This is a table of type quadgram and their frequencies. Use it to search & browse the list to learn more about your study carrel.
quadgram | frequency |
---|---|
feline infectious peritonitis virus | 326 |
of feline infectious peritonitis | 284 |
with feline infectious peritonitis | 69 |
infectious peritonitis virus infection | 67 |
in the presence of | 47 |
pathogenesis of feline infectious | 44 |
in feline infectious peritonitis | 42 |
feline infectious peritonitis in | 36 |
severe acute respiratory syndrome | 36 |
against feline infectious peritonitis | 33 |
to feline infectious peritonitis | 33 |
sequence analysis of the | 32 |
in cats with fip | 32 |
types i and ii | 28 |
the pathogenesis of fip | 28 |
peritonitis virus infection in | 28 |
cats with feline infectious | 27 |
dependent enhancement of feline | 25 |
f i p v | 25 |
enhancement of feline infectious | 25 |
at an moi of | 24 |
in the pathogenesis of | 24 |
on the basis of | 24 |
in the present study | 23 |
of cats with feline | 23 |
and feline infectious peritonitis | 22 |
on the other hand | 22 |
of the s protein | 22 |
strains of feline infectious | 22 |
feline infectious peritonitis viruses | 22 |
at the time of | 21 |
the s protein of | 21 |
the feline infectious peritonitis | 20 |
feline infectious peritonitis and | 20 |
the p mapk pathway | 20 |
review of feline infectious | 19 |
by mutation from endemic | 19 |
by feline infectious peritonitis | 19 |
feline infectious peritonitis feline | 19 |
a review of feline | 19 |
human immunodeficiency virus type | 18 |
endemic feline enteric coronaviruses | 18 |
mutation from endemic feline | 18 |
has been shown to | 18 |
peritonitis viruses arise by | 18 |
infectious peritonitis viruses arise | 18 |
viruses arise by mutation | 18 |
in the s protein | 18 |
arise by mutation from | 18 |
of cats with fip | 18 |
from endemic feline enteric | 18 |
an important role in | 18 |
of the feline coronavirus | 17 |
on feline infectious peritonitis | 17 |
cell differentiation survival factors | 17 |
feline infectious peritonitis is | 17 |
protein of feline infectious | 17 |
the presence or absence | 17 |
presence or absence of | 17 |
virus infection in feline | 17 |
of feline coronavirus isolates | 16 |
porcine transmissible gastroenteritis virus | 16 |
type i feline coronavirus | 16 |
infection in feline macrophages | 16 |
of feline coronaviruses in | 16 |
of feline enteric coronavirus | 16 |
feline enteric coronavirus infection | 16 |
play an important role | 16 |
cats infected with fipv | 16 |
of the feline infectious | 15 |
the cells were washed | 15 |
acute respiratory syndrome coronavirus | 15 |
infectious peritonitis virus and | 15 |
peritonitis feline infectious peritonitis | 15 |
in feline macrophages by | 15 |
in the feces of | 15 |
relationship to feline infectious | 15 |
and feline enteric coronavirus | 15 |
infectious peritonitis feline infectious | 15 |
of hcq and rfifn | 15 |
the orf a b | 14 |
of cats against feline | 14 |
of transmissible gastroenteritis virus | 14 |
of mouse hepatitis virus | 14 |
the spike protein of | 14 |
to human cancer cells | 14 |
felis catus whole fetus | 14 |
comparative sequence analysis of | 14 |
infection of feline macrophages | 14 |
an enteric coronavirus infection | 14 |
enteric coronavirus infection of | 14 |
and pathogenesis of feline | 14 |
the effusive form of | 14 |
and its relationship to | 14 |
on the surface of | 14 |
diagnosis of feline infectious | 14 |
infection of cats and | 14 |
peripheral blood mononuclear cells | 14 |
its relationship to feline | 14 |
in peripheral blood monocytes | 14 |
of the orf a | 14 |
was added to the | 14 |
of naturally occurring feline | 14 |
coronavirus infection of cats | 14 |
used in this study | 14 |
the pathogenesis of feline | 14 |
of feline peritoneal macrophages | 13 |
a feline enteric coronavirus | 13 |
isolated from immunocompromised cats | 13 |
the molecular biology of | 13 |
are shown in table | 13 |
in the culture supernatant | 13 |
cats and its relationship | 13 |
feline coronavirus infections in | 13 |
cats against feline infectious | 13 |
feline coronavirus spike protein | 13 |
i and type ii | 13 |
in vitro and in | 13 |
pathogenicity studies of feline | 13 |
intrinsic resistance of feline | 13 |
the mechanism of antibody | 13 |
related strains of feline | 13 |
nucleotide sequence of the | 13 |
type i and type | 13 |
for the presence of | 13 |
in the absence of | 13 |
immunocompromised cats infected with | 13 |
of cats and its | 13 |
from immunocompromised cats infected | 13 |
two related strains of | 13 |
american type culture collection | 13 |
of human immunodeficiency virus | 13 |
genetics of feline coronaviruses | 12 |
or sublethal amounts of | 12 |
coronavirus infection correlates with | 12 |
in the case of | 12 |
infectious peritonitis and feline | 12 |
with in vivo virulence | 12 |
unit of different biotypes | 12 |
virus isolated from immunocompromised | 12 |
studies of feline coronavirus | 12 |
occurring feline infectious peritonitis | 12 |
the fcov c je | 12 |
with a feline enteric | 12 |
naturally occurring feline infectious | 12 |
transcription unit of different | 12 |
school of veterinary medicine | 12 |
infectious peritonitis virus isolated | 12 |
vitro and in vivo | 12 |
sublethal amounts of virulent | 12 |
orf a b transcription | 12 |
attempted immunization of cats | 12 |
feline infectious peritonitis coronavirus | 12 |
feline peritoneal macrophages to | 12 |
molecular genetics of feline | 12 |
amounts of virulent virus | 12 |
correlates with in vivo | 12 |
ade of fipv infection | 12 |
infectious peritonitis virus in | 12 |
of fipv and fecv | 12 |
virus or sublethal amounts | 12 |
peritonitis virus isolated from | 12 |
to coronavirus infection correlates | 12 |
of porcine transmissible gastroenteritis | 12 |
during the pathogenesis of | 12 |
infected with a feline | 12 |
the peplomer protein of | 12 |
macrophages to coronavirus infection | 12 |
from cats with fip | 12 |
b transcription unit of | 12 |
infection correlates with in | 12 |
of type ii fipv | 12 |
genomic rna sequence of | 12 |
analysis of the orf | 12 |
of splenocytes cultured with | 12 |
the molecular genetics of | 12 |
the development of fip | 12 |
the sequence of the | 12 |
peritoneal macrophages to coronavirus | 12 |
live virus or sublethal | 12 |
of the peplomer protein | 12 |
cats infected with a | 12 |
resistance of feline peritoneal | 12 |
immunization of cats against | 12 |
a multiplicity of infection | 12 |
a b transcription unit | 12 |
at a multiplicity of | 12 |
the feline coronavirus spike | 12 |
avirulent live virus or | 12 |
of the virus in | 12 |
of feline coronavirus infection | 11 |
structural and accessory genes | 11 |
it has been reported | 11 |
mutations in the feline | 11 |
cells were infected with | 11 |
determined by mutations in | 11 |
cats experimentally infected with | 11 |
for feline infectious peritonitis | 11 |
cells infected with fipv | 11 |
by mutations in the | 11 |
peritonitis is determined by | 11 |
in the development of | 11 |
of feline coronavirus in | 11 |
of types i and | 11 |
produced by feline infectious | 11 |
role in the pathogenesis | 11 |
important role in the | 11 |
infectious peritonitis is determined | 11 |
acquisition of macrophage tropism | 11 |
tropism during the pathogenesis | 11 |
in the feline coronavirus | 11 |
of macrophage tropism during | 11 |
in the effusive form | 11 |
mixture of fipv and | 11 |
have been shown to | 11 |
with a mixture of | 11 |
is determined by mutations | 11 |
has been reported that | 11 |
work was supported by | 11 |
infected with feline coronavirus | 11 |
macrophage tropism during the | 11 |
were infected with fipv | 11 |
and the role of | 11 |
quantitatively analyzed in terms | 10 |
of feline coronaviruses with | 10 |
the housekeeping gene gapdh | 10 |
it has been suggested | 10 |
the combination of hcq | 10 |
antigenic relationship of the | 10 |
new strains of feline | 10 |
form of feline infectious | 10 |
as well as the | 10 |
three new strains of | 10 |
analyzed in terms of | 10 |
in the presence or | 10 |
the amino acid sequence | 10 |
the s proteins of | 10 |
a member of the | 10 |
of type i fipv | 10 |
detection of feline coronavirus | 10 |
experimental studies with three | 10 |
of the family coronaviridae | 10 |
has been suggested that | 10 |
in the supernatant of | 10 |
kindly provided by dr | 10 |
the s domain of | 10 |
the presence of the | 10 |
the supernatant of splenocytes | 10 |
supernatant of splenocytes cultured | 10 |
this work was supported | 10 |
on the mechanism of | 10 |
porcine epidemic diarrhea virus | 10 |
relationship of the feline | 10 |
feline coronavirus type i | 10 |
as shown in figure | 10 |
combination of hcq and | 10 |
sequence of the peplomer | 10 |
in the s gene | 10 |
coronaviruses to human cancer | 10 |
the antiviral activity of | 10 |
from feline infectious peritonitis | 10 |
in peripheral blood lymphocytes | 10 |
type i fipv black | 10 |
one of the most | 10 |
with three new strains | 10 |
of f i p | 10 |
and baff mrna expression | 10 |
the antiviral effects of | 10 |
a study on the | 10 |
human coronaviruses to human | 10 |
spf and fip cats | 10 |
effusive form of feline | 10 |
using avirulent live virus | 10 |
studies with three new | 10 |
diseased tissues of cats | 9 |
i and canine coronavirus | 9 |
combination of these drugs | 9 |
molecular biology of coronaviruses | 9 |
supernatants were collected and | 9 |
feline infectious peritonitis the | 9 |
macrophages by monoclonal antibodies | 9 |
differences between various feline | 9 |
of disease in feline | 9 |
experimental inoculation of cats | 9 |
the pre post treatment | 9 |
i feline coronavirus infection | 9 |
enhancement of disease in | 9 |
pathogenesis of feline coronavirus | 9 |
coronavirus infection and the | 9 |
