quadgram

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
porcine reproductive and respiratory168
reproductive and respiratory syndrome167
and respiratory syndrome virus142
porcine epidemic diarrhea virus55
of porcine reproductive and38
nkp high nk cells32
the mab d group30
they have no competing30
authors declare that they30
that they have no30
the authors declare that30
declare that they have30
have no competing interests30
in the present study29
approved the final manuscript28
gds and gds strains28
read and approved the28
authors read and approved28
and approved the final28
of newcastle disease virus27
in the mab d26
all authors read and26
of influenza a virus25
the end of the25
of the ns protein24
cats in group a24
in the case of24
the gds and gds23
peripheral blood mononuclear cells22
in the infected pigs21
the development of bnp21
highly pathogenic avian influenza21
h n influenza virus21
an important role in21
in the lungs of21
pcr and western blotting20
the vero cells and20
as shown in figure20
cells were treated with20
as a negative control19
one of the most19
the other two groups19
splenic nkp high nk19
was used as a19
cats in group b18
in the united states18
at hpi and hpi18
the cells were fixed17
figures a and b17
in cats in group17
in the absence of16
the cells were washed16
the cells were collected16
cells were incubated with16
was performed as described16
in the presence of16
in the vero cells16
bnp and bnp dams16
in the development of16
during the course of16
as well as the15
was observed in the15
with inactivated h n15
nature remains neutral with15
of hpai h n15
in the current study15
to jurisdictional claims in15
used in this study15
regard to jurisdictional claims15
used as a negative15
with porcine reproductive and15
with regard to jurisdictional15
in published maps and15
claims in published maps15
jurisdictional claims in published15
of porcine epidemic diarrhea15
published maps and institutional15
neutral with regard to15
vero cells and ipec15
remains neutral with regard15
springer nature remains neutral15
maps and institutional affiliations15
rna was extracted from14
was added to the14
at weeks of age14
influenza a virus infection14
the mhc class i14
important role in the14
at the end of14
pathogenic avian influenza virus14
was no significant difference14
and then infected with14
the results showed that14
note springer nature remains14
there was no significant14
were detected in the13
from cats without fip13
of the infected pigs13
bovine viral diarrhea virus13
faecal samples from cats13
has been shown to13
feline infectious peritonitis virus13
mhc class i alleles13
the invasion rates of13
in the pathogenesis of13
of newcastle disease viruses12
of the gds and12
with pedv strains at12
care and use committee12
were observed in the12
cells were transfected with12
animal care and use12
the passively immunized cats12
in any of the12
a high density of12
the expression levels of12
for the detection of12
innate and adaptive immune12
treated with mab d12
newcastle disease viruses isolated12
samples from cats with12
play a role in12
play an important role12
h n avian influenza12
to porcine reproductive and11
terminal domain of alpha11
there were no significant11
washed three times with11
participated in the design11
compared to the other11
fragment of alpha toxin11
heart and skeletal muscle11
then infected with pedv11
cells were seeded in11
cells were collected at11
the vero and ipec11
replaced with fresh dmem11
for the presence of11
in proteinase k treated11
samples from cats without11
newcastle disease virus isolated11
for h and then11
bovine respiratory disease complex11
of feline infectious peritonitis11
classical swine fever virus11
the invasion efficiency of11
cells were infected with11
terminal fragment of alpha11
a better understanding of11
for min at room11
bovine respiratory syncytial virus11
as well as in11
mice treated with mab11
the m l substitution11
innate and adaptive immunity11
against porcine reproductive and11
infected with pedv strains11
institutional animal care and11
at the time of11
disease viruses isolated from11
in accordance with the11
development of bnp in11
domain of alpha toxin11
and the development of11
this study was to10
inactivated h n and10
no vac no cha10
were collected at hpi10
and in the ipec10
little is known about10
version of this article10
of mhc class i10
at room temperature for10
and adaptive immune responses10
next manuscript to biomed10
of this study was10
total rna was extracted10
in the passively immunized10
your next manuscript to10
which is available to10
is available to authorized10
compared to the sav10
the online version of10
h at room temperature10
manuscript to biomed central10
during the second wave10
n avian influenza virus10
differentiated respiratory epithelial cells10
at each time point10
design of the study10
respiratory syndrome virus infection10
to biomed central and10
were infected with pedv10
than that in the10
submit your next manuscript10
min at room temperature10
figures c and d10
disease virus isolated from10
and irrelevant mab igg10
online version of this10
in the other two10
rates of the gds10
available to authorized users10
and in the vero10
it is possible that10
were no significant differences10
three times with pbs10
was performed in triplicate10
of the immune response9
citations maximum visibility for9
with and without fip9
large and complex data9
maximum visibility for your9
it has been shown9
the innate immune response9
a role in the9
nkp and nkp nk9
fosters wider collaboration and9
with the other two9
influenza a virus in9
in the ns protein9
visibility for your research9
the hpai h n9
and infected with pedv9
the culture medium was9
to the other two9
supplementary information accompanies this9
high nk cells showed9
and gds strains were9
including large and complex9
strains at h after9
over m website views9
which fosters wider collaboration9
the host immune response9
website views per year9
studies are needed to9
m website views per9
and increased citations maximum9
collaboration and increased citations9
from cats with fip9
h and h challenge9
of avian paramyxovirus type9
cells were fixed and9
and complex data types9
accompanies this paper at9
results showed that the9
invasion efficiency of pedv9
was detected in the9
in the spread of9
the risk of hpai9
access which fosters wider9
at the age of9
increased citations maximum visibility9
open access which fosters9
information accompanies this paper9
for h at room9
this paper at https9
gold open access which9
compared with the other9
wider collaboration and increased9
at days and pi9
the course of infection9
at h after the9
could be due to8
detected in proteinase k8
complete genome sequence of8
of h n influenza8
and h challenge strains8
are involved in the8
were approved by the8
of the alpha toxin8
on the surface of8
of influenza a viruses8
on the other hand8
could be detected in8
medium was replaced with8
peer review by experienced8
hpi and hpi for8
proteinase k treated tadv8
rapid publication on acceptance8
been shown to be8
cells and and in8
in vitro and in8
at different time points8
vero cells and and8
experienced researchers in your8
pedv strains at h8
no significant difference in8
mice in the mab8
of bnp in calves8
the ns protein of8
review by experienced researchers8
of infectious bronchitis virus8
the virus from the8
a member of the8
and hpi for qrt8
mhc class i haplotypes8
respiratory syndrome virus and8
