quadgram

This is a table of type quadgram and their frequencies. Use it to search & browse the list to learn more about your study carrel.

quadgram	frequency
of vesicular stomatitis virus	141
in the presence of	60
severe acute respiratory syndrome	54
recombinant vesicular stomatitis virus	52
in the absence of	42
reproductive and respiratory syndrome	38
porcine reproductive and respiratory	38
middle east respiratory syndrome	37
acute respiratory syndrome coronavirus	34
on the surface of	33
and respiratory syndrome virus	33
cells were infected with	29
congo hemorrhagic fever virus	28
the antiviral activity of	28
east respiratory syndrome coronavirus	27
vitro and in vivo	26
in vitro and in	25
vesicular stomatitis virus glycoprotein	25
human immunodeficiency virus type	25
the vesicular stomatitis virus	24
as shown in figure	23
in the case of	23
on the other hand	23
vesicular stomatitis virus vectors	22
of host protein synthesis	22
the transcriptional activity of	21
transcriptional activity of irf	21
and the cells were	21
the surface of the	20
cells were transfected with	19
for the first time	18
a vesicular stomatitis virus	18
wt and ifit mice	18
h at room temperature	18
and cellular immune responses	18
has been shown to	17
humoral and cellular immune	17
ebov gp pseudotyped hiv	17
for h at room	17
for h and then	16
the cells were washed	16
glycoprotein of vesicular stomatitis	16
vesicular stomatitis virus g	16
recombinant vesicular stomatitis viruses	16
of porcine reproductive and	15
of ebov gp pseudotyped	15
stomatitis virus vectors expressing	15
in the present study	15
as well as the	15
the total number of	15
the reaction mixture was	15
and then infected with	14
were detected by q	14
in the current study	14
min at room temperature	14
west nile virus infection	14
the central nervous system	14
added to each well	14
highly pathogenic avian influenza	14
in vesicular stomatitis virus	14
of middle east respiratory	14
it is possible that	13
to the plasma membrane	13
were washed twice with	13
of the vesicular stomatitis	13
of the g protein	13
the cells were then	13
attenuated vesicular stomatitis virus	13
as shown in fig	13
the cytoplasmic tail of	13
protein of vesicular stomatitis	13
in the brains of	13
with vesicular stomatitis virus	13
a recombinant vesicular stomatitis	13
at a multiplicity of	13
of west nile virus	13
cells were treated with	12
described in materials and	12
was added to the	12
it is likely that	12
inhibition of host protein	12
as described in the	12
at the plasma membrane	12
the ebov gp pseudotyped	12
ebov gp pseudotyped vsv	12
incubated for h at	12
was used as a	12
a single dose of	12
to the cell surface	12
a multiplicity of infection	12
in materials and methods	12
in the golgi complex	12
the golgi exclusion zone	12
the resulting residue was	12
at h post transfection	12
the top of the	11
on the cell surface	11
of protein synthesis in	11
the wnv e glycoprotein	11
of the viral envelope	11
these results indicate that	11
for min at room	11
of hepatitis c virus	11
of bv or mlt	11
in cells infected with	11
as described in materials	11
at a dilution of	11
the inhibitory effect of	11
g protein of vsv	11
then infected with vsv	11
with severe acute respiratory	11
inhibited the replication of	11
type i ifn signaling	11
vesicular stomatitis virus and	11
washed three times with	11
antiviral activity of rfeifn	11
of recombinant vesicular stomatitis	11
of rous sarcoma virus	11
the presence of the	11
a consequence of the	11
herpes simplex virus type	11
and the reaction mixture	11
vesicular stomatitis virus expressing	11
vesicular stomatitis virus matrix	10
of type i ifn	10
syndrome coronavirus spike protein	10
were obtained from the	10
by vesicular stomatitis virus	10
residue was purified by	10
at the level of	10
resulting residue was purified	10
respiratory syndrome coronavirus spike	10
gel column chromatography using	10
by silica gel column	10
used in this study	10
cells were washed twice	10
vesicular stomatitis virus infection	10
cells were seeded in	10
reaction mixture was stirred	10
were washed with pbs	10
vesicular stomatitis virus recombinants	10
stomatitis virus g protein	10
was purified by silica	10
m a b s	10
purified by silica gel	10
the vsv g protein	10
expression of p y	10
silica gel column chromatography	10
the antiviral activities of	10
cells were inoculated with	10
were shown to be	10
of human immunodeficiency virus	10
of influenza a viruses	10
of the viral genome	10
of the stacking gel	9
these results suggest that	9
cells were fixed with	9
as the eluent to	9
at the end of	9
for h before being	9
can be activated by	9
the neutralization test using	9
the glycoprotein of vesicular	9
have been shown to	9
in mice immunized with	9
the reciprocal of the	9
from the endoplasmic reticulum	9
ripa branch of irf	9
the size of the	9
had no effect on	9
the inhibition of host	9
was significantly stronger than	9
surface of the er	9
was added to each	9
cells were washed with	9
to be associated with	9
a stirred solution of	9
stomatitis virus matrix protein	9
in prok treated virions	9
rna replicates were detected	9
of the host cell	9
to a stirred solution	9
were washed three times	9
removed and the cells	9
for the development of	9
the eluent to give	9
an important role in	9
antiviral activities of rfeifn	9
the ebola virus glycoprotein	9
the severe acute respiratory	9
against fcov and vsv	9
replicates were detected by	9
stronger than that of	9
in the viral envelope	9
cells were then washed	9
significantly stronger than that	9
was removed and the	9
at the restrictive temperature	9
top of the stacking	9
position in the genome	8
cells were washed three	8
pretreated or not with	8
studies have shown that	8
p y and p	8
based on a replication	8
of a novel coronavirus	8
been shown to be	8
supplemented with fetal bovine	8
as a positive control	8
for host cell entry	8
incubated for min at	8
reads that map to	8
mutation of the gxxxg	8
in comparison to the	8
and nhei restriction sites	8
of the lipid bilayer	8
were infected with vsv	8
the first position in	8
a small amount of	8
was found to be	8
mice per infected group	8
t cells were transfected	8
in the transmembrane domain	8
vesicular stomatitis virus is	8
number of er buds	8
with a single dose	8
to each well and	8
female balb c mice	8
retained in the golgi	8
animal care and use	8
mechanism of host shutoff	8
no effect on the	8
is consistent with the	8
s pseudoparticle neutralization assay	8
genes of vesicular stomatitis	8
regions of the brain	8
and vesicular stomatitis virus	8
of the gxxxg motif	8
sites were analyzed by	8
y and p y	8
were carried out in	8
proteolytic cleavage of the	8
three times with pbs	8
with fetal bovine serum	8
of viral protein synthesis	8
were pretreated or not	8
a single immunization with	8
of severe acute respiratory	8
for the treatment of	8
as a result of	8
the first aug codon	8
institutional animal care and	8
host protein synthesis is	8
first position in the	8
isolation and characterization of	8
the end of the	8
the inoculum was removed	8
the ripa branch of	8
vesicular stomatitis virus in	8
the replication of vsv	8
the g protein of	8
stomatitis virus vectors in	7
by standard plaque assay	7
column chromatography using hexane	7
in the context of	7
mlt h n treated	7
a final concentration of	7
in contrast to the	7
national institutes of health	7
h n treated mice	7
cell lines from the	7
in the development of	7
for the study of	7
the surface of baculovirus	7
chromatography using hexane and	7
balb c mice were	7
untreated with the ifns	7
competent vesicular stomatitis virus	7
cells were washed and	7
use of laboratory animals	7
of the recombinant feifn	7
based on live attenuated	7
mixture was stirred at	7
on the viral surface	7
cells were extensively washed	7
against lethal challenge with	7
an effective aids vaccine	7
the west nile virus	7
cells untreated with the	7
respiratory syndrome coronavirus infection	7
in the neutralization test	7
viruses as vaccine vectors	7
centers for disease control	7
hexane and ethyl acetate	7
viral and cellular mrnas	7
vaccine based on live	7
plotted as mean sd	7
these data suggest that	7
do not affect the	7
nucleotide sequence of the	7
vsv replication in the	7
of the influenza virus	7
evaporated under reduced pressure	7
neutralization test using vsv	7
of the ebola virus	7