de groot et a | 9 |
the viral spike protein | 9 |
in the pre post | 9 |
an update on feline | 9 |
the culture supernatant of | 9 |
lower than that of | 9 |
the incidence of fip | 9 |
and ii feline coronavirus | 9 |
virus titer in the | 9 |
of these drugs strongly | 9 |
ii feline coronavirus infections | 9 |
of severe acute respiratory | 9 |
inoculation of cats with | 9 |
feline infectious peritonitis among | 9 |
i and ii feline | 9 |
peplomer protein of feline | 9 |
phenomena in the effusive | 9 |
induction in peripheral blood | 9 |
than in that of | 9 |
coronavirus infection in cats | 9 |
pathogenic differences between various | 9 |
of fcov c je | 9 |
feline coronavirus c gene | 9 |
studies have shown that | 9 |
type i and canine | 9 |
peripheral blood lymphocytes of | 9 |
study on the mechanism | 9 |
disease in feline infectious | 9 |
induced feline infectious peritonitis | 9 |
fipv type i viruses | 9 |
after inoculation with fipv | 9 |
immunologic aspects of feline | 9 |
protection against feline infectious | 9 |
the macrophages from the | 9 |
infectious peritonitis virus type | 9 |
with dengue hemorrhagic fever | 9 |
protein of feline coronavirus | 9 |
was obtained from the | 9 |
in terms of the | 9 |
mediated enhancement of disease | 9 |
feline macrophages by monoclonal | 9 |
the upper respiratory tract | 9 |
antigenic relationship between feline | 9 |
feline coronavirus infection and | 9 |
the combination of these | 9 |
the virus titer in | 9 |
coronavirus type i and | 9 |
play a role in | 9 |
the feline coronavirus c | 9 |
in apoptosis induction in | 9 |
immunologic phenomena in the | 9 |
blood lymphocytes of cats | 9 |
and transmissible gastroenteritis virus | 9 |
update on feline infectious | 9 |
lymphocytes of cats with | 9 |
apoptosis induction in peripheral | 9 |
been shown to be | 9 |
x g for minutes | 9 |
virologic and immunologic aspects | 9 |
and immunologic aspects of | 9 |
of the fipv genome | 9 |
aspects of feline infectious | 9 |
was used as a | 9 |
an equal volume of | 8 |
higher than in that | 8 |
in contrast to the | 8 |
before inoculating with fipv | 8 |
alpha in apoptosis induction | 8 |
a recurrent feline coronavirus | 8 |
upon isolates from resident | 8 |
resident and adopted shelter | 8 |
fcov n gene expression | 8 |
a mixture of fipv | 8 |
the american type culture | 8 |
coronaviruses of other species | 8 |
natural history of a | 8 |
risk factors for feline | 8 |
double recombination between feline | 8 |
form of the disease | 8 |
between feline infectious peritonitis | 8 |
between various feline coronavirus | 8 |
from two cats with | 8 |
immunity in survival and | 8 |
peritonitis virus to coronaviruses | 8 |
recombination between feline coronavirus | 8 |
to coronaviruses of other | 8 |
was performed as described | 8 |
for h at c | 8 |
it is possible that | 8 |
infectious peritonitis pathogenicity studies | 8 |
in survival and disease | 8 |
peritonitis pathogenicity studies of | 8 |
role of cellular immunity | 8 |
infection and the role | 8 |
recurrent feline coronavirus infection | 8 |
feline coronaviruses in peripheral | 8 |
protein cleavage site and | 8 |
c gene in intestinal | 8 |
coronaviruses in peripheral blood | 8 |
isolation of feline coronaviruses | 8 |
from a double recombination | 8 |
experimentally induced feline infectious | 8 |
can be used to | 8 |
role of the feline | 8 |
in spike protein cleavage | 8 |
that died of fip | 8 |
mrna expression levels in | 8 |
the relative density value | 8 |
similar to that of | 8 |
between feline coronavirus type | 8 |
three times with pbs | 8 |
and subsequent challenge with | 8 |
cleavage site and pathogenesis | 8 |
macrophages from the ascites | 8 |
of the p mapk | 8 |
isolates from resident and | 8 |
of the relative density | 8 |
tropism and pathogenicity based | 8 |
in that of splenocytes | 8 |
feline infectious peritonitis pathogenicity | 8 |
pathogenesis of feline enteric | 8 |
activation of the p | 8 |
various feline coronavirus isolates | 8 |
mutation in spike protein | 8 |
and type ii feline | 8 |
pathogenicity based upon isolates | 8 |
for h before inoculating | 8 |
in the upper respiratory | 8 |
lesions in feline infectious | 8 |
and adopted shelter cats | 8 |
history of a recurrent | 8 |
h before inoculating with | 8 |
propagated in cell culture | 8 |
originate from a double | 8 |
and pathogenicity based upon | 8 |
coronavirus type ii strains | 8 |
cells were incubated with | 8 |
coronavirus c gene in | 8 |
of cats suffering from | 8 |
infectious peritonitis among cats | 8 |
crandell feline kidney cells | 8 |
from the american type | 8 |
peritonitis virus and its | 8 |
were quantitatively analyzed in | 8 |
induced p mapk activation | 8 |
terms of the relative | 8 |
virus to coronaviruses of | 8 |
receptor feline aminopeptidase n | 8 |
infectious peritonitis virus to | 8 |
a double recombination between | 8 |
infected monocytes and macrophages | 8 |
feline coronavirus type ii | 8 |
of a recurrent feline | 8 |
subsequent challenge with feline | 8 |
were inoculated with fipv | 8 |
site and pathogenesis of | 8 |
based upon isolates from | 8 |
experimental feline infectious peritonitis | 8 |
intestinal tropism and pathogenicity | 8 |
th and th epitopes | 8 |
spike protein cleavage site | 8 |
analysis of feline coronaviruses | 8 |
coronavirus infections in cats | 8 |
activation of p mapk | 8 |
from resident and adopted | 8 |
significantly higher than in | 8 |
is involved in the | 8 |
human cancer cells t | 8 |
the role of cellular | 8 |
compared to that of | 8 |
pathologic changes and immunofluorescence | 8 |
replication of feline coronaviruses | 8 |
challenge with feline infectious | 8 |
cellular immunity in survival | 8 |
of cellular immunity in | 8 |
of viral proteins in | 8 |
gene in intestinal tropism | 8 |
in intestinal tropism and | 8 |
college of veterinary medicine | 8 |
related to transmissible gastroenteritis | 7 |
feline coronavirus persistence in | 7 |
infectious peritonitis virus replication | 7 |
studies of naturally occurring | 7 |
virus type ii and | 7 |
natural type i feline | 7 |
a role in the | 7 |
aminopeptidase n in feline | 7 |
in the spike protein | 7 |
peptides derived from the | 7 |
persistence in healthy cats | 7 |
to the spike protein | 7 |
expression of type ii | 7 |
comparisons with dengue hemorrhagic | 7 |
of the infected cells | 7 |
mrna expression levels were | 7 |
both serotypes of fipv | 7 |
antiviral activity of hcq | 7 |
the treatment of fip | 7 |
for the diagnosis of | 7 |
baff mrna expression levels | 7 |
this study was to | 7 |
the s and m | 7 |
end of the genome | 7 |
protein fusion peptide and | 7 |
prevalence of types i | 7 |
persistence and transmission of | 7 |
persistence and evolution of | 7 |
sites of feline coronavirus | 7 |
virus propagated in cell | 7 |
of monoclonal antibodies against | 7 |
susceptibility to feline infectious | 7 |
upregulates expression of type | 7 |
the majority of the | 7 |
either sb or sc | 7 |
the specificity of the | 7 |
naturally occurring feline coronavirus | 7 |
monoclonal antibodies to the | 7 |
monocyte cell line u | 7 |
of gc or npi | 7 |
feline coronavirus in a | 7 |
phylogenetic analysis of feline | 7 |
transmission of natural type | 7 |
experimentally infected with feline | 7 |
suffering from feline infectious | 7 |
of naturally infected cats | 7 |
coronavirus persistence in healthy | 7 |
antibodies against feline infectious | 7 |
has been reported to | 7 |
of serotype ii feline | 7 |
for the detection of | 7 |
of feline coronavirus persistence | 7 |
of the viral genome | 7 |
in crfk cells and | 7 |
of the fcov c | 7 |
fipv receptor feline aminopeptidase | 7 |
cats that died of | 7 |
in cats experimentally infected | 7 |
were cultured in medium | 7 |
human monocyte cell line | 7 |
to protect cats against | 7 |
of coronavirus mutants in | 7 |
of fipv and mab | 7 |
peptide and feline coronavirus | 7 |
it has been shown | 7 |
the diagnosis of feline | 7 |
of natural type i | 7 |
the gene encoding the | 7 |
ii and antigenic relationship | 7 |
it remains to be | 7 |
replication in monocytes macrophages | 7 |
avirulent feline infectious peritonitis | 7 |
the reason for this | 7 |
and feline coronavirus virulence | 7 |
peritonitis virus type ii | 7 |
been reported to be | 7 |
type ii and antigenic | 7 |
was found to be | 7 |
infection studies in kittens | 7 |
tissues of cats suffering | 7 |
from transmissible gastroenteritis virus | 7 |
of the s gene | 7 |
and antigenic relationship between | 7 |
serotype ii feline coronaviruses | 7 |
has been described for | 7 |
produced by macrophages in | 7 |
was added to each | 7 |
prevalence of feline coronavirus | 7 |
added to each well | 7 |
of p mapk by | 7 |
feline coronaviruses from two | 7 |
and transmission of natural | 7 |
monoclonal antibodies against feline | 7 |
type ii fipv receptor | 7 |
of a coronavirus from | 7 |
activity of hcq and | 7 |
of this study was | 7 |
spike protein fusion peptide | 7 |
in a closed cat | 7 |
of feline coronavirus rna | 7 |
the type i fipv | 7 |
the s s cleavage | 7 |
type ii feline coronavirus | 7 |
of feline coronaviruses from | 7 |
coronaviruses from two cats | 7 |
cultured in medium containing | 7 |
serologic studies of naturally | 7 |
and fcov n genes | 7 |
feline aminopeptidase n in | 7 |
serotype ii fipv strain | 7 |
n in feline macrophages | 7 |
infectious peritonitis in cats | 7 |
by macrophages in cats | 7 |
the prevalence of types | 7 |
cells were treated with | 7 |
spike protein of feline | 7 |
infectious peritonitis virus propagated | 7 |
fusion peptide and feline | 7 |
which were pretreated with | 7 |
fipv type ii and | 7 |
mouse hepatitis virus strain | 7 |
peritonitis virus propagated in | 7 |
cats suffering from feline | 7 |
de groot et al | 7 |
in the c gene | 7 |
used in the present | 7 |