and skeletal muscle inflammation8
in mdm at hpi8
for the development of8
the mdbk cell line8
of the virus in8
and and in the8
of the apmv serotypes8
a final concentration of8
end of the experiment8
and drafted the manuscript8
take full advantage of8
is one of the8
the cells were then8
severe acute respiratory syndrome8
codon was identified in8
biomed central and take8
dmso was used as8
a leucine codon was8
nasal swabs and balf8
low pathogenic avian influenza8
support for research data8
regulated deg at hpi8
researchers in your field8
and institutional affiliations the8
by experienced researchers in8
thorough peer review by8
were washed three times8
is known about the8
the cells were incubated8
and take full advantage8
invasion rates of the8
in the control group8
in the lungs and8
plays an important role8
observed in the infected8
central and take full8
the occurrence of bnp8
mhc class i haplotype8
the phenotype of the8
vitro and in vivo8
and the cells were7
j cells were transfected7
shown in figure a7
h n canine influenza7
human immunodeficiency virus type7
respiratory syncytial virus infection7
was performed using the7
dams not vaccinated with7
studies have shown that7
to better understand the7
the acute phase of7
blood nkp nk cells7
in the cytoplasm of7
have been isolated from7
test the invasion efficiency7
the expression of the7
to the development of7
the second wave of7
were washed with pbs7
were significantly higher than7
cat jhw was excluded7
has been shown that7
the extracellular part of7
cells were fixed with7
the surface of the7
against bovine necrohemorrhagic enteritis7
were used for the7
between the two groups7
at days of age7
avian influenza h n7
the development of the7
cats with and without7
well plates until confluence7
this is the first7
spore h n group7
h n and or7
characterization of newcastle disease7
p and g p7
cd and cd t7
no significant differences in7
the false discovery rate7
in contrast to the7
maintenance and target hosts7
virus porcine reproductive and7
was kindly provided by7
end of the study7
to test the invasion7
the spread of hpai7
of the relative risk7
the native alpha toxin7
than those in the7
g for min at7
may contribute to the7
has been reported that7
cells were washed with7
was performed using a7
in a previous study7
the chemokine receptor cxcr7
infected mdm at hpi7
culture medium was replaced7
collected at hpi and7
the pandemic h n7
of the development of7
in addition to the7
the development of a7
wild and domestic birds7
added to each well7
heritability of the development7
performed as described in7
between the gds and7
college of veterinary medicine7
g p and g7
the design of the7
the pbs control group7
the results indicated that7
was excluded from the7
to prevent and control7
newcastle disease virus in7
the bovine respiratory disease7
with gds or gds7
and mab igg group7
the spore h n7
were fixed and stained7
to infection by brsv7
h and then infected7
did not show any7
the age of the7
were not detected in7
compared with the control7
and western blotting assay7
our results showed that7
level in the mab7
the severity of the7
the infected pigs at7
in the challenge group7
the mrna levels of7
of the virus from7
influenza virus h n7
group and mab igg7
with different concentrations of7
identified in this study7
was replaced with fresh7
for chickens and ducks7
that in the control7
with the exception of7
were significantly higher in7
the reciprocal of the7
tissue samples from cats7
against necrotic enteritis in7
the female reproductive system7
immune response in pigs7
at h after transfection7
pcr was performed using7
spread of h n7
was used as the7
in the respiratory tract7
mab d group at7
k of the ns7
against porcine epidemic diarrhea7
when cat jhw was7
spread of the virus7
the wiv treatment groups7
clearance of the virus7
these results indicate that7
be due to the7
mhc class i genes7
in the amount of7
at the same time7
and western blotting at7
hpai h n virus7
to cats in group7
an increase in the7
compared to cats in7
as the reciprocal of7
the differences in the7
institutional affiliations the authors7
avian infectious bronchitis virus7
it has been reported7
relative risk of hpai7
significant difference between the7
all animal experiments were6
available at the end6
n highly pathogenic avian6
mhc class i allele6
the heterologous aut com6
each experiment was performed6
information is available at6
of avian influenza virus6
of the epithelial barrier6
bovine viral diarrhoea virus6
mdck and a cells6
the maintenance of the6
a key role in6
jhw was excluded from6
and revised the manuscript6
treated with different concentrations6
the clearance of the6
incubated for h at6
were added to the6
were found to be6
the spread of h6
with a high density6
j cells were pre6
was identified in samples6
both chickens and ducks6
be related to the6
subtilis spores as adjuvants6
complete genome sequences of6
for both chickens and6
the results are expressed6
both h and h6
the best of our6
incubated with gds or6
it is clear that6
the analysis of the6
as the negative control6
the infected pigs compared6
the upper and lower6
mhc class i typing6
effect of tomatidine on6
virus was detected in6
in the bvdv bhv6
nk cells are in6
with a mixture of6
a highly activated state6
epidemic diarrhea virus infection6
of human immunodeficiency virus6
the spread of the6
identity with reference strain6
immune responses in pigs6
the course of the6
and mhc class i6
infected with porcine reproductive6
was found in the6
porcine respiratory disease complex6
mice in the virus6
infectious pancreatic necrosis virus6
influenza a viruses in6
cells were grown in6
g p at the6
expressed as the mean6
replication and pathogenicity of6
incubated with pedv at6
significant difference in the6
most of the virus6
in the design of6
in a recent study6
the intestinal loop model6
repeated outbreaks of diarrhea6
shown in figure b6
list of author information6
are expressed as the6
in a highly activated6
was significantly lower in6
a total volume of6
in group a compared6
with significance reached at6
significantly higher than those6
room temperature for min6
that the development of6
than in the other6
of acute myocardial necrosis6
nk cells showed a6
end of the article6
aim of this study6
other two groups at6
no significant difference between6
in the clearance of6
infected pigs compared with6
to the sav controls6
full list of author6
viral loads in the6
levels of pedv n6
at an moi of6
a methionine codon was6
with feline infectious peritonitis6
the movement of poultry6
foot and mouth disease6
then washed with pbs6
of avian influenza viruses6
is available at the6
subtype iiaa g r6
distilled water was used6
of the mhc class6
direct and indirect contact6
newcastle disease virus from6
no vac cha pigs6
h n influenza a6
influenza a h n6
n influenza virus infection6
it is likely that6
development of bnp within6
the relative risk of6
as well as to6
data are expressed as6
cells were then washed6
immunized with inactivated h6
lower than that in6
approximately and in the6
swabs and balf samples6
of the gar strains6
virulent newcastle disease virus6
was used to analyze6
h n highly pathogenic6
the replication and pathogenicity6
was approved by the6
immune responses induced by6
were obtained from the6
of broiler and layer6
differences between the two6
to be associated with6
was found to be6
avian influenza virus in6
in a humidified atmosphere6
analysis of newcastle disease6
is important for the6
