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
the presence of387
in this study371
infectious bronchitis virus305
porcine epidemic diarrhea303
epidemic diarrhea virus255
analysis of the234
as well as228
and respiratory syndrome221
arch virol doi216
of the virus212
reproductive and respiratory202
porcine reproductive and201
mouse hepatitis virus201
of the s200
based on the196
feline infectious peritonitis183
in the presence173
the present study171
respiratory syndrome virus169
the cells were166
a n d163
the s protein161
data not shown151
the detection of147
according to the145
of porcine epidemic143
the s gene139
transmissible gastroenteritis virus136
of infectious bronchitis132
avian infectious bronchitis132
one of the132
as described previously129
in the present129
t h e127
the number of126
sequence of the122
shown in fig119
end of the118
for h at117
it has been116
found to be114
sequences of the113
the absence of110
was detected in110
as shown in110
amino acid sequence109
in the s107
polymerase chain reaction107
has been reported104
phylogenetic analysis of104
a and b103
the united states103
members of the102
of the viral102
been shown to101
the amino acid101
due to the100
detected in the98
for the detection96
in order to95
amino acid sequences94
for min at94
showed that the93
and characterization of93
at room temperature93
to determine the93
the use of92
were obtained from91
the effect of90
in the absence90
all of the90
to that of90
region of the89
the end of89
acute respiratory syndrome88
that of the88
has been shown88
respiratory syndrome coronavirus88
severe acute respiratory88
closely related to88
infectious peritonitis virus86
was used to86
in the united84
p and p83
sequence analysis of83
the role of82
was performed using82
were infected with82
was carried out81
r n a81
found in the81
herpes simplex virus80
influenza a virus80
a total of80
were found to78
the prevalence of78
involved in the78
in the same78
characterization of a77
was used as77
characterization of the76
a t e76
was added to76
to those of76
of porcine reproductive75
as described above75
the development of75
of the genome74
a number of74
member of the73
were detected in72
this study was72
cells infected with71
of avian infectious71
the addition of70
of the family70
hepatitis c virus69
the production of69
of a novel69
a member of68
the surface of68
were used to67
the pathogenesis of67
rna was extracted67
shown to be67
used as a67
have been reported67
the replication of66
used in this66
t h a66
e n t66
most of the66
was extracted from66
in cell culture65
as previously described65
in addition to65
a n t65
was found to64
the results of64
the ability of64
s gene of64
to investigate the64
mouth disease virus64
those of the64
any of the63
vesicular stomatitis virus63
h n influenza62
the middle east62
used in the62
shown in table61
cells were washed61
obtained from the61
of the n61
changes in the60
indicated that the60
of feline infectious60
of the orf60
nucleotide sequence of60
middle east respiratory60
of the two60
differences in the59
there was no59
were inoculated with59
for detection of59
pcr products were59
east respiratory syndrome59
t e d59
part of the58
on the other58
were observed in58
was used for57
of these viruses57
related to the57
present in the56
of influenza virus56
were collected from56
were carried out56
similar to that56
the sequence of56
was isolated from56
the level of56
the cell surface55
antiviral activity of55
were subjected to55
to be a55
was obtained from55
of mouse hepatitis54
were used as54
the n protein54
of the genus54
observed in the54
were positive for54
has not been54
were treated with54
the lack of54
the other hand54
comparison of the54
this work was53
cells were infected53
molecular characterization of53
compared to the53
and stored at53
on the surface53
similar to those53
and phylogenetic analysis52
could not be52
structural proteins of52
was supported by52
infectious bursal disease52
are shown in52
respiratory syncytial virus52
than that of51
of influenza a51
structure of the51
the virus was51
conflict of interest51
similar to the51
was observed in51
i t h51
infected cells were51
were used for51
w i t51
an important role51
of transmissible gastroenteritis50
associated with the50
the majority of50
infected with the50
the amount of50
have shown that50
s and s49
was determined by49
three times with49
genome sequence of49
the plates were49
the expression of48
equine arteritis virus48
h a t48
with those of48
in the case48
virus infection in48
in patients with48
virus in the48
in the middle48
s protein of47
the most common47
suggest that the47
none of the47
of bovine coronavirus47
the emergence of47
were isolated from47
washed three times47
respiratory tract infections47
isolation and characterization47
the case of47
appears to be46
incubated for h46
the formation of46
hemorrhagic fever virus46
of a new46
were added to46
nucleotide sequences of45
indicate that the45
important role in45
was found in45
it is possible45
of respiratory viruses45
t r a45
the genbank database45
the genome of45
added to the45
binding domain of45
in response to45
samples were collected45
each of the45
vero cells were45
there was a44
regions of the44
and h n44
was not detected44
h n viruses44
when compared to44
the samples were43
been reported to43
of viral rna43
portion of the43
results showed that43
of the same43
of the porcine43
in the cytoplasm43
identification of a43
isolated from the43
the fact that43
we found that43
and incubated at43
of the coronavirus42
be due to42
were incubated for42
fetal bovine serum42
viral rna was42
of the viruses42
the sequences of42
a and cv42
work was supported42
the n gene42
the percentage of42
in vitro and41
acid sequences of41
monoclonal antibodies to41
the ability to41
were incubated at41
