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
transmissible gastroenteritis virus	718
of transmissible gastroenteritis	304
porcine epidemic diarrhea	302
epidemic diarrhea virus	256
the presence of	223
in this study	217
transmissible gastroenteritis coronavirus	203
the s protein	202
porcine respiratory coronavirus	195
mouse hepatitis virus	147
of the s	146
the expression of	143
according to the	137
of the tgev	130
infected with tgev	127
for h at	125
as well as	122
the cells were	119
for min at	116
of the virus	114
porcine transmissible gastroenteritis	113
in the presence	110
of porcine epidemic	105
data not shown	101
end of the	100
was used to	100
reproductive and respiratory	98
and respiratory syndrome	97
porcine reproductive and	97
tgev and prcv	94
infectious bronchitis virus	94
cells infected with	94
the s gene	93
feline infectious peritonitis	92
at room temperature	89
in the s	87
of tgev and	87
results showed that	87
respiratory syndrome virus	86
as shown in	86
that tgev infection	85
the use of	82
the detection of	82
in order to	81
of the coronavirus	80
were infected with	79
the role of	79
the absence of	78
it has been	78
in the tgev	78
analysis of the	77
the effect of	76
compared with the	76
shown in fig	76
based on the	76
a and b	76
we found that	74
sequence of the	73
were used to	71
cells were infected	70
the level of	70
the present study	69
were transfected with	69
the leader rna	69
the m protein	69
intestinal epithelial cells	69
involved in the	68
were incubated with	68
showed that the	68
tgev n protein	67
pedv and tgev	67
acute respiratory syndrome	67
severe acute respiratory	67
due to the	66
used as a	65
in cell culture	64
for the detection	63
was used as	63
the small intestine	62
j cells were	61
the levels of	61
has been shown	60
cell cycle arrest	59
been shown to	59
tgev and pedv	59
an important role	59
cells were transfected	58
in st cells	58
to transmissible gastroenteritis	58
the effects of	57
of tgev in	56
to determine the	56
the development of	55
of porcine transmissible	55
the percentage of	55
strain of tgev	55
important role in	54
cells were washed	54
gastroenteritis virus and	54
the amount of	54
of tgev infection	53
in the present	53
in the absence	53
role in the	53
the results showed	52
were treated with	52
the production of	52
infectious peritonitis virus	52
the surface of	51
washed three times	51
three times with	51
of mouse hepatitis	51
of the viral	51
t cells were	51
the cell membrane	50
and porcine respiratory	50
have shown that	50
was detected in	50
a receptor for	50
hek t cells	50
the transmissible gastroenteritis	50
were analyzed by	50
the number of	49
expression of the	49
of the genome	49
respiratory syndrome coronavirus	49
with tgev at	49
virus and porcine	49
most of the	48
detected in the	48
porcine epidemic diarrhoea	48
the formation of	48
observed in the	48
than that of	48
the activation of	48
the cell surface	48
of the porcine	47
cells were incubated	47
derived from the	47
that of the	47
cells in the	47
is required for	47
one of the	47
protein of tgev	46
tgev s protein	46
the tgev s	45
the united states	45
are shown in	45
region of the	45
was added to	45
were used as	44
on the surface	44
binding to the	44
the ability of	44
as a receptor	44
as previously described	44
cells were fixed	43
st cells were	43
in addition to	43
has not been	43
of tgev was	43
is involved in	43
the spike protein	43
a role in	43
at h post	42
the n protein	42
as described previously	42
responsible for the	42
structure of the	42
three independent experiments	42
the regulation of	41
the binding of	41
were inoculated with	41
were grown in	41
were purchased from	41
by tgev infection	41
expression levels of	41
there was no	40
s protein of	40
the replication of	40
and g m	40
was carried out	40
was observed in	40
compared to the	40
the loss of	39
the end of	39
during tgev infection	39
a variety of	39
porcine aminopeptidase n	39
for min and	39
characterization of a	39
a member of	39
found to be	39
any of the	39
to that of	39
lactic acid bacteria	39
used in this	38
were fixed with	38
the genomic rna	38
cells were treated	38
in the cytoplasm	38
the sensitivity of	38
virus in the	38
results suggest that	38
activation of p	38
antibody binding to	38
in the united	38
were observed in	37
present in the	37
to determine whether	37
consistent with the	37
member of the	37
at h p	37
detection of tgev	37
of the n	37
rna was extracted	37
the results of	37
in the viral	36
the cell cycle	36
has been reported	36
fetal bovine serum	36
was isolated from	36
against transmissible gastroenteritis	36
of the cell	36
g for min	36
on the cell	36
of the leader	36
cov n proteins	36
indicating that the	36
of the spike	36
conjugated goat anti	36
cells transfected with	35
changes in the	35
cells treated with	35
of the two	35
the e protein	35
was determined by	35
shown to be	35
in the intestinal	35
diarrhea virus in	35
results indicate that	35
open reading frame	35
min at room	35
sequence analysis of	35
development of a	35
was performed using	35
higher than that	35
coronavirus transmissible gastroenteritis	35
were stained with	35
was detected by	35
is a major	34
found in the	34
infected st cells	34
the mechanism of	34
play an important	34
total rna was	34
the interaction between	34
with pbs and	34
times with pbs	34
were washed three	34
of porcine respiratory	34
a total of	34
the induction of	34
has also been	34
gastroenteritis virus in	33
days after infection	33
from transmissible gastroenteritis	33
molecular biology of	33
significantly higher than	33
domain of the	33
used for the	33
wang et al	33
of the three	33
s and g	33
were obtained from	33
associated with the	33
cd t cells	33
to investigate the	33
for tgev and	33
in our study	33
were added to	33
aminopeptidase n is	33
epidemic diarrhoea virus	33
was supported by	33
demonstrated that the	32
by centrifugation at	32
in the small	32
the control of	32
in the cells	32
between tgev and	32
and porcine epidemic	32
and incubated with	32
was used for	32
in transgenic plants	31
epidermal growth factor	31
to those of	31
the sequence of	31
laude et al	31
in infected cells	31
isolated from the	31
in the same	31
of the m	31
strand rna synthesis	31
in the gut	31
receptor for the	31
in the cell	31
of infected cells	31
added to the	31
incubated for h	31
the synthesis of	31
