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
vesicular stomatitis virus	453
of vesicular stomatitis	147
the presence of	120
the cells were	87
recombinant vesicular stomatitis	70
as well as	64
in the presence	64
of influenza virus	63
of the viral	62
west nile virus	61
respiratory syndrome coronavirus	61
the absence of	60
for h at	56
at room temperature	55
severe acute respiratory	54
acute respiratory syndrome	54
in this study	54
the plasma membrane	47
as shown in	46
cells were washed	46
in the absence	45
of the vsv	45
for min at	45
the expression of	44
the surface of	44
of the virus	44
ebov gp pseudotyped	43
human immunodeficiency virus	43
herpes simplex virus	42
type i ifn	42
the replication of	42
antiviral activity of	42
in order to	42
cells infected with	40
vero e cells	40
were infected with	39
host protein synthesis	39
porcine reproductive and	38
the cell surface	38
middle east respiratory	38
and respiratory syndrome	38
due to the	38
reproductive and respiratory	38
data not shown	37
east respiratory syndrome	37
infected with vsv	36
at h post	36
associated with the	36
the g protein	35
congo hemorrhagic fever	35
surface of the	35
the number of	35
on the surface	35
the viral envelope	34
as described above	34
respiratory syndrome virus	34
the synthesis of	34
cells were infected	34
compared to the	32
the development of	32
and in vivo	32
a variety of	32
in infected cells	31
t cells were	31
hela cells were	31
the use of	31
in vitro and	31
as described in	31
in addition to	30
was added to	30
according to the	29
the antiviral activity	29
the golgi complex	29
the host cell	29
hemorrhagic fever virus	29
vesicular stomatitis viruses	28
to determine the	28
been shown to	28
the fact that	28
the vsv g	28
the ability of	28
structure of the	28
protein synthesis in	28
analysis of the	27
expression of the	27
were treated with	27
based on the	27
influenza a virus	27
the role of	27
activity of irf	27
inhibition of host	26
shown in figure	26
vitro and in	26
of protein synthesis	26
consistent with the	26
the production of	26
the translation of	26
and incubated at	25
wt and ifit	25
murine leukemia virus	25
was used to	25
stomatitis virus glycoprotein	25
of host protein	25
immunodeficiency virus type	25
on the other	25
in which the	25
the vesicular stomatitis	25
one of the	25
of the virion	25
shown to be	24
used as a	24
the level of	24
cells were transfected	24
activity of the	24
we found that	24
cells were then	24
in the golgi	24
hepatitis c virus	24
shown in fig	24
than that of	23
the mechanism of	23
the case of	23
in the case	23
the inhibition of	23
the other hand	23
of influenza a	23
a and b	23
was used as	23
was determined by	23
for h and	23
stomatitis virus vectors	22
influenza a viruses	22
cellular immune responses	22
of a novel	22
the activity of	22
transcriptional activity of	22
the transcriptional activity	22
the lipid bilayer	22
were detected by	21
part of the	21
end of the	21
ebola virus glycoprotein	21
were transfected with	21
as compared to	21
has been shown	21
adp p y	21
of enveloped viruses	21
in the cell	21
the glycoproteins of	21
and the cells	21
of g protein	21
materials and methods	21
antiviral activities of	21
as previously described	21
the effect of	20
similar to the	20
bv or mlt	20
prok treated virions	20
protein synthesis by	20
in the viral	20
as described previously	20
in the present	20
were obtained from	20
of the er	20
vsv g protein	20
sequence of the	20
the present study	20
it is possible	20
the ebov gp	20
it has been	20
from the er	20
then infected with	20
has not been	20
of ebola virus	20
detected by q	20
were analyzed by	20
cells were fixed	19
a consequence of	19
and cellular immune	19
and incubated for	19
in the same	19
found to be	19
the formation of	19
a vesicular stomatitis	19
central nervous system	19
added to the	19
of the cell	19
the infectivity of	19
the amount of	19
in the brain	19
of type i	19
of the host	19
for the first	19
is required for	19
were carried out	19
and ifit mice	19
thermo fisher scientific	19
kindly provided by	18
the viral genome	18
of the g	18
balb c mice	18
of acid sphingomyelinase	18
the first time	18
a number of	18
of ebov gp	18
viral protein synthesis	18
obtained from the	18
of vsv g	18
in hela cells	18
in the vsv	18
were able to	18
cells were treated	18
regions of the	18
the transmembrane domain	18
h at room	18
semliki forest virus	18
in contrast to	18
have shown that	18
results indicate that	18
attenuated vesicular stomatitis	18
supplementary figure s	18
and p y	17
the m protein	17
incubated for h	17
host cell entry	17
were inoculated with	17
high levels of	17
the distribution of	17
the reaction mixture	17
gp pseudotyped hiv	17
of viral mrna	17
portion of the	17
the endoplasmic reticulum	17
in cells infected	17
to assess the	17
were used to	17
the brains of	17
were added to	17
the current study	17
carried out in	17
mediated antiviral activities	17
humoral and cellular	17
a single dose	17
nucleotide sequence of	16
were shown to	16
type i interferon	16
h and then	16
rvsv vectors expressing	16
based on a	16
of the golgi	16
the spike protein	16
the ability to	16
live ebov neutralisation	16
were determined by	16
the lack of	16
glycoprotein of vesicular	16
stomatitis virus g	16
of host cell	16
gp and gp	16
b and c	16
development of a	16
the addition of	16
of infected cells	16
appear to be	16
to the cells	16
of the sars	16
were used as	16
was removed and	16
role of the	16
cd t cells	16
the cotton rat	16
the inhibitory effect	16
to determine whether	16
was carried out	16
was observed in	16
treated with adp	15
virus vectors expressing	15
that of the	15
washed twice with	15
is essential for	15
cells were incubated	15
to each well	15
cleavage of the	15
vectors pseudotyped with	15
cells were seeded	15
cytoplasmic tail of	15
was shown to	15
immune responses to	15
multiplicity of infection	15
of p y	15
size of the	15
the cytoplasmic tail	15
in vesicular stomatitis	15
well as the	15
m a b	15
is consistent with	15
composition of the	15
was performed using	15
care and use	15
for h before	15
added to each	15
analyzed by sds	15
of the membrane	15
washed with pbs	15
nile virus infection	15
of porcine reproductive	15
g protein of	15
the total number	15
