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 the ebola virus99
ebola virus disease in81
the ebola virus glycoprotein76
republic of the congo65
democratic republic of the64
ebola and marburg viruses61
severe acute respiratory syndrome59
of ebola virus disease57
middle east respiratory syndrome56
of ebola hemorrhagic fever52
in the absence of52
east respiratory syndrome coronavirus48
in the presence of45
of ebola virus infection45
the democratic republic of37
ebola virus infection in37
as well as the35
for the treatment of34
in the context of34
of ebola and marburg34
in the democratic republic31
acute respiratory syndrome coronavirus29
on the cell surface28
human immunodeficiency virus type28
treatment of ebola virus27
ebola hemorrhagic fever in27
in the case of26
in vitro and in26
vitro and in vivo24
with ebola virus disease23
recombinant vesicular stomatitis virus23
against ebola virus infection22
for ebola virus infection22
patients with ebola virus22
have been shown to22
on the surface of21
virus disease in guinea21
in the united states21
democratic republic of congo21
been shown to be20
has been shown to20
of type i ifn20
ebola virus entry requires20
of severe acute respiratory20
on the other hand20
of ebola virus glycoprotein20
of ebola virus in20
ebola virus glycoprotein is20
virus entry requires the20
cells were transfected with20
a wide range of19
against lethal ebola virus19
one of the most19
in vero e cells19
centers for disease control18
for the detection of18
ebola and marburg virus18
colored fruit bat cells18
to the plasma membrane18
analysis of ebola virus18
marburg and ebola viruses18
structure of the ebola17
of marburg hemorrhagic fever17
for disease control and17
proteolysis of the ebola17
of middle east respiratory17
essential for ebola virus17
disease control and prevention17
ebov gp pseudotyped hiv17
an important role in17
min at room temperature16
c is essential for16
pathogenesis of ebola hemorrhagic16
pick c is essential16
lethal ebola virus infection16
the cholesterol transporter niemann16
is essential for ebola16
processing of the ebola16
for ebola virus disease16
from a human survivor15
of ebov gp pseudotyped15
requires the cholesterol transporter15
type i ifn signaling15
entry requires the cholesterol15
by the ebola virus15
play a role in15
of ebola virus vp15
during the course of15
lethal ebola virus challenge14
vaccine protects nonhuman primates14
protects nonhuman primates against14
safety and immunogenicity of14
the ebola virus vp14
in the treatment of14
protection against ebola virus14
of ebov and marv14
of zaire ebola virus14
ebola virus vp protein14
a u a u14
small molecule inhibitors reveal14
the course of the14
molecule inhibitors reveal niemann14
for min at room14
it is possible that14
ebola virus infection with14
the presence of the14
t cells were seeded14
to ebov gp cl13
added to each well13
emergence of zaire ebola13
after the onset of13
equine antisera and f13
on the plasma membrane13
to the cell surface13
the extent of fusion13
of ebola virus entry13
fever in cynomolgus macaques13
cells were treated with13
gp on the cell13
zaire ebola virus disease13
ebola and marburg hemorrhagic13
during the west african13
hemorrhagic fever in cynomolgus13
the ebov gp pseudotyped12
a case fatality rate12
is necessary for infection12
it is likely that12
a single amino acid12
in a mouse model12
virus disease in west12
of the ebov gp12
play an important role12
glycoprotein is necessary for12
virus glycoprotein by the12
outbreak in west africa12
of patients with ebola12
virus glycoprotein is necessary12
ebov gp on the12
the world health organization12
ebola haemorrhagic fever in12
fusion of the viral12
ebola virus glycoprotein by12
and marburg hemorrhagic fever12
transmission of ebola virus12
highly pathogenic avian influenza12
the west african outbreak12
in the development of12
is one of the12
endosomal proteolysis of the12
ebov gp pseudotyped vsv12
venezuelan equine encephalitis virus12
it is important to12
a broad range of11
compendium of years of11
case fatality rate of11
can be used to11
entry mediated by the11
a lethal dose of11
for the development of11
ebola virus infection is11
proteolytic processing of the11
of years of epidemiological11
at the plasma membrane11
is associated with an11
increasing or decreasing trend11
a compendium of years11
the role of the11
for h at room11
in the present study11
a single dose of11
national institutes of health11
of ebola virus and11
h at room temperature11
compared with pbs group11
of human immunodeficiency virus11
bind to ebov gp11
cells were infected with11
of ebola virus is11
virion glycoproteins of ebola11
disease in west africa11
infection is associated with11
by ebola and marburg11
work was supported by10
on the basis of10
pick c small molecule10
virus glycoprotein bound to10
c small molecule inhibitors10
glycoprotein bound to an10
and marburg virus infections10
to an antibody from10
the viral life cycle10
the antiviral activity of10
rift valley fever virus10
cell immunoglobulin and mucin10
an antibody from a10
virus disease in the10
the host immune response10
of the ebov genome10
the type i interferon10
early and sustained targets10
in the current study10
over the course of10
were found to be10
african green monkey kidney10
vero e cells were10
vp is essential for10
ebola virus glycoprotein bound10
bound to an antibody10
persistence of ebola virus10
was added to the10
for the first time10
as seen in figure10
ebola virus entry by10
of the viral envelope10
virus infection is associated10
antibody from a human10
of advanced ebola virus10
food and drug administration10
of vesicular stomatitis virus10
outbreak of ebola virus10
immunoglobulin and mucin domain10
cellular entry by ebola10
gp of ebola virus9
diagnosis of ebola hemorrhagic9
from the cell surface9
into the host cell9
cathepsins b and l9
role of type i9
not required for ebola9
of marburg virus disease9
infection and vlp entry9
vero e and huh9
required for ebola virus9
elucidates ebola virus origin9
trvlp infection and vlp9
with massive lymphocyte apoptosis9
the structure of the9
it is conceivable that9
first months of the9
in the exporting country9
in the plasma membrane9
antibodies against ebola virus9
virus infection ebola virus9
genomic surveillance elucidates ebola9
treatment of ebola hemorrhagic9
of the epidemic and9
the united states and9
of the type i9
of the ifn system9
these results suggest that9
it should be noted9
associated with an aberrant9
an aberrant innate immunity9
infected with ebola virus9
this work was supported9
of proinflammatory cytokines and9
cells were seeded in9
are early and sustained9
at h post transfection9
e and huh cells9
surveillance elucidates ebola virus9
origin and transmission during9
are not required for9
peripheral blood mononuclear cells9
a large number of9
immunity and with massive9
analysis and interpretation of9
at the time of9
cleavage of ebov gp9
and sustained targets of9
at an moi of9
and interpretation of data9
transmission during the outbreak9
aberrant innate immunity and9
virus origin and transmission9
ebola virus origin and9
and with massive lymphocyte9
with fetal bovine serum9
infection ebola virus entry9
and vesicular stomatitis virus9
proportion of the year9
and transmission during the9
months of the epidemic9
liberia and sierra leone9
ebola virus infection by9
to bind to ebov9
the absence of other9
the inoculum was removed9
effector and target cells9
innate immunity and with9
with an aberrant innate9
a high degree of9
luciferase reporter gene inhibition8
the human ebov infection8
reservoirs of ebola virus8
this study was to8
of marburg virus and8
in the pathogenesis of8
contact with bodily fluids8
ebola virus can be8
on vero e cells8
fruit bats as reservoirs8
the total number of8
the plasma membrane and8
like particles produced in8
as a result of8
of the immune system8
a final concentration of8
that dendritic cells are8
the end of the8
we found that a8
nonhuman primates against ebola8
human fatal zaire ebola8
is not required for8
outbreaks of ebola virus8