was significantly higher	31
cloned into the	31
gastroenteritis virus infection	31
coronavirus spike protein	31
detection of transmissible	31
shown in table	31
all of the	31
similar to that	30
after tgev infection	30
the tgev group	30
in vitro and	30
infected with the	30
was found to	30
be involved in	30
to be a	30
western blot analysis	30
to evaluate the	30
found that tgev	30
used in the	30
transmissible gastroenteritis of	30
presence of the	29
was purchased from	29
in tgev infection	29
p and jnk	29
the case of	29
a number of	29
results indicated that	29
each of the	29
that in the	29
play a role	29
n is a	29
activation of the	29
with transmissible gastroenteritis	29
the plasma membrane	29
then incubated with	29
high levels of	29
transmissible gastroenteritis in	28
to study the	28
the coronavirus transmissible	28
to the cell	28
were used for	28
multiplicity of infection	28
this work was	28
to assess the	28
monoclonal antibodies to	28
and transmissible gastroenteritis	28
were detected in	28
zhang et al	28
of a coronavirus	28
similar to the	28
sialic acid binding	28
induced by tgev	28
such as the	28
b and c	28
indicated that the	28
the cell culture	28
the tgev genome	28
by western blotting	27
the expression levels	27
the respiratory tract	27
was analyzed by	27
li et al	27
the basis of	27
genome sequence of	27
avian infectious bronchitis	27
the family coronaviridae	27
in the regulation	27
growth factor receptor	27
in the case	27
showed that tgev	27
shown in figure	27
the degree of	27
amino acid sequence	27
related to transmissible	27
the leader sequence	27
of a novel	27
found that the	27
sites of the	27
strains of tgev	27
the virus was	27
rapid detection of	27
amino acid changes	27
hemagglutinating encephalomyelitis virus	27
related to the	27
in transmissible gastroenteritis	27
it is not	27
of murine coronavirus	27
and incubated at	27
of the e	27
and incubated for	27
the viral genome	27
in contrast to	27
are involved in	27
swine transmissible gastroenteritis	26
lower than that	26
is associated with	26
has been demonstrated	26
with the tgev	26
similar to those	26
inoculated with tgev	26
and st cells	26
supplemented with fetal	26
infection with tgev	26
for h and	26
characterization of the	26
is responsible for	26
in our laboratory	26
diarrhea virus and	26
have been developed	26
was performed with	26
in the us	26
suggesting that the	26
with fetal bovine	26
biology of coronaviruses	26
of the small	26
s protein was	26
of the cells	26
in a co	26
swine enteric coronaviruses	26
and in the	25
between the two	25
of porcine reproductive	25
with tgev and	25
tgev spike protein	25
g m phase	25
coronavirus nucleocapsid protein	25
for detection of	25
open reading frames	25
s protein is	25
tgev infection in	25
in agreement with	25
room temperature for	25
been reported to	25
samples were collected	25
studies have shown	25
gene of tgev	25
the host cell	25
as described above	25
to be the	25
coronavirus infectious bronchitis	25
the n gene	25
performed as described	25
the pathogenesis of	25
of tgev n	25
the authors declare	25
were detected by	25
comparison of the	25
fetal calf serum	25
been shown that	25
these results suggest	25
suggests that the	25
delmas et al	25
can be used	25
hepatitis c virus	25
complete genome sequence	25
differences in the	25
major antigenic sites	25
receptor for tgev	25
gastroenteritis of swine	25
of enteric tropism	25
previous studies have	25
colon epithelial cells	25
in tissue culture	25
cells were grown	24
and of the	24
terminal domain of	24
control of the	24
of neutralizing antibodies	24
and characterization of	24
specificity of the	24
the specificity of	24
amino acid sequences	24
the immune response	24
the molecular biology	24
on the basis	24
at the end	24
washed with pbs	24
porcine intestinal epithelial	24
is essential for	24
loss of enteric	24
colostrum and milk	24
of feline infectious	24
mucosal immune responses	24
were incubated for	24
closely related to	24
work was supported	24
the construction of	24
was resuspended in	24
kim et al	24
at the same	24
detection of porcine	24
could not be	24
in which the	24
virulent and attenuated	24
of viral rna	24
type i interferon	24
than that in	24
located in the	24
c for min	24
washed twice with	24
cell lysates were	24
the supernatant was	24
depending on the	24
cells were cultured	23
in the lp	23
of the genomic	23
antigenic sites of	23
well as the	23
fixed with paraformaldehyde	23
ileum and colon	23
the s and	23
the golgi complex	23
min at rt	23
appears to be	23
those of the	23
in gnotobiotic pigs	23
a porcine respiratory	23
assay was performed	23
both tgev and	23
pigs inoculated with	23
cells which were	23
vesicular stomatitis virus	23
ileum epithelial cells	23
gastroenteritis in pigs	23
were washed with	23
were determined by	23
suggested that the	23
the structure of	23
the concentration of	23
and then incubated	23
coronavirus mouse hepatitis	23
nucleotide sequence of	23
data indicate that	23
in response to	23
this study was	23
identification of a	23
to analyze the	23
of antibody binding	23
but not in	22
some of the	22
bovine serum albumin	22
the infection of	22
chen et al	22
part of the	22
of e protein	22
by transmissible gastroenteritis	22
have not been	22
in the n	22
acid binding activity	22
apn and egfr	22
the nucleoprotein gene	22
is consistent with	22
garwes et al	22
of the prcv	22
pcr assay for	22
plays an important	22
the s glycoprotein	22
virus infection induces	22
was obtained from	22
the di rna	22
the ability to	22
of severe acute	22
of the same	22
sodium dodecyl sulfate	22
the virus in	22
used to detect	22
and the virus	22
in the virus	22
size of the	22
inserted into the	22
of st cells	22
epithelial cells of	22
in the intestine	22
pi k akt	22
viral rna synthesis	22
with respect to	22
because of the	22
of s protein	22
to confirm the	22
the nature of	22
of a porcine	22
n protein of	22
as described by	21
with ml of	21
have been reported	21
and tgev infection	21
linked immunosorbent assay	21
infected cells were	21
these results indicate	21
g m phases	21
m protein was	21
cellular receptor for	21
was found in	21
swine enteric coronavirus	21
were subjected to	21
gene of transmissible	21
cells were then	21
after h of	21
shown that the	21
and stained with	21
were found to	21
and stored at	21
has been described	21
the spike gene	21
of p and	21