primary structure of the | 7 |
with diverse disease manifestations | 7 |
age at the time | 7 |
the structural and accessory | 7 |
macrophages were infected with | 7 |
ii fipv receptor feline | 7 |
factors for feline infectious | 7 |
serotypes i and ii | 7 |
peritonitis and feline enteric | 7 |
of the gene encoding | 7 |
and fecv type ii | 7 |
transcriptase polymerase chain reaction | 7 |
from fecv by mutation | 6 |
of a field strain | 6 |
virus and its growth | 6 |
fipv infection of feline | 6 |
and physical characteristics of | 6 |
in the none group | 6 |
naturally infected cats by | 6 |
i and ii in | 6 |
of fipv infection of | 6 |
genetic analysis of the | 6 |
a small number of | 6 |
cats with canine coronavirus | 6 |
cats with diverse disease | 6 |
the feline coronavirus fipv | 6 |
on genetic analysis of | 6 |
the infiltration of neutrophils | 6 |
these drugs strongly decreased | 6 |
derived feline mononuclear cells | 6 |
orf a and orf | 6 |
feline and canine coronaviruses | 6 |
with an equal volume | 6 |
immunized with an avirulent | 6 |
cells were cultured in | 6 |
mrna and fcov n | 6 |
been associated with the | 6 |
of splenocytes derived from | 6 |
fip and spf cats | 6 |
and phylogenetic analysis of | 6 |
amino acid changes in | 6 |
of feline coronaviruses and | 6 |
analysis of neutralization and | 6 |
and epidemiology based on | 6 |
was significantly inhibited by | 6 |
in the macrophages from | 6 |
biological diversity of feline | 6 |
the feline coronavirus genome | 6 |
of the peplomer gene | 6 |
has not yet been | 6 |
and evolution of feline | 6 |
coronavirus mutants in feces | 6 |
we evaluated the antiviral | 6 |
infected with fipv and | 6 |
the m protein of | 6 |
between the s and | 6 |
the concentration of il | 6 |
u m a n | 6 |
was significantly higher than | 6 |
infectious peritonitis in a | 6 |
to play an important | 6 |
insights into feline coronavirus | 6 |
feline infectious peritonitis cases | 6 |
the end of the | 6 |
of a type i | 6 |
effects of the combination | 6 |
decreased the replication of | 6 |
in feces and diseased | 6 |
inhibited by hcq and | 6 |
mutants in feces and | 6 |
the internal mutation theory | 6 |
the role of the | 6 |
in the small intestine | 6 |
class i virus fusion | 6 |
monoclonal antibody analysis of | 6 |
feline coronavirus pathobiogenesis and | 6 |
canine coronavirus and subsequent | 6 |
as a therapeutic drug | 6 |
by hcq and rfifn | 6 |
the sensitivity of the | 6 |
splenocytes cultured with or | 6 |
and its growth in | 6 |
analyzed by western blot | 6 |
mutations in the s | 6 |
the s and s | 6 |
antigenic and biological diversity | 6 |
remains to be determined | 6 |
fipv replication in vitro | 6 |
evolution of feline coronavirus | 6 |
characterization of monoclonal antibodies | 6 |
outbreak of feline infectious | 6 |
coronavirus rna in feces | 6 |
of dengue virus infection | 6 |
fipv replication was significantly | 6 |
s protein of the | 6 |
protein levels of fipv | 6 |
washed three times with | 6 |
diversity of feline coronaviruses | 6 |
were obtained from the | 6 |
in the s and | 6 |
of the m gene | 6 |
in cats infected with | 6 |
method of takano et | 6 |
coronavirus spike protein is | 6 |
these results suggest that | 6 |
enteric coronavirus infection in | 6 |
was observed in the | 6 |
obtained from the american | 6 |
has been shown that | 6 |
study of naturally occurring | 6 |
nature and development of | 6 |
the survival rate of | 6 |
after virus adsorption at | 6 |
infiltration of neutrophils into | 6 |
feces and diseased tissues | 6 |
antibody analysis of neutralization | 6 |
replication was significantly inhibited | 6 |
domain of the s | 6 |
a study of naturally | 6 |
previous studies have shown | 6 |
group was comprised of | 6 |
morphologic and physical characteristics | 6 |
of the pathogenesis of | 6 |
at room temperature for | 6 |
rna was extracted from | 6 |
antigens on the surface | 6 |
avian infectious bronchitis virus | 6 |
of monocytes and macrophages | 6 |
for the treatment of | 6 |
cultured with or without | 6 |
for the identification of | 6 |
coronavirus pathobiogenesis and epidemiology | 6 |
associated with feline infectious | 6 |
antigenic relationships among homologous | 6 |
inoculated with feline infectious | 6 |
gene of feline infectious | 6 |
inflammatory cytokine production in | 6 |
between fipv and fecv | 6 |
antiviral effects of the | 6 |
inoculated with a mixture | 6 |
expression of viral proteins | 6 |
of the viral c | 6 |
pathogenesis of fip is | 6 |
and fcov n gene | 6 |
of the amino acid | 6 |
coronavirus and subsequent challenge | 6 |
either one of the | 6 |
the cells were incubated | 6 |
neutrophils into granulomatous lesions | 6 |
and biological diversity of | 6 |
and characterization of a | 6 |
the expression of viral | 6 |
characteristics of feline infectious | 6 |
of neutralization and antibody | 6 |
occurring feline coronavirus infections | 6 |
and diseased tissues of | 6 |
cats by reverse transcriptase | 6 |
analysis of the viral | 6 |
characterization of a coronavirus | 6 |
of takano et al | 6 |
the culture supernatant was | 6 |
of cats with canine | 6 |
therapeutic drug for fip | 6 |
a therapeutic drug for | 6 |
molecular weight of the | 6 |
significance of coronavirus mutants | 6 |
mrna for the housekeeping | 6 |
from cats infected with | 6 |
detection of feline coronaviruses | 6 |
of fipv and anti | 6 |
a wide range of | 6 |
infected with feline infectious | 6 |
strongly decreased the replication | 6 |
of the combination of | 6 |
as shown in fig | 6 |
the nucleotide sequence of | 6 |
a recombinant vaccinia virus | 6 |
significantly inhibited by hcq | 6 |
were inoculated intraperitoneally with | 6 |
and the number of | 6 |
cells were washed three | 6 |
based on genetic analysis | 6 |
h u m a | 6 |
to that of the | 6 |
the time of exposure | 6 |
coronavirus transmissible gastroenteritis virus | 6 |
increased plasma levels of | 6 |
transmissible gastroenteritis virus and | 6 |
an incubation period of | 6 |
deletions in orf b | 6 |
of the viral spike | 6 |
cells were washed with | 6 |
two cats with diverse | 6 |
deletions in the a | 6 |
experimentally infected with fipv | 6 |
feline infectious peritonitis tnf | 6 |
infected tissue culture fluid | 6 |
it was shown that | 6 |
infected cats by reverse | 6 |
pathobiogenesis and epidemiology based | 6 |
in medium containing chloroquine | 6 |
of the infected cats | 6 |
by reverse transcriptase pcr | 6 |
fcov n genes were | 6 |
of ade of fipv | 6 |
the method of takano | 6 |
were washed three times | 6 |
vascular endothelial growth factor | 6 |
of the e glycoprotein | 6 |
feline coronavirus rna in | 6 |
epidemiology based on genetic | 6 |
is a member of | 6 |
coronavirus in a closed | 6 |
s domain of the | 6 |
in view of the | 6 |
the four related cats | 6 |
the e glycoprotein of | 6 |
relative density value to | 6 |
naturally infected with feline | 6 |
between fecv and fipv | 6 |
the peplomer gene of | 6 |
with canine coronavirus and | 6 |
drugs strongly decreased the | 6 |
infection enhancement of dengue | 6 |
for the housekeeping gene | 6 |
the viral c gene | 6 |
as a result of | 6 |
studies are required to | 6 |
that of splenocytes derived | 6 |
of neutrophils into granulomatous | 6 |
was provided by dr | 6 |
it is necessary to | 6 |
cats in this study | 6 |
physical characteristics of feline | 6 |
into feline coronavirus pathobiogenesis | 6 |
against the clpro of | 6 |
of a cat with | 6 |
the antigenic relationship of | 6 |
was supported by a | 6 |
at a concentration of | 6 |
containing fetal bovine serum | 6 |
than that of cq | 6 |
are more likely to | 5 |
centrifuged at g for | 5 |
cd and cd t | 5 |
among homologous structural polypeptides | 5 |
disease outcome and cytokine | 5 |
the fipv orf b | 5 |
its growth in autochthonous | 5 |
in this study were | 5 |
have been used to | 5 |
the th and th | 5 |
the circular tfo rnas | 5 |
strain feline coronaviruses with | 5 |
the differences in the | 5 |
in cats with histopathologically | 5 |
with hcq and rfifn | 5 |
cats with fip and | 5 |
and respiratory syndrome virus | 5 |
survival time and quality | 5 |
culture an enteric coronavirus | 5 |
infectious peritonitis and porcine | 5 |
and post treatment groups | 5 |
feline alveolar macrophages were | 5 |
not yet been clarified | 5 |
during feline infectious peritonitis | 5 |
the vast majority of | 5 |
of the faecal samples | 5 |
derived from the fp | 5 |
a final concentration of | 5 |
with neutralizing activity against | 5 |
reproductive and respiratory syndrome | 5 |
a standardized plaque assay | 5 |
in cell culture an | 5 |
of ltb and pge | 5 |
by the method of | 5 |
coronaviruses with peptidyl compounds | 5 |
of the fusion core | 5 |
homologous structural polypeptides of | 5 |
analysis of feline coronavirus | 5 |
amino acids in the | 5 |
did not show significant | 5 |
in cats immunized with | 5 |
in cell culture and | 5 |
clinical and pathological findings | 5 |
present in the s | 5 |
for min and then | 5 |
there was no significant | 5 |
of life of cats | 5 |
the fusion core complex | 5 |
cell culture an enteric | 5 |
through the directed deletion | 5 |
and infectious peritonitis virus | 5 |
findings in cats experimentally | 5 |
of a modified live | 5 |
of feline coronavirus strain | 5 |
recombinant vaccinia virus vtf | 5 |
of the accessory proteins | 5 |
pbml isolated from cats | 5 |
i p v infection | 5 |
comparison with the sequence | 5 |
characterization of a feline | 5 |
cytokine production in primary | 5 |
with an epidemic of | 5 |
mapk by feline infectious | 5 |
cells and in pbmcs | 5 |
p mapk by feline | 5 |
was kindly provided by | 5 |
coronavirus mouse hepatitis virus | 5 |
samples were collected from | 5 |
of porcine coronavirus tgev | 5 |
pcr for the diagnosis | 5 |
cells were grown in | 5 |
the genome of porcine | 5 |