with diarrhea in41
the h n41
f i p41
cells were incubated41
congo hemorrhagic fever41
results suggest that41
role in the41
influenza a viruses40
bursal disease virus40
in contrast to40
t t t40
and in vivo40
be involved in40
has also been40
were grown in40
for the presence40
of the three40
clinical signs of40
of this study40
between the two40
pi k akt40
mouse spleen cells40
of h n40
were tested for40
and amino acid40
responsible for the39
were determined by39
t i o39
i o n39
the s glycoprotein39
added to each39
a variety of39
the cleavage site39
some of the39
from the same39
the infected cells39
the s subunit39
a role in38
the small intestine38
is possible that38
belonging to the38
development of a38
the sensitivity of38
compared with the38
to evaluate the38
g for min38
n t i38
is involved in38
in our study38
expression of the38
revealed that the38
protein of the38
upper respiratory tract38
of the protein38
specificity of the38
the s and37
studies on the37
the induction of37
the nucleotide sequence37
lower respiratory tract37
in which the37
the effects of37
been reported in37
genetic diversity of37
the nucleotide sequences37
the viral rna37
to confirm the37
suggested that the37
balb c mice37
located in the37
results indicate that37
expressed as the37
identification of the37
difference in the37
were analyzed by37
newcastle disease virus37
the levels of37
molecular epidemiology of37
r a t37
of the highest36
were performed using36
were washed with36
of human metapneumovirus36
h n and36
mutations in the36
the mechanism of36
a t i36
could be detected36
the antiviral activity36
for min and36
has been suggested36
proteins of the36
listed in table36
vitro and in36
the existence of36
in cell cultures36
by electron microscopy36
a i n36
is the first36
the structural proteins36
were found in36
considered to be35
h after infection35
the basis of35
the viral genome35
of the spike35
b and c35
the complete genome35
on the basis35
nm in diameter35
a multiplicity of35
cells in the35
to be the35
is associated with35
for h and35
fetal calf serum35
the course of35
the phylogenetic tree35
hepatitis a virus35
as a result35
have also been35
have not been34
by centrifugation at34
and identification of34
appeared to be34
p h a34
multiplicity of infection34
the pi k34
to determine whether34
was detected by34
open reading frame34
in vero cells34
to each well34
h n virus34
kindly provided by34
used as the34
reciprocal of the34
the reciprocal of34
indicating that the34
the synthesis of34
but not in34
an outbreak of34
a concentration of34
well as the34
were used in34
appear to be34
was shown to33
at the end33
studies have shown33
the identification of33
as described in33
a result of33
g and g33
understanding of the33
activation of the33
at the same33
are associated with33
resulted in a33
isolated from a33
of the disease33
with pbs and33
the family coronaviridae33
open reading frames33
western blot analysis33
i and ii33
such as the33
t e r33
as the reciprocal33
the orf gene33
increase in the33
domain of the33
in infected cells33
an moi of33
at a multiplicity33
to identify the33
of the small33
the origin of33
pedv s protein33
this is the32
of a coronavirus32
of the infected32
and the other32
viruses of the32
used for the32
found that the32
were incubated with32
to assess the32
were purchased from32
suggests that the32
in the feces32
study was to32
p a r32
c and d32
were maintained in32
alignment of the32
inoculated with the32
p e d32
m i n32
at an moi32
at a concentration32
minute virus of32
prrsv and pedv32
of the rna32
this suggests that31
p e r31
in south korea31
provided by dr31
deduced amino acid31
the current study31
belongs to the31
cells were grown31
of this article31
approved by the31
neonatal calf diarrhea31
the nucleocapsid protein31
of infected cells31
korean ibv isolates31
demonstrated that the31
strand rna viruses31
diarrhea virus in31
in the field31
play an important31
suggesting that the31
function of the31
of the p31
the plasma membrane31
dependent rna polymerase31
of the other31
as determined by31
the possibility that31
processing of the31
have been shown31
neutralizing antibody titers31
shown that the31
in the genbank31
the specificity of31
the time of31
per cent of30
virus isolated from30
is available to30
included in the30
of amino acids30
of the complete30
be used to30
sensitivity of the30
contains supplementary material30
at the time30
which is available30
on the s30
available to authorized30
igg and iga30
times with pbs30
version of this30
cells were then30
washed twice with30
analysis based on30
consistent with the30
as described by30
the efficacy of30
the online version30
online version of30
have been identified30
antibodies to the30
nucleotide and amino30
viruses in the30
the method of30
amino acid changes30
and centrifuged at30
mice infected with30
of infectious virus30
was used in30
to authorized users30
derived from the30
of the virion30
the spike protein29
have been described29
terminus of the29
in the pathogenesis29
is one of29
room temperature for29
of infectious bursal29
with acute respiratory29
bovine serum albumin29
domain of hdag29
linked immunosorbent assay29
molecular evolutionary genetics29
coding region of29
in the first29
be detected in29
were collected and29
these results suggest29
minimum essential medium29
taxonomy of viruses29
presence of the29
high levels of29
amino acid residues29
of herpes simplex29
higher than that29
recombinant s protein29
the pedv s29
children with acute29
with respect to29
this study were29
evolutionary genetics analysis29
a phylogenetic tree29
of hepatitis c29
international committee on29
the supernatant was29
the structure of29
with the same29
on the cell29
the international committee28
porcine respiratory coronavirus28
e d v28
the ratio of28
an increase in28