in the early	21
of three independent	21
orf a and	21
have been used	21
terminus of the	21
at an moi	21
the samples were	21
no significant difference	21
the course of	21
by flow cytometry	21
ingezim corona diferencial	21
wesley et al	21
the generation of	21
immune response to	21
pcv and tgev	21
and cloned into	21
the lack of	21
m and s	21
under the control	21
a multiplicity of	21
of tgev to	21
the coronaviridae family	21
intestinal epithelial cell	21
tgev infection and	21
suggest that the	21
were cultured in	21
innate immune response	21
different time points	21
tgev in the	20
viral genomic rna	20
cells were collected	20
in newborn piglets	20
were pretreated with	20
in suckling piglets	20
an moi of	20
protein is a	20
by western blot	20
liu et al	20
two types of	20
murine hepatitis virus	20
is a member	20
the same time	20
of the protein	20
and orf b	20
have been described	20
expressed as the	20
study showed that	20
supported by the	20
there is a	20
in the study	20
that the tgev	20
in comparison with	20
c for h	20
the plates were	20
increase in the	20
in the control	20
was incubated with	20
c and d	20
for pedv and	20
the amino acid	20
a series of	20
replication in the	20
downstream of the	20
at a multiplicity	20
the m gene	20
the possibility of	20
a transmissible gastroenteritis	20
vitro and in	20
of the disease	20
at different time	20
of maternal antibodies	20
leader rna sequence	20
of the orf	20
to the s	20
herpes simplex virus	20
were fixed in	20
human coronavirus e	20
were carried out	20
paraformaldehyde for min	20
the site of	20
infected with rtgev	20
of all ages	20
polymerase chain reaction	20
f i p	20
the tgev rbd	20
was performed in	20
were found in	20
immune responses in	19
mutations in the	19
there is no	19
detection of the	19
treated with lp	19
gastroenteritis virus by	19
the fact that	19
revealed that the	19
the control group	19
as described in	19
of p mapk	19
the tgev nucleoprotein	19
incubated with the	19
godet et al	19
corresponding to the	19
the nucleocapsid protein	19
of the villi	19
the culture medium	19
enteric and respiratory	19
in the spike	19
was extracted from	19
tgev for h	19
was no significant	19
to tgev infection	19
n protein was	19
were cloned into	19
song et al	19
tgev m protein	19
to the n	19
related porcine respiratory	19
added to each	19
tgev and pcv	19
protein expressed in	19
than in the	19
deletion in the	19
resulting in the	19
required for the	19
mucosal immune system	19
and in vivo	19
risco et al	19
induced by the	19
with or without	19
the piglets were	19
a mixture of	19
not essential for	19
from three independent	19
polyacrylamide gel electrophoresis	19
the sialic acid	19
cycle arrest and	19
the addition of	19
protein of transmissible	19
indicates that the	19
nature of the	19
sensitivity of the	19
may be a	19
coronavirus related to	19
in the infection	19
dna and rna	19
a and orf	19
probably due to	19
the viral rna	19
of cell cycle	19
interaction between the	19
were washed twice	19
m protein is	19
the ratio of	19
of the intestinal	19
the importance of	18
arrest and apoptosis	18
of the assay	18
of the pedv	18
degree of antibody	18
that the virus	18
pcr products were	18
obtained from the	18
understanding of the	18
tgev n gene	18
the gene encoding	18
indicate that the	18
the porcine epidemic	18
used as the	18
compared to that	18
we investigated the	18
ren et al	18
level of p	18
sequences of the	18
in cell cultures	18
immune responses to	18
human immunodeficiency virus	18
and that the	18
sites a and	18
the influence of	18
site of the	18
to detect the	18
in ml of	18
at the indicated	18
epithelial cells and	18
the in vitro	18
the porcine transmissible	18
the possibility that	18
tgev infection induced	18
is an important	18
hepatitis virus strain	18
the enteric tropism	18
of bovine coronavirus	18
piglets in the	18
have been identified	18
were isolated from	18
of the recombinant	18
expressed in transgenic	18
antibodies in the	18
have been shown	18
the inhibition of	18
were performed in	18
the study of	18
role in tgev	18
mouth disease virus	18
the difference in	18
pigs infected with	18
ding et al	18
of orf a	18
as a control	18
of a new	18
for the expression	18
in the serum	18
at the n	18
p mapk pathway	18
ranging from to	18
essential for the	18
surface of the	18
the villous enterocytes	17
belong to the	17
to the cells	17
is a highly	17
of this study	17
structure of transmissible	17
of the transmissible	17
functional receptor for	17
ortego et al	17
on the other	17
expression in the	17
for the first	17
bind to the	17
the infectivity of	17
is the most	17
half of the	17
corona diferencial elisa	17
the m and	17
and colon epithelial	17
in a dose	17
in the respiratory	17
with paraformaldehyde for	17
demonstrated that tgev	17
appear to be	17
and evolution of	17
important roles in	17
was confirmed by	17
cell culture adapted	17
s gene of	17
levels in the	17
was performed by	17
transcription of tgev	17
is a receptor	17
tgev replication in	17
was inserted into	17
cells were seeded	17
was lower than	17
to the tgev	17
cells per well	17
performed using the	17
conflict of interest	17
the detection limit	17
was performed as	17
identification of the	17
be used for	17
be detected in	17
with tgev for	17
binding of the	17
cells were pretreated	17
the intestinal epithelium	17
incubated for min	17
it is possible	17
in the usa	17
thirds of the	17
replication of tgev	17
relative to the	17
of glycoprotein s	17
svanovir tgev prcv	17
is not essential	17
pedv s protein	17
included in the	17
vennema et al	17
processing of the	17
transferred to a	17
infected cells and	17
to the nucleus	17
were compared with	17
with a virulent	17
were collected at	17
were performed using	17
mediated by the	17
experiments were performed	17
of a recombinant	17
the growth of	17
were used in	17
crystal structure of	17
result in the	17
difference in the	17
the mucosal immune	17
the purdue strain	16
was significantly lower	16
the phosphorylation of	16
with bound tgev	16
is the first	16
transfected with the	16
located within the	16
enjuanes et al	16
did not show	16
of tgev gene	16
the tgev m	16
of tgev is	16
major structural proteins	16
leader rna sequences	16
were cotransfected with	16
aynaud et al	16
the clinical signs	16
neutralizing antibody titers	16
sethna et al	16
to infection with	16
coronavirus is a	16
the release of	16
