trigram

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
and respiratory syndrome169
porcine reproductive and168
reproductive and respiratory168
respiratory syndrome virus142
as well as111
the cells were110
in this study103
mhc class i99
influenza a virus97
the presence of85
the development of77
newcastle disease virus76
of the virus66
porcine epidemic diarrhea66
in the lungs66
the number of59
compared to the58
according to the57
based on the57
epidemic diarrhea virus55
the role of53
was used to52
the expression of48
of influenza a47
the ns protein46
one of the46
feline infectious peritonitis45
observed in the45
role in the44
the present study44
avian influenza virus44
a and b42
analysis of the42
cats in group42
vet res doi41
of newcastle disease40
compared with the40
detected in the40
the infected pigs39
to determine the39
due to the38
of porcine reproductive38
the use of38
data not shown38
for min at38
the immune response37
involved in the37
of alpha toxin37
high nk cells37
and in the37
it has been36
h n influenza36
nkp high nk36
in order to35
at room temperature35
mab d group35
in the infected35
of the study35
the other two35
the effect of35
the mab d35
was observed in34
as previously described34
was used as34
in group a33
was performed using33
the induction of33
infected with pedv32
of h n32
no competing interests32
h n virus32
in group b32
respiratory syncytial virus32
were incubated with32
the authors declare32
pathogenic avian influenza31
they have no31
were infected with31
used as a31
the vero cells31
in the present31
weeks of age31
results showed that31
the course of30
were observed in30
have no competing30
infectious bronchitis virus30
expression of the30
innate immune responses30
authors declare that30
declare that they30
of the infected30
in the mab30
polymerase chain reaction30
that they have30
at hpi and29
end of the29
cells in the29
showed that the29
the united states29
were treated with28
authors read and28
gds and gds28
the final manuscript28
approved the final28
and gds strains28
and approved the28
of viral rna28
vero cells and28
in additional file28
the control group28
read and approved28
the pathogenesis of28
shown in figure27
cd t cells27
the end of27
the detection of27
as shown in27
all authors read27
any of the27
a previous study27
at day pi27
were detected in27
innate and adaptive27
the production of26
was detected in26
hpai h n26
for h at26
expression levels of26
there was no26
newcastle disease viruses26
has been shown26
inactivated h n26
influenza a viruses26
a total of25
the case of25
in response to25
than in the25
j cells were25
as described previously25
samples were collected25
the lungs of25
the spread of25
differences in the25
swine influenza virus24
immune responses in24
nkp nk cells24
samples from cats24
in the case24
of the ns24
risk of hpai23
with regard to23
porcine circovirus type23
in the virus23
an important role23
g for min23
type i interferon23
was added to23
were used as23
in addition to23
the gds and23
blood mononuclear cells23
the amount of23
bvd vaccinated dams22
peripheral blood mononuclear22
n influenza virus22
adaptive immune responses22
were used to22
innate immune response22
there were no22
of the most22
differences between the22
found in the22
added to the22
the absence of22
for h and21
pcr and western21
were collected at21
vero and ipec21
highly pathogenic avian21
approved by the21
splenic nkp high21
in the lung21
in the same21
a number of21
cells were washed21
cells were treated21
associated with the21
immune response in21
pigs in the21
development of bnp21
influenza virus infection21
and western blotting21
we found that21
important role in21
related to the21
in the vero21
cells were fixed21
and characterization of20
cats without fip20
hpi and hpi20
been shown to20
of this study20
a negative control20
in accordance with20
mdm at hpi20
the current study20
bvd vaccinated non20
h n and20
this study was20
bnp and bnp20
contribute to the20
and stored at20
changes in the20
were carried out20
t cells were20
most of the20
the results of20
in terms of20
vero cells were20
participated in the20
performed as described20
of the pigs19
the activation of19
as a negative19
in the control19
the ability of19
the respiratory tract19
the alpha toxin19
the age of19
cells were collected19
part of the19
mouth disease virus19
other two groups19
followed by a19
chickens and ducks19
was performed as19
used for the19
cells were incubated19
proteinase k treated19
in the presence19
of the host19
the relative risk18
in the united18
respiratory disease complex18
virus infection in18
was used for18
respiratory epithelial cells18
h and h18
was performed on18
mice in the18
has been reported18
the prevalence of18
used in the18
mab igg group18
the lack of18
cd and cd18
in the ipec18
in cats in18
all of the18
classical swine fever18
the risk of18
in our study18
understanding of the18
figures a and18
the level of18
was performed in18
of the immune18
of porcine epidemic18
washed with pbs18
present in the18
a role in18
iiaa g r18
then infected with18
of infected cells17
of clostridium perfringens17
were collected and17
cells of the17
to infection by17
between the two17
infected with apmv17
to prrsv infection17
at h after17
in the absence17
native alpha toxin17
nk cells showed17
did not show17
swine fever virus17
of the experiment17
influenza virus in17
were used for17
in the co17
can be used17
in contrast to17
no significant difference17
the percentage of17
intestinal epithelial cells17
the immune system17
t cell responses17
the invasion rates17
rna was extracted17
were subjected to17
days and pi17
be detected in17
and stained with17
the innate immune17
is important for17
of the viral17
cells were pre17
and bnp dams17
an increase in17
has also been17
nkp and nkp17
response in the17
avian influenza viruses17
used in this17
the virus was17
the importance of17
the effects of16
in both groups16