feline infectious peritonitis two | 5 |
coronaviruses with small deletions | 5 |
control and infected samples | 5 |
viral rna level in | 5 |
both fipv and fecv | 5 |
the presence of a | 5 |
in accordance with the | 5 |
rna was isolated from | 5 |
associated with an epidemic | 5 |
peritonitis and feline enteritis | 5 |
comparison with the genome | 5 |
to be responsible for | 5 |
sequences are shown in | 5 |
plasma levels occurred in | 5 |
peplomer gene of porcine | 5 |
relationships among homologous structural | 5 |
the cells were fixed | 5 |
is a class i | 5 |
and development of viremia | 5 |
is similar to that | 5 |
at c for min | 5 |
r i and ii | 5 |
on the cell surface | 5 |
characterization of the fusion | 5 |
cloning and sequence analysis | 5 |
recombinant vaccinia virus expressing | 5 |
and in naturally fcov | 5 |
specific genes provide protection | 5 |
in orf b associated | 5 |
infection of cats with | 5 |
b associated with both | 5 |
immunodeficiency virus type infection | 5 |
outcome and cytokine responses | 5 |
at this time point | 5 |
environments with endemic feline | 5 |
derived from the s | 5 |
structural polypeptides of porcine | 5 |
type i and ii | 5 |
peritonitis and porcine transmissible | 5 |
feline enteric coronavirus and | 5 |
porcine reproductive and respiratory | 5 |
an epidemic of feline | 5 |
from fip diagnosed cats | 5 |
of the virus to | 5 |
transmissible gastroenteritis virus by | 5 |
despite absence of clinical | 5 |
with peptidyl compounds targeting | 5 |
through the oral route | 5 |
the nucleocapsid protein of | 5 |
verified feline infectious peritonitis | 5 |
coronavirus feline infectious peritonitis | 5 |
center for companion animal | 5 |
feline infectious peritonitis antibody | 5 |
feline coronavirus associated with | 5 |
results of this study | 5 |
centrifuged for min at | 5 |
density value to the | 5 |
both control and infected | 5 |
crfk cells infected with | 5 |
and body fluids of | 5 |
spike protein is a | 5 |
or without fipv antigen | 5 |
antibodies recognizing different epitopes | 5 |
of a feline infectious | 5 |
crandell rees feline kidney | 5 |
persistent feline enteric coronavirus | 5 |
associated with both enteric | 5 |
and the nucleocapsid protein | 5 |
exposed with virulent fipv | 5 |
fipv type ii strain | 5 |
from the s domain | 5 |
and ii in cats | 5 |
called feline infectious peritonitis | 5 |
the results of this | 5 |
and functional characterization of | 5 |
infectious peritonitis virus infections | 5 |
of feline coronavirus associated | 5 |
to experimental feline infectious | 5 |
evidence for markedly different | 5 |
provide protection against feline | 5 |
the plates were incubated | 5 |
members of the family | 5 |
pretreated with dmso alone | 5 |
infected with fipv strain | 5 |
orf b associated with | 5 |
of feline coronavirus types | 5 |
of the two viruses | 5 |
for markedly different peplomer | 5 |
cats infected with feline | 5 |
with the outcome of | 5 |
to manipulate the feline | 5 |
evaluation of a modified | 5 |
cells were removed by | 5 |
and quality of life | 5 |
of persistent feline enteric | 5 |
the directed deletion of | 5 |
of circular tfo rna | 5 |
and cytokine responses in | 5 |
infection of monocytes and | 5 |
of fipv infection is | 5 |
that the incidence of | 5 |
directed deletion of group | 5 |
titer in the culture | 5 |
mixed with an equal | 5 |
infectious peritonitis virus mediate | 5 |
small deletions in orf | 5 |
related group was comprised | 5 |
the biology of coronaviruses | 5 |
the origin of the | 5 |
phosphorylation of p mapk | 5 |
the plasma drug concentrations | 5 |
field strains of fipv | 5 |
well culture chamber slides | 5 |
feline coronavirus serotypes and | 5 |
university college of veterinary | 5 |
pathological findings in cats | 5 |
at different time points | 5 |
of both serotypes of | 5 |
life of cats with | 5 |
an avirulent feline infectious | 5 |
viral loads despite absence | 5 |
cats that developed fip | 5 |
and pathological findings in | 5 |
these results indicate that | 5 |
are listed in table | 5 |
tissue culture fluid was | 5 |
in the a orf | 5 |
feline coronavirus infection in | 5 |
the concentrations of ifn | 5 |
and feline enteritis virus | 5 |
in cats naturally infected | 5 |
quality of life of | 5 |
were washed with hbss | 5 |
the indirect fluorescent antibody | 5 |
and analyzed by western | 5 |
an effective way to | 5 |
after an incubation period | 5 |
the development of a | 5 |
were fixed in absolute | 5 |
of the feline coronaviruses | 5 |
cytokine responses in cats | 5 |
of a porcine respiratory | 5 |
body fluids of naturally | 5 |
and sequence analysis of | 5 |
an overview of feline | 5 |
can be used for | 5 |
neutralizing monoclonal antibodies recognizing | 5 |
time and quality of | 5 |
rna level in the | 5 |
inflammatory cytokine mrna expression | 5 |
peritonitis attempted immunization of | 5 |
due to the lack | 5 |
activation in cats with | 5 |
the binding of the | 5 |
ii in cats with | 5 |
pathogenic characteristics of persistent | 5 |
the severe acute respiratory | 5 |
have been implicated in | 5 |
ade of fipv infectivity | 5 |
peritonitis two related strains | 5 |
and association with disease | 5 |
to transmissible gastroenteritis virus | 5 |
infection and feline infectious | 5 |
inoculated with the virus | 5 |
fixed in absolute acetone | 5 |
a orf of feline | 5 |
and in pbmcs from | 5 |
pfbm cells were treated | 5 |
independent evaluation of a | 5 |
peptidyl compounds targeting coronavirus | 5 |
field strain feline coronaviruses | 5 |
with the sequence of | 5 |
kill human cancer cells | 5 |
protein is a class | 5 |
enhancement and neutralization of | 5 |
isolation and characterization of | 5 |
ml of growth medium | 5 |
the hybridoma cell line | 5 |
i and in naturally | 5 |
of the spike glycoprotein | 5 |
feline coronavirus types i | 5 |
the coronavirus spike protein | 5 |
on the s protein | 5 |
among cats in multiple | 5 |
the mrna for the | 5 |
manipulate the feline coronavirus | 5 |
it has been proposed | 5 |
and type ii fipv | 5 |
histopathologically verified feline infectious | 5 |
on the one hand | 5 |
of different biotypes feline | 5 |
involved in immune signaling | 5 |
it is unclear whether | 5 |
feline coronaviruses with small | 5 |
studies between feline infectious | 5 |
and replication of coronaviruses | 5 |
orf of feline coronavirus | 5 |
gene of porcine transmissible | 5 |
samples from healthy cats | 5 |
porcine transmissible gastroenteritis viruses | 5 |
peritonitis among cats in | 5 |
feline coronaviruses with peptidyl | 5 |
enhancement of infection of | 5 |
markedly different peplomer glycoproteins | 5 |
be attributed to the | 5 |
experimentally infected with the | 5 |
of type i and | 5 |
upper respiratory tract and | 5 |
entry of feline infectious | 5 |
epidemic of feline infectious | 5 |
pre post treatment group | 5 |
antigenically related group was | 5 |
was calculated using the | 5 |
cats with histopathologically verified | 5 |
receptor for type i | 5 |
way to manipulate the | 5 |
can be seen in | 5 |
both enteric infection and | 5 |
isolation and cdna preparation | 5 |
rna isolation and cdna | 5 |
different regions of the | 5 |
antibodies to the spike | 5 |
phylogenetic analysis of the | 5 |
mabs with neutralizing activity | 5 |
feline coronaviruses and the | 5 |
potent inhibition of feline | 5 |
protection studies between feline | 5 |
cells were maintained in | 5 |
coronavirus associated with an | 5 |
s s cleavage site | 5 |
containing fetal calf serum | 5 |
it was suggested that | 5 |
vaccine under experimental conditions | 5 |
antiviral treatment was started | 5 |
seroprevalence and association with | 5 |
compounds targeting coronavirus c | 5 |
the s gene of | 5 |
in the treatment of | 5 |
number of infected cells | 5 |
responses in cats immunized | 5 |
feline enteric coronavirus infections | 5 |
molecular weights of the | 5 |
macrophages by neutralizing monoclonal | 5 |
with endemic feline enteric | 5 |
mrna expression level was | 5 |
it is difficult to | 5 |
peritonitis virus regulates pro | 5 |
may be important in | 5 |
cells were inoculated with | 5 |
have not yet been | 5 |
c t values of | 5 |
type i and in | 5 |
human and animal coronaviruses | 5 |
were kindly provided by | 5 |
coronavirus infections in kittens | 5 |
monoclonal antibodies recognizing different | 5 |
coronavirus types i and | 5 |
between fecvs and fipvs | 5 |
of infection of feline | 5 |
loads despite absence of | 5 |
in pbmcs from fip | 5 |
as shown in table | 5 |
estimating fifty percent endpoints | 5 |
the plasma membrane of | 5 |
using feline infectious peritonitis | 5 |
virus in tissue culture | 5 |
p mapk pathway is | 5 |
with small deletions in | 5 |
in well culture chamber | 5 |
structural and functional characterization | 5 |
has also been reported | 5 |
min at room temperature | 5 |
with an avirulent feline | 5 |
infect and replicate in | 5 |
the a orf of | 5 |
cornell university college of | 5 |
the detection limit of | 5 |
were pretreated with dmso | 5 |
were used for the | 5 |
genome of porcine coronavirus | 5 |
have been described for | 5 |
treatment of cats with | 5 |
and porcine transmissible gastroenteritis | 5 |
inhibition of feline coronaviruses | 5 |
effective way to manipulate | 5 |
enhancement of human immunodeficiency | 5 |
from the four related | 5 |
by neutralizing monoclonal antibodies | 5 |
effusive form of fip | 5 |
high viral loads despite | 5 |
value to the mrna | 5 |
these factors act on | 5 |
cases of feline infectious | 5 |
porcine coronavirus tgev reveals | 5 |
feline infectious peritonitis by | 5 |
with disease in switzerland | 5 |
recovery and characterization of | 5 |
and feline enteric coronaviruses | 5 |
mrna pcr for the | 5 |
of fecvs and fipvs | 5 |
infectious peritonitis virus regulates | 5 |
regions of the s | 5 |