protect nonhuman primates against8
at the level of8
reporter gene inhibition assay8
the spike protein of8
it has been shown8
from discovery to vaccine8
incubated for h at8
and the cells were8
dendritic cells are early8
infection of rhesus macaques8
the causative agent of8
factor viia tissue factor8
nematode anticoagulant protein c8
pathology of experimental ebola8
replication of the ebov8
the treatment of ebov8
disease in the united8
a member of the8
the host cell cytoplasm8
ebov entry and infection8
mutation of the gxxxg8
with a lethal dose8
recombinant nematode anticoagulant protein8
particles produced in insect8
cells are early and8
for the production of8
the transcription and replication8
cis and in trans8
of marburg and ebola8
produced in insect cells8
in humans and nonhuman8
the surface of the8
of the ebov infection8
in patients with ebola8
rapid diagnosis of ebola8
the size of the8
against ebola and marburg8
fatal zaire ebola virus8
the probability of introduction8
zaire ebola virus infection8
was found to be8
the epidemic and forward8
used in this study8
of the gxxxg motif8
cells by macropinocytosis and8
the authors declare no8
should be noted that8
sustained targets of infection8
evidence that dendritic cells8
outbreak in the democratic8
to ebola virus glycoprotein8
a u and a8
scientific and technical committee8
the human immunodeficiency virus8
has been detected in8
bats as reservoirs of8
at least in part8
balb c mice were8
acute respiratory distress syndrome8
antibodies to ebola virus8
in the endoplasmic reticulum8
for the identification of8
epidemic and forward projections8
haemorrhagic fever in zaire8
of experimental ebola virus8
in cis and in8
protection from ebola virus8
in addition to the8
of the marburg virus8
transcription and replication of8
in the mouse model8
to a lesser extent8
to the development of8
of this study was8
to that of the8
generation of therapeutic antisera8
of personal protective equipment8
for h at rt8
in an outbreak setting8
by marburg and ebola8
as reservoirs of ebola8
mediated by the ebola8
selective estrogen receptor modulators8
the average number of8
against a lethal challenge8
international scientific and technical8
entry of ebola virus8
mediate cellular entry by7
by using pseudotyped viruses7
in the formation of7
glycoproteins of ebola viruses7
t cells were transfected7
inoculum was removed and7
outbreak setting and assessment7
a role in the7
mpxv infection resulted in7
zaire ebolavirus and lake7
ebola viruses are encoded7
among the three areas7
against a lethal ebola7
the receptor binding domain7
nonhuman primates from filovirus7
ebov gp is cleaved7
of type i ifns7
ebola hemorrhagic fever by7
a small animal model7
setting and assessment of7
for the determination of7
cathepsins in entry mediated7
probability of introduction for7
of the ebov in7
from egyptian fruit bats7
the ebola virus disease7
the recent outbreak of7
virus entry by using7
innate and adaptive immune7
are expressed through transcriptional7
epidemic in western africa7
course of the experiment7
frames and are expressed7
advanced ebola virus disease7
pcr in an outbreak7
humans and nonhuman primates7
viruses from egyptian fruit7
g for min at7
of ebola virus from7
neutral with regard to7
virus infection with a7
and a u a7
live ebov neutralisation assay7
of patient viral load7
cd and cd t7
nature remains neutral with7
by ebola virus in7
published maps and institutional7
protects nonhuman primates from7
similar to that of7
role of endosomal cathepsins7
virus in cis and7
could be due to7
the virion glycoproteins of7
of endosomal cathepsins in7
proinflammatory cytokines and chemokines7
a lethal ebola virus7
macrophages and dendritic cells7
to jurisdictional claims in7
are encoded in two7
prophylaxis protects nonhuman primates7
host cells by macropinocytosis7
characterization of ebola virus7
based on these data7
enters host cells by7
as a predictor of7
and lake victoria marburgvirus7
virus and marburg virus7
viruses are encoded in7
at the cell surface7
springer nature remains neutral7
of ebola viruses are7
antibody prophylaxis protects nonhuman7
remains neutral with regard7
in entry mediated by7
medium was replaced by7
entry by using pseudotyped7
an outbreak setting and7
disease in nonhuman primates7
were observed in the7
at a concentration of7
crystal structure of the7
with regard to jurisdictional7
ebolavirus and lake victoria7
three viral data sets7
against ebola virus in7
jurisdictional claims in published7
claims in published maps7
was shown to be7
inhibit ebola virus infection7
these results demonstrate that7
institute of infectious diseases7
type i interferon response7
was used for the7
a receptor for zaire7
or revising the article7
single amino acid change7
mice and guinea pigs7
ebola virus in cis7
primates from filovirus disease7
and supplementary figure s7
protection against lethal challenge7
entry of the ebov7
maps and institutional affiliations7
two reading frames and7
is safe and immunogenic7
assessment of patient viral7
during the recovery process7
virus disease in nonhuman7
in the form of7
can be used as7
receptor for zaire ebolavirus7
patient viral load as7
the onset of symptoms7
the early stages of7
in two reading frames7
and functional characterization of7
the ability of the7
drafting or revising the7
recombinant inhibitor of factor7
hek t cells were7
load as a predictor7
initial viral load on7
diverse marburg viruses from7
of the family filoviridae7
a lethal ebov challenge7
of ebola virus during7
has not yet been7
recombinant human activated protein7
a mouse model of7
viral load as a7
the ebov infection in7
species of ebola virus7
as a surrogate for7
the centers for disease7
ebola virus enters host7
ebola virus and marburg7
in published maps and7
endosomal cathepsins in entry7
supplemented with fetal bovine7
may not be a7
safe and immunogenic in7
of gp and gp7
enhancement of ebola virus7
of influenza a virus7
the us department of7
and are expressed through7
fever by reverse transcription7
for ebola virus replication7
have been associated with7
regard to jurisdictional claims7
and tumor necrosis factor7
and assessment of patient7
the vesicular stomatitis virus7
responses in ebola virus7
during the outbreak in7
remains to be determined7
expressed through transcriptional editing7
have been detected in7
were obtained from the7
marburg viruses from egyptian7
encoded in two reading7
reading frames and are7
the matrix protein vp7
a predictor of outcome7
virus entry and infection7
a critical role in7
the first months of7
in the respiratory tract7
and replication of the7
binding in the presence7
isolation of genetically diverse7
influenza a h n7
fecal samples were collected7
both ebov and marv7
hemorrhagic fever by reverse7
sign mediate cellular entry7
genetically diverse marburg viruses7
as a function of7
sequence analysis of the7
activity against ebola virus7
virus and ebola virus7
infection in rhesus macaques7
for zaire ebolavirus and7
of host immune responses7
of genetically diverse marburg7
entry by ebola virus7
virus enters host cells7
postexposure antibody prophylaxis protects7
human activated protein c7
is a receptor for7
ebola virus disease outbreak7
the west african ebola7
ge healthcare life sciences6
was based on the6
of the envelope glycoprotein6
successful treatment of ebola6
employ different strategies to6
therapy prolongs survival in6
by antibody produced in6
in ebov infected mice6
there is no evidence6
the gp of the6
inhibitor of factor viia6
on the raw product6
was associated with a6
macrophages and endothelial cells6
is not essential for6
prolongs survival in rhesus6
covalent modifications of the6
of ebola virus nucleocapsid6
not included in the6
an average weight loss6
transfusions from convalescent patients6
the ebola virus polymerase6
of the ebov trailer6
functional analysis of ebola6
reversion of advanced ebola6
polymerase and by t6
disease in sierra leone6
therapeutic antisera for emerging6
congo hemorrhagic fever virus6
the base of the6
host cells via macropinocytosis6
role of vp in6
modifications of the ebola6
are thought to be6