of ctf virus28
causative agent of28
complete genome sequence28
due to a28
associated with a28
to each other28
the relationship between28
in the virus28
large number of28
and stained with28
data suggest that28
electronic supplementary material28
total rna was28
the results showed28
on taxonomy of28
were cultured in28
not detected in28
serum samples were28
followed by a28
performed using the28
and subjected to28
i n e28
gene of the28
virus replication in28
differentially expressed genes28
of severe acute27
of the four27
was confirmed by27
a series of27
that had been27
in terms of27
of the most27
committee on taxonomy27
human immunodeficiency virus27
can be used27
the cell culture27
were washed twice27
in the viral27
an equal volume27
results of the27
in agreement with27
supported by the27
has been described27
in our laboratory27
fecal samples were27
the recombinant s27
the isolation of27
corresponding to the27
the pcr products27
the pathogenicity of27
analysis was performed27
is essential for27
the porcine epidemic27
depending on the27
with the virus27
m a n27
activity of the27
the incidence of27
of the cell27
been shown that27
cleavage of the27
from that of27
infected with a26
were shown to26
are listed in26
cells were cultured26
based on a26
in children with26
plates were incubated26
prior to infection26
compared to those26
supplemented with fetal26
of the gene26
the evolution of26
of the m26
the spread of26
is the most26
sequencing of the26
were detected by26
analysis showed that26
the in vitro26
orf and orf26
k akt pathway26
differences between the26
were stained with26
a mixture of26
the purpose of26
of porcine deltacoronavirus26
were washed three26
in the n26
of the present26
the most important26
n and h26
of the structural26
experimental infection of26
is important for26
may be a26
of the cells26
respiratory tract infection26
i t y26
a previous study26
half of the26
of the amino26
was performed by26
determined by the26
are involved in26
seen in the26
of vesicular stomatitis26
t a n26
by western blot26
phylogenetic analysis based25
type culture collection25
pedv belgorod dom25
of the host25
the vp gene25
of the pedv25
the he protein25
and expression of25
has been demonstrated25
results indicated that25
were stored at25
cells of the25
cells were inoculated25
cells were maintained25
american type culture25
binding to the25
i p v25
carried out in25
a and o25
been isolated from25
the mixture was25
x g for25
respiratory viruses in25
and incubated with25
nucleotide sequence identity25
clarified by centrifugation25
days after infection25
is required for25
infection in the25
previous studies have25
the binding of25
the function of25
virus of canines25
of the first25
identified in the25
of the mabs25
the appearance of25
of the e25
m a b25
c o n25
of the vp25
the viral envelope25
in accordance with25
fipv and fecv25
and that the25
amino acid identity25
the activation of25
from patients with25
in the family25
with ml of25
report of the25
h at room24
as a receptor24
has been proposed24
that they have24
by treatment with24
are known to24
been found to24
pandemic h n24
by the addition24
of neutralizing antibodies24
of the h24
study of the24
pedv field isolates24
the respiratory tract24
avian influenza viruses24
been reported for24
in the serum24
of virus particles24
equal volume of24
of equine arteritis24
to the virus24
deletion in the24
cells were treated24
a large number24
acute gastroenteritis in24
is similar to24
sequence of a24
the degree of24
well tissue culture24
in the netherlands24
proteolytic cleavage of24
years of age24
days after inoculation24
strain of tgev24
tree based on24
polyacrylamide gel electrophoresis24
detection of the24
the authors declare24
tobacco mosaic virus24
as a control24
reported to be24
n e d24
of canine parvovirus24
e t h24
not yet been24
and incubated for24
authors declare that24
antigenically related to24
in a previous23
during the first23
that the virus23
semliki forest virus23
well as in23
were expressed as23
performed using a23
by the method23
be associated with23
in suckling mice23
of the authors23
antigenic relationship between23
simplex virus type23
movement proteins of23
relationship between the23
samples collected from23
cells treated with23
a titer of23
is characterized by23
in the number23
is consistent with23
most closely related23
no significant difference23
piglets born to23
were able to23
are summarized in23
properties of the23
in the region23
that were positive23
remains to be23
hepatitis b virus23
of the human23
in the respiratory23
in st cells23
the cytoplasm of23
s protein was23
for minutes at23
of the samples23
with fetal bovine23
antiviral effect of23
nature of the23
evolution of the23
the results are23
in the intestinal23
in hong kong23
were fixed in23
it is not23
ha and na23
u m a23
in cultured cells23
agarose gel electrophoresis23
fragment length polymorphism23
were fixed with23
compared with those23
pcr assay for23
coronavirus spike protein23
difference between the22
a c t22
extracted from the22
porcine alveolar macrophages22
canine distemper virus22
complete nucleotide sequence22
evaluation of the22
e d in22
a comparison of22
and eya virus22
and in the22
pcr was performed22
hek t cells22
the genomes of22
i n g22
at a dilution22
in recent years22
in mouse spleen22
referred to as22
c for min22
isolation of a22
be responsible for22
the negative control22
for the first22
occurred in the22
summarized in table22
the interaction of22
c t i22
upstream of the22
been detected in22
and analyzed by22
by any of22
in the current22
surface of the22
binding of the22
human coronavirus e22
the infectivity of22
n a t22
effect of the22
a dilution of22
size of the22
the reaction was22
these two viruses22
were compared with22
a receptor for22
porcine epidemic diarrhoea22