have been reported to6
the age of weeks6
to the best of6
bnp in the calf6
the heritability of the6
mrna levels of pedv6
were significantly lower than6
syndrome virus and porcine6
a virus in swine6
author information is available6
high nk cells are6
best of our knowledge6
can be used to6
immune response in the6
were washed twice with6
were found in the6
was significantly higher than6
toxin and perfringolysin o6
gds or gds strains6
group a compared to6
in the small intestine6
in the form of6
no vac cha group6
results are expressed as6
n influenza a virus6
were incubated with pedv6
porcine epidemic diarrhoea virus6
and incubated with gds6
of author information is6
but there was no6
water was used as6
test was used to6
it is important to6
the plates were incubated6
maintenance and target populations6
to determine whether the6
have been associated with6
in the maintenance of6
at all time points6
are in a highly6
identified in samples from6
the apical surface of6
would like to thank6
lungs and nasal turbinates6
n and or b6
excluded from the analyses6
way anova followed by6
experiment was performed in6
has not yet been6
of the most important6
was collected from the5
type porcine reproductive and5
in the spore h5
was expressed as the5
followed by a friedman5
upper and lower respiratory5
the pathogenicity of tw5
virus was isolated from5
african swine fever virus5
of peripheral blood mononuclear5
the empty shuttle vector5
as the mean values5
confirmed by western blotting5
our results suggest that5
n and gapdh in5
research which is freely5
two tailed simple t5
against experimental gas gangrene5
weeks of age with5
nk cells showed the5
chickens immunized with inactivated5
of intestinal epithelial cells5
with the presence of5
was supported by the5
diarrhea among suckling pigs5
approved by the institutional5
by the institutional animal5
when compared to the5
the case of apmv5
a significant decrease in5
influenza a virus ns5
in blood and spleen5
myocardial degeneration and inflammation5
current status and future5
bovine mhc class i5
were inoculated oronasally with5
g and p genotypes5
gds strains were and5
homologous challenge with mhf5
cats in both groups5
tissue culture infectious dose5
the pigs in the5
of pedv cl protease5
pathogenicity of tw i5
by the addition of5
cells were cultured in5
found in the majority5
for h and incubated5
the sav control groups5
tissue and faecal samples5
group compared with the5
significant differences between the5
the plates were washed5
class i alleles was5
threshold and all p5
pandemic h n influenza5
the cells were treated5
the lungs and nasal5
human respiratory syncytial virus5
which is freely available5
the basal region of5
samples were collected at5
the understanding of the5
and colostrum of bnp5
replication and virulence of5
was used in the5
by a friedman test5
have been shown to5
an in vitro model5
results showed that pedv5
h n and b5
with goat t cells5
is shown in figure5
with mean titers of5
codon was found in5
immediate publication on acceptance5
colostrum of bnp dams5
until the end of5
comparison of the vp5
during the acute phase5
detection of viral rna5
atlantic salmon salmo salar5
no space constraints or5
of faecal samples from5
and approved by the5
may have contributed to5
on the cell surface5
at least one pathogen5
no effect on the5
for h in a5
broiler and layer ducks5
were purchased from the5
or gds strains for5
treated with proteinase k5
cd t lymphocyte counts5
play a key role5
viral rna detection in5
serum and colostrum of5
caused by tw i5
were provided by the5
mdbk mhc class i5
plates were infected with5
could be used for5
the role of the5
pedv n and gapdh5
h and incubated with5
of porcine proliferative enteropathy5
at the first outbreak5
cd high nk cells5
fixed and stained with5
second wave of the5
it has been suggested5
epidemic diarrhea virus in5
animals infected with apmv5
as indicated by the5
by chang et al5
alpha toxin and perfringolysin5
adaptive immune responses to5
to the culture medium5
pigs in this group5
in feline infectious peritonitis5
an intestinal loop model5
the different lung compartments5
the ns protein is5
compared with the virus5
fecv ucd and fecv5
in serum and colostrum5
data collection and analysis5
made it possible to5
respiratory dc macrophage network5
of viral rna in5
the respiratory dc macrophage5
risk of hpai h5
has been suggested that5
were randomly assigned to5
can be used as5
and t cell responses5
analysis was performed using5
were collected from the5
the most commonly used5
is freely available for5
and respiratory syndrome viruses5
the porcine reproductive and5
or color figure charges5
pigs compared with the5
were treated with the5
play important roles in5
gds strains for h5
of cd and cd5
respiratory syndrome virus porcine5
as compared to the5
in the context of5
in the induction of5
infected group and mab5
significance threshold and all5
was added to each5
higher than those of5
the changes in the5
ucd and fecv rm5
to adjust for multiple5
constraints or color figure5
the mechanisms involved in5
space constraints or color5
is required for the5
geometric mean fluorescent intensity5
value lower than its5
bvd vaccinated bnp dams5
in a total volume5
lower than in the5
calves vaccinated with the5
were confirmed by western5
at a concentration of5
experiments were performed in5
the institutional animal care5
through the activation of5
compared to the nkp5
the clearance of prrsv5
newcastle disease virus strains5
the lungs of mice5
tomatidine for h and5
a wide range of5
of bnp in the5
has been observed in5
syndrome virus porcine reproductive5
can be found in5
was used to compare5
the number of samples5
in the porcine respiratory5
an equal volume of5
as a marker for5
scopus and google scholar5
sequence of avian paramyxovirus5
incubated at room temperature5
western blotting at hpi5
on the basis of5
type i and type5
associated with respiratory diseases5
the replication and virulence5
the virus in the5
in chickens immunized with5
and gapdh in the5
cells were maintained in5
these results suggest that5
derived significance threshold and5
with respiratory diseases in5
the fourth transcription unit5
the united states and5
vac no cha pigs5
and characterization of a5
the effect of tomatidine5
influenza virus infection in5
to the spread of5
embedded in paraffin wax5
activated cd t lymphocyte5
stimulated with inactivated h5
g b live vaccine5
the binding energy of5
after the second transfection5
after the first transfection5
and porcine circovirus type5
of the vp gene5
further studies are needed5
against porcine viral infections5
for the first time5
immune responses in the5
of the s protein5
infected cells in the5
mab d group were5
with fresh dmem containing5
ns protein of influenza5
uninfected and infected pigs5
freely available for redistribution5
was carried out in5
and the number of5
the presence of a5
density of broiler and5
on ice for min5
the viability of the5
status and future direction5
in the total lung5
the active pocket of5
strains identified in this5
differentiated airway epithelial cells5
the aim of this5
clearance of prrsv from5
lesions were observed in5
invasion rates of pedv5
gene expression levels were5
were then washed with5
the prrsv envelope proteins5
other swine disease viruses5
the sav control group5
groups a and b5
of the host immune5
at k of the5
and western blotting analysis5
the type i interferon5
anova followed by a5
with the immune system5
changes consistent with fip5