ebola virus is edited6
cells were grown in6
the proprotein convertase furin6
infection by a potently6
of the west african6
virus glycoprotein is not6
have been used in6
to ebola and marburg6
lectin specific for galactose6
eye and male reproductive6
t and vaccinia virus6
with a recombinant inhibitor6
a vesicular stomatitis virus6
the inhibition of the6
boosted and weeks later6
risk of human infection6
i ifn signaling in6
respiratory syndrome coronavirus infection6
gp mrna of ebola6
of ebov and other6
direct effect of virus6
glycoproteins of marburg and6
the envelope glycoprotein gp6
seasonal pulses of marburg6
phase i clinical trial6
by a potently neutralizing6
is assumed to be6
as described in the6
has been shown that6
the rule of six6
human asymptomatic ebola infection6
and boosted and weeks6
cells were maintained in6
structure of the ebov6
with blood transfusions from6
during the recent outbreak6
has been used to6
in rhesus macaque models6
gxxxg motif in the6
time to clinical signs6
macaque models of ebola6
ebola hemorrhagic fever with6
dronedarone and verapamil inhibit6
of a number of6
glycoprotein by the proprotein6
the treatment was given6
average weight loss of6
virus disease in sierra6
infection prevention and control6
cd t cell responses6
the ratio of the6
marburg virus circulation in6
for host cell entry6
the treatment of ebola6
after the first immunization6
infection and strong inflammatory6
in contrast to the6
studies have demonstrated that6
for the presence of6
at a dilution of6
into host cells via6
induced cytolysis of endothelial6
for marburg hemorrhagic fever6
replication in cell culture6
system for functional analysis6
to secondary lymphoid tissues6
of the viral genome6
protective efficacy of neutralizing6
the outbreak in kikwit6
ebolavirus is internalized into6
pathogenic avian influenza virus6
host cell entry of6
of the zaire ebov6
imported case of marburg6
the absence of any6
case of marburg hemorrhagic6
human ebola virus infection6
vaccine expressing ebola virus6
the glycan cap and6
k akt mtor signaling6
of npc domain c6
inhibitors of ebola virus6
virus infection in monkeys6
coincide with periods of6
edited by the ebola6
as shown in fig6
ebola virus envelope glycoprotein6
fig a and b6
no competing interests were6
nonhuman primates with zmapp6
in the viral envelope6
are associated with fatal6
glycoprotein sgp of ebola6
use of personal protective6
the acute phase of6
entry into cell lines6
type lectin specific for6
circulation in juvenile rousettus6
by t and vaccinia6
we show that the6
in nonhuman primates with6
the length of the6
rousettus aegyptiacus bats coincide6
of therapeutic antisera for6
with an average weight6
ebola virus infection ebola6
binding to ebola virus6
study in rhesus monkeys6
and male reproductive tract6
pseudotyped virus neutralisation assays6
macropinocytosis in a viral6
sgp of ebola virus6
the fact that the6
pi k akt mtor6
with ebola and marburg6
dependent enhancement of ebola6
survival in rhesus macaque6
nonstructural small glycoprotein sgp6
mechanism of binding to6
threat to public health6
nonhuman primates against infection6
the formation of the6
against the ebov infection6
virus is edited by6
cathepsin l and b6
of the virus in6
u and a u6
antibody produced in natural6
as compared to the6
ebola virus infection of6
is internalized into host6
were added to each6
a recombinant inhibitor of6
with increasing amounts of6
juvenile rousettus aegyptiacus bats6
increased risk of human6
internalized into host cells6
with periods of increased6
and vaccinia virus polymerases6
during ebola virus infection6
with the endosomal membrane6
approved selective estrogen receptor6
virus polymerase and by6
glycoprotein by the zmapp6
neutralized by antibody produced6
the eye and male6
are given in table6
bats coincide with periods6
cytolysis of endothelial cells6
of factor viia tissue6
as a worst case6
receptor modulators inhibit ebola6
have been reported to6
rhesus macaque models of6
protection against lethal ebola6
protective monotherapy against lethal6
have been found to6
cellular entry of ebola6
of increased risk of6
detection of antibodies to6
ebola virus polymerase and6
samples were collected from6
virus disease in humans6
virus disease outbreak in6
in juvenile rousettus aegyptiacus6
has been associated with6
fold serial dilutions of6
fever with blood transfusions6
growth in human cells6
a system for functional6
small glycoprotein sgp of6
asymptomatic ebola infection and6
to each well and6
virus infection by a6
hemorrhagic fever with blood6
is edited by the6
in humans and animals6
were found in the6
in jui government hospital6
of marburg virus glycoprotein6
monotherapy against lethal ebola6
the nonstructural small glycoprotein6
in the ebola virus6
the s protein of6
virus circulation in juvenile6
blood transfusions from convalescent6
the authors declare that6
pick type c disease6
terminal heptad repeat region6
is thought to be6
different strategies to counteract6
pulses of marburg virus6
and by t and6
guinea pigs against a6
competing interests were disclosed6
the pathogenesis of ebola6
ebola virus during the6
ebola infection and strong6
cells via macropinocytosis in6
aegyptiacus bats coincide with6
ebola in sierra leone6
virus prevalence in bats6
in natural human infection6
regarded as sl reference6
of binding to ebola6
by the proprotein convertase6
be effectively neutralized by6
rhesus macaques infected with6
of the immune response6
the stability of the6
for functional analysis of6
protection of nonhuman primates6
virus can be effectively6
infection with a recombinant6
viral transcription and replication6
the internal fusion loop6
the medium was removed6
in a phase i6
at a dose of6
estrogen receptor modulators inhibit6
was performed as described6
with a case fatality6
of three independent experiments6
modulators inhibit ebola virus6
of the risk of6
effectively neutralized by antibody6
the absence of a6
primates against infection with6
of ebola virus gp6
ebola virus glycoprotein gp6
vaccine for ebola virus6
in humans infected with6
produced in natural human6
of marburg virus circulation6
in the range of6
a potently neutralizing antibody6
as a positive control6
and strong inflammatory response6
copies of ebov gp6
at the end of6
viral spread in tetherin6
a worst case scenario6
can be effectively neutralized6
of the human immunodeficiency6
macaques with monoclonal antibodies6
models of ebola and6
cynomolgus macaques with monoclonal6
the protective efficacy of6
via macropinocytosis in a6
cell entry of ebola6
periods of increased risk6
a study in rhesus6
ebov gp pseudotyped virus6
mrna of ebola virus6
recognition of an intracellular5
available as supplementary data5
a small nonhuman primate5
were washed with pbs5
to be effective in5
the second luminal domain5
has been suggested that5
to ebola virus in5
version of this article5
factor in primate monocytes5
protection against the ebov5
glycoprotein structure and mechanism5
glycoproteins for efficient entry5
and inhibit ebola virus5
clinical management of ebola5
trafficking through early and5
primates against ebola and5
is the use of5
the proportion of the5
by the addition of5
inhibit ebola virus entry5
to impact the course5
and extensive intravascular apoptosis5
a direct effect of5
folate receptor alpha and5
cells were washed with5
virus binding and infectivity5
plays an important role5
and rift valley fever5
of the congo and5
of hepatitis c virus5
region of ebov gp5
protein of marburg virus5
effects of ebola virus5
clinical features of patients5
lsectin interacts with filovirus5
fasman beta turn prediction5
are available from the5
were transfected with the5
at the same time5
spike protein of sars5
viraly r schmidt et5
and a mtd of5
the course of ebola5
hemorrhagic fever in primate5
is composed of a5
the ebola virus glycoproteins5
endothelial cell activation and5
cells were stained with5
clinical observations in patients5
rvsv ebola vaccine in5
hepatitis c virus infection5
background level of neutralisation5
is not a direct5
ebola virus disease ebola5
were infected with ebov5
