11 |
translocation to the | 11 |
with the exception | 11 |
antiviral responses the | 11 |
found in arenavirus | 11 |
virus c protease | 11 |
activate antiviral signaling | 11 |
zhao et al | 11 |
a signaling role | 11 |
alexopoulou et al | 11 |
a molecular signature | 11 |
together with the | 11 |
response by the | 11 |
context of viral | 11 |
large number of | 11 |
impact on the | 11 |
of immune cells | 11 |
jiang et al | 11 |
the jak stat | 11 |
interaction between ns | 11 |
of cellular proteins | 11 |
and the induction | 11 |
virus core protein | 11 |
result in the | 11 |
activation by rig | 11 |
an endoplasmic reticulum | 11 |
basis for dsrna | 11 |
plays a crucial | 11 |
needs to be | 11 |
is composed of | 11 |
the case for | 11 |
activate and propagate | 11 |
of ifn genes | 11 |
rna viruses such | 11 |
as a consequence | 11 |
is a common | 11 |
of the situation | 11 |
into the cytosol | 11 |
in the cns | 11 |
central nervous system | 11 |
evades host restriction | 11 |
of the tlr | 11 |
the translocation of | 11 |
of cytokines and | 11 |
propagate antiviral innate | 11 |
course of infection | 11 |
could not be | 11 |
restriction by ifit | 11 |
and propagate antiviral | 11 |
under positive selection | 11 |
adaptor inducing ifn | 11 |
activation of ikk | 11 |
previous studies have | 11 |
like aggregates to | 11 |
detected by the | 11 |
in the first | 11 |
role in regulating | 11 |
may contribute to | 11 |
habjan et al | 11 |
was purchased from | 11 |
important to note | 11 |
rna helicase domain | 11 |
high levels of | 11 |
t cell responses | 11 |
in influenza a | 11 |
mavs forms functional | 11 |
been linked to | 11 |
used as a | 11 |
differentiation primary response | 11 |
proteins such as | 11 |
a reduction in | 11 |
binding protein that | 11 |
induced expression of | 11 |
required for rig | 11 |
syncytial virus ns | 11 |
to avoid rig | 11 |
of h n | 11 |
were immunoprecipitated with | 11 |
domain and a | 11 |
the text belongs | 11 |
the same time | 11 |
insights into rna | 11 |
data not shown | 11 |
response to poly | 11 |
nonstructural protein a | 11 |
is required to | 11 |
ifn signaling pathway | 11 |
the mechanisms of | 11 |
in the viral | 11 |
in an atp | 11 |
were collected from | 11 |
at least three | 11 |
and antiviral signal | 11 |
observing the word | 11 |
v proteins of | 11 |
recognition and innate | 11 |
recognition and activation | 11 |
i ifns in | 11 |
the top words | 11 |
g allele of | 11 |
role of trim | 11 |
and mda in | 11 |
the ebola virus | 11 |
by inhibition of | 11 |
shown in figure | 11 |
on the expression | 11 |
the trim family | 11 |
cap evades host | 11 |
viral evasion of | 11 |
was responsible for | 11 |
of the meaning | 11 |
like receptors in | 11 |
systemic lupus erythematosus | 11 |
of dexd h | 11 |
have been found | 11 |
the presence or | 11 |
the actin cytoskeleton | 11 |
to be activated | 11 |
mrna cap evades | 11 |
rna interference in | 11 |
induced by ifn | 11 |
a result of | 11 |
kumar et al | 11 |
cpg motifs in | 11 |
to the induction | 11 |
in accordance with | 11 |
in hcv replication | 11 |
the molecular mechanism | 11 |
recruited to the | 11 |
of viral rnas | 11 |
prrsv n protein | 11 |
coronavirus m protein | 11 |
viruses to avoid | 11 |
unusual viral rna | 11 |
in the lung | 11 |
at room temperature | 11 |
of the manuscript | 11 |
to promote viral | 11 |
upon infection with | 11 |
in antiviral defense | 11 |
of which are | 11 |
activation of protein | 11 |
sendai virus c | 11 |
upon rsv infection | 11 |
in uninfected cells | 11 |
the iav control | 11 |
to form an | 11 |
immune system is | 11 |
the endosomal compartment | 11 |