in the swine	16
of tgev were	16
a negative control	16
to of the	16
which is a	16
led to the	16
major receptor for	16
presence of a	16
of these viruses	16
the epithelial cells	16
with the exception	16
was evaluated by	16
virus infection in	16
with diarrhea in	16
in cells infected	16
sglt and glut	16
followed by a	16
jejunum and ileum	16
a major receptor	16
of tgev pl	16
in the pig	16
terminal half of	16
that had been	16
differentially expressed lncrnas	16
of the human	16
with n protein	16
authors declare that	16
to tgev and	16
the sa protein	16
zhou et al	16
spike gene of	16
results demonstrated that	16
results suggested that	16
apn positive cells	16
results show that	16
apn negative cells	16
were incubated at	16
cavanagh et al	16
the largest rna	16
lactogenic immunity against	16
leading to the	16
the activity of	16
of the purdue	16
for viral replication	16
sites on the	16
of the mhv	16
and the tgev	16
the recombinant lactobacillus	16
detection limit of	16
are essential for	16
in the pbs	16
mucosal and systemic	16
glucose uptake in	16
this study were	16
binding of tgev	16
coe and rlppg	16
the mortality rate	16
four major antigenic	16
be due to	16
was expressed in	16
the jejunum of	16
epithelial cell line	16
early in infection	16
after infection with	16
were significantly higher	16
influenza a virus	16
cs a fibrillae	16
and e proteins	16
the s proteins	16
absence of e	16
pcr was performed	16
gene of the	16
tropism of the	16
of p signaling	16
virulent strain of	16
as a result	16
were able to	16
evidence for a	16
demonstrates that the	16
virus replication in	16
in the nucleus	16
the isolation of	16
that there is	16
to amplify the	16
virus binding to	16
similar results were	16
is not known	16
when compared to	16
clinical signs of	16
that tgev n	16
and immunogenicity of	16
the majority of	16
cells of the	16
virus spike protein	16
to each well	16
of epithelial cells	15
and treated with	15
is difficult to	15
of viral replication	15
were expressed as	15
effect on the	15
interact with the	15
with regard to	15
located at the	15
the distribution of	15
with tgev antigen	15
were transferred to	15
two amino acid	15
antigenic structure of	15
in the porcine	15
the orf gene	15
molecular basis of	15
mesenteric lymph node	15
members of the	15
the efficiency of	15
was shown to	15
cruz et al	15
higher in the	15
were removed by	15
indirect fluorescent antibody	15
stranded rna genome	15
small intestine and	15
j cells treated	15
suggest that tgev	15
as a negative	15
addition to the	15
cells were used	15
in dmem containing	15
recombinant s protein	15
of pedv and	15
tgev at a	15
cell cycle progression	15
makino et al	15
in terms of	15
i and ii	15
the assembly of	15
the viral membrane	15
and expression of	15
interacts with the	15
jiang et al	15
is possible that	15
the insertion of	15
the time of	15
the membrane protein	15
for porcine epidemic	15
the structural proteins	15
a polypeptide of	15
entry into cells	15
the viral envelope	15
identified in the	15
in the loss	15
of the papn	15
compared with that	15
of the coronaviridae	15
evolution of the	15
levels of the	15
in the field	15
zhu et al	15
and differentiation of	15
carried out in	15
not required for	15
pathogenesis of transmissible	15
antibodies against the	15
with the cell	15
weeks of age	15
tgev infection induces	15
was removed and	15
cells were cotransfected	15
prcv and tgev	15
tgev s gene	15
the tropism of	15
of monoclonal antibodies	15
binds to the	15
the design of	15
a titer of	15
tropism and virulence	15
has been used	15
neutralizing antibodies in	15
our results showed	15
protein in the	15
analysis was performed	15
n proteins from	15
was detected with	15
none of the	15
between the leader	15
economic losses in	15
receptor for pdcov	15
the exception of	15
a co incubator	15
of differentially expressed	15
balb c mice	15
been detected in	15
in all cases	15
were performed as	15
and porcine deltacoronavirus	15
the recovery of	15
of the rbd	15
for more than	15
the dko pigs	15
and used to	15
a cellular receptor	15
induced mitochondrial damage	15
and identification of	15
were collected from	15
the efficacy of	15
on st cells	15
tgev has been	15
the finding that	15
ml of pbs	15
to identify the	15
and rlppg f	15
the tgev n	15
have also been	15
spike protein is	15
upstream of the	15
was able to	15
of the membrane	15
the virus to	15
virus strain a	15
are presented as	15
has been previously	15
the cellular receptor	15
the accumulation of	15
huang et al	15
epithelial cells were	15
morbidity and mortality	15
against tgev and	15
their ability to	15
kindly provided by	15
the application of	14
the slides were	14
animals immunized with	14
rna genome of	14
serum samples were	14
the membrane was	14
bernard et al	14
data suggest that	14
synthesis of the	14
be used to	14
for virus replication	14
ability of the	14
be related to	14
the size of	14
the other hand	14
been used to	14
cv vero adapted	14
that the s	14
and the other	14
yang et al	14
materials and methods	14
and phylogenetic analysis	14
leader rna and	14
yuan et al	14
middle east respiratory	14
function of the	14
cells were harvested	14
antibodies to the	14
there was a	14
the function of	14
and rna viruses	14
the he protein	14
primary porcine enterocytes	14
clinical signs and	14
at least three	14
a determinant of	14
bca protein assay	14
against tgev in	14
m protein of	14
belongs to the	14
tgev strain purdue	14
a functional receptor	14
the epidermal growth	14
of the pfcrn	14
swinecheck tgev prcv	14
characteristics of a	14
virus titers were	14
proteins in the	14
were challenged with	14
for the tgev	14
tgev infection was	14
incubated with tgev	14
more sensitive than	14
by plaque assay	14
deletions in the	14
spike protein of	14
villous enterocytes of	14
there were no	14
the negative control	14
at the time	14
some of these	14
or tgev n	14
supplemented with fbs	14
culture medium was	14
east respiratory syndrome	14
did not neutralize	14
for the development	14
and infected with	14
enteric tropism and	14
tgev at moi	14
the pellet was	14
c in a	14
a dilution of	14
h at room	14
is not clear	14
proteins have been	14
epidemic diarrhea in	14
at the cell	14
virus entry into	14
the swine industry	14
agreement with the	14
that they have	14
t cells in	14
the subgenomic mrnas	14
with that of	14
required for viral	14
inoculated with the	14
e protein is	14