care and use of	7
and analyzed by sds	7
of the vsv g	7
mice immunized with n	7
higher than that of	7
a wide range of	7
the absence of a	7
care and use committee	7
live ebov neutralisation assay	7
and use of laboratory	7
immunized with n ct	7
at the top of	7
our results demonstrate that	7
used as a control	7
with a recombinant vesicular	7
eluent to give the	7
vaccination with a recombinant	7
than that of rfeifn	7
as a vaccine vector	7
at the cell surface	7
the start of the	7
the medium was removed	7
and heterologous animal cells	7
using hexane and ethyl	7
aids vaccine based on	7
the spike protein of	7
cells infected with vsv	7
the synthesis of a	7
the expression of p	7
m and g proteins	7
pseudotyped with severe acute	7
of cap binding factor	7
host protein synthesis by	7
each well and incubated	7
h and then infected	7
are shown as mean	6
medium was replaced by	6
virus vectors expressing glycoproteins	6
with a lethal dose	6
live attenuated vesicular stomatitis	6
see materials and methods	6
host cell protein synthesis	6
cells were grown in	6
in addition to the	6
the major surface glycoprotein	6
we found that the	6
was used as the	6
in vivo and in	6
were analyzed by sds	6
of the glycoproteins of	6
in cells infected by	6
from the first position	6
disease control and prevention	6
of semliki forest virus	6
the matrix protein of	6
x for peer review	6
were incubated for h	6
it is important to	6
are included in the	6
and vsv was significantly	6
on the transcriptional activity	6
cells were then infected	6
is not required for	6
the m g cap	6
translation of viral mrnas	6
the interior of the	6
vivo and in vitro	6
similar to that of	6
of vero e cells	6
in adp p y	6
the major enu start	6
washed twice with pbs	6
a significant difference between	6
of the spike protein	6
antiviral activity of the	6
was not required for	6
were then infected with	6
of newcastle disease virus	6
vesicular stomatitis virus pseudotype	6
protein synthesis in cells	6
the plates were incubated	6
on vero e cells	6
synthesis in cells infected	6
one of the most	6
gxxxg motif in the	6
oncolytic vesicular stomatitis virus	6
for the presence of	6
of influenza a virus	6
in dmem containing fbs	6
for disease control and	6
host cell plasma membrane	6
was detected by q	6
to the golgi complex	6
for peer review of	6
that the inhibitory effect	6
viral spread in tetherin	6
on live attenuated vesicular	6
guide for the care	6
than that of intercat	6
vectors expressing glycoproteins of	6
pseudotyped virus neutralisation assays	6
major surface glycoprotein of	6
total number of er	6
was kindly provided by	6
of herpes simplex virus	6
were treated with adp	6
of the cytoplasmic tail	6
for the production of	6
into the plasma membrane	6
of wt and ifit	6
have shown that the	6
the external surface of	6
inoculum was removed and	6
infection of hela cells	6
also inhibited the replication	6
the replication of both	6
persistently or latently infected	6
expressing glycoproteins of filoviruses	6
modified vaccinia virus ankara	6
retention in the golgi	6
were collected from the	6
vesicular stomatitis viruses from	6
the cells were treated	6
fold serial dilutions of	6
cells were obtained from	6
the results showed that	6
epitopes on g protein	6
infected wt and ifit	6
fcov and vsv was	6
that of intercat ifn	6
as a colorless oil	6
for the care and	6
an additional transcription unit	6
and evaporated under reduced	6
a library of fda	6
autographa californica nuclear polyhedrosis	6
the care and use	6
vesicular stomatitis virus as	6
vsv was significantly stronger	6
of host cell protein	6
mrnas with increased polysome	6
n mice per infected	6
inhibitory effect of pis	6
shutoff of host protein	6
in this study were	6
effective aids vaccine based	6
were metabolically labeled for	6
of filoviruses and arenaviruses	6
a consequence of a	6
and supplementary figure s	6
strongly inhibited by doxorubicin	6
these results demonstrate that	6
from the e r	6
by the presence of	6
vesicular stomatitis virus by	6
glycoproteins of filoviruses and	6
were analyzed by the	6
were found to be	6
of the virus in	6
shown in figure a	6
matrix protein of vesicular	6
major enu start site	6
the cells were extensively	6
a lethal dose of	6
generation of vsv pseudotypes	6
californica nuclear polyhedrosis virus	6
the mechanism by which	6
of vsv pseudotypes using	5
throughput screen of a	5
incorporated efficiently into virus	5
revealed the presence of	5
that pis do not	5
observed when comparing the	5
with an moi of	5
bars represent the mean	5
transfection medium was replaced	5
type i and i	5
functional receptor for the	5
of the influenza virion	5
of a vesicular stomatitis	5
at h post infection	5
virus infection of the	5
initiation of protein synthesis	5
between groups compared by	5
were carried out by	5
ebov gp pseudotyped virus	5
type ii transmembrane serine	5
mrna was detected by	5
efficiently into virus particles	5
inhibition of host cell	5
on ace and tmprss	5
and immune responses to	5
for studies on virus	5
used to assess the	5
virus and vesicular stomatitis	5
matrix protein inhibits host	5
vesicular stomatitis viruses as	5
of the leader sequence	5
west nile virus encephalitis	5
either immediately or after	5
surface glycoprotein of vesicular	5
h and then intraperitoneally	5
and tmprss and is	5
fig a and b	5
of attenuated vesicular stomatitis	5
were observed when comparing	5
to the use of	5
on the viral envelope	5
of a library of	5
it is not known	5
are associated with the	5
antiviral activity against vsv	5
used as negative controls	5
cell protein synthesis by	5
coronavirus infection conferred by	5
of the central nervous	5
the highest dilution of	5
hela cells were treated	5
vsv for studies on	5
stomatitis virus infection of	5
intraperitoneally injected with vsv	5
would like to thank	5
g pseudotyped lentiviral vectors	5
the guide for the	5
dmem supplemented with fbs	5
of antibody with the	5
compared to the control	5
a functional receptor for	5
the type i ifn	5
immunization with an attenuated	5
average number of buds	5
surface of the virion	5
are incorporated efficiently into	5
internal surface of the	5
of cargo from the	5
supplementary figure s a	5
influenza a h n	5
transport of vesicular stomatitis	5
the endoplasmic reticulum to	5
this work was supported	5
single immunization with an	5
at a moi of	5
the lumenal domain of	5
were used as negative	5
vsv rna replicates were	5
play an important role	5
and ifit mice at	5
er to golgi transport	5
we were able to	5
hela cells expressing gml	5
by a clinically proven	5
spike protein of sars	5
studies on virus entry	5
depends on ace and	5
sars coronavirus infection conferred	5
ripa contributes to the	5
stomatitis viruses as vaccine	5
the prrsv envelope proteins	5
t cell responses in	5
as shown in table	5
i and i glycopeptides	5
difference between groups compared	5
the interaction of antibody	5
i ifn signaling competent	5
attenuated vesicular stomatitis viruses	5
reciprocal of the highest	5
the authors declare that	5
from host to viral	5
ifit mice at d	5
foreign glycoproteins expressed from	5
using intercat ifn for	5
immune responses to vaccines	5
before being treated with	5
the fourth transcription unit	5
compared to the only	5
viruses are incorporated efficiently	5
of the type i	5
is a functional receptor	5
with the exception of	5
the vsv g gene	5
the expression of the	5
it has been suggested	5
cells were incubated at	5
the translation of viral	5
of the golgi complex	5
were determined to be	5
and downstream of the	5
regulation of protein synthesis	5
against a variety of	5
in their soluble forms	5
as a bioisostere of	5
by host cell proteases	5
from sars coronavirus infection	5
is blocked by a	5
described in the results	5
the background level of	5
the erk signaling pathway	5
from recombinant vesicular stomatitis	5
ni affinity column chromatography	5
in line with the	5
characterization of a novel	5
number of buds per	5
titers were determined by	5
antiviral activity of doxorubicin	5
work was supported by	5
was carried out in	5
by a single immunization	5
protection from sars coronavirus	5
the centers for disease	5
vaccine vector based on	5
viral mrna cap methylation	5
complete nucleotide sequence of	5
of ebola virus glycoprotein	5
in three independent experiments	5
balance between pathogenesis and	5
cells infected with a	5