rnase l pathway | 11 |
acids by retinoic | 11 |
order rna structures | 11 |
role of mda | 11 |
for the first | 11 |
resulted in the | 11 |
differences in the | 11 |
play important roles | 11 |
reveals a signaling | 11 |
by acting as | 11 |
involvement of the | 11 |
viruses can also | 11 |
acting on rna | 11 |
we demonstrated that | 10 |
by a viral | 10 |
of a variety | 10 |
with clustalw implemented | 10 |
detects cytosolic dna | 10 |
and contributes to | 10 |
in the rna | 10 |
of the mechanisms | 10 |
are presented in | 10 |
from ensembl and | 10 |
ifn production is | 10 |
a strategy of | 10 |
reveals a novel | 10 |
lymphocytic choriomeningitis virus | 10 |
from observing the | 10 |
the molecular level | 10 |
mrna dependent on | 10 |
indicated that the | 10 |
is an e | 10 |
acid and encephalomyocarditis | 10 |
is interesting to | 10 |
ns interacts with | 10 |
contrast to the | 10 |
mechanism of action | 10 |
role of trims | 10 |
or b c | 10 |
as a signal | 10 |
transcriptional activation of | 10 |
an moi of | 10 |
not belong to | 10 |
processing of genome | 10 |
in the lsc | 10 |
not affected by | 10 |
ns protein in | 10 |
dependent sensing of | 10 |
after viral infection | 10 |
a cytosolic dna | 10 |
acts as an | 10 |
domain is the | 10 |
host immune responses | 10 |
immune recognition of | 10 |
tank binding kinase | 10 |
expression of cytokines | 10 |
inhibits the activation | 10 |
which is an | 10 |
factor activation by | 10 |
regulate the expression | 10 |
adaptor that facilitates | 10 |
represented by a | 10 |
sun et al | 10 |
authors declare no | 10 |
mechanism for the | 10 |
a is a | 10 |
the virus replication | 10 |
indicate that the | 10 |
of the mavs | 10 |
and ncbi databases | 10 |
cytokine production in | 10 |
hcv rna replication | 10 |
and stress granules | 10 |
by inhibiting the | 10 |
levels of the | 10 |
in a similar | 10 |
upon recognition of | 10 |
the form of | 10 |
ns a cleaves | 10 |
signal transduction by | 10 |
is mediated through | 10 |
effect on the | 10 |
the sars coronavirus | 10 |
may be a | 10 |
rna structures generated | 10 |
the initiation of | 10 |
and encephalomyocarditis picornavirus | 10 |
inhibition of irf | 10 |
the mitochondria to | 10 |
the adaptor mavs | 10 |
may be due | 10 |
in the toll | 10 |
i interferons through | 10 |
nuclear factor kappa | 10 |
of pkr by | 10 |
to avoid the | 10 |
such as rig | 10 |
the dengue virus | 10 |
deletion in the | 10 |
can be considered | 10 |
stimulated gene factor | 10 |
to those of | 10 |
the three rlr | 10 |
liu et al | 10 |
generated during virus | 10 |
interferon signaling pathway | 10 |
into rna recognition | 10 |
trim and trim | 10 |
inhibition of virus | 10 |
and m j | 10 |
melanoma differentiation associated | 10 |
card domains and | 10 |
likely to be | 10 |
the respiratory tract | 10 |
is expected to | 10 |
depend on the | 10 |
card and rd | 10 |
of the hcv | 10 |
immune responses against | 10 |
the signaling pathways | 10 |
recognition receptor rig | 10 |
is dispensable for | 10 |
gene expression in | 10 |
kappab by toll | 10 |
signaling by rna | 10 |
version of the | 10 |
of mitochondrial antiviral | 10 |
to trigger ifn | 10 |
of inflammatory cytokines | 10 |
in human monocytes | 10 |
of eif a | 10 |
polymerase iii detects | 10 |
signature for the | 10 |
proteins interact with | 10 |
infected a cells | 10 |
some of these | 10 |
in a sequence | 10 |
can lead to | 10 |
provides a molecular | 10 |
riplet and trim | 10 |
termini as a | 10 |
stimulated with ifn | 10 |
immunoprecipitated with anti | 10 |
influenza virus and | 10 |
of irf activation | 10 |
shown in fig | 10 |
of the c | 10 |
dna and induces | 10 |