differences in the	15
total number of	15
were incubated with	15
reaction mixture was	15
studies on the	15
some of the	14
and then infected	14
the ebola virus	14
used for the	14
pathogenic avian influenza	14
to that of	14
there was no	14
serial dilutions of	14
coronavirus spike protein	14
of the brain	14
to the cell	14
there was a	14
highly pathogenic avian	14
of er buds	14
respiratory syncytial virus	14
of eif e	14
the central nervous	14
in the current	14
the end of	14
of middle east	14
consequence of the	14
were incubated at	14
of host mrnas	14
detected in the	14
the possibility that	14
present in the	14
neutralization test using	14
all of the	14
the wnv e	14
viral and cellular	14
min at room	14
as a result	14
appears to be	14
of the total	14
a multiplicity of	14
green fluorescent protein	14
cov s protein	14
on the viral	14
results demonstrate that	14
protein of vsv	14
fetal bovine serum	14
cells were grown	14
cells in the	14
described in the	14
from infected cells	14
the aug codon	13
the size of	13
it is likely	13
used in this	13
removal of the	13
is likely that	13
in cell culture	13
the effects of	13
was detected by	13
lucas et al	13
was detected in	13
vsv replication in	13
rous sarcoma virus	13
that the vsv	13
cell lines from	13
antiviral activity in	13
remains to be	13
immune responses in	13
of viral proteins	13
or not with	13
were incubated for	13
a recombinant vesicular	13
and characterization of	13
on the cell	13
of the vesicular	13
none of the	13
vaccine based on	13
were challenged with	13
at a multiplicity	13
three times with	13
there is no	13
supernatants were harvested	13
included in the	13
is possible that	13
proteolytic cleavage of	13
mice immunized with	13
the influenza virus	13
as a control	13
the function of	13
bat cell lines	13
of west nile	13
to test the	13
was used for	13
the kinetics of	13
showed that the	13
to the plasma	13
with pfu of	13
in the brains	13
were washed with	13
the results of	13
were washed twice	13
inhibitory effect of	13
of host shutoff	13
with vesicular stomatitis	13
protein of vesicular	13
m and g	13
of cellular mrnas	13
production of infectious	13
mabs to ep	13
the resulting residue	13
has been reported	13
t cell responses	13
of the most	13
immune responses against	13
in the cytoplasm	13
the extent of	12
of the influenza	12
of viral protein	12
pfu of vsv	12
described in materials	12
budding from the	12
related to the	12
in materials and	12
single dose of	12
of the spike	12
washed three times	12
were used for	12
of the cytoplasmic	12
gp pseudotyped vsv	12
top of the	12
at the plasma	12
after infection with	12
inserted into the	12
the activation of	12
neutralizing antibody titers	12
viral mrnas are	12
we used a	12
characterization of a	12
can be used	12
infected cells and	12
the generation of	12
were grown in	12
antiviral activity against	12
of the lipid	12
pseudotyped virus neutralisation	12
to investigate whether	12
no effect on	12
the idea that	12
found in the	12
and incubated with	12
bv and mlt	12
indicating that the	12
referred to as	12
dmem containing fbs	12
cap binding factor	12
a novel coronavirus	12
contribute to the	12
h n virus	12
a dilution of	12
region of the	12
of viral replication	12
translation of viral	12
of the mrna	12
component of the	12
of the glycoproteins	12
to identify the	12
s ribosomal subunits	12
results suggest that	12
by western blot	12
not required for	12
the golgi apparatus	12
similar to that	12
of the envelope	12
the golgi exclusion	12
resulting residue was	12
cell protein synthesis	12
as vaccine vectors	12
the binding of	12
identification of a	12
suggest that the	12
of the cells	12
characterization of the	12
activation of the	12
the induction of	12
virus infection in	12
suggesting that the	12
golgi exclusion zone	12
stomatitis virus and	12
three independent experiments	12
is responsible for	12
proteins on the	12
position of the	12
h post transfection	12
of the recombinant	12
of sindbis virus	12
of pseudotyped virus	12
it is not	12
of the proteins	12
presence of the	12
of viral mrnas	12
the intercat ifn	12
of recombinant vesicular	11
these results indicate	11
of bv or	11
hek t cells	11
data suggest that	11
i ifn signaling	11
shutoff of host	11
virus matrix protein	11
due to its	11
viral gene expression	11
were fixed with	11
a series of	11
upstream aug codons	11
of rous sarcoma	11
indicate that the	11
the first aug	11
vaccination with a	11
to be the	11
was performed in	11
in mammalian cells	11
kapadia et al	11
activity of rfeifn	11
protein in the	11
of the mice	11
in figure a	11
and cells were	11
aridor et al	11
with respect to	11
is the most	11
the site of	11
replication of vsv	11
of cotton rats	11
at a dilution	11
position in the	11
could be detected	11
of host translation	11
to the golgi	11
the translational machinery	11
pseudotyped lentiviral vectors	11
pseudotyped with the	11
for generation of	11
that can be	11
the gxxxg motif	11
was found to	11
and vesicular stomatitis	11
be used to	11
incubated for min	11
any of the	11
infected cells were	11
the virus was	11
the abundance of	11
with severe acute	11
were performed in	11
was obtained from	11
simplex virus type	11
open reading frames	11
viruses such as	11
and stored at	11
an important role	11
results in the	11
involved in the	11
infection of the	11
of the human	11
stomatitis virus expressing	11
the efficiency of	11
wnv e glycoprotein	11
of hepatitis c	11
in the genome	11
members of the	11
in the future	11
of the s	11
the concentration of	11
inhibited the replication	11
the medium was	11
to the viral	11
of the oligomer	11
and the reaction	11
the neutralization test	11
the top of	11
by centrifugation at	11
of the antiviral	11
with a recombinant	11
an moi of	11
of viral glycoproteins	11
the viral surface	11
and analyzed by	11
of the two	11
syndrome coronavirus spike	10
plates were incubated	10
to vsv infection	10
in transfected cells	10
to investigate the	10
mixture was stirred	10
of viral rna	10
used as the	10
fold serial dilutions	10
for the treatment	10
vero cells were	10
retained in the	10
was supported by	10
for use in	10
a b s	10
protein synthesis is	10
their ability to	10
were measured by	10
pind et al	10
at the same	10
were seeded in	10