infectious peritonitis detection of | 5 |
infectious peritonitis attempted immunization | 5 |
c protein of feline | 5 |
is thought to be | 5 |
neutralization of feline infectious | 5 |
from spf and fip | 5 |
crfk cells and in | 5 |
splenocytes derived from wild | 5 |
i virus fusion protein | 5 |
absence of clinical and | 5 |
the center for companion | 5 |
feline infectious peritonitis detection | 5 |
a feline infectious peritonitis | 5 |
is likely to be | 5 |
m a b s | 5 |
but not in the | 5 |
cells which were pretreated | 5 |
cats naturally infected with | 5 |
cats immunized with an | 5 |
functional characterization of the | 5 |
the growth curves of | 5 |
culture supernatants were collected | 5 |
were found to be | 5 |
feline macrophages by neutralizing | 5 |
vaccines through the directed | 5 |
in cats inoculated with | 5 |
production in primary blood | 5 |
from military dogs with | 5 |
the structural proteins of | 5 |
with or without fipv | 5 |
of neutrophil survival factors | 5 |
cats with naturally occurring | 5 |
infection in crfk cells | 5 |
the ability of the | 5 |
against the replication of | 5 |
with the genome of | 5 |
association with disease in | 5 |
dmso for h before | 5 |
with that of the | 5 |
the serotype i fcov | 5 |
and hemagglutinating encephalomyelitis virus | 5 |
characteristics of persistent feline | 5 |
of the immune system | 5 |
a class i virus | 5 |
fluids of naturally infected | 5 |
in the serum of | 5 |
at x g for | 5 |
the n protein of | 5 |
with both enteric infection | 5 |
of clinical and pathological | 5 |
of the c gene | 5 |
viral rna was isolated | 5 |
with histopathologically verified feline | 5 |
shedding of feline coronavirus | 5 |
cat environments with endemic | 5 |
for companion animal health | 5 |
growth in autochthonous peritoneal | 5 |
feline alveolar macrophages and | 5 |
enteric infection and feline | 5 |
porcine and canine coronaviruses | 5 |
to the s protein | 5 |
coronavirus tgev reveals large | 5 |
to the lack of | 5 |
endemic feline enteric coronavirus | 5 |
infectious peritonitis two related | 5 |
a possible involvement of | 5 |
the replication of fipv | 5 |
for h in the | 5 |
feline infectious peritonitis attempted | 5 |
of cells were positive | 5 |
feline immunodeficiency virus infection | 5 |
of the disease and | 5 |
genes provide protection against | 5 |
and neutralization of feline | 5 |
a mrna pcr for | 5 |
was subcutaneously administered every | 4 |
a modified live fipv | 4 |
infection and syncytium formation | 4 |
of the viral rna | 4 |
df at an moi | 4 |
was amplified by pcr | 4 |
that the p mapk | 4 |
infectious peritonitis in specific | 4 |
of the type i | 4 |
standard error of the | 4 |
type ii viruses are | 4 |
the s subunit of | 4 |
changes in the spike | 4 |
target cells of fipv | 4 |
western blot with the | 4 |
a tenfold virus dilution | 4 |
placed in each well | 4 |
head of bacteriophage t | 4 |
the feces of a | 4 |
the molecular weights of | 4 |
of granulomatous vasculitis in | 4 |
overnight at room temperature | 4 |
fcov c je genome | 4 |
by the indirect fluorescent | 4 |
culture supernatant was measured | 4 |
peritonitis detection of feline | 4 |
coronavirus vaccines through the | 4 |
antigen was significantly higher | 4 |
to mouse hepatitis virus | 4 |
pre post treatment and | 4 |
novel tool for the | 4 |
rnas of the feline | 4 |
the strips were then | 4 |
the molecular pathogenesis of | 4 |
ade of virus infectivity | 4 |
the nine structural and | 4 |
discriminate between fipv strain | 4 |
strips and incubated at | 4 |
veterinary medical teaching hospitals | 4 |
in absolute acetone after | 4 |
a type i feline | 4 |
have been associated with | 4 |
depletion during feline infectious | 4 |
from the feces of | 4 |
the efficiency of the | 4 |
has been demonstrated to | 4 |
is released into the | 4 |
induces vascular permeability and | 4 |
after experimental infection with | 4 |
monocytes from cats with | 4 |
ii feline infectious peritonitis | 4 |
the presence of fcov | 4 |
and effusion in cats | 4 |
in the level of | 4 |
the effect of chloroquine | 4 |
mabs which discriminate between | 4 |
permeability and effusion in | 4 |
i and ii of | 4 |
of the recombinant rna | 4 |
pfbm cells is regulated | 4 |
objective of this study | 4 |
t values of the | 4 |
serotype i fcov strain | 4 |
antigenic analysis of feline | 4 |
of cq and hcq | 4 |
in macrophages inoculated with | 4 |
at h post inoculation | 4 |
epidemiology of feline infectious | 4 |
for peer review of | 4 |
fipv arises from fecv | 4 |
and the development of | 4 |
the supernatant was removed | 4 |
in an epizootic outbreak | 4 |
of the spike protein | 4 |
a wide variety of | 4 |
of infected cells was | 4 |
effect of feline interferon | 4 |
rna sequence of feline | 4 |
blood samples from healthy | 4 |
the cats were housed | 4 |
encoding the peplomer protein | 4 |
the ec value of | 4 |
infectious peritonitis virus a | 4 |
h in the presence | 4 |
against type i fipv | 4 |
method of estimating fifty | 4 |
in cells infected with | 4 |
the highest dilution of | 4 |
indirect fluorescent antibody technique | 4 |
dry form of fip | 4 |
porcine coronavirus transmissible gastroenteritis | 4 |
cats passively immunized with | 4 |
had been experimentally infected | 4 |
a temperature sensitive feline | 4 |
the supernatant was collected | 4 |
referred to as feline | 4 |
i p v to | 4 |
for weeks or months | 4 |
the purpose of this | 4 |
fipv vaccine under experimental | 4 |
to the presence of | 4 |
reverse genetic analysis of | 4 |
with fipv type ii | 4 |
glycoprotein of murine coronavirus | 4 |
novel type ii feline | 4 |
in crandell feline kidney | 4 |
feline coronaviruses with monoclonal | 4 |
sequence of a field | 4 |
in tissue culture and | 4 |
care and use committee | 4 |
type ii feline coronaviruses | 4 |
viral proteins in the | 4 |
attenuated coronavirus vaccines through | 4 |
ability to infect macrophages | 4 |
proteolytic cleavage of the | 4 |
been experimentally infected with | 4 |
coronavirus from military dogs | 4 |
the amino acid sequences | 4 |
at veterinary medical teaching | 4 |
slides were fixed in | 4 |
overview of feline enteric | 4 |
protein derived from the | 4 |
amino acid sequences are | 4 |
feline infectious peritonitis a | 4 |
peritonitis pathogenesis of feline | 4 |
the envelope protein of | 4 |
of cells infected with | 4 |
using the following formula | 4 |
the od in the | 4 |
and evidence for the | 4 |
v a q k | 4 |
the role of orf | 4 |
and expression of the | 4 |
as the reciprocal of | 4 |
differs from transmissible gastroenteritis | 4 |
viral replication in the | 4 |
minimum essential medium containing | 4 |
lesions in the small | 4 |
dengue hemorrhagic fever pathogenesis | 4 |
sensitive feline infectious peritonitis | 4 |
end of the canine | 4 |
was placed in each | 4 |
cell differentiation survival factor | 4 |
cytokine patterns in association | 4 |
fmhv in the presence | 4 |
of human coronavirus e | 4 |
of the canine and | 4 |
added to the culture | 4 |
in addition to the | 4 |
calculated using the following | 4 |
by hohdatsu et al | 4 |
as demonstrated by immunoblotting | 4 |
the medium was removed | 4 |
of the circular tfo | 4 |
contribute to the pathogenesis | 4 |
any of the other | 4 |
of viral rna in | 4 |
genes that were sequenced | 4 |
arises from fecv by | 4 |
not neutralize the fipv | 4 |
of the serotype ii | 4 |
the pathogenesis of fipv | 4 |
the identical serotype virus | 4 |
is known as feline | 4 |
on the day of | 4 |
enterotropic mouse hepatitis virus | 4 |
with either sb or | 4 |
viral mrna expression level | 4 |
cell depletion during feline | 4 |
was then added to | 4 |
was quantified by anti | 4 |
a simple method of | 4 |
feline coronavirus strains in | 4 |
the immune complex pathogenesis | 4 |
animal care and use | 4 |
by monoclonal antibodies enhancement | 4 |
from the jejunum of | 4 |
for the s protein | 4 |
to the development of | 4 |
to the culture and | 4 |
were added to the | 4 |
to the normal state | 4 |
the reason for the | 4 |
of differentially expressed genes | 4 |
blot with the anti | 4 |
evidence for the immune | 4 |
feline infectious peritonitis using | 4 |
more likely to be | 4 |
treatment was started at | 4 |
in cats with feline | 4 |
room temperature for h | 4 |
th tc epitopes in | 4 |
the number of infected | 4 |
inoculated intraperitoneally with a | 4 |
to a final concentration | 4 |
reverse transcriptase polymerase chain | 4 |
causes feline infectious peritonitis | 4 |
washed twice with pbs | 4 |
complex pathogenesis of feline | 4 |
to feline alveolar macrophages | 4 |
genetics and pathogenesis of | 4 |
studies are needed to | 4 |
prevalence of korean cats | 4 |
preparation of mabs which | 4 |
as well as for | 4 |
amino acid differences in | 4 |
differentiation into plasma cells | 4 |
the biology and pathogenesis | 4 |
were maintained in a | 4 |
subcutaneously administered every days | 4 |
of the fecv genome | 4 |
cats were inoculated intraperitoneally | 4 |
inoculated at an moi | 4 |
amplified by pcr using | 4 |
the presence of scfv | 4 |
were collected from fip | 4 |
cell activation in cats | 4 |
coronavirus strains in an | 4 |
n genes were quantitatively | 4 |
in the majority of | 4 |
presence of gc or | 4 |
natural feline coronavirus infection | 4 |
in each well of | 4 |
cells were incubated for | 4 |
infectious peritonitis virus isolates | 4 |
the laboratory strain fcov | 4 |
presence of scfv f | 4 |
reciprocal of the highest | 4 |
national institutes of health | 4 |
involved in the pathogenesis | 4 |
can be detected in | 4 |
peritoneal and pleural effusions | 4 |
cells were stained with | 4 |
for viral replication in | 4 |
and the supernatant was | 4 |
in an atmosphere of | 4 |
cultured with medium alone | 4 |
of the porcine transmissible | 4 |
the peplomer protein e | 4 |
infected pfbm cells is | 4 |