associated with fatal ebola5
ebola virus challenge with5
the survival of filoviruses5
by the observation that5
r schmidt et al5
b and l activate5
outbreak of marburg hemorrhagic5
marburg virus glycoproteins for5
vaccine in africa and5
host immune responses in5
used for the determination5
mice against a lethal5
emini surface accessibility prediction5
humoral responses and extensive5
the gp subunit is5
infection of macrophages and5
national institute of allergy5
nonhuman primates against lethal5
a percentage of the5
glycoprotein gp of ebola5
evaluated in this study5
assays have been developed5
a mouse model for5
type i ifn induction5
expressing ebola virus gp5
small nonhuman primate model5
mice that received vlps5
of type i interferons5
clomiphene and its isomers5
a phase i clinical5
l activate ebola but5
extents of fusion were5
the time to recovery5
is a key event5
of antibodies to ebola5
for the selection of5
a novel mechanism of5
a wide variety of5
to play an important5
programmed recognition of an5
and marburg viruses in5
virus assembly and budding5
responses and extensive intravascular5
host for the reston5
swine as a host5
data at jac online5
was used as a5
a dose of mg5
of filovirus entry into5
essential data or reagents5
at h post infection5
transfection medium was replaced5
dose of mg kg5
with fatal outcome in5
beta therapy prolongs survival5
the activity of the5
inhibition of ebola virus5
of swine as a5
the cells were washed5
stretch of tnc mutations5
the viral envelope with5
recombinant vesicular stomatitis viruses5
virus glycoproteins for efficient5
ebola virus persistence in5
the international committee on5
humans infected with sudan5
at the base of5
phase trials of rvsv5
how ebola and marburg5
in the transmission of5
as a host for5
nonhuman primate model for5
virus involves uptake by5
macrophages independent of tmprss5
available therapeutic agents that5
determined by plaque assay5
of the influenza virus5
a lethal challenge of5
a host for the5
a luciferase reporter gene5
clinically approved drugs amiodarone5
filovirus glycoproteins and the5
in ebola hemorrhagic fever5
in patients with evd5
was removed and the5
primate monocytes macrophages is5
against a lethal ebov5
of ebola virus transmission5
available to authorized users5
defective humoral responses and5
and l activate ebola5
committee on taxonomy of5
the binding of the5
were collected from the5
from bodily fluids and5
interacts with filovirus glycoproteins5
by interfering with the5
in an animal model5
caveolae are not required5
development and evaluation of5
the background level of5
in this study were5
specific for galactose and5
recombinant vaccine protects nonhuman5
read and approved the5
protein of sars coronavirus5
that they have no5
an important step in5
error of the mean5
the virus in the5
respiratory syndrome coronavirus in5
marburg virus infection in5
least one introduction event5
factors that influence ebola5
of ebov gp and5
macrophages is a key5
protection of guinea pigs5
and macrophages independent of5
wag and np i5
authors declare that they5
were added to the5
immunogenic in healthy adults5
and mechanism of entry5
the ebola virus envelope5
declare that they have5
the relative importance of5
may be able to5
ebov gp pseudotyped viruses5
ad vaccine expressing ebola5
it is assumed that5
the online version of5
and caveolae are not5
ebola virus mediated by5
and subsequent trafficking through5
the active microfluidic cartridge5
that does not require5
and verapamil inhibit filovirus5
it is plausible that5
and severe acute respiratory5
intravascular apoptosis are associated5
clinical illness and outcomes5
antisera for emerging viraly5
a neutralizing human antibody5
likely due to the5
in multiple cell types5
ebola virus involves uptake5
the protein data bank5
up of convalescent ebola5
of the role of5
entry requires the host5
infection in an animal5
at least one introduction5
of ebov infection in5
antibodies in scfv format5
be due to the5
has the potential to5
budding of vp virus5
common increasing or decreasing5
into cell lines and5
in a viral glycoprotein5
of the host cell5
in the nhp model5
screen of approved drugs5
recombinant ad vaccine expressing5
the antiviral factor tetherin5
of marburg virus is5
risk of ebola virus5
is available to authorized5
discovery of swine as5
glycoproteins and the spike5
infection results in substantial5
for both ebov and5
from lethal ebov infection5
that is critical for5
impact the course of5
strain of marburg virus5
the national institutes of5
are part of the5
are one of the5
vp to budding of5
of convalescent ebola hemorrhagic5
prophylaxis of ebola virus5
multiple cationic amphiphiles induce5
it has been suggested5
fails to impact the5
course of ebola virus5
mechanisms underlying coagulation abnormalities5
alpha and caveolae are5
associated with fatal outcome5
with ebola in sierra5
as part of the5
mutable targets of the5
glycoproteins of ebola virus5
no conflict of interest5
n and h n5
abnormalities in ebola hemorrhagic5
virus in sierra leone5
of gp on the5
efficient growth in human5
decay in the environment5
at the significance level5
cells were transduced with5
may play a role5
enhances virus binding and5
have an impact on5
bodily fluids and fomites5
members of the filoviridae5
hemorrhagic fever in kikwit5
to budding of vp5
live attenuated recombinant vaccine5
stored at room temperature5
in the course of5
viruses battle the immune5
a multiplicity of infection5
marburg viruses battle the5
the cells were then5
is able to inhibit5
and immunogenic in healthy5
both humoral and cellular5
was dependent on the5
evaluated in our study5
the cathepsin b inhibitor5
at the higher ah5
viral rna polymerase inhibitor5
to counteract the antiviral5
subsequent trafficking through early5
in africa and europe5
of ebov infection and5
the vp protein of5
mechanism and subsequent trafficking5
the majority of the5
t cell responses to5
pick c phenotype and5
short stretch of tnc5
through a sucrose cushion5
virus structure of the5
of rvsv ebola vaccine5
it has been reported5
and increased vascular permeability5
particles from infected cells5
and evaluation of a5
virus gp is safe5
genome replication and transcription5
infected cynomolgus macaques with5
has been isolated from5
virus decay in the5
of allergy and infectious5
ebolavirus glycoprotein structure and5
indicating that it is5
infection in nonhuman primates5
the mean hospitalization time5
antiviral activities in cell5
ebola virus glycoprotein and5
and outcomes in patients5
cd t cell response5
to be required for5
phenotype and inhibit ebola5
entry driven by both5
chou and fasman beta5
in ebola virus disease5
rna secondary structures in5
and enhance infection of5
cell lines and macrophages5
structure and mechanism of5
mean hospitalization time for5
marburg hemorrhagic fever in5
ebola virus infection results5
entry of ebola and5
a retrospective cohort study5
with sudan ebola virus5
of ebov gp on5
type i ifn antagonist5
with middle east respiratory5
an outbreak of ebola5
which is available to5
of tissue factor in5
in gabonese bat populations5
attenuated recombinant vaccine protects5
fatal outcome in ebola5
had no effect on5
primates against a lethal5
the development of new5
institute of allergy and5
of filoviruses in liquids5
ebola virus glycoprotein as5
virus transmission from bodily5
core structure of the5
in response to the5
not a direct effect5
subunits gp and gp5
for galactose and n5
with fatal ebola virus5
characterization of the ebola5
persistence in semen of5
culture supernatants were harvested5
for emerging viraly r5
the ebola virus genome5
minimize the risk of5
verapamil inhibit filovirus cell5
vpu employ different strategies5
h n and h5
for the generation of5
receptor alpha and caveolae5
virus infection results in5
tissue factor in primate5
that influence ebola antiviral5
enhance infection of macrophages5
may also contribute to5
a final volume of5
the extents of fusion5
specific for the viral5
an animal model by5
vp is involved in5
primate model for filovirus5
in a small animal5
of respiratory syncytial virus5