course of the experiment5
lower than its fdr5
a virus ns protein5
a primary prv infection5
of pedv n and5
we would like to5
in the intestinal loop5
between bnp and non5
mhc class i protein5
nk cells in the5
tenfold serial dilutions of5
is a heritable trait5
were performed using the5
from blood and spleen5
pigs were challenged with5
of pedv rna in5
cells were washed twice5
blotting at hpi and5
and use committee of5
significance reached at days5
bacillus subtilis spores as5
the levels of ifn5
of hpai in thailand5
the ability of the5
of the innate immune5
the immune response in5
h after the first5
and stained with anti5
of proteinase k treated5
on the viability of5
and g p strains5
strains were and in5
of alpha toxin in5
pigs from no vac5
spread of hpai h5
with fetal bovine serum5
mab d group was5
tests for unequal variance5
were and in the5
cells are in a5
figure a and b5
reciprocal of the highest5
between mdbk cells and5
high density of broiler5
acute phase of infection5
newcastle disease viruses in5
the early stage of5
detected in any of5
strong innate immune responses5
respiratory syndrome virus in4
bnp and bnp calves4
any of the other4
pigs porcine reproductive and4
fold serial dilutions of4
bmc and benefit from4
in the swine industry4
performed using graphpad prism4
cd a cd low4
revealed the presence of4
room temperature for h4
difference between the gds4
is a member of4
have resulted in a4
the pcr products were4
error of the mean4
nk cells from spleen4
used as negative controls4
increased expression of the4
the results show that4
are the most common4
choose bmc and benefit4
the data collection and4
pigs in laiv none4
significantly higher than in4
pedv entry relies on4
control and infected animals4
had no effect on4
a broad range of4
different letters on each4
the results of the4
depicts the overall average4
the other two viruses4
and reemerging epizootic swine4
were included in the4
of the respiratory tract4
virus titers in the4
that mab d could4
in the balf of4
in terms of mean4
could be observed for4
and lung viral loads4
in the sav control4
higher than in the4
with the seeder pigs4
bnp within the calf4
mdbk and paternally inherited4
the prevalence of cryptosporidium4
research and development of4
during the pathogenesis of4
under the accession numbers4
in the late co4
the dam rather than4
wave of the epidemic4
remained within the reference4
you to find the4
vero cells were treated4
values smaller are significant4
compared to g b4
number of samples with4
are susceptible to infection4
ecology and epidemiology of4
oral and cloaca swabs4
been reported to be4
with a combination of4
porcine respiratory coronavirus in4
viral titers of the4
significantly higher in the4
not detected in any4
against other swine disease4
the innate and adaptive4
performed in accordance with4
replication of the virus4
the mice in the4
mab d reacted with4
mdm at hpi and4
our results indicate that4
was controlled at using4
in combination with cd4
for influenza a virus4
differences in the amount4
the other two splenic4
the splenic nkp high4
was associated with a4
the g p and4
the oral and cloaca4
with a signal above4
with tenfold serial dilutions4
for differentiated respiratory epithelial4
of the expression of4
the exact role of4
were approximately and in4
vivo and in vitro4
each group denote a4
dpi in all tissues4
and institutional affiliations we4
innate immune responses in4
basal region of the4
the number above the4
friedman test corrected by4
with the control group4
of goat t cells4
the protective efficacy of4
irrelevant mab igg groups4
outbreaks of diarrhea among4
samples that did not4
both groups remained within4
was detected by qrt4
production compared to the4
nkp nk cells showed4
heritable trait of the4
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the hamsters infected with4
pigs vaccinated with the4
the relative risk for4
the pathogenesis of feline4
the use of the4
and nasal turbinates of4
the inflammatory response to4
experiments were approved by4
performed as previously described4
serum and lung viral4
in mouse and human4
in an intestinal loop4
in samples from fip4
nasal turbinates of all4
were kindly provided by4
significantly lower than in4
and pathogenicity of apmv4
in pbs for min4
of the immune responses4
reduce the need for4
pigs at different ages4
in the vero and4
study are included in4
adjust for multiple comparisons4
chicken type i interferon4
of the other two4
in this study were4
ready to submit your4
role of alpha toxin4
identified as differentially regulated4
in a given ecosystem4
figure on next page4
clinical signs of disease4
the samples were collected4
subdistricts with a high4
splenocytes or monocytes macrophages4
there were no differences4
l substitution in the4
in group a showed4
strains of h n4
kegg terms related to4
to plasma transfusion and4
inhibited the activity of4
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letters on each group4
on each group denote4
drafting of the manuscript4
the no vac cha4
with cats in group4
highly pathogenic h n4
the immunogenicity of the4
detected in the serum4
multiple comparison test was4
fipv replication in vitro4
mean log number of4
with the target host4
protective immune response in4
and the mdbk cell4
the cells were stained4
than or equal to4
of each serum sample4
levels of viral rna4
with the indicated concentrations4
the duration of the4
passively immunized and control4
sus scrofa and chlorocebus4
influenza a viruses from4
helps you to find4
the mixtures were then4
knockdown of the expression4
monocytes macrophages stimulated with4
by all three technologies4
coordination of the study4
proteinase k treated purified4
we did not observe4
study was supported by4
virus replication in the4
group denote a significant4
using the principle from4
for the duration of4
for a review see4
tool helps you to4
the onset of peak4
in the production of4
alloantibody binding of pbmc4
are shown in table4
number above the plots4
nkp nk cells in4
salmonella enterica serovar typhimurium4
rna and dna viruses4
samples in four replicates4
the activation of the4
were incubated with the4
j cells were treated4
of bnp within the4
pathogenic avian influenza h4
genome sequence of avian4
the control pigs at4
hamsters infected with apmv4
strains have been isolated4
leucine codon was identified4
th and th responses4
plots describes the number4
via mhc class ii4
expression levels were higher4
was calculated using the4
our results show that4
and incubated for h4
relative copy numbers in4
of age with a4
pigs in the wiv4
rna was detected in4
important to note that4
to provide protection against4
selector tool helps you4
onset of peak bacteremia4
balb c mice were4
in additional file e4
with hematoxylin and eosin4
of the study and4
to find the most4
results of this study4
cell subsets in blood4
were then further incubated4
the influenza a virus4
critical role in the4
agents associated with respiratory4
in vivo and in4
denote a significant difference4
in the transmission function4
trait of the dam4
cd a cd int4
our understanding of the4
to each well and4
samples with a signal4
in a humidified chamber4
was supported by grants4
it is noteworthy that4
in this study to4
above the plots describes4
infected with tenfold serial4
plates were incubated for4
applied to the apical4
a high level of4
the amount of virus4
the course of a4
pathogenesis and interaction with4
infectious hematopoietic necrosis virus4
and nm emissions every4
