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 the ebola virus | 99 |
ebola virus disease in | 81 |
the ebola virus glycoprotein | 76 |
republic of the congo | 65 |
democratic republic of the | 64 |
ebola and marburg viruses | 61 |
severe acute respiratory syndrome | 59 |
of ebola virus disease | 57 |
middle east respiratory syndrome | 56 |
of ebola hemorrhagic fever | 52 |
in the absence of | 52 |
east respiratory syndrome coronavirus | 48 |
in the presence of | 45 |
of ebola virus infection | 45 |
the democratic republic of | 37 |
ebola virus infection in | 37 |
as well as the | 35 |
for the treatment of | 34 |
in the context of | 34 |
of ebola and marburg | 34 |
in the democratic republic | 31 |
acute respiratory syndrome coronavirus | 29 |
on the cell surface | 28 |
human immunodeficiency virus type | 28 |
treatment of ebola virus | 27 |
ebola hemorrhagic fever in | 27 |
in the case of | 26 |
in vitro and in | 26 |
vitro and in vivo | 24 |
with ebola virus disease | 23 |
recombinant vesicular stomatitis virus | 23 |
against ebola virus infection | 22 |
for ebola virus infection | 22 |
patients with ebola virus | 22 |
have been shown to | 22 |
on the surface of | 21 |
virus disease in guinea | 21 |
in the united states | 21 |
democratic republic of congo | 21 |
been shown to be | 20 |
has been shown to | 20 |
of type i ifn | 20 |
ebola virus entry requires | 20 |
of severe acute respiratory | 20 |
on the other hand | 20 |
of ebola virus glycoprotein | 20 |
of ebola virus in | 20 |
ebola virus glycoprotein is | 20 |
virus entry requires the | 20 |
cells were transfected with | 20 |
a wide range of | 19 |
against lethal ebola virus | 19 |
one of the most | 19 |
in vero e cells | 19 |
centers for disease control | 18 |
for the detection of | 18 |
ebola and marburg virus | 18 |
colored fruit bat cells | 18 |
to the plasma membrane | 18 |
analysis of ebola virus | 18 |
marburg and ebola viruses | 18 |
structure of the ebola | 17 |
of marburg hemorrhagic fever | 17 |
for disease control and | 17 |
proteolysis of the ebola | 17 |
of middle east respiratory | 17 |
essential for ebola virus | 17 |
disease control and prevention | 17 |
ebov gp pseudotyped hiv | 17 |
an important role in | 17 |
min at room temperature | 16 |
c is essential for | 16 |
pathogenesis of ebola hemorrhagic | 16 |
pick c is essential | 16 |
lethal ebola virus infection | 16 |
the cholesterol transporter niemann | 16 |
is essential for ebola | 16 |
processing of the ebola | 16 |
for ebola virus disease | 16 |
from a human survivor | 15 |
of ebov gp pseudotyped | 15 |
requires the cholesterol transporter | 15 |
type i ifn signaling | 15 |
entry requires the cholesterol | 15 |
by the ebola virus | 15 |
play a role in | 15 |
of ebola virus vp | 15 |
during the course of | 15 |
lethal ebola virus challenge | 14 |
vaccine protects nonhuman primates | 14 |
protects nonhuman primates against | 14 |
safety and immunogenicity of | 14 |
the ebola virus vp | 14 |
in the treatment of | 14 |
protection against ebola virus | 14 |
of ebov and marv | 14 |
of zaire ebola virus | 14 |
ebola virus vp protein | 14 |
a u a u | 14 |
small molecule inhibitors reveal | 14 |
the course of the | 14 |
molecule inhibitors reveal niemann | 14 |
for min at room | 14 |
it is possible that | 14 |
ebola virus infection with | 14 |
the presence of the | 14 |
t cells were seeded | 14 |
to ebov gp cl | 13 |
added to each well | 13 |
emergence of zaire ebola | 13 |
after the onset of | 13 |
equine antisera and f | 13 |
on the plasma membrane | 13 |
to the cell surface | 13 |
the extent of fusion | 13 |
of ebola virus entry | 13 |
fever in cynomolgus macaques | 13 |
cells were treated with | 13 |
gp on the cell | 13 |
zaire ebola virus disease | 13 |
ebola and marburg hemorrhagic | 13 |
during the west african | 13 |
hemorrhagic fever in cynomolgus | 13 |
the ebov gp pseudotyped | 12 |
a case fatality rate | 12 |
is necessary for infection | 12 |
it is likely that | 12 |
a single amino acid | 12 |
in a mouse model | 12 |
virus disease in west | 12 |
of the ebov gp | 12 |
play an important role | 12 |
glycoprotein is necessary for | 12 |
virus glycoprotein by the | 12 |
outbreak in west africa | 12 |
of patients with ebola | 12 |
virus glycoprotein is necessary | 12 |
ebov gp on the | 12 |
the world health organization | 12 |
ebola haemorrhagic fever in | 12 |
fusion of the viral | 12 |
ebola virus glycoprotein by | 12 |
and marburg hemorrhagic fever | 12 |
transmission of ebola virus | 12 |
highly pathogenic avian influenza | 12 |
the west african outbreak | 12 |
in the development of | 12 |
is one of the | 12 |
endosomal proteolysis of the | 12 |
ebov gp pseudotyped vsv | 12 |
venezuelan equine encephalitis virus | 12 |
it is important to | 12 |
a broad range of | 11 |
compendium of years of | 11 |
case fatality rate of | 11 |
can be used to | 11 |
entry mediated by the | 11 |
a lethal dose of | 11 |
for the development of | 11 |
ebola virus infection is | 11 |
proteolytic processing of the | 11 |
of years of epidemiological | 11 |
at the plasma membrane | 11 |
is associated with an | 11 |
increasing or decreasing trend | 11 |
a compendium of years | 11 |
the role of the | 11 |
for h at room | 11 |
in the present study | 11 |
a single dose of | 11 |
national institutes of health | 11 |
of ebola virus and | 11 |
h at room temperature | 11 |
compared with pbs group | 11 |
of human immunodeficiency virus | 11 |
bind to ebov gp | 11 |
cells were infected with | 11 |
of ebola virus is | 11 |
virion glycoproteins of ebola | 11 |
disease in west africa | 11 |
infection is associated with | 11 |
by ebola and marburg | 11 |
work was supported by | 10 |
on the basis of | 10 |
pick c small molecule | 10 |
virus glycoprotein bound to | 10 |
c small molecule inhibitors | 10 |
glycoprotein bound to an | 10 |
and marburg virus infections | 10 |
to an antibody from | 10 |
the viral life cycle | 10 |
the antiviral activity of | 10 |
rift valley fever virus | 10 |
cell immunoglobulin and mucin | 10 |
an antibody from a | 10 |
virus disease in the | 10 |
the host immune response | 10 |
of the ebov genome | 10 |
the type i interferon | 10 |
early and sustained targets | 10 |
in the current study | 10 |
over the course of | 10 |
were found to be | 10 |
african green monkey kidney | 10 |
vero e cells were | 10 |
vp is essential for | 10 |
ebola virus glycoprotein bound | 10 |
bound to an antibody | 10 |
persistence of ebola virus | 10 |
was added to the | 10 |
for the first time | 10 |
as seen in figure | 10 |
ebola virus entry by | 10 |
of the viral envelope | 10 |
virus infection is associated | 10 |
antibody from a human | 10 |
of advanced ebola virus | 10 |
food and drug administration | 10 |
of vesicular stomatitis virus | 10 |
outbreak of ebola virus | 10 |
immunoglobulin and mucin domain | 10 |
cellular entry by ebola | 10 |
gp of ebola virus | 9 |
diagnosis of ebola hemorrhagic | 9 |
from the cell surface | 9 |
into the host cell | 9 |
cathepsins b and l | 9 |
role of type i | 9 |
not required for ebola | 9 |
of marburg virus disease | 9 |
infection and vlp entry | 9 |
vero e and huh | 9 |
required for ebola virus | 9 |
elucidates ebola virus origin | 9 |
trvlp infection and vlp | 9 |
with massive lymphocyte apoptosis | 9 |
the structure of the | 9 |
it is conceivable that | 9 |
first months of the | 9 |
in the exporting country | 9 |
in the plasma membrane | 9 |
antibodies against ebola virus | 9 |
virus infection ebola virus | 9 |
genomic surveillance elucidates ebola | 9 |
treatment of ebola hemorrhagic | 9 |
of the epidemic and | 9 |
the united states and | 9 |
of the type i | 9 |
of the ifn system | 9 |
these results suggest that | 9 |
it should be noted | 9 |
associated with an aberrant | 9 |
an aberrant innate immunity | 9 |
infected with ebola virus | 9 |
this work was supported | 9 |
of proinflammatory cytokines and | 9 |
cells were seeded in | 9 |
are early and sustained | 9 |
at h post transfection | 9 |
e and huh cells | 9 |
surveillance elucidates ebola virus | 9 |
origin and transmission during | 9 |
are not required for | 9 |
peripheral blood mononuclear cells | 9 |
a large number of | 9 |
immunity and with massive | 9 |
analysis and interpretation of | 9 |
at the time of | 9 |
cleavage of ebov gp | 9 |
and sustained targets of | 9 |
at an moi of | 9 |
and interpretation of data | 9 |
transmission during the outbreak | 9 |
aberrant innate immunity and | 9 |
virus origin and transmission | 9 |
ebola virus origin and | 9 |
and with massive lymphocyte | 9 |
with fetal bovine serum | 9 |
infection ebola virus entry | 9 |
and vesicular stomatitis virus | 9 |
proportion of the year | 9 |
and transmission during the | 9 |
months of the epidemic | 9 |
liberia and sierra leone | 9 |
ebola virus infection by | 9 |
to bind to ebov | 9 |
the absence of other | 9 |
the inoculum was removed | 9 |
effector and target cells | 9 |
innate immunity and with | 9 |
with an aberrant innate | 9 |
a high degree of | 9 |
luciferase reporter gene inhibition | 8 |
the human ebov infection | 8 |
reservoirs of ebola virus | 8 |
this study was to | 8 |
of marburg virus and | 8 |
in the pathogenesis of | 8 |
contact with bodily fluids | 8 |
ebola virus can be | 8 |
on vero e cells | 8 |
fruit bats as reservoirs | 8 |
the total number of | 8 |
the plasma membrane and | 8 |
like particles produced in | 8 |
as a result of | 8 |
of the immune system | 8 |
a final concentration of | 8 |
that dendritic cells are | 8 |
the end of the | 8 |
we found that a | 8 |
nonhuman primates against ebola | 8 |
human fatal zaire ebola | 8 |
is not required for | 8 |
outbreaks of ebola virus | 8 |