for ebola and marburg5
coagulation abnormalities in ebola5
its w a mutant5
assessment of the risk5
challenge with rna interference5
from the surface of5
lethal dose of ebov5
that the expression of5
of severe ebola virus5
motif in the transmembrane5
neutralizing antibody fails to5
in patients with severe5
that a fraction of5
with filovirus glycoproteins and5
protection against ebov infection5
proteins vp and vp5
the highest probability of5
at a multiplicity of5
no conflicts of interest5
and cd t cells5
sudan ebola hemorrhagic fever5
but not marburg virus5
viruses such as hiv5
convalescent ebola hemorrhagic fever5
and the spike protein5
c phenotype and inhibit5
entry into target cells5
the cells were incubated5
virus glycoproteins enhances virus5
lifecycle in host cells5
independent of tmprss expression5
fatal ebola virus infection5
the amount of cleaved5
hemorrhage is not a5
t cell responses are5
postexposure prophylaxis of ebola5
contribution of ebola virus5
used to assess the5
patients infected with ebov5
kolaskar and tongaonkar antigenicity5
bind ebola glycoproteins and5
guinea pigs and nonhuman5
of human peripheral blood5
the ph dependence of5
h n influenza virus5
ebola virus by using5
then added to each5
for the viral nucleoprotein5
of the viral rna5
the reciprocal of the5
antibody fails to impact5
that hemorrhage is not5
model by passive transfer5
on the day of5
ebola virus glycoproteins enhances5
marburg virus and ebola5
was assumed to be5
laboratory diagnosis of ebola5
of the filoviridae family5
lines and macrophages independent5
infected with sudan ebola5
have no competing interests5
overexpression of tissue factor5
common among the three5
based vaccine design against5
plays a role in5
that are important for5
the molecular basis of5
glycoproteins and enhance infection5
influence ebola antiviral activities5
case of ebola virus5
of marburg virus in5
ebola glycoproteins and enhance5
apoptosis are associated with5
of at least one5
to cleave ebov gp5
and middle east respiratory5
survival of filoviruses in5
samples were collected in5
the efficacy of remdesivir5
on taxonomy of viruses5
ebola virus transmission from5
of macrophages and endothelial5
with the exception of5
has been reported to5
unpublished essential data or5
involves uptake by a5
as supplementary data at5
and fasman beta turn5
transfer of a neutralizing5
underlying coagulation abnormalities in5
standard error of the5
of ebola virus involves5
in primate monocytes macrophages5
were used to infect5
the role of this5
in substantial immune activation5
the hepatitis c virus5
outcomes in patients with5
elevated levels of interferon5
note springer nature remains5
management of ebola virus5
the transfection medium was5
the binding site for5
for the reston ebolavirus5
illness and outcomes in5
which is important for5
amphiphiles induce a niemann5
in a variety of5
the risk of ebola5
and the role of5
ebola antiviral activities in5
functional characterization of the5
cell fusion mediated by5
authors declare no competing5
in a manner that5
and influenza a virus5
have been developed for5
and marburg viruses using5
trials of rvsv ebola5
the transmembrane domain of5
of a neutralizing human5
under the age of5
is required for the5
extensive intravascular apoptosis are5
type calcium channel blocker5
and marburg viruses battle5
erk mapk and pi5
cationic amphiphiles induce a5
online version of this5
due to the lack5
been detected in the5
has yet to be5
vesicular stomatitis virus vectors5
in sierra leone ebola5
signr bind ebola glycoproteins5
pigs and nonhuman primates5
ebola virus entry and5
dynamics of ebola virus5
for efficient entry into5
in liver and spleen5
strategies to counteract the5
of an intracellular receptor5
virus glycoprotein as the5
in the common marmoset5
mapk and pi k5
cells were then incubated5
ebola virus gp is5
animal model by passive5
and samples were collected5
a u u a5
the clinically approved drugs5
of the disease and5
ebola virus in sierra5
as a type i5
due to their ability5
outbreak in western africa5
by ebola virus glycoprotein5
by macropinocytosis and clathrin5
during an outbreak of5
evidence that hemorrhage is5
number of years to5
the a u mutant5
it is clear that5
by passive transfer of5
for ebola virus glycoprotein5
in a co incubator5
inhibit filovirus cell entry5
mediated cell entry of5
hemorrhagic fever associated with5
ebov infection in nhps5
acetylgalactosamine promotes filovirus entry5
treatment with recombinant nematode5
humoral and cellular immunity5
transmission from bodily fluids5
were immunized intramuscularly with5
to the fact that5
and vp to budding5
ebov lifecycle in host5
ebov or marv gp5
and immunogenicity of a5
of nonhuman primates against5
ebola but not marburg5
ebola virus matrix protein5
results in substantial immune5
pigs against a lethal5
to their ability to5
average number of years5
of the viral and5
contributed unpublished essential data5
rna viruses such as5
the significance level of5
supplementary data at jac5
to the release of5
of equine antisera and5
twice daily for days5
monocytes macrophages is a5
virus challenge with rna5
volume of pbs as5
mediated protection against ebov5
of ebola virus ebola5
vp protein of ebola5
international committee on taxonomy5
efficient entry into cell5
and pi k akt5
of viral hemorrhagic fever5
virus infection in an5
not marburg virus glycoproteins5
ebola virus disease patients5
passive transfer of a5
activate ebola but not5
the percentage of ebov5
gp is safe and5
were regarded as sl5
gorilla fecal samples were5
marburg virus surface protein5
fever in primate models5
in the transmembrane domain5
the replication of the5
causative agent of the5
patients with ebola in5
markedly elevated levels of5
have the potential to5
glycoproteins enhances virus binding5
emerging viraly r schmidt5
ebola vaccine in africa5
battle the immune system5
detection of neutralizing antibodies4
to nonhuman primates complete4
the creative commons license4
of dendritic cells and4
undergo a subsequent fusion4
nucleoprotein of ebola virus4
implications for a role4
not be sufficient to4
from the same patient4
internal fusion loop of4
for inhibitors of biological4
viruses replicate in monocyte4
filovirus entry into vero4
it is not clear4
when march was expressed4
site of ebov fusion4
does not require tetherin4
the lineage dual model4
for formation of the4
monitoring and human ebola4
of convalescent plasma for4
to be important for4
and in trans dc4
you give appropriate credit4
a type i ifn4
clomiphene and enclomiphene in4
who ebola response team4
will need to obtain4
a significant threat to4
cytotoxic t lymphocytes specific4
of the year bats4
groups of mice were4
intended use is not4
a standardized nomenclature for4
of vascular cell cytotoxicity4
ebola virus counters the4
your intended use is4
for replication in cell4
virus vp protein functions4
health and human services4
allergy and infectious diseases4
of bushmeat is bats4
nonhuman primate model of4
uniform standard error of4
cytokines and full maturation4
from the envelope glycoprotein4
the virus and the4
direct exposure to fruit4
alpha associated with fatal4
globulin and recombinant interferon4
tested negative for anti4
axl enhances macropinocytosis of4
activation of type i4
were infected with a4
virus and the s4
receptor kinase axl enhances4
ebolavirus in humans and4
of filoviral hemorrhagic fever4
and neutralizing antibody responses4
are included in the4
united states and europe4
a type i transmembrane4
with one or more4
b l are not4
is used as a4
clinical efficacy of remdesivir4
was to assess the4
lethal infection in mice4
innate immune responses in4
through the use of4
in the early stages4
assays were used to4
ebola virus secrete mip4
not permitted by statutory4
against ebov infection in4
is consistent with previous4
for the introduction of4
association with the lipid4
glycan cap and the4
these data the initial4
figure a and b4
require endosomal cysteine proteases4
the role of siglec4
of ebola virus triggers4
and is associated with4
pathogenesis and treatment with4
detected in a common4
the main viral determinant4