some important disorders of | 4 |
genome organization and reverse | 4 |
with natural feline coronavirus | 4 |
remains to be elucidated | 4 |
cdna was amplified by | 4 |
prevalence of feline infectious | 4 |
culture and adsorbed to | 4 |
which discriminate between fipv | 4 |
were used to design | 4 |
detected in the feces | 4 |
is able to detect | 4 |
pbmcs from fip diagnosed | 4 |
incubated at c for | 4 |
a cat with a | 4 |
all of the cats | 4 |
is one of the | 4 |
live fipv vaccine under | 4 |
differences in cytokine patterns | 4 |
in a mouse model | 4 |
ii and fecv type | 4 |
cleavage of structural proteins | 4 |
the fipv and fecv | 4 |
production of progeny virus | 4 |
very closely related to | 4 |
differentiation survival factor production | 4 |
the reaction was stopped | 4 |
and c for min | 4 |
the igg a mabs | 4 |
porcine respiratory coronavirus differs | 4 |
the survival time and | 4 |
expression level of the | 4 |
nine structural and accessory | 4 |
used in the study | 4 |
length cdna copy of | 4 |
genomic organization and expression | 4 |
the fipv type i | 4 |
cats with natural feline | 4 |
peritonitis in purebred catteries | 4 |
cats with experimental feline | 4 |
the presence of virus | 4 |
was performed using a | 4 |
growth in cell culture | 4 |
the presence of fmhv | 4 |
in as few as | 4 |
to the pathogenesis of | 4 |
enhancement of dengue virus | 4 |
survival rate of neutrophils | 4 |
act on neutrophils and | 4 |
that susceptibility to fip | 4 |
feline infectious peritonitis after | 4 |
naturally and experimentally infected | 4 |
study has shown that | 4 |
of the e gene | 4 |
is responsible for the | 4 |
in order to determine | 4 |
the genomic rna sequence | 4 |
the type ii fipv | 4 |
guidelines on prevention and | 4 |
at the same time | 4 |
of the head of | 4 |
of the fcov genome | 4 |
infectious peritonitis virus contribute | 4 |
genes were quantitatively analyzed | 4 |
may be responsible for | 4 |
as well as in | 4 |
a total volume of | 4 |
in the b gene | 4 |
the authors concluded that | 4 |
macrophages and virulence in | 4 |
an intact orf c | 4 |
cells is regulated by | 4 |
the porcine coronavirus transmissible | 4 |
the susceptibility of the | 4 |
the winn feline foundation | 4 |
omega on the survival | 4 |
infection with the identical | 4 |
pellets were resuspended in | 4 |
virus infection in crfk | 4 |
antigenic sites of the | 4 |
antibodies enhancement and neutralization | 4 |
from healthy cats and | 4 |
was supported by the | 4 |
granulomatous vasculitis in feline | 4 |
the spike proteins of | 4 |
and these factors act | 4 |
feline infectious peritonitis experimental | 4 |
in association with the | 4 |
of feline c and | 4 |
the size of the | 4 |
the porcine transmissible gastroenteritis | 4 |
by a few genomic | 4 |
the fecv and fipv | 4 |
levels of ltb and | 4 |
in monocytes macrophages and | 4 |
in peripheral blood mononuclear | 4 |
in monocytes from cats | 4 |
cells were positive when | 4 |
organization and expression of | 4 |
in a total volume | 4 |
of korean cats with | 4 |
of the mabs was | 4 |
of the porcine coronavirus | 4 |
of the highest dilution | 4 |
of the domestic cat | 4 |
coronavirus differs from transmissible | 4 |
all mabs in group | 4 |
was carried out by | 4 |
and adsorbed to the | 4 |
the cells were stained | 4 |
of fip in cats | 4 |
a v k q | 4 |
a novel type ii | 4 |
the fecv b protein | 4 |
coronavirus in multicat environments | 4 |
to the mrna of | 4 |
by western blot with | 4 |
c for min and | 4 |
identical serotype virus in | 4 |
in the fipv antigenic | 4 |
the canine and feline | 4 |
experimental infection with fipv | 4 |
disease of the felidae | 4 |
type ii and fecv | 4 |
by a number of | 4 |
the fipv b protein | 4 |
in this study are | 4 |
virus replication in macrophages | 4 |
with either one of | 4 |
of a virus in | 4 |
the open reading frames | 4 |
challenge with virulent fipv | 4 |
response to experimental feline | 4 |
possible involvement of tnf | 4 |
virus feline infectious peritonitis | 4 |
strains in an epizootic | 4 |
b and prostaglandin e | 4 |
and characterization of feline | 4 |
lower part of the | 4 |
of feline coronavirus strains | 4 |
the central nervous system | 4 |
of the murine coronavirus | 4 |
cdna cloning and sequence | 4 |
in cytokine patterns in | 4 |
to that of fipv | 4 |
in the cell culture | 4 |
the detection of feline | 4 |
and development of granulomatous | 4 |
mrna of the housekeeping | 4 |
c and evidence for | 4 |
gene encoding the peplomer | 4 |
s protein of fipv | 4 |
epizootic outbreak of feline | 4 |
effusive form of the | 4 |
has been proposed that | 4 |
surface of infected cells | 4 |
the surface of infected | 4 |
did not neutralize the | 4 |
the virus in the | 4 |
infectious peritonitis virus isolate | 4 |
modified live fipv vaccine | 4 |
the cells were then | 4 |
cats inoculated with feline | 4 |
of structural proteins during | 4 |
glycoprotein of feline infectious | 4 |
cells has not been | 4 |
feline c and evidence | 4 |
was used as the | 4 |
middle east respiratory syndrome | 4 |
of murine hepatitis virus | 4 |
as well as from | 4 |
effect of chloroquine on | 4 |
region of the s | 4 |
canine and feline enteric | 4 |
x for peer review | 4 |
an epizootic outbreak of | 4 |
production was quantified by | 4 |
enteric coronavirus and infectious | 4 |
did not react with | 4 |
the in vivo efficacy | 4 |
infectious peritonitis pathogenesis of | 4 |
respiratory coronavirus differs from | 4 |
profiling of feline infectious | 4 |
plasma levels of ltb | 4 |
epithelial cells of the | 4 |
and cells were collected | 4 |
in the s domain | 4 |
transcriptional profiling of feline | 4 |
sequence of feline coronavirus | 4 |
enhancement of dengue viruses | 4 |
analysis of a type | 4 |
of a tenfold virus | 4 |
the objective of this | 4 |
tumor necrosis factor alpha | 4 |
neutralize the fipv type | 4 |
assembly of the head | 4 |
peritonitis virus mediate antibody | 4 |
reverse genetics approach to | 4 |
temperature sensitive feline infectious | 4 |
natural feline coronavirus infections | 4 |
to the method of | 4 |
vivo cytokine response to | 4 |
that the s protein | 4 |
of the s domain | 4 |
myosin light chain kinase | 4 |
of orf a and | 4 |
of a novel type | 4 |
the target cells of | 4 |
coronavirus and infectious peritonitis | 4 |
treatment and post treatment | 4 |
of the housekeeping gene | 4 |
the region of the | 4 |
did not show any | 4 |
the lower part of | 4 |
with the identical serotype | 4 |
gc at mg kg | 4 |
peritonitis virus infection of | 4 |
hemorrhagic fever pathogenesis of | 4 |
hepatitis virus strain a | 4 |
cytokine response to experimental | 4 |
antiviral effects of hcq | 4 |
feline leukemia virus infection | 4 |
the s gene and | 4 |
the active site of | 4 |
virus immunologic phenomena in | 4 |
end of the feline | 4 |
dependent enhancement of human | 4 |
amino acid sequences of | 4 |
it was concluded that | 4 |
fever pathogenesis of feline | 4 |
of virulent virus experimental | 4 |
at the present time | 4 |
structure and genome expression | 4 |
the fip disease process | 4 |
coronavirus related to transmissible | 4 |
site downstream of the | 4 |
the genes that were | 4 |
pbs containing fetal calf | 4 |
susceptibility of the cheetah | 4 |
e glycoprotein of murine | 4 |
at g for min | 4 |
immune complex pathogenesis of | 4 |
as feline enteric coronavirus | 4 |
the assembly of the | 4 |
features and development of | 4 |
of mice infected with | 4 |
acid changes in the | 4 |
the plasma hcq level | 4 |
added to the cells | 4 |
the outcome of infection | 4 |
and experimentally infected cats | 4 |
of feline coronavirus by | 4 |
for the immune complex | 4 |
simple method of estimating | 4 |
abcd guidelines on prevention | 4 |
to be associated with | 4 |
of the laboratory strain | 4 |
observed in cats with | 4 |
the mrna of the | 4 |
virus in cats with | 4 |
rna sequence of a | 4 |
in vitro growth of | 4 |
i fcov strain black | 4 |
and reverse genetic analysis | 4 |
monocytes inoculated with a | 4 |
the reciprocal of the | 4 |
autochthonous peritoneal cell cultures | 4 |
and ml of growth | 4 |
was determined by the | 4 |
incidence of fip in | 4 |
g for minutes at | 4 |
was based on the | 4 |
in vivo cytokine response | 4 |
the method of reed | 4 |
rna sequence of fcov | 4 |
in the face of | 4 |
of mabs which discriminate | 4 |
morphologic features and development | 4 |
the small intestine of | 4 |
feline infectious peritonitis date | 4 |
peritonitis virus contribute to | 4 |
the jejunum of a | 4 |
type ii fipv strain | 4 |
is believed to be | 4 |
on prevention and management | 4 |
qpcr c t values | 4 |
association with the outcome | 4 |
in macrophages from all | 4 |
virus experimental studies with | 4 |
virulent virus experimental studies | 4 |
of the s s | 4 |
cats with passive immunization | 4 |
extraperitoneal lesions in feline | 4 |
a difference in the | 4 |
type i fipv ku | 4 |
the infected cells were | 4 |
development of granulomatous vasculitis | 4 |
gastroenteritis virus by a | 4 |
on the survival time | 4 |
effusion in cats with | 4 |
screening and identification of | 4 |
are located in the | 4 |
in vitro have been | 4 |
the nucleoside analog gs | 4 |
organization and reverse genetic | 4 |
analysis of the gene | 4 |
to inhibit fipv replication | 4 |
feline infectious peritonitis pathogenesis | 4 |
which is involved in | 4 |
fipv infected crfk cells | 4 |
fipv and fecv isolates | 4 |
in the form of | 4 |
melting points of the | 4 |
macrophages in cats infected | 4 |
blood samples were collected | 4 |
sequence of fcov c | 4 |
apoptosis during fipv infection | 4 |
of hcq in cats | 4 |
at am and pm | 4 |
a virus in cats | 4 |
and the pathogenesis of | 4 |
amino acid sequence and | 4 |
strips were then washed | 4 |
feline infectious peritonitis natural | 4 |
cdna copy of the | 4 |