protect nonhuman primates against | 8 |
at the level of | 8 |
reporter gene inhibition assay | 8 |
the spike protein of | 8 |
it has been shown | 8 |
from discovery to vaccine | 8 |
incubated for h at | 8 |
and the cells were | 8 |
dendritic cells are early | 8 |
infection of rhesus macaques | 8 |
the causative agent of | 8 |
factor viia tissue factor | 8 |
nematode anticoagulant protein c | 8 |
pathology of experimental ebola | 8 |
replication of the ebov | 8 |
the treatment of ebov | 8 |
disease in the united | 8 |
a member of the | 8 |
the host cell cytoplasm | 8 |
ebov entry and infection | 8 |
mutation of the gxxxg | 8 |
with a lethal dose | 8 |
recombinant nematode anticoagulant protein | 8 |
particles produced in insect | 8 |
cells are early and | 8 |
for the production of | 8 |
the transcription and replication | 8 |
cis and in trans | 8 |
of marburg and ebola | 8 |
produced in insect cells | 8 |
in humans and nonhuman | 8 |
the surface of the | 8 |
of the ebov infection | 8 |
in patients with ebola | 8 |
rapid diagnosis of ebola | 8 |
the size of the | 8 |
against ebola and marburg | 8 |
fatal zaire ebola virus | 8 |
the probability of introduction | 8 |
zaire ebola virus infection | 8 |
was found to be | 8 |
the epidemic and forward | 8 |
used in this study | 8 |
of the gxxxg motif | 8 |
cells by macropinocytosis and | 8 |
the authors declare no | 8 |
should be noted that | 8 |
sustained targets of infection | 8 |
evidence that dendritic cells | 8 |
outbreak in the democratic | 8 |
to ebola virus glycoprotein | 8 |
a u and a | 8 |
scientific and technical committee | 8 |
the human immunodeficiency virus | 8 |
has been detected in | 8 |
bats as reservoirs of | 8 |
at least in part | 8 |
balb c mice were | 8 |
acute respiratory distress syndrome | 8 |
antibodies to ebola virus | 8 |
in the endoplasmic reticulum | 8 |
for the identification of | 8 |
epidemic and forward projections | 8 |
haemorrhagic fever in zaire | 8 |
of experimental ebola virus | 8 |
in cis and in | 8 |
protection from ebola virus | 8 |
in addition to the | 8 |
of the marburg virus | 8 |
transcription and replication of | 8 |
in the mouse model | 8 |
to a lesser extent | 8 |
to the development of | 8 |
of this study was | 8 |
to that of the | 8 |
generation of therapeutic antisera | 8 |
of personal protective equipment | 8 |
for h at rt | 8 |
in an outbreak setting | 8 |
by marburg and ebola | 8 |
as reservoirs of ebola | 8 |
mediated by the ebola | 8 |
selective estrogen receptor modulators | 8 |
the average number of | 8 |
against a lethal challenge | 8 |
international scientific and technical | 8 |
entry of ebola virus | 8 |
mediate cellular entry by | 7 |
by using pseudotyped viruses | 7 |
in the formation of | 7 |
glycoproteins of ebola viruses | 7 |
t cells were transfected | 7 |
inoculum was removed and | 7 |
outbreak setting and assessment | 7 |
a role in the | 7 |
mpxv infection resulted in | 7 |
zaire ebolavirus and lake | 7 |
ebola viruses are encoded | 7 |
among the three areas | 7 |
against a lethal ebola | 7 |
the receptor binding domain | 7 |
nonhuman primates from filovirus | 7 |
ebov gp is cleaved | 7 |
of type i ifns | 7 |
ebola hemorrhagic fever by | 7 |
a small animal model | 7 |
setting and assessment of | 7 |
for the determination of | 7 |
cathepsins in entry mediated | 7 |
probability of introduction for | 7 |
of the ebov in | 7 |
from egyptian fruit bats | 7 |
the ebola virus disease | 7 |
the recent outbreak of | 7 |
virus entry by using | 7 |
innate and adaptive immune | 7 |
are expressed through transcriptional | 7 |
epidemic in western africa | 7 |
course of the experiment | 7 |
frames and are expressed | 7 |
advanced ebola virus disease | 7 |
pcr in an outbreak | 7 |
humans and nonhuman primates | 7 |
viruses from egyptian fruit | 7 |
g for min at | 7 |
of ebola virus from | 7 |
neutral with regard to | 7 |
virus infection with a | 7 |
and a u a | 7 |
live ebov neutralisation assay | 7 |
of patient viral load | 7 |
cd and cd t | 7 |
nature remains neutral with | 7 |
by ebola virus in | 7 |
published maps and institutional | 7 |
protects nonhuman primates from | 7 |
similar to that of | 7 |
role of endosomal cathepsins | 7 |
virus in cis and | 7 |
could be due to | 7 |
the virion glycoproteins of | 7 |
of endosomal cathepsins in | 7 |
proinflammatory cytokines and chemokines | 7 |
a lethal ebola virus | 7 |
macrophages and dendritic cells | 7 |
to jurisdictional claims in | 7 |
are encoded in two | 7 |
prophylaxis protects nonhuman primates | 7 |
host cells by macropinocytosis | 7 |
characterization of ebola virus | 7 |
based on these data | 7 |
enters host cells by | 7 |
as a predictor of | 7 |
and lake victoria marburgvirus | 7 |
virus and marburg virus | 7 |
viruses are encoded in | 7 |
at the cell surface | 7 |
springer nature remains neutral | 7 |
of ebola viruses are | 7 |
antibody prophylaxis protects nonhuman | 7 |
remains neutral with regard | 7 |
in entry mediated by | 7 |
medium was replaced by | 7 |
entry by using pseudotyped | 7 |
an outbreak setting and | 7 |
disease in nonhuman primates | 7 |
were observed in the | 7 |
at a concentration of | 7 |
crystal structure of the | 7 |
with regard to jurisdictional | 7 |
ebolavirus and lake victoria | 7 |
three viral data sets | 7 |
against ebola virus in | 7 |
jurisdictional claims in published | 7 |
claims in published maps | 7 |
was shown to be | 7 |
inhibit ebola virus infection | 7 |
these results demonstrate that | 7 |
institute of infectious diseases | 7 |
type i interferon response | 7 |
was used for the | 7 |
a receptor for zaire | 7 |
or revising the article | 7 |
single amino acid change | 7 |
mice and guinea pigs | 7 |
ebola virus in cis | 7 |
primates from filovirus disease | 7 |
and supplementary figure s | 7 |
protection against lethal challenge | 7 |
entry of the ebov | 7 |
maps and institutional affiliations | 7 |
two reading frames and | 7 |
is safe and immunogenic | 7 |
assessment of patient viral | 7 |
during the recovery process | 7 |
virus disease in nonhuman | 7 |
in the form of | 7 |
can be used as | 7 |
receptor for zaire ebolavirus | 7 |
patient viral load as | 7 |
the onset of symptoms | 7 |
the early stages of | 7 |
in two reading frames | 7 |
and functional characterization of | 7 |
the ability of the | 7 |
drafting or revising the | 7 |
recombinant inhibitor of factor | 7 |
hek t cells were | 7 |
load as a predictor | 7 |
initial viral load on | 7 |
diverse marburg viruses from | 7 |
of the family filoviridae | 7 |
a lethal ebov challenge | 7 |
of ebola virus during | 7 |
has not yet been | 7 |
recombinant human activated protein | 7 |
a mouse model of | 7 |
viral load as a | 7 |
the ebov infection in | 7 |
species of ebola virus | 7 |
as a surrogate for | 7 |
the centers for disease | 7 |
ebola virus enters host | 7 |
ebola virus and marburg | 7 |
in published maps and | 7 |
endosomal cathepsins in entry | 7 |
supplemented with fetal bovine | 7 |
may not be a | 7 |
safe and immunogenic in | 7 |
of gp and gp | 7 |
enhancement of ebola virus | 7 |
of influenza a virus | 7 |
the us department of | 7 |
and are expressed through | 7 |
fever by reverse transcription | 7 |
for ebola virus replication | 7 |
have been associated with | 7 |
regard to jurisdictional claims | 7 |
and tumor necrosis factor | 7 |
and assessment of patient | 7 |
the vesicular stomatitis virus | 7 |
responses in ebola virus | 7 |
during the outbreak in | 7 |
remains to be determined | 7 |
expressed through transcriptional editing | 7 |
have been detected in | 7 |
were obtained from the | 7 |
marburg viruses from egyptian | 7 |
encoded in two reading | 7 |
reading frames and are | 7 |
the matrix protein vp | 7 |
a predictor of outcome | 7 |
virus entry and infection | 7 |
a critical role in | 7 |
the first months of | 7 |
in the respiratory tract | 7 |
and replication of the | 7 |
binding in the presence | 7 |
isolation of genetically diverse | 7 |
influenza a h n | 7 |
fecal samples were collected | 7 |
both ebov and marv | 7 |
hemorrhagic fever by reverse | 7 |
sign mediate cellular entry | 7 |
genetically diverse marburg viruses | 7 |
as a function of | 7 |
sequence analysis of the | 7 |
activity against ebola virus | 7 |
virus and ebola virus | 7 |
infection in rhesus macaques | 7 |
for zaire ebolavirus and | 7 |
of host immune responses | 7 |
of genetically diverse marburg | 7 |
entry by ebola virus | 7 |
virus enters host cells | 7 |
postexposure antibody prophylaxis protects | 7 |
human activated protein c | 7 |
is a receptor for | 7 |
ebola virus disease outbreak | 7 |
the west african ebola | 7 |
ge healthcare life sciences | 6 |
was based on the | 6 |
of the envelope glycoprotein | 6 |
successful treatment of ebola | 6 |
employ different strategies to | 6 |
therapy prolongs survival in | 6 |
by antibody produced in | 6 |
in ebov infected mice | 6 |
there is no evidence | 6 |
the gp of the | 6 |
inhibitor of factor viia | 6 |
on the raw product | 6 |
was associated with a | 6 |
macrophages and endothelial cells | 6 |
is not essential for | 6 |
prolongs survival in rhesus | 6 |
covalent modifications of the | 6 |
of ebola virus nucleocapsid | 6 |
not included in the | 6 |
an average weight loss | 6 |
transfusions from convalescent patients | 6 |
the ebola virus polymerase | 6 |
of the ebov trailer | 6 |
functional analysis of ebola | 6 |
reversion of advanced ebola | 6 |
polymerase and by t | 6 |
disease in sierra leone | 6 |
therapeutic antisera for emerging | 6 |
congo hemorrhagic fever virus | 6 |
the base of the | 6 |
host cells via macropinocytosis | 6 |
role of vp in | 6 |
modifications of the ebola | 6 |