in this case	14
of the host	14
of the receptor	14
glycoprotein s polypeptides	14
nchez et al	14
comparison with the	14
with porcine respiratory	14
the tgev strain	14
protein of the	14
for mouse hepatitis	14
was assessed by	14
innate immune responses	14
involved in tgev	14
were selected for	14
was similar to	14
no effect on	14
systemic immune responses	14
mediated isothermal amplification	14
play important roles	14
these results indicated	14
the tgev and	14
have demonstrated that	14
of pigs with	14
structural proteins of	14
side of the	14
lee et al	14
into host cells	14
is an enveloped	14
and avian coronaviruses	14
resulting in a	14
tgev and pdcov	14
oral administration of	14
a and d	14
in the culture	14
dmem supplemented with	14
the s domain	14
using monoclonal antibodies	14
was expressed as	14
is not required	14
diarrhea in swine	14
of newborn piglets	14
efficacy of a	14
mechanism of tgev	14
e and e	14
course of the	14
the extent of	14
dependent rna polymerase	14
located on the	14
tgev at an	14
when cells were	14
purdue strain of	14
the cytoplasm of	14
assay for the	14
the antigenic sites	14
tgev is an	14
mouse monoclonal anti	14
to the viral	14
infected cells per	14
cell culture medium	14
role of the	14
copy number of	14
sequences in the	13
these data indicate	13
expressed in the	13
hu et al	13
the existence of	13
the emergence of	13
the process of	13
infection of the	13
the lamina propria	13
the ingezim corona	13
the in vivo	13
were seeded in	13
cells and the	13
declare that they	13
differences between the	13
in the infected	13
they have no	13
recombinant vaccinia virus	13
days of age	13
mucosal immune response	13
passages in tissue	13
we demonstrated that	13
and it is	13
pfu ml in	13
by the coronavirus	13
with the results	13
infection with the	13
and western blot	13
an increase in	13
to test the	13
transfected into pk	13
complex with the	13
and systemic immune	13
was performed on	13
well plates and	13
compared with those	13
on tgev replication	13
diarrhea in pigs	13
studies showed that	13
tgev prcv recombinant	13
may have been	13
are consistent with	13
infected cells was	13
of the other	13
phylogenetic analysis of	13
and pathogenesis of	13
st cells and	13
these results suggested	13
analysis of porcine	13
ibv and mhv	13
at days post	13
results in the	13
ra plus tgev	13
immunized with rlppg	13
in pbs for	13
when the cells	13
those in the	13
days after the	13
was consistent with	13
against challenge with	13
antigenic sites a	13
entry of ribosomes	13
were collected and	13
is present in	13
of pedv n	13
the age of	13
chang et al	13
tgev was detected	13
is caused by	13
were identified as	13
been demonstrated to	13
i i f	13
induced cell cycle	13
two of the	13
and has been	13
the results obtained	13
in the golgi	13
serves as a	13
the transcription of	13
for h in	13
the orf a	13
the proliferation of	13
responses induced by	13
not significantly different	13
losses in the	13
with the s	13
the result of	13
viral replication and	13
of the wt	13
were mixed with	13
regardless of the	13
of the piglets	13
with lysis buffer	13
due to a	13
was performed to	13
of clinical signs	13
associated with diarrhea	13
c for s	13
determination of the	13
the murine coronavirus	13
a highly contagious	13
of cells in	13
the copy number	13
related to tgev	13
with the same	13
and prcv strains	13
is mediated by	13
changes at the	13
virus and transmissible	13
of the virion	13
antigenic relationship of	13
early stage of	13
subgenomic mrna species	13
orally immunized with	13
were then incubated	13
at g for	13
the genome of	13
were collected for	13
viruses such as	13
natural science foundation	13
miller and purdue	13
approved by the	13
the tgev spike	13
tips of the	13
isolation of a	13
in neonatal piglets	13
gastroenteritis virus spike	13
protein is not	13
for tgev infection	13
by fluorescence microscopy	13
of orf b	13
was measured by	13
in mammalian cells	13
sequence at the	13
cd and papn	13
and n genes	13
of the gene	13
of the murine	13
the tips of	13
was higher than	13
the gastrointestinal tract	13
infectious cdna clone	13
the infected cells	13
antibody responses to	13
m and n	13
in complex with	13
that the spike	13
in any of	13
the coronavirus infectious	13
the assay was	13
pensaert et al	13
conjugated secondary antibodies	13
significantly increased the	13
antigenic relationship between	13
plates were washed	13
and table s	13
the pbs group	13
s gene sequences	13
analyzed by western	13
saif and wesley	13
cells at h	13
is capable of	13
with the control	13
of apn positive	13
only in the	13
to the m	13
which is the	13
pellet was resuspended	13
shedding of prcv	13
induces cell cycle	13
a concentration of	13
was derived from	13
the nucleotide sequence	13
coronavirus infection in	13
acid changes at	13
the differentially expressed	13
of di rna	13
have been detected	13
tgev and the	13
significantly lower than	13
is a functional	13
antibodies for h	13
infected cell lysates	13
in the first	13
nuclei were stained	13
but not the	13
via activation of	13
to that in	12
human and animal	12
the n terminus	12
antibodies to tgev	12
immunogenicity of the	12
integral membrane protein	12
are required for	12
and did not	12
equine influenza virus	12
of pedv in	12
mrna expression levels	12
may play a	12
in cultured cells	12
critical epitopes in	12
contrast to the	12
coronaviruses as the	12
virus with a	12
sense rna genome	12
the glycoprotein s	12
m and m	12
the immunogenicity of	12
may be involved	12
of the rna	12
by using the	12
gene in the	12
the enteric tract	12
against tgev infection	12
and centrifuged at	12
by neutralizing antibodies	12
of the p	12
cells that were	12
virus on the	12
were as follows	12
in accordance with	12
result showed that	12
of prcv was	12
used to infect	12
is a determinant	12
the endoplasmic reticulum	12
of diarrhea in	12
no competing interests	12
expression of tgev	12
the pfcrn gene	12
experimentally infected with	12
in the immunized	12
differentially expressed proteins	12
role of apn	12
the af mab	12
described in the	12
plays a role	12
national natural science	12
assays were performed	12
the papn ectodomain	12
were tested for	12
on the day	12
considered statistically significant	12
by means of	12
of the four	12
the intestinal contents	12
with tgev strain	12
the complete genome	12
it may be	12
cells were inoculated	12