of virus infection | 10 |
it has also | 10 |
the combination of | 10 |
the establishment of | 10 |
and activation by | 10 |
loss of rig | 10 |
myeloid immune cells | 10 |
of nuclear factor | 10 |
has shown that | 10 |
transcription of ifn | 10 |
also able to | 10 |
response to virus | 10 |
marq et al | 10 |
lund et al | 10 |
of viruses and | 10 |
site model a | 10 |
essential component of | 10 |
the attachment of | 10 |
mediated antiviral immunity | 10 |
also been reported | 10 |
transcription factor irf | 10 |
a complex with | 10 |
like receptor in | 10 |
and proteasomal degradation | 10 |
activation of a | 10 |
has not yet | 10 |
responses to polyriboinosinic | 10 |
one or two | 10 |
a platform for | 10 |
sensing mechanism of | 10 |
interactions with the | 10 |
the ctd and | 10 |
there is a | 10 |
lysates were immunoprecipitated | 10 |
identification of a | 10 |
to identify the | 10 |
mutations in the | 10 |
a signaling cascade | 10 |
ability of the | 10 |
of the dsrna | 10 |
may not be | 10 |
the probability that | 10 |
mediated antiviral signal | 10 |
drv or b | 10 |
infected with svv | 10 |
a regulator of | 10 |
the effects of | 10 |
the study of | 10 |
collected from ensembl | 10 |
proteins encoded by | 10 |
gene expression and | 10 |
iii detects cytosolic | 10 |
the surface of | 10 |
and viral infection | 10 |
of innate and | 10 |
ube l and | 10 |
for the top | 10 |
induction of innate | 10 |
is a target | 10 |
which is required | 10 |
analysis revealed that | 10 |
interferons through the | 10 |
syndrome coronavirus m | 10 |
mda signaling by | 10 |
xu et al | 10 |
to the mitochondrial | 10 |
were able to | 10 |
are required to | 10 |
trim family proteins | 10 |
regulation of rlr | 10 |
in immune cells | 10 |
production by interfering | 10 |
essential role in | 10 |
domains of the | 10 |
the innate immunity | 10 |
antiviral defense and | 10 |
interact with mavs | 10 |
which is essential | 10 |
in the field | 10 |
clustalw implemented in | 10 |
host defense against | 10 |
and jev infection | 10 |
polyubiquitination of rig | 10 |
h n viruses | 10 |
it is well | 10 |
negatively regulates tlr | 10 |
was found that | 10 |
regulation of type | 10 |
i and sting | 10 |
molecular signature for | 10 |
baum et al | 10 |
c virus nonstructural | 10 |
role for the | 10 |
have evolved to | 10 |
j and m | 10 |
all of which | 10 |
be associated with | 10 |
the exact mechanism | 10 |
used in this | 10 |
for the treatment | 10 |
w j in | 10 |
during influenza virus | 10 |
the viral ns | 10 |
i detects viral | 10 |
required for its | 10 |
response to rna | 10 |
in the last | 10 |
ensembl and ncbi | 10 |
influenza virus ns | 10 |
regions of the | 10 |
wu et al | 10 |
derived dendritic cells | 10 |
in these cells | 10 |
antiviral immunity and | 10 |
it was reported | 10 |
and negative regulation | 10 |
chiu et al | 10 |
implemented in bioedit | 10 |
the results of | 10 |
essential components of | 10 |
studies have demonstrated | 10 |
honda et al | 10 |
infected cells by | 10 |
aligned with clustalw | 10 |
ubiquitination and deubiquitination | 10 |
box rna helicases | 10 |
with the rig | 10 |
which results in | 10 |
antiviral response is | 10 |
and rnase l | 10 |
mechanism through which | 10 |
been proposed that | 10 |
i recognition of | 10 |
cui et al | 10 |
been observed in | 10 |
activation by mda | 10 |
a direct interaction | 10 |
be considered as | 10 |
are found in | 10 |
nucleic acid sensing | 10 |
in this way | 10 |
a negative feedback | 10 |
is also involved | 10 |
a large number | 10 |
polyribocytidylic acid and | 10 |
mediated by rig | 10 |
blood mononuclear cells | 10 |
mice infected with | 10 |