have been reported16
was identified in16
no significant differences16
were performed using16
in the current16
when compared to16
of avian influenza16
three times with16
no vac cha16
was extracted from16
considered to be16
for min and16
was detected by16
of influenza virus16
are involved in16
the passively immunized16
to evaluate the16
bovine respiratory disease16
were significantly higher16
was significantly higher16
gp and gp16
host immune response16
nk cells in16
the plates were16
such as the16
serial dilutions of16
of feline coronavirus16
with mab d16
was supported by16
of avian paramyxovirus16
bovine viral diarrhea16
in the development16
could not be16
during the course16
of the three16
to be the16
significantly higher than15
c and d15
of hpai h15
in published maps15
the levels of15
regard to jurisdictional15
the host immune15
cell subsets in15
spore h n15
of the other15
is associated with15
maps and institutional15
jurisdictional claims in15
were collected from15
with porcine reproductive15
intestinal loop model15
claims in published15
of nk cells15
and institutional affiliations15
virus in the15
higher levels of15
nature remains neutral15
remains neutral with15
the clearance of15
with inactivated h15
virus isolated from15
responsible for the15
to test the15
none of the15
cells were infected15
pandemic h n15
a leucine codon15
springer nature remains15
was isolated from15
has not been15
bovine necrohemorrhagic enteritis15
in the first15
the culture medium15
gene expression levels15
airway epithelial cells15
experiments were performed15
kindly provided by15
with pedv strains15
that in the15
was found in15
by western blotting15
the fact that15
in the pig15
well as the15
in the early15
cells and ipec15
the expression levels15
to jurisdictional claims15
found to be15
published maps and15
of the disease15
cats with fip15
to identify the15
of the animals15
neutral with regard15
total rna was15
are expressed as14
comparison of the14
to the other14
in the pathogenesis14
republic of korea14
the s protein14
note springer nature14
difference between the14
depending on the14
acute myocardial necrosis14
could be detected14
the lungs and14
infectious peritonitis virus14
terminal domain of14
were found in14
washed three times14
mhc class ii14
were stained with14
results indicate that14
heart and skeletal14
at weeks of14
a virus infection14
the results showed14
the most common14
a bridge host14
the severity of14
the occurrence of14
terminal fragment of14
and then infected14
faecal samples from14
animal care and14
are needed to14
the epithelial barrier14
of the manuscript14
of bnp in14
was no significant14
was carried out14
at the end14
characterization of a14
indicated that the14
experimental infection of14
were identified in14
cd a cd14
to be a14
were transfected with14
expressed as the14
the mhc class14
viral loads in14
salmo salar l14
of the vp14
the time of13
a methionine codon13
study was to13
of a novel13
group at dpi13
each of the13
shown to be13
in vitro and13
of mhc class13
was determined by13
is required for13
in proteinase k13
invasion rates of13
class i alleles13
bovine neonatal pancytopenia13
care and use13
from cats without13
respiratory disease in13
analysis was performed13
the virus in13
play an important13
it is possible13
at the time13
a combination of13
with the same13
immune responses and13
a review of13
were washed with13
thorough peer review13
higher in the13
of the vaccine13
and skeletal muscle13
thermo fisher scientific13
for the detection13
passively immunized cats13
because of the13
spread of the13
goat t cells13
surface of the13
in the other13
viral diarrhea virus13
maintenance and target13
only in the13
in the cytoplasm13
of the samples13
in which the13
immune responses to13
included in the13
the replication of13
publication on acceptance13
obtained from the13
and incubated at13
a high density13
irrelevant mab igg13
role of the13
been reported to13
viruses isolated from13
with the virus13
was significantly lower13
human immunodeficiency virus13
is the most13
the release of13
convenient online submission13
replaced with fresh13
replication in vitro13
levels of ifn13
m l substitution13
response in pigs13
the need for13
the onset of13
activity of the13
immune responses against13
member of the13
as described in13
were performed in13
of these cells12
those in the12
with pedv at12
found that the12
performed in triplicate12
the most important12
tumor necrosis factor12
cells were seeded12
are shown in12
against necrotic enteritis12
in any of12
against h n12
in exhibition swine12
and adaptive immune12
cells were transfected12
design of the12
at and hpi12
immune response to12
high density of12
is an important12
carried out the12
room temperature for12
the m l12
and incubated with12
of haemonchus contortus12
each time point12
pcr products were12
in the sav12
the bridge host12
herpes simplex virus12
from cats with12
cells and the12
play a role12
at the same12
accordance with the12
the bvdv bhv12
is caused by12
development of a12
and use committee12
isolated from the12
rates of the12
in the maintenance12
need to be12
the samples were12
was found to12
consistent with the12
activation of the12
to investigate the12
was performed by12
on day pi12
h n civ12
be used to12
showed that pedv12
performed using the12
h n in12
lesions in the12
treated with mab12
of this article12
infection in the12
of monoclonal antibodies12
associated with a12
levels in the12
than that in12
the results are12
disease viruses isolated12
clinical signs of12
a better understanding12
days of age12
isolated from a12
n avian influenza12
and infected with12
of tw i12
cell proliferation and12
hepatitis c virus12
mice treated with12
results suggest that12
the secretion of12
a significant difference12
h n avian12
the phenotype of12
as described above12
and in vivo12
incubated with pedv12
were confirmed by12
proteomic analysis of12
age of the12