the differences in22
method for the22
antiviral activity against22
have been found22
virus particles were22
in ml of22
followed by the22
genome sequences of22
may be due22
each other and22
n influenza virus22
the feces of22
murine hepatitis virus22
colorado tick fever22
a r e22
of fipv infection22
eya virus strain22
indirect fluorescent antibody22
in of the22
known to be22
and it was22
simultaneous detection of22
addition to the22
infected cells at22
the significance of22
were performed in22
genetic characterization of22
spike protein of22
in situ hybridization22
did not show22
with each other22
assays were performed22
samples that were22
korean pedv field21
it is also21
in the usa21
dilutions of the21
of virus replication21
were collected at21
the orf la21
play a role21
would like to21
c for minutes21
care and use21
genbank accession number21
m o n21
was performed as21
is not a21
are the most21
of antibodies to21
is an important21
the host cell21
g for minutes21
washed with pbs21
data indicate that21
a simple method21
and it is21
of amino acid21
amplification of the21
cells were used21
the endoplasmic reticulum21
electron microscopy of21
n d t21
the concentration of21
strain of porcine21
cloned into the21
terminal region of21
to detect the21
positive samples were21
is critical for21
infected vero cells21
tested positive for21
the same as21
are closely related21
detection of bovine21
n t a21
samples from the21
molecular biology of21
there is no21
may also be21
those of other21
serial dilutions of21
be detected by21
and then incubated21
to examine the21
hepatitis delta virus21
been reported that21
of the international21
the rate of21
in the lung21
acute respiratory tract21
the causative agent21
canine parvovirus type21
neutralizing antibodies in21
r p h21
morbidity and mortality21
we have previously21
the cultures were21
were examined for21
intestinal epithelial cells21
have been used21
t h o21
been observed in21
likely to be21
the e protein21
and analysis of21
in both the21
with acute gastroenteritis21
was purchased from21
orf la protein21
to the cell21
and sequence analysis21
which had been21
cell lysates were21
the study of21
of monoclonal antibodies21
associated with diarrhea21
thought to be20
and the results20
in the orf20
cent of the20
n i n20
detection of respiratory20
the two isolates20
or absence of20
h n viral20
of the major20
need to be20
does not contain20
is present in20
phosphate buffered saline20
the distribution of20
collected from the20
used to determine20
virus attachment and20
phylogenetic tree based20
these results indicate20
genes of the20
hepatitis virus strain20
was associated with20
suckling mouse brain20
prior to the20
carried out at20
the age of20
h a n20
cells were fixed20
is known to20
and compared with20
s gene sequences20
antibody titers were20
located at the20
pcr assay panel20
with an equal20
the two viruses20
b i t20
sequence identity with20
the nucleotide and20
colostrum and milk20
p r e20
purified using a20
to the same20
it would be20
may have been20
n t r20
in a dose20
and evolution of20
possible that the20
t e s20
this study are20
the presence or20
viral infections in20
strains from the20
s genes of20
is shown in20
assay for the20
primers and probes20
m e t20
r a n20
viral rna in20
complete genome sequences20
the vaccine strain20
the same time20
of porcine parvovirus20
m h v20
of influenza viruses20
in vivo and20
viruses have been20
d t h20
was resuspended in20
in the small20
in the culture20
and found that20
were present in20
and the virus20
they have no20
t a i20
have been isolated20
assay was performed20
of the experiment20
thermo fisher scientific20
more closely related20
very similar to20
it was found20
in the cell20
were the most20
to bind to20
influenza viruses in20
immune response to20
and of the20
of infant mice20
the first report19
tissue culture plates19
that have been19
was performed on19
were prepared from19
the analysis of19
b b i19
p b s19
d e d19
these data suggest19
to determine if19
was the most19
cell differentiation survival19
a b b19
was isolated in19
to be involved19
at h post19
only in the19
infectious bronchitis viruses19
cells were collected19
of murine coronavirus19
the culture supernatant19
was significantly higher19
has been used19
h u m19
and has been19
of antibody to19
were not detected19
of middle east19
were analyzed using19
results not shown19
the occurrence of19
with per cent19
n influenza viruses19
inhibition of the19
not due to19
is not known19
of adult cattle19
submitted to the19
coronavirus infectious bronchitis19
at different time19
o n t19
effect on the19
experimentally infected with19
with that of19
it can be19
molecular weights of19
by means of19
available in the19
the region of19
was similar to19
in per cent19
snap or la19
antibodies in the19
in gnotobiotic pigs19
infected with prrsv19
declare that they19
sequences in the19
mediated isothermal amplification19
the hmg box19
at h after19
were mixed with19
of the patients19
of the animals19
phylogenetic trees were19
of the positive19
expression levels of19
were seen in19
in the study19
were determined using19
results show that19
that in the19
vereflu tm assay19
in central china19
in the second19
derived from a19
were identified in19
site of the19
that there are19
plates were washed19
porcine transmissible gastroenteritis19
no conflict of19
used to detect19
of pedv in19
the immune response19
was not observed19
to analyze the19
the difference in19
and ll of19
after inoculation with19
origin of the19
characteristics of the19
vp and vp19
present study was19
then incubated with19
the cause of19
r a b19
pleural effusion disease19
was kindly provided19
bhm and bj19
role of the19
infection of the19
in the pcag19
trees were constructed19
presence or absence19
restriction fragment length19