compared with the	10
of the glycoprotein	10
with n ct	10
effect on the	10
alonso and carrasco	10
number of buds	10
signs of disease	10
determined by the	10
had no effect	10
be associated with	10
c and d	10
to examine the	10
of human immunodeficiency	10
in response to	10
found that the	10
endoplasmic reticulum to	10
to a stirred	10
for host cell	10
ebola virus infection	10
the control of	10
monoclonal antibodies against	10
viral spread in	10
replication in the	10
has also been	10
a moi of	10
but not in	10
role in the	10
times with pbs	10
of mammalian cells	10
supplemented with fetal	10
followed by a	10
can be activated	10
was able to	10
expression of p	10
have been shown	10
cells per well	10
virus infection of	10
the interaction of	10
are shown in	10
stomatitis virus matrix	10
error bars indicate	10
the type i	10
p y and	10
the e glycoprotein	10
gel column chromatography	10
by vesicular stomatitis	10
as a colorless	10
have not been	10
the release of	10
the glycoprotein of	10
a result of	10
the amino acid	10
server at http	10
adjacent to the	10
the viral mrnas	10
at the level	10
in prok treated	10
rna replicates were	10
in vero cells	10
the antiviral activities	10
was purified by	10
avian influenza viruses	10
of a protein	10
purified by silica	10
for the development	10
l g a	10
of hela cells	10
the recombinant feifn	10
virus g protein	10
with a single	10
column chromatography using	10
were then washed	10
feline leukemia virus	10
the preparation of	10
stomatitis virus infection	10
both lentiviral vectors	10
nef g c	10
h n treated	10
the treatment of	10
were maintained in	10
approved by the	10
truncated g protein	10
cells were inoculated	10
expression of a	10
no antiviral activity	10
was confirmed by	10
virus replication in	10
cellular mrnas that	10
the s protein	10
relative to the	10
this work was	10
were washed and	10
residue was purified	10
that could be	10
in comparison to	10
stomatitis virus recombinants	10
cell culture supernatant	10
cap binding protein	10
have been identified	10
the first position	10
silica gel column	10
to be translated	10
g or vsv	10
on day pi	10
with the viral	10
of infectious virus	10
by silica gel	10
mechanism by which	9
the severe acute	9
are associated with	9
the structure of	9
medium was removed	9
a stirred solution	9
as a vaccine	9
was detected using	9
of the gml	9
at the end	9
is necessary for	9
the rate of	9
resulting in the	9
safety and immunogenicity	9
the h n	9
because it is	9
our results demonstrate	9
not affect the	9
lethal challenge with	9
mrna cap methylation	9
doxorubicin inhibits the	9
ifit mice were	9
translation of the	9
we have previously	9
with the anti	9
g protein was	9
were collected from	9
important role in	9
creative commons license	9
those of the	9
recombinant feline interferon	9
the vaccinated mice	9
was performed as	9
s pseudoparticle neutralization	9
pseudoparticle neutralization assay	9
of the ha	9
mutation of the	9
information is available	9
and g proteins	9
nakamura and compans	9
airway epithelial cells	9
ifit and ifit	9
mlt h n	9
attenuated rvsv vectors	9
ripa branch of	9
inoculum was removed	9
with vsv g	9
the infection of	9
with the virus	9
were washed three	9
in the neutralization	9
n and g	9
was analyzed by	9
lymphocytic choriomeningitis virus	9
were found to	9
appeared to be	9
viral protein expression	9
stronger than that	9
these results suggest	9
with pbs containing	9
cells with vsv	9
to be associated	9
on day after	9
upstream from the	9
corresponding to the	9
eluent to give	9
expression plasmids for	9
the vsv genome	9
branch of irf	9
mutations in the	9
inhibition of the	9
be due to	9
the study of	9
we showed that	9
derived from the	9
the west nile	9
was replaced with	9
h after infection	9
membrane fusion activity	9
small amount of	9
determined to be	9
comparison of the	9
apilimod and vacuolin	9
for min and	9
at the restrictive	9
in mice immunized	9
neutralization assay for	9
motif in the	9
from the endoplasmic	9
the immune system	9
each well and	9
for analysis of	9
higher than that	9
from the first	9
supplemented with fbs	9
a single immunization	9
infected hela cells	9
the inoculum was	9
prime boost vaccination	9
the stacking gel	9
is known to	9
heterologous animal cells	9
between the two	9
mouse hepatitis virus	9
as the eluent	9
of the mean	9
prrsv envelope proteins	9
and cellular mrnas	9
in saudi arabia	9
the restrictive temperature	9
the authors declare	9
the process of	9
one or more	9
the eluent to	9
er to golgi	9
latently infected rn	9
neutralizing antibodies against	9
may not be	9
conjugated goat anti	9
hispidus cell lines	9
the assembly of	9
the boosted group	9
spike protein of	9
open reading frame	9
against fcov and	9
the highest dilution	9
led us to	9
removed and the	9
national institute of	9
reciprocal of the	9
that p y	9
newcastle disease virus	9
significantly stronger than	9
activities of rfeifn	9
in the transmembrane	9
treated with trypsin	9
cov neutralizing antibodies	9
h n viruses	9
medium was replaced	9
against lethal challenge	9
attenuation of vsv	9
by plaque assay	9
and it is	9
effect of the	9
a type i	9
replicates were detected	9
synthesis of the	9
final concentration of	9
plutner et al	9
the reciprocal of	9
synthesis of a	9
acid sphingomyelinase and	9
of vsv in	9
studies have shown	9
results showed that	9
a positive control	9
fcov and vsv	9
of the m	9
are involved in	9
of the same	9
the cells with	9
a mw of	9
at the cell	9
to produce a	9
was significantly stronger	9
h before being	9
stirred solution of	9
type i and	9
influenza virus mrnas	9
of the stacking	9
single immunization with	9
the leader sequence	9
mechanism of host	9
the potential of	9
in a cell	9
be activated by	9
of the protein	9
and nhei restriction	8
shown in the	8
in a dose	8
first aug codon	8
its ability to	8
of vsv infection	8
in line with	8
a t the	8
in dromedary camels	8
displayed on the	8
shown in table	8
is not a	8
cells infected by	8
location of the	8
phosphate buffered saline	8
components of the	8
more potent than	8
to the vsv	8
that it is	8
responsible for the	8
influenza virus hemagglutinin	8
stomatitis virus in	8
based neutralization assay	8
protective immune response	8
in the host	8
log pfu ml	8
batfluav surface proteins	8
