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1 us, Murray Valley virus, Powassan virus, and yellow fever virus).
2 , such as dengue virus, West Nile virus, and yellow fever virus.
3 lustered substitutions in the NS1 protein of yellow fever virus.
4 uch as hepatitis C virus, dengue viruses and yellow fever virus.
5 NV), Zika virus (ZIKV), West Nile virus, and yellow fever virus.
6 nd-concomitantly-protective immunity against yellow fever virus.
7 dengue virus (DENV), Zika virus (ZIKV), and yellow fever virus.
8 rica to understand and predict the spread of yellow fever virus.
9 es or West Nile virus, or vaccinated against yellow fever virus.
10 iated mosquito-borne flaviviruses, including yellow fever virus.
11 munodeficiency virus, influenza A virus, and yellow fever virus.
12 s, including pathogens such as influenza and yellow fever virus.
13 nfection and cell death by DENV-2, ZIKV, and yellow fever virus.
14 EN) 4 virus was chimerized with the WT Asibi yellow fever virus.
15 ansmission of dengue, chikungunya, Zika, and yellow fever viruses.
16 ce, including Zika, chikungunya, dengue, and yellow fever viruses.
17 NS4B biogenesis extends to the West Nile and Yellow Fever viruses.
18 hich transmit Zika, chikungunya, dengue, and yellow fever viruses.
19 ain vector of dengue, Zika, chikungunya, and yellow fever viruses.
20 ot neutralize or immune-precipitate mumps or yellow fever viruses.
21 diseases that include West Nile, dengue and yellow fever viruses.
22 of other flaviviruses, including dengue and yellow fever viruses.
23 nction of NS4B is conserved in West Nile and yellow fever viruses.
24 he related mosquito-transmitted flaviviruses yellow fever virus 17D (YFV) and dengue virus type 2 (DE
26 wing ex vivo exposure to the live attenuated yellow fever virus 17D strain vaccine, a virus that we s
27 s of the flavivirus dengue virus (DV) and by yellow fever virus 17D were cholesterol independent, and
28 ift Valley fever virus, West Nile virus, and yellow fever virus), 8 bacteria (Bartonella spp., Brucel
29 The capsid proteins of two flaviviruses, yellow fever virus and dengue virus, were expressed in E
32 sis of CD8(+) T cells responding to the live yellow fever virus and smallpox vaccines--two highly suc
33 include the 2 flaviviruses dengue virus and yellow fever virus and the alphavirus chikungunya virus,
35 ding vesicular stomatitis virus, poliovirus, yellow fever virus, and herpes simplex virus type 1, rep
38 vectors of African malaria, dengue fever and yellow fever viruses, and lymphatic filariasis, respecti
39 oflaviviruses, including West Nile virus and yellow fever virus, but not to the broader Flaviviridae
41 es from melanoma, CMV, influenza A, EBV, and yellow fever viruses, but they were of low frequency and
43 ae family, including dengue virus (DENV) and yellow fever virus, cause serious disease in humans, whi
44 y-important viruses, including dengue virus, yellow fever virus, chikungunya virus, and Zika virus, a
45 nd other flaviviruses, such as West Nile and yellow fever viruses, contain a 5' m7GpppN-capped positi
46 curred in NS2B-NS3 recombinant proteins from yellow fever virus, dengue virus types 2 and 4, and Japa
47 ing three members of the family Flaviviridae(yellow fever virus, dengue virus, and bovine viral diarr
49 cutive plaque purifications of four chimeric yellow fever virus-dengue virus (ChimeriVax-DEN) vaccine
50 revaccination or natural infection with wild yellow fever virus during a 2011-12 outbreak in northern
51 rm persistence of neutralising antibodies to yellow fever virus following routine vaccination in infa
52 f 18 nucleotides (residues 146 to 163 of the yellow fever virus genome, which encode amino acids 9 to
53 ucleotide sequence found in the 5' region of yellow fever virus genomic RNA that is required for RNA
55 A vaccine against the prototype flavivirus, yellow fever virus, has been deployed for 85 years and i
56 s such as Zika virus, chikungunya virus, and yellow fever virus have drawn attention toward other coc
58 ssessed neutralizing antibody titers against yellow fever virus in blood samples obtained before vacc
60 eplication of infectious West Nile virus and yellow fever virus in cell culture with low toxicity.