pedv strains at12
of proinflammatory cytokines12
for at least12
were challenged with12
domain of alpha12
antiviral activity against12
disease virus in12
with the other12
in the respiratory12
the surface of12
of the gds12
the existence of12
the proliferation of12
and development of12
immune response against12
we speculated that12
results indicated that12
avian paramyxovirus type11
in the design11
were analyzed by11
have also been11
be used as11
as the mean11
suggest that the11
tissue samples from11
alternatives to antibiotics11
were approved by11
virus from the11
was defined as11
vesicular stomatitis virus11
well as in11
the transmission function11
better understanding of11
results show that11
in a humidified11
the n protein11
blood and spleen11
figures c and11
on the contrary11
antibodies against the11
the small intestine11
min at room11
the invasion efficiency11
were seeded in11
of the infection11
protective immunity against11
were determined by11
disease virus isolated11
be due to11
the gds strain11
the analysis of11
significantly higher in11
the sav controls11
the activity of11
institutional animal care11
the pigs were11
been associated with11
of the chicken11
at dpi and11
with h n11
a variety of11
occurrence of bnp11
with fresh dmem11
provide protection against11
against porcine reproductive11
of dynamin ii11
the difference in11
were no significant11
the dynamics of11
incubated for h11
the outcome of11
region of the11
the replication and11
the differences in11
invasion efficiency of11
molecular epidemiology of11
h and then11
of the dam11
vaccinated with the11
used as the11
differentiated respiratory epithelial11
and adaptive immunity11
bovine respiratory syncytial11
mediated immune responses11
and the development11
to those of11
is known to11
hpi for qrt11
the maintenance of11
a member of11
see additional file11
were purchased from11
contributed to the11
tissue samples were11
provided by the11
of feline infectious11
and t cell11
during prrsv infection11
of the porcine11
monoclonal antibodies against11
bacillus subtilis spores11
have been identified11
collected from the11
to porcine reproductive11
been isolated from11
th and th11
viral rna detection11
with and without11
of the same11
the generation of11
blood nkp nk11
in chicken mdm11
for the presence11
regulatory t cells11
significant difference in11
results of the11
is known about11
the inhibition of11
the pathogenicity of11
alloantibody binding of11
collected at hpi11
the negative control11
infected pigs at11
as indicated by11
in a dose11
ability of the11
to determine whether11
based on a11
and pathogenicity of11
that the virus11
of the lung11
fragment of alpha11
times with pbs11
the vero and11
the sav control11
the two groups10
submit your next10
be associated with10
after prrsv infection10
is responsible for10
electronic supplementary material10
of veterinary medicine10
immune response and10
no vac no10
showed the highest10
the challenge group10
pcr was performed10
clearance of the10
can also be10
were performed with10
treated with the10
false discovery rate10
cells infected with10
from the same10
your next manuscript10
the viability of10
bnp and non10
is available to10
the binding of10
a mixture of10
analyses were performed10
replication and virulence10
to authorized users10
and incubated for10
and target hosts10
the aim of10
the second wave10
of the animal10
throughout the study10
during the second10
manuscript to biomed10
and centrifuged at10
resulted in a10
in the porcine10
syndrome virus infection10
by flow cytometry10
important for the10
of the two10
at dpv dpc10
significantly lower than10
under field conditions10
course of infection10
final concentration of10
by dpv dpc10
to biomed central10
g b challenge10
natural killer cell10
the online version10
supported by the10
the control of10
genome sequence of10
located in the10
the maintenance function10
of the respiratory10
the supernatant was10
prevalence of cryptosporidium10
was replaced with10
in the transmission10
three virus strains10
the virus from10
strains in the10
to analyze the10
titers in the10
insights into the10
to compare the10
suggested that the10
the target population10
biomed central and10
subtilis spores as10
infected cells were10
culture medium was10
is the first10
a series of10
to enter cells10
additional file a10
vac no cha10
derived dendritic cells10
epithelial cells are10
little is known10
of immune responses10
ducks and geese10
which is available10
with the control10
in relation to10
serum samples were10
virus replication and10
was measured by10
were inoculated with10
the target host10
specific immune responses10
with a high10
prv and sav10
identification of a10
is possible that10
the university of10
the same animal10
of infectious bronchitis10
of the cats10
studies have shown10
in the ns10
at each time10
pedv g b10
were significantly lower10
mice infected with10
significant differences in10
influenza h n10
host immune responses10
broiler and layer10
the apical surface10
cells were then10
in the field10
at and dpi10
in the different10
in both the10
and g p10
significant difference between10
to the sav10
is shown in10
immune responses of10
the h n10
next manuscript to10
characterization of the10
alpha toxin activity10
belonging to the10
were fixed and10
version of this10
of the viruses10
serum and colostrum10
available to authorized10
the emergence of10
infectious bursal disease10
contains supplementary material10
innate immune cells10
to the target10
in the passively10
that of the10
h at room10
nkp and cd10
infected with the10
at days and10
in figure a10
of group a10
and irrelevant mab10
online version of10
of the ifn10
and subjected to9
infection of the9
and without fip9
an moi of9
virulent newcastle disease9
responses in pigs9
and the number9
cd t cell9
not detected in9
including large and9
as described elsewhere9
in the spread9
normal rat igg9
citations maximum visibility9