it is important to | 4 |
and quantitation of fcov | 4 |
immune system of the | 4 |
korean cats with natural | 4 |
vasculitis in feline infectious | 4 |
causes a fatal disease | 4 |
by the fact that | 4 |
pathogenesis of granulomatous lesions | 4 |
type i feline coronaviruses | 4 |
patterns in association with | 4 |
according to the method | 4 |
leukotriene b and prostaglandin | 4 |
levels and body temperature | 4 |
in the molecular weights | 4 |
genome copies of fcov | 4 |
the presence of gc | 4 |
in the gastrointestinal tract | 4 |
established at cornell university | 4 |
passively immunized with anti | 4 |
am and pm for | 4 |
plays an important role | 4 |
in specific pathogen free | 4 |
morphogenesis of a virus | 4 |
genetic analysis of a | 4 |
replication of coronaviruses the | 4 |
the case of the | 4 |
of a temperature sensitive | 4 |
s subunit of the | 4 |
the culture and adsorbed | 4 |
virus contribute to the | 4 |
the circulating virulent avirulent | 4 |
infectious peritonitis in purebred | 4 |
cleavage of the e | 4 |
with dmso alone showed | 4 |
in monocytes and macrophages | 4 |
the only gene that | 4 |
which is able to | 4 |
faculty of veterinary medicine | 4 |
in cats with experimental | 4 |
may be due to | 4 |
was shown to be | 4 |
feline coronavirus in multicat | 4 |
we investigated whether hcq | 4 |
are involved in the | 4 |
it can be concluded | 4 |
coronaviruses with monoclonal antibodies | 4 |
as described by the | 4 |
or a mixture of | 4 |
in the gut but | 4 |
the pathogenesis of granulomatous | 4 |
of virulent virus immunologic | 4 |
of the mechanism of | 4 |
was not detected in | 4 |
for the pathogenesis of | 4 |
route of fipv infection | 4 |
the s protein and | 4 |
characterization of feline c | 4 |
a few genomic deletions | 4 |
were detected in the | 4 |
a coronavirus from military | 4 |
the head of bacteriophage | 4 |
proteins abc and ab | 4 |
total volume of ml | 4 |
for the biotype switch | 4 |
detection limit of the | 4 |
in autochthonous peritoneal cell | 4 |
cats and cats with | 4 |
canine and porcine coronaviruses | 4 |
fipv antigen was significantly | 4 |
common for all cats | 4 |
supernatant was removed and | 4 |
dependent enhancement of infection | 4 |
that fipv arises from | 4 |
also found to be | 4 |
virus by a few | 4 |
feline coronavirus infection the | 4 |
vascular permeability and effusion | 4 |
deleterious c gene mutations | 4 |
to the plasma membrane | 4 |
post treatment and post | 4 |
to per cent of | 4 |
the fipv spike protein | 4 |
at mg kg dose | 4 |
virus replication in the | 4 |
centrifuged at x g | 4 |
the nature of the | 4 |
simple method for estimating | 3 |
is critical for the | 3 |
as described above and | 3 |
the purdue strain of | 3 |
of different biotypes a | 3 |
the antiviral effect of | 3 |
significantly higher viral loads | 3 |
with fip than in | 3 |
cats with clinical feline | 3 |
differential role for low | 3 |
the authors declare no | 3 |
peritonitis virus and feline | 3 |
crfk cells were infected | 3 |
s protein of a | 3 |
it is tempting to | 3 |
infected crfk cells and | 3 |
for animal experiments of | 3 |
and stained with crystal | 3 |
of recombinant vaccinia viruses | 3 |
in monocytes inoculated with | 3 |
of a calf diarrheal | 3 |
the vesicular stomatitis virus | 3 |
part of the s | 3 |
dmso alone showed significant | 3 |
for measurement of the | 3 |
the action of csa | 3 |
display accelerated viral growth | 3 |
between transmissible gastroenteritis virus | 3 |
fipv and type ii | 3 |
in severe acute respiratory | 3 |
of crandell rees feline | 3 |
amplification of cdna ends | 3 |
i fipvs in fcwf | 3 |
results indicate the applicability | 3 |
monoclonal antibodies in antibody | 3 |
of the same cat | 3 |
purdue strain of tgev | 3 |
collected and analyzed by | 3 |
fipv peplomer protein induces | 3 |
there is also a | 3 |
as a member of | 3 |
the structure and replication | 3 |
to hr after heat | 3 |
aminopeptidase n as a | 3 |
pcr products were sequenced | 3 |
produced maximum fluorescence by | 3 |
amino acid sequence identity | 3 |
in the envelope protein | 3 |
atpase phospholipid transporting b | 3 |
be used for the | 3 |
cells in the presence | 3 |
infected with the virus | 3 |
with the development of | 3 |
fluctuations in kittens with | 3 |
safety and efficacy of | 3 |
viral rna genome copy | 3 |
circulating virulent avirulent theory | 3 |
cells for a prolonged | 3 |
that fipv can employ | 3 |
in a previous study | 3 |
the effects of the | 3 |
would like to thank | 3 |
to members of the | 3 |
positive correlation was found | 3 |
of fipv and fmhv | 3 |
taken up by the | 3 |
cancer cells expressing the | 3 |
than that of fipv | 3 |
selected for this study | 3 |
fipv and fecv can | 3 |
it is interesting to | 3 |
pcr assay to detect | 3 |
results suggest that fipv | 3 |
hr after heat shock | 3 |
was detected in the | 3 |
culture supernatants and cells | 3 |
of gc and npi | 3 |
by indirect fluorescent antibody | 3 |
and weeks of age | 3 |
p and p were | 3 |
is located in the | 3 |
curves of fipv and | 3 |
months of age were | 3 |
to further investigate the | 3 |
virus isolated from the | 3 |
just upstream of the | 3 |
of e in rm | 3 |
immune response of the | 3 |
which is caused by | 3 |
subclass of mouse monoclonal | 3 |
atmosphere of co in | 3 |
and u ml of | 3 |
in the same manner | 3 |
treatment group than in | 3 |
protein genes of feline | 3 |
cats with experimentally induced | 3 |
post mortem from the | 3 |
acid sequence identity of | 3 |
for the improved diagnosis | 3 |
ii fipv replication was | 3 |
coronaviruses acquisition of macrophage | 3 |
and immunopathogenesis a review | 3 |
of fip in cheetahs | 3 |
appears to be the | 3 |
activate the p mapk | 3 |
mabs in group iv | 3 |
the same field strain | 3 |
have been detected in | 3 |
associated with the fecv | 3 |
antigenic comparison of feline | 3 |
human cancer cells expressing | 3 |
a and orf b | 3 |
of serotype i fipv | 3 |
i feline infectious peritonitis | 3 |
and their sources are | 3 |
structure and replication of | 3 |
protein a of feline | 3 |
upregulated genes common for | 3 |
cats with cutaneous viral | 3 |
is regulated by p | 3 |
the hr and hr | 3 |
involved in cell cycle | 3 |
that fipv and fecv | 3 |
was quantified under appropriate | 3 |
from rectal swab samples | 3 |
approach to study feline | 3 |
anti cv hyperimmune serum | 3 |
transmissible gastroenteritis in pigs | 3 |
to be involved in | 3 |
entry of feline coronaviruses | 3 |
pbmcs from fip cats | 3 |
or absence of the | 3 |
in cats with passive | 3 |
to evaluate and assess | 3 |
for fipv replication in | 3 |
glycosylation of the severe | 3 |
genome organisation and predictions | 3 |
that fipv infection is | 3 |
in the infected cells | 3 |
of the gastrointestinal tract | 3 |
of fipv black virus | 3 |
nucleocapsid protein of feline | 3 |
study was to determine | 3 |
s and s domains | 3 |
stained with crystal violet | 3 |
were inoculated at an | 3 |
for type i and | 3 |
were used in this | 3 |
viability was calculated using | 3 |
characteristics of a coronavirus | 3 |
supernatants and cells were | 3 |
untreated cells was below | 3 |
of blood samples from | 3 |
of fipv or fmhv | 3 |
described by the manufacturer | 3 |
groups were analyzed by | 3 |
recombinant coronavirus spike proteins | 3 |
of respiratory syncytial virus | 3 |
of cats infected with | 3 |
type i fipv and | 3 |
of the e protein | 3 |
sequence and phylogenetic analysis | 3 |
in the replication of | 3 |
interferon on feline infectious | 3 |
of vesicular stomatitis virus | 3 |
the basis of this | 3 |
these data indicate that | 3 |
replication of the virus | 3 |
classified as fipv type | 3 |
for s and c | 3 |
tgev reveals large insertions | 3 |
virus titers in the | 3 |
downregulated in all macrophages | 3 |
the mixtures were incubated | 3 |
feline infectious peritonitis morphologic | 3 |
which is equivalent with | 3 |
on beamline bl u | 3 |
in purebred catteries risk | 3 |
that orf b is | 3 |
inhibits feline infectious peritonitis | 3 |
fipv interstructural gene region | 3 |
performed as described above | 3 |
differences in virus receptor | 3 |
cells derived from the | 3 |
were used as the | 3 |
by the neutralization test | 3 |
sequence of the fipv | 3 |
s and s pockets | 3 |
been the subject of | 3 |
no conflict of interest | 3 |
inducing factors have not | 3 |
a d e of | 3 |
a reverse genetics system | 3 |
of the fipv ku | 3 |
with fipv or fecv | 3 |
coronaviruses and the circulating | 3 |
appear to be very | 3 |
region of the m | 3 |
of t helper and | 3 |
fip is associated with | 3 |
were analyzed using a | 3 |
evaluate and assess the | 3 |
tissue culture infectious dose | 3 |
the c t values | 3 |
infection in the cheetah | 3 |
from the ascites and | 3 |
virion polypeptide specificity of | 3 |
isolation of a porcine | 3 |
pretreated with hcq or | 3 |
weaker than that of | 3 |
virus infection of feline | 3 |
presence of fcov in | 3 |
from the surface of | 3 |
which are known to | 3 |
we showed that virus | 3 |
leucine zipper transcriptional factor | 3 |
a positive correlation was | 3 |
feline coronavirus by healthy | 3 |
of this study also | 3 |
found between ltb plasma | 3 |
protein in infected cells | 3 |
the membrane and nucleocapsid | 3 |
are known to be | 3 |
fatal disease of cats | 3 |
succumbed with feline infectious | 3 |
c je genomic rna | 3 |
detected in the cells | 3 |
macrophages were obtained from | 3 |
genetic susceptibility to feline | 3 |
in the hr region | 3 |
feline enteric coronaviruses feline | 3 |
monoclonal antibodies enhancement and | 3 |
but the exact mutation | 3 |
on of the infected | 3 |
in cats with cutaneous | 3 |
gc or npi were | 3 |
mutation of neutralizing antibody | 3 |
water and stored at | 3 |
supernatant of cells pretreated | 3 |
a ml reaction containing | 3 |
it has been demonstrated | 3 |