63 g dengue, chikungunya, and Zika viruses, and yellow fever virus in urban settings, pose an escalating
64 tion of Zika, Ebola, dengue, chikungunya and yellow fever viruses in plasma samples from infected pat
66 ogistic model to infer the district-specific yellow fever virus infection risk during the course of t
67 aviviruses, including West Nile, dengue, and yellow fever viruses, is capable of inducing variable de
69 ephalitis virus, norovirus, metapneumovirus, yellow fever virus, Japanese encephalitis virus, parainf
70 elp uncover the causes of three outbreaks as yellow fever virus, monkeypox virus, and a noninfectious
72 that the E protein is a critical factor for yellow fever virus neuropathogenesis in the SCID mouse m
77 NV), Zika virus (ZIKV), West Nile virus, and yellow fever virus, pose significant public health threa
81 protein) is essential for replication of the yellow fever virus replicon and that a slightly longer s
82 30451, specifically blocked translation of a yellow fever virus replicon but not a Sindbis virus repl
83 l four organ recipients by identification of yellow fever virus RNA consistent with the 17D vaccine s
84 ed nucleotide and that the error rate of the yellow fever virus RNA polymerase employed by the chimer
86 d mosquito-borne flaviviruses, which include yellow fever virus, Sepik virus, Saboya virus, and other
87 wide range of viruses, including DENV, WNV, yellow fever virus, Sindbis virus, Venezuelan equine enc
88 sed analyses of mass cytometry data, we show yellow fever virus-specific cCXCR5 T cells elicited by v
89 o many flavivirus types including Dengue and yellow fever viruses, the nonstructural NS3 multifunctio
90 timated timing, source, and likely routes of yellow fever virus transmission and dispersion during on
92 till require vaccination in areas at risk of yellow fever virus transmission to achieve the 80% popul
93 s constructed from the genetic backbone of a yellow fever virus vaccine strain 17D (YFV-17D) and the
100 ax-II), rotavirus (Rotateq and Rotarix), and yellow fever virus were negative for XMRV and highly rel
101 animal viruses, including hepatitis C virus, yellow fever virus, West Nile virus, chikungunya virus,
104 ysis of the nonstructural protein 1 (NS1) of yellow fever virus (YF) has implicated it in viral RNA r
106 y, of bovine viral diarrhea virus (BVDV) and yellow fever virus (YF), members of the other two establ
107 e a high mosquito infectivity phenotype, the yellow fever virus (YFV) 17D backbone of the ChimeriVax-
110 f the replication-competent, live-attenuated yellow fever virus (YFV) 17D vaccine provides lifelong i
111 phosphorylation sites of the NS5 proteins of yellow fever virus (YFV) and dengue virus (DENV), two fl
113 tricts two medically important flaviviruses, yellow fever virus (YFV) and dengue virus serotype 2 (DE
114 ncy extends to the NS4A and NS4B proteins of Yellow Fever virus (YFV) and West Nile virus (WNV), whic
116 out metagenomic sequencing which implicated yellow fever virus (YFV) as the etiology of this outbrea
117 In the present study we characterize the Yellow Fever Virus (YFV) associated with this outbreak i
120 etime recommendation for vaccination against yellow fever virus (YFV) has been controversial, leading
122 e previously demonstrated to be required for yellow fever virus (YFV) infection and others subsequent
124 the considerable morbidity and mortality of yellow fever virus (YFV) infections in Brazil, our under
131 sequencing is presented using as a model the yellow fever virus (YFV) live vaccine strain 17D-204 and
132 It was previously reported that mutations in yellow fever virus (YFV) nonstructural protein NS2A bloc
133 gue virus (DENV), West Nile virus (WNV), and yellow fever virus (YFV) NS1 attenuate classical and lec
135 verexpressed DNAJC14 is targeted to sites of yellow fever virus (YFV) replication complex (RC) format
136 Here we describe a two-component genome yellow fever virus (YFV) replication system in which eac
137 s-packaging system that involved packaging a yellow fever virus (YFV) replicon into pseudo-infectious