virus replication in9
for your research9
of t cells9
website views per9
wider collaboration and9
according to a9
viruses such as9
of the epithelial9
caused by the9
blood samples were9
the apmv serotypes9
at least one9
in combination with9
in this group9
virus infection of9
bnp dams and9
human nk cells9
in case of9
the pbs group9
accompanies this paper9
ns protein of9
strains at h9
supplementary information accompanies9
in the host9
western blotting assay9
h after the9
in atlantic salmon9
extracted from the9
the sections were9
in humans and9
from blood and9
at the fourth9
ryanae and c9
were maintained in9
cells from the9
indicating that the9
gold open access9
the acute phase9
h challenge strains9
by western blot9
efficiency of pedv9
cell lysates were9
infected mdm at9
of the cells9
expression of cd9
of the s9
no virus was9
of highly pathogenic9
the majority of9
as compared to9
at the age9
to the development9
the study of9
are summarized in9
a virus in9
in a previous9
serum or colostrum9
fosters wider collaboration9
the definition of9
open access which9
were isolated from9
chickens immunized with9
virus was detected9
the animals were9
phenotype of the9
significant differences between9
and additional file9
that pedv entry9
to protect against9
on the other9
at different time9
access which fosters9
in the blood9
this paper at9
the cytoplasm of9
h n group9
study of the9
was associated with9
nature of the9
of t cell9
results are expressed9
were cultured in9
and cd t9
a recent study9
severe acute respiratory9
and nkp nk9
infection with the9
information accompanies this9
the authors thank9
the efficiency of9
increased citations maximum9
hemolysis in nacl9
m website views9
with or without9
the clinical signs9
in some cases9
maximum visibility for9
are associated with9
paper at https9
dpi in the9
views per year9
virus ns protein9
genes in the9
attributed to the9
protective immune response9
porcine alveolar macrophages9
gds strains were9
out of the9
collaboration and increased9
in vero cells9
african swine fever9
as a result9
for this purpose9
of the pathogen9
were analysed using9
the impact of9
excluded from the9
and complex data9
experimentally infected with9
were not detected9
in the balf9
increase in the9
drafted the manuscript9
were used in9
the identification of9
shown in table9
test was performed9
level in the9
carried out in9
hamsters infected with9
in lymphoid organs9
different time points9
visibility for your9
due to their9
complex data types9
that mab d9
with ml of9
natural killer cells9
of innate immune9
k treated tadv9
is one of9
we used the9
prior to the9
nk cells are9
large and complex9
were euthanized at9
of faecal samples9
the late co9
and h challenge9
studies are needed9
for detection of9
over m website9
the hpai h9
for animal health9
lungs and nasal9
we investigated the9
which fosters wider9
pigs from the9
of type i9
were found to9
in lymphoid tissues9
were obtained from9
have to be9
prrsv envelope proteins9
higher than those9
the design of9
and h n9
in the us9
were grown in9
and increased citations9
plasmacytoid dendritic cells9
of the alpha9
were associated with9
contact with the9
were identified as9
have not been9
the control pigs9
porcine proliferative enteropathy9
several studies have9
some of the9
in cell culture8
derived from the8
peer review by8
in pbs and8
in the serum8
the cell surface8
in pigs is8
in agreement with8
in figure b8
genetic diversity of8
indicated by the8
in blood and8
effect of the8
genbank accession no8
revised the manuscript8
replication and pathogenicity8
porcine viral infections8
are known to8
the efficacy of8
group and mab8
reported to be8
and hpi for8
this is the8
swabs and balf8
alpha toxin and8
was performed with8
codon was identified8
period of time8
difference in the8
entry into cells8
reactions were performed8
medium was replaced8
the other hand8
pigs at dpc8
and take full8
class i haplotypes8
inhibition of the8
each group were8
different concentrations of8
the viral loads8
rapid publication on8
perfringens alpha toxin8
in the nkp8
used to determine8
of bnp dams8
of a new8
after iav infection8
and virulence of8
of pedv n8
avian influenza h8
blood was collected8
neutralizing antibodies and8
full advantage of8
plays an important8
antigenic differences between8
and drafted the8
h after transfection8
were housed in8
fetal bovine serum8
remains to be8
was also observed8
the mdbk cell8
cell responses in8
known about the8
of the apmv8
be related to8
of cd and8
a h n8
replication in the8
in all tissues8
mdbk cells and8
the mechanisms of8
host gene expression8
for min to8
g b isolates8
dmso was used8
and nasal turbinates8
could be due8
the amino acid8
the influenza virus8
sav rna levels8
at dpi in8
at and wpc8
severity of the8
of relative risk8
in disease ecology8
and can be8
antigen presenting cells8
regulated deg at8
like to thank8
the potential of8
of virus in8
wt and gfp8
of this virus8
may contribute to8
of the different8
as a potential8
detected in any8
were then washed8
been reported that8
infected pigs were8
expression levels were8
of the enteroid8
rna levels in8
of the prrsv8
on the surface8
t cell proliferation8
in vivo and8
more than one8
complete genome sequence8
differentiated epithelial cells8
viral rna in8
have shown that8
mrna levels of8
review by experienced8
susceptible to infection8
the maintenance and8
canine influenza virus8
replication of the8
had significantly higher8
to each well8
relative copy numbers8
of pigs with8
have been isolated8
titers of the8
porcine nk cells8
vitro and in8
detected in proteinase8
that hcesp stimuli8
balb c mice8
and control of8
loads in the8
pigs vaccinated with8
with pbs and8
by experienced researchers8
previous studies have8
virus h n8
outbreaks of diarrhea8
central and take8
in swine at8
to detect the8
were fixed with8
observed for the8
low pathogenic avian8
to explore the8
morbidity and mortality8
indicate that the8