are thought to be | 6 |
ebola virus is edited | 6 |
cells were grown in | 6 |
the proprotein convertase furin | 6 |
infection by a potently | 6 |
of the west african | 6 |
virus glycoprotein is not | 6 |
have been used in | 6 |
to ebola and marburg | 6 |
lectin specific for galactose | 6 |
eye and male reproductive | 6 |
t and vaccinia virus | 6 |
with a recombinant inhibitor | 6 |
a vesicular stomatitis virus | 6 |
the inhibition of the | 6 |
boosted and weeks later | 6 |
risk of human infection | 6 |
i ifn signaling in | 6 |
respiratory syndrome coronavirus infection | 6 |
gp mrna of ebola | 6 |
of ebov and other | 6 |
direct effect of virus | 6 |
glycoproteins of marburg and | 6 |
the envelope glycoprotein gp | 6 |
seasonal pulses of marburg | 6 |
phase i clinical trial | 6 |
by a potently neutralizing | 6 |
is assumed to be | 6 |
as described in the | 6 |
has been shown that | 6 |
the rule of six | 6 |
human asymptomatic ebola infection | 6 |
and boosted and weeks | 6 |
cells were maintained in | 6 |
structure of the ebov | 6 |
with blood transfusions from | 6 |
during the recent outbreak | 6 |
has been used to | 6 |
in rhesus macaque models | 6 |
gxxxg motif in the | 6 |
time to clinical signs | 6 |
macaque models of ebola | 6 |
ebola hemorrhagic fever with | 6 |
dronedarone and verapamil inhibit | 6 |
of a number of | 6 |
glycoprotein by the proprotein | 6 |
the treatment was given | 6 |
average weight loss of | 6 |
virus disease in sierra | 6 |
infection prevention and control | 6 |
cd t cell responses | 6 |
the ratio of the | 6 |
marburg virus circulation in | 6 |
for host cell entry | 6 |
the treatment of ebola | 6 |
after the first immunization | 6 |
infection and strong inflammatory | 6 |
in contrast to the | 6 |
studies have demonstrated that | 6 |
for the presence of | 6 |
at a dilution of | 6 |
into host cells via | 6 |
induced cytolysis of endothelial | 6 |
for marburg hemorrhagic fever | 6 |
replication in cell culture | 6 |
system for functional analysis | 6 |
to secondary lymphoid tissues | 6 |
of the viral genome | 6 |
protective efficacy of neutralizing | 6 |
the outbreak in kikwit | 6 |
ebolavirus is internalized into | 6 |
pathogenic avian influenza virus | 6 |
host cell entry of | 6 |
of the zaire ebov | 6 |
imported case of marburg | 6 |
the absence of any | 6 |
case of marburg hemorrhagic | 6 |
human ebola virus infection | 6 |
vaccine expressing ebola virus | 6 |
the glycan cap and | 6 |
k akt mtor signaling | 6 |
of npc domain c | 6 |
inhibitors of ebola virus | 6 |
virus infection in monkeys | 6 |
coincide with periods of | 6 |
edited by the ebola | 6 |
as shown in fig | 6 |
ebola virus envelope glycoprotein | 6 |
fig a and b | 6 |
no competing interests were | 6 |
nonhuman primates with zmapp | 6 |
in the viral envelope | 6 |
are associated with fatal | 6 |
glycoprotein sgp of ebola | 6 |
use of personal protective | 6 |
the acute phase of | 6 |
entry into cell lines | 6 |
type lectin specific for | 6 |
circulation in juvenile rousettus | 6 |
by t and vaccinia | 6 |
we show that the | 6 |
in nonhuman primates with | 6 |
the length of the | 6 |
rousettus aegyptiacus bats coincide | 6 |
of therapeutic antisera for | 6 |
with an average weight | 6 |
ebola virus infection ebola | 6 |
binding to ebola virus | 6 |
study in rhesus monkeys | 6 |
and male reproductive tract | 6 |
pseudotyped virus neutralisation assays | 6 |
macropinocytosis in a viral | 6 |
sgp of ebola virus | 6 |
the fact that the | 6 |
pi k akt mtor | 6 |
with ebola and marburg | 6 |
dependent enhancement of ebola | 6 |
survival in rhesus macaque | 6 |
nonstructural small glycoprotein sgp | 6 |
mechanism of binding to | 6 |
threat to public health | 6 |
nonhuman primates against infection | 6 |
the formation of the | 6 |
against the ebov infection | 6 |
virus is edited by | 6 |
cathepsin l and b | 6 |
of the virus in | 6 |
u and a u | 6 |
antibody produced in natural | 6 |
as compared to the | 6 |
ebola virus infection of | 6 |
is internalized into host | 6 |
were added to each | 6 |
a recombinant inhibitor of | 6 |
with increasing amounts of | 6 |
juvenile rousettus aegyptiacus bats | 6 |
increased risk of human | 6 |
internalized into host cells | 6 |
with periods of increased | 6 |
and vaccinia virus polymerases | 6 |
during ebola virus infection | 6 |
with the endosomal membrane | 6 |
approved selective estrogen receptor | 6 |
virus polymerase and by | 6 |
glycoprotein by the zmapp | 6 |
neutralized by antibody produced | 6 |
the eye and male | 6 |
are given in table | 6 |
bats coincide with periods | 6 |
cytolysis of endothelial cells | 6 |
of factor viia tissue | 6 |
as a worst case | 6 |
receptor modulators inhibit ebola | 6 |
have been reported to | 6 |
rhesus macaque models of | 6 |
protection against lethal ebola | 6 |
protective monotherapy against lethal | 6 |
have been found to | 6 |
cellular entry of ebola | 6 |
of increased risk of | 6 |
detection of antibodies to | 6 |
ebola virus polymerase and | 6 |
samples were collected from | 6 |
virus disease in humans | 6 |
virus disease outbreak in | 6 |
in juvenile rousettus aegyptiacus | 6 |
has been associated with | 6 |
fold serial dilutions of | 6 |
fever with blood transfusions | 6 |
growth in human cells | 6 |
a system for functional | 6 |
small glycoprotein sgp of | 6 |
asymptomatic ebola infection and | 6 |
to each well and | 6 |
virus infection by a | 6 |
hemorrhagic fever with blood | 6 |
is edited by the | 6 |
in humans and animals | 6 |
were found in the | 6 |
in jui government hospital | 6 |
of marburg virus glycoprotein | 6 |
monotherapy against lethal ebola | 6 |
the nonstructural small glycoprotein | 6 |
in the ebola virus | 6 |
the s protein of | 6 |
virus circulation in juvenile | 6 |
blood transfusions from convalescent | 6 |
the authors declare that | 6 |
pick type c disease | 6 |
terminal heptad repeat region | 6 |
is thought to be | 6 |
different strategies to counteract | 6 |
pulses of marburg virus | 6 |
and by t and | 6 |
guinea pigs against a | 6 |
competing interests were disclosed | 6 |
the pathogenesis of ebola | 6 |
ebola virus during the | 6 |
ebola infection and strong | 6 |
cells via macropinocytosis in | 6 |
aegyptiacus bats coincide with | 6 |
ebola in sierra leone | 6 |
virus prevalence in bats | 6 |
in natural human infection | 6 |
regarded as sl reference | 6 |
of binding to ebola | 6 |
by the proprotein convertase | 6 |
be effectively neutralized by | 6 |
rhesus macaques infected with | 6 |
of the immune response | 6 |
the stability of the | 6 |
for functional analysis of | 6 |
protection of nonhuman primates | 6 |
virus can be effectively | 6 |
infection with a recombinant | 6 |
viral transcription and replication | 6 |
the internal fusion loop | 6 |
the medium was removed | 6 |
in a phase i | 6 |
at a dose of | 6 |
estrogen receptor modulators inhibit | 6 |
was performed as described | 6 |
with a case fatality | 6 |
of three independent experiments | 6 |
modulators inhibit ebola virus | 6 |
of the risk of | 6 |
effectively neutralized by antibody | 6 |
the absence of a | 6 |
primates against infection with | 6 |
of ebola virus gp | 6 |
ebola virus glycoprotein gp | 6 |
vaccine for ebola virus | 6 |
in humans infected with | 6 |
produced in natural human | 6 |
of marburg virus circulation | 6 |
in the range of | 6 |
a potently neutralizing antibody | 6 |
as a positive control | 6 |
and strong inflammatory response | 6 |
copies of ebov gp | 6 |
at the end of | 6 |
viral spread in tetherin | 6 |
a worst case scenario | 6 |
can be effectively neutralized | 6 |
of the human immunodeficiency | 6 |
macaques with monoclonal antibodies | 6 |
models of ebola and | 6 |
cynomolgus macaques with monoclonal | 6 |
the protective efficacy of | 6 |
via macropinocytosis in a | 6 |
cell entry of ebola | 6 |
periods of increased risk | 6 |
a study in rhesus | 6 |
ebov gp pseudotyped virus | 6 |
mrna of ebola virus | 6 |
recognition of an intracellular | 5 |
available as supplementary data | 5 |
a small nonhuman primate | 5 |
were washed with pbs | 5 |
to be effective in | 5 |
the second luminal domain | 5 |
has been suggested that | 5 |
to ebola virus in | 5 |
version of this article | 5 |
factor in primate monocytes | 5 |
protection against the ebov | 5 |
glycoprotein structure and mechanism | 5 |
glycoproteins for efficient entry | 5 |
and inhibit ebola virus | 5 |
clinical management of ebola | 5 |
trafficking through early and | 5 |
primates against ebola and | 5 |
is the use of | 5 |
the proportion of the | 5 |
by the addition of | 5 |
inhibit ebola virus entry | 5 |
to impact the course | 5 |
and extensive intravascular apoptosis | 5 |
a direct effect of | 5 |
folate receptor alpha and | 5 |
cells were washed with | 5 |
virus binding and infectivity | 5 |
plays an important role | 5 |
and rift valley fever | 5 |
of the congo and | 5 |
of hepatitis c virus | 5 |
region of ebov gp | 5 |
protein of marburg virus | 5 |
effects of ebola virus | 5 |
clinical features of patients | 5 |
lsectin interacts with filovirus | 5 |
fasman beta turn prediction | 5 |
are available from the | 5 |
were transfected with the | 5 |
at the same time | 5 |
spike protein of sars | 5 |
viraly r schmidt et | 5 |
and a mtd of | 5 |
the course of ebola | 5 |
hemorrhagic fever in primate | 5 |
is composed of a | 5 |
the ebola virus glycoproteins | 5 |
endothelial cell activation and | 5 |
cells were stained with | 5 |
clinical observations in patients | 5 |
rvsv ebola vaccine in | 5 |
hepatitis c virus infection | 5 |
background level of neutralisation | 5 |
is not a direct | 5 |
ebola virus disease ebola | 5 |
were infected with ebov | 5 |