h prior to	12
inhibition of tgev	12
egfp expression vector	12
based on a	12
at seven days	12
of the bovine	12
which can be	12
of the negative	12
l a and	12
cd ssc low	12
gastroenteritis coronavirus is	12
the spike glycoprotein	12
pan et al	12
regions of the	12
it is difficult	12
st cells was	12
vero adapted strain	12
was cloned into	12
cd cd t	12
the percentages of	12
we conclude that	12
listed in table	12
functions as a	12
prior to infection	12
gastroenteritis virus of	12
study of the	12
evidence that the	12
and western blotting	12
is shown in	12
infected with a	12
were negative for	12
early in tgev	12
contribute to the	12
in this paper	12
dependent on the	12
released from the	12
a deletion of	12
the tgev infection	12
presence of tgev	12
lower than the	12
a new coronavirus	12
of viral proteins	12
the susceptibility of	12
wt pigs were	12
of the samples	12
to bind to	12
the virus and	12
may also be	12
cells with bound	12
resulted in the	12
the gene source	12
of the total	12
was based on	12
domains in the	12
not affect the	12
the results were	12
and used as	12
attenuated and virulent	12
had no effect	12
a previous study	12
anpep ko pigs	12
to the virus	12
g g phase	12
with porcine epidemic	12
gene source of	12
the differences in	12
cells were lysed	12
recombinase polymerase amplification	12
protein levels of	12
in the colostrum	12
prrsv m protein	12
and the cell	12
of the virulent	12
transmissible gastroenteritis and	12
temperature for h	12
the analysis of	12
component of the	12
fipv type i	12
h post infection	12
was detected using	12
in porcine intestinal	12
four structural proteins	12
explained by the	12
the pcr products	12
at a dilution	12
higher than the	12
levels of p	12
woo et al	12
strains of the	12
is important to	12
receptor for pedv	12
as the gene	12
of swine enteric	12
tropism of tgev	12
are required to	12
the svanovir tgev	12
is critical for	12
the e glycoprotein	12
the two viruses	12
is characterized by	12
were positive for	12
of the heterologous	12
structures of the	12
diarrhea virus infection	12
amino acid residues	12
during the first	12
the relationship between	12
the beginning of	12
of the ibv	12
was identified as	12
intestinal stem cells	12
phosphate buffered saline	12
recombinant swinepox virus	12
portion of the	12
cells released from	12
rasschaert et al	12
has been identified	12
nsp and nsp	12
are located within	12
from the same	12
nucleocapsid protein of	12
for the rapid	12
stat signaling pathway	12
a fluorescence microscope	12
is believed to	12
the causative agent	12
cycle arrest at	12
epitopes in transmissible	12
the total rna	12
of suspect results	12
expressed in e	12
diarrhea virus strain	12
ma et al	12
in situ hybridization	12
acid sequences of	12
virus replication and	12
s protein and	12
tgev infection on	12
were examined by	11
the membranes were	11
the preparation of	11
de groot et	11
sequencing of the	11
the difference between	11
after infection and	11
in the di	11
difference between the	11
were randomly divided	11
was measured at	11
the spread of	11
of the nucleoprotein	11
st cell monolayers	11
il rap and	11
were analyzed using	11
cd ssc high	11
the proportion of	11
the porcine reproductive	11
s and s	11
virus in porcine	11
can be found	11
it is likely	11
into three groups	11
complementary to the	11
in both the	11
were synthesized by	11
by electron microscopy	11
glycoprotein s from	11
by the viral	11
of tge virus	11
taxonomy of viruses	11
the interpretation of	11
been identified in	11
in the spleen	11
is similar to	11
are located on	11
peng et al	11
to the intestinal	11
calculated using the	11
luytjes et al	11
ends of the	11
isolated from a	11
or the full	11
proteins were identified	11
gastroenteritis virus on	11
hepatitis b virus	11
s protein in	11
it should be	11
or negative control	11
immunogenicity of recombinant	11
deletion of the	11
s gene was	11
the cell lines	11
cycle arrest in	11
immunized with tgev	11
simultaneous detection of	11
s proteins from	11
aminopeptidase n and	11
as high as	11
hofmann et al	11
cv fecal suspension	11
the human coronavirus	11
antibody titers in	11
more than one	11
virus and its	11
of aminopeptidase n	11
were stored at	11
be associated with	11
that eif a	11
the attachment of	11
and canine coronaviruses	11
the rate of	11
twice with pbs	11
of the structural	11
detection of pedv	11
different from the	11
u ml penicillin	11
carried out using	11
the fusion of	11
immune response in	11
performed according to	11
in the order	11
expression of apn	11
determined by the	11
from tgev and	11
in the ileum	11
a consequence of	11
method for the	11
tgev infection is	11
foundation of china	11
in of the	11
lymph node cells	11
tgev is a	11
for rapid detection	11
gastroenteritis virus neutralization	11
well plates were	11
provided by dr	11
the identification of	11
of apn and	11
have been demonstrated	11
been demonstrated that	11
to the golgi	11
with the virus	11
obtained from a	11
is likely that	11
to examine the	11
and the results	11
the secretory pathway	11
discovery of a	11
porcine enteric coronaviruses	11
transfected with n	11
entry of tgev	11
in the formation	11
in the feces	11
seems to be	11
of tgev has	11
using trizol reagent	11
from the viral	11
of spike protein	11
enteric coronavirus related	11
the virus is	11
are listed in	11
infection with a	11
fragment of the	11
in each group	11
protein a g	11
analysis showed that	11
limit of the	11
saif and fernandez	11
group was significantly	11
followed by the	11
of the target	11
were maintained in	11
it is a	11
of apn in	11
was removed by	11
and m proteins	11
prcv recombinant elisa	11
the optical density	11
on the s	11
zhao et al	11
virus in vitro	11
cell entry receptor	11
causative agent of	11
was calculated using	11
relationship of the	11
tgev nucleoprotein gene	11
experimental infection of	11
the serum of	11
accordance with the	11
fecal and nasal	11
the day of	11
the three commercial	11
acts as a	11
of the peplomer	11
parts of the	11
swine fever virus	11
the pedv s	11
was amplified by	11
replicates in the	11
pedv n and	11
the replicase gene	11
the supernatant of	11
to protect against	11
cells compared to	11
cells with tgev	11
with those of	11
effects of tgev	11
detected by the	11
and in vitro	11
fusion of the	11
and h post	11
led to a	11
of m protein	11
antibody responses in	11
its enteric tropism	11