were exposed to19
better understanding of19
tract infections in19
recovered in the18
s t r18
to study the18
ibv isolates were18
dq ck ch18
protein of pedv18
isolated in the18
was performed with18
kipyv and wupyv18
characterization of porcine18
the virus is18
in cats with18
n protein of18
of the cleavage18
performed as described18
there is a18
acid sequence identity18
the vereflu tm18
the f gene18
been identified in18
to replicate in18
it may be18
is thought to18
h o d18
and vero cells18
clone infected cells18
of cellular cholesterol18
with the exception18
viral replication in18
length genome sequence18
of the original18
from those of18
is responsible for18
to the s18
the onset of18
were identified as18
as a template18
of patients with18
no effect on18
hepatitis virus type18
the s genes18
by plaque assay18
rpm for min18
in the phylogenetic18
than those of18
arg dq ck18
of the proteins18
ml of the18
their ability to18
significantly higher than18
infection with the18
were observed for18
in fecal samples18
are similar to18
synthesized in the18
feline alveolar macrophages18
relative to the18
antibodies were detected18
by monoclonal antibodies18
infected cell lysates18
epithelial cells of18
in the supernatant18
virus infection of18
cell monolayers were18
ctf virus and18
there have been18
to mouse hepatitis18
result in the18
korean ibv strains18
because of the18
were as follows18
the immunogenicity of18
the medium was18
has been found18
of the mhv18
of the isolates18
d n a18
viruses isolated in18
in this paper18
further studies are18
detected by the18
that there was18
of this virus18
sequence similarity between18
we did not18
directed against the18
dependent on the18
the swine industry18
the control of18
bind to the18
hemagglutinating encephalomyelitis virus18
respiratory disease in18
been suggested to18
was present in18
with mouse hepatitis18
virus and the18
for an additional18
are essential for18
belong to the18
major structural proteins18
influenza virus and18
with the cell18
two of the18
of tobacco mosaic18
was extracted using18
of canine coronavirus18
was prepared from18
in the control18
in each group18
of viral antigen18
detection of human18
the virus in18
a per cent18
of the full18
of hepatitis a18
a b s18
t i v18
u t e18
children with artis18
the slides were18
the american type18
of prrsv and18
cleavage recognition site18
the virus titer17
were purified using17
pedv vaccine strain17
it was shown17
and development of17
r e d17
of a virus17
epidemic diarrhea viruses17
transmissible gastroenteritis coronavirus17
a m i17
field isolates of17
rna in the17
final concentration of17
the entry of17
and molecular characterization17
i m m17
at hours p17
majority of the17
acid sequence of17
was identified in17
were similar to17
vero e cells17
rna was detected17
in association with17
accordance with the17
the association of17
position of the17
with regard to17
in any of17
virus titers were17
the authors thank17
of the strains17
r e p17
article does not17
bovine viral diarrhea17
m e d17
after treatment with17
samples were obtained17
described in the17
e d i17
amino acid mutations17
of the sars17
the highest dilution17
was mixed with17
were obtained by17
have been observed17
of the wild17
of the a17
needs to be17
of the capsid17
was treated with17
final extension at17
crystal structure of17
r e a17
min at room17
isolated in korea17
sensitivity and specificity17
of feline coronaviruses17
detection of porcine17
in cells infected17
at least one17
e p a17
stage of infection17
strains isolated in17
are required to17
are needed to17
s proteins of17
of the sequence17
a better understanding17
and function of17
the proportion of17
like to thank17
the natural host17
in combination with17
n t e17
a source of17
were negative for17
dependent enhancement of17
the supernatants were17
we report the17
calf diarrhea coronavirus17
ranging from to17
of the antiviral17
also detected in17
may be the17
a protein of17
the s proteins17
u t a17
mrna expression levels17
of virus in17
and pathogenesis of17
the spike glycoprotein17
the influenza virus17
contrast to the17
h and h17
each group were17
the molecular biology17
was assessed by17
strains of ibv17
by reverse transcription17
a new coronavirus17
of the genomic17
the vp protein17
performed by any17
of other species17
gene sequences of17
the first time17
multiple sequence alignment17
change in the17
pandemic influenza a17
cov and mers17
b u t17
in some cases17
titers in the17
the results obtained17
a group of17
biological properties of17
in relation to17
has been observed17
products of the17
inhibitory effect on17
replication of the17
antibodies against the17
of human adenovirus17
viruses belonging to17
was determined using17
feline enteric coronavirus17
been associated with17
products were analyzed17
the location of17
the proteins were17
minimal essential medium17
molecular weight of17
high degree of17
the m protein17
type i interferon17
epidemic diarrhoea virus17
replication in the17
conjugated goat anti17
bronchitis virus in17
e d b17
was prepared by17
to the family17
were challenged with16
the phylogenetic analysis16
in the early16
influenza b virus16
were examined by16
sequence alignments were16
was replaced with16
gastroenteritis virus and16
of the korean16
a d e16
spread of the16
of the sequences16
of all ages16
disease in the16
downstream of the16
suckling mouse brains16
are susceptible to16
were resuspended in16
in this report16
the chimeric vlps16
were observed between16
it is likely16
encoded by the16
was incubated at16
together with the16
the alignment of16
of the murine16
o d y16
n viral infection16
which have been16
the highest serum16
also been reported16
there are no16
of viruses in16
after infection and16
infected cells was16
presence of a16
korean field isolates16
using the maximum16