loads in the lungs4
virulence of influenza virus4
in the s protein4
from domestic ducks in4
associated with an increased4
interaction with the immune4
measured by flow cytometry4
the growth rate of4
the total number of4
involved in the maintenance4
a signal above the4
with pbs to remove4
design and coordination of4
can enter cells through4
this study to those4
of highly pathogenic avian4
against influenza a virus4
cytokines locally in the4
to the apical surface4
and coordination of the4
the protective role of4
nm excitation and nm4
compared with cats in4
and cellular immune responses4
organisation for animal health4
of african swine fever4
against alpha toxin alone4
newcastle disease virus strain4
the internalization rates of4
than the gds strain4
above the horizontal line4
number of copies g4
a large number of4
of mice treated with4
any clinical signs of4
were used as negative4
figure and additional file4
form of the virus4
pcr was carried out4
principle from benjamini and4
influenza h n virus4
virus belonging to the4
and the presence of4
both the upper and4
against native alpha toxin4
the most relevant journal4
the early induction of4
a multiplicity of infection4
cells were stained with4
lower compared with the4
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at final concentrations of4
to the target population4
infection with porcine reproductive4
h n and h4
of copies g of4
that the m l4
a vital role in4
the highest serum dilution4
the other apmv serotypes4
can be divided into4
cell subsets in the4
in the wiv treatment4
the samples collected at4
recruitment of nk cells4
may have resulted in4
in the sera and4
significantly increased in alv4
related to immune responses4
were infected with tenfold4
viruses associated with the4
dotted line depicts the4
data were analysed using4
transfer of antibodies from4
the results of this4
and interaction with the4
phenotype of the calf4
study to those of4
methionine codon was identified4
immune cells in the4
of antibodies from mhf4
the guidelines of the4
copies g of rna4
i and type ii4
in most of the4
see figure on next4
pellets were resuspended in4
pathogenic avian influenza viruses4
alveolar and vascular areas4
in the female reproductive4
the horizontal dotted line4
better understanding of the4
university institutional animal care4
indicated concentrations of tomatidine4
were used as a4
the receptor binding domain4
h n oil vaccine4
statistical analysis was performed4
turbinates of all three4
samples were collected from4
reached at day pi4
necrotic enteritis in broiler4
characterization of a new4
the indicated concentrations of4
groups remained within the4
dam rather than the4
group than in the4
of the virus into4
to further explore the4
excitation and nm emissions4
a mhc class i4
fourth transcription unit of4
genes of the gar4
mixtures were then further4
the specificity of the4
did not result in4
for porcine epidemic diarrhea4
cells were inoculated with4
find the most relevant4
the lumen of the4
infectious bronchitis virus strain4
h n swine influenza4
in the number of4
by targeting cl protease4
swine at agricultural exhibitions4
blood samples were collected4
were harvested and the4
no virus was isolated4
infectious peritonitis virus infection4
receptor family member cd4
than the calf and4
of porcine circovirus type4
no significant differences between4
alpha toxin activity was4
human influenza a viruses4
the development of fip4
against h and h4
with pedv at moi4
are listed in table4
and virulence of influenza4
stained with hematoxylin and4
lower than those in4
this protocol was performed4
were measured using qrt4
j replication in mdm4
to the sav control4
relative copy numbers were4
the cells were harvested4
h after the second4
gar strains identified in4
and then incubated with4
one of the main4
of the chicken genome4
performed as described elsewhere4
for the mab d4
as the number of4
of mice in the4
efficacy under field conditions4
carrying the empty shuttle4
live bird markets in4
shown in additional file4
the university of minnesota4
mrna expression levels of4
vaccines against porcine reproductive4
of all three animals4
as a result of4
be detected in the4
we found that the4
as well as a4
was responsible for the4
to g b isolates4
the gar strains identified4
which is consistent with4
the respiratory tract of4
strain was more sensitive4
of the influenza virus4
the porcine respiratory disease4
humoral and cellular immune4
cd t cell proliferation4
of the vp genes4
described in the above4
recombinant vesicular stomatitis virus4
effects of hcesps on4
risk of hpai in4
of the dam rather4
j infection in mdm4
density of native chickens4
with that of the4
for min and then4
white leghorn chickens were4
to determine the significance4
nm emissions every minute4
line depicts the overall4
pigs in the laiv4
analysis of proteinase k4
differences in mhc class4
following homologous challenge with4
amount of viral rna4
reviewed and approved by4
antigenic differences between the4
faecal virus shedding and4
infectious bursal disease virus4
the cd cell population4
gds strain was more4
the calf as a4
the mucosal immune system4
the experiments were performed4
nucleotide sequences of the4
xx xx xx xx4
virus replication and virulence4
at nm excitation and4
broiler and layer chickens4
epidemic diarrhea virus strains4
our selector tool helps4
the acetylated k residue4
the activity of pedv4
pcr reactions were performed4
on the immune response4
and the number above4
could not be detected4
the authors concluded that4
with reference strain dq4
d the vero cells4
are summarized in table4
porcine hemagglutinating encephalomyelitis virus4
high nk cells from4
the same results were4
respiratory syndrome virus induces4
a significant difference at4
the length of the4
comparison test was performed4
be attributed to the4
the location of the4
role in the clearance4
blocked with bsa in4
difference in protein sequence4
well plates were infected4
blood as well as4
at using the principle4
to influenza a virus4
an aliquot of the4
were performed as described4
was isolated from lungs4
susceptible to infection by4
in the netherlands and4
of diarrhea among suckling4
of the bvdv bhv4
in the nasal turbinates4
the cd a cd4
describes the number of4
to submit your research4
in response to infection4
of the pigs in4
immunized and control cats4
were inserted into the4
was significantly inhibited by4
vp genes of the4
significant difference at p4
the induction of ifn4
n and h n4
enteritis in broiler chickens4
cats in this study4
in each group were4
approved by the animal4
standard error of the4
the plots describes the4
bnp in calves is4
rather than the calf4
was used to determine4
the principle from benjamini4
data and drafted the4
in both the upper4
interpretation of data and4
to the closest highway4
of the extracellular part4
m l substitution in4
to the target host4
the amount of viral4
by the university of4
than those of the4
revealed that hcesp stimuli4
locally in the balf4
the cells from the4
showed a significant decrease4
within the reference interval4
titers in the lungs4
exclude the possibility that4
in this study was4
the three virus strains4
transcriptase polymerase chain reaction4
the gds strain was4
the sav rna level4
blood was collected from4
results were confirmed by4
used to analyze the4
and phylogenic analysis of4
were fixed with paraformaldehyde4
the sav rna levels4
the effects of the4
of the infected flock4
showed an increase in4
a heritable trait of4
