This is a table of type quadgram and their frequencies. Use it to search & browse the list to learn more about your study carrel.
quadgram | frequency |
---|---|
of influenza a virus | 165 |
n and h n | 116 |
h n and h | 115 |
influenza a virus infection | 89 |
has been shown to | 83 |
in the presence of | 74 |
h n influenza virus | 72 |
memory cd t cells | 69 |
influenza a h n | 63 |
in the absence of | 61 |
middle east respiratory syndrome | 59 |
h n influenza a | 57 |
severe acute respiratory syndrome | 54 |
of influenza a viruses | 53 |
h n influenza viruses | 52 |
have been shown to | 51 |
east respiratory syndrome coronavirus | 47 |
pandemic h n influenza | 46 |
cells were infected with | 44 |
influenza a virus in | 44 |
in vitro and in | 43 |
highly pathogenic avian influenza | 40 |
cd t cells in | 40 |
in the united states | 40 |
the influenza a virus | 40 |
and h n viruses | 39 |
in the context of | 39 |
vitro and in vivo | 39 |
acute respiratory syndrome coronavirus | 37 |
been shown to be | 37 |
to display the preprint | 35 |
is the author funder | 35 |
the preprint in perpetuity | 35 |
license to display the | 35 |
a h n virus | 35 |
for the treatment of | 35 |
medrxiv a license to | 35 |
has granted medrxiv a | 35 |
granted medrxiv a license | 35 |
display the preprint in | 35 |
who has granted medrxiv | 35 |
a license to display | 35 |
in the case of | 35 |
of ha and na | 34 |
acute respiratory distress syndrome | 33 |
specific cd t cells | 33 |
t cells in the | 33 |
of the influenza virus | 33 |
n influenza a virus | 33 |
in the upper respiratory | 32 |
influenza virus infection in | 31 |
of the h n | 31 |
of the influenza a | 31 |
an important role in | 31 |
h n viruses were | 31 |
the upper respiratory tract | 31 |
on the surface of | 31 |
in influenza a virus | 31 |
were found to be | 30 |
of the nlrp inflammasome | 30 |
h n virus was | 29 |
as shown in fig | 29 |
of h n virus | 28 |
to influenza a virus | 28 |
of cd t cells | 28 |
h n virus in | 28 |
on the other hand | 27 |
cells were transfected with | 26 |
against influenza a virus | 26 |
respiratory syncytial virus infection | 26 |
not certified by peer | 25 |
certified by peer review | 25 |
which was not certified | 25 |
was not certified by | 25 |
the lower respiratory tract | 25 |
as well as the | 25 |
of h n influenza | 24 |
cd t cell responses | 24 |
the first report of | 24 |
influenza a and b | 24 |
of pandemic h n | 23 |
in a mouse model | 23 |
h n swine influenza | 23 |
influenza a virus replication | 23 |
during influenza virus infection | 23 |
a cells were infected | 23 |
the ha and na | 23 |
in the pathogenesis of | 23 |
holder for this preprint | 22 |
this preprint this version | 22 |
copyright holder for this | 22 |
the h n virus | 22 |
the copyright holder for | 22 |
preprint this version posted | 22 |
the pandemic h n | 22 |
for this preprint this | 22 |
human airway epithelial cells | 22 |
human immunodeficiency virus type | 21 |
influenza a viruses in | 21 |
h n virus isolates | 21 |
in the lungs of | 21 |
the activation of the | 21 |
no reuse allowed without | 20 |
reuse allowed without permission | 20 |
has been reported to | 20 |
with influenza a virus | 20 |
a mouse model of | 20 |
n influenza a viruses | 20 |
one of the most | 19 |
cd t cell response | 19 |
specific memory cd t | 19 |
cells were treated with | 19 |
able to bind to | 19 |
have been reported to | 18 |
influenza a virus and | 18 |
at a moi of | 18 |
n influenza virus infection | 18 |
influenza a virus hemagglutinin | 18 |
influenza h n virus | 18 |
were detected in swine | 18 |
for influenza virus replication | 18 |
oxidative medicine and cellular | 17 |
reproductive and respiratory syndrome | 17 |
as a result of | 17 |
of the immune system | 17 |
porcine reproductive and respiratory | 17 |
a and b viruses | 17 |
the h n and | 17 |
protein of influenza a | 17 |
min at room temperature | 17 |
influenza a virus from | 17 |
of influenza virus infection | 17 |
h n viruses in | 17 |
play a role in | 17 |
medicine and cellular longevity | 17 |
of h n pdm | 17 |
activation of the nlrp | 16 |
also been shown to | 16 |
of human influenza a | 16 |
in the lower respiratory | 16 |
of middle east respiratory | 16 |
and h n influenza | 16 |
for the development of | 16 |
highly pathogenic h n | 16 |
of respiratory syncytial virus | 16 |
h n avian influenza | 16 |
and respiratory syndrome virus | 16 |
for min at room | 16 |
of the innate immune | 16 |
response to iav infection | 16 |
the innate immune response | 16 |
reassortant h n virus | 16 |
of human immunodeficiency virus | 16 |
memory cd t cell | 16 |
specific cd t cell | 15 |
studies have shown that | 15 |
play an important role | 15 |
the expression of the | 15 |
of avian h n | 15 |
a wide range of | 15 |
had no effect on | 15 |
of influenza viruses in | 15 |
van eijk et al | 15 |
has also been shown | 15 |
n swine influenza virus | 15 |
was found to be | 15 |
iav h n pdm | 15 |
the surface of the | 15 |
has been demonstrated to | 15 |
at the nucleotide level | 15 |
innate immune response to | 15 |
avian influenza h n | 15 |
in a murine model | 15 |
it is possible that | 15 |
h n virus infection | 15 |
plays an important role | 15 |
origin h n influenza | 15 |
type i and type | 14 |
the network data exchange | 14 |
the host immune response | 14 |
on the expression of | 14 |
viruses were detected in | 14 |
these results suggest that | 14 |
was detected in the | 14 |
made available under a | 14 |
in addition to the | 14 |
of swine influenza virus | 14 |
presence or absence of | 14 |
it has been shown | 14 |
to influenza virus infection | 14 |
n influenza viruses in | 14 |
to the activation of | 14 |
proteins a and d | 14 |
surfactant proteins a and | 14 |
type i and iii | 14 |
a murine model of | 14 |
is known to be | 14 |
for influenza a virus | 14 |
in the respiratory tract | 14 |
h n pdm virus | 14 |
of tumor necrosis factor | 14 |
is also able to | 14 |
type i ifn signaling | 14 |
was shown to be | 14 |
ha and na genes | 14 |
of severe acute respiratory | 14 |
a and mdck cells | 13 |
cd t cells are | 13 |
a is the author | 13 |
of avian influenza a | 13 |
under a is the | 13 |
infected with h n | 13 |
h n pdm and | 13 |
is able to bind | 13 |
the innate immune system | 13 |
it is made available | 13 |
license it is made | 13 |
this version posted may | 13 |
h n virus antibodies | 13 |
in contrast to the | 13 |
is made available under | 13 |
is involved in the | 13 |
the nucleotide level and | 13 |
in the treatment of | 13 |
h n and a | 13 |
international license it is | 13 |
cells in the lung | 13 |
swine influenza a virus | 13 |
a virus infection by | 13 |
of h n and | 13 |
for the detection of | 13 |
followed by infection with | 13 |
influenza virus h n | 13 |
influenza viruses in pigs | 13 |
avian h n and | 13 |
available under a is | 13 |
virus was detected in | 13 |
as shown in figure | 13 |
the authors declare no | 13 |
the presence or absence | 13 |
influenza a virus ns | 13 |
is one of the | 13 |
infection with pr virus | 13 |
of influenza virus hemagglutinin | 13 |
of influenza a h | 13 |
the amino acid level | 13 |
has also been reported | 12 |
a critical role in | 12 |
avian influenza a h | 12 |
to the cell surface | 12 |
at the amino acid | 12 |
of swine influenza viruses | 12 |
were infected with iav | 12 |
of surfactant protein a | 12 |
in agreement with the | 12 |
the cd t cell | 12 |
were found infected with | 12 |
innate and adaptive immunity | 12 |
were found positive for | 12 |
response to influenza a | 12 |
on the cell surface | 12 |
the nuclear export of | 12 |
pathogenic avian influenza virus | 12 |
virus infection in mice | 12 |
the highest number of | 12 |
of three independent experiments | 12 |
at an moi of | 12 |
human h n virus | 12 |
immune response to influenza | 12 |
with respiratory syncytial virus | 12 |
the treatment of iav | 12 |
of pandemic influenza a | 12 |
as well as in | 12 |
the initial binding rate | 12 |
infected with pr virus | 12 |
in response to iav | 12 |
of influenza c virus | 12 |
and pandemic h n | 12 |
were transfected with a | 12 |
i and type iii | 11 |
the nlrp inflammasome in | 11 |
transmission of avian influenza | 11 |
cd t cells and | 11 |
the h n influenza | 11 |
morbidity and mortality in | 11 |
likely due to the | 11 |
of influenza virus infections | 11 |
induction of type i | 11 |
of type i ifn | 11 |
in the regulation of | 11 |
this is the first | 11 |
of cd t cell | 11 |
influenza virus m protein | 11 |
in the presence or | 11 |
human bronchial epithelial cells | 11 |
has the potential to | 11 |
in human airway epithelial | 11 |
the development of novel | 11 |
response to viral infection | 11 |
against influenza virus infection | 11 |
of the inflammatory response | 11 |
n viruses were detected | 11 |
in the induction of | 11 |
of memory cd t | 11 |
cells infected with iav | 11 |
characterization of h n | 11 |
n influenza virus in | 11 |
the protective role of | 11 |
in the development of | 11 |
influenza virus infection of | 11 |
cd t cell effector | 11 |
inflammatory cytokines and chemokines | 11 |
of type i interferon | 11 |