the epithelial cells8
leucine codon was8
calculated using the8
were incubated for8
of atlantic salmon8
in your field8
were incubated at8
cells and and8
molecular characterization of8
a significant decrease8
were provided by8
of age with8
between and dpi8
the ability to8
cells showed a8
the maintenance host8
in recent years8
of the lungs8
we did not8
the frequency of8
in mdm at8
and and in8
haydon et al8
in wild birds8
identification of the8
cells cultured in8
in the prv8
decrease in the8
deg at hpi8
low levels of8
strains for h8
in pedv entry8
that can be8
specific antibody responses8
washed twice with8
syndrome virus and8
take full advantage8
evaluation of the8
in the study8
necrotic enteritis in8
a final concentration8
resulting in the8
the sav rna8
then washed with8
nasal swabs and8
were washed three8
virus was isolated8
the reference interval8
as in the8
lower than those8
samples with a8
skeletal muscle inflammation8
class i haplotype8
infected group and8
identified in this8
the supernatants were8
of the relative8
of calves with8
inserted into the8
infection in pigs8
heterologous aut com8
institutional affiliations the8
addition to the8
western blotting analysis8
in each group8
for chickens and8
the mechanisms involved8
the three viruses8
development of the8
no effect on8
experienced researchers in8
resulting in a8
as determined by8
and mab igg8
a set of8
required for the8
the magnitude of8
infection and the8
wiv treatment groups8
infection by brsv8
and mycoplasma hyopneumoniae8
of the innate8
in ovo vaccination8
immunized with the8
avian infectious bronchitis8
clinical signs and8
ranged from to8
k r substitution8
incubated with gds8
high levels of8
the decrease in8
is important to8
responses induced by8
nk cells from8
at any time8
been shown that8
virus in swine8
cells were cultured8
researchers in your8
the movement of8
the no vac8
mdbk cell line8
p and g8
for research data8
t cells in8
would like to8
acute respiratory syndrome8
direct and indirect8
indicates that the8
western blotting at8
dilutions of the8
were added to8
support for research8
bnp in calves8
are the most8
the pigs in8
for the development8
western blot analysis8
in pbs containing7
cat jhw was7
the immunogenicity of7
vaccines against porcine7
after stimulation with7
of the primary7
in the mouse7
cd t lymphocyte7
chemokine receptor cxcr7
with the anti7
with the exception7
female reproductive system7
both chickens and7
in mice and7
even in the7
those of the7
and the cells7
and infected pigs7
pbs control group7
humoral immune response7
identified as a7
from the waterfowl7
in serum and7
cats that had7
for virus strain7
in the poultry7
was shown to7
dams not vaccinated7
against bovine necrohemorrhagic7
in the sera7
spread of hpai7
enter cells through7
in the immune7
faecal virus shedding7
lower respiratory tract7
porcine respiratory disease7
around the world7
pigs compared with7
has recently been7
compared to cats7
the results indicated7
all pigs were7
of hpai in7
we hypothesized that7
after the last7
relative risk of7
performed using a7
in chicken macrophages7
e and f7
of prrsv infection7
not yet been7
inoculated with the7
of bnp within7
as the reciprocal7
of gfp nsp7
not vaccinated with7
j replication in7
to assess the7
of our knowledge7
in the intestinal7
prior to challenge7
plates until confluence7
increases in the7
transmission of the7
in the late7
alpha toxin was7
extracellular part of7
information is available7
t cells and7
and did not7
of infection in7
heritability of the7
in the nucleus7
bacteria such as7
protective efficacy of7
the false discovery7
all animal experiments7
has been suggested7
college of veterinary7
lower than that7
the changes in7
to study the7
from each group7
early stage of7
response to influenza7
immune responses induced7
by the institutional7
in new zealand7
added to each7
in the netherlands7
be found in7
in the challenge7
prevent and control7
h n canine7
fixed and stained7
design and coordination7
vp and vp7
than those of7
reduction in the7
effect on the7
socs and socs7
porcine respiratory coronavirus7
the range of7
detection of viral7
cells treated with7
production compared to7
it is important7
transmissible gastroenteritis virus7
with the indicated7
depends on the7
of mab d7
spread of h7
acute phase of7
plates were incubated7
virus porcine reproductive7
were stored at7
and indirect contact7
to prevent and7
the location of7
in peripheral blood7
a key role7
than those in7
n canine influenza7
the most commonly7
on the cell7
the wiv treatment7
amount of virus7
serum samples from7
the vp gene7
of porcine circovirus7
except for the7
to cats in7
clostridium perfringens alpha7
the possibility that7
d group at7
and p genotypes7
number of samples7
water was used7
it is clear7
salmonella enterica serovar7
the intestinal loop7
the addition of7
multiplicity of infection7
the interactions between7
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response to infection7
and analysis of7
experimental infection with7
j infection in7
were stimulated with7
g and p7
bvdv and bhv7
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signs of disease7
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forward and reverse7
of the development7
the regulation of7
the heterologous prime7
the interaction between7
specific pathogen free7
these results indicate7
not show any7
embedded in paraffin7
lesions were observed7
the female reproductive7
levels of pedv7
responses in the7
were washed twice7
b and c7
gp and m7
one or more7
dc macrophage network7
gp gp gp7
for h with7
upper and lower7
and mouth disease7
according to their7
were included in7
in vascular areas7
in chickens and7
the site of7
have been used7
test the invasion7
flow cytometric analysis7
to elucidate the7
were measured using7
in of the7
type ii pneumocytes7
it possible to7
in the majority7
sequence analysis of7
induced by alv7
been reported in7
genes of the7
gds or gds7