respiratory tract disease16
and the cells16
has not yet16
s e r16
replication of prrsv16
the antiviral effect16
n gene of16
the complete nucleotide16
and the rna16
amino acid substitutions16
control and prevention16
cats with fip16
blood mononuclear cells16
were prepared in16
strains of infectious16
of interest the16
of the infection16
with and without16
h e n16
in the future16
the family reoviridae16
s and n16
our understanding of16
in the lungs16
fecal samples from16
these results indicated16
federal republic of16
as a source16
transcription polymerase chain16
determined using a16
the m gene16
cloning and sequencing16
the rest of16
for min in16
strains have been16
reported that the16
analysis of a16
structure and function16
there were no16
virus replication and16
to be positive16
completion of the16
of the b16
aminopeptidase n is16
hepatitis e virus16
with feline infectious16
the size of16
i n u16
detected in this16
viral rna and16
of diarrhea in16
the importance of16
of ibv in16
when compared with16
n d e16
m a t16
cell monolayers in16
e a t16
porcine deltacoronavirus strain16
different time points16
cell cultures were16
we investigated the16
it is a16
to infection with16
were also observed16
was found that16
porcine nidovirus infection16
movement protein of16
of the pcr16
carried out by16
to the genus16
of the d16
the culture medium16
on the complete16
epitopes on the16
this article does16
were compared to16
plays an important16
with the plasma16
accession numbers are16
was based on16
of the six16
red blood cells16
tested for the16
and in vitro16
these results are16
was defined as16
found to have16
not i site16
studies of the16
rna recombination in16
to note that16
carried out with16
virus in a16
were classified into16
in the spike16
a final extension16
that the two16
much higher than16
like particles in16
is dependent on16
not contain any16
to improve the16
resulting in the16
of viral replication16
pcr products of16
central nervous system16
may not be16
close to the16
provided by the16
and those of16
of the cellular16
have indicated that16
the control group16
antigen positive cells16
syndrome virus in16
and sg mrna16
the d strain16
s protein is16
kb in length16
viruses isolated from16
some of these16
infection of cells16
of the various16
p r o16
were submitted to16
using trizol reagent15
recent studies have15
the same group15
lower than that15
positive and negative15
identical to that15
the detection and15
were infected at15
m u n15
acid sequence similarity15
t r e15
m m u15
of hepatitis delta15
observed for the15
virus was isolated15
expressed on the15
defined as the15
in serum and15
in clinical samples15
nde i fragment15
based on these15
a panel of15
e and e15
of fipv and15
comparison with the15
time reverse transcription15
interest the authors15
s glycoprotein of15
phylogenetic tree was15
i b o15
materials and methods15
t i b15
tree was constructed15
analysis revealed that15
has been identified15
tick fever virus15
was shown that15
f gene dna15
first report of15
was first reported15
to our knowledge15
b o d15
w a s15
medium supplemented with15
of a recombinant15
to per cent15
of the manuscript15
been found in15
sodium dodecyl sulfate15
pcd and vero15
detection and genetic15
length of the15
were clarified by15
indirect immunofluorescence assay15
were coated with15
level of the15
parts of the15
in the p15
in pbs and15
gene encoding the15
recombination within the15
was performed in15
the virus to15
the murine coronavirus15
is related to15
member viruses of15
its ability to15
the simultaneous detection15
to the mhv15
viruses associated with15
the fecal samples15
prevalence of respiratory15
it should be15
a set of15
of the nucleotide15
of the polymerase15
were included in15
antigenic relationship of15
the possibility of15
epidemic diarrhea in15
republic of germany15
incidence of covid15
after infection with15
the nature of15
except for the15
and genetic characterization15
and sequencing of15
the positive control15
could be demonstrated15
with ll of15
observed in this15
have no conflict15
c e n15
the preparation of15
isolated in japan15
pigs inoculated with15
antibody titers to15
of the surface15
were isolated in15
was also observed15
of emc virus15
which has been15
virus and eya15
genomic rna and15
could be used15
protein gene of15
and use of15
respiratory distress syndrome15
under the conditions15
the duration of15
early stage of15
bronchitis virus isolates15
course of the15
due to their15
the need for15
reverse transcription polymerase15
were performed with15
of the different15
a template for15
a negative control15
incubated for min15
by using the15
was collected from15
the generation of15
of the g15
with other viruses15
are responsible for15
classification and nomenclature15
were identified by15
in the genus15
higher than those15
use of a15
than that in15
national institute of15
of cats with15
be important for15
disease control and15
from the american15
induction of ifn15
viral protein synthesis15
carried out using15
swabs were collected15
study on the15
for h with15
days after the15
virus has been15
the p region15
indicates that the15
h e m15
be used for15
results in the15
purpose of this15
in peripheral blood15
detection of a15
for at least15
by using a15
correlation between the15
that h n15
more than one15
in china and15
amino acids in15
n u t15
highest serum dilution15
were transfected with15
virus strain fr15
in infant mice15
and genetic diversity15
calculated using the15
classical and novel15
diarrhea in swine15
activity in the15
by cycles of15
isolates from the15
of virus infection15
at least two15
influenza a and15
of at least15
of the feline15
supplied by dr15
were allowed to15
kindly supplied by15
the genome and15
diarrhea virus infection15
of the putative15
differentiation survival factors15