associated with fatal ebola | 5 |
ebola virus challenge with | 5 |
the survival of filoviruses | 5 |
by the observation that | 5 |
r schmidt et al | 5 |
b and l activate | 5 |
outbreak of marburg hemorrhagic | 5 |
marburg virus glycoproteins for | 5 |
vaccine in africa and | 5 |
host immune responses in | 5 |
used for the determination | 5 |
mice against a lethal | 5 |
emini surface accessibility prediction | 5 |
humoral responses and extensive | 5 |
the gp subunit is | 5 |
infection of macrophages and | 5 |
national institute of allergy | 5 |
nonhuman primates against lethal | 5 |
a percentage of the | 5 |
glycoprotein gp of ebola | 5 |
evaluated in this study | 5 |
assays have been developed | 5 |
a mouse model for | 5 |
type i ifn induction | 5 |
expressing ebola virus gp | 5 |
small nonhuman primate model | 5 |
mice that received vlps | 5 |
of type i interferons | 5 |
clomiphene and its isomers | 5 |
a phase i clinical | 5 |
l activate ebola but | 5 |
extents of fusion were | 5 |
the time to recovery | 5 |
is a key event | 5 |
of antibodies to ebola | 5 |
for the selection of | 5 |
a novel mechanism of | 5 |
a wide variety of | 5 |
to play an important | 5 |
programmed recognition of an | 5 |
and marburg viruses in | 5 |
virus assembly and budding | 5 |
responses and extensive intravascular | 5 |
host for the reston | 5 |
swine as a host | 5 |
data at jac online | 5 |
was used as a | 5 |
a dose of mg | 5 |
of filovirus entry into | 5 |
essential data or reagents | 5 |
at h post infection | 5 |
transfection medium was replaced | 5 |
dose of mg kg | 5 |
with fatal outcome in | 5 |
beta therapy prolongs survival | 5 |
the activity of the | 5 |
inhibition of ebola virus | 5 |
of swine as a | 5 |
the cells were washed | 5 |
stretch of tnc mutations | 5 |
the viral envelope with | 5 |
recombinant vesicular stomatitis viruses | 5 |
virus glycoproteins for efficient | 5 |
ebola virus persistence in | 5 |
the international committee on | 5 |
humans infected with sudan | 5 |
at the base of | 5 |
phase trials of rvsv | 5 |
how ebola and marburg | 5 |
in the transmission of | 5 |
as a host for | 5 |
nonhuman primate model for | 5 |
virus involves uptake by | 5 |
macrophages independent of tmprss | 5 |
available therapeutic agents that | 5 |
determined by plaque assay | 5 |
of the influenza virus | 5 |
a lethal challenge of | 5 |
a host for the | 5 |
a luciferase reporter gene | 5 |
clinically approved drugs amiodarone | 5 |
filovirus glycoproteins and the | 5 |
in ebola hemorrhagic fever | 5 |
in patients with evd | 5 |
was removed and the | 5 |
primate monocytes macrophages is | 5 |
against a lethal ebov | 5 |
of ebola virus transmission | 5 |
available to authorized users | 5 |
defective humoral responses and | 5 |
and l activate ebola | 5 |
committee on taxonomy of | 5 |
the binding of the | 5 |
were collected from the | 5 |
from bodily fluids and | 5 |
interacts with filovirus glycoproteins | 5 |
by interfering with the | 5 |
in an animal model | 5 |
caveolae are not required | 5 |
development and evaluation of | 5 |
the background level of | 5 |
in this study were | 5 |
specific for galactose and | 5 |
recombinant vaccine protects nonhuman | 5 |
read and approved the | 5 |
protein of sars coronavirus | 5 |
that they have no | 5 |
an important step in | 5 |
error of the mean | 5 |
the virus in the | 5 |
respiratory syndrome coronavirus in | 5 |
marburg virus infection in | 5 |
least one introduction event | 5 |
factors that influence ebola | 5 |
of ebov gp and | 5 |
macrophages is a key | 5 |
protection of guinea pigs | 5 |
and macrophages independent of | 5 |
wag and np i | 5 |
authors declare that they | 5 |
were added to the | 5 |
immunogenic in healthy adults | 5 |
and mechanism of entry | 5 |
the ebola virus envelope | 5 |
declare that they have | 5 |
the relative importance of | 5 |
may be able to | 5 |
ebov gp pseudotyped viruses | 5 |
ad vaccine expressing ebola | 5 |
it is assumed that | 5 |
the online version of | 5 |
and caveolae are not | 5 |
ebola virus mediated by | 5 |
and subsequent trafficking through | 5 |
the active microfluidic cartridge | 5 |
that does not require | 5 |
and verapamil inhibit filovirus | 5 |
it is plausible that | 5 |
and severe acute respiratory | 5 |
intravascular apoptosis are associated | 5 |
clinical illness and outcomes | 5 |
antisera for emerging viraly | 5 |
a neutralizing human antibody | 5 |
likely due to the | 5 |
in multiple cell types | 5 |
ebola virus involves uptake | 5 |
the protein data bank | 5 |
up of convalescent ebola | 5 |
of the role of | 5 |
entry requires the host | 5 |
infection in an animal | 5 |
at least one introduction | 5 |
of ebov infection in | 5 |
antibodies in scfv format | 5 |
be due to the | 5 |
has the potential to | 5 |
budding of vp virus | 5 |
common increasing or decreasing | 5 |
into cell lines and | 5 |
in a viral glycoprotein | 5 |
of the host cell | 5 |
in the nhp model | 5 |
screen of approved drugs | 5 |
recombinant ad vaccine expressing | 5 |
the antiviral factor tetherin | 5 |
of marburg virus is | 5 |
risk of ebola virus | 5 |
is available to authorized | 5 |
discovery of swine as | 5 |
glycoproteins and the spike | 5 |
infection results in substantial | 5 |
for both ebov and | 5 |
from lethal ebov infection | 5 |
that is critical for | 5 |
impact the course of | 5 |
strain of marburg virus | 5 |
the national institutes of | 5 |
are part of the | 5 |
are one of the | 5 |
vp to budding of | 5 |
of convalescent ebola hemorrhagic | 5 |
prophylaxis of ebola virus | 5 |
multiple cationic amphiphiles induce | 5 |
it has been suggested | 5 |
fails to impact the | 5 |
course of ebola virus | 5 |
mechanisms underlying coagulation abnormalities | 5 |
alpha and caveolae are | 5 |
associated with fatal outcome | 5 |
with ebola in sierra | 5 |
as part of the | 5 |
mutable targets of the | 5 |
glycoproteins of ebola virus | 5 |
no conflict of interest | 5 |
n and h n | 5 |
abnormalities in ebola hemorrhagic | 5 |
virus in sierra leone | 5 |
of gp on the | 5 |
efficient growth in human | 5 |
decay in the environment | 5 |
at the significance level | 5 |
cells were transduced with | 5 |
may play a role | 5 |
enhances virus binding and | 5 |
have an impact on | 5 |
bodily fluids and fomites | 5 |
members of the filoviridae | 5 |
hemorrhagic fever in kikwit | 5 |
to budding of vp | 5 |
live attenuated recombinant vaccine | 5 |
stored at room temperature | 5 |
in the course of | 5 |
viruses battle the immune | 5 |
a multiplicity of infection | 5 |
marburg viruses battle the | 5 |
the cells were then | 5 |
is able to inhibit | 5 |
and immunogenic in healthy | 5 |
both humoral and cellular | 5 |
was dependent on the | 5 |
evaluated in our study | 5 |
the cathepsin b inhibitor | 5 |
at the higher ah | 5 |
viral rna polymerase inhibitor | 5 |
to counteract the antiviral | 5 |
subsequent trafficking through early | 5 |
in africa and europe | 5 |
of ebov infection and | 5 |
the vp protein of | 5 |
mechanism and subsequent trafficking | 5 |
the majority of the | 5 |
t cell responses to | 5 |
pick c phenotype and | 5 |
short stretch of tnc | 5 |
through a sucrose cushion | 5 |
virus structure of the | 5 |
of rvsv ebola vaccine | 5 |
it has been reported | 5 |
and increased vascular permeability | 5 |
particles from infected cells | 5 |
and evaluation of a | 5 |
virus gp is safe | 5 |
genome replication and transcription | 5 |
infected cynomolgus macaques with | 5 |
has been isolated from | 5 |
virus decay in the | 5 |
of allergy and infectious | 5 |
ebolavirus glycoprotein structure and | 5 |
indicating that it is | 5 |
infection in nonhuman primates | 5 |
the mean hospitalization time | 5 |
antiviral activities in cell | 5 |
ebola virus glycoprotein and | 5 |
and outcomes in patients | 5 |
cd t cell response | 5 |
to be required for | 5 |
phenotype and inhibit ebola | 5 |
entry driven by both | 5 |
chou and fasman beta | 5 |
in ebola virus disease | 5 |
rna secondary structures in | 5 |
and enhance infection of | 5 |
cell lines and macrophages | 5 |
structure and mechanism of | 5 |
mean hospitalization time for | 5 |
marburg hemorrhagic fever in | 5 |
ebola virus infection results | 5 |
entry of ebola and | 5 |
a retrospective cohort study | 5 |
with sudan ebola virus | 5 |
of ebov gp on | 5 |
type i ifn antagonist | 5 |
with middle east respiratory | 5 |
an outbreak of ebola | 5 |
which is available to | 5 |
of tissue factor in | 5 |
in gabonese bat populations | 5 |
attenuated recombinant vaccine protects | 5 |
fatal outcome in ebola | 5 |
had no effect on | 5 |
primates against a lethal | 5 |
the development of new | 5 |
institute of allergy and | 5 |
of filoviruses in liquids | 5 |
ebola virus glycoprotein as | 5 |
virus transmission from bodily | 5 |
core structure of the | 5 |
in response to the | 5 |
not a direct effect | 5 |
subunits gp and gp | 5 |
for galactose and n | 5 |
with fatal ebola virus | 5 |
characterization of the ebola | 5 |
persistence in semen of | 5 |
culture supernatants were harvested | 5 |
for emerging viraly r | 5 |
the ebola virus genome | 5 |
minimize the risk of | 5 |
verapamil inhibit filovirus cell | 5 |
vpu employ different strategies | 5 |
h n and h | 5 |
for the generation of | 5 |
receptor alpha and caveolae | 5 |
virus infection results in | 5 |
tissue factor in primate | 5 |
that influence ebola antiviral | 5 |
enhance infection of macrophages | 5 |
may also contribute to | 5 |
a final volume of | 5 |
the extents of fusion | 5 |
specific for the viral | 5 |
an animal model by | 5 |
vp is involved in | 5 |
primate model for filovirus | 5 |
in a small animal | 5 |
of respiratory syncytial virus | 5 |