that had been7
characterization of newcastle7
by centrifugation at7
in the amount7
at days of7
gd and sd7
when cat jhw7
the extracellular part7
their ability to7
similar to the7
university of minnesota7
samples collected at7
of the epithelium7
and days post7
and balf samples7
in bronchiolar areas7
in another study7
in the cell7
pedv rna in7
of all three7
was kindly provided7
the same time7
to the best7
virus shedding and7
n and or7
virus neutralizing antibodies7
the second transfection7
the duration of7
the t cell7
after the second7
of these viruses7
ml of the7
between the gds7
effects of the7
the pathogen to7
then incubated with7
calves born to7
were resuspended in7
of tomatidine with7
was used in7
the poultry industry7
prior to infection7
in the gut7
between tomatidine and7
the pandemic h7
a highly activated7
against alpha toxin7
the exception of7
locally in the7
with proteinase k7
related to immune7
jhw was excluded7
second wave of7
viral replication and7
associated with an7
for the first7
associated with respiratory7
of tomatidine on7
cats with and7
of infection and7
the potential to7
epithelial cells and7
g p and7
was collected from7
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component of the7
was excluded from7
total protein concentrations7
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lung viral loads7
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the kinetics of7
wild and domestic7
avian leukosis virus7
was observed at7
the reciprocal of7
in egg production7
response to porcine7
influenza virus h7
for unequal variance7
for each tissue7
the early co7
type i ifn7
of lawsonia intracellularis7
can be found7
the cytokine levels7
animals infected with7
the disease is7
immunodeficiency virus type7
assays were performed7
human influenza a7
were approximately and7
and domestic birds7
in the calf7
in the environment7
in ml of7
well plates until7
protein of influenza7
class i genes7
with those of7
in the intestine7
showed a significant7
in this work7
and mhc class7
the mrna levels7
k of the7
animal experiments were7
with different concentrations7
to induce a7
the seeder pigs7
table and figure7
sav and sav7
reciprocal of the7
flow cytometry analysis7
and revised the7
influenza virus and7
sequences of the7
better understand the7
pigs were challenged7
lungs of mice7
in the two7
alveolar epithelial cells7
it can be7
leading to the7
the bovine respiratory7
with gds or7
pb and pa7
have been described7
the antibody response7
of mdbk cells7
fecv ucd and7
the concept of7
the pbs control7
the transmission of7
demonstrated that the7
affiliations the authors7
were also observed7
white leghorn chickens7
large number of7
to obtain a7
infected with porcine7
significantly lower in7
the spore h7
chicken and duck7
with an increased7
the concentration of7
porcine epidemic diarrhoea7
from the body7
stages of infection7
the g b7
diarrhea virus infection7
mutations in the7
stained with anti7
nk cells into7
well plates were7
used as an7
against porcine epidemic7
an h n7
in infected cells7
disease in pigs7
the chemokine receptor7
was expressed as7
the native alpha7
infected cells in7
our results showed7
for s and7
farmed atlantic salmon7
be used for7
syncytial virus infection7
cut lung slices7
activated cd t7
summarized in table7
terms related to7
to better understand7
type i and7
sav control groups7
the form of6
h n highly6
of innate immunity6
g strains comprising6
depend on the6
available at the6
for both chickens6
red blood cells6
pancreatic necrosis virus6
pedv cl protease6
ctrl means control6
virus and porcine6
were inoculated oronasally6
other swine disease6
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epithelial cells were6
its ability to6
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secreting cells in6
a decrease in6
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mab d could6
the study was6
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the upper and6
these findings were6
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the infected flock6
both inoculated groups6
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subtype iiaa g6
feed and water6
using graphpad prism6
of viral particles6
the acetylated k6
and in vitro6
the most relevant6
chang et al6
in serum samples6
antibody response in6
hepatitis e virus6
in a highly6
findings suggest that6
triggered by the6
at h post6
the heterologous aut6
epidemic diarrhoea virus6
a total volume6
aim of this6
levels of nkp6
to viral infection6
cell monolayers were6
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group a compared6
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to activate pdc6
there is a6
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the extent of6
were considered positive6
in the clearance6
under the accession6
in samples from6
until day pi6
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of immune cells6
the experiments were6
the he proteins6
for vaccine development6
infected with rvv6
bnp in the6
for each sample6
of the first6
some of these6
genetic differences between6
to virus infection6
xx xx xx6
pigs in each6
cells are in6
in association with6
none of these6
key role in6
viral replication in6
the porcine respiratory6
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swabs were collected6
total number of6
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codon at position6
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binding energy of6
the need to6
from pigs in6
recent advances in6
were able to6
sequence of the6
the vp genes6
with respiratory diseases6
have resulted in6
chickens in the6
of neutralizing antibodies6
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and dpi in6
is characterized by6
rna was detected6
genbank accession number6
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a commercial inactivated6
used to analyze6
major histocompatibility complex6