and then intraperitoneally injected	5
rna and dna viruses	5
clinically proven protease inhibitor	5
of acid sphingomyelinase and	5
vesicular stomatitis virus pseudotypes	5
replication of the virus	5
the cells were fixed	5
endoplasmic reticulum to golgi	5
against ebola and marburg	5
the presence of a	5
the cells were incubated	5
antibody with the major	5
the transmembrane domain of	5
pathogenic avian influenza virus	5
identification of entry inhibitors	5
of the golgi exclusion	5
added and incubated for	5
vsvs with mutated m	5
the activity of the	5
as well as for	5
control of protein synthesis	5
expressed from recombinant vesicular	5
during the preparation of	5
than that of the	5
motif in the transmembrane	5
then intraperitoneally injected with	5
ebov gp pseudotyped viruses	5
that adp p y	5
in order to assess	5
tmprss and is blocked	5
has been suggested that	5
of the vaccinated mice	5
on vesicular stomatitis virus	5
frozen in liquid nitrogen	5
does not appear to	5
with pfu of vsv	5
by herpes simplex virus	5
switch from host to	5
protects nonhuman primates against	5
viral protein synthesis in	5
and incubated for min	5
results indicate that the	5
in vitro antiviral activity	5
ace and tmprss and	5
cytoplasmic tail of gml	5
activation of acid sphingomyelinase	5
results led us to	5
as a consequence of	5
subtypes of feline ifn	5
against west nile virus	5
performed using graphpad prism	5
tag ni affinity column	5
pis do not affect	5
at the time of	5
vaccine based on a	5
screen of a library	5
treated or not with	5
cells were pretreated or	5
and then chased for	5
gml or vsv g	5
the cellular mrnas that	5
plates were incubated for	5
was removed and cells	5
whether the antiviral activities	5
the plane of the	5
stomatitis viruses from dna	5
the ability of the	5
glycoproteins expressed from recombinant	5
lentiviral vectors pseudotyped with	5
infection conferred by a	5
the transfection medium was	5
by proteolytic cleavage of	5
background level of neutralisation	5
a mw of approximately	5
the human immunodeficiency virus	5
off host protein synthesis	5
interaction of antibody with	5
the airway epithelial cells	5
vesicular stomatitis virus replicon	5
g n and g	5
at room temperature for	5
y mrna was detected	5
of the ifn system	5
washed with pbs containing	5
virus matrix protein inhibits	5
after infection with a	5
removed and cells were	5
the renal epithelial cells	5
when comparing the rfeifn	5
is thought to be	5
a final volume of	5
hela cells were transfected	5
n and g c	5
blocked by a clinically	5
vsv pseudotypes using recombinant	5
the normal shutoff mechanism	5
in vsv infected cells	5
intercat ifn for comparison	5
hek t cells were	5
the average number of	5
with west nile virus	5
the brains of ifit	5
stomatitis viruses are incorporated	5
dmem containing fbs and	5
enveloped viruses such as	5
indicates a significant difference	5
at the elevated temperature	5
supernatants were harvested and	5
virus vectors in non	5
to the intercat ifn	5
significant difference between groups	5
a comparison of the	5
it remains to be	5
nonhuman primates against ebola	5
of infectious virus particles	5
in the central nervous	5
and is blocked by	5
surface area of the	5
at an moi of	5
inhibition of host translation	5
metabolically radiolabeled for min	5
with the major surface	5
vesicular stomatitis viruses are	5
error bars indicate the	5
these findings suggest that	5
sars vaccine based on	5
inhibits the replication of	5
data are shown as	5
retroviral vectors pseudotyped with	5
viral envelope with the	5
g or vsv m	5
with a moi of	5
attenuated vsvs with mutated	5
at room temperature with	5
ebola and marburg viruses	5
the total cytoplasmic fraction	5
sem for each group	5
the host cell and	5
conferred by a single	5
vaccine protects nonhuman primates	5
the innate antiviral response	5
a clinically proven protease	5
medium was removed and	5
whole and prok treated	5
a wide variety of	5
p y mrna was	5
mean sd on log	4
to give the corresponding	4
amino acid composition of	4
cytoplasmic accumulation of late	4
of s ribosomal subunits	4
of pseudotyped virus input	4
and titrated for the	4
a variety of viruses	4
the presence of pis	4
virus expressing an influenza	4
vesicular stomatitis virus vector	4
of bat cell lines	4
infection with an moi	4
respiratory syndrome coronavirus s	4
a portion of the	4
inhibit acid sphingomyelinase activity	4
assays were carried out	4
term protection from sars	4
mice were intraperitoneally treated	4
of the gml oligomer	4
were separated by sds	4
may contribute to the	4
values were normalized to	4
mice were anesthetized with	4
associated with the interior	4
was defined as the	4
series of concentric shells	4
stomatitis virus expressing an	4
in uitro translation of	4
was observed in the	4
particles was assessed h	4
mutated m and or	4
cleavage of the hemagglutinin	4
and or g proteins	4
and the plates were	4
the overall translational capacity	4
the infectivity of the	4
fourth transcription unit of	4
and vero e cells	4
accumulation of late viral	4
cellular immune responses against	4
the volume of the	4
the genes encoding feifn	4
involved in promoting ripa	4
characterization of vesicular stomatitis	4
primates against ebola and	4
inhibited the transcriptional activity	4
susceptible to vsv infection	4
grown in these cells	4
in the formation of	4
doxorubicin inhibits the replication	4
signal promotes stable expression	4
from the plasma membrane	4
viral protein expression led	4
the switch from host	4
release of cytochrome c	4
assay for detection of	4
from triplicate in three	4
robust increase in rlr	4
virus entirely from cdna	4
both g and m	4
host protein synthesis and	4
l p r e	4
the cells were infected	4
institute of allergy and	4
attenuated recombinant vaccine protects	4
incorporate high levels of	4
the absence of va	4
sd on log scale	4
we conclude that budding	4
the activation of acid	4
and incubated for h	4
of the genes of	4
with an attenuated vsv	4
recovery of infectious vesicular	4
to a final concentration	4
be associated with the	4
infectious virus particle release	4
using previously described procedures	4
the authors would like	4
african green monkey kidney	4
medium at a final	4
cells were fixed and	4
vesicular stomatitis virus with	4
our results show that	4
the replication competent construct	4
we have previously shown	4
the world health organization	4
added to the cells	4
gp pseudotyped virus neutralisation	4
a novel coronavirus associated	4
is more potent than	4
the exterior of the	4
m and or g	4
the live ebov neutralisation	4
c into the cytosol	4
the distribution of vsv	4
that viral mrnas are	4
to as export complexes	4
organization of er export	4
the expression of vsv	4
cells were challenged with	4
nipah virus fusion protein	4
cells were further incubated	4
the caudal thigh muscle	4
were intraperitoneally treated with	4
being exposed to adp	4
a protective immune response	4
analysis was performed using	4
stirred at room temperature	4
plaque reduction neutralization test	4
mg ml of bsa	4
stirred at the same	4
values obtained from triplicate	4
viruses in vitro and	4
host to viral translation	4
positive in the neutralization	4
the molecular weights of	4
using vesicular stomatitis virus	4
of the serum samples	4
to resume virus production	4
were added to the	4
for their ability to	4
with increased polysome association	4
expressing an influenza virus	4
to that of the	4
the virus life cycle	4
a and b viruses	4
the volatiles were removed	4
is sufficient to mediate	4
foreign gene in vesicular	4
presence of gtp s	4
cell entry depends on	4
in homologous and heterologous	4
under a co atmosphere	4
markers nestin and sox	4
from the cotton rat	4
other values were normalized	4
it is known that	4
inhibition of protein synthesis	4
virus particle release from	4
p r o o	4
of cytochrome c into	4
after the volatiles were	4
recombinants that express and	4
a novel coronavirus from	4
detected by western blotting	4
cov neutralizing antibody titers	4
of the virus to	4
cells were incubated for	4
intraperitoneally treated with adp	4
treatment with cytochalasin d	4
the antiviral action of	4
between viral and cellular	4
as evidenced by the	4
the antiviral function of	4
of the hemagglutinin polypeptide	4
cells were incubated with	4
presence of the sarl	4
are highly susceptible to	4
was added and incubated	4