for ebola and marburg | 5 |
coagulation abnormalities in ebola | 5 |
its w a mutant | 5 |
assessment of the risk | 5 |
challenge with rna interference | 5 |
from the surface of | 5 |
lethal dose of ebov | 5 |
that the expression of | 5 |
of severe ebola virus | 5 |
motif in the transmembrane | 5 |
neutralizing antibody fails to | 5 |
in patients with severe | 5 |
that a fraction of | 5 |
with filovirus glycoproteins and | 5 |
protection against ebov infection | 5 |
proteins vp and vp | 5 |
the highest probability of | 5 |
at a multiplicity of | 5 |
no conflicts of interest | 5 |
and cd t cells | 5 |
sudan ebola hemorrhagic fever | 5 |
but not marburg virus | 5 |
viruses such as hiv | 5 |
convalescent ebola hemorrhagic fever | 5 |
and the spike protein | 5 |
c phenotype and inhibit | 5 |
entry into target cells | 5 |
the cells were incubated | 5 |
virus glycoproteins enhances virus | 5 |
lifecycle in host cells | 5 |
independent of tmprss expression | 5 |
fatal ebola virus infection | 5 |
the amount of cleaved | 5 |
hemorrhage is not a | 5 |
t cell responses are | 5 |
postexposure prophylaxis of ebola | 5 |
contribution of ebola virus | 5 |
used to assess the | 5 |
patients infected with ebov | 5 |
kolaskar and tongaonkar antigenicity | 5 |
bind ebola glycoproteins and | 5 |
guinea pigs and nonhuman | 5 |
of human peripheral blood | 5 |
the ph dependence of | 5 |
h n influenza virus | 5 |
ebola virus by using | 5 |
then added to each | 5 |
for the viral nucleoprotein | 5 |
of the viral rna | 5 |
the reciprocal of the | 5 |
antibody fails to impact | 5 |
that hemorrhage is not | 5 |
model by passive transfer | 5 |
on the day of | 5 |
ebola virus glycoproteins enhances | 5 |
marburg virus and ebola | 5 |
was assumed to be | 5 |
laboratory diagnosis of ebola | 5 |
of the filoviridae family | 5 |
lines and macrophages independent | 5 |
infected with sudan ebola | 5 |
have no competing interests | 5 |
overexpression of tissue factor | 5 |
common among the three | 5 |
based vaccine design against | 5 |
plays a role in | 5 |
that are important for | 5 |
the molecular basis of | 5 |
glycoproteins and enhance infection | 5 |
influence ebola antiviral activities | 5 |
case of ebola virus | 5 |
of marburg virus in | 5 |
ebola glycoproteins and enhance | 5 |
apoptosis are associated with | 5 |
of at least one | 5 |
to cleave ebov gp | 5 |
and middle east respiratory | 5 |
survival of filoviruses in | 5 |
samples were collected in | 5 |
the efficacy of remdesivir | 5 |
on taxonomy of viruses | 5 |
ebola virus transmission from | 5 |
of macrophages and endothelial | 5 |
with the exception of | 5 |
has been reported to | 5 |
unpublished essential data or | 5 |
involves uptake by a | 5 |
as supplementary data at | 5 |
and fasman beta turn | 5 |
transfer of a neutralizing | 5 |
underlying coagulation abnormalities in | 5 |
standard error of the | 5 |
of ebola virus involves | 5 |
in primate monocytes macrophages | 5 |
were used to infect | 5 |
the role of this | 5 |
in substantial immune activation | 5 |
the hepatitis c virus | 5 |
outcomes in patients with | 5 |
elevated levels of interferon | 5 |
note springer nature remains | 5 |
management of ebola virus | 5 |
the transfection medium was | 5 |
the binding site for | 5 |
for the reston ebolavirus | 5 |
illness and outcomes in | 5 |
which is important for | 5 |
amphiphiles induce a niemann | 5 |
in a variety of | 5 |
the risk of ebola | 5 |
and the role of | 5 |
ebola antiviral activities in | 5 |
functional characterization of the | 5 |
cell fusion mediated by | 5 |
authors declare no competing | 5 |
in a manner that | 5 |
and influenza a virus | 5 |
have been developed for | 5 |
and marburg viruses using | 5 |
trials of rvsv ebola | 5 |
the transmembrane domain of | 5 |
of a neutralizing human | 5 |
under the age of | 5 |
is required for the | 5 |
extensive intravascular apoptosis are | 5 |
type calcium channel blocker | 5 |
and marburg viruses battle | 5 |
erk mapk and pi | 5 |
cationic amphiphiles induce a | 5 |
online version of this | 5 |
due to the lack | 5 |
been detected in the | 5 |
has yet to be | 5 |
vesicular stomatitis virus vectors | 5 |
in sierra leone ebola | 5 |
signr bind ebola glycoproteins | 5 |
pigs and nonhuman primates | 5 |
ebola virus entry and | 5 |
dynamics of ebola virus | 5 |
for efficient entry into | 5 |
in liver and spleen | 5 |
strategies to counteract the | 5 |
of an intracellular receptor | 5 |
virus glycoprotein as the | 5 |
in the common marmoset | 5 |
mapk and pi k | 5 |
cells were then incubated | 5 |
ebola virus gp is | 5 |
animal model by passive | 5 |
and samples were collected | 5 |
a u u a | 5 |
the clinically approved drugs | 5 |
of the disease and | 5 |
ebola virus in sierra | 5 |
as a type i | 5 |
due to their ability | 5 |
outbreak in western africa | 5 |
by ebola virus glycoprotein | 5 |
by macropinocytosis and clathrin | 5 |
during an outbreak of | 5 |
evidence that hemorrhage is | 5 |
number of years to | 5 |
the a u mutant | 5 |
it is clear that | 5 |
by passive transfer of | 5 |
for ebola virus glycoprotein | 5 |
in a co incubator | 5 |
inhibit filovirus cell entry | 5 |
mediated cell entry of | 5 |
hemorrhagic fever associated with | 5 |
ebov infection in nhps | 5 |
acetylgalactosamine promotes filovirus entry | 5 |
treatment with recombinant nematode | 5 |
humoral and cellular immunity | 5 |
transmission from bodily fluids | 5 |
were immunized intramuscularly with | 5 |
to the fact that | 5 |
and vp to budding | 5 |
ebov lifecycle in host | 5 |
ebov or marv gp | 5 |
and immunogenicity of a | 5 |
of nonhuman primates against | 5 |
ebola but not marburg | 5 |
ebola virus matrix protein | 5 |
results in substantial immune | 5 |
pigs against a lethal | 5 |
to their ability to | 5 |
average number of years | 5 |
of the viral and | 5 |
contributed unpublished essential data | 5 |
rna viruses such as | 5 |
the significance level of | 5 |
supplementary data at jac | 5 |
to the release of | 5 |
of equine antisera and | 5 |
twice daily for days | 5 |
monocytes macrophages is a | 5 |
virus challenge with rna | 5 |
volume of pbs as | 5 |
mediated protection against ebov | 5 |
of ebola virus ebola | 5 |
vp protein of ebola | 5 |
international committee on taxonomy | 5 |
efficient entry into cell | 5 |
and pi k akt | 5 |
of viral hemorrhagic fever | 5 |
virus infection in an | 5 |
not marburg virus glycoproteins | 5 |
ebola virus disease patients | 5 |
passive transfer of a | 5 |
activate ebola but not | 5 |
the percentage of ebov | 5 |
gp is safe and | 5 |
were regarded as sl | 5 |
gorilla fecal samples were | 5 |
marburg virus surface protein | 5 |
fever in primate models | 5 |
in the transmembrane domain | 5 |
the replication of the | 5 |
causative agent of the | 5 |
patients with ebola in | 5 |
markedly elevated levels of | 5 |
have the potential to | 5 |
glycoproteins enhances virus binding | 5 |
emerging viraly r schmidt | 5 |
ebola vaccine in africa | 5 |
battle the immune system | 5 |
detection of neutralizing antibodies | 4 |
to nonhuman primates complete | 4 |
the creative commons license | 4 |
of dendritic cells and | 4 |
undergo a subsequent fusion | 4 |
nucleoprotein of ebola virus | 4 |
implications for a role | 4 |
not be sufficient to | 4 |
from the same patient | 4 |
internal fusion loop of | 4 |
for inhibitors of biological | 4 |
viruses replicate in monocyte | 4 |
filovirus entry into vero | 4 |
it is not clear | 4 |
when march was expressed | 4 |
site of ebov fusion | 4 |
does not require tetherin | 4 |
the lineage dual model | 4 |
for formation of the | 4 |
monitoring and human ebola | 4 |
of convalescent plasma for | 4 |
to be important for | 4 |
and in trans dc | 4 |
you give appropriate credit | 4 |
a type i ifn | 4 |
clomiphene and enclomiphene in | 4 |
who ebola response team | 4 |
will need to obtain | 4 |
a significant threat to | 4 |
cytotoxic t lymphocytes specific | 4 |
of the year bats | 4 |
groups of mice were | 4 |
intended use is not | 4 |
a standardized nomenclature for | 4 |
of vascular cell cytotoxicity | 4 |
ebola virus counters the | 4 |
your intended use is | 4 |
for replication in cell | 4 |
virus vp protein functions | 4 |
health and human services | 4 |
allergy and infectious diseases | 4 |
of bushmeat is bats | 4 |
nonhuman primate model of | 4 |
uniform standard error of | 4 |
cytokines and full maturation | 4 |
from the envelope glycoprotein | 4 |
the virus and the | 4 |
direct exposure to fruit | 4 |
alpha associated with fatal | 4 |
globulin and recombinant interferon | 4 |
tested negative for anti | 4 |
axl enhances macropinocytosis of | 4 |
activation of type i | 4 |
were infected with a | 4 |
virus and the s | 4 |
receptor kinase axl enhances | 4 |
ebolavirus in humans and | 4 |
of filoviral hemorrhagic fever | 4 |
and neutralizing antibody responses | 4 |
are included in the | 4 |
united states and europe | 4 |
a type i transmembrane | 4 |
with one or more | 4 |
b l are not | 4 |
is used as a | 4 |
clinical efficacy of remdesivir | 4 |
was to assess the | 4 |
lethal infection in mice | 4 |
innate immune responses in | 4 |
through the use of | 4 |
in the early stages | 4 |
assays were used to | 4 |
ebola virus secrete mip | 4 |
not permitted by statutory | 4 |
against ebov infection in | 4 |
is consistent with previous | 4 |
for the introduction of | 4 |
association with the lipid | 4 |
glycan cap and the | 4 |
these data the initial | 4 |
figure a and b | 4 |
require endosomal cysteine proteases | 4 |
the role of siglec | 4 |
of ebola virus triggers | 4 |
and is associated with | 4 |
pathogenesis and treatment with | 4 |
detected in a common | 4 |