viruses in gabonese bat4
and nonfatal cases of4
there are a number4
cells were obtained from4
c region of ebov4
ebola virus infection complicated4
infection in african straw4
immune globulin and recombinant4
and the evolution of4
at the point of4
life cycle modeling system4
adaptation of ebov during4
the terms and conditions4
glycoprotein of marburg virus4
specific cd t cells4
absence of thermolysin treatment4
be used as a4
biochemical analysis of the4
sequence and residues critical4
study had high estimates4
of the external solution4
ad and protect nonhuman4
able to inhibit the4
of ebola virus makona4
expression of type i4
in the republic of4
and weight change for4
the specificity of the4
was similar to that4
immunity to ad and4
progress in the development4
decline of central african4
and vero e cells4
assumed that c min4
stability of ebola virus4
gp is cleaved by4
for emerging infectious diseases4
through early and late4
has been reported for4
if changes were made4
and conditions of the4
primates against ebola virus4
commons license and your4
systematic screen of fda4
on ice for min4
using artificial replication systems4
a paucity of information4
cells infected with ebola4
and the gp subunit4
cellular host range of4
have a uniform standard4
and weeks after the4
contaminated in eu ms4
are known to be4
with the glycoprotein of4
of plants and animals4
and approved the final4
are a number of4
of the transcription and4
alpha and inhibit poly4
regulation or exceeds the4
under a creative commons4
cells without inducing the4
with the lipid bilayer4
of biological threat agents4
years of marburg virus4
single amino acid residue4
the immune epitope database4
based ebola vaccine is4
production of cytokines and4
cell fusion induced by4
vesicular stomatitis virus vaccine4
of the experiment and4
the angola strain of4
inducing the production of4
but exhibit distinct protease4
infection by ebola and4
in the selection of4
in rhesus macaques infected4
and three species of4
blood samples were collected4
domains of lake victoria4
any medium or format4
ebola vaccine in healthy4
enveloped viruses such as4
if material is not4
and peripheral blood mononuclear4
load on raw product4
rhesus macaque model of4
neutralizing antibody responses against4
directly from the copyright4
mixture of two stereoisomers4
of hpai h n4
filoviruses require endosomal cysteine4
when compared to the4
early and late endosomes4
vector mediates postexposure protection4
and support vector machines4
among ehf patients in4
this is an important4
of emerging and re4
of health and sanitation4
human primates against a4
this is consistent with4
from ebola virus mediated4
titers were determined by4
ic for clomiphene was4
resulting from direct exposure4
in human dendritic cells4
linked immunosorbent assay for4
the sudv outbreak in4
comprehensive analysis of ebola4
structure of the envelope4
should be addressed to4
of the infected cell4
and laboratory features of4
of the congo in4
monitored for additional days4
was performed using the4
authors declare no conflict4
use is not permitted4
and nitric oxide levels4
vaccine vectors bypass immunity4
the late stages of4
with ebola virus secrete4
that one or more4
permission directly from the4
analysis of the ebola4
cells were seeded at4
or exceeds the permitted4
high seroprevalence of both4
starting at or dpi4
a systematic screen of4
underestimation of branch lengths4
variance log tcid ml4
with the ifn system4
hepatitis c virus entry4
a preventive vaccine for4
by a novel broad4
the therapeutic efficacy of4
of west nile virus4
marburg virus disease in4
dendritic cell stimulating activity4
infection prevalence in exporting4
structure of ebov gp4
for antibodies to ebola4
west african evd outbreak4
give appropriate credit to4
credit line to the4
obtain permission directly from4
the a u a4
of the sars coronavirus4
as you give appropriate4
blood ebov turned negative4
immunization of ebola virus4
in the biosafety level4
a potent inhibitor of4
cell entry mediated by4
the national institute for4
protein of severe acute4
vaccine in healthy adults4
treatment of experimental ebola4
mononuclear cells infected with4
resistant to ebov infection4
removed and cells were4
class i fusion proteins4
virus glycoprotein to undergo4
cells were fixed with4
epidemic in west africa4
hemorrhagic fever patients and4
monkeys with immunoglobulin from4
protects immunocompromised nonhuman primates4
derived human macrophages and4
hemorrhagic fever ebola virus4
lake victoria marburgvirus and4
in insect cells exhibit4
adaptation of ebola virus4
after the second boost4
the ns protein of4
ebov negative reference serum4
and ad vaccine vectors4
in the same way4
early stages of infection4
sexual transmission of ebola4
hemorrhagic fever in nonhuman4
genetics demonstrates that proteolytic4
primary human monocytes and4
and rapid decline of4
of ebola haemorrhagic fever4
year bats may shed4
in the endocytic pathway4
the ebola virus matrix4
for signs of disease4
worst case scenario it4
the nih aids reagent4
using a combination of4
to the original author4
in vivo during infection4
and the use of4
of an antioxidant small4
blocked with bovine serum4
these results indicate that4
acidification of the external4
and there was no4
the most promising candidates4
monkeys by aerosolized ebola4
have been implicated in4
remdesivir reduces the time4
of ebola viruses causing4
phi may not be4
virus glycoprotein counteracts bst4
clinical virology of ebola4
the envelope glycoprotein of4
like mechanism and subsequent4
gp from ebola virus4
to the lack of4
the use of the4
as the main viral4
domain of marburg virus4
to obtain permission directly4
humans and animals in4
on these data the4
replication strategies of marburg4
gabon and republic of4
in the induction of4
survival and weight change4
the use of different4
cathepsin b l are4
ebola virus glycoproteins on4
manner that does not4
the gp gene and4
induced particle formation and4
infected with ebov mak4
were cloned into the4
fusion induced by cleaved4
within the plasma membrane4
igg ebov negative reference4
due to the presence4
and replication strategies of4
representative of three independent4
fever in nonhuman primates4
the zaire strain of4
entry inhibitor for filoviruses4
structure of ebola virus4
binding domains of lake4
in the design of4
of both viruses in4
for treatment of experimental4
antiviral activity in vitro4
not necessarily reflect the4
for a role in4
identification of the ebola4
for compartmentalized trafficking of4
main viral determinant of4
vaccine design against ebov4
this article are included4
virus mediated by cytotoxic4
human monocytes and macrophages4
hemorrhagic fever in humans4
virus glycoprotein and hiv4
has been demonstrated in4
marburgvirus and zaire ebolavirus4
consider product contaminated in4
line to the material4
important role in the4
unless indicated otherwise in4
ebola virus nonstructural glycoprotein4
it was shown that4
log tcid ml in4
the ebola virus nucleocapsid4
its endosomal receptor niemann4
molecules of the ifn4
haemorrhagic fever ebola virus4
and is required for4
female balb c mice4
new ebola virus nonstructural4
at an early stage4
cells exhibit dendritic cell4
infected cynomolgus monkeys with4
glycoprotein is not essential4
rapid decline of central4
posttranslational modification of nucleoprotein4
vesicular stomatitis virus vector4
antiviral activity of a4
it is difficult to4
was removed and replaced4
postexposure protection against sudan4
in west africa from4
and effectiveness of an4
virus nonstructural glycoprotein expressed4
preventive vaccine for ebola4
and ebolavirus cell entry4
supernatants were harvested at4
virus by using artificial4
a h n virus4
the ebola virus outbreak4
was removed from the4
vectors bypass immunity to4
defective recombinant ad vaccine4
is believed to be4
molecular evidence of sexual4
of sexual transmission of4
an impact on the4
against sudan ebola hemorrhagic4
gp on the plasma4
role in virus assembly4
cathepsin b and l4
open access article distributed4
pubmed abstract publisher full4
mechanism of action of4