the antiviral activity of | 11 |
by infection with pr | 11 |
and lower respiratory tract | 11 |
has been shown that | 11 |
been shown to inhibit | 11 |
resident memory cd t | 11 |
increase in the ifitm | 11 |
by influenza a virus | 11 |
have been associated with | 11 |
viruses in pigs in | 11 |
the iav control group | 11 |
models of acute pneumonia | 11 |
been reported to be | 11 |
on the viral surface | 11 |
versus the iav control | 11 |
innate and adaptive immune | 11 |
the mechanism by which | 11 |
the authors declare that | 10 |
and h n virus | 10 |
transmission of influenza a | 10 |
the release of viral | 10 |
the role of the | 10 |
the h n pandemic | 10 |
at week and week | 10 |
identification and characterization of | 10 |
influenza virus ns protein | 10 |
no conflict of interest | 10 |
in the antigenic sites | 10 |
upper respiratory tract of | 10 |
as compared to the | 10 |
and influenza a virus | 10 |
and h n subtypes | 10 |
a virus ns protein | 10 |
be involved in the | 10 |
these results indicate that | 10 |
induced by pr virus | 10 |
no vac no cha | 10 |
for the generation of | 10 |
upper and lower respiratory | 10 |
a virus infection in | 10 |
mouse models of acute | 10 |
of an h n | 10 |
suggesting that pa may | 10 |
in comparison with pr | 10 |
cells in response to | 10 |
inhibition of iav infection | 10 |
at different time points | 10 |
the h n pdm | 10 |
by the addition of | 10 |
of mice infected with | 10 |
n virus isolates were | 10 |
during influenza a virus | 10 |
ha and na proteins | 10 |
pandemic h n virus | 10 |
of influenza virus in | 10 |
in the activation of | 10 |
swine in the united | 10 |
i and iii ifns | 10 |
pi k akt pathway | 10 |
been shown to have | 10 |
restricts influenza a virus | 10 |
sequences obtained from pigs | 10 |
in the response to | 10 |
in line with this | 10 |
a strong nuclear np | 10 |
innate immunity to influenza | 10 |
for the production of | 10 |
in iav infected cells | 10 |
human h n influenza | 10 |
for the first time | 10 |
have been identified in | 10 |
were infected with a | 10 |
west nile virus infection | 10 |
was used as a | 10 |
by the presence of | 10 |
is thought to be | 9 |
cells were incubated with | 9 |
of the immune response | 9 |
with adnrf followed by | 9 |
respiratory syndrome coronavirus infection | 9 |
influenza virus in a | 9 |
of surfactant protein d | 9 |
required for influenza virus | 9 |
n avian influenza virus | 9 |
claims in published maps | 9 |
the immune response to | 9 |
and other respiratory viruses | 9 |
of influenza b virus | 9 |
influenza virus infections in | 9 |
of the ha protein | 9 |
t cell response to | 9 |
published maps and institutional | 9 |
following respiratory virus infection | 9 |
the presence of serum | 9 |
in the immune system | 9 |
n viruses were identified | 9 |
ind entry of iav | 9 |
systematic review and meta | 9 |
during respiratory syncytial virus | 9 |
nature remains neutral with | 9 |
strains of h n | 9 |
and activator of transcription | 9 |
in published maps and | 9 |
avian and human iavs | 9 |
signal transducer and activator | 9 |
has been implicated in | 9 |
with pr virus alone | 9 |
of the pandemic h | 9 |
ha and na subtypes | 9 |
is consistent with the | 9 |
influenza a virus infections | 9 |
in the lung airways | 9 |
cells were seeded in | 9 |
with regard to jurisdictional | 9 |
transducer and activator of | 9 |
and the h n | 9 |
were found to have | 9 |
to the h n | 9 |
it is likely that | 9 |
response to cov infection | 9 |
springer nature remains neutral | 9 |
have been reported in | 9 |
at the site of | 9 |
jurisdictional claims in published | 9 |
h n and pandemic | 9 |
reported in swine in | 9 |
influenza a virus m | 9 |
the context of viral | 9 |
a role in the | 9 |
a cells infected with | 9 |
similar to that of | 9 |
it has been reported | 9 |
was performed using the | 9 |
to influenza a h | 9 |
of the viral genome | 9 |
in influenza virus infection | 9 |
remains neutral with regard | 9 |
in accordance with the | 9 |
neutral with regard to | 9 |
of type i ifns | 9 |
respiratory viral infections in | 9 |
like and atii cells | 9 |
in the present study | 9 |
and respiratory syncytial virus | 9 |
both in vitro and | 9 |
at the same time | 9 |
to jurisdictional claims in | 9 |
the presence of the | 9 |
mdck cells were infected | 9 |
maps and institutional affiliations | 9 |
lower respiratory tract of | 9 |
obtained from pigs sampled | 9 |
of surfactant proteins a | 9 |
the course of infection | 9 |
the lungs of mice | 9 |
respiratory syncytial virus and | 9 |
this version posted april | 9 |
a wide variety of | 9 |
n influenza viruses from | 9 |
a single amino acid | 9 |
h and h challenge | 9 |
regard to jurisdictional claims | 9 |
response to sars infection | 9 |
been shown to bind | 9 |
the presence of fcs | 9 |
a broad spectrum of | 9 |
influenza viruses in swine | 8 |
also able to bind | 8 |
the inhibitory effect of | 8 |
generation of recombinant influenza | 8 |
role of nrf in | 8 |
through the activation of | 8 |
note springer nature remains | 8 |
that they have no | 8 |
an influenza a virus | 8 |
the viral polymerase complex | 8 |
the specificity of the | 8 |
of the virus to | 8 |
and cd t cells | 8 |
influenza virus isolated from | 8 |
has been reported that | 8 |
iav infected a cells | 8 |
like h n and | 8 |
with h n pdm | 8 |
human influenza a viruses | 8 |
strong nuclear np signal | 8 |
effects of curcumin derivatives | 8 |
virus was isolated from | 8 |
resistance to influenza a | 8 |
origin h n virus | 8 |
the treatment of influenza | 8 |
authors declare no conflict | 8 |
the end of the | 8 |
has been associated with | 8 |
to the induction of | 8 |
in this study were | 8 |
nasal swabs and balf | 8 |
for the evaluation of | 8 |
isolation and characterization of | 8 |
and the cells were | 8 |
influenza a virus entry | 8 |
closely related to the | 8 |
on influenza a virus | 8 |
production of type i | 8 |
cd t cells is | 8 |
play a critical role | 8 |
the ha na balance | 8 |
was obtained from the | 8 |
mortality associated with influenza | 8 |
pfu cell pr virus | 8 |
of wdnhbe cells with | 8 |
of influenza a and | 8 |
h n or h | 8 |
was added to the | 8 |
of avian and human | 8 |
the magnitude of the | 8 |
our understanding of the | 8 |
against h n and | 8 |
and type iii ifn | 8 |
n virus was reported | 8 |
for min at uc | 8 |
and characterization of the | 8 |
iav infection in a | 8 |
treated with or without | 8 |
used in this study | 8 |
t cell effector functions | 8 |
pandemic influenza a h | 8 |
responses to influenza a | 8 |
a type ii transmembrane | 8 |
swine influenza virus in | 8 |
declare no conflict of | 8 |
of hepatitis c virus | 8 |
authors declare that they | 8 |
of cytokines and chemokines | 8 |
to swine transmission of | 8 |
a virus in swine | 8 |
pig id at week | 8 |
in lung epithelial cells | 8 |
our data suggest that | 8 |
of iav infection in | 8 |
to be able to | 8 |
respiratory virus infection in | 8 |
and h challenge strains | 8 |
pulmonary surfactant protein a | 8 |
the emergence of a | 8 |
both h n and | 8 |
was also shown to | 8 |
the pathogenesis of iav | 8 |
the activation of nf | 8 |
the case of sars | 8 |
the pathogenesis of influenza | 8 |
n or h n | 8 |
cytokines and chemokines in | 8 |
of swine influenza a | 8 |
pathogenic avian influenza h | 8 |
rift valley fever virus | 8 |
a large number of | 8 |
comparison with pr virus | 8 |
of the role of | 8 |
influenza viruses from pigs | 8 |
in cd t cell | 8 |
from apparently healthy swine | 8 |
complete genome sequence of | 8 |
type i ifn production | 8 |
surfactant protein d in | 8 |
associated with severe influenza | 8 |
formation of fusion pores | 8 |
n pdm and poly | 8 |
at the cell surface | 8 |
prior to infection with | 8 |
structure of the haemagglutinin | 8 |
shown to increase the | 8 |
to the plasma membrane | 8 |
and its role in | 8 |
of the cd t | 8 |
of highly pathogenic avian | 8 |
the generation of recombinant | 8 |
the plasma membrane of | 8 |
declare that they have | 8 |
the upper and lower | 8 |
ns protein of influenza | 8 |
respiratory tract of humans | 8 |
influenza a virus nucleoprotein | 8 |
like h n viruses | 8 |
with h n influenza | 8 |
at later time points | 8 |
in the supernatants of | 8 |
the formation of fusion | 8 |
van asbeck et al | 8 |
blunt the cytokine storm | 8 |
cells were fixed with | 8 |
influenza a viruses from | 8 |
avian h n influenza | 8 |
to be involved in | 8 |
infections in hospitalized children | 8 |
been shown to increase | 8 |
of a number of | 8 |
iav infection in the | 8 |
of avian influenza virus | 8 |
to be associated with | 7 |
replication and gene transcription | 7 |
pandemic influenza a virus | 7 |
we were able to | 7 |
the unfolded protein response | 7 |
a better understanding of | 7 |
was shown to decrease | 7 |
animal care and use | 7 |
to the presence of | 7 |
is likely due to | 7 |
shown to bind to | 7 |
against respiratory syncytial virus | 7 |
was shown to increase | 7 |
it has also been | 7 |
we found that the | 7 |
the length of the | 7 |
h n iav infection | 7 |
swine h n virus | 7 |
at the plasma membrane | 7 |
work was supported by | 7 |