the main viral determinant | 4 |
viruses in gabonese bat | 4 |
and nonfatal cases of | 4 |
there are a number | 4 |
cells were obtained from | 4 |
c region of ebov | 4 |
ebola virus infection complicated | 4 |
infection in african straw | 4 |
immune globulin and recombinant | 4 |
and the evolution of | 4 |
at the point of | 4 |
life cycle modeling system | 4 |
adaptation of ebov during | 4 |
the terms and conditions | 4 |
glycoprotein of marburg virus | 4 |
specific cd t cells | 4 |
absence of thermolysin treatment | 4 |
be used as a | 4 |
biochemical analysis of the | 4 |
sequence and residues critical | 4 |
study had high estimates | 4 |
of the external solution | 4 |
ad and protect nonhuman | 4 |
able to inhibit the | 4 |
of ebola virus makona | 4 |
expression of type i | 4 |
in the republic of | 4 |
and weight change for | 4 |
the specificity of the | 4 |
was similar to that | 4 |
immunity to ad and | 4 |
progress in the development | 4 |
decline of central african | 4 |
and vero e cells | 4 |
assumed that c min | 4 |
stability of ebola virus | 4 |
gp is cleaved by | 4 |
for emerging infectious diseases | 4 |
through early and late | 4 |
has been reported for | 4 |
if changes were made | 4 |
and conditions of the | 4 |
primates against ebola virus | 4 |
commons license and your | 4 |
systematic screen of fda | 4 |
on ice for min | 4 |
using artificial replication systems | 4 |
a paucity of information | 4 |
cells infected with ebola | 4 |
and the gp subunit | 4 |
cellular host range of | 4 |
have a uniform standard | 4 |
and weeks after the | 4 |
contaminated in eu ms | 4 |
are known to be | 4 |
with the glycoprotein of | 4 |
of plants and animals | 4 |
and approved the final | 4 |
are a number of | 4 |
of the transcription and | 4 |
alpha and inhibit poly | 4 |
regulation or exceeds the | 4 |
under a creative commons | 4 |
cells without inducing the | 4 |
with the lipid bilayer | 4 |
of biological threat agents | 4 |
years of marburg virus | 4 |
single amino acid residue | 4 |
the immune epitope database | 4 |
based ebola vaccine is | 4 |
production of cytokines and | 4 |
cell fusion induced by | 4 |
vesicular stomatitis virus vaccine | 4 |
of the experiment and | 4 |
the angola strain of | 4 |
inducing the production of | 4 |
but exhibit distinct protease | 4 |
infection by ebola and | 4 |
in the selection of | 4 |
in rhesus macaques infected | 4 |
and three species of | 4 |
blood samples were collected | 4 |
domains of lake victoria | 4 |
any medium or format | 4 |
ebola vaccine in healthy | 4 |
enveloped viruses such as | 4 |
if material is not | 4 |
and peripheral blood mononuclear | 4 |
load on raw product | 4 |
rhesus macaque model of | 4 |
neutralizing antibody responses against | 4 |
directly from the copyright | 4 |
mixture of two stereoisomers | 4 |
of hpai h n | 4 |
filoviruses require endosomal cysteine | 4 |
when compared to the | 4 |
early and late endosomes | 4 |
vector mediates postexposure protection | 4 |
and support vector machines | 4 |
among ehf patients in | 4 |
this is an important | 4 |
of emerging and re | 4 |
of health and sanitation | 4 |
human primates against a | 4 |
this is consistent with | 4 |
from ebola virus mediated | 4 |
titers were determined by | 4 |
ic for clomiphene was | 4 |
resulting from direct exposure | 4 |
in human dendritic cells | 4 |
linked immunosorbent assay for | 4 |
the sudv outbreak in | 4 |
comprehensive analysis of ebola | 4 |
structure of the envelope | 4 |
should be addressed to | 4 |
of the infected cell | 4 |
and laboratory features of | 4 |
of the congo in | 4 |
monitored for additional days | 4 |
was performed using the | 4 |
authors declare no conflict | 4 |
use is not permitted | 4 |
and nitric oxide levels | 4 |
vaccine vectors bypass immunity | 4 |
the late stages of | 4 |
with ebola virus secrete | 4 |
that one or more | 4 |
permission directly from the | 4 |
analysis of the ebola | 4 |
cells were seeded at | 4 |
or exceeds the permitted | 4 |
high seroprevalence of both | 4 |
starting at or dpi | 4 |
a systematic screen of | 4 |
underestimation of branch lengths | 4 |
variance log tcid ml | 4 |
with the ifn system | 4 |
hepatitis c virus entry | 4 |
a preventive vaccine for | 4 |
by a novel broad | 4 |
the therapeutic efficacy of | 4 |
of west nile virus | 4 |
marburg virus disease in | 4 |
dendritic cell stimulating activity | 4 |
infection prevalence in exporting | 4 |
structure of ebov gp | 4 |
for antibodies to ebola | 4 |
west african evd outbreak | 4 |
give appropriate credit to | 4 |
credit line to the | 4 |
obtain permission directly from | 4 |
the a u a | 4 |
of the sars coronavirus | 4 |
as you give appropriate | 4 |
blood ebov turned negative | 4 |
immunization of ebola virus | 4 |
in the biosafety level | 4 |
a potent inhibitor of | 4 |
cell entry mediated by | 4 |
the national institute for | 4 |
protein of severe acute | 4 |
vaccine in healthy adults | 4 |
treatment of experimental ebola | 4 |
mononuclear cells infected with | 4 |
resistant to ebov infection | 4 |
removed and cells were | 4 |
class i fusion proteins | 4 |
virus glycoprotein to undergo | 4 |
cells were fixed with | 4 |
epidemic in west africa | 4 |
hemorrhagic fever patients and | 4 |
monkeys with immunoglobulin from | 4 |
protects immunocompromised nonhuman primates | 4 |
derived human macrophages and | 4 |
hemorrhagic fever ebola virus | 4 |
lake victoria marburgvirus and | 4 |
in insect cells exhibit | 4 |
adaptation of ebola virus | 4 |
after the second boost | 4 |
the ns protein of | 4 |
ebov negative reference serum | 4 |
and ad vaccine vectors | 4 |
in the same way | 4 |
early stages of infection | 4 |
sexual transmission of ebola | 4 |
hemorrhagic fever in nonhuman | 4 |
genetics demonstrates that proteolytic | 4 |
primary human monocytes and | 4 |
and rapid decline of | 4 |
of ebola haemorrhagic fever | 4 |
year bats may shed | 4 |
in the endocytic pathway | 4 |
the ebola virus matrix | 4 |
for signs of disease | 4 |
worst case scenario it | 4 |
the nih aids reagent | 4 |
using a combination of | 4 |
to the original author | 4 |
in vivo during infection | 4 |
and the use of | 4 |
of an antioxidant small | 4 |
blocked with bovine serum | 4 |
these results indicate that | 4 |
acidification of the external | 4 |
and there was no | 4 |
the most promising candidates | 4 |
monkeys by aerosolized ebola | 4 |
have been implicated in | 4 |
remdesivir reduces the time | 4 |
of ebola viruses causing | 4 |
phi may not be | 4 |
virus glycoprotein counteracts bst | 4 |
clinical virology of ebola | 4 |
the envelope glycoprotein of | 4 |
like mechanism and subsequent | 4 |
gp from ebola virus | 4 |
to the lack of | 4 |
the use of the | 4 |
as the main viral | 4 |
domain of marburg virus | 4 |
to obtain permission directly | 4 |
humans and animals in | 4 |
on these data the | 4 |
replication strategies of marburg | 4 |
gabon and republic of | 4 |
in the induction of | 4 |
survival and weight change | 4 |
the use of different | 4 |
cathepsin b l are | 4 |
ebola virus glycoproteins on | 4 |
manner that does not | 4 |
the gp gene and | 4 |
induced particle formation and | 4 |
infected with ebov mak | 4 |
were cloned into the | 4 |
fusion induced by cleaved | 4 |
within the plasma membrane | 4 |
igg ebov negative reference | 4 |
due to the presence | 4 |
and replication strategies of | 4 |
representative of three independent | 4 |
fever in nonhuman primates | 4 |
the zaire strain of | 4 |
entry inhibitor for filoviruses | 4 |
structure of ebola virus | 4 |
binding domains of lake | 4 |
in the design of | 4 |
of both viruses in | 4 |
for treatment of experimental | 4 |
antiviral activity in vitro | 4 |
not necessarily reflect the | 4 |
for a role in | 4 |
identification of the ebola | 4 |
for compartmentalized trafficking of | 4 |
main viral determinant of | 4 |
vaccine design against ebov | 4 |
this article are included | 4 |
virus mediated by cytotoxic | 4 |
human monocytes and macrophages | 4 |
hemorrhagic fever in humans | 4 |
virus glycoprotein and hiv | 4 |
has been demonstrated in | 4 |
marburgvirus and zaire ebolavirus | 4 |
consider product contaminated in | 4 |
line to the material | 4 |
important role in the | 4 |
unless indicated otherwise in | 4 |
ebola virus nonstructural glycoprotein | 4 |
it was shown that | 4 |
log tcid ml in | 4 |
the ebola virus nucleocapsid | 4 |
its endosomal receptor niemann | 4 |
molecules of the ifn | 4 |
haemorrhagic fever ebola virus | 4 |
and is required for | 4 |
female balb c mice | 4 |
new ebola virus nonstructural | 4 |
at an early stage | 4 |
cells exhibit dendritic cell | 4 |
infected cynomolgus monkeys with | 4 |
glycoprotein is not essential | 4 |
rapid decline of central | 4 |
posttranslational modification of nucleoprotein | 4 |
vesicular stomatitis virus vector | 4 |
antiviral activity of a | 4 |
it is difficult to | 4 |
was removed and replaced | 4 |
postexposure protection against sudan | 4 |
in west africa from | 4 |
and effectiveness of an | 4 |
virus nonstructural glycoprotein expressed | 4 |
preventive vaccine for ebola | 4 |
and ebolavirus cell entry | 4 |
supernatants were harvested at | 4 |
virus by using artificial | 4 |
a h n virus | 4 |
the ebola virus outbreak | 4 |
was removed from the | 4 |
vectors bypass immunity to | 4 |
defective recombinant ad vaccine | 4 |
is believed to be | 4 |
molecular evidence of sexual | 4 |
of sexual transmission of | 4 |
an impact on the | 4 |
against sudan ebola hemorrhagic | 4 |
gp on the plasma | 4 |
role in virus assembly | 4 |
cathepsin b and l | 4 |
open access article distributed | 4 |
pubmed abstract publisher full | 4 |