surface of infected cells4
with activity against ebola4
found that a single4
virus nomenclature below the4
seen in figure a4
can be inhibited by4
of the virus from4
projected data have a4
the primed ebolavirus glycoprotein4
of the gp gene4
environment and during transport4
probability of introduction of4
in domestic pigs in4
analysis of the secreted4
expressed through rna editing4
for transcription and replication4
glycoprotein gp from ebola4
both innate and adaptive4
primates complete protection against4
is at present unknown4
activated protein c for4
have been reported in4
mediated by cytotoxic t4
army medical research institute4
log normal distribution with4
in ocular fluid during4
in decay rates between4
you will need to4
macropinocytosis of zaire ebolavirus4
the effects of clomiphene4
cell stimulating activity and4
counteract the antiviral factor4
determinant of vascular cell4
model of ebola virus4
fresh medium was added4
and human ebola outbreaks4
long as you give4
in the replication cycle4
lower than that of4
the resistance of mice4
and virion glycoproteins of4
for viral transcription and4
target of ebov infection4
has been used for4
is an open access4
outbreak resulting from direct4
human macrophages and peripheral4
follows a log normal4
viruses in rousettus aegyptiacus4
the same volume of4
shown to be effective4
the secondary structure of4
and residues critical for4
fatal and nonfatal cases4
in a wide range4
the development of a4
of its body weight4
ebola virus virulence in4
of hemorrhagic fever virus4
from the copyright holder4
against infection with marburg4
can be explained by4
induce the expression of4
in the live ebov4
essential for replication in4
in the protein data4
cysteine proteases for entry4
exposure treatment of ebola4
a uniform standard error4
fusion was independent of4
weight over the course4
and igm antibody findings4
both viruses in rousettus4
caused by the ongoing4
like filovirus in europe4
the images or other4
derived dendritic cells without4
domain c of npc4
results of this study4
was independent of ph4
bypass immunity to ad4
they have no competing4
to confer to nonhuman4
human ebola outbreak resulting4
exhibit dendritic cell stimulating4
ebola virus nucleocapsid requires4
a log normal distribution4
design against ebov gp4
identification of a small4
virus transmission events and4
same volume of pbs4
virus virulence in mice4
west africa from to4
and may result in4
the virus from the4
transmission events and rapid4
a guinea pig model4
rna editing of the4
of lake victoria marburgvirus4
western african evd outbreak4
angola strain of marburg4
randomly assigned into groups4
against filovirus diseases by4
for a variety of4
is shown in fig4
functions as a type4
van damme et al4
treatment was given ip4
proteases for entry but4
virus vector mediates postexposure4
to a final concentration4
survey showing cocirculation of4
research institute of infectious4
its body weight over4
text free full text4
counters the interferon system4
results from the guinea4
guinea pigs from lethal4
of ebola virus glycoproteins4
features of filoviral hemorrhagic4
the determination of cut4
link to the creative4
there was evidence of4
within the respiratory tract4
marburg virus and three4
with the plasma membrane4
in the middle east4
receptors on the surface4
vivo during infection by4
a complementary role to4
hydroxyl acylation analyzed by4
the potential of the4
virus infection in rodents4
viral hemorrhagic fever in4
the surface of infected4
in dcs and macrophages4
a link to the4
evidence of sexual transmission4
demonstrates that proteolytic processing4
prevalence of infection in4
is often associated with4
directed against the mutable4
infection detected in a4
were randomly assigned into4
modified vaccinia virus ankara4
essential for transcription and4
drugs inhibiting the ebola4
in the three areas4
at room temperature with4
not be a suitable4
zaire ebolavirus bind a4
is not included in4
and evolution during seven4
seroprevalence of both viruses4
of interferon regulatory factor4
calcium channel blocker verapamil4
it is believed that4
of ebola virus fusion4
the replication cycle of4
reston ebolavirus in humans4
absence of any other4
replication cycle of the4
experimental ebola virus infections4
of the glycoprotein gp4
bats may shed active4
the expression of ifn4
antibody findings among ehf4
of enclomiphene and zuclomiphene4
the viral fusion world4
model of filovirus infection4
the equine antisera and4
marburg and ebola virus4
novelty in the viral4
to minimize the risk4
a new ebola virus4
highlights the importance of4
findings among ehf patients4
endosomal cysteine proteases for4
in liberia and sierra4
in the resistance of4
virus disease in johannesburg4
in vero e and4
in cellular cholesterol trafficking4
detection limit of the4
abstract publisher full text4
not essential for replication4
in humans and other4
full text free full4
potentiates the ebola virus4
ebola virus fusion triggering4
the ability of these4
for detection of antibodies4
this article is an4
of the different ebov4
in the viral fusion4
efficacy and effectiveness of4
of ebov gp by4
into vero e cells4
and a high seroprevalence4
as shown in figure4
and tongaonkar antigenicity scale4
entry into vero e4
from ebola virus at4
a normal distribution of4
fresh growth medium containing4
based vaccine protects nonhuman4
and incubated for h4
reproduction in any medium4
of host cell entry4
with recombinant nematode anticoagulant4
successful treatment of advanced4
of cytokines and full4
large serological survey showing4
as a percentage of4
removed and the cells4
was observed in the4
the cell surface is4
high estimates of d4
envelope glycoprotein gp from4
inhibiting the ebola virus4
mg kg loading dose4
have a complementary role4
changes were accompanied by4
to the creative commons4
amount of cleaved gp4
diseases by a novel4
ad vaccine vectors bypass4
a role in virus4
stomatitis virus vector mediates4
factors that influence the4
the initial viral load4
prevalence in exporting country4
the projected data have4
protection against multistrain ebola4
changes in gene expression4
is known about the4
required for inhibition of4
the production of cytokines4
a limited number of4
serological survey showing cocirculation4
and ebola virus by4
from direct exposure to4
of the evd patients4
the van der waals4
the initial concentration of4
on endothelial cell activation4
article is an open4
role of the type4
are found in the4
dendritic cells without inducing4
in the infected host4
against multistrain ebola and4
by factors such as4
highest probability of introduction4
in virus assembly and4
entry of enveloped viruses4
virus infection in a4
glycoprotein in viral entry4
a case of ebola4
in the environment and4
can be detected in4
the mechanism by which4
probability of at least4
the secreted and virion4
of the virus particles4
for the prediction of4
kinase axl enhances macropinocytosis4
growth medium containing scs4
plants and animals with4
immune activation and increased4
to its endosomal receptor4
was supported by the4
stimulating activity and induce4
cells were cotransfected with4
the onset of illness4
evaluation of immune globulin4
patients and their household4
filovirus diseases by a4
ebola outbreak resulting from4
gp in viral entry4
there is also evidence4
declare no competing interests4
entry but exhibit distinct4
for host cell binding4
samples were collected at4
under positive selection in4
rate of up to4
dcs and macrophages in4
assigned into groups of4
using inhibitors of endocytosis4
samples from fatal and4
have been developed to4
necessary for infection ebola4
immunoglobulin from hyperimmune horses4
uptake by a macropinocytosis4
infection complicated by gram4
residues critical for host4
to ad and protect4
bind a common receptor4
enhances macropinocytosis of zaire4
i interferon response in4
virus and three species4
with live ebov neutralisation4
cells were cultured in4
in accordance with the4
nonstructural glycoprotein expressed through4
and treatment with recombinant4
in the viral life4
collected in zone b4
under the terms and4