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defective interfering particles6
in broiler chickens6
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of the article6
naturally infected cats6
in pbs for6
the infected group6
cells in a6
surveillance and control6
a heritable trait6
of the gut6
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the potential for6
from the lungs6
viral loads and6
in the pbmc6
together with the6
open access correspondence6
relative risk for6
in the total6
genome sequences of6
of swine influenza6
viral diarrhoea virus6
details of the6
is that the6
effect of tomatidine6
blns and tonsils6
nitric oxide synthase6
of nkp and6
were kept in6
as bridge hosts6
g p at6
infected with prrsv6
during the study6
of the epidemic6
in the nasal6
to investigate whether6
the calf and6
could be a6
emerging and re6
members of the6
age of weeks6
is composed of6
spf chicken eggs6
this study were6
with reference strain6
the basis of6
the recipient cats6
and of the6
it is likely6
protection against c6
of cytokine signaling6
group a showed6
equal volume of6
observed at hpi6
cd cell population6
the relationship between6
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foot and mouth6
genetic analysis of6
of peripheral blood6
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days post inoculation6
immune responses by6
the epidemiology of6
protein in the6
types of cells6
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the control cats6
three independent experiments6
virus in chickens6
a marker for6
in calves is6
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the best of6
of ml of6
maintenance of the6
of the calf6
were analyzed using6
a compared to6
the shedding of6
rates of pedv6
production of the6
of the mhc6
different types of6
of the influenza6
to influenza virus6
copy numbers were6
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through the activation6
incubated with the6
nk cells and6
specificity of the6
in the pigs6
at and dpc6
a lack of6
bovine viral diarrhoea6
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different lung compartments6
the virus shedding6
increased expression of6
no differences in6
experiment was performed6
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the nasal turbinates6
but there was6
was determined using6
of cryptosporidium infection6
among suckling pigs6
ucd and fecv6
north american strain6
there are no6
best of our6
test was used6
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has not yet6
cells were grown6
this work was6
bovine mhc class6
to the nkp6
density gradient centrifugation6
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antibody response against6
mdck and a6
vac cha group6
sav in the6
t cells was6
challenge with mhf6
a humidified atmosphere6
the tissue samples6
our understanding of6
in comparison with6
anova followed by6
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data are expressed6
the first weeks6
intestinal loop experiments6
cellular immune responses6
piglets from litter6
complete genome sequences6
full list of6
and porcine circovirus6
approximately and in6
confirmed by western6
the growth rate6
diarrhea virus in6
the influenza a6
epithelial cells in6
treated with different6
interact with the6
from the analyses6
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g b strain6
activated protein kinase6
of all the6
and that the6
at the first6
plates were washed6
significance reached at6
to viral replication6
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to the apical6
the distribution of6
to control the6
the type of6
induced enteric diseases6
consistent with fip6
scale bars indicate6
identified in samples6
disease virus from6
the binding energy6
active pocket of6
influenza a h6
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that the development6
current status and6
at different ages6
suggests that the6
of acute myocardial6
bnp dams are6
of the calves6
in contact with6
infected with either6
both h and6
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repeated outbreaks of6
at an moi6
the protective effect6
in tne buffer6
total volume of6
up to day6
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the gene expression6
the proportion of6
or gds strains6
levels of the6
to understand the6
cells in vitro6
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all time points6
due to its6
which is the6
h in a6
response to the6
at hpi were6
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body weight gain6
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after washing with6
and target populations6
in the upper6
of pedv clpro6
cd t lymphocytes6
and application of6
vac cha pigs6
of the local6
way anova followed6
of pedv rna6
at the second6
and it is6
in veterinary medicine6
to the c6
influenza d virus6
and the virus6
gene specific primers6
of the hamsters6
the involvement of6
time pcr system6
list of author6
n influenza a6
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interaction with the6
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each treatment group6
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class i typing6
p at the6
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in vitro model6
expression of il6
pigs in a6
placed in the6
to prevent the6
lead to the6
protection against experimental6
concentrations of tomatidine6
movement of poultry6
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the early stage6
control and infected6
in the bvdv6
to the lungs6
in vitro culture6
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the immune responses6
at peak viremia6
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cd high nk6
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class i allele6
see figure on6
alpha toxin in6
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used to evaluate6
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temperature for min6