inhibition of influenza virus | 7 |
influenza virus replication and | 7 |
a virus infection and | 7 |
infected with a pr | 7 |
to be required for | 7 |
as shown in table | 7 |
cells were inoculated with | 7 |
from a pig in | 7 |
fusion of the viral | 7 |
influenza virus infection a | 7 |
sibu and kapit hospitals | 7 |
cells and alveolar macrophages | 7 |
has been proposed to | 7 |
and ali bx zhou | 7 |
was determined by real | 7 |
fusion in virus entry | 7 |
as well as by | 7 |
with influenza a viruses | 7 |
it was demonstrated that | 7 |
cells in the presence | 7 |
were reported in swine | 7 |
peripheral blood mononuclear cells | 7 |
type i interferon signaling | 7 |
lower respiratory tract infection | 7 |
of type i and | 7 |
was used to assess | 7 |
physiologic levels of gm | 7 |
the induction of macropinocytosis | 7 |
the airway epithelium in | 7 |
care and use committee | 7 |
mbl is able to | 7 |
nl and hl nl | 7 |
several studies have shown | 7 |
structure and function of | 7 |
and genetic characteristics of | 7 |
was reported to be | 7 |
avian influenza a virus | 7 |
induces apoptosis in human | 7 |
transmission of h n | 7 |
frontiers in immunology www | 7 |
swine h n influenza | 7 |
at the time of | 7 |
the spatial organization of | 7 |
and characterization of a | 7 |
entry by blocking the | 7 |
immunity to influenza a | 7 |
viruses were identified in | 7 |
infection with adnrf followed | 7 |
receptor binding and membrane | 7 |
of h n iav | 7 |
was detected in swine | 7 |
is responsible for the | 7 |
ac and muc b | 7 |
that cd t cells | 7 |
of pig id at | 7 |
virus infection in a | 7 |
approximately log decrease at | 7 |
of type i interferons | 7 |
analysis was performed using | 7 |
activates the nlrp inflammasome | 7 |
response to h n | 7 |
cellular pi k akt | 7 |
growth factor receptor tyrosine | 7 |
were approved by the | 7 |
influenza a virus the | 7 |
of iav in swine | 7 |
respiratory syncytial virus in | 7 |
inflammation and ali bx | 7 |
in mice infected with | 7 |
between iav infection and | 7 |
cells were fixed and | 7 |
this work was supported | 7 |
it is clear that | 7 |
antigenic and genetic characteristics | 7 |
the host cell surface | 7 |
of influenza virus at | 7 |
the presence of a | 7 |
the type i interferon | 7 |
is well known that | 7 |
se of three independent | 7 |
van iwaarden et al | 7 |
immunity to influenza virus | 7 |
and membrane fusion in | 7 |
the results showed that | 7 |
characterization of a novel | 7 |
to that of the | 7 |
important role in the | 7 |
the integrity of the | 7 |
of h n avian | 7 |
cells in the lungs | 7 |
the viruses and their | 7 |
were infected with pr | 7 |
in the inhibition of | 7 |
hl nl and hl | 7 |
was also observed in | 7 |
for disease control and | 7 |
membrane fusion in virus | 7 |
threat to public health | 7 |
were treated with curcumin | 7 |
in the endoplasmic reticulum | 7 |
association between iav infection | 7 |
detection of influenza a | 7 |
bhb was shown to | 7 |
in the lung and | 7 |
of pi k akt | 7 |
a systematic review and | 7 |
avian h n virus | 7 |
the role of nrf | 7 |
induced inflammation and ali | 7 |
does not appear to | 7 |
the human cathelicidin ll | 7 |
been implicated in the | 7 |
to h n pdm | 7 |
pathogenic avian influenza a | 7 |
cells of the immune | 7 |
diversity of swine influenza | 7 |
antiviral effects of curcumin | 7 |
structure of the influenza | 7 |
of a novel influenza | 7 |
alveolar type ii cells | 7 |
the wiv treatment groups | 7 |
of avian influenza viruses | 7 |
in the culture supernatants | 7 |
genome replication and gene | 7 |
membrane glycoprotein of influenza | 7 |
the ns protein of | 7 |
on the host cell | 7 |
was supported by the | 7 |
type i ifn in | 7 |
the role of host | 7 |
for treatment of influenza | 7 |
was a gift from | 7 |
a broad range of | 7 |
in cells infected with | 7 |
on the role of | 7 |
influenza and other respiratory | 7 |
the periphery of the | 7 |
with or without pa | 7 |
are expressed as the | 7 |
the carbohydrate recognition domain | 7 |
the site of infection | 7 |
the middle east respiratory | 7 |
is also involved in | 7 |
factor receptor tyrosine kinases | 7 |
lower respiratory tract infections | 7 |
it is well known | 7 |
the antiviral potential of | 7 |
of the airway epithelium | 7 |
data are expressed as | 7 |
iav strains in swine | 7 |
glycoprotein of influenza virus | 7 |
in the current study | 7 |
and one h n | 7 |
the host immune system | 7 |
washed three times with | 7 |
h n influenza in | 7 |
both h and h | 7 |
inhibition of np expression | 7 |
muc ac and muc | 7 |
our results show that | 7 |
divergent at the nucleotide | 7 |
cells in the absence | 7 |
hepatitis c virus infection | 7 |
to blunt the cytokine | 7 |
in patients with severe | 7 |
and h n iav | 7 |
virus hemagglutinin and neuraminidase | 7 |
of viral respiratory infections | 7 |
vivo and in vitro | 7 |
disease control and prevention | 7 |
of swine influenza in | 7 |
binding and membrane fusion | 7 |
hek cells were transfected | 7 |
of seasonal and pandemic | 7 |
the infectious diseases ward | 7 |
viruses and their replication | 7 |
detected by western blotting | 6 |
and na genes of | 6 |
are shown in figure | 6 |
of acute respiratory distress | 6 |
for the activation of | 6 |
these data suggest that | 6 |
the apical surface of | 6 |
of severe influenza in | 6 |
n highly pathogenic avian | 6 |
authors declare no competing | 6 |
pdm virus isolates were | 6 |
of the viral polymerase | 6 |
an avian h n | 6 |
g cell cycle arrest | 6 |
has been linked to | 6 |
can lead to the | 6 |
and h n in | 6 |
for efficient influenza virus | 6 |
decrease at lg ml | 6 |
viruses have been reported | 6 |
inhibition of influenza a | 6 |
severe influenza virus infection | 6 |
into the mitochondrial matrix | 6 |
host factors crucial for | 6 |
used to determine the | 6 |
from pig id at | 6 |
identifies human host factors | 6 |
added to each well | 6 |
promoter is associated with | 6 |
is dependent on the | 6 |
the extent to which | 6 |
influenza viruses isolated from | 6 |
highly pathogenic strains of | 6 |
to play a role | 6 |
the first evidence of | 6 |
type i interferon production | 6 |
cd t cells to | 6 |
expression was detected by | 6 |
in the airway epithelium | 6 |
of acute lung injury | 6 |
at weeks of age | 6 |
in the course of | 6 |
cd t cells also | 6 |
with the plasma membrane | 6 |
blocking the formation of | 6 |
mediated activation of the | 6 |
on the infectious diseases | 6 |
seroprevalence of h n | 6 |
were negative for the | 6 |
an increased ifitm signal | 6 |
iav h n infection | 6 |
infection with h n | 6 |
the h n viruses | 6 |
associated with influenza a | 6 |
has been proven to | 6 |
pathology of influenza virus | 6 |
of influenza virus replication | 6 |
has been found to | 6 |
no significant difference in | 6 |
and the expression of | 6 |
efficient influenza virus propagation | 6 |
the increased expression of | 6 |
type i interferon and | 6 |
isolated from pigs in | 6 |
lung surfactant protein d | 6 |
influenza a virus through | 6 |
human influenza a h | 6 |
protein expression was detected | 6 |
novel reassortant h n | 6 |
would like to thank | 6 |
outbreak of influenza a | 6 |
prevalence of iav in | 6 |
the nature of the | 6 |
ifitm restricts the morbidity | 6 |
injury induced by pr | 6 |
new world bats harbor | 6 |
apoptosis in human airway | 6 |
mediate cellular resistance to | 6 |
the nlrp inflammasome and | 6 |
may contribute to the | 6 |
leads to the activation | 6 |
and mortality associated with | 6 |
the survival rate of | 6 |
no effect on the | 6 |
rnai screen identifies human | 6 |
the ifitm proteins mediate | 6 |
as well as to | 6 |
factors crucial for influenza | 6 |
human alveolar epithelial cells | 6 |
by type i ifn | 6 |
for h at room | 6 |
strains of influenza a | 6 |
human respiratory syncytial virus | 6 |
the plasma membrane and | 6 |
the s r mutation | 6 |
expressed as the mean | 6 |
wide rnai screen identifies | 6 |
induction of innate immune | 6 |
susceptible to iav infection | 6 |
the production of infectious | 6 |
was detected by western | 6 |
infected with influenza a | 6 |
diverse influenza a viruses | 6 |
treatment of iav infection | 6 |
cd t cells following | 6 |
induced acute lung injury | 6 |
network data exchange sars | 6 |
induced lung injury and | 6 |
in an elementary school | 6 |
an overview of the | 6 |
virus entry by blocking | 6 |
we did not observe | 6 |
were included in the | 6 |
detected in swine sera | 6 |
and the united states | 6 |
the protective effect of | 6 |
h n highly pathogenic | 6 |
consensomes and hct intersection | 6 |
of fusion pores following | 6 |
the acute respiratory distress | 6 |
the influenza virus hemagglutinin | 6 |
shown to inhibit the | 6 |
pi k akt signaling | 6 |
sitosterol on the expression | 6 |
in response to viral | 6 |
evolution and ecology of | 6 |
hek t cells were | 6 |
were significantly dysregulated by | 6 |
it is believed that | 6 |
expression was determined by | 6 |
national institutes of health | 6 |
and were found to | 6 |
the expression of rig | 6 |
test was used to | 6 |
of influenza virus is | 6 |
in a and mdck | 6 |