mechanism of action of | 4 |
surface of infected cells | 4 |
with activity against ebola | 4 |
found that a single | 4 |
virus nomenclature below the | 4 |
seen in figure a | 4 |
can be inhibited by | 4 |
of the virus from | 4 |
projected data have a | 4 |
the primed ebolavirus glycoprotein | 4 |
of the gp gene | 4 |
environment and during transport | 4 |
probability of introduction of | 4 |
in domestic pigs in | 4 |
analysis of the secreted | 4 |
expressed through rna editing | 4 |
for transcription and replication | 4 |
glycoprotein gp from ebola | 4 |
both innate and adaptive | 4 |
primates complete protection against | 4 |
is at present unknown | 4 |
activated protein c for | 4 |
have been reported in | 4 |
mediated by cytotoxic t | 4 |
army medical research institute | 4 |
log normal distribution with | 4 |
in ocular fluid during | 4 |
in decay rates between | 4 |
you will need to | 4 |
macropinocytosis of zaire ebolavirus | 4 |
the effects of clomiphene | 4 |
cell stimulating activity and | 4 |
counteract the antiviral factor | 4 |
determinant of vascular cell | 4 |
model of ebola virus | 4 |
fresh medium was added | 4 |
and human ebola outbreaks | 4 |
long as you give | 4 |
in the replication cycle | 4 |
lower than that of | 4 |
the resistance of mice | 4 |
and virion glycoproteins of | 4 |
for viral transcription and | 4 |
target of ebov infection | 4 |
has been used for | 4 |
is an open access | 4 |
outbreak resulting from direct | 4 |
human macrophages and peripheral | 4 |
follows a log normal | 4 |
viruses in rousettus aegyptiacus | 4 |
the same volume of | 4 |
shown to be effective | 4 |
the secondary structure of | 4 |
and residues critical for | 4 |
fatal and nonfatal cases | 4 |
in a wide range | 4 |
the development of a | 4 |
of its body weight | 4 |
ebola virus virulence in | 4 |
of hemorrhagic fever virus | 4 |
from the copyright holder | 4 |
against infection with marburg | 4 |
can be explained by | 4 |
induce the expression of | 4 |
in the live ebov | 4 |
essential for replication in | 4 |
in the protein data | 4 |
cysteine proteases for entry | 4 |
exposure treatment of ebola | 4 |
a uniform standard error | 4 |
fusion was independent of | 4 |
weight over the course | 4 |
and igm antibody findings | 4 |
both viruses in rousettus | 4 |
caused by the ongoing | 4 |
like filovirus in europe | 4 |
the images or other | 4 |
derived dendritic cells without | 4 |
domain c of npc | 4 |
results of this study | 4 |
was independent of ph | 4 |
bypass immunity to ad | 4 |
they have no competing | 4 |
to confer to nonhuman | 4 |
human ebola outbreak resulting | 4 |
exhibit dendritic cell stimulating | 4 |
ebola virus nucleocapsid requires | 4 |
a log normal distribution | 4 |
design against ebov gp | 4 |
identification of a small | 4 |
virus transmission events and | 4 |
same volume of pbs | 4 |
virus virulence in mice | 4 |
west africa from to | 4 |
and may result in | 4 |
the virus from the | 4 |
transmission events and rapid | 4 |
a guinea pig model | 4 |
rna editing of the | 4 |
of lake victoria marburgvirus | 4 |
western african evd outbreak | 4 |
angola strain of marburg | 4 |
randomly assigned into groups | 4 |
against filovirus diseases by | 4 |
for a variety of | 4 |
is shown in fig | 4 |
functions as a type | 4 |
van damme et al | 4 |
treatment was given ip | 4 |
proteases for entry but | 4 |
virus vector mediates postexposure | 4 |
to a final concentration | 4 |
survey showing cocirculation of | 4 |
research institute of infectious | 4 |
its body weight over | 4 |
text free full text | 4 |
counters the interferon system | 4 |
results from the guinea | 4 |
guinea pigs from lethal | 4 |
of ebola virus glycoproteins | 4 |
features of filoviral hemorrhagic | 4 |
the determination of cut | 4 |
link to the creative | 4 |
there was evidence of | 4 |
within the respiratory tract | 4 |
marburg virus and three | 4 |
with the plasma membrane | 4 |
in the middle east | 4 |
receptors on the surface | 4 |
vivo during infection by | 4 |
a complementary role to | 4 |
hydroxyl acylation analyzed by | 4 |
the potential of the | 4 |
virus infection in rodents | 4 |
viral hemorrhagic fever in | 4 |
the surface of infected | 4 |
in dcs and macrophages | 4 |
a link to the | 4 |
evidence of sexual transmission | 4 |
demonstrates that proteolytic processing | 4 |
prevalence of infection in | 4 |
is often associated with | 4 |
directed against the mutable | 4 |
infection detected in a | 4 |
were randomly assigned into | 4 |
modified vaccinia virus ankara | 4 |
essential for transcription and | 4 |
drugs inhibiting the ebola | 4 |
in the three areas | 4 |
at room temperature with | 4 |
not be a suitable | 4 |
zaire ebolavirus bind a | 4 |
is not included in | 4 |
and evolution during seven | 4 |
seroprevalence of both viruses | 4 |
of interferon regulatory factor | 4 |
calcium channel blocker verapamil | 4 |
it is believed that | 4 |
of ebola virus fusion | 4 |
the replication cycle of | 4 |
reston ebolavirus in humans | 4 |
absence of any other | 4 |
replication cycle of the | 4 |
experimental ebola virus infections | 4 |
of the glycoprotein gp | 4 |
bats may shed active | 4 |
the expression of ifn | 4 |
antibody findings among ehf | 4 |
of enclomiphene and zuclomiphene | 4 |
the viral fusion world | 4 |
model of filovirus infection | 4 |
the equine antisera and | 4 |
marburg and ebola virus | 4 |
novelty in the viral | 4 |
to minimize the risk | 4 |
a new ebola virus | 4 |
highlights the importance of | 4 |
findings among ehf patients | 4 |
endosomal cysteine proteases for | 4 |
in liberia and sierra | 4 |
in the resistance of | 4 |
virus disease in johannesburg | 4 |
in vero e and | 4 |
in cellular cholesterol trafficking | 4 |
detection limit of the | 4 |
abstract publisher full text | 4 |
not essential for replication | 4 |
in humans and other | 4 |
full text free full | 4 |
potentiates the ebola virus | 4 |
ebola virus fusion triggering | 4 |
the ability of these | 4 |
for detection of antibodies | 4 |
this article is an | 4 |
of the different ebov | 4 |
in the viral fusion | 4 |
efficacy and effectiveness of | 4 |
of ebov gp by | 4 |
into vero e cells | 4 |
and a high seroprevalence | 4 |
as shown in figure | 4 |
and tongaonkar antigenicity scale | 4 |
entry into vero e | 4 |
from ebola virus at | 4 |
a normal distribution of | 4 |
fresh growth medium containing | 4 |
based vaccine protects nonhuman | 4 |
and incubated for h | 4 |
reproduction in any medium | 4 |
of host cell entry | 4 |
with recombinant nematode anticoagulant | 4 |
successful treatment of advanced | 4 |
of cytokines and full | 4 |
large serological survey showing | 4 |
as a percentage of | 4 |
removed and the cells | 4 |
was observed in the | 4 |
the cell surface is | 4 |
high estimates of d | 4 |
envelope glycoprotein gp from | 4 |
inhibiting the ebola virus | 4 |
mg kg loading dose | 4 |
have a complementary role | 4 |
changes were accompanied by | 4 |
to the creative commons | 4 |
amount of cleaved gp | 4 |
diseases by a novel | 4 |
ad vaccine vectors bypass | 4 |
a role in virus | 4 |
stomatitis virus vector mediates | 4 |
factors that influence the | 4 |
the initial viral load | 4 |
prevalence in exporting country | 4 |
the projected data have | 4 |
protection against multistrain ebola | 4 |
changes in gene expression | 4 |
is known about the | 4 |
required for inhibition of | 4 |
the production of cytokines | 4 |
a limited number of | 4 |
serological survey showing cocirculation | 4 |
and ebola virus by | 4 |
from direct exposure to | 4 |
of the evd patients | 4 |
the van der waals | 4 |
the initial concentration of | 4 |
on endothelial cell activation | 4 |
article is an open | 4 |
role of the type | 4 |
are found in the | 4 |
dendritic cells without inducing | 4 |
in the infected host | 4 |
against multistrain ebola and | 4 |
by factors such as | 4 |
highest probability of introduction | 4 |
in virus assembly and | 4 |
entry of enveloped viruses | 4 |
virus infection in a | 4 |
glycoprotein in viral entry | 4 |
a case of ebola | 4 |
in the environment and | 4 |
can be detected in | 4 |
the mechanism by which | 4 |
probability of at least | 4 |
the secreted and virion | 4 |
of the virus particles | 4 |
for the prediction of | 4 |
kinase axl enhances macropinocytosis | 4 |
growth medium containing scs | 4 |
plants and animals with | 4 |
immune activation and increased | 4 |
to its endosomal receptor | 4 |
was supported by the | 4 |
stimulating activity and induce | 4 |
cells were cotransfected with | 4 |
the onset of illness | 4 |
evaluation of immune globulin | 4 |
patients and their household | 4 |
filovirus diseases by a | 4 |
ebola outbreak resulting from | 4 |
gp in viral entry | 4 |
there is also evidence | 4 |
declare no competing interests | 4 |
entry but exhibit distinct | 4 |
for host cell binding | 4 |
samples were collected at | 4 |
under positive selection in | 4 |
rate of up to | 4 |
dcs and macrophages in | 4 |
assigned into groups of | 4 |
using inhibitors of endocytosis | 4 |
samples from fatal and | 4 |
have been developed to | 4 |
necessary for infection ebola | 4 |
immunoglobulin from hyperimmune horses | 4 |
uptake by a macropinocytosis | 4 |
infection complicated by gram | 4 |
residues critical for host | 4 |
to ad and protect | 4 |
bind a common receptor | 4 |
enhances macropinocytosis of zaire | 4 |
i interferon response in | 4 |
virus and three species | 4 |
with live ebov neutralisation | 4 |
cells were cultured in | 4 |
in accordance with the | 4 |
nonstructural glycoprotein expressed through | 4 |
and treatment with recombinant | 4 |
in the viral life | 4 |
collected in zone b | 4 |