the virus is6
n highly pathogenic6
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the prrsv envelope6
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the gar strains6
primary and secondary6
differential expression of6
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influenza a infection6
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to verify the6
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identity with reference6
the most prevalent6
the interaction of6
coordination of the6
bovine serum albumin6
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turkeys infected with6
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bvd vaccinated bnp6
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of tissue samples6
methionine codon was6
the formation of6
suggesting that the6
acetylation of k6
analysis of newcastle6
t cell binding6
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to neutralize the6
inhibition of pedv6
after the first6
from no vac6
of broiler and6
pathogenesis of feline6
mechanisms involved in6
different levels of6
virus infection and6
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most commonly used6
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spores as adjuvants6
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a viruses in6
origin h n6
highly activated state6
viral rna was6
conjugated goat anti6
on nasal swabs6
pigs infected with6
the study period6
using the same6
the indicated concentrations6
the first outbreak6
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infectious pancreatic necrosis6
the adaptive immune6
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of human immunodeficiency6
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two groups at6
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replication and pathogenesis6
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the heritability of6
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wild birds in6
levels of il6
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potential bridge hosts6
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ms ms analysis6
the different nk6
to the maintenance6
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author information is6
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of author information6
subsets in blood6
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nanjing agricultural university6
respiratory tract and6
the hi test6
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the type i6
important roles in6
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experimental infection studies6
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samples that were6
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substitution in the6
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the blood nkp6
infections in pigs6
the lipid raft6
we compared the6
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vaccinated bnp dams6
h n subtype6
at days post6
the degree of6
day and day6
has to be6
toxin and perfringolysin6
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with vrp expressing6
h or h6
activity of tomatidine6
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shows that the6
each experiment was6
distilled water was6
cells such as6
in the cells6
infected pigs compared6
after infection with6
in the s6
days post infection6
subdistricts with a6
laiv com treatment6
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diseases such as6
influenza viruses in6
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threshold and all5
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cytokine production and5
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pcr master mix5
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research which is5
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the feline coronavirus5
virus in wild5
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infectious diseases in5
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the data were5
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strains were and5
sequences and the5
a vital role5
feline enteric coronavirus5
and the results5
were compared to5
at a concentration5
weeks after the5
humoral and cell5
homologous challenge with5
the pulmonary parenchyma5
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carried out to5
form of the5
is crucial for5
expression in the5
antiviral activity of5
between the different5
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of cryptosporidium in5
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differentially expressed genes5
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virus with the5
infection in chicken5
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the animal study5
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the incidence of5
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virus strains in5
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pathogenicity of apmv5
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cell surface staining5
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the nasal swabs5
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induction of the5
phase of infection5
in pigs and5
of defective interfering5
from tissue samples5
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multiple comparison test5
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virus in pigs5
the institutional animal5
calves immunized with5
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scopus and google5
salmon salmo salar5
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animal and human5
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epithelial cells of5
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the influence of5
potential role of5
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