peritonitis natural fcov infection | 3 |
fip than in spf | 3 |
the virology and pathogenesis | 3 |
with fipv strain wsu | 3 |
of the membrane and | 3 |
from the fipv ku | 3 |
of fipv significantly decreased | 3 |
pharmacokinetic data on chloroquine | 3 |
strongly inhibits feline infectious | 3 |
at post mortem from | 3 |
dengue strains by monoclonal | 3 |
in this group are | 3 |
suppressed the replication of | 3 |
biology and pathogenesis of | 3 |
were found in the | 3 |
and immunostained for the | 3 |
were pretreated with either | 3 |
predictions made for the | 3 |
antibodies in cats inoculated | 3 |
for low ph and | 3 |
on the susceptibility of | 3 |
inoculate feline alveolar macrophages | 3 |
i and ii fipvs | 3 |
mixture was then inoculated | 3 |
proposed that fipv arises | 3 |
characterization of type i | 3 |
that most e was | 3 |
the fipv antigenic group | 3 |
in conferring resistance to | 3 |
cells were lysed in | 3 |
compared to those in | 3 |
ii feline coronavirus in | 3 |
washed with hbss and | 3 |
induces cell fusion and | 3 |
for min and the | 3 |
a coronavirus from laboratoryinduced | 3 |
most e was retained | 3 |
that encode type ii | 3 |
fcov c je genomic | 3 |
clinical signs of fip | 3 |
studies on transmissible gastroenteritis | 3 |
both biotypes of type | 3 |
a simple method for | 3 |
cent fcs in well | 3 |
restoration of orf c | 3 |
of type i fipvs | 3 |
cleavage of the viral | 3 |
pathogenesis of fip and | 3 |
biotypes a study on | 3 |
is divided into two | 3 |
accessory protein a of | 3 |
feline coronaviruses in vitro | 3 |
from cats succumbed with | 3 |
each other and to | 3 |
end of the leader | 3 |
of fecv type ii | 3 |
collected from fip cats | 3 |
the experiment using feline | 3 |
using a heparinized syringe | 3 |
when compared to the | 3 |
uv exposure by video | 3 |
the virus and to | 3 |
have no competing interests | 3 |
and altered receptor usage | 3 |
role of accessory proteins | 3 |
used to inoculate feline | 3 |
coronavirus by healthy cats | 3 |
blood samples from cats | 3 |
viral antigens on the | 3 |
performed according to the | 3 |
days before fipv inoculation | 3 |
of infected tissue culture | 3 |
during the assembly of | 3 |
clinical feline infectious peritonitis | 3 |
the basis of the | 3 |
in macrophages infected with | 3 |
isolates from the same | 3 |
feline leukemia virus and | 3 |
and nucleocapsid protein genes | 3 |
coronavirus characterization of a | 3 |
from laboratoryinduced cases of | 3 |
qiaamp viral rna mini | 3 |
type i fipv replication | 3 |
reaction for monitoring the | 3 |
removed and cells were | 3 |
from cat to cat | 3 |
for the development of | 3 |
and sequencing of the | 3 |
and elicits neutralizing antibodies | 3 |
of the assay was | 3 |
further studies are required | 3 |
has been suggested to | 3 |
used as a source | 3 |
peritonitis experimental studies with | 3 |
infected cells has not | 3 |
of the accessory gene | 3 |
the present study recognizes | 3 |
cells was below the | 3 |
polypeptide specificity of immune | 3 |
molecular characterization of type | 3 |
immune responses in cats | 3 |
of newborn pigs inoculated | 3 |
the three major structural | 3 |
with recombinant vaccinia virus | 3 |
applicability of the new | 3 |
the mechanism of ade | 3 |
the cellular entry of | 3 |
s gene and the | 3 |
to fipv and fecv | 3 |
not result in the | 3 |
the virus titers of | 3 |
of dengue strains by | 3 |
ade of virus infection | 3 |
peplomer protein e of | 3 |
identify epitopes that mediate | 3 |
were collected at the | 3 |
the effectiveness of the | 3 |
different biotypes feline coronavirus | 3 |
virus receptor for type | 3 |
is in contrast to | 3 |
peripheral blood monocytes feline | 3 |
the replication of viruses | 3 |
in wild and domestic | 3 |
and the potential for | 3 |
analysis of the accessory | 3 |
significantly decreased in the | 3 |
and were used for | 3 |
with hcq or rfifn | 3 |
the fipv peplomer gene | 3 |
determining the outcome of | 3 |
for min at r | 3 |
antivirals against c or | 3 |
may function as a | 3 |
that mediate immune infection | 3 |
the stained cells were | 3 |
than healthy infected cats | 3 |
cats succumbed with feline | 3 |
in minimal essential medium | 3 |
the cells h after | 3 |
of type ii viruses | 3 |
were identified in the | 3 |
the fcov n genes | 3 |
and identification of t | 3 |
fipv evolves from fecv | 3 |
pcr was performed using | 3 |
viral infections in free | 3 |
replication of fipv in | 3 |
these drugs strongly suppressed | 3 |
of infection enhancement of | 3 |
of infectious bronchitis virus | 3 |
particles in the feces | 3 |
l and baff mrna | 3 |
in viral rna and | 3 |
domestic and wild cats | 3 |
also been reported to | 3 |
of a virus suspension | 3 |
and assess the antiviral | 3 |
were antigenically unrelated to | 3 |
rapid amplification of cdna | 3 |
of cells pretreated with | 3 |
spectrum antivirals against c | 3 |
chimeric feline coronaviruses that | 3 |
the relationship between fipv | 3 |
herpes simplex virus type | 3 |
cells were collected after | 3 |
serotype i and serotype | 3 |
is considered to be | 3 |
strains of feline coronavirus | 3 |
expression of feline infectious | 3 |
of type ii fcov | 3 |
of fip can be | 3 |
i fipv and type | 3 |
reaction of blood samples | 3 |
test was used to | 3 |
infection with type i | 3 |
is the od in | 3 |
been implicated in the | 3 |
dependent enhancement of hiv | 3 |
fipv infection causes a | 3 |
fip exhibit significantly higher | 3 |
of the cells was | 3 |
every days from days | 3 |
closely related to fipv | 3 |
cats at the time | 3 |
serotypes of fipv significantly | 3 |
does not appear to | 3 |
that are involved in | 3 |
localization of antigenic sites | 3 |
antibodies in feline infectious | 3 |
whether hcq and rfifn | 3 |
cat with feline infectious | 3 |
accessory proteins in the | 3 |
fcov is classified into | 3 |
part of the viral | 3 |
the respiratory tract and | 3 |
moloney murine leukemia virus | 3 |
limit of the assay | 3 |
the structural proteins are | 3 |
fipv not causing fip | 3 |
a calf diarrheal coronavirus | 3 |
the ability of a | 3 |
to inoculate feline alveolar | 3 |
cytokine mrna levels were | 3 |
from untreated cells was | 3 |
viral replication in feline | 3 |
the paradox of feline | 3 |
in determining the outcome | 3 |
cats with fip than | 3 |
expressed fipv peplomer protein | 3 |
this is in contrast | 3 |
and the circulating virulent | 3 |
when cats passively immunized | 3 |
identification of t helper | 3 |
we investigated the expression | 3 |
in the crfk cells | 3 |
in fip incidence between | 3 |
could not be detected | 3 |
east respiratory syndrome coronavirus | 3 |
mouse monoclonal antibodies in | 3 |
protein induces cell fusion | 3 |
biotypes feline coronavirus type | 3 |
role for low ph | 3 |
in infected cells has | 3 |
normal state at hpi | 3 |
improved diagnosis of feline | 3 |
of the present study | 3 |
the activity of the | 3 |
of the two fcov | 3 |
at h after infection | 3 |
the immune system of | 3 |
virus and feline enteric | 3 |
relationship of f i | 3 |
virus and immunogenicity of | 3 |
had a titer of | 3 |
i genetic background display | 3 |
in order to evaluate | 3 |
cell fusion and elicits | 3 |
has not been investigated | 3 |
quantified under appropriate uv | 3 |
between and h post | 3 |
detected in as few | 3 |
organ samples of perished | 3 |
determine whether or not | 3 |
healthy spf cats of | 3 |
bl u of the | 3 |
purebred catteries risk factors | 3 |
of the center for | 3 |
type i fipv after | 3 |
in the detection of | 3 |
is independent of the | 3 |
alone showed significant production | 3 |
were present in the | 3 |
encode type ii spike | 3 |
significantly lower in the | 3 |
implications for virus assembly | 3 |
at months of age | 3 |
were fixed and stained | 3 |
pathological consequences of feline | 3 |
found in the feces | 3 |
were then washed times | 3 |
mutations in the c | 3 |
at the optimal temperature | 3 |
in a final volume | 3 |
enhancement occurs upon re | 3 |
dependent enhancement of viral | 3 |
spread throughout the body | 3 |
from p and p | 3 |
peritonitis in birman cats | 3 |
to those of the | 3 |
of accessory proteins in | 3 |
virus titers of both | 3 |
comparison of feline coronavirus | 3 |
there are presently no | 3 |
outcome of fipv infection | 3 |
of the cellular receptor | 3 |
and virulence in cats | 3 |
the feline coronaviruses in | 3 |
of the target cells | 3 |
cells were washed and | 3 |
of fip and the | 3 |
and the rna was | 3 |
can be concluded that | 3 |
a sublethal dose of | 3 |
cultivation of a coronavirus | 3 |
in the in vivo | 3 |
heterogeneity of infection enhancement | 3 |
s domain of fipv | 3 |
was measured by the | 3 |
ii spike protein on | 3 |
mean plasma levels of | 3 |
fusion and elicits neutralizing | 3 |
were maintained in rpmi | 3 |
ascites and the omentum | 3 |
on spike protein and | 3 |
had been treated with | 3 |
treated with chloroquine at | 3 |
i fipv after viral | 3 |
virulent virus immunologic phenomena | 3 |
of the role of | 3 |
drug concentrations were measured | 3 |
is tempting to speculate | 3 |
feline coronaviruses that encode | 3 |
the ratio of peripheral | 3 |
plates were incubated at | 3 |
days of antiviral treatment | 3 |
and predictions made for | 3 |
exposure by video densitometry | 3 |
secreting hybridoma cultures were | 3 |
terminal part of the | 3 |
vitro cultivation of a | 3 |
in an equal volume | 3 |
shanghai synchrotron radiation facility | 3 |
was first described by | 3 |
viral growth and altered | 3 |
been proposed that fipv | 3 |
incubated with or without | 3 |
to each other and | 3 |
the faculty of veterinary | 3 |
lethal systemic granulomatous disease | 3 |
mrna responses in pbmcs | 3 |
an atmosphere of co | 3 |
igg a mabs enhanced | 3 |
of recombinant coronavirus spike | 3 |
neutralizing antibodies in mice | 3 |