before being exposed to	4
moloney murine leukemia virus	4
against yersinia pestis challenge	4
induction conditions for rfeifn	4
perfusion with ml of	4
rna polymerase of vesicular	4
for the prevention of	4
play a more important	4
at a final volume	4
under a fluorescence microscope	4
spectrum antiviral activities of	4
defined as the highest	4
is known to be	4
be a consequence of	4
vaccine vectors in a	4
in the serum of	4
was assessed h after	4
expression were an iptg	4
has the potential to	4
protection against yersinia pestis	4
a single amino acid	4
an antibody titer of	4
membrane fusion activity of	4
by batfluav surface proteins	4
generation of vesicular stomatitis	4
saturated nahco aqueous solution	4
results demonstrate that the	4
ebola virus glycoprotein is	4
during vesicular stomatitis virus	4
a colorless sticky oil	4
events in the viral	4
of the plasma membrane	4
of bv and mlt	4
favorable immune cell targeting	4
which is essential for	4
in wt and ifit	4
as the reciprocal of	4
the mean surface of	4
stirred solution of alcohol	4
supernatants were harvested at	4
the antiviral effects of	4
the parainfluenza virus sv	4
minimal conserved transcription stop	4
budding from the er	4
a foreign gene in	4
vesicular stomatitis virus envelope	4
glycosylation sites were analyzed	4
a l p r	4
cell markers nestin and	4
more important role than	4
virus is more potent	4
signal peptide cleavage sites	4
to intranasal vsv infection	4
the host cell membrane	4
served as negative control	4
a gxxxg motif in	4
we refer to as	4
safety and immunogenicity of	4
vectors expressing antigens from	4
of mammalian cells by	4
efficient recovery of infectious	4
a type i ifn	4
the surface of infected	4
replication in the absence	4
of the mrna cap	4
which is known to	4
high levels of hepatitis	4
is responsible for the	4
for vesicular stomatitis virus	4
new subtypes of feline	4
is not included in	4
these observations suggest that	4
interior of the virion	4
under the control of	4
the national institutes of	4
hepatitis c virus glycoproteins	4
syndrome coronavirus infection in	4
viral mrnas are present	4
of hpai h n	4
infected with vsv and	4
pattern of codon usage	4
and a small amount	4
dependent on eif e	4
may not be the	4
of host translation in	4
translation of poliovirus rna	4
the innate immune response	4
nd and th fractions	4
protein expression led to	4
of infectious vesicular stomatitis	4
h before being treated	4
of the human immunodeficiency	4
of the population of	4
activity was detected in	4
for min in the	4
expressed in their soluble	4
on the external surface	4
as a danger signal	4
a low dose of	4
the culture medium was	4
and incorporate high levels	4
as the highest dilution	4
were added to each	4
mean surface of the	4
endoplasmic reticulum to the	4
immune response in mice	4
based on recombinant vesicular	4
vectors pseudotyped with severe	4
levels of hepatitis c	4
epithelial cell lines from	4
we examined whether doxorubicin	4
the location of the	4
the use of live	4
vsv and influenza virus	4
to determine whether the	4
was not due to	4
solubilized either immediately or	4
of the virus and	4
domain of vsv g	4
of the ha spike	4
infectious vesicular stomatitis virus	4
infected insect cells and	4
u r n a	4
by titration of supernatants	4
bars indicate the range	4
that budding from the	4
r n a l	4
approved by the institutional	4
vsv rna levels in	4
pathogenic avian influenza viruses	4
of the endoplasmic reticulum	4
well and incubated at	4
of this study was	4
order of transcription of	4
entirely from cdna clones	4
on recombinant vesicular stomatitis	4
external surface of the	4
of influenza a and	4
from influenza virus challenge	4
obtained from triplicate in	4
influenza virus hemagglutinin provides	4
of allergy and infectious	4
for the generation of	4
of values obtained from	4
metabolically labeled for min	4
it was shown that	4
and not the transcriptional	4
is not known which	4
a starting dilution of	4
to investigate whether the	4
the jak stat pathway	4
as compared to the	4
authors would like to	4
rna was isolated from	4
were normalized to this	4
demonstrate that doxorubicin inhibits	4
plates were incubated at	4
o u r n	4
gfp expression levels were	4
the prokaryotic soluble expression	4
lethal ebola virus infection	4
at the same temperature	4
gfp expression at hpi	4
promoted the ripa branch	4
are available upon request	4
as well as in	4
associated with export complexes	4
indiana and new jersey	4
analyses were performed using	4
refer to as export	4
after infection by titration	4
a beckman sw ti	4
novel coronavirus associated with	4
the range of values	4
and virus infection without	4
triplicate in three independent	4
in the polysome fraction	4
at the permissive temperature	4
stomatitis virus recombinants that	4
it is difficult to	4
of alfalfa mosaic virus	4
with phosphate buffered saline	4
complete protection from influenza	4
and an induction time	4
the minimal conserved transcription	4
were observed between rfeifn	4
or vsv g were	4
on g protein of	4
ripa by activating the	4
and the expression of	4
displayed on the surface	4
enhanced green fluorescent protein	4
by the addition of	4
the lipid bilayer of	4
g and vsv m	4
were fixed with paraformaldehyde	4
expressing the wnv e	4
hemagglutinin provides complete protection	4
an induction time of	4
were metabolically radiolabeled for	4
an equal volume of	4
a bioisostere of lamivudine	4
at the same time	4
recombinant vsvs expressing the	4
the presence of measles	4
in a biosafety level	4
vesicular stomatitis virus pseudotyped	4
was determined to be	4
to differences in the	4
with the lipid bilayer	4
statistical analyses were performed	4
similar results were obtained	4
transport from the endoplasmic	4
prime boost vaccination with	4
detected in mice immunized	4
and they are not	4
are shown in fig	4
antiviral activity of bv	4
as indicated in the	4
potent than one based	4
cells were grown on	4
not included in the	4
is required for efficient	4
optimal induction conditions for	4
to be the most	4
the outcome of the	4
j o u r	4
our study provides a	4
national institute of allergy	4
h before being exposed	4
stomatitis virus is more	4
but not the transcriptional	4
as compared to wild	4
it is possible to	4
no significant differences in	4
compared to wt mice	4
more potent than one	4
to those of the	4
the portion of the	4
the removal of the	4
because it is the	4
microdose cytopathic effect inhibition	4
in the mouse model	4
production of high titer	4
directed expression of tetherin	4
significantly higher than that	4
and herpes simplex virus	4
the replication of hsv	4
in vero e cells	4
work was funded by	4
expression of epac was	4
and expressed as log	4
cytoplasmic tail of vsv	4
cd cd cd low	4
protection from influenza virus	4
medium and the cells	4
results demonstrate that doxorubicin	4
r o o f	4
that express and incorporate	4
live attenuated recombinant vaccine	4
in hek t cells	4
and prok treated virions	4
the authors declare no	4
infection was determined by	4
vesicular stomatitis virus mrnas	4
the absence of irf	4
t cells were seeded	4
cells were lysed in	4
beckman sw ti rotor	4
different attenuated vsvs with	4
a more important role	4
induction time of h	4
figure d and e	4
than one based on	4
the supernatants were harvested	4
with truncated g protein	4
in a suboptimal context	4
polymerase of vesicular stomatitis	4
is likely to be	4
in balb c mice	4
was a consequence of	4
as a colorless sticky	4
with mutated m and	4
protein expression were an	4
the development of vaccines	4
of uninfected or vsv	4
influenza a and b	4
we then tested whether	4
the envelope proteins of	4
blocked formation of sds	4
vesicular stomatitis virus to	4
of the ebov gp	4
the characteristics of the	4
stomatitis virus entirely from	4
then infected with hsv	4
virus and host cell	4
were used for the	4
were an iptg concentration	4
infection with a moi	4
can be used to	4
with the negative control	4
test using live mers	4
determined by standard plaque	4
alfalfa mosaic virus rna	4
the rna expression of	4
of a foreign gene	4
cells were plated in	4
the presence or absence	4
the organic layer was	4
the cells were transfected	4
the addition of the	4
cells were stained with	4
range of values obtained	4
transduction of mammalian cells	4
in different regions of	4
were identified based on	4
their antiviral activities were	4