of the hpai h4
and cd t cells4
compared to the cd4
virus and porcine circovirus4
guidelines of the animal4
up to day pi4
the cell lysates were4
research was supported by4
in swine at exhibitions4
of samples with a4
aliquot of plasma pool4
world organisation for animal4
or mab igg group4
fecv ucd infected cats4
in which the pathogen4
a friedman test corrected4
then further incubated at4
of pigs infected with4
prior to plasma transfusion4
respiratory syndrome virus replication4
groups compared to the4
samples from fip cats4
binding of mdbk cells4
as subtype iiaa g4
monitored at nm excitation4
cat in group b4
alloantibody binding of mdbk4
respiratory syndrome virus vaccines4
horizontal dotted line depicts4
of viral rna were4
calf mhc class i4
an emerging and reemerging4
n swine influenza virus4
g strains comprising lineage4
has been reported to4
of severe acute respiratory4
calves immunized with the4
a critical role in4
of mean log number4
is important to note4
protocol was performed as4
the no vac no4
the laiv treatment groups4
the vp fragment of4
from benjamini and hochberg4
protein of influenza a4
to a final concentration4
of clostridium perfringens alpha4
log number of copies4
to a lesser extent4
a protective immune response4
mimic k r substitution4
to those of reference4
the difference in protein4
scrofa and chlorocebus sabaeus4
work was supported by4
and then shifted to4
serial dilutions of the4
of h n virus4
the secretion of il4
emerging and reemerging epizootic4
terms of mean log4
cells were washed three4
suppressor of cytokine signaling4
the blood nkp nk4
h n influenza viruses4
the mab igg group4
controlled at using the4
reemerging epizootic swine virus4
cme to enter cells4
was monitored at nm4
animal and public health4
of respiratory syncytial virus4
was extracted from the4
signal above the horizontal4
vaccines for porcine epidemic4
previous reports showed that3
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national institutes of health3
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protein sequences and the3
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of the samples collected3
were in agreement with3
rare occurrence of bnp3
commercial inactivated g b3
of mhc class ii3
splenocytes were stained with3
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the proteins are colored3
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cats in groups a3
the number of hydrogen3
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in serum or colostrum3
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visualized using western blot3
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was significantly lower than3
new approaches and potential3
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for porcine reproductive and3
enhance antigen uptake by3
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cells from blood and3
found no differences in3
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the nature of the3
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represent the three mice3
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expression levels of nkp3
summarized in additional file3
samples and nasal swabs3
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counts in cats in3
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based on the corresponding3
distantly related to human3
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the highest levels of3
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the prevalence of this3
viral loads in terms3
vp and vp genes3
the identification of bridge3
of group a rotaviruses3
method of estimating fifty3
inflammatory cytokines tumor necrosis3
of classical swine fever3
insights into the mechanisms3
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play a critical role3
tuberculosis in new zealand3
enter cells through the3
early stage of infection3
vp genes from the3
and the influx of3
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defective interfering influenza virus3
are expressed in terms3
the same time point3
known about the mechanisms3
transcription polymerase chain reaction3
detected at the first3
a methionine codon at3
contact with infected animals3
of tomatidine with pedv3
protective immune response against3
respiratory epithelial cells are3
commercial h n oil3
of pedv entry into3
respiratory epithelial cells in3
be used as an3
gds strains in the3
peritonitis is determined by3
differences in the ability3
from no vac cha3
infectious peritonitis is determined3
of local immune responses3
the nkp and nkp3
the role of alpha3
in the virusinfected group3
via the apical membrane3
macrophage tropism during the3
reaction was performed using3
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and months of age3
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mabs reacted with ha3
from pigs at different3
protective immune responses against3
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activity of tomatidine against3
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nkp and nkg d3
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compared to the control3
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position in the s3
need for antibiotic use3
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a significant difference between3
gfp nsp encoding plasmid3
effect on the viability3
presented in additional file3
are shown as a3
pedv iga antibodies in3
it is the most3
value less than or3
to kag vaccine controls3
it has also been3
pbmc irrespective of total3
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was considered to be3
as early as dpc3
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infectious diseases in animal3
of hepatitis c virus3
the release of cytokines3
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findings suggest that the3
high morbidity and mortality3
the plasma membrane of3
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over the course of3
cytokines chemokines in the3
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were randomly divided into3
prevalence of cryptosporidium in3
the sav and sav3
the university of bristol3
day and on days3
after the onset of3
been used as a3
the pigs were challenged3
the absence of neutralization3
previous study demonstrated that3
response to porcine reproductive3
compounds are colored green3
be detected in proteinase3
in the peripheral blood3
were fixed at hpi3
in case of gp3
were observed at hpi3
samples were collected and3
pigs infected with prrsv3
need to be further3
at pathway in fcwf3
we speculated that alv3
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second transfection was carried3
strain of porcine epidemic3
indicated by different superscripts3
live porcine reproductive and3
the virusinfected group and3
pathogenic h n influenza3
as described in the3
had a methionine codon3
was supported by a3
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was characterised by a3
by porcine reproductive and3
levels were significantly higher3
the development of novel3
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swabs were collected from3
within the calf as3
fixed at hpi and3
the amount of infectious3
is important for virus3
and represent the three3
influenza a virus replication3
against both he proteins3
from bsc cells infected3
showed the highest nes3
protein of haemonchus contortus3
well plates were co3