single amino acid	8
to promote ripa	8
the population of	8
of measles virus	8
after h of	8
assembly of the	8
shown that the	8
not the transcriptional	8
spread in tetherin	8
under reduced pressure	8
mice per infected	8
y and p	8
serve as a	8
of the hemagglutinin	8
proteolytic activation of	8
in ifit mice	8
that map to	8
host cell protein	8
as a model	8
to be a	8
and stained with	8
demonstrated that the	8
and use of	8
per infected group	8
of the genome	8
the ha spike	8
were unable to	8
expression of epac	8
of sialic acids	8
the results from	8
for the study	8
mosaic virus rna	8
nhei restriction sites	8
inhibited vsv replication	8
of the first	8
were pretreated or	8
to analyze the	8
previous studies have	8
nonhuman primates against	8
serum samples were	8
irf s s	8
in our study	8
of monoclonal antibodies	8
whether the antiviral	8
and in vitro	8
using graphpad prism	8
alfalfa mosaic virus	8
a mechanism for	8
h n challenge	8
were stained with	8
institutional animal care	8
were harvested at	8
in l cells	8
observed in the	8
isolation and characterization	8
most of the	8
virus envelope glycoprotein	8
the cell culture	8
absence of a	8
of the major	8
gold particles per	8
has been demonstrated	8
in tissue culture	8
rna levels in	8
rose et al	8
contributes to the	8
cellular mrnas with	8
in these cells	8
proteins identified in	8
used in the	8
a library of	8
of laboratory animals	8
sites were analyzed	8
bound to the	8
doms et al	8
or vsv m	8
defined as the	8
reduction in the	8
in wt mice	8
h n influenza	8
this study was	8
is thought to	8
for hr at	8
animal care and	8
analysis was performed	8
of viral envelope	8
of vsv and	8
genes of vesicular	8
as indicated by	8
and in the	8
the ripa branch	8
g and vsv	8
the replication competent	8
be involved in	8
of cellular proteins	8
of severe acute	8
translation of capped	8
the lumenal domain	8
that of rfeifn	8
correlation between the	8
the course of	8
of the ifn	8
could not be	8
viral mrnas in	8
to measure the	8
are known to	8
well and incubated	8
by standard plaque	8
of the gxxxg	8
pretreated or not	8
effect of pis	8
to the control	8
the nuclear envelope	8
which can be	8
with fetal bovine	8
protects mice from	8
by a single	8
standard plaque assay	8
the finding that	8
for detection of	8
thought to be	8
at days post	8
a combination of	8
gag and pol	8
did not show	8
on a replication	8
as evidenced by	8
of the other	8
stomatitis virus is	8
antiviral effect of	8
the density of	8
was replaced by	8
has been suggested	8
body weight loss	8
as a positive	8
the antiviral effect	8
comparison to the	8
on g protein	8
is that the	8
have been reported	8
of hal and	8
for influenza virus	8
with pbs and	8
for this purpose	8
nature of the	8
host cell shut	8
mdck cells were	8
to be an	8
and the resulting	8
female balb c	8
to study the	8
or vsv g	8
of these proteins	8
expression in the	8
in dmem containing	8
with a lethal	8
neutralizing antibody response	8
regulation of the	8
expression of vsv	8
and influenza virus	8
to golgi transport	8
of infectious vsv	8
has previously been	8
competent vesicular stomatitis	8
in table i	8
of cap binding	8
proteins associated with	8
a small amount	8
reads that map	8
cells were used	8
on sucrose gradients	8
generation of vsv	8
in vivo and	8
in the hiv	8
infection with a	8
in the cytoplasmic	8
in extracts from	8
in the first	8
the potential for	8
number of er	8
el and e	8
the positive control	8
figure s a	8
immune response to	8
the supernatants were	8
required for efficient	8
a lethal dose	8
of host proteins	8
first position in	8
the specificity of	8
g protein in	8
vsv rna replicates	8
based on live	8
the cellular mrnas	8
the outcome of	8
is not known	7
analyses were performed	7
titers were determined	7
start of the	7
of eif a	7
a vaccine vector	7
provides complete protection	7
in pbs for	7
infected with the	7
cells were extensively	7
is not required	7
for disease control	7
on vero cells	7
evaporated under reduced	7
a second bud	7
as negative control	7
sorensen et al	7
a cell line	7
the volume of	7
using live mers	7
cells challenged with	7
was isolated from	7
animal model for	7
interaction with the	7
of the corresponding	7
is inhibited by	7
in the mouse	7
figure s c	7
fresh culture medium	7
were separated by	7
of the replication	7
of a viral	7
the efficacy of	7
at the time	7
the appearance of	7
metabolically labeled for	7
by authentic sars	7
we evaluated the	7
in agreement with	7
com scientificreports www	7
are likely to	7
a gift from	7
are required for	7
these data suggest	7
the envelope of	7
were extensively washed	7
the membrane of	7
vectors expressing hiv	7
intraperitoneally injected with	7
studies of the	7
mrna in the	7
the negative control	7
t cells and	7
dmem supplemented with	7
n treated mice	7
of wt mice	7
plotted as mean	7
the impact of	7
and ethyl acetate	7
protein of sars	7
with wt vsv	7
carried out by	7
sequences of the	7
mice at d	7
pbs h n	7
a sucrose cushion	7
pseudotyped with severe	7
associated with a	7
cells were analyzed	7
it is the	7
in hek t	7
by the point	7
effective aids vaccine	7
and can be	7
need to be	7
the pi treatment	7
gp gp gp	7
enu start site	7
the total cytoplasmic	7
these results demonstrate	7
e and f	7
of the bv	7
hela cells expressing	7
a monoclonal antibody	7
interact with the	7
envelope glycoproteins of	7
the external surface	7
infected insect cells	7
acid sphingomyelinase activity	7
of vaccinia virus	7
were grown on	7
specific antibody responses	7
in the development	7
infection with pp	7
t rna polymerase	7
neutralizing antibodies in	7
by using a	7
viral infection in	7
wide range of	7
host shutoff is	7
centers for disease	7
do not affect	7
immunogenicity of the	7
was required for	7
at the top	7
hal and nal	7
host translation is	7
investigation of the	7
binds to the	7
analyzed by the	7
the incorporation of	7
bernstein et al	7
the live ebov	7
collected from the	7
influenza virus replication	7
did not affect	7
was added and	7
which is a	7
the gene encoding	7
the virus in	7
shown as mean	7
a wide range	7
untreated with the	7
a comparison of	7
viral infections in	7
influenza h n	7
syndrome coronavirus infection	7
broad spectrum of	7
viral rna was	7
different concentrations of	7
which is the	7