using the immunodiffusion protocol	4
different regions of the	4
being treated with adp	4
in the course of	4
xhoi and nhei restriction	4
for hour at room	4
or not with esi	4
n a l p	4
did not result in	4
bv or mlt against	4
express and incorporate high	4
doxorubicin inhibits the transcriptional	4
analysis of ebola virus	4
virus recombinants that express	4
h after infection by	4
one based on a	4
carried out in a	4
shutoff of host translation	4
human t cell leukemia	4
cap binding protein complex	4
neutralizing antibody titers in	4
the shutoff of host	4
was stirred at the	4
promotes stable expression of	4
cytochrome c into the	4
for the induction of	4
rna was extracted from	4
described in the materials	4
but it is not	4
based neutralization assay for	4
stem cell markers nestin	4
experiments were performed in	4
of mabs to ep	4
increase in ge copies	4
formed in the presence	4
in place of the	4
hela and mdck cells	4
reticulum to the golgi	4
gene in vesicular stomatitis	4
we were unable to	4
was determined using the	4
the optimal induction conditions	4
at the nuclear margin	4
stable expression of a	4
ii transmembrane serine proteases	4
for the renal epithelial	4
in a variety of	4
indicate the range of	4
the translation of capped	4
in the figure legends	4
hela cells were infected	4
upstream and downstream of	4
novel vesicular stomatitis virus	4
identified in whole virions	4
recombinant vaccine protects nonhuman	4
expression of a foreign	4
start signal promotes stable	4
were expressed as mean	4
further attenuated rvsv vectors	4
of the virus life	4
production of monoclonal antibodies	4
further incubated for h	4
provides complete protection from	4
hour at room temperature	4
have previously shown that	4
homologous and heterologous animal	4
rpm and uc for	4
following lethal ebov challenge	4
of approximately kda and	4
the infectivity of influenza	4
ideal balance between pathogenesis	4
by the fact that	4
with the interior of	4
in both sample types	4
with live ebov neutralisation	4
both in vitro and	4
the presence of cytosol	4
in pbs for h	4
an influenza virus hemagglutinin	4
syndrome coronavirus s protein	4
through a sucrose cushion	4
the synthesis of viral	4
titration of supernatants on	4
fbs was added to	4
in type i ifn	4
a variety of different	4
at a starting dilution	4
the negative control pnhs	4
is one of the	4
cells were maintained in	4
cellular mrnas that exhibit	4
virus hemagglutinin provides complete	4
host cell gene expression	4
vero e cells were	4
has been reported to	4
presence or absence of	4
assessed h after infection	4
with expression plasmids for	4
as mean sd on	4
an iptg concentration of	4
as a mechanism for	4
based on vesicular stomatitis	4
were performed using graphpad	4
entry depends on ace	4
vesicular stomatitis virus entirely	4
a dose of pfu	4
of influenza virus glycoproteins	4
was approved by the	4
central nervous system of	4
protein inhibits host cell	4
associated with the viral	4
were further incubated for	4
infection by titration of	4
the internal surface of	4
the mechanism of host	4
ebola virus entry requires	3
were washed and then	3
a credit line to	3
antibody at a dilution	3
gloma multi dectection luminometer	3
have been described previously	3
differences were observed between	3
is licensed under a	3
the number of elements	3
release from infected cells	3
entirely within the cytoplasm	3
the stem cell markers	3
or may not be	3
and murine leukemia virus	3
and data not shown	3
single immunization with a	3
transcription of genes of	3
for the rapid and	3
panel of human sera	3
stomatitis virus expressing cottontail	3
for the preparation of	3
have a mw of	3
the rate of viral	3
of the severe acute	3
you will need to	3
transport and translation of	3
of influenza virus mrnas	3
type i ifn family	3
the attenuation of vsv	3
may be involved in	3
genes identified in this	3
virus pseudotyped with severe	3
translated more efficiently than	3
replication in tissue culture	3
method of estimating fifty	3
although there was a	3
of influenza c virus	3
and the antiviral activities	3
terminal portion of the	3
neutralization test using live	3
and entry of the	3
stomatitis virus as an	3
and intramuscular vaccination routes	3
carbohydrate composition of the	3
virus vectors expressing herpes	3
with equal volumes of	3
groups i and ii	3
rest of the brain	3
papillomavirus l protein provides	3
budding from the e	3
protection of nonhuman primates	3
inserted into the fourth	3
of nihon university were	3
or decreased polysome association	3
cells were harvested at	3
in the viral genome	3
a human immunodeficiency virus	3
of genes of vesicular	3
used as the antigen	3
to be translated in	3
neutralise the ebov gp	3
have been isolated from	3
were expressed as the	3
the fusion of viral	3
the competitive binding assay	3
synthesis and assembly of	3
activation of influenza a	3
treated cells than the	3
emanating from the er	3
against ebov gp pseudotyped	3
were heat inactivated at	3
contributes to the optimal	3
at a density of	3
mutations in the rvsv	3
to the rbd of	3
challenge in macaques by	3
in the same context	3
for the emerging human	3
a second bud in	3
s c and d	3
were immunoprecipitated using anti	3
of the viral proteins	3
treated cells as compared	3
in the prefusion conformation	3
expression in the wt	3
animals in each group	3
our results indicate that	3
fusion between viral envelope	3
is not involved in	3
the same temperature for	3
line to the material	3
titers in supernatants were	3
their evolutionary relationship to	3
of ebola virus entry	3
the institutional animal care	3
with vrp expressing the	3
the first aug triplet	3
complete sequence of the	3
supplementary figure s e	3
complete protection against papillomavirus	3
n and h n	3
by intramuscular injection of	3
were determined by plaque	3
antibody titers in the	3
by gloma multi dectection	3
accreditation of laboratory animal	3
enhancement of the infectivity	3
can induce immune responses	3
which can be activated	3
cells expressing gml or	3
fusion activity of the	3
small amount of methanol	3
black creek canal virus	3
buds emanating from the	3
with cytochalasin d blocked	3
were prepared as described	3
identified in this study	3
neurovirulence properties of recombinant	3
protective humoral and cellular	3
it was reported that	3
is necessary for infection	3
hamsters against lethal challenge	3
transfected with increasing amounts	3
previous work demonstrated that	3
to drive efficient budding	3
cells were used for	3
was no antiviral activity	3
increase in viral rna	3
a novel vesicular stomatitis	3
mice were im vaccinated	3
surface of infected cells	3
surface density of vsv	3
and reproduction in any	3
a high throughput screen	3
th immune responses and	3
evolution and ecology of	3
bvdv or pedv by	3
type i and type	3
permission directly from the	3
with fbs was added	3
to a monolayer of	3
em structure of the	3
we wanted to investigate	3
efficient than host mrnas	3
were extensively washed and	3
of the total number	3
spectrum of enveloped viruses	3
article are included in	3
virus entry by using	3
of these cell lines	3
of the vaccinia virus	3
neutralization tests using vsv	3
and all other values	3
the release of ceramide	3
statistical analysis was performed	3
grown in the presence	3
component of the oligomer	3
monoclonal antibodies to the	3
attenuation of vsv m	3
first line of defense	3
in the materials and	3
eukaryotic ribosomes can initiate	3
immune responses in mice	3
the cytoplasmic accumulation of	3
due to differences in	3
challenge with a lethal	3
at a concentration of	3
in the control of	3
guinea pigs immunized with	3
more resistant than host	3
gml were metabolically labeled	3
a variety of pathogens	3
article is licensed under	3
fresh medium was added	3
immunoblotting with hybridoma antibodies	3
titer was determined as	3
washed six times in	3
a mechanism for their	3
of the distribution of	3
appropriate credit to the	3
induced high levels of	3
between wt and ifit	3
of the parainfluenza virus	3
entry requires the cholesterol	3
of radiolabeled vsv to	3
mice from lethal challenge	3
and incubated for hr	3
with saturated nahco aqueous	3
multiplication in and transmission	3
in our previous study	3
these data demonstrated that	3
the carboxyl terminus of	3
during the course of	3
to the creative commons	3
efficiency as compared to	3