of the respiratory tract | 6 |
the possible role of | 6 |
virus was reported in | 6 |
reassortment between avian and | 6 |
to the production of | 6 |
have no competing interests | 6 |
iav infection in mice | 6 |
entry into host cells | 6 |
ecology of influenza a | 6 |
was performed using a | 6 |
fusion pores following virus | 6 |
by focus formation assay | 6 |
of human and animal | 6 |
infected a cells were | 6 |
to the expression of | 6 |
in absence of oc | 6 |
chronic obstructive pulmonary disease | 6 |
id at week and | 6 |
an increasing number of | 6 |
virus isolated from pigs | 6 |
human host factors crucial | 6 |
comparative histopathology of mouse | 6 |
the induction of type | 6 |
were identified in the | 6 |
log decrease at lg | 6 |
receptor specificity of the | 6 |
swine influenza a viruses | 6 |
cd t cells that | 6 |
cd and cd t | 6 |
the total number of | 6 |
the antigenic sites of | 6 |
acute lung injury in | 6 |
the severity of the | 6 |
hemagglutinin and neuraminidase activities | 6 |
linear ubiquitin chain assembly | 6 |
pandemic a h n | 6 |
can also bind to | 6 |
carbohydrate recognition domain of | 6 |
in hospitalized children in | 6 |
screen identifies human host | 6 |
ifitm restricts influenza a | 6 |
and human h n | 6 |
and h n avian | 6 |
influenza other respir viruses | 6 |
risk of severe influenza | 6 |
n swine influenza viruses | 6 |
the expression of proinflammatory | 6 |
sialic acids on the | 6 |
influenza a virus blocks | 6 |
virus titers in the | 6 |
of human influenza viruses | 6 |
cells infected with pandemic | 6 |
of the plasma membrane | 6 |
h n and human | 6 |
h n dk variant | 6 |
the morbidity and mortality | 6 |
and severe acute respiratory | 6 |
infection of mice with | 6 |
were identified in swine | 6 |
human influenza viruses to | 6 |
declare no competing interests | 6 |
of swine h n | 6 |
novel influenza a virus | 6 |
induced by iav infection | 6 |
van de wetering et | 6 |
in the lung during | 6 |
relationship and antiviral effects | 6 |
seasonal and pandemic influenza | 6 |
cellular resistance to influenza | 6 |
a virus in mice | 6 |
the cells were lysed | 6 |
may be involved in | 6 |
virus at a moi | 6 |
the molecular basis of | 6 |
viral titers in the | 6 |
a virus entry by | 6 |
ifitm proteins mediate cellular | 6 |
read and approved the | 6 |
the antiviral effects of | 6 |
detected in swine in | 6 |
the nlrp inflammasome by | 6 |
the pandemic potential of | 6 |
histopathology of mouse models | 6 |
morbidity and mortality associated | 6 |
in the direction of | 6 |
is important for the | 6 |
the last two decades | 6 |
be explained by the | 6 |
n virus in swine | 6 |
inhibitor of apoptosis protein | 6 |
the pathology of influenza | 6 |
susceptibility to influenza a | 6 |
bind to sialic acid | 6 |
the expression of il | 6 |
as part of the | 6 |
washed and incubated with | 6 |
an increase in the | 6 |
of innate immune responses | 6 |
rna and dna viruses | 6 |
the adaptive immune response | 6 |
will be required to | 6 |
incubated for min at | 6 |
harbor diverse influenza a | 6 |
as well as their | 6 |
restricts the morbidity and | 6 |
in the peripheral blood | 6 |
the ifitm signal intensity | 6 |
as well as a | 6 |
hepatitis c virus p | 6 |
of mouse models of | 6 |
we were unable to | 6 |
have also been reported | 6 |
to the lack of | 6 |
by blocking the formation | 6 |
in response to the | 6 |
and antiviral effects of | 6 |
by both h n | 6 |
type ii transmembrane protein | 6 |
can be induced by | 6 |
atii cells and am | 6 |
of defective interfering particles | 6 |
these studies indicate that | 6 |
in figshare file f | 6 |
crucial for influenza virus | 6 |
is located in the | 6 |
host immune response to | 6 |
human transmission of avian | 6 |
de wetering et al | 6 |
h n viruses reported | 6 |
reassortant h n viruses | 6 |
is associated with severe | 6 |
pathogenic potential of interferon | 6 |
h at room temperature | 6 |
cd t cells from | 6 |
in combination with the | 6 |
from three independent experiments | 6 |
proteins mediate cellular resistance | 6 |
h n influenza pandemic | 6 |
and the number of | 6 |
of porcine reproductive and | 6 |
antibodies were detected in | 6 |
treated with curcumin derivatives | 6 |
vesicular stomatitis virus infection | 6 |
cells were maintained in | 6 |
a cells were transfected | 6 |
h n virus and | 6 |
cells are critical for | 6 |
in response to influenza | 6 |
no vac cha group | 6 |
influenza viruses have been | 6 |
eukaryotic translation initiation factor | 6 |
could be due to | 6 |
d is also able | 6 |
effect of h n | 6 |
and is able to | 6 |
pr virus at a | 6 |
in swine in the | 6 |
origin iav strains in | 6 |
a virus replication in | 6 |
cd t cells play | 6 |
and adaptive immune responses | 6 |
was added to each | 6 |
this is consistent with | 6 |
pathogenic avian influenza viruses | 6 |
reassortant h n influenza | 6 |
of iav h n | 6 |
pb e k mutation | 6 |
they have no competing | 6 |
are required for the | 6 |
prevention and control of | 6 |
influenza virus infection and | 6 |
the fact that the | 6 |
swabs and balf samples | 6 |
in line with the | 6 |
at the end of | 6 |
and approved the final | 6 |
was approved by the | 6 |
protects mice from lethal | 6 |
of influenza virus a | 6 |
a h n viruses | 6 |
may be able to | 6 |
play important roles in | 6 |
n virus antibodies in | 6 |
can also be used | 6 |
human to swine transmission | 6 |
a h n influenza | 6 |
and ecology of influenza | 6 |
world bats harbor diverse | 6 |
bats harbor diverse influenza | 6 |
in acute influenza infection | 6 |
we would like to | 6 |
ha and na on | 6 |
the heterologous aut com | 6 |
h n infection in | 6 |
to the initial binding | 6 |
response to influenza virus | 6 |
the fusion of the | 6 |
the human respiratory tract | 6 |
of viral infection and | 6 |
novel avian influenza a | 6 |
of recombinant influenza viruses | 6 |
of the viral and | 6 |
natural science foundation of | 6 |
authors read and approved | 6 |
divergent at the amino | 6 |
virus in swine in | 6 |
a key role in | 6 |
no vac cha pigs | 6 |
the emergence of new | 6 |
be due to the | 6 |
the uptake of fdx | 6 |
transport of influenza a | 6 |
shown in figure a | 6 |
a subset of the | 6 |
infected a cells at | 6 |
with the help of | 6 |
samples were collected from | 6 |
it is known that | 6 |
in the human population | 6 |
the h n dk | 6 |
of respiratory viral infections | 5 |
of reactive oxygen species | 5 |
with the exception of | 5 |
defense against influenza a | 5 |
an increased risk of | 5 |
the mitochondrial inner membrane | 5 |
at the indicated time | 5 |
of the haemagglutinin membrane | 5 |
the phosphorylation of stat | 5 |
n and human h | 5 |
h and h influenza | 5 |
target for antiviral therapy | 5 |
cells in the airways | 5 |
to be caused by | 5 |
and hepatitis c virus | 5 |
human and avian influenza | 5 |
followed by pr virus | 5 |
was used as the | 5 |
apoptosis in influenza virus | 5 |
genetic diversity of swine | 5 |
pkr and eif a | 5 |
replication of the iav | 5 |
h n virus which | 5 |
immune responses to influenza | 5 |
consistent with previous reports | 5 |
iav strains in the | 5 |
of the m protein | 5 |
linkages abundantly present on | 5 |
not included in the | 5 |
determined by western blotting | 5 |
id at weeks and | 5 |
in a range of | 5 |
c motif chemokine ligand | 5 |
the cytoplasmic tail of | 5 |
respiratory tract infection in | 5 |
use of laboratory animals | 5 |
acute lower respiratory tract | 5 |
amino acid change in | 5 |
the emergence of novel | 5 |
the activation of pi | 5 |
influenza a virus h | 5 |
airway epithelial cells and | 5 |
of the iav infection | 5 |
of pulmonary surfactant protein | 5 |
the results of a | 5 |
respiratory syndrome coronavirus spike | 5 |
the type i ifn | 5 |
type a influenza virus | 5 |
on the susceptibility of | 5 |
cells infected with pr | 5 |
in swine sera samples | 5 |
infection in a cells | 5 |
inhibits influenza a virus | 5 |
viruses from pigs in | 5 |
of a cells with | 5 |
the potential use of | 5 |
is essential for the | 5 |
the haemagglutinin membrane glycoprotein | 5 |
similarly as described previously | 5 |
an alternative entry pathway | 5 |
targeting ha of iavs | 5 |
human influenza a virus | 5 |
distinct lineage of influenza | 5 |
intracellular m ion channel | 5 |
a cells transfected with | 5 |
to protect mice from | 5 |
used to assess statistical | 5 |
shown in figure b | 5 |
are responsible for the | 5 |
recent studies have shown | 5 |
the pb e k | 5 |
nuclear export of viral | 5 |
curcumin derivatives and neuraminidase | 5 |
in a model of | 5 |
the effective replication of | 5 |
avian influenza virus h | 5 |
with fetal bovine serum | 5 |
by neutrophils and macrophages | 5 |
is considered to be | 5 |
study was supported by | 5 |
either rsv or iav | 5 |
in the promoter region | 5 |
and acute lung injury | 5 |
activates inflammasomes via its | 5 |
influenza a puerto rico | 5 |
infected as well as | 5 |
avian h n iavs | 5 |
is associated with high | 5 |
of influenza h n | 5 |
influenza virus at a | 5 |
ubiquitin chain assembly complex | 5 |
in the guinea pig | 5 |
mouse model of influenza | 5 |
swine influenza virus from | 5 |