mice infected with ebov4
variation in selection pressures4
determinants of ebola virus4
the tyro receptor kinase4
it has also been4
of any other data4
of the viral membrane4
nomenclature below the species4
the medium was replaced4
used in our study4
have been identified as4
blood samples from fatal4
and error bars indicate4
of the virus to4
virus infection in primates4
normal distribution with mean4
negative reference serum panel4
party material in this4
injection vaccine protects nonhuman4
the natural history of4
has also been shown4
resistance of mice to4
the entry of the4
patients with severe covid4
as well as in4
to consider product contaminated4
analysis of human peripheral4
marburg viruses in gabonese4
apoptosis induced in vitro4
article are included in4
experimental infections of rhesus4
igm antibody findings among4
the site of ebov4
the ebola virus nucleoprotein4
prophylaxis and therapy of4
c min log tcid4
insights from ebola virus4
h n highly pathogenic4
is essential for the4
and cd t cell4
the innate immune response4
to the sites of4
glycoprotein as the main4
as long as you4
shedding of the glycoprotein4
the cellular host range4
is cleaved by the4
reduces the time to4
material is not included4
absence of other information4
it is thought that4
and igg and igm4
virus infection with t4
variant of ebola virus4
we were unable to4
was calculated as the4
a severe haemorrhagic fever4
case of severe ebola4
direct contact with bodily4
is involved in the4
glycoprotein to undergo a4
of the conserved region4
and the s protein4
were then incubated for4
the gps of the4
ebola virus in ocular4
the recent west african4
gp pseudotyped virus neutralisation4
virus gp in viral4
transcription polymerase chain reaction4
scenario it is assumed4
of rhesus macaques with4
second luminal domain of4
is likely that the4
ebola haemorrhagic fever virus4
vascular cell cytotoxicity and4
activation and increased vascular4
the results of the4
the expression of type4
binding to ebov gp4
experimental inoculation of plants4
clinical and laboratory features4
primates against lethal ebola4
the nature of the4
view a copy of4
and huh cells were4
angola infection of rhesus4
that type i ifns4
provide a link to4
advanced ebola virus infection4
other third party material4
the low ph pulse4
phase i clinical trials4
is assumed that c4
animal mortality monitoring and4
an open access article4
tetherin restriction in a4
human immunodeficiency virus and4
ebov entry into the4
and their household contacts4
minimum viral load to4
a high seroprevalence of4
single particle image analysis4
animals in the philippines4
infection with marburg virus4
for ebov and marv4
from the guinea ring4
replication and transcription of4
the clinical efficacy of4
induced in vitro and4
ebola virus glycoprotein to4
were transferred to a4
the highest serum dilution4
is responsible for the4
four fda approved drugs4
that are required for4
that proteolytic processing of4
all animals were monitored4
ml in the absence4
was monitored for additional4
the guinea ring vaccination4
contact with an infected4
a creative commons attribution4
by the national institutes4
the presence of vp4
in a credit line4
blood mononuclear cells infected4
virus infection complicated by4
of ebov gp that4
fever patients and their4
evolution during seven months4
in wild great apes4
results suggest that the4
and your intended use4
the year bats may4
epidemic of ebola virus4
experiment and none survived4
and detection of neutralizing4
the activity of cathepsins4
visualization of ebola virus4
directed expression of tetherin4
lymphocytes specific for the4
marburgvirus and ebolavirus cell4
particle formation and association4
molecular basis for ebola4
wild animal mortality monitoring4
compartmentalized trafficking of ebola4
nonfatal cases of ebola4
rates of up to4
to binding in the4
cytokine and chemokine expression4
exposure to fruit bats4
during infection by ebola4
drugs for inhibitors of4
in the eye and4
fever ebola virus disease4
analysis of filovirus entry4
and disseminated intravascular coagulation4
and indicate if changes4
virus angola infection of4
their ability to inhibit4
to interfere with the4
ebola virus glycoprotein counteracts4
vaccine to confer to4
given the same volume4
with marburg virus and4
victoria marburgvirus and zaire4
of health and human4
s protein of severe4
postexposure treatment of ebola4
trafficking of ebola and4
images or other third4
newborn balb c mice4
that c min log4
severe ebola virus infection4
data suggest that the4
in the ebov lifecycle4
class i fusion protein4
antiviral activity against ebov4
n highly pathogenic avian4
to fruit bats in4
are located in the4
favorable immune cell targeting4
is a type i4
during the acute phase4
there have been a4
cocirculation of ebola and4
article distributed under the4
alpha b for treatment4
material in this article4
a suitable surrogate for4
basic clinical and laboratory4
survival was monitored for4
outbreak in south korea4
critical for host cell4
development of a preventive4
cell lines were maintained4
of the most promising4
secreted and virion glycoproteins4
a variety of different4
to ebola virus disease4
statutory regulation or exceeds4
data have a uniform4
protection against a lethal4
monoclonal antibodies against ebola4
a replication defective recombinant4
that vp and vp4
of type i interferon4
molecular determinants of ebola4
of disseminated intravascular coagulation4
not require tetherin surface4
ebola hemorrhagic fever patients4
mortality monitoring and human4
the ebov outbreak in4
supernatant was removed and4
the threat posed by4
or in combination with4
virus matrix protein vp4
and in vivo during4
of pseudotyped virus input4
access article distributed under4
strategies of marburg virus4
susceptible to infection by4
the sites of budding4
by using artificial replication4
case scenario it is4
our results suggest that4
extent of fusion was4
in any medium or4
a function of time4
there was no significant4
patients with confirmed evd4
in the african straw4
require tetherin surface removal4
the glycoprotein of marburg4
distributed under the terms4
mediates postexposure protection against4
seven months in sierra4
ebolavirus bind a common4
against lethal challenge in4
been found to be4
the nucleoprotein of ebola4
approved drugs for inhibitors4
inoculation of plants and4
department of health and4
appropriate credit to the4
with an infected person4
protection against sudan ebola4
and incorporation into virions4
glycoproteins on endothelial cell4
terms and conditions of4
little is known about4
peptide immunoadhesins inhibit marburgvirus4
characterization of host immune4
for a wide range4
binding of gp to4
entry into host cells4
ready form of the4
mice to filovirus infection4
bound to its endosomal4
the incubation period of4
doses as low as4
and marburg viruses replicate4
virus nucleocapsid requires virion4
the role of type4
marburg virus and the4
a nonhuman primate model4
a credit line to4
gateway for compartmentalized trafficking4
entry into the host4
fever in humans and4
virus glycoproteins on endothelial4
indicate if changes were4
passive immunization of ebola4
and animals in the4
human peripheral blood samples4
paucity of information regarding4
igg and igm antibody4
patients treated with remdesivir4
these data indicate that4
a novelty in the4
these findings suggest that4
that they are modified4
in this article are4
confer to nonhuman primates4
with immunoglobulin from hyperimmune4
medical research institute of4
from the plasma membrane4
the cells were transfected4
lethal experimental infections of4
product contaminated in eu4
basis for ebola virus4
the glycoprotein gp of4
b for treatment of4
bat infection prevalence in4
l are not required4
when the drug was4
proteins and and posttranslational4
in the management of4
these data suggest that4
mouse model of ebola4
by the fact that4
amino acid change in4
t lymphocytes specific for4
and association with the4
associated proteins and and4
the environment and during4
for entry but exhibit4
of a preventive vaccine4
the development of antiviral4