and expression of	7
and found that	7
were expressed as	7
to determine if	7
virus envelope proteins	7
thymidine kinase gene	7
and heterologous animal	7
mediated cell fusion	7
cell culture supernatants	7
chromatography using hexane	7
that has been	7
of a library	7
expression levels were	7
between viral and	7
on virus entry	7
replication of both	7
with cytochalasin d	7
cell plasma membrane	7
for in vitro	7
was generated by	7
virus vectors in	7
of vsv replication	7
of the prrsv	7
using hexane and	7
the cell membrane	7
insect cells and	7
on live attenuated	7
out of the	7
lethal dose of	7
the plates were	7
structural proteins of	7
rvsv vaccine vectors	7
used to assess	7
the probability of	7
in insect cells	7
these cell lines	7
were observed in	7
gxxxg motif in	7
after a single	7
induction of ifit	7
national institutes of	7
phosphorylation of eif	7
cellular protein synthesis	7
of the vaccinated	7
is sufficient for	7
increase in the	7
infected ifit mice	7
of a foreign	7
were purchased from	7
a final concentration	7
from the same	7
mrnas with increased	7
to test whether	7
epithelial cell lines	7
is shown in	7
activity of doxorubicin	7
the s subunit	7
in the context	7
lines from the	7
tetherin antagonism by	7
the importance of	7
and vero cells	7
expressed as the	7
d and e	7
recombinant vaccinia virus	7
the virus and	7
spectrum antiviral activities	7
have been used	7
as negative controls	7
of wt and	7
of the eif	7
hafl or vsv	7
for membrane fusion	7
is difficult to	7
test using vsv	7
we demonstrate that	7
of the cap	7
of a given	7
cells were obtained	7
inhibition of viral	7
the major enu	7
not appear to	7
after infection by	7
of the rfeifn	7
the virus is	7
in the nucleus	7
decreased polysome association	7
in vitro models	7
results demonstrated that	7
aids vaccine based	7
cells were pretreated	7
in ml of	7
area of the	7
c mice were	7
hexane and ethyl	7
in vivo studies	7
the interior of	7
of cellular mrna	7
been reported to	7
antiviral action of	7
to give the	7
the potential to	7
recombinant vsv with	7
of the ebola	7
as determined by	7
rna expression of	7
by proteolytic cleavage	7
of bv and	7
cells expressing gml	7
abl tyrosine kinase	7
the n ct	7
a significant difference	7
virus neutralisation assays	7
with the major	7
the pool of	7
immune responses and	7
immunoprecipitated using anti	7
the presence or	7
a subset of	7
of a single	7
the context of	7
at a final	7
has been described	7
of the manuscript	7
an increase in	7
and that the	7
in viral rna	7
mouth disease virus	7
into the cytosol	7
with mutated m	7
to be determined	7
is sufficient to	7
of neutralizing antibodies	7
as mean sd	7
institutes of health	7
an effective aids	7
and use committee	7
showed a high	7
characteristics of the	7
equipped with a	7
immunized with n	7
known to be	7
for treatment of	7
synthesis in cells	7
rna was extracted	7
surface of baculovirus	7
compared to control	7
cells untreated with	7
contrast to the	7
of viral particles	7
the e r	7
ability of the	7
was determined using	7
of these viruses	7
show that the	7
of herpes simplex	7
as an experimental	7
of a recombinant	7
induction of ifn	7
mediated immune responses	7
of virus particles	7
and assembly of	7
to inhibit the	7
at and hpi	7
understanding of the	7
with the ifns	7
with the exception	7
found on the	7
and development of	7
of influenza viruses	7
transmembrane domain of	7
of semliki forest	7
viruses as vaccine	7
the control group	7
cd t cell	7
library of fda	7
in some cases	7
in each group	7
use of laboratory	7
we determined the	7
the start of	7
was stirred at	7
aug codon in	7
the culture medium	7
the genome of	7
a portion of	7
vectors expressing glycoproteins	7
indicated that the	7
machamer et al	7
major surface glycoprotein	7
than host mrnas	7
significantly higher than	7
saquinavir and nelfinavir	7
avian influenza virus	7
vaccination with vsv	7
ebov neutralisation assay	7
many of the	7
and identification of	7
a large oligomer	7
and then chased	7
is similar to	7
infection of vsv	7
by western blotting	7
changes in the	7
that viral mrnas	7
immediately or after	7
to this end	7
the matrix protein	7
with the vsv	7
against ebola virus	7
in cotton rats	7
renal epithelial cells	7
recombinant vsvs expressing	7
for the presence	6
of the serum	6
increased polysome association	6
attenuated recombinant vaccine	6
were anesthetized with	6
external surface of	6
interior of the	6
of poliovirus rna	6
complete protection from	6
this study were	6
transcription of the	6
it would be	6
of ifit and	6
the onset of	6
based vaccine protects	6
virus titer was	6
the c terminus	6
has been obtained	6
the care and	6
supported by the	6
from the e	6
average number of	6
the fraction of	6
difference between the	6
added and incubated	6
we conclude that	6
for quantification of	6
cells were pre	6
proteins that are	6
mediated by the	6
of viral and	6
pis do not	6
as long as	6
gene in the	6
o f the	6
in a single	6
both vsv and	6
g and m	6
the immunogenicity of	6
in keeping with	6
were performed using	6
of gtp s	6
proteins found in	6
into virus particles	6
have been described	6
infected wt and	6
tobacco mosaic virus	6
by host cell	6
similar to those	6
into the plasma	6
with decreased polysome	6
different regions of	6
levels of viral	6
blocked with bsa	6
and subjected to	6
ml of bv	6
baby hamster kidney	6
virus as a	6
to evaluate the	6
infected with hsv	6
to examine whether	6
inhibition of vsv	6
were observed when	6
vaccinated and mock	6
was achieved by	6
vaccinia virus ankara	6
focused on the	6
addition to the	6
er buds in	6
were analyzed for	6
amino acid sequence	6
in the infected	6
g in a	6
is likely to	6
rvsv vector expressing	6
for hour at	6
specific for the	6
may be a	6
polyacrylamide gel electrophoresis	6
we sought to	6
a value of	6
of ifnar mice	6
were then infected	6
release of ceramide	6
the vsv glycoprotein	6
an additional transcription	6
the majority of	6
there are no	6
upon infection with	6
lentiviral pseudotyped vectors	6
to viral spread	6
ebola and marburg	6
vsv was significantly	6
of vero e	6
were metabolically labeled	6
enveloped rna viruses	6
cooper and moss	6
in well plates	6
performed in a	6
assays were performed	6
in animal models	6
in the membrane	6
vsv g gene	6
but not the	6
the shutoff of	6