influenza a virus surveillance | 5 |
viral load and hypercytokinemia | 5 |
at a density of | 5 |
antiviral activity of dips | 5 |
associated with severe iav | 5 |
type i interferons in | 5 |
type i interferon induction | 5 |
been demonstrated to be | 5 |
like h n virus | 5 |
in the extranuclear space | 5 |
with h n and | 5 |
the mechanism of ifitm | 5 |
into the host cell | 5 |
by the lack of | 5 |
in the formation of | 5 |
after treatment with pa | 5 |
associated with susceptibility to | 5 |
influenza a virus influenza | 5 |
compared to a cells | 5 |
to acute respiratory distress | 5 |
transmission of iav was | 5 |
or in pbs containing | 5 |
the replication of multiple | 5 |
time pcr and normalised | 5 |
different time points after | 5 |
t cells were transfected | 5 |
and avian influenza viruses | 5 |
severe influenza in humans | 5 |
h n pdm infection | 5 |
virus infections in swine | 5 |
of the adaptive immune | 5 |
at h and h | 5 |
over the course of | 5 |
report of h n | 5 |
of iav and ibv | 5 |
with risk of severe | 5 |
pathogenesis of avian influenza | 5 |
of the epidemiology of | 5 |
the primary site of | 5 |
n influenza a epidemic | 5 |
viral infection in mice | 5 |
associated with high viral | 5 |
respiratory syndrome coronavirus envelope | 5 |
were washed and incubated | 5 |
between curcumin derivatives and | 5 |
and evolution of influenza | 5 |
to an increase in | 5 |
context of viral infection | 5 |
t cells to the | 5 |
antiviral activity of ifitm | 5 |
between avian and swine | 5 |
mice infected with a | 5 |
the hemagglutinin of influenza | 5 |
haemagglutinin membrane glycoprotein of | 5 |
in swine at agricultural | 5 |
human lung epithelial cells | 5 |
activation of dendritic cells | 5 |
immune response to iav | 5 |
at least one pathogen | 5 |
influenza viruses in mice | 5 |
wdnhbe cells infected with | 5 |
the absence of standard | 5 |
interaction between iav and | 5 |
in the bronchoalveolar lavage | 5 |
a viruses isolated from | 5 |
or absence of the | 5 |
resident memory t cells | 5 |
pr virus for h | 5 |
a virus in wild | 5 |
pdm and h n | 5 |
induced by influenza a | 5 |
expression of proinflammatory cytokines | 5 |
the bronchoalveolar lavage fluid | 5 |
in addition to its | 5 |
and the formation of | 5 |
in health and disease | 5 |
in the sars consensome | 5 |
the cells were then | 5 |
swine influenza viruses in | 5 |
infection influenza a virus | 5 |
cd domain of ifitm | 5 |
biology of influenza viruses | 5 |
with high viral load | 5 |
a cells were treated | 5 |
genome sequence of a | 5 |
virus infection in vitro | 5 |
origin h n viruses | 5 |
viruses were reported in | 5 |
virus and dengue virus | 5 |
characterization of influenza virus | 5 |
in the last two | 5 |
by h n infection | 5 |
are involved in the | 5 |
alveolar epithelial cell injury | 5 |
as a receptor for | 5 |
of an influenza a | 5 |
an important determinant of | 5 |
pigs sampled between week | 5 |
was not observed in | 5 |
due to the presence | 5 |
phosphorylation of stat tyr | 5 |
system for production of | 5 |
virus in wild birds | 5 |
and hrv were the | 5 |
t cell responses in | 5 |
as well as of | 5 |
of natural killer cells | 5 |
strain of h n | 5 |
a respiratory disease outbreak | 5 |
that memory cd t | 5 |
the ha protein of | 5 |
epithelial cells of the | 5 |
effective replication of the | 5 |
by memory cd t | 5 |
used for the detection | 5 |
in the lung following | 5 |
innate immune responses to | 5 |
evolutionary genomics of the | 5 |
generation of influenza a | 5 |
carried out as described | 5 |
is the first report | 5 |
virus m ion channel | 5 |
infection with influenza a | 5 |
due to the lack | 5 |
in the viral genome | 5 |
n virus was isolated | 5 |
a virus from bats | 5 |
the inhibition of iav | 5 |
an h n virus | 5 |
of the ketogenic diet | 5 |
virus infection of mice | 5 |
of innate immune response | 5 |
to the emergence of | 5 |
the context of the | 5 |
as we previously described | 5 |
between week and week | 5 |
and function of the | 5 |
are in agreement with | 5 |
iav in swine in | 5 |
the antiviral activities of | 5 |
be one of the | 5 |
also involved in the | 5 |
lineage of influenza a | 5 |
infection of human cells | 5 |
the cells were treated | 5 |
can be used for | 5 |
of acute respiratory viral | 5 |
a virus h n | 5 |
to cd t cells | 5 |
alveolar epithelial cells and | 5 |
number of iav positive | 5 |
sampled between week and | 5 |
in mouse models of | 5 |
for middle east respiratory | 5 |
of programmed cell death | 5 |
a h n pdm | 5 |
infection with influenza virus | 5 |
nuclear export of vrnp | 5 |
is also known to | 5 |
protein induces apoptosis in | 5 |
of seasonal influenza a | 5 |
a reassortant h n | 5 |
to the influenza virus | 5 |
the case of iav | 5 |
a past exposure of | 5 |
high levels of gm | 5 |
in the mbl gene | 5 |
vac no cha pigs | 5 |
absence of standard virus | 5 |
influenza a viruses isolated | 5 |
akt and erk mapk | 5 |
infection of pigs with | 5 |
between bat and conventional | 5 |
inflammasomes via its intracellular | 5 |
as a positive control | 5 |
between cov infection and | 5 |
and na on the | 5 |
the development of live | 5 |
a number of studies | 5 |
amino acid sequences of | 5 |
and a decrease in | 5 |
the response to cov | 5 |
to a lesser extent | 5 |
in embryonated chicken eggs | 5 |
influenza virus infection by | 5 |
and swine influenza viruses | 5 |
influenza a virus transmission | 5 |
it is not clear | 5 |
all authors read and | 5 |
were negative for iav | 5 |
following respiratory virus infections | 5 |
antigenic structure of the | 5 |
single nucleotide polymorphisms in | 5 |
ha of the h | 5 |
influenza viruses in the | 5 |
the ability of the | 5 |
the influenza virus nucleoprotein | 5 |
of iav in the | 5 |
pandemic h n and | 5 |
for the induction of | 5 |
the creative commons attribution | 5 |
ifitm promoter is associated | 5 |
adnrf followed by pr | 5 |
in this study we | 5 |
virus infection results in | 5 |
activation of pi k | 5 |
human nasal epithelial cells | 5 |
the supernatants of a | 5 |
the influenza virus genome | 5 |
its intracellular m ion | 5 |
in control and ifitm | 5 |
in pbs containing fcs | 5 |
and use of laboratory | 5 |
iav infection has been | 5 |
in the control group | 5 |
origins and evolutionary genomics | 5 |
to test this hypothesis | 5 |
supernatants of a cells | 5 |
in respiratory virus infections | 5 |
cationic host defence peptides | 5 |
surfactant protein a binds | 5 |
was reported from a | 5 |
is essential for efficient | 5 |
influence of curcumin derivatives | 5 |
t cells play a | 5 |
binding of surfactant protein | 5 |
fatal outcome of human | 5 |
the protective effects of | 5 |
cell pr virus for | 5 |
pandemic influenza a viruses | 5 |
to induce apoptosis in | 5 |
a swine farm in | 5 |
human host factors required | 5 |
the promoter region of | 5 |
influenza virus replication by | 5 |
role of ap m | 5 |
a significant increase in | 5 |
outcome of human influenza | 5 |
increase the expression of | 5 |
a cells at different | 5 |
iav replication in vitro | 5 |
with a pr at | 5 |
n virus antibodies were | 5 |
in the blood of | 5 |
mice were infected with | 5 |
k akt and erk | 5 |
are more likely to | 5 |
was observed in the | 5 |
the absence of iav | 5 |
cells such as macrophages | 5 |
presence of fcs and | 5 |
is not required for | 5 |
in bronchoalveolar lavage fluid | 5 |
by any of the | 5 |
pi k akt and | 5 |
for influenza a viruses | 5 |
in the lung tissues | 5 |
an essential role in | 5 |
characterization of the human | 5 |
and vesicular stomatitis virus | 5 |
patients with h n | 5 |
lung epithelial a cells | 5 |
avian influenza virus in | 5 |
care and use of | 5 |
infection was shown to | 5 |
the ic activity of | 5 |
the lectin complement pathway | 5 |
as a ratio to | 5 |
of iav positive swine | 5 |
was found in the | 5 |
pneumonia symptoms in iav | 5 |
characterization of influenza a | 5 |
of the virus and | 5 |
in the human lung | 5 |
an innate immune response | 5 |
was isolated from the | 5 |
with avian and human | 5 |
host factors required for | 5 |
herpes simplex virus type | 5 |
and evolutionary genomics of | 5 |
the size of the | 5 |
genetic characterization of h | 5 |
involved in iav replication | 5 |
ns protein induces apoptosis | 5 |
at the ifitm promoter | 5 |
a pivotal role in | 5 |
high viral load and | 5 |
trail and sfas ligand | 5 |
between human and swine | 5 |
it is worth noting | 5 |
nlrp inflammasome activation in | 5 |
t cells are critical | 5 |
it was shown that | 5 |
in vivo and in | 5 |
syndrome coronavirus envelope protein | 5 |
two tailed paired students | 5 |
of the viral infection | 5 |
virus infection dynamics in | 5 |
as an alternative entry | 5 |
is closely related to | 5 |
also been associated with | 5 |
shown to decrease the | 5 |
virus activates inflammasomes via | 5 |
protein ion channel activity | 5 |
to assess statistical significance | 5 |
could be used to | 5 |
the inhibition of rig | 5 |
is worth noting that | 5 |
the ifitm promoter is | 5 |
via its intracellular m | 5 |
in cell culture and | 5 |
is required for efficient | 5 |
also been reported to | 5 |
the potential to be | 5 |