science foundation of	11
mice orally immunized	11
cell proliferation and	11
the indicated time	11
spike glycoprotein s	11
within the same	11
of its enteric	11
mrna and protein	11
of the control	11
the antigenic relationship	11
cells stably expressing	11
protein and the	11
the piglets in	11
m and e	11
cleavage of the	11
in some cases	11
significantly higher in	11
no conflict of	11
could be detected	11
total number of	11
identified as a	11
small intestine of	11
the ectodomain of	11
at s and	11
required for efficient	11
and high mortality	11
monoclonal antibodies against	11
rna helicase ddx	11
is a key	11
consistent with a	11
virus in cell	11
not affected by	11
the same conditions	11
the sequences of	11
were resuspended in	11
the molecular basis	11
a t the	11
porcine hemagglutinating encephalomyelitis	11
three major structural	11
that tgev pl	11
into virus particles	11
and maintained in	11
of the large	11
egfp empty vector	11
the size and	11
caused by the	11
been identified as	11
significant differences in	11
is the main	11
the enteropathogenicity of	11
in each well	11
function as a	11
of ibv and	11
pcr using the	11
that the leader	11
cells compared with	11
rna and dna	11
to each other	11
of lgr iscs	11
of the family	11
of subgenomic mrnas	11
pigs in the	11
determinant of its	11
the porcine respiratory	11
in recent years	11
observed between the	11
the tgev purdue	11
and the cells	11
is not yet	11
in host cells	11
because of its	11
results of the	11
in neonatal pigs	11
appeared to be	11
of sows with	11
of newborn pigs	11
the origin of	11
the viral nucleocapsid	11
and h p	11
under a fluorescence	11
the appearance of	11
the differentiation of	11
did not affect	11
in tgev replication	11
that apn is	11
strain of transmissible	11
on the amino	11
from the cell	11
than those in	11
the immune system	11
the interaction of	11
cells were stained	11
partial protection against	11
group than in	11
the helper virus	11
mechanism by which	11
moi of tgev	11
tgev or prcv	11
was used in	11
the viability of	11
which has been	11
and could be	11
h of incubation	11
enteric tropism of	11
were considered significant	11
in the induction	11
of the respiratory	11
except for the	11
percentage of apn	11
in vero cells	11
were characterized by	10
were obtained by	10
the online version	10
b cells and	10
wu et al	10
were interpreted as	10
be detected by	10
be responsible for	10
and the expression	10
porcine kidney cells	10
quantitative proteomic analysis	10
as a vaccine	10
the cells released	10
in serum and	10
mrna start sites	10
of the present	10
target of mir	10
is one of	10
tgev inactivated vaccine	10
in the supernatants	10
reactivity between tgev	10
jung et al	10
n and m	10
are associated with	10
a sialic acid	10
compared to mock	10
activated protein kinase	10
th and th	10
number of the	10
studies on transmissible	10
the swinecheck tgev	10
propagation of the	10
moi for h	10
basis of the	10
on the viral	10
green fluorescent protein	10
was identified in	10
high level of	10
lamphear et al	10
localization of the	10
position of the	10
of tgev strains	10
a function of	10
higher than those	10
immune responses and	10
internal entry of	10
was mixed with	10
vaccine on days	10
cells using the	10
would be expected	10
incubated with mouse	10
titers were determined	10
enterocytes of newborn	10
activity of the	10
s and n	10
cells were co	10
was prepared in	10
of eif a	10
were measured by	10
and tgev was	10
different concentrations of	10
of host cells	10
that the recombinant	10
and n proteins	10
this is the	10
immune response against	10
a monoclonal antibody	10
also showed that	10
the university of	10
it is worth	10
has been observed	10
in a swine	10
influenza c virus	10
fixed with acetone	10
with the porcine	10
and cultured for	10
different types of	10
were also observed	10
yokomori et al	10
the s subunit	10
length glycoprotein s	10
greater than that	10
and analysis of	10
known to be	10
in a humidified	10
systemic and mucosal	10
on transmissible gastroenteritis	10
after centrifugation at	10
of virus infection	10
virus are located	10
responses in the	10
renewal and differentiation	10
to develop a	10
amplified by pcr	10
from porcine transmissible	10
of the enteric	10
of the sequence	10
gastroenteritis virus from	10
to explore the	10
amino acids of	10
and evaluation of	10
the coronavirus mouse	10
that the expression	10
clarified by centrifugation	10
hepatitis b surface	10
occurs in the	10
sites c and	10
at and h	10
gastroenteritis coronavirus spike	10
be explained by	10
for min in	10
samples were tested	10
the potential of	10
mg ml streptomycin	10
no significant differences	10
at and hpi	10
groot et al	10
infected cells which	10
molecular characterization and	10
results not shown	10
were verified by	10
at a concentration	10
the international committee	10
performed in triplicate	10
data indicated that	10
there are no	10
of this article	10
the mrna start	10
by incubation with	10
interpretation of suspect	10
the small intestinal	10
close to the	10
receptor for mouse	10
and replication of	10
been described in	10
apn is a	10
gfp and tgev	10
pdcov and tgev	10
infection in the	10
for use in	10
proteins of the	10
were harvested and	10
feline enteric coronavirus	10
treated with the	10
iga antibodies in	10
results demonstrate that	10
integrin and ccr	10
the translation of	10
and attenuated strains	10
attached to the	10
were consistent with	10
as templates for	10
of the immune	10
a result of	10
significant difference in	10
humoral immune response	10
used to confirm	10
and subjected to	10
protein that is	10
neonatal calf diarrhea	10
a co atmosphere	10
stained with hoechst	10
differential diagnosis of	10
that it is	10
was digested with	10
the early stage	10
sequence of a	10
and amino acid	10
of the different	10
correlated with the	10
suspect results were	10
are responsible for	10
rna was isolated	10
modified live virus	10
results were obtained	10
of the corresponding	10
studies of the	10
after h incubation	10
protective lactogenic immunity	10
beginning of the	10
time reverse transcription	10
from porcine respiratory	10
sawicki and sawicki	10
the oral route	10
followed by goat	10
t cells to	10
bacterial artificial chromosome	10
pedv n cells	10
committee on taxonomy	10
antigens on the	10
standard deviation for	10
after infection of	10
b and d	10