with the same enzymes	3
strong humoral and cellular	3
of intranasal and intramuscular	3
while the boosted group	3
and the occurrence of	3
drive efficient budding of	3
previous studies have shown	3
protects hamsters against lethal	3
virus and modified vaccinia	3
of the synthesis of	3
vector and vaccine candidate	3
a m o n	3
neutral with regard to	3
have not yet been	3
sterilizing immunity against heterologous	3
statistically significant difference in	3
adp p y restricts	3
responses and are protective	3
guinea pig and nhp	3
either one or both	3
antiviral properties of bv	3
of the transmembrane domain	3
were removed in vacuo	3
the production of high	3
virus vectors expressing avian	3
of cellular protein synthesis	3
a panel of human	3
vesicular stomatitis virus the	3
between vesicular stomatitis virus	3
of the cytoplasmic mrna	3
proteins of zaire ebolavirus	3
and the release of	3
models of vaginal challenge	3
resulting plasmid was designated	3
the antiviral effect of	3
and cells were washed	3
to address this question	3
stomatitis virus and modified	3
broad spectrum of enveloped	3
low concentration of cycloheximide	3
the complete sequence of	3
for min before inoculating	3
the membrane proteins of	3
recombinant feline interferon omega	3
gp of porcine reproductive	3
m o n g	3
is based on the	3
give appropriate credit to	3
and hela cells were	3
in which host protein	3
bud in the cell	3
antibody responses were detected	3
protective in mouse and	3
in mouse and guinea	3
on day after vaccination	3
rvsv vectors expressing antigens	3
more efficient than host	3
rna and protein synthesis	3
simplex virus type gd	3
that they have no	3
infectivity of influenza a	3
stomatitis viruses expressing respiratory	3
in pancreatic acinar cells	3
by the number of	3
plates were coated with	3
viruses by trypsin treatment	3
important role than m	3
in the caudal thigh	3
and p y receptors	3
entry into host cells	3
both lentiviral vectors transduced	3
were immunized three times	3
the fraction of cells	3
in minimum essential medium	3
regulation or exceeds the	3
portion of the ha	3
a man with pneumonia	3
to the host cell	3
antiviral activity detected in	3
by plaque assay on	3
of vsv has been	3
poliovirus rna in uitro	3
env and siv gag	3
nature remains neutral with	3
the dominance of viral	3
the gene expressing the	3
under normal incubation conditions	3
of female balb c	3
the interface between the	3
a potent inhibitor of	3
was performed using the	3
published in the genbank	3
bacteriophage t rna polymerase	3
in order to determine	3
as a model for	3
vesicular stomatitis virus gives	3
monoclonal antibodies against ebola	3
from a human survivor	3
supernatant was removed and	3
exceeds the permitted use	3
nile virus infection in	3
the mean cell volume	3
as is the case	3
by centrifugation at x	3
cd t cells were	3
robust cd th immune	3
kit according to the	3
tetherin counteraction by vsv	3
were cloned into the	3
the safety and immunogenicity	3
the ha and na	3
linked by disulfide bonds	3
viruses such as enterovirus	3
ifit isg and ifit	3
fig b and d	3
reticulum to golgi transport	3
of pseudotyped virus neutralisation	3
virus infection without any	3
cytopathic effect inhibition assays	3
especially strong against fcov	3
at different time points	3
out with the supernatant	3
is retained in the	3
there is no evidence	3
bioassay for the rapid	3
in a credit line	3
the host plasma membrane	3
consequence of the inhibition	3
monolayer of vero e	3
it is not clear	3
the onset of viral	3
in the amount of	3
for the airway epithelial	3
vesicular stomatitis viruses expressing	3
inhibits vsv replication in	3
in a positive way	3
surface of the lipid	3
antibodies against ebola virus	3
small fraction of the	3
buried within the lipid	3
type env and siv	3
the average of three	3
having proximity to a	3
rvsv vectors expressing hiv	3
biochemical studies revealed that	3
using methylene chloride and	3
view a copy of	3
expressing gml or vsv	3
cottontail rabbit papillomavirus l	3
we sought to determine	3
pfu g at days	3
vectors expressing avian influenza	3
to jurisdictional claims in	3
to inhibit virus infection	3
vaccinia virus ankara vaccine	3
with pneumonia in saudi	3
endosomal proteolysis of the	3
collected from the top	3
for influenza a virus	3
is not permitted by	3
for transcription but not	3
plates at a density	3
the viral life cycle	3
ml after infection with	3
with pbs and fixed	3
incorporation of a foreign	3
immunity against heterologous challenge	3
statutory regulation or exceeds	3
as described above and	3
in the first position	3
and the reverse primer	3
the most widely used	3
p y mediated antiviral	3
expression plasmids for the	3
were especially strong against	3
and b viruses by	3
the limit of detection	3
production of infectious virus	3
a novel recombinant vsv	3
chromatography using methylene chloride	3
mlui and nhei restriction	3
of hela cell protein	3
from the copyright holder	3
development of a new	3
figure s c and	3
an optimal signalase cleavage	3
an optimized vaccine vector	3
replication in the brain	3
rate limiting factor for	3
after infection with an	3
ebola virus entry by	3
which host protein synthesis	3
springer nature remains neutral	3
one log lower than	3
no role in the	3
gold particles corresponding to	3
wt and mutant lxxxl	3
hpai h n virus	3
endocytosis of viral particles	3
of avian sarcoma virus	3
using the superscript iii	3
the transmembrane domains of	3
lethal challenge with the	3
innate and adaptive immune	3
the presence of vsv	3
further studies on the	3
cells were labeled with	3
determined to be the	3
pig models of vaginal	3
of the tripartite leader	3
treating viral infections in	3
cov s protein was	3
in vitro in the	3
ifit and ifnar mice	3
the major capsid protein	3
may be related to	3
the creative commons license	3
in ge copies was	3
both wt and ifit	3
for the detection of	3
the e gene was	3
activation of hal and	3
old mice were intraperitoneally	3
this strongly suggests that	3
obtain permission directly from	3
of the virus from	3
range of different viruses	3
into the prokaryotic soluble	3
cells infected with herpes	3
neutralization assay for nipah	3
by a variety of	3
cytochalasin d blocked formation	3
were then added to	3
tetherin in transfected cells	3
for vero e cells	3
polypeptide chains from the	3
is a versatile tool	3
grown in mdbk cells	3
attenuated recombinant vesicular stomatitis	3
the role of the	3
published maps and institutional	3
quantities were chosen so	3
of the cell projection	3
in the translational machinery	3
and immunogenicity of the	3
on distantly connected er	3
at the c terminus	3
remain to be determined	3
group also indicated significant	3
journal of infectious diseases	3
credit to the original	3
measured by gloma multi	3
vaccine vector and vaccine	3
immune responses against a	3
the functional template for	3
was removed from the	3
production of type i	3
an antibody specific for	3
room temperature with slow	3
washed and further incubated	3
ability to activate irf	3
h ha induce cross	3
grown on glass coverslips	3
p protein was approximately	3
cardiac perfusion with ml	3
the effect of vsv	3
in a favorable context	3
cell culture supernatant was	3
expression of viral genes	3
platform technologies for assaying	3
titers were expressed as	3
elicit robust cd th	3
is similar to the	3
the nature of the	3
g protein cytoplasmic tail	3
of transcription of genes	3
susceptible to intranasal vsv	3
semliki forest virus membrane	3
indicated otherwise in a	3
were transfected with increasing	3
from the national institutes	3
antiviral activities of both	3
material in this article	3
min before inoculating to	3
of the corresponding protein	3
mixtures were incubated for	3
need to obtain permission	3
structure of viral mrnas	3
of p y and	3
viral rna ge copies	3
domain was not required	3
evidence in support of	3
transduced normal brain cells	3
to the positive control	3
able to form hetero	3
wnv e glycoprotein were	3
membranes were blocked in	3
ankara vaccine vectors in	3
signs of disease following	3
of the infectivity of	3
for the inhibition of	3
methylene chloride and methanol	3
capacity to resume virus	3
glycoproteins of enveloped viruses	3
influenza h ha induce	3
copy of this license	3
the ubiquitination of irf	3
spikeless vesicular stomatitis virus	3
that appears to be	3
not depend on the	3