at an moi | 10 |
several studies have | 10 |
a dexd h | 10 |
through the rig | 10 |
and ns a | 10 |
for induction of | 10 |
it is interesting | 10 |
of porcine reproductive | 10 |
each word is | 10 |
phosphorylation and activation | 10 |
to the ifn | 10 |
the endolysosomal compartment | 10 |
the retinoic acid | 10 |
disruption of the | 10 |
the unfolded protein | 10 |
role in innate | 10 |
amino acid sequence | 10 |
antagonize type i | 10 |
an essential component | 10 |
unmethylated cpg motifs | 10 |
pi k akt | 10 |
it remains to | 10 |
irf activation by | 10 |
patients with chronic | 10 |
interferon pathway by | 10 |
in some cases | 10 |
the indicated antibodies | 10 |
is based on | 10 |
in the present | 10 |
swine fever virus | 10 |
it should be | 10 |
release of the | 10 |
the phosphatase pp | 10 |
which is also | 10 |
is a potent | 10 |
data indicate that | 10 |
of host proteins | 10 |
to hepatitis c | 10 |
syndrome coronavirus nsp | 10 |
with the host | 10 |
illustrated by the | 10 |
to elucidate the | 10 |
and signal transduction | 9 |
like receptor activation | 9 |
and figure s | 9 |
role of rnase | 9 |
it is unclear | 9 |
i ifn pathway | 9 |
was able to | 9 |
the requirement for | 9 |
has been observed | 9 |
activation of p | 9 |
by rnase l | 9 |
to the cell | 9 |
the ns b | 9 |
i and the | 9 |
as a positive | 9 |
the most important | 9 |
modulates type i | 9 |
foreign nucleic acid | 9 |
through the induction | 9 |
and effector functions | 9 |
response in the | 9 |
i ifn receptor | 9 |
deaminase acting on | 9 |
and as a | 9 |
off the mitochondria | 9 |
distribution or reproduction | 9 |
induce the formation | 9 |
induction during the | 9 |
virus infection by | 9 |
in viral infection | 9 |
was associated with | 9 |
suppression of innate | 9 |
be necessary to | 9 |
is noteworthy that | 9 |
these viral proteins | 9 |
rna binding proteins | 9 |
were purchased from | 9 |
of the family | 9 |
play a critical | 9 |
the family of | 9 |
as an important | 9 |
the nsd complex | 9 |
ability to induce | 9 |
stimulation of the | 9 |
belonging to the | 9 |
that has been | 9 |
studies will be | 9 |
are resistant to | 9 |
innate immunity in | 9 |
a range of | 9 |
this is a | 9 |
in regulating the | 9 |
for degradation by | 9 |
crucial for the | 9 |
and control of | 9 |
and innate antiviral | 9 |
be used to | 9 |
with type i | 9 |
i to promote | 9 |
with drv or | 9 |
self nucleic acids | 9 |
immunity induced by | 9 |
indicate that ns | 9 |
signaling protein off | 9 |
and mda activates | 9 |
due to their | 9 |
positive regulation of | 9 |
transcribed rna intermediate | 9 |
in spite of | 9 |
that of the | 9 |
and aligned with | 9 |
and expression of | 9 |
change in the | 9 |
of emcv and | 9 |
inhibited by the | 9 |
which binds to | 9 |
inhibits the type | 9 |
host response to | 9 |
g bp and | 9 |
innate immune pathways | 9 |
in the release | 9 |
sensor of rig | 9 |
further studies are | 9 |
in pathogen recognition | 9 |
of the pathogen | 9 |
receptors in the | 9 |
factors such as | 9 |
i has been | 9 |
of the eif | 9 |
each of these | 9 |
or empty vector | 9 |
deduced protein sequences | 9 |
the antiviral rig | 9 |
of trim with | 9 |
the interaction with | 9 |
innate immune activation | 9 |
for the detection | 9 |
evidence suggests that | 9 |
sensing of poly | 9 |
against rna viruses | 9 |
stranded rna via | 9 |
no conflict of | 9 |
through inhibition of | 9 |
dna sensing by | 9 |
to provide a | 9 |
identified in the | 9 |
to be further | 9 |
on the molecular | 9 |
during iav infection | 9 |
interaction of rig | 9 |
the er to | 9 |
of these genes | 9 |
during infection with | 9 |