recombination demonstrates that	10
j cells infected	10
c and b	10
dilutions of the	10
before and after	10
in tgev infected	10
be used as	10
each sample was	10
as a consequence	10
the modified live	10
carried out by	10
has shown that	10
it is important	10
of a probiotic	10
specific for tgev	10
effect of tgev	10
or infected with	10
in escherichia coli	10
alignment of the	10
the s region	10
in the lamina	10
is a common	10
membrane protein of	10
the animals were	10
by goat anti	10
been associated with	10
the variant tgev	10
with tgev or	10
that the levels	10
recombinant plasmid ppg	10
orf l a	10
of the sars	10
antibodies were detected	10
studies on the	10
and the resulting	10
the heterologous gene	10
st cells infected	10
international committee on	10
for h with	10
pigs of all	10
piglets born to	10
formation of the	10
as evidenced by	10
restriction endonuclease sites	10
schultze et al	10
as a model	10
determine whether the	10
of murine hepatitis	10
findings suggest that	10
protection against tgev	10
the viral genomic	10
the titers of	10
whether or not	10
distinct from the	10
as a template	10
effects of the	10
of virus in	10
immune response of	10
expression of small	10
of tgev s	10
this suggests that	10
which were fixed	10
confirmed that the	10
of the jejunum	10
the introduction of	10
of virus particles	10
the intensity of	10
penzes et al	10
significantly increase the	10
j cells by	10
coronaviruses such as	10
to interact with	10
tissue culture fluid	10
divided into four	10
the stimulation of	10
rna virus genome	10
after passages in	10
the stability of	10
deduced amino acid	10
by the addition	10
protein expression of	10
homing receptors on	10
for the study	10
in the coronavirus	10
of apn negative	10
of murine coronaviruses	10
expression of p	10
isolation and identification	10
of viral antigens	10
analysis of variance	10
may be an	10
we determined the	10
sites in the	10
spike protein result	10
virus isolation and	10
the involvement of	10
protein result in	10
h post transfection	10
targeted recombination demonstrates	10
to n protein	10
insight into the	10
b surface antigen	10
the rna genome	10
largest rna virus	10
correa et al	10
in a variety	10
it is the	10
and the supernatant	10
h and h	10
of lactic acid	10
phase of the	10
construction of a	10
of the nucleocapsid	10
is a type	10
gastroenteritis coronavirus genome	10
with the indicated	10
pigs were used	10
three of the	10
significantly different from	10
phosphorylation of p	10
on pedv replication	10
using the same	10
summarized in table	10
is also a	10
of human coronavirus	10
the first time	10
tgev and ccv	10
of recombinant lactobacillus	10
level of tgev	10
expression levels in	10
the animals immunized	10
tgev strain miller	10
divided into three	10
the absorbance was	10
porcine circovirus type	10
the innate immune	10
sturman and holmes	10
to form a	10
supernatants were collected	10
purdue and miller	10
classical swine fever	10
the lactobacillus vaccine	10
the basis for	10
mammalian and avian	10
is expressed in	10
prior to farrowing	10
reed and muench	10
were harvested at	10
the characteristics of	10
of the infected	10
the secondary antibody	10
from that of	10
for h prior	10
all piglets were	10
show that the	10
is known to	10
cells from the	10
considered to be	10
and found that	9
for pcv and	9
the order nidovirales	9
amount of viral	9
e and f	9
disruption of the	9
gastroenteritis and porcine	9
emergence of porcine	9
determinants are located	9
g e v	9
a review of	9
infection by tgev	9
antigenic homology among	9
of the first	9
immunity against transmissible	9
tgev infection of	9
the neutralizing antibody	9
were separated by	9
may be the	9
was collected and	9
the intestinal tract	9
of protection against	9
is necessary for	9
half of spike	9
by pcr using	9
is able to	9
product of the	9
it is interesting	9
smith et al	9
by the national	9
piglets infected with	9
infection in vitro	9
be able to	9
to detect tgev	9
as the target	9
different from those	9
bound to the	9
domains of the	9
fixed cells were	9
mpi to mpi	9
days after inoculation	9
at h after	9
single amino acid	9
and mucosal immune	9
de diego et	9
protein was expressed	9
enteric tropism in	9
tgev infection could	9
was determined using	9
reactive oxygen species	9
of up to	9
of the viruses	9
m protein and	9
virus of swine	9
ssc low cells	9
cells did not	9
coronavirus infections in	9
randomly divided into	9
and resuspended in	9
humoral and cellular	9
in this region	9
to inhibit the	9
this could be	9
in the development	9
were classified as	9
viral rna was	9
with rlppg f	9
structural components from	9
of the full	9
evaluation of the	9
are needed to	9
of the animals	9
use of a	9
the method of	9
was not affected	9
by a few	9
the viral replication	9
as shown by	9
it was not	9
coronavirus defective interfering	9
belouzard et al	9
results were interpreted	9
mabs specific for	9
were examined for	9
samples were taken	9
cells were maintained	9
this protein is	9
stages of the	9
virus by rt	9
tooze et al	9
when suspect results	9
of the serum	9
of the infection	9
for tgev replication	9
were observed between	9
de haan et	9
to the leader	9
the wt group	9
of influenza a	9
was tested by	9
diego et al	9
evaluated in this	9
c and f	9
number of cd	9
dko pigs and	9
presented as the	9
cell line was	9
the region of	9
and c antigen	9
the severity of	9
the functions of	9
in target cells	9
the enteric and	9
hoechst for min	9
of swine transmissible	9
viral replication in	9
purchased from sigma	9
act as a	9
used to analyze	9
has been detected	9
on taxonomy of	9
kidney cell line	9
neutralizing antibodies against	9
sensitivity and specificity	9
was detected at	9
of the replication	9
t g e	9
seen in the	9
h and then	9
of the genus	9
bos et al	9
in the correct	9
been reported that	9
selected characteristics of	9
s protein has	9
diarrhea virus strains	9
interaction between tgev	9
way analysis of	9
gp and gp	9
from the tgev	9
is worth noting	9
isolated from tgev	9
clone and evolution	9
by the use	9
diarrhea in piglets	9
in cells transfected	9
yu et al	9
data demonstrate that	9
the cells in	9
fecal shedding of	9
to the small	9
these findings suggest	9
that the m	9
oral corn vaccine	9
of amino acids	9
the feces of	9
mice immunized with	9
orally inoculated with	9
followed by dylight	9
and nasal swabs	9
have no competing	9
is important for	9
is composed of	9