pig id at weeks | 5 |
during the course of | 5 |
the expression of ifitm | 5 |
a and d in | 5 |
are one of the | 5 |
macrophages and dendritic cells | 5 |
the viral life cycle | 5 |
of growth factor receptor | 5 |
a novel interaction between | 5 |
cells were pretreated with | 5 |
been shown to induce | 5 |
might be due to | 5 |
moi of pfu cell | 5 |
g g cell cycle | 5 |
performed as previously described | 5 |
on the pathogenesis of | 5 |
approved the final manuscript | 5 |
restrict the replication of | 5 |
pigs from no vac | 5 |
against h n influenza | 5 |
a key regulator of | 5 |
a negative regulator of | 5 |
susceptible to infection with | 5 |
cd t cells can | 5 |
tailed paired students t | 5 |
any of the h | 5 |
in response to sars | 5 |
inducing the expression of | 5 |
roles in the response | 5 |
the severe acute respiratory | 5 |
factors required for influenza | 5 |
in the influenza virus | 5 |
are recruited to the | 5 |
for h prior to | 5 |
through the inhibition of | 5 |
for the emergence of | 5 |
as a model for | 5 |
the pi k akt | 5 |
at weeks and were | 5 |
this study was supported | 5 |
in host defense against | 5 |
the hemagglutinin and neuraminidase | 5 |
production of defective interfering | 5 |
and erk mapk signaling | 5 |
airway epithelium in vitro | 5 |
influenza virus a pr | 5 |
distributed under the terms | 5 |
induction of proinflammatory cytokines | 5 |
under the age of | 5 |
primary human airway epithelial | 5 |
the first months of | 5 |
pcr and normalised to | 5 |
infected with pandemic iav | 5 |
of the nrf pathway | 5 |
involved in the anti | 5 |
virus isolates were reported | 5 |
against influenza a viruses | 5 |
for each of the | 5 |
viruses isolated from pigs | 5 |
such as iav and | 5 |
than years of age | 5 |
that the presence of | 5 |
to increase the expression | 5 |
associated with risk of | 5 |
vaccines for use in | 5 |
the biology of influenza | 5 |
our data showed that | 5 |
protection against h n | 5 |
including inhibition of the | 5 |
of influenza virus and | 5 |
from pigs sampled between | 5 |
in dmem supplemented with | 5 |
were washed twice with | 5 |
the inhibition of the | 5 |
has been suggested to | 5 |
was reported in swine | 5 |
are included in the | 5 |
of the creative commons | 5 |
in response to h | 5 |
cells were grown in | 5 |
of h n swine | 5 |
activity relationship and antiviral | 5 |
with severe influenza in | 5 |
from march to may | 5 |
avian influenza virus a | 5 |
cells at different time | 5 |
by cd t cells | 5 |
was carried out as | 5 |
viral and endosomal membranes | 5 |
in swine in china | 5 |
influenza a virus infected | 5 |
the viral replication cycle | 5 |
in the production of | 5 |
in iav infected mice | 5 |
based swine farm in | 5 |
the inhibitory effects of | 5 |
of human influenza virus | 5 |
in order to determine | 5 |
have been reported from | 5 |
to inhibit replication of | 5 |
glycoprotein of influenza c | 5 |
a novel influenza a | 5 |
h n pdm on | 5 |
of influenza virus ns | 5 |
recent study showed that | 5 |
influenza viruses circulating in | 5 |
have also been shown | 5 |
b on iav infection | 5 |
antibodies against h n | 5 |
the ifitm expression was | 5 |
of the virus with | 5 |
the effect of iav | 5 |
with pr virus at | 5 |
data are presented as | 5 |
a gift from dr | 5 |
virus at a resolution | 5 |
was performed as previously | 5 |
organization of ha and | 5 |
type i ifn response | 5 |
ha of h n | 5 |
on the plasma membrane | 5 |
strain of influenza a | 5 |
a distinct lineage of | 5 |
of na on the | 5 |
pulmonary surfactant protein d | 5 |
immunity against iav infection | 5 |
of the host cell | 5 |
genomics of the swine | 5 |
erk mapk signaling pathways | 5 |
the cd domain of | 5 |
antigenic drift and shift | 5 |
viruses using reverse genetics | 5 |
isolates were retrieved from | 5 |
results suggest that the | 5 |
in presence of oc | 5 |
of proinflammatory cytokines in | 5 |
avian and swine influenza | 5 |
due to the low | 5 |
induced by highly pathogenic | 5 |
influenza virus activates inflammasomes | 5 |
and h n pdm | 5 |
cells were then infected | 5 |
in cells treated with | 5 |
have not been identified | 5 |
as an opsonin for | 4 |
a is also able | 4 |
mortality from iav infection | 4 |
to be closely related | 4 |
ifitm proteins restrict viral | 4 |
in the viral membrane | 4 |
type ii cells and | 4 |
supplemented with fetal bovine | 4 |
h n virus were | 4 |
avian and swine iav | 4 |
impact of cov infection | 4 |
cells lacking a strong | 4 |
to middle east respiratory | 4 |
of ifitm is required | 4 |
a virus infections in | 4 |
involved in activation of | 4 |
reduced lung viral titers | 4 |
immune response and the | 4 |
confluent mdck cells were | 4 |
from pigs sampled at | 4 |
to be critical in | 4 |
of the use of | 4 |
sections were incubated with | 4 |
reassortant h n swine | 4 |
enhanced type i ifn | 4 |
in a human lung | 4 |
the concerted action of | 4 |
the uninfected a cells | 4 |
number of infected cells | 4 |
for iav h n | 4 |
under the terms and | 4 |
ifitm clustering at vesicular | 4 |
role of cd t | 4 |
ifn trail signaling axis | 4 |
factors associated with influenza | 4 |
gene segments from the | 4 |
role in innate immunity | 4 |
a specific inhibitor of | 4 |
severity and prognosis of | 4 |
pdm virus was reported | 4 |
it is conceivable that | 4 |
influenza a penetrates host | 4 |
also contribute to the | 4 |
the indicated concentration of | 4 |
update on the susceptibility | 4 |
the location of the | 4 |
of viral m protein | 4 |
a virus replication by | 4 |
small airway epithelial cells | 4 |
intranasal administration of pa | 4 |
a more recent study | 4 |
in the levels of | 4 |
the avian influenza virus | 4 |
followed by cycles of | 4 |
in severe influenza virus | 4 |
in a manner that | 4 |
were positive for the | 4 |
from a swine in | 4 |
epithelial to mesenchymal transition | 4 |
pulmonary hypersensitivity induced by | 4 |
they can also be | 4 |
the absence or presence | 4 |
first report of h | 4 |
research has shown that | 4 |
to infection with iav | 4 |
pigs in the laiv | 4 |
infected with respiratory syncytial | 4 |
a crucial role in | 4 |
swine was documented during | 4 |
group infected with iav | 4 |
syncytial virus infection in | 4 |
binding at the ifitm | 4 |
the binding of influenza | 4 |
of novel treatment strategies | 4 |
animal and public health | 4 |
in hospitalized children with | 4 |
in mice critical role | 4 |
influenza a virus inhibits | 4 |
the basis of the | 4 |
sow and nursery sites | 4 |
and critical care medicine | 4 |
in response to infection | 4 |
of high levels of | 4 |
in the mitochondrial matrix | 4 |
the emergence of the | 4 |
a swine h n | 4 |
isolates were reported in | 4 |
of hepatitis b virus | 4 |
inhibits the activation of | 4 |
were upregulated by pr | 4 |
plays a key role | 4 |
role of the nlrp | 4 |
avian and human type | 4 |
to bind to the | 4 |
and conditions of the | 4 |
and genome uncoating are | 4 |
procedures were approved by | 4 |
medium was replaced with | 4 |
of double or triple | 4 |
been associated with the | 4 |
of the human genome | 4 |
infection of influenza a | 4 |
to h n virus | 4 |
in this study was | 4 |
of acute lower respiratory | 4 |
opsonin for influenza a | 4 |
the level of the | 4 |
the studies conducted in | 4 |
terms and conditions of | 4 |
np and hsp in | 4 |
had the highest sequence | 4 |
after a respiratory disease | 4 |
of p ipk from | 4 |
the results of the | 4 |
for the effective replication | 4 |
in this article are | 4 |
in the ifitm signal | 4 |
of the viral envelope | 4 |
vaccines need to be | 4 |
influenza a virus endocytic | 4 |
were found seropositive for | 4 |
treatment of influenza viral | 4 |
were shown to bind | 4 |
and swine influenza a | 4 |
immune responses such as | 4 |
for use in the | 4 |
initial virus binding rate | 4 |
in the nuclear export | 4 |
of influenza b viruses | 4 |
ifitms restrict the replication | 4 |
the group infected with | 4 |
can be infected with | 4 |
a virus endocytic routes | 4 |
the ifn trail signaling | 4 |
c is associated with | 4 |
viruses such as iav | 4 |
in addition to iav | 4 |
neuraminidase of influenza virus | 4 |
for apoptosis induction on | 4 |
the course of iav | 4 |
antiviral effector ifitm disrupts | 4 |
the laiv treatment groups | 4 |
adnrf followed by infection | 4 |
swine influenza virus isolated | 4 |
susceptibility of human influenza | 4 |
p ipk from hsp | 4 |
the case of the | 4 |
were infected with h | 4 |
influenza virus infection is | 4 |
the development of influenza | 4 |
t cell responses against | 4 |
the immune response against | 4 |
with the severity of | 4 |
infection in vitro and | 4 |
to the effects of | 4 |
periphery of the lobes | 4 |
on the basis of | 4 |
iav h n and | 4 |
in the globular head | 4 |
rsv or iav infection | 4 |
contribution of na to | 4 |
in both ams and | 4 |
consent was obtained from | 4 |
with h n virus | 4 |
the h n subtype | 4 |
in both mice and | 4 |
and epidemiological characteristics of | 4 |
tumor necrosis factor receptor | 4 |
virus from eight plasmids | 4 |
infection of a cells | 4 |
impact of influenza on | 4 |
proteins were upregulated by | 4 |