response to viruses | 9 |
the current study | 9 |
as the reference | 9 |
meylan et al | 9 |
it was also | 9 |
regions of zbrig | 9 |
the emergence of | 9 |
adenosine deaminase acting | 9 |
for proteasomal degradation | 9 |
the host cells | 9 |
effect of the | 9 |
production by targeting | 9 |
stranded ribonucleic acids | 9 |
with mavs and | 9 |
zhong et al | 9 |
to detect and | 9 |
the ring domain | 9 |
closely related to | 9 |
referred to as | 9 |
viral rna is | 9 |
of interferon signaling | 9 |
a gap or | 9 |
well plates were | 9 |
in the supernatants | 9 |
and the helicase | 9 |
basis for viral | 9 |
the ubiquitin system | 9 |
mda activates antiviral | 9 |
one or more | 9 |
i is a | 9 |
viral innate immune | 9 |
of ifn signaling | 9 |
protein inhibits the | 9 |
infected epithelial cells | 9 |
rna by the | 9 |
for interaction with | 9 |
farrell et al | 9 |
is the rna | 9 |
by viral infection | 9 |
genomic rna during | 9 |
ifn antiviral activity | 9 |
and evolution of | 9 |
decrease in the | 9 |
was proposed to | 9 |
and induction of | 9 |
in the future | 9 |
peripheral blood mononuclear | 9 |
self and nonself | 9 |
b c at | 9 |
host type i | 9 |
of antiviral immunity | 9 |
hcv ns a | 9 |
of the infection | 9 |
in the alignment | 9 |
the reference sequence | 9 |
by means of | 9 |
study suggests that | 9 |
be the case | 9 |
virus protease ns | 9 |
it is noteworthy | 9 |
rna during negative | 9 |
and inhibits the | 9 |
synthesis of unanchored | 9 |
the antiviral innate | 9 |
host antiviral responses | 9 |
a cap structure | 9 |
gap or deletion | 9 |
viral rna in | 9 |
serves as an | 9 |
the creative commons | 9 |
sense rna viruses | 9 |
i helicase and | 9 |
regulation of gene | 9 |
depends on the | 9 |
the middle east | 9 |
this results in | 9 |
in the form | 9 |
nucleotide polymorphisms of | 9 |
of rna virus | 9 |
conjugation to target | 9 |
word is represented | 9 |
this is an | 9 |
induced oligomerization of | 9 |
dependent type i | 9 |
the capacity of | 9 |
to block the | 9 |
or deletion in | 9 |
mouse embryonic fibroblasts | 9 |
be recognized by | 9 |
to investigate the | 9 |
is not the | 9 |
and ns b | 9 |
located on the | 9 |
in this context | 9 |
double stranded rna | 9 |
any of the | 9 |
in the myd | 9 |
interference in mammalian | 9 |
binding of rig | 9 |
of long double | 9 |
detects viral genomic | 9 |
is an endoplasmic | 9 |
be targeted by | 9 |
protein involved in | 9 |
immune evasion by | 9 |
mediated antiviral innate | 9 |
the supernatants of | 9 |
remain to be | 9 |
is recruited to | 9 |
ikkepsilon and tbk | 9 |
transfected with the | 9 |
interferon stimulated gene | 9 |
transcription and translation | 9 |
i and ii | 9 |
to promote interferon | 9 |
small interfering rnas | 9 |
by the fact | 9 |
e ligase trim | 9 |
on type i | 9 |
by plasmacytoid dendritic | 9 |
outside of the | 9 |
huang et al | 9 |
ubiquitin ligase activity | 9 |
species were collected | 9 |
i signaling pathway | 9 |
was dependent on | 9 |
cells such as | 9 |
cells via the | 9 |
of middle east | 9 |
was confirmed by | 9 |
borna disease virus | 9 |
of downstream signaling | 9 |
and interferon antagonism | 9 |
membrane association and | 9 |
virus infection the | 9 |
higher levels of | 9 |
of the respiratory | 9 |
leading to a | 9 |
represents the same | 9 |
structures generated during | 9 |
in the intracellular | 9 |
regulatory domain is | 9 |
to be an | 9 |
mass spectrometry analysis | 9 |
protein off the | 9 |
in recent years | 9 |
c virus protease | 9 |
mammalian species were | 9 |
triphosphate sensor of | 9 |
of the indicated | 9 |
stimulator of ifn | 9 |
in the er | 9 |
was also found | 9 |
the ctd of | 9 |