cov spike protein	6
guide for the	6
we used the	6
detected using a	6
to some extent	6
data demonstrated that	6
the yield of	6
hpai h n	6
the time of	6
t cells in	6
matrix protein inhibits	6
volume of the	6
in wt and	6
mrnas are translated	6
virus infection and	6
is associated with	6
strongly inhibited by	6
and not the	6
replication competent construct	6
host shutoff by	6
determined using the	6
of the nucleocapsid	6
x for peer	6
reduction neutralization test	6
at the permissive	6
in a highly	6
viral and host	6
antiviral activities were	6
molecular weights of	6
the f glycoprotein	6
and host cell	6
proteins of the	6
export from the	6
that of intercat	6
in accordance with	6
in the results	6
vivo and in	6
the regulation of	6
infection of hela	6
the insertion of	6
antibodies against mers	6
on the transcriptional	6
we wanted to	6
ifit mice at	6
influenza a h	6
intranasal vsv infection	6
or g proteins	6
vsv mrnas are	6
is important to	6
by activating the	6
the nucleocapsid protein	6
the effectiveness of	6
in this experiment	6
fraction of the	6
the sequence of	6
the virus to	6
by vaccinia virus	6
incorporation of a	6
demonstrate that doxorubicin	6
for the vsv	6
vector based on	6
stomatitis virus as	6
disruption of the	6
replication of the	6
in the liver	6
we focused on	6
of human sera	6
use of a	6
the envelope proteins	6
was used in	6
of recombinant vsv	6
infected with a	6
in support of	6
m protein is	6
linked immunosorbent assay	6
lodish and porter	6
californica nuclear polyhedrosis	6
mediated immune response	6
entry driven by	6
host range and	6
with dmem containing	6
matrix protein of	6
positive cells were	6
of the genes	6
as a potential	6
polymerase chain reaction	6
fig a and	6
was measured by	6
of the bilayer	6
there is a	6
a fluorescence microscope	6
the prrsv envelope	6
coding for the	6
identification of the	6
for min in	6
available upon request	6
antibody responses to	6
infection in humans	6
in patients with	6
etchison et al	6
with vsv and	6
homologous and heterologous	6
fractions were collected	6
expression of tetherin	6
it may be	6
and immunogenicity of	6
tani et al	6
for peer review	6
highly susceptible to	6
and hela cells	6
in the figure	6
the best studied	6
whole and prok	6
the removal of	6
see materials and	6
to address this	6
properties of replication	6
polysome association of	6
were detected in	6
metabolically radiolabeled for	6
the results showed	6
of filoviruses and	6
the major surface	6
cap binding proteins	6
of n ct	6
of uninfected or	6
the virion and	6
lumenal domain of	6
levels were measured	6
cells by the	6
were lysed in	6
the mixtures were	6
disease control and	6
cells treated with	6
of vsv is	6
are shown as	6
normal brain cells	6
all of which	6
interfere with the	6
of infectious diseases	6
of the hiv	6
to mammalian cells	6
protective efficacy of	6
dose of vsv	6
challenged with a	6
on the external	6
virus glycoprotein is	6
these proteins are	6
viruses have been	6
and l proteins	6
by use of	6
inhibited by doxorubicin	6
the association of	6
gives rise to	6
cells as a	6
and prok treated	6
of the study	6
specific immune response	6
disease in humans	6
strand rna virus	6
values obtained from	6
and vsv m	6
proteins in the	6
revealed that the	6
an influenza virus	6
h post infection	6
blocked by a	6
the extracellular domain	6
consistent with this	6
was kindly provided	6
supernatants were collected	6
dose of the	6
isolated from a	6
klenk et al	6
promoted the ripa	6
hela cells with	6
and vsv was	6
virus in the	6
presented in the	6
would like to	6
of ifit mice	6
are present in	6
the ml domain	6
cells at the	6
in previous studies	6
by the same	6
nasal epithelial cells	6
amino acid sequences	6
envelope proteins of	6
and m proteins	6
cells in vitro	6
demonstrate that the	6
in place of	6
proteomic analysis of	6
alterations in the	6
to explain the	6
vaccine vector and	6
primates against ebola	6
in this context	6
with the endosomal	6
protein on the	6
viral envelope and	6
hal and hal	6
required for the	6
infection results in	6
dried over mgso	6
old mice were	6
effect of mlt	6
of the plasma	6
cells were stained	6
lethal ebov challenge	6
function of the	6
stomatitis viruses from	6
nuss et al	6
neutralizing antibodies to	6
host cell plasma	6
with the envelope	6
yellow fever virus	6
stomatitis virus by	6
only in the	6
was determined as	6
that they are	6
the mechanism by	6
of rvsv vectors	6
results in a	6
the er membrane	6
the sensitivity of	6
ep and ep	6
based on recombinant	6
g pseudotyped vectors	6
the results were	6
that the inhibitory	6
transcription and translation	6
viral mrna cap	6
retention in the	6
pseudotyped virus input	6
was purchased from	6
for the care	6
the loss of	6
degradation of host	6
to the virus	6
of a second	6
samples were collected	6
of the rvsv	6
correlates of protection	6
vaccinated mice had	6
on the virion	6
the mixture was	6
cells were lysed	6
surface glycoproteins of	6
mice were intraperitoneally	6
peer review of	6
or latently infected	6
to estimate the	6
control and prevention	6
were observed between	6
innate antiviral response	6
in the serum	6
in adp p	6
likely due to	6
provided by the	6
heat shock protein	6
likely to be	6
sites in the	6
in pbs and	6
of viral membrane	6
major enu start	6
may contribute to	6
incubation in vitro	6
also inhibited the	6
for minutes at	6
rna and dna	6
safety and efficacy	6
gp and m	6
the types of	6
significant difference between	6
significant differences in	6
for rain at	6
the center of	6
twice with pbs	6
the location of	6
ebola virus entry	6
the percentage of	6
host cell membrane	6
was not required	6
ii transmembrane serine	6
medium supplemented with	6
additional transcription unit	6
depend on the	6
stomatitis virus pseudotype	6
off of host	6
transferred to a	6
oncolytic vesicular stomatitis	6
to the host	6
used to determine	6
difference in the	6
protective immune responses	6
to a single	6
synthesis of viral	6
of vsv pseudotypes	6
of this study	6
the viral rna	6
in the polysome	6
of translation of	6
for production of	6
type i ifns	6
it is important	6
cells transfected with	6
the m g	6
of the e	6
after intranasal infection	6
of cells with	6
more efficient than	6
virus grown in	6
for min before	6
avian influenza a	6