expression levels were measured	3
technologies for assaying antibody	3
lumenal domain of vsv	3
required for assembly of	3
is not essential for	3
these results suggested that	3
vsv with only truncated	3
active site of the	3
in a number of	3
obtained from the american	3
virus vectors expressing hiv	3
times higher than the	3
seven distinct epitopes on	3
all other values were	3
insect and mammalian cells	3
of a recombinant vesicular	3
neutralizing antibodies against mers	3
the virucidal activity of	3
the green fluorescent protein	3
in whole and prok	3
division of intramural research	3
step of the viral	3
and are protective in	3
of the cell membrane	3
nonpropagating vesicular stomatitis viruses	3
activities were especially strong	3
chosen so that the	3
of the immune system	3
compared to control groups	3
of oncolytic vesicular stomatitis	3
case of enveloped viruses	3
h n and h	3
we found that a	3
cultured in dmem containing	3
viruses expressing respiratory syncytial	3
unless indicated otherwise in	3
driven by batfluav surface	3
examined under a fluorescence	3
the second aug codon	3
apilimod blocks infection of	3
this work was funded	3
against porcine reproductive and	3
blood was removed from	3
standard deviations of the	3
of hal and hal	3
centrifugation for minutes at	3
only type i glycopeptides	3
were treated or not	3
for quantification of infectious	3
the camp epac signal	3
pbs h n treated	3
erns t et al	3
an aids virus challenge	3
activity in both homologous	3
expressing respiratory syncytial virus	3
wt and ifit ob	3
d blocked formation of	3
to view a copy	3
cells as well as	3
claims in published maps	3
your intended use is	3
the difference between the	3
of plasma from evd	3
measuring the gfp expression	3
pbs h n or	3
cells were imaged using	3
does not depend on	3
hiv type env and	3
the m protein is	3
of a novel virus	3
one of the main	3
with the spike protein	3
of poliovirus rna in	3
by virtue of its	3
this article are included	3
and characterization of a	3
the distribution of the	3
in vitro models of	3
using a wide range	3
c bl embryonic stem	3
of a new vaccine	3
the impact of the	3
avian influenza h ha	3
would open the way	3
was removed from organs	3
results are expressed as	3
pbs and fixed with	3
neutralizing antibody responses to	3
extracts from infected cells	3
and allowed to incubate	3
doxorubicin promoted ripa by	3
result in any significant	3
the ectodomain of gp	3
pseudotyped virus neutralisation assay	3
that the cellular mrnas	3
wanted to investigate whether	3
off of host cell	3
foreign proteins on the	3
from an additional transcription	3
inhibit the activity of	3
brains of uninfected or	3
recovered from cytochalasin d	3
cell pellet was cut	3
the assembly of the	3
amino acid substitutions in	3
that replicate in the	3
in the production of	3
was shown to be	3
proteins showed antiviral activity	3
the o subunit of	3
control of an aids	3
the nucleotide sequence of	3
l wt and vsv	3
neutralizing antibody response to	3
the polysome association of	3
influenza virus assembly of	3
antiviral activities were especially	3
the population of cellular	3
access this article is	3
in ether and a	3
regard to jurisdictional claims	3
were obtained from sigma	3
the replication of many	3
with lymphocytic choriomeningitis virus	3
transmembrane and cytoplasmic domains	3
this paper at https	3
cells infected with wt	3
pedv were significantly higher	3
glycoprotein is necessary for	3
portion of the eif	3
the absence of antiviral	3
for influenza h n	3
of foreign proteins on	3
only one of the	3
the transcriptional induction of	3
a single vaccination with	3
at the nonpermissive temperature	3
vsv pseudotyped with mers	3
was determined as described	3
a new vaccine for	3
mcias using a wide	3
based on these results	3
were used as a	3
and sensitive determination of	3
lumenal domain was not	3
peptidase is a functional	3
to be susceptible to	3
via the intranasal route	3
export of cargo from	3
were inserted into the	3
protein is responsible for	3
licensed under a creative	3
in the cytoplasm of	3
attaches to the host	3
that are defective in	3
suitability of ebov gp	3
expressing avian influenza h	3
metabolically labeled for rain	3
polypeptide of influenza virus	3
be used as a	3
these results demonstrated that	3
virus glycoprotein hef for	3
cells were seeded into	3
bearing vesicular stomatitis virus	3
golgi retention of gml	3
mrnas that remain polysome	3
vesicular stomatitis virus rna	3
inhibit the translation of	3
approximately kda and kda	3
in vitro synthesis of	3
based assay for detection	3
mabs to ep and	3
the gag and pol	3
overall translational capacity is	3
proteolytic cleavage of hal	3
rna levels in brains	3
material is not included	3
support the idea that	3
were used in this	3
challenged with a lethal	3
vectors expressing hiv type	3
in a cell line	3
a viruses by trypsin	3
of the infected mice	3
expressed as the percentage	3
mice against rsv challenge	3
the fluidity of the	3
the potential role of	3
the rapid and sensitive	3
the idea that pis	3
vectors expressing ebovgp from	3
from the er through	3
of the autographa californica	3
the cholesterol transporter niemann	3
and nhp challenge studies	3
the development of an	3
of the n gene	3
proximity to a second	3
findings suggest that the	3
sought to determine whether	3
the surface area of	3
transcription unit of pvsv	3
attenuated rvsv vectors expressing	3
intranasal with pfu of	3
the glycoproteins into the	3
the studies described above	3
using a beckman sw	3
intranasally infected with vsv	3
could serve as a	3
were used to assess	3
l protein provides complete	3
virus type gd elicit	3
antigens protect mice against	3
known subtypes of feifn	3
camp epac signal pathway	3
are protective in mouse	3
by the centers for	3
and in vitro models	3
or latently infected rn	3
to the absence of	3
in vivo gene delivery	3
adenovirus early region a	3
in the total cytoplasmic	3
better than that of	3
f and supplementary figure	3
ether and a small	3
mlt treatments were used	3
although some of the	3
antiviral activity against bvdv	3
optimising pseudotyped virus neutralisation	3
with the fact that	3
mouse and guinea pig	3
dipeptidyl peptidase is a	3
medium only and virus	3
plays an important role	3
was performed as described	3
and modified vaccinia virus	3
optimized vaccine vector based	3
effective control of an	3
in different cell types	3
notable differences were observed	3
isolation of a novel	3
simple method of estimating	3
envelope with the endosomal	3
a simple method of	3
cytotoxicity of the peptide	3
the presence of sialic	3
mediated antiviral activities are	3
of the envelope protein	3
in macaques by using	3
influenza virus mrnas are	3
from the fact that	3
ripa in multiple cell	3
macaques by using vesicular	3
in addition to vsv	3
between viral envelope and	3
sphingomyelinase and the release	3
with different concentrations of	3
expressing hiv type env	3
mem buffered with mm	3
c virus glycoprotein hef	3
well plates at a	3
the standard deviation from	3
of the m glycoprotein	3
plasma from evd survivors	3
of acid sphingomyelinase in	3
the ability of rvsv	3
in the golgi region	3
the cell culture supernatant	3
a variety of viral	3
and indicate if changes	3
we validated these results	3
protective immune responses in	3
were treated with trypsin	3
protein on the surface	3
the composition of the	3
of recombinant feline interferon	3
of further attenuated rvsv	3
in the same way	3
third party material in	3
mediated pathway of apoptosis	3
preventing vesicular stomatitis disease	3
of viral protein expression	3
activities of the recombinant	3
and embedded in epon	3
ml of bv or	3
fusion of viral envelope	3
declare that they have	3
were anesthetized with ketamine	3
by the use of	3
this article is licensed	3
a copy of this	3
was cut with a	3
the virucidal effect of	3
proteolytic activation of hal	3
activity of the recombinant	3
temperature with slow shaking	3
jurisdictional claims in published	3
y mediated antiviral activities	3
spike protein by the	3
a promising vaccine vector	3
density of er buds	3
participation of sulfur atom	3
regions of the er	3
against bvdv or pedv	3
cd th immune responses	3
the host cell plasma	3
comparison of intranasal and	3
dilution of purified mab	3
are present in the	3
or the presence of	3
the probability of encountering	3
highlights the importance of	3