under the terms and | 4 |
mice infected with ebov | 4 |
variation in selection pressures | 4 |
determinants of ebola virus | 4 |
the tyro receptor kinase | 4 |
it has also been | 4 |
of any other data | 4 |
of the viral membrane | 4 |
nomenclature below the species | 4 |
the medium was replaced | 4 |
used in our study | 4 |
have been identified as | 4 |
blood samples from fatal | 4 |
and error bars indicate | 4 |
of the virus to | 4 |
virus infection in primates | 4 |
normal distribution with mean | 4 |
negative reference serum panel | 4 |
party material in this | 4 |
injection vaccine protects nonhuman | 4 |
the natural history of | 4 |
has also been shown | 4 |
resistance of mice to | 4 |
the entry of the | 4 |
patients with severe covid | 4 |
as well as in | 4 |
to consider product contaminated | 4 |
analysis of human peripheral | 4 |
marburg viruses in gabonese | 4 |
apoptosis induced in vitro | 4 |
article are included in | 4 |
experimental infections of rhesus | 4 |
igm antibody findings among | 4 |
the site of ebov | 4 |
the ebola virus nucleoprotein | 4 |
prophylaxis and therapy of | 4 |
c min log tcid | 4 |
insights from ebola virus | 4 |
h n highly pathogenic | 4 |
is essential for the | 4 |
and cd t cell | 4 |
the innate immune response | 4 |
to the sites of | 4 |
glycoprotein as the main | 4 |
as long as you | 4 |
shedding of the glycoprotein | 4 |
the cellular host range | 4 |
is cleaved by the | 4 |
reduces the time to | 4 |
material is not included | 4 |
absence of other information | 4 |
it is thought that | 4 |
and igg and igm | 4 |
virus infection with t | 4 |
variant of ebola virus | 4 |
we were unable to | 4 |
was calculated as the | 4 |
a severe haemorrhagic fever | 4 |
case of severe ebola | 4 |
direct contact with bodily | 4 |
is involved in the | 4 |
glycoprotein to undergo a | 4 |
of the conserved region | 4 |
and the s protein | 4 |
were then incubated for | 4 |
the gps of the | 4 |
ebola virus in ocular | 4 |
the recent west african | 4 |
gp pseudotyped virus neutralisation | 4 |
virus gp in viral | 4 |
transcription polymerase chain reaction | 4 |
scenario it is assumed | 4 |
of rhesus macaques with | 4 |
second luminal domain of | 4 |
is likely that the | 4 |
ebola haemorrhagic fever virus | 4 |
vascular cell cytotoxicity and | 4 |
activation and increased vascular | 4 |
the results of the | 4 |
the expression of type | 4 |
binding to ebov gp | 4 |
experimental inoculation of plants | 4 |
clinical and laboratory features | 4 |
primates against lethal ebola | 4 |
the nature of the | 4 |
view a copy of | 4 |
and huh cells were | 4 |
angola infection of rhesus | 4 |
that type i ifns | 4 |
provide a link to | 4 |
advanced ebola virus infection | 4 |
other third party material | 4 |
the low ph pulse | 4 |
phase i clinical trials | 4 |
is assumed that c | 4 |
animal mortality monitoring and | 4 |
an open access article | 4 |
tetherin restriction in a | 4 |
human immunodeficiency virus and | 4 |
ebov entry into the | 4 |
and their household contacts | 4 |
minimum viral load to | 4 |
a high seroprevalence of | 4 |
single particle image analysis | 4 |
animals in the philippines | 4 |
infection with marburg virus | 4 |
for ebov and marv | 4 |
from the guinea ring | 4 |
replication and transcription of | 4 |
the clinical efficacy of | 4 |
induced in vitro and | 4 |
ebola virus glycoprotein to | 4 |
were transferred to a | 4 |
the highest serum dilution | 4 |
is responsible for the | 4 |
four fda approved drugs | 4 |
that are required for | 4 |
that proteolytic processing of | 4 |
all animals were monitored | 4 |
ml in the absence | 4 |
was monitored for additional | 4 |
the guinea ring vaccination | 4 |
contact with an infected | 4 |
a creative commons attribution | 4 |
by the national institutes | 4 |
the presence of vp | 4 |
in a credit line | 4 |
blood mononuclear cells infected | 4 |
virus infection complicated by | 4 |
of ebov gp that | 4 |
fever patients and their | 4 |
evolution during seven months | 4 |
in wild great apes | 4 |
results suggest that the | 4 |
and your intended use | 4 |
the year bats may | 4 |
epidemic of ebola virus | 4 |
experiment and none survived | 4 |
and detection of neutralizing | 4 |
the activity of cathepsins | 4 |
visualization of ebola virus | 4 |
directed expression of tetherin | 4 |
lymphocytes specific for the | 4 |
marburgvirus and ebolavirus cell | 4 |
particle formation and association | 4 |
molecular basis for ebola | 4 |
wild animal mortality monitoring | 4 |
compartmentalized trafficking of ebola | 4 |
nonfatal cases of ebola | 4 |
rates of up to | 4 |
to binding in the | 4 |
cytokine and chemokine expression | 4 |
exposure to fruit bats | 4 |
during infection by ebola | 4 |
drugs for inhibitors of | 4 |
in the eye and | 4 |
fever ebola virus disease | 4 |
analysis of filovirus entry | 4 |
and disseminated intravascular coagulation | 4 |
and indicate if changes | 4 |
virus angola infection of | 4 |
their ability to inhibit | 4 |
to interfere with the | 4 |
ebola virus glycoprotein counteracts | 4 |
vaccine to confer to | 4 |
given the same volume | 4 |
with marburg virus and | 4 |
victoria marburgvirus and zaire | 4 |
of health and human | 4 |
s protein of severe | 4 |
postexposure treatment of ebola | 4 |
trafficking of ebola and | 4 |
images or other third | 4 |
newborn balb c mice | 4 |
that c min log | 4 |
severe ebola virus infection | 4 |
data suggest that the | 4 |
in the ebov lifecycle | 4 |
class i fusion protein | 4 |
antiviral activity against ebov | 4 |
n highly pathogenic avian | 4 |
to fruit bats in | 4 |
are located in the | 4 |
favorable immune cell targeting | 4 |
is a type i | 4 |
during the acute phase | 4 |
there have been a | 4 |
cocirculation of ebola and | 4 |
article distributed under the | 4 |
alpha b for treatment | 4 |
material in this article | 4 |
a suitable surrogate for | 4 |
basic clinical and laboratory | 4 |
survival was monitored for | 4 |
outbreak in south korea | 4 |
critical for host cell | 4 |
development of a preventive | 4 |
cell lines were maintained | 4 |
of the most promising | 4 |
secreted and virion glycoproteins | 4 |
a variety of different | 4 |
to ebola virus disease | 4 |
statutory regulation or exceeds | 4 |
data have a uniform | 4 |
protection against a lethal | 4 |
monoclonal antibodies against ebola | 4 |
a replication defective recombinant | 4 |
that vp and vp | 4 |
of type i interferon | 4 |
molecular determinants of ebola | 4 |
of disseminated intravascular coagulation | 4 |
not require tetherin surface | 4 |
ebola hemorrhagic fever patients | 4 |
mortality monitoring and human | 4 |
the ebov outbreak in | 4 |
supernatant was removed and | 4 |
the threat posed by | 4 |
or in combination with | 4 |
virus matrix protein vp | 4 |
and in vivo during | 4 |
of pseudotyped virus input | 4 |
access article distributed under | 4 |
strategies of marburg virus | 4 |
susceptible to infection by | 4 |
the sites of budding | 4 |
by using artificial replication | 4 |
case scenario it is | 4 |
our results suggest that | 4 |
extent of fusion was | 4 |
in any medium or | 4 |
a function of time | 4 |
there was no significant | 4 |
patients with confirmed evd | 4 |
in the african straw | 4 |
require tetherin surface removal | 4 |
the glycoprotein of marburg | 4 |
distributed under the terms | 4 |
mediates postexposure protection against | 4 |
seven months in sierra | 4 |
ebolavirus bind a common | 4 |
against lethal challenge in | 4 |
been found to be | 4 |
the nucleoprotein of ebola | 4 |
approved drugs for inhibitors | 4 |
inoculation of plants and | 4 |
department of health and | 4 |
appropriate credit to the | 4 |
with an infected person | 4 |
protection against sudan ebola | 4 |
and incorporation into virions | 4 |
glycoproteins on endothelial cell | 4 |
terms and conditions of | 4 |
little is known about | 4 |
peptide immunoadhesins inhibit marburgvirus | 4 |
characterization of host immune | 4 |
for a wide range | 4 |
binding of gp to | 4 |
entry into host cells | 4 |
ready form of the | 4 |
mice to filovirus infection | 4 |
bound to its endosomal | 4 |
the incubation period of | 4 |
doses as low as | 4 |
and marburg viruses replicate | 4 |
virus nucleocapsid requires virion | 4 |
the role of type | 4 |
marburg virus and the | 4 |
a nonhuman primate model | 4 |
a credit line to | 4 |
gateway for compartmentalized trafficking | 4 |
entry into the host | 4 |
fever in humans and | 4 |
virus glycoproteins on endothelial | 4 |
indicate if changes were | 4 |
passive immunization of ebola | 4 |
and animals in the | 4 |
human peripheral blood samples | 4 |
paucity of information regarding | 4 |
igg and igm antibody | 4 |
patients treated with remdesivir | 4 |
these data indicate that | 4 |
a novelty in the | 4 |
these findings suggest that | 4 |
that they are modified | 4 |
in this article are | 4 |
confer to nonhuman primates | 4 |
with immunoglobulin from hyperimmune | 4 |
medical research institute of | 4 |
from the plasma membrane | 4 |
the cells were transfected | 4 |
lethal experimental infections of | 4 |
product contaminated in eu | 4 |
basis for ebola virus | 4 |
the glycoprotein gp of | 4 |
b for treatment of | 4 |
bat infection prevalence in | 4 |
l are not required | 4 |
when the drug was | 4 |
proteins and and posttranslational | 4 |
in the management of | 4 |
these data suggest that | 4 |
mouse model of ebola | 4 |
by the fact that | 4 |
amino acid change in | 4 |
t lymphocytes specific for | 4 |
and association with the | 4 |
associated proteins and and | 4 |
the environment and during | 4 |
for entry but exhibit | 4 |
of a preventive vaccine | 4 |
the development of antiviral | 4 |