is likely to15
seems to be15
carried out as15
in the nucleus15
amino acids of15
was centrifuged at15
in the fecal15
infected with pedv14
of the primers14
the extent of14
and treated with14
for the virus14
and transmissible gastroenteritis14
the length of14
type and mutant14
clinical signs and14
virus nucleocapsid protein14
united states and14
and nasal swabs14
by the neighbor14
viral antigen was14
different types of14
viral particles were14
containing per cent14
of the mouse14
stranded rna viruses14
on bhk cells14
i n t14
the deduced amino14
of less than14
h prior to14
of the hexon14
suggested to be14
study showed that14
of veterinary medicine14
contain any studies14
the spike gene14
of the l14
of the villi14
a novel coronavirus14
determination of the14
nt sequence identity14
to serve as14
determined to be14
the partial s14
of eya virus14
followed by cycles14
e r a14
patients with acute14
a portion of14
on day p14
h e d14
of viral infection14
linked to the14
virus infection and14
cytopathic effect in14
that the s14
of a canine14
that they are14
a p p14
contribute to the14
was expressed as14
using the same14
of viral dna14
of ibv is14
of avian influenza14
i m a14
strains in the14
presence of trypsin14
of the new14
as a negative14
of avian coronavirus14
cells at hpi14
not been reported14
pellet was resuspended14
transferred to a14
in the other14
is a member14
of the predicted14
of mice with14
resulted in the14
molecular characterization and14
three independent experiments14
in these experiments14
capable of inducing14
supported by a14
cells were harvested14
for disease control14
t i n14
d b y14
the site of14
hsp and hsp14
of t h14
was observed with14
to be important14
the stockholm agent14
at least three14
we thank dr14
was conducted using14
rna replication and14
of the anti14
the inhibition of14
around the world14
confirmed that the14
effects of the14
to that in14
was provided by14
significant difference in14
multisystemic wasting syndrome14
human and animal14
to test the14
was first detected14
knu cells were14
for h in14
large amounts of14
t a t14
domestic ducks in14
carried out to14
small intestine of14
be attributed to14
within the same14
not be detected14
specific for the14
rna extracted from14
the care and14
the monolayers were14
the detection limit14
are consistent with14
was able to14
were calculated using14
the complete orf14
for hours at14
of the infectious14
infected with mhv14
serve as a14
in fip cats14
in the central14
in the natural14
cells were seeded14
mixture was incubated14
been used to14
in a co14
infectious virus was14
reproductive failure in14
only a few14
sequences available in14
that there is14
and baff mrna14
cell culture fluids14
were tested by14
the inhibitory effect14
rna genome of14
distribution of the14
genbank accession no14
of these two14
chain reaction and14
of g protein14
titers were expressed14
without affinity for14
examined using a14
multiple sequence alignments14
of the fusion14
the kinetics of14
divided into three14
within the s14
s protein gene14
a previous report14
was no significant14
n genes of14
stranded rna genome14
of in vitro14
analysis of porcine14
in a humidified14
performed according to14
viral diarrhea virus14
it is unclear14
the upper respiratory14
porcine aminopeptidase n14
monoclonal antibodies against14
hours after inoculation14
a t t14
and tested for14
this indicates that14
for rain at14
the serum of14
serum samples from14
the early stage14
t h r14
i u m14
the form of14
was observed between14
incubated at room14
resulting in a14
first reported in14
production of infectious14
by indirect immunofluorescence14
neutralizing antibodies against14
at kennel a14
studies are needed14
for the development14
the dub activity14
we demonstrated that14
of these proteins14
not appear to14
in this region14
a review of14
are present in14
fragment of the14
associated with severe14
t u r14
peripheral blood mononuclear14
is an enveloped14
of the ap14
is the only14
tissue culture fluid14
by western blotting14
h r o14
is likely that14
constructed using the14
one of these14
the virus and14
in ll of14
of the five14
an additional h14
divided into two14
medium was replaced14
using polymerase chain14
the major structural14
is based on14
for the care14
ml of a14
it is important13
terminal amino acids13
animals performed by13
economic losses in13
the severity of13
positive cells were13
at intervals of13
peritonitis virus infection13
as compared to13
reduction in the13
was measured by13
in the liver13
wide variety of13
genes of porcine13
virus spike protein13
i i f13
in the form13
the diagnosis of13
positive in the13
was approved by13
titer in the13
of the fecal13
to reduce the13
most similar to13
serum samples collected13
proteins encoded by13
and the two13
and cells were13
p h f13
consistent with previous13
the homologous virus13
immunodeficiency virus type13
gene of infectious13
were closely related13
by the end13
compared to that13
the e glycoprotein13
detection of antibody13
deposited in the13
as in the13
inoculated orally with13
hours after infection13
might be a13
genome of the13
was performed at13
of which are13
excellent technical assistance13
and iga antibodies13
plays a role13
of members of13
between the s13
was amplified using13
respiratory tract of13
is located in13
detection of canine13
with human participants13
characteristics of a13
of feline coronavirus13
of both the13
protein could be13
to be determined13
with respiratory tract13
c for sec13
h and then13
was the only13
in other countries13
for the n13
viral protein expression13
s oligo ibv13
relationship of the13
to the viral13
treated with trypsin13
protein in the13
from each other13
clustered with the13
were cloned into13
were then washed13
virus isolation and13
led to the13
in the jejunum13
in the c13