the nuclear translocation | 9 |
results demonstrate that | 9 |
immune cells and | 9 |
was performed using | 9 |
methylation provides a | 9 |
is known about | 9 |
positive strand rna | 9 |
of unanchored k | 9 |
reference sequence of | 9 |
of host immune | 9 |
to contribute to | 9 |
directly or indirectly | 9 |
cells were incubated | 9 |
detection of foreign | 9 |
many of the | 9 |
in the cells | 9 |
infected cells were | 9 |
mechanisms used by | 9 |
results indicated that | 9 |
to the identification | 9 |
immunodeficiency virus type | 9 |
viruses have developed | 9 |
protease domain of | 9 |
proteins and their | 9 |
been described as | 9 |
to evade the | 9 |
viruses in innate | 9 |
variant allele of | 9 |
terminal regulatory domain | 9 |
as mentioned above | 9 |
been demonstrated that | 9 |
implications for the | 9 |
the nucleus where | 9 |
the nuclear factor | 9 |
mitochondria to evade | 9 |
that leads to | 9 |
trim and rig | 9 |
and dengue virus | 9 |
the plasma membrane | 9 |
suppresses type i | 9 |
c virus core | 9 |
innate immunity induced | 9 |
viral rna sensing | 9 |
a cleaves mitochondrial | 9 |
card domain of | 9 |
are expressed in | 9 |
jak stat signaling | 9 |
recognition of hepatitis | 9 |
ifn signaling pathways | 9 |
are critical for | 9 |
interacts with traf | 9 |
of translation initiation | 9 |
was determined by | 9 |
like receptor lgp | 9 |
to viral rna | 9 |
cells were treated | 9 |
the secretion of | 9 |
viral infection is | 9 |
murine hepatitis virus | 9 |
effectors of the | 9 |
well as in | 9 |
ligase activity of | 9 |
mediated ubiquitination of | 9 |
for viral rna | 9 |
by the rig | 9 |
to the viral | 9 |
cleaves mitochondrial antiviral | 9 |
proteins ns and | 9 |
inhibition of type | 9 |
helicase and activation | 9 |
gene induction by | 9 |
evidence for the | 9 |
be able to | 9 |
a viral deubiquitinase | 9 |
and b cells | 9 |
ubiquitin and ubiquitin | 9 |
similar to that | 9 |
an rna polymerase | 9 |
strategy of negative | 9 |
interesting to note | 9 |
the rna exosome | 9 |
considered to be | 9 |
used in the | 9 |
induced proteins with | 9 |
a distinct role | 9 |
nod and nod | 9 |
sequence of human | 9 |
cytoplasmic viral rna | 9 |
bronchial epithelial cells | 9 |
rna and inhibits | 9 |
adaptor protein trif | 9 |
is a critical | 9 |
viral proteins and | 9 |
filaments in an | 9 |
rna replication and | 9 |
cov orf b | 9 |
of interferon genes | 9 |
inhibitor of the | 9 |
regulation of ifn | 9 |
rd regions of | 9 |
the restriction of | 9 |
of the receptor | 9 |
triggered type i | 9 |
i repressor domain | 9 |
the corresponding category | 9 |
oligomerization of the | 9 |
dependent interferon induction | 9 |
antiviral response to | 9 |
signal transduction pathways | 9 |
c k and | 9 |
will focus on | 9 |
detected in the | 9 |
was observed in | 8 |
i for k | 8 |
occurs in the | 8 |
cell lines and | 8 |
and k of | 8 |
the linker region | 8 |
containing the word | 8 |
representation of the | 8 |
in the lungs | 8 |
viruses and the | 8 |
and antiviral signaling | 8 |
the results showed | 8 |
viruses in the | 8 |
a broad range | 8 |
of the mitochondrial | 8 |
molecules such as | 8 |
involved in ifn | 8 |
activation in response | 8 |
activation by innate | 8 |
in nucleic acid | 8 |
that there are | 8 |
cytokines such as | 8 |
is likely to | 8 |
of stat and | 8 |
of the duck | 8 |
dimerization and nuclear | 8 |
as a vector | 8 |
transcription factor activation | 8 |
in human antiviral | 8 |
t cells in | 8 |
adenosine deaminase adar | 8 |
host protein synthesis | 8 |
of traf in | 8 |
the c pro | 8 |
absence of a | 8 |
the c terminus | 8 |
and severe acute | 8 |
that in the | 8 |