luciferase activity was	6
to the n	6
in vitro antiviral	6
the permissive temperature	6
vsv g or	6
was removed from	6
cloned into the	6
a colorless oil	6
used to generate	6
of h n	6
epitopes on g	6
presence of a	6
proteins can be	6
cov neutralizing antibody	6
persistently or latently	6
of newcastle disease	6
as the highest	6
cells were plated	6
tail of gml	6
size and shape	6
surface area of	6
the range of	6
influenza virus proteins	6
we examined the	6
of viral translation	6
inhibition of translation	6
dependent rna polymerase	6
by the presence	6
protect mice against	6
on vero e	6
dilution of the	6
was not detected	6
no significant differences	6
for the prevention	6
surface glycoprotein of	6
on log scale	6
a functional receptor	6
influenza virus glycoproteins	6
high degree of	6
and supplementary figure	6
glycoproteins of filoviruses	6
cancer stem cells	6
fixed with paraformaldehyde	6
host cell proteases	6
were harvested and	6
modified vaccinia virus	6
initiation factor eif	6
the mean surface	6
glycoproteins of the	6
antiviral effects of	6
proven to be	6
is not the	6
vsv has been	6
xhoi and nhei	6
and viral rna	6
in p y	6
cells were further	6
cd and cd	6
organization of the	6
of late viral	6
autographa californica nuclear	6
are included in	6
or in the	6
domain of vsv	6
to the only	6
of the gag	6
half of the	6
mammalian cells by	6
effects of the	6
protection from sars	6
nuclear polyhedrosis virus	6
the safety of	6
mice were anesthetized	6
titers in the	6
of gold particles	6
neutralizing antibody responses	6
n mice per	6
with vrp expressing	6
mg ml of	6
of these compounds	6
all cell lines	6
mm tris ph	6
isolated from the	6
a co atmosphere	6
a terminator codon	6
doxorubicin treatment inhibited	6
by vsv m	6
avian sarcoma virus	6
to the same	6
neutralizing antibodies and	6
expressing glycoproteins of	6
suppression of the	6
african green monkey	6
truncation of the	6
with increased polysome	6
of intercat ifn	6
for the production	6
filoviruses and arenaviruses	6
were collected and	6
the erk signaling	6
the n protein	6
evidence that the	6
consequence of a	6
virus fusion protein	6
is defective in	6
and evaporated under	6
vaccine vectors in	6
m g cap	6
neutralization tests using	6
bars indicate the	6
belonging to the	6
i and i	6
were prepared as	6
live attenuated vesicular	6
were found in	6
experiments were performed	6
dose of pfu	6
in a way	6
gfp infected cells	6
play a role	6
mice were vaccinated	6
response to the	6
inhibits the replication	6
the titer of	6
high concentrations of	6
glycoprotein exchange vectors	6
g protein cytoplasmic	5
final volume of	5
initiation of protein	5
homologous animal cells	5
cell responses in	5
approaches have been	5
of these sera	5
reduction in rlu	5
is dependent on	5
we hypothesized that	5
erk signaling pathway	5
the cells in	5
off host protein	5
tmprss and is	5
a final volume	5
reticulum to golgi	5
antibody directed against	5
the prototypic rvsv	5
the pseudotyped hiv	5
p and l	5
activation of influenza	5
in the virus	5
with a moi	5
in relation to	5
bars represent the	5
the combination of	5
and marburg viruses	5
against a variety	5
the average number	5
of the rat	5
and entry of	5
the virion surface	5
of antibody with	5
cleavage of p	5
injected with vsv	5
the virus from	5
fusion activity of	5
cell monolayers in	5
in the virion	5
of the four	5
occur in the	5
of sialic acid	5
it remains to	5
the position of	5
before being treated	5
that the feifn	5
we examined whether	5
at the indicated	5
upstream and downstream	5
binding protein complex	5
of imatinib to	5
of the main	5
with live ebov	5
g protein is	5
we observed no	5
significant reduction in	5
recovery of infectious	5
been isolated from	5
viral envelope with	5
monoclonal antibodies to	5
either immediately or	5
has been previously	5
western blot analysis	5
glycoproteins expressed from	5
a h n	5
and vero e	5
prepared as described	5
we constructed a	5
with the nucleocapsid	5
difference between groups	5
separated by sds	5
innate immune responses	5
on glass coverslips	5
plane of the	5
inhibition of virus	5
virus infection without	5
in most instances	5
humoral immune responses	5
pseudotypes using recombinant	5
infectious virus particles	5
the gml oligomer	5
ni affinity column	5
receptor for the	5
g for min	5
of the sarl	5
were determined to	5
viral replication cycle	5
of attenuated vesicular	5
specific immune responses	5
coronavirus infection conferred	5
labeled for min	5
of a vesicular	5
expression was detected	5
levels in the	5
was treated with	5
vsv infected cells	5
tag ni affinity	5
griffiths et al	5
cell lines and	5
of host mrna	5
eukaryotic initiation factor	5
h influenza virus	5
g pseudotyped lentiviral	5
been described previously	5
wide variety of	5
in nonhuman primates	5
in our previous	5
were injected into	5
in whole virions	5
the viral glycoproteins	5
a replication competent	5
lethal ebola virus	5
responses to vaccines	5
for expression of	5
foreign gene in	5
the binding medium	5
in combination with	5
efficacy of the	5
the contribution of	5
in the vaccinated	5
the adsorption of	5
revealed the presence	5
with ml of	5
influenza a and	5
in vsv m	5
continuous cell lines	5
medium was added	5
liu et al	5
vector expressing the	5
and then intraperitoneally	5
the viral genes	5
virus particles in	5
extracts from infected	5
using a vsv	5
be attributed to	5
the n gene	5
were coated with	5
of supernatants on	5
in three independent	5
is based on	5
and challenged with	5
amplification of the	5
the vaccinated group	5
these findings suggest	5
the most abundant	5
data indicate that	5
fourth transcription unit	5
of buds per	5
lentiviral vectors pseudotyped	5
ebola virus disease	5
frame with the	5
and downstream of	5
were plated in	5
was performed by	5
removal of sialic	5
carrasco and lacal	5
vectors in non	5
of cells in	5
cd cd low	5
fold increase in	5
s protein in	5
the airway epithelial	5
the most important	5
immediately after synthesis	5
results led us	5
form of the	5
of the large	5
of the ribosomes	5
using a wide	5
we performed mcias	5
identification of entry	5
replaced with the	5
the media was	5
of infectious particles	5
rna polymerase of	5
modification of the	5
vsv pseudotypes using	5
from sars coronavirus	5
ml recombinant human	5