hare coltivirus s13
virus titer was13
induced by the13
did not neutralize13
like particles were13
twice with pbs13
can be detected13
when synthesized in13
california hare coltivirus13
the action of13
of newcastle disease13
any studies with13
with cold pbs13
the exception of13
the observation that13
sites of the13
v e r13
significant differences in13
v i t13
number of virus13
fatal and nonfatal13
by the presence13
the cell lysates13
the peplomer protein13
was also detected13
the isolates were13
it is interesting13
considered statistically significant13
bronchitis virus and13
the cellular receptor13
performed with the13
bovine enteric coronavirus13
of the substrate13
the pattern of13
the kakegawa strain13
interferon induction in13
by pcr using13
virus in vitro13
influenza h n13
and pathogenicity of13
the construction of13
immune responses in13
of each virus13
u r e13
identical to the13
be related to13
obtained from dr13
distinct from the13
of bovine torovirus13
the growth of13
and cloned into13
fusion of the13
of the entire13
cell culture adapted13
to those in13
it was also13
constructed by the13
other members of13
synthesis of the13
entry into cells13
the coat protein13
in north america13
emergence of a13
under the same13
ability of the13
f infected cells13
results were obtained13
for m i13
showed that all13
at the indicated13
the tissue culture13
was obtained by13
and analyzed using13
of acute respiratory13
are able to13
the mpcr method13
nucleocapsid protein of13
is necessary for13
the th passage13
dna and rna13
gene dna vaccine13
from each group13
these viruses in13
i n i13
virus titers in13
the titer of13
nucleic acids were13
t t e13
of p e13
induction of interferon13
infection resulted in13
strain with a13
t g e13
a high degree13
b and b13
i v i13
the size and13
primers were designed13
in this experiment13
to amplify the13
days of age13
pcr product was13
the n and13
in suckling mouse13
embryonated chicken eggs13
from this study13
from the other13
using monoclonal antibodies13
is a major13
bovine coronavirus in13
nucleotide sequences were13
in a few13
of the recombinant13
to the high13
variation in the13
were unable to13
ibv isolates in13
designed based on13
studies with human13
comparative analysis of13
or infected with13
isolates and the13
the mice were13
should be considered13
mabs to ep13
in sera of13
decrease in the13
at the nucleotide13
in the sera13
lesions in the13
a wide variety13
national center for13
hepatitis virus infection13
r u m13
the genomic rna13
cells in a13
and application of13
was propagated in13
structural protein of13
cell cultures and13
the university of13
ck ch ldl13
virulent and attenuated13
the question of13
were amplified by13
of the movement13
of orf and13
were collected in13
of the piglets13
were examined using13
cell fusion activity13
the range of13
strains of the13
the virus particles13
of human cytomegalovirus13
school of medicine13
significant economic losses13
of pdcov in13
all of these13
from fip cats13
than in the13
as described elsewhere13
predicted amino acid13
was derived from13
wide range of13
sites in the13
the discovery of13
a r a13
a lack of13
of semliki forest13
related to those13
fold dilutions of13
result of the13
the nucleic acid13
unique amino acid13
the efficiency of13
chinese ibv isolates13
of n protein13
losses to the13
this study showed13
the replication cycle13
respiratory infections in13
and used to13
caused by the13
first detected in13
infection in a13
proteins in the13
presented in fig12
not found in12
blood samples were12
findings indicate that12
c mice were12
on the viral12
the genome sequence12
the virulence of12
the first passage12
viral rna synthesis12
with the other12
of the peplomer12
viral dna synthesis12
were also detected12
replication in vitro12
of the control12
large numbers of12
detected in of12
classified into the12
of the bcv12
reacted with the12
dilution of the12
the a and12
the orf a12
removal of the12
as a new12
a consequence of12
but not at12
isolated from an12
in comparison to12
little is known12
of the ha12
washed once with12
infection in vitro12
of up to12
were incubated in12
virus was detected12
in the b12
avian influenza virus12
within the family12
m a r12
with the rna12
on days and12
the same manner12
f ep group12
using the following12
expression of a12
of movement proteins12
the other two12
pcr assay was12
p a n12
identical to those12
was amplified by12
in p b12
e r u12
nucleotide sequence and12
e m o12
evidence that the12
cell culture and12
nt and aa12
and comparison with12
of the assay12
in suckling piglets12
and n genes12
of this protein12
out of the12
o u n12
the genetic diversity12
belonged to the12
been reported previously12
neutrophil survival factors12
pcr purification kit12
the first week12
in the u12
born to immunized12
a combination of12
in tissue culture12
cells were examined12
tumor necrosis factor12
f and ifb12
infected cp mice12
of the vaccine12
of the nucleocapsid12
isolation of the12
the region between12
were calculated by12
h n avian12
mabs to the12
prepared from the12
was prepared as12
associated with acute12
and typing of12
m u t12
the membrane was12
be found in12
the antigenic relationship12
r d e12
a n y12
was identified by12
after incubation for12
the loss of12
after incubation at12
cells were observed12
e d a12
a maximum of12
ethical approval this12
has been detected12
the mhv n12
present on the12
of human coronavirus12
lower than the12
variations in the12
cultures were incubated12
the wells were12
avian coronavirus ibv12
virus is a12
replication of porcine12
genetic analysis of12
immune responses to12
at the amino12
the molecular epidemiology12
field strains from12
different from that12
c and c12
of the rdrp12
sasa quelpaertensis nakai12
protein and the12
deletions in the12
basic amino acids12