tropism during the pathogenesis3
the vero cells were3
and clinical disease following3
the magnitude of rna3
these results demonstrate that3
ipd bovine mhc class3
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mhc class i proteins3
fathered by the same3
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at rt for min3
pcr using the forward3
tomatidine and the active3
binding energy of the3
occurrence of bnp in3
after heterologous virus challenge3
sites of enzyme pockets3
most similar mdbk and3
animal and human health3
the thermal cycling profile3
of sera obtained from3
compared with that of3
inoculated with virus strain3
given birth to a3
in the splenic nkp3
magnitude of rna copies3
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as described for mhc3
pigs in each group3
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that hcesp stimuli induced3
no statistically significant differences3
of key genes in3
inflammatory mediators released by3
of the immune system3
thereafter up to day3
infection has been shown3
the relative copy numbers3
significantly lower than that3
in the control cats3
infectious bronchitis virus in3
of the airway epithelium3
and fluorescence was monitored3
the three experimental groups3
none of the pigs3
of virulent newcastle disease3
exposure was avoided throughout3
against g b challenge3
showed that the virus3
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cells infected with rvv3
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neutralizing antibodies were not3
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the emergence of highly3
across the epithelial barrier3
to transmit the pathogen3
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released into the supernatant3
a commercial inactivated pedv3
test was performed in3
that tomatidine inhibits pedv3
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of the control group3
with repeated outbreaks of3
participated in its design3
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mucosal iga antibody response3
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the gene expression levels3
of the four designated3
and the location of3
infected pigs at dpc3
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progress has been made3
each well and incubated3
the expression of cd3
cells were isolated by3
of the infected cells3
pigs were euthanized at3
more than one pathogen3
prevalence of cryptosporidium infection3
of the amount of3
from lungs and nasal3
an increased cytokine production3
from the department of3
clinical outcome of the3
in groups a and3
of poultry and poultry3
was used to calculate3
from kd to kd3
an optimal signalase cleavage3
toxin of clostridium perfringens3
nk cells from blood3
the data are presented3
pedv g b at3
rotavirus classification working group3
more details of the3
prevention and control of3
in the nucleus of3
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to account for the3
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a review of feline3
feline coronavirus infections in3
after incubation for h3
cells were collected and3
all three virus strains3
virusinfected group and mab3
group and irrelevant mab3
three cats in group3
and subunit vaccines against3
the three viral strains3
recognised genes were identified3
a and b at3
results suggest that the3
bnp as a sire3
this study are included3
of tomatidine on clpro3
vero cells cultured in3
the clinical outcome of3
symposium on alternatives to3
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docked conformations of tomatidine3
growth rate of the3
represents viral loads in3
cell subset compared to3
polymerase chain reaction assay3
mice inoculated with virus3
the design and coordination3
severity of the disease3
sera obtained from pigs3
cd a cd high3
as a sire trait3
compared to each other3
in farmed atlantic salmon3
previous studies have shown3
group or mab igg3
feline coronavirus spike protein3
of influenza a infection3
into the phenotype of3
associated with a high3
in laiv none group3
economic losses in the3
the alpha toxin activity3
in each of the3
the present study we3
the pulmonary parenchyma of3
of the faecal samples3
replication by targeting cl3
the world organisation for3
compared by two tailed3
on alternatives to antibiotics3
the authors thank the3
the onset of maximal3
vaccine based on a3
with porcine circovirus type3
as adjuvants in chickens3
the reed and muench3
with the aim of3
is essential for the3
shanghai jiao tong university3
the following thermal profile3
used as a control3
generation and characterization of3
of enzyme pockets are3
induction of necrotic lesions3
environmental and management conditions3
this study was supported3
were confirmed negative for3
genes were identified as3
the k r mutation3
proteinase k treated or3
the passively immunized and3
fresh dmem containing tomatidine3
amount of infectious virus3
experiments were performed with3
by haydon et al3
influenza virus ns protein3
and porcine g strains3
nkp nk cells from3
influenza virus in chickens3
disease is caused by3
at position in the3
activity of alpha toxin3
the need for antibiotics3
percentage of cells in3
was isolated from any3
for each of the3
in the above section3
cells treated with the3
b pigs by dpv3
have been carried out3
expressed in terms of3
the primers and probe3
with h n influenza3
it is possible to3
for the diagnosis of3
observed in three cats3
reverse transcription polymerase chain3
the pathogenesis of the3
different values for a3
in dams not vaccinated3
acid changes in the3
absorbance was measured at3
expressed as the reciprocal3
contact with the virus3
the clinical signs and3
and protective efficacy of3
enhance the proliferation of3
sav rna levels in3
in order to determine3
observed in the cytoplasm3
and the supernatants were3
swine influenza virus in3
is involved in the3
the majority of the3
the presence of antibodies3
in accordance with a3
the lack of an3
may have played a3
of host proteins in3
significant differences between groups3
for min and the3
ns protein in the3
we speculated that tomatidine3
pedv g b vaccine3
using a power sybr3
were used to determine3
of porcine nk cells3
times with pbs to3
specific antibody and t3
endothelial cytotoxicity in vitro3
laiv com and laiv3
located in the nucleus3
half of the pigs3
pathogen to the target3
were blocked with bsa3
parts of the world3
were designed and synthesized3
higher than that of3
is the use of3
in the course of3
significantly higher than that3
at the fourth outbreak3
the supernatant was collected3
of the virus was3
from animals infected with3
that completely inhibited hemagglutination3
clinical signs such as3
showing a positive signal3
total of ml of3
based vaccine delivery platforms3
sections were incubated with3
the odds of bnp3
used to compare the3
protein a g plus3
in the poultry industry3
economic losses to the3
compounds and proteins are3
tomatidine on clpro activity3
on human nk cells3
conformations of tomatidine with3
be found in the3
institute for animal health3
pattern was less pronounced3
was in accordance with3
excretory and secretory proteins3
infected with tw i3
played a role in3
loads in terms of3
statistical analyses were performed3
are included in this3
viruses isolated from domestic3
lipid raft enrichment layer3
carried out at h3
induced endothelial cytotoxicity in3
of mice infected with3
for the emergence of3
that genetic differences between3
the effect of the3
treated with the indicated3