and s fig	5
for each group	5
viral rna levels	5
in export complexes	5
throughput screen of	5
responses in the	5
of pseudotyped viruses	5
is mediated by	5
on ace and	5
which may be	5
toxicity was observed	5
gp on the	5
domain of the	5
amino acid substitutions	5
amino acid residues	5
than the average	5
translated more efficiently	5
for min with	5
well as for	5
may also be	5
antibodies to the	5
this article is	5
of tumor cells	5
the viral proteins	5
gene transfer into	5
inhibit viral replication	5
were described previously	5
accumulation of late	5
could be used	5
expressing the wnv	5
transport from the	5
luciferase reporter gene	5
the e gene	5
detected by western	5
the attenuation of	5
that the viral	5
led to a	5
mutated m and	5
were further incubated	5
incorporated efficiently into	5
to develop a	5
they are not	5
properties of recombinant	5
infection of human	5
with a c	5
significant difference in	5
extracts from uninfected	5
expression of viral	5
the fourth transcription	5
comparing the rfeifn	5
are incorporated efficiently	5
a dose of	5
immunized with vsv	5
protection against lethal	5
initiate a t	5
infection was determined	5
and sec p	5
minimum essential medium	5
with the highest	5
is the only	5
room temperature with	5
we demonstrated that	5
the observation that	5
sars coronavirus infection	5
and used for	5
gml or vsv	5
transduction of the	5
cells expressing the	5
and tmprss and	5
schneider et al	5
and herpes simplex	5
vectors expressing ebovgp	5
was seen in	5
response in mice	5
pfu of the	5
that the pi	5
strong immune responses	5
from which the	5
immunization with an	5
schwarz et al	5
was determined to	5
a and c	5
rna in uitro	5
not included in	5
and immune responses	5
indicates a significant	5
host to viral	5
of an influenza	5
attenuated vsvs with	5
morbidity and mortality	5
be used as	5
of ifn and	5
equine encephalitis virus	5
change in the	5
in vivo gene	5
pancreatic acinar cells	5
release of the	5
in vsv infected	5
stomatitis viruses are	5
was observed for	5
enveloped viruses such	5
sodium dodecyl sulfate	5
gp pseudotyped virus	5
functional receptor for	5
with an attenuated	5
the suppression of	5
present on the	5
have also been	5
were analyzed using	5
the only ev	5
spectrum antiviral activity	5
the upstream aug	5
transfection medium was	5
with truncated g	5
the infected cells	5
mw of approximately	5
the optimal induction	5
as described by	5
and dna viruses	5
and accumulation of	5
of the na	5
hepatitis b virus	5
they do not	5
vsv titers in	5
the characteristics of	5
the creative commons	5
frozen in liquid	5
of doxorubicin was	5
ripa contributes to	5
for translational regulation	5
buds per ixm	5
is blocked by	5
a foreign gene	5
a clinically proven	5
highest dilution of	5
simian immunodeficiency virus	5
molecular weight of	5
inhibits virus replication	5
protein inhibits host	5
at the elevated	5
in the central	5
the polysome fraction	5
can be translated	5
interaction of antibody	5
proteins encoded by	5
c virus glycoprotein	5
day post challenge	5
be required to	5
host and viral	5
viruses are incorporated	5
by titration of	5
protein expression were	5
of the virions	5
with an moi	5
groups to the	5
work was supported	5
vsv vectors expressing	5
covalently linked to	5
expressing the sars	5
observed in vivo	5
active site of	5
vsv g and	5
the reduction in	5
vsv g were	5
competitive binding assay	5
transport of the	5
membrane of the	5
by using the	5
into host cells	5
virus and vesicular	5
one of these	5
biological activities of	5
filtered through a	5
sensitive mutants of	5
vitro antiviral activity	5
as a consequence	5
inhibits vsv replication	5
of cargo from	5
cells were maintained	5
with west nile	5
immune response in	5
envelope with the	5
and the other	5
coronavirus s protein	5
authors declare that	5
proteins were identified	5
based pseudotyped virus	5
x g for	5
stomatitis virus replicon	5
and fixed with	5
from influenza virus	5
regulation of protein	5
protein synthesis and	5
type ii transmembrane	5
more than one	5
figure d and	5
with two different	5
and h n	5
level of neutralisation	5
from a single	5
the human immunodeficiency	5
for help with	5
performed using graphpad	5
indicated by the	5
the wsn strain	5
the renal epithelial	5
complete nucleotide sequence	5
the spread of	5
of mers coronavirus	5
of influenza viral	5
of the section	5
of the leader	5
we did not	5
the ripa activity	5
the mabs to	5
ml of pbs	5
in out of	5
only a few	5
studies demonstrate that	5
the exception of	5
glycoproteins of influenza	5
the cleavage of	5
sharpe and fields	5
reads in the	5
results show that	5
type i glycopeptides	5
in humans and	5
innate immune response	5
against west nile	5
the optimal antiviral	5
on eif e	5
stomatitis virus pseudotypes	5
of entry inhibitors	5
version of the	5
brains of ifit	5
cells were either	5
from that of	5
when comparing the	5
were transferred to	5
positive and negative	5
of this virus	5
transfected cells were	5
of the gp	5
host translation by	5
production of high	5
protein of the	5
infection and the	5
that adp p	5
the receptor molecule	5
antibody with the	5
might be a	5
represent the mean	5
prompted us to	5
immunoprecipitated with anti	5
the plane of	5
when compared to	5
the occurrence of	5
ifn signaling competent	5
doxorubicin did not	5
cargo from the	5
and mdck cells	5
of vsv m	5
further incubated for	5
in the bv	5
infection of cells	5
each of the	5
the organization of	5
of zoonotic viruses	5
the pseudotyped virus	5
induced cell fusion	5
mrnas have been	5
play an important	5
the viral replication	5
groups compared by	5
that contribute to	5
during the preparation	5
translation of cellular	5
as indicated in	5
be important for	5
observed when comparing	5
like to thank	5
and is blocked	5
mouse pems were	5
rna was isolated	5
with vsv m	5
viruses can be	5
gene from the	5
been suggested that	5
membrane proteins of	5
evidence for the	5
protein is a	5
vsv for studies	5
of tetherin expression	5
into the vsv	5
that is required	5
findings suggest that	5
activation of acid	5
virus with the	5
the normal shutoff	5
strand rna viruses	5
membranes were blocked	5
a ratio of	5
associated with export	5
cell lysates were	5
the safety and	5
distribution of the	5
was extracted from	5