fusion and genome uncoating | 4 |
acute respiratory infections in | 4 |
on the presence of | 4 |
to its inhibition of | 4 |
the lack of a | 4 |
disruption of ctcf binding | 4 |
metabolic state of the | 4 |
shown to induce the | 4 |
d can also bind | 4 |
identity to a swine | 4 |
the avian iav strains | 4 |
in the uninfected a | 4 |
and sfas ligand levels | 4 |
of cleaved sialic acid | 4 |
of the influenza viruses | 4 |
to the development of | 4 |
the presence of iav | 4 |
characterization of an h | 4 |
the sow and nursery | 4 |
of cov infection on | 4 |
mice infected with respiratory | 4 |
contributes to severe pathophysiology | 4 |
with a novel avian | 4 |
with type i ifn | 4 |
be caused by the | 4 |
in mice treated with | 4 |
been shown to possess | 4 |
highest number of iav | 4 |
is strongly dependent on | 4 |
science foundation of china | 4 |
acid change in the | 4 |
polymorphisms in the mbl | 4 |
which is activated by | 4 |
reassortant iav strains in | 4 |
reproduction in any medium | 4 |
respiratory tract infections in | 4 |
the structural and functional | 4 |
cell infection with adnrf | 4 |
been shown to stimulate | 4 |
express high levels of | 4 |
it is important to | 4 |
the pathogenesis of avian | 4 |
before being stimulated with | 4 |
influenza virus hemagglutinin to | 4 |
analyzed the effect of | 4 |
nlrp inflammasome by iav | 4 |
generation and characterization of | 4 |
firefly luciferase activity was | 4 |
cells and atii cells | 4 |
virus assembly and budding | 4 |
of equine influenza virus | 4 |
the impact of cov | 4 |
acid sequences of the | 4 |
led to a significant | 4 |
and luciferase activity was | 4 |
of airborne influenza virus | 4 |
the level of ifitm | 4 |
in the viral replication | 4 |
the hepatitis c virus | 4 |
clustering at vesicular structures | 4 |
in an attempt to | 4 |
the adaptive immune system | 4 |
national natural science foundation | 4 |
had no role in | 4 |
the pigs in the | 4 |
of patients with severe | 4 |
which is essential for | 4 |
in the ifitm expression | 4 |
to recognise and bind | 4 |
h influenza virus isolates | 4 |
a binds to the | 4 |
of the a cells | 4 |
bat influenza a viruses | 4 |
against injury induced by | 4 |
stimulated by viroporin ion | 4 |
cd memory t cells | 4 |
time point of examination | 4 |
assay for rapid screening | 4 |
canine kidney cell line | 4 |
weight loss and mortality | 4 |
risk allele associated with | 4 |
influenza virus hemagglutinin and | 4 |
viruses with pandemic potential | 4 |
nuclear export of the | 4 |
five active curcumin derivatives | 4 |
similar results were obtained | 4 |
mouse model of infection | 4 |
or in the presence | 4 |
acids in cell culture | 4 |
a recent study showed | 4 |
at the concentrations of | 4 |
in the spp knowledgebase | 4 |
its ability to inhibit | 4 |
of influenza virus by | 4 |
pigs in laiv none | 4 |
to block viral entry | 4 |
with curcumin derivatives at | 4 |
for at least one | 4 |
influenza h n viruses | 4 |
human infection with a | 4 |
understanding of the epidemiology | 4 |
the hexosamine biosynthesis pathway | 4 |
the cells were transfected | 4 |
and antigenic diversity of | 4 |
cell responses against influenza | 4 |
a risk factor for | 4 |
in one out of | 4 |
influenza virus activity in | 4 |
american journal of respiratory | 4 |
alveolar type ii epithelial | 4 |
infection with a novel | 4 |
like swine h n | 4 |
autophagosome fusion with lysosomes | 4 |
be used as a | 4 |
inhibits influenza virus replication | 4 |
killed approximately two million | 4 |
a virus m ion | 4 |
in alveolar epithelial cells | 4 |
from lethal h n | 4 |
the expression level of | 4 |
plays a role in | 4 |
cd t cells provide | 4 |
the antiviral effector ifitm | 4 |
protein of iav is | 4 |
influenza a virus neuraminidase | 4 |
cellular networks involved in | 4 |
the highly pathogenic h | 4 |
the m segment of | 4 |
porcine respiratory disease complex | 4 |
protein a binds to | 4 |
epithelial cells infected with | 4 |
evidence of avian influenza | 4 |
a virus blocks autophagosome | 4 |
by grants from the | 4 |
uncoating are required for | 4 |
need to be reformulated | 4 |
infection has also been | 4 |
in the defense against | 4 |
way anova followed by | 4 |
supernatants were collected and | 4 |
are known to be | 4 |
responses against influenza virus | 4 |
no increase in the | 4 |
the first time that | 4 |
influenza a virus by | 4 |
the transcriptional response to | 4 |
involved in the activation | 4 |
course of iav infection | 4 |
in the generation of | 4 |
an interacting partner of | 4 |
obtained using the geneoverlap | 4 |
m ion channel activity | 4 |
replication of middle east | 4 |
in this context are | 4 |
upper respiratory tracts of | 4 |
can bind to the | 4 |
is assumed for z | 4 |
of the ha and | 4 |
demonstrated that overexpression of | 4 |
primary antibody and alexa | 4 |
associated with an increased | 4 |
the collagen region of | 4 |
of the presence of | 4 |
interferon alphabeta in acute | 4 |
pigs in the wiv | 4 |
collected from children years | 4 |
infection prevention and control | 4 |
may be used to | 4 |
of the lung and | 4 |
dependent on the lipid | 4 |
and alveolar epithelial cells | 4 |
was not able to | 4 |
cells during infection with | 4 |
nucleoprotein of influenza a | 4 |
epithelial cells and macrophages | 4 |
restrict viral membrane hemifusion | 4 |
cleavage of sialic acid | 4 |
in pregnant women is | 4 |
and european h n | 4 |
alphabeta in acute influenza | 4 |
such as the h | 4 |
proteins restrict viral membrane | 4 |
infect a wide range | 4 |
the vrna packaging signals | 4 |
h and h subtypes | 4 |
effects of type i | 4 |
ha and na are | 4 |
the release of inflammatory | 4 |
viruses circulating in humans | 4 |
is supported by a | 4 |
expressed as a ratio | 4 |
iav strains of h | 4 |
lung epithelial apoptosis in | 4 |
all the ha sequences | 4 |
first report of a | 4 |
in immunity to iav | 4 |
proinflammatory cytokine production in | 4 |
a high seroprevalence of | 4 |
nrf sirna followed by | 4 |
influenza a virus nuclear | 4 |
hemagglutinin of influenza a | 4 |
fig a and fig | 4 |
detection of influenza viruses | 4 |
treatment of iav infections | 4 |
was used to determine | 4 |
in swine populations of | 4 |
the expression of np | 4 |
spatial organization of ha | 4 |
statistically significant risk factor | 4 |
facilitate the emergence of | 4 |
linked inhibitor of apoptosis | 4 |
high levels of cd | 4 |
and h n are | 4 |
release of viral particles | 4 |
with disease severity in | 4 |
may be due to | 4 |
similar trends to apical | 4 |
a a a a | 4 |
entry of influenza a | 4 |
alexa conjugated secondary antibody | 4 |
host factors involved in | 4 |
influenza viruses target different | 4 |
from those in the | 4 |
evidence for a role | 4 |
of viral infections in | 4 |
found that pr virus | 4 |
the terms and conditions | 4 |
up to h p | 4 |
may lead to a | 4 |
effect on the expression | 4 |
associated death domain protein | 4 |
and p mapk signaling | 4 |
as an interacting partner | 4 |
known to interact with | 4 |
in the iav group | 4 |
outbreak of swine influenza | 4 |
influenza viruses during viral | 4 |
with pr virus decreased | 4 |
the nrf pathway in | 4 |
mice were randomly divided | 4 |
influenza research and surveillance | 4 |
the potential of a | 4 |
the airway epithelium was | 4 |
in the human airway | 4 |
of invasive pulmonary aspergillosis | 4 |
of seasonal influenza vaccines | 4 |
that the h n | 4 |
it is estimated that | 4 |
macropinocytosis as an alternative | 4 |
respiratory syncytial virus subtype | 4 |
over a h period | 4 |
d can bind to | 4 |
influenza type b virus | 4 |
forms of cell death | 4 |
was determined by tcid | 4 |
increases susceptibility to secondary | 4 |
institutional animal care and | 4 |
determine the effects of | 4 |
proportion of the population | 4 |
in the central seven | 4 |
influenza virus due to | 4 |
a high mutation rate | 4 |
the h n strain | 4 |
as a target for | 4 |
were collected from children | 4 |
sirna followed by infection | 4 |
examined the effect of | 4 |
as a function of | 4 |
the pandemic influenza virus | 4 |
ctcf binding at the | 4 |
the neuraminidase of influenza | 4 |
host mucus by cleaving | 4 |
rna polymerase i promoter | 4 |
of ctcf binding at | 4 |
the master regulator of | 4 |
detrimental to the host | 4 |
of influenza virus rna | 4 |
a weak ifitm signal | 4 |
pigs in southern china | 4 |
sequence identity to a | 4 |
better understanding of the | 4 |
the globular head of | 4 |
along the length of | 4 |
sialic acids with neuraminidase | 4 |
virus in swine at | 4 |
ifitm disrupts intracellular cholesterol | 4 |
of the pandemic influenza | 4 |
were randomly divided into | 4 |
diet was shown to | 4 |
blocks autophagosome fusion with | 4 |
an h n influenza | 4 |
the severity of pandemic | 4 |
reported in chinese swine | 4 |
it is hypothesized that | 4 |
in influenza virus pneumonia | 4 |
avian influenza virus infection | 4 |
was isolated from a | 4 |
at uc for min | 4 |
a highly pathogenic h | 4 |
the detection of iav | 4 |
the cells were harvested | 4 |
inflammasome by iav virulence | 4 |
influenza a virus date | 4 |