to the loss of	3
it has been reported	3
virus expressing cottontail rabbit	3
virus entry requires the	3
only truncated g protein	3
we performed mcias using	3
it is conceivable that	3
of vsv replication in	3
of the evd survivor	3
remains neutral with regard	3
we demonstrate that p	3
assay for nipah virus	3
supplementary figure s c	3
antagonism in transfected cells	3
antiviral activity of mlt	3
did not observe any	3
an eif e dependent	3
gp pseudotyped vsv neutralisation	3
in any of the	3
was measured at nm	3
maps and institutional affiliations	3
to the original author	3
the amount of the	3
may be due to	3
high throughput screen of	3
acid sphingomyelinase ceramide system	3
a broad range of	3
serotype of vesicular stomatitis	3
inserted into the plasma	3
from a variety of	3
proteins were also broad	3
the optimal antiviral activity	3
correlation between the two	3
viral rna levels in	3
aids virus challenge in	3
the production of camp	3
hela cells were pretreated	3
infectivity of the virus	3
well cell culture plates	3
highlighting the potential of	3
to ep and ep	3
and ecology of influenza	3
rna virus belonging to	3
on the presence of	3
translation of capped mrnas	3
before inoculating to the	3
viral budding and packaging	3
structure of the sars	3
to the golgi apparatus	3
virus ankara vaccine vectors	3
no statistically significant difference	3
inoculating to the cells	3
with increasing amounts of	3
in a small volume	3
only and virus infection	3
dmem medium only and	3
was detected in the	3
by fusion to the	3
to restore translation to	3
pseudotyped with lymphocytic choriomeningitis	3
the mixture was partitioned	3
pathway of vesicular stomatitis	3
pig and nhp challenge	3
mixed with an equal	3
the amino acid composition	3
prime only group had	3
that the level of	3
lethal challenge with andes	3
estimation of the mean	3
of zoonotic viruses in	3
in a way that	3
might be able to	3
the first and second	3
evaluation of a novel	3
to the cells and	3
the gfp expression at	3
gives rise to and	3
cells were cotransfected with	3
surface of the bilayer	3
novel coronavirus from a	3
first and second aug	3
from the surface of	3
as an experimental animal	3
added to the wells	3
as a large oligomer	3
density of gold particles	3
of the west nile	3
of the golgi apparatus	3
were injected into the	3
to desired cell types	3
vaccine for the prevention	3
in this article are	3
highly effective control of	3
negative strand rna virus	3
with the supernatant at	3
surface of the cell	3
as determined by the	3
at the study endpoint	3
in the cell lines	3
virus thymidine kinase gene	3
was supported by the	3
were anesthetized with pentobarbital	3
after h of adsorption	3
log increase in ge	3
mechanism for their retention	3
in infected cells and	3
the production of type	3
the absence of rlr	3
a link to the	3
and found that the	3
viral titers were determined	3
continued to migrate as	3
study indicated that p	3
the h n challenge	3
rauscher murine leukemia virus	3
challenge with andes virus	3
size of the oligomer	3
the type i interferon	3
vesicular stomatitis virus phenotypic	3
culture supernatants were removed	3
aspirated out with the	3
that doxorubicin did not	3
infectious virus particles in	3
there was no antiviral	3
performed using previously described	3
the brains of nude	3
on the baculoviral surface	3
viruses such as influenza	3
under a creative commons	3
are shown in the	3
both type i and	3
infected with wt vsv	3
s protein pseudotyped vsv	3
optimal signalase cleavage site	3
for golgi retention of	3
are involved in the	3
hela cell protein synthesis	3
was stirred at room	3
a quantitative analysis of	3
long as you give	3
min in the presence	3
the ability of imatinib	3
in homologous animal cells	3
certain bat cell lines	3
of pigs with vrp	3
in cells challenged with	3
further evidence that the	3
antiviral activities of the	3
in accordance with the	3
entry by using pseudotyped	3
titers in the serum	3
the fact that the	3
four hours prior to	3
obtained through the nih	3
pcr was performed using	3
after removal of the	3
mem medium at a	3
inhibition of translation of	3
of feline leukemia virus	3
in mammalian cell lines	3
bv or mlt was	3
rnas encoded by epstein	3
aug codon occurs in	3
have been suggested to	3
it is worthy to	3
the envelope glycoproteins of	3
of an antiviral state	3
centrifugation at x g	3
outside of the golgi	3
ecology of influenza a	3
a previous study indicated	3
respiratory syndrome virus vaccines	3
of p y was	3
of gold particles per	3
prompted us to test	3
of cytosol and atp	3
cargo from the er	3
spread of the virus	3
c mice were im	3
the viral replication cycle	3
mouse pems were pretreated	3
absence or the presence	3
of an influenza virion	3
or other third party	3
properties of recombinant vesicular	3
that the presence of	3
to assess the effect	3
as depicted in fig	3
organic layer was washed	3
viral proteins on the	3
a live ebov neutralisation	3
rlu number in triplicate	3
strong against fcov and	3
bovine viral diarrhea virus	3
in er to golgi	3
average rlu number in	3
the position of the	3
shown to be associated	3
and ifnar mice at	3
prevention of lassa fever	3
infection of cells with	3
with decreased polysome association	3
were chosen so that	3
coronavirus from a man	3
into the vsv genome	3
all animal experiments were	3
kindly provided by g	3
using the suicide gene	3
virus challenge attenuated vesicular	3
on the sugar ring	3
was found in the	3
were blocked with bsa	3
in multiple cell types	3
association of host mrnas	3
synthesis of a protein	3
with dmem containing fbs	3
open access this article	3
virus challenge in macaques	3
are also being developed	3
if changes were made	3
in and transmission by	3
in published maps and	3
stomatitis virus glycoprotein g	3
incubated at room temperature	3
not appear to be	3
in the liver of	3
induced p y expression	3
the transmembrane and cytoplasmic	3
results suggest that vsv	3
coronavirus associated with severe	3
the viruses and their	3
an internal aug codon	3
supernatants were collected and	3
cells as compared to	3
brains of nude rats	3
and your intended use	3
the possibility that the	3
both displayed in vitro	3
hef for generation of	3
stomatitis virus gives high	3
a monolayer of vero	3
no antiviral activity detected	3
defective recombinant vesicular stomatitis	3
size and shape of	3
in the absence or	3
directly from the copyright	3
doxorubicin was expanded to	3
the sequence of the	3
or mlt h n	3
an upstream aug codon	3
term protection against yersinia	3
with only truncated g	3
the results obtained in	3
the binding kinetics of	3
t cells in vaccinated	3
that both lentiviral vectors	3
xn vsv m vsv	3
were challenged with ng	3
prevention and treatment of	3
in each group were	3
by interfering with its	3
ifit and wt mice	3
of the virion and	3
were aspirated out with	3
cleared by centrifugation at	3
and identification of a	3
in the membrane of	3
of viral envelope with	3
you give appropriate credit	3
no antiviral activity against	3
culture medium and the	3
vsv or influenza virus	3
mrnas to be translated	3
of viral gene expression	3
were transfected with the	3
license and your intended	3
was found according to	3
infected with ts vsv	3
recombinant vsv with only	3
been reported to be	3
into the fourth transcription	3
vectors pseudotyped with lymphocytic	3
vsv rna replicates in	3
virus with the envelope	3
of the e glycoprotein	3
mice were divided into	3
in triplicate wells with	3
were infected with the	3
otherwise in a credit	3
the presence of gtp	3
sialic acid from the	3
we observed no antiviral	3
the cytoplasmic tails of	3
identification of a novel	3
credit line to the	3
the intercat ifn group	3
g protein of vesicular	3
antiviral activity of irf	3
viruses and their replication	3
ability of imatinib to	3
cells and incubated at	3
apilimod also inhibits infection	3
of bv against vsv	3
effects of bee venom	3
the g protein cytoplasmic	3
an experimental animal model	3
in the live ebov	3
with regard to jurisdictional	3
containing mg ml of	3
entry driven by batfluav	3
second bud in the	3
following challenge infection with	3
be activated by doxorubicin	3
to a second bud	3
with a mixture of	3
vectors pseudotyped with the	3
of vsv g was	3
creative commons license and	3
treated cells compared to	3
in the plane of	3
by using pseudotyped viruses	3
in the fraction of	3