estimating fifty per cent3
studies have demonstrated that3
the g b virus3
bacteremia and clinical disease3
was defined as a3
significantly lower in the3
subunit vaccines against porcine3
leucine codon was found3
in cats with fip3
of the virus by3
and the control group3
the integrity of the3
birth to a calf3
tissue samples were collected3
with any of the3
avian influenza virus infection3
reactivity of sera obtained3
three viruses of the3
see materials and methods3
a higher number of3
use of laboratory animals3
into protein sequences and3
at the level of3
each group at different3
mutations in the feline3
united states and the3
losses in the swine3
in this published article3
from calves immunized with3
in porcine reproductive and3
related to immune signalling3
in the cells were3
direct contact with infected3
extracellular part of the3
transcription unit of pvsv3
in swine at agricultural3
binding energy of tomatidine3
spread of the hpai3
experiments were carried out3
higher levels of ifn3
on the same farm3
to determine the effect3
swine influenza a virus3
act as bridge hosts3
been performed to identify3
power sybr green kit3
energy of the tomatidine3
analysis was performed on3
cells were labelled with3
spread of the disease3
involved in pedv entry3
pigs were exposed to3
in response to influenza3
the nadir reached at3
of natural killer cells3
risk for both chickens3
protocols were approved by3
and transforming growth factor3
a significant effect on3
from each group were3
samples that were positive3
from the same animal3
per year ready to3
of bnp dams compared3
the s a substitution3
genbank under the accession3
united states porcine epidemic3
t cells treated with3
after ph n infection3
performed as described previously3
disease virus strains isolated3
nasal turbinate infected with3
responses to prrsv infection3
in the nucleus and3
a showed significantly higher3
decrease in egg production3
as alternatives to antibiotics3
cells were fixed at3
were identified as differentially3
the compounds are colored3
pathogenesis of feline infectious3
these findings suggest that3
the absence of the3
were infected with the3
irrespective of total alloantibody3
immunofluorescence was evident primarily3
sequences were detected in3
no vac cha and3
in chicken and duck3
in the epidemiology of3
and the production of3
has been identified as3
during influenza virus infection3
the need for antibiotic3
among the pigs at3
the humoral immune response3
of prrsv from pigs3
immunized with spore h3
th and th immune3
pedv entry into cells3
airway epithelial cells are3
harvested and the cleaved3
of the economic impact3
genotype viid newcastle disease3
antibodies against porcine epidemic3
those in the other3
bovine airway epithelial cells3
antigen was detected by3
available for redistribution this3
paternally inherited calf mhc3
cells were stimulated with3
dpc are indicated by3
was detectable in the3
fragment of gfp nsp3
the united states department3
euthanized by cervical dislocation3
genechip chicken genome array3
of innate and adaptive3
cleaved fragment of gfp3
influenza a virus by3
dc macrophage network in3
was measured by flow3
feces and blood of3
evade the host immune3
the nucleotide identities of3
by two tailed simple3
were prepared as described3
of the tissue samples3
less than or equal3
washed with pbs containing3
the essential role of3
goat t cells were3
was isolated from the3
the passive transfer of3
newcastle disease virus isolates3
in both inoculated groups3
of health and human3
sequences were deposited in3
are represented as sticks3
the first step in3
as risk factors for3
alone was found at3
commercial inactivated pedv g3
at day pi in3
against the n protein3
from the lungs and3
at the same settings3
mab d and irrelevant3
and weeks of age3
injuring the cell monolayer3
at dpi in all3
transfused with a ml3
of tumor necrosis factor3
were inoculated intranasally with3
also present in the3
were immunized twice with3
are indicated by different3
thermal profile was used3
colored according to their3
using an unpaired t3
differences between mdbk cells3
passive transfer of antibodies3
detected among the pigs3
alpha toxin activity and3
following thermal profile was3
the viability of goat3
three mice euthanized from3
shown as a mesh3
level was set to3
for s followed by3
acetylation at k of3
fifty per cent endpoints3
was lower than that3
viid newcastle disease virus3
was detected in any3
samples of mice inoculated3
serum dilution that completely3
of porcine alveolar macrophages3
was also found in3
fmdv isolates to activate3
of nasal virus shedding3
blood and spleen were3
with different functional properties3
splenic nkp nk cells3
raised against native alpha3
nsp was visualized using3
united states department of3
due to differences in3
or normal rat igg3
of bovine necrohemorrhagic enteritis3
rates in the gds3
to the fact that3
turbinate infected with apmv3
the tissue samples were3
a virulent newcastle disease3
the supernatants were collected3
antibody response against the3
gd and sd were3
between the most similar3
of the united states3
most different to the3
hpi and stained for3
stained for confocal analysis3
viral titers in the3
for mhc class i3
were suspended in serum3
the basal side of3
from blood and cd3
of influenza a h3
response to porcine respiratory3
the outcome of a3
of feline coronaviruses in3
of avian infectious bronchitis3
with an increased risk3
of macrophage tropism during3
of avian paramyxovirus serotype3
cattle mhc class i3
a combination of both3
at the c terminus3
natural killer cells in3
sera from calves immunized3
rna detection in collected3
analyses were performed with3
sucrose density gradient centrifugation3
and mouth disease virus3
origin human influenza a3
in the infected mice3
of estimating fifty per3
in the transmission of3
of sus scrofa and3
western blotting showed that3
this research was supported3
results are expressed in3
against h n civ3
to the respiratory tract3
that the presence of3
any of the tissues3
in spf chicken eggs3
tended to be higher3
dam mhc class i3
com com and aut3
from the no vac3
not differ significantly from3
and bnp dams are3
terms related to viral3
platelet aggregation in the3
stranded dna virus of3
the cytoplasm of the3
in bronchiolar areas at3
between the dam and3
all of the animals3
of the viruses and3
the mechanism by which3
and performed in accordance3
and pi compared with3
in the spike protein3
detection in collected samples3
of mice inoculated with3
a major role in3
key role in activating3
of the most devastating3
cryptosporidium parvum infection in3
iav in swine at3
of nkp nk cells3
lesions in any of3
a decrease in the3
comparison with other paramyxoviruses3
from splenocytes or monocytes3
at a final concentration3
essential genes in the3
was set to p3
leukosis virus subgroup j3
be caused by the3
hpai h n in3
was provided by the3
cells via the clathrin3
in pancreas and acute3
this pattern was less3
were collected from pigs3
of mdbk cells by3
respiratory coronavirus in pigs3
expression level of cd3
at a multiplicity of3
levels were higher in3
influenza virus in pigs3
week and weekly thereafter3
the pathogen to the3
in the final model3
were replaced with fresh3
in naturally infected cats3
invasion rate of pedv3
accession numbers gu to3
to prevent the virus3
in the gds and3
the two he lineages3
proposed by chang et3
to the mucosal immune3
of broiler chickens against3
supernatants were replaced with3
at a ratio of3
when most of the3