virus isolates were retrieved | 4 |
as described in the | 4 |
ketogenic diet activates protective | 4 |
the determination of the | 4 |
penetrates host mucus by | 4 |
t cell responses to | 4 |
may be responsible for | 4 |
ifitm is required for | 4 |
activation in response to | 4 |
a virus genomic rna | 4 |
detection and isolation of | 4 |
journal of respiratory and | 4 |
of nlrp inflammasome activation | 4 |
influenza viruses to neuraminidase | 4 |
between avian and human | 4 |
is released from the | 4 |
in these primary cells | 4 |
influenza vaccine virus selection | 4 |
the interaction between respiratory | 4 |
to influenza a infection | 4 |
like cells and atii | 4 |
is a determinant of | 4 |
of the host immune | 4 |
of iav in pigs | 4 |
with h n iav | 4 |
the innate and adaptive | 4 |
apparently healthy swine in | 4 |
of the antiviral protein | 4 |
studies have also shown | 4 |
younger than years of | 4 |
these studies suggest that | 4 |
mediated inhibition of iav | 4 |
or h n subtypes | 4 |
strongly dependent on the | 4 |
that this effect is | 4 |
the amplitude of the | 4 |
using the geneoverlap analysis | 4 |
in upper respiratory tract | 4 |
the antiviral properties of | 4 |
of cd t lymphocytes | 4 |
at one of the | 4 |
of curcumin derivatives on | 4 |
at h post transfection | 4 |
in different cell types | 4 |
in each of the | 4 |
the seasonal influenza virus | 4 |
at least two different | 4 |
of the ns protein | 4 |
to the site of | 4 |
of influenza and other | 4 |
the distribution of the | 4 |
host immune response is | 4 |
is proportional to the | 4 |
involved in the influenza | 4 |
dimensional structure of the | 4 |
limited understanding of the | 4 |
which appeared to have | 4 |
have been demonstrated to | 4 |
protection against influenza virus | 4 |
pathogenesis of influenza a | 4 |
emergence of influenza a | 4 |
in type i interferon | 4 |
h n virus having | 4 |
a major role in | 4 |
time points after infection | 4 |
the capacity of the | 4 |
with iav before being | 4 |
which is known to | 4 |
fcs and mm dynasore | 4 |
global update on the | 4 |
a decrease in the | 4 |
influenza virus life cycle | 4 |
in immune response to | 4 |
compared with the control | 4 |
decrease the expression of | 4 |
avian and human influenza | 4 |
pa may be able | 4 |
with pandemic influenza a | 4 |
conditions of the creative | 4 |
animal and human health | 4 |
a and b virus | 4 |
a cells were pretreated | 4 |
and genetic characterization of | 4 |
sialic acid on the | 4 |
highest sequence identity to | 4 |
macrophages and neutrophils in | 4 |
detected in swine samples | 4 |
and porcine reproductive and | 4 |
h n and avian | 4 |
determined by tcid assay | 4 |
n and pandemic h | 4 |
cells infected with influenza | 4 |
cd t cell subsets | 4 |
the cleavage of sialic | 4 |
related to its inhibition | 4 |
respiratory and critical care | 4 |
in pigs in the | 4 |
in influenza virus infected | 4 |
ha and na in | 4 |
viruses the role of | 4 |
rna viruses such as | 4 |
of the hemagglutinin and | 4 |
influenza virus avian influenza | 4 |
have shown that the | 4 |
influenza viruses from swine | 4 |
iav replication through the | 4 |
inhibits the function of | 4 |
a vital role in | 4 |
in the first round | 4 |
a virus surveillance in | 4 |
type i ifn induction | 4 |
n influenza virus by | 4 |
were shown to be | 4 |
identified in this study | 4 |
in cells transfected with | 4 |
mediated disruption of ctcf | 4 |
avian and human iav | 4 |
article is an open | 4 |
sampled at week and | 4 |
did not result in | 4 |
research is needed to | 4 |
positive for at least | 4 |
lethal influenza virus challenge | 4 |
pig id sampled at | 4 |
shown to be a | 4 |
virus endocytic routes reveals | 4 |
pigs sampled at week | 4 |
surfactant protein d and | 4 |
and pandemic influenza a | 4 |
african green monkey kidney | 4 |
the replication cycle of | 4 |
was found to have | 4 |
the activity of na | 4 |
and four h n | 4 |
four h n viruses | 4 |
viruses to neuraminidase inhibitors | 4 |
respiratory disease outbreak in | 4 |
both the upper and | 4 |
for the pathogenesis of | 4 |
is an open access | 4 |
specific intercellular adhesion molecule | 4 |
homeostasis to block viral | 4 |
and na subtypes of | 4 |
of inflammatory cytokines and | 4 |
the increase in the | 4 |
cells with a strong | 4 |
n virus was detected | 4 |
in the influenza a | 4 |
and influenza susceptibility and | 4 |
virus isolated from a | 4 |
there is an urgent | 4 |
the no vac no | 4 |
identification of a novel | 4 |
the source of the | 4 |
absence or presence of | 4 |
acts as a receptor | 4 |
and to a lesser | 4 |
cells in the upper | 4 |
with pandemic h n | 4 |
be related to its | 4 |
of avian and mammalian | 4 |
the antigenic structure of | 4 |
percentage of necrotic cells | 4 |
to iav h n | 4 |
system for generation of | 4 |
glycosylation of the hemagglutinin | 4 |
the influenza virus disease | 4 |
m ion channel blockers | 4 |
respiratory syndrome coronavirus and | 4 |
is associated with risk | 4 |
and human iav binding | 4 |
in tissue culture cells | 4 |
results are expressed as | 4 |
lectin pathway of complement | 4 |
in swine at exhibitions | 4 |
intracellular cholesterol homeostasis to | 4 |
studies are needed to | 4 |
in the human respiratory | 4 |
in mediating viral clearance | 4 |
h n pdm subtypes | 4 |
is required for the | 4 |
found infected with h | 4 |
these data demonstrate that | 4 |
pr mtsin and wsn | 4 |
potential of interferon alphabeta | 4 |
human upper respiratory tract | 4 |
a penetrates host mucus | 4 |
the role of macrophage | 4 |
influenza a virus with | 4 |
virus from pigs in | 4 |
disrupts intracellular cholesterol homeostasis | 4 |
increased ifitm signal intensity | 4 |
ifitm restriction of viral | 4 |
by the influenza a | 4 |
hct intersection networks in | 4 |
cellular signaling pathway nodes | 4 |
the metabolic state of | 4 |
and activation of the | 4 |
for min followed by | 4 |
involved in regulation of | 4 |
of mbl in the | 4 |
ifitm signal intensity in | 4 |
cells transfected with vrna | 4 |
samples were negative for | 4 |
used for the treatment | 4 |
actin filaments of the | 4 |
dissection of the influenza | 4 |
analysis package in r | 4 |
genes in wdnhbe cells | 4 |
localization of ifitm and | 4 |
our results showed that | 4 |
iav has been shown | 4 |
the release of iav | 4 |
the impact of the | 4 |
the activity of the | 4 |
in mice challenged with | 4 |
syncytial virus and influenza | 4 |
the care and use | 4 |
on apparently vesicular structures | 4 |
f contributes to severe | 4 |
the sialic acid binding | 4 |
of the h hemagglutinin | 4 |
been found to be | 4 |
of the cytokine storm | 4 |
we will discuss the | 4 |
infected with iav at | 4 |
results showed that pa | 4 |
isolated from a swine | 4 |
gene of influenza a | 4 |
viral membrane fusion and | 4 |
into the mechanisms of | 4 |
lacking a strong nuclear | 4 |
system development and function | 4 |
there was no difference | 4 |
approaches for the development | 4 |
the cytokine storm in | 4 |
is a type ii | 4 |
and type iii interferons | 4 |
virus and influenza a | 4 |
fold by h n | 4 |
upon influenza virus infection | 4 |
the ratios of the | 4 |
a mouse model for | 4 |
consistent with our previous | 4 |
cytokine and chemokine secretion | 4 |
production of infectious dips | 4 |
detected in swine nasal | 4 |
influenza virus infected cells | 4 |
the iav m protein | 4 |
rsv and hrv were | 4 |
the first time the | 4 |
experiments were performed in | 4 |
nlg site at position | 4 |
with severe iav infection | 4 |
of the common cold | 4 |
known to be an | 4 |
initial binding rate by | 4 |
detection of influenza virus | 4 |
protective effects of the | 4 |
of the proinflammatory cytokines | 4 |
iav infection has also | 4 |
was observed during the | 4 |
of apoptotic cells in | 4 |
matrix protein of influenza | 4 |
reported to be required | 4 |
innate immune response and | 4 |
needed to determine the | 4 |
was determined by using | 4 |
lethal h n infection | 4 |
report of iav in | 4 |
is similar to that | 4 |
defective interfering influenza virus | 4 |
with iav h n | 4 |
of lung surfactant protein | 4 |
mucus by cleaving sialic | 4 |
replication of influenza a | 4 |
of influenza virus neuraminidase | 4 |
total rna was isolated | 4 |
the vast majority of | 4 |
prior to iav infection | 4 |
dengue and zika viruses | 4 |
to injury induced by | 4 |
cases of h n | 4 |
of interferon alphabeta in | 4 |
the top of the | 4 |
with an h n | 4 |
to a number of | 4 |
virus infection by preventing | 4 |
is likely to be | 4 |
activation of the interferon | 4 |
pdm viruses were reported | 4 |
protective role of nrf | 4 |
according to previously described | 4 |
we analyzed the effect | 4 |
genome uncoating are required | 4 |
routes reveals macropinocytosis as | 4 |
viruses during viral entry | 4 |
associated with the first | 4 |
mice infected with iav | 4 |
the inoculum was removed | 4 |
of the epidemiology and | 4 |
around individual influenza viruses | 4 |
a type i ifn | 4 |
cov infection on human | 4 |
sitosterol on the ifn | 4 |
of vdid dequenching in | 4 |
the origin of the | 4 |
cov e protein is | 4 |
and acute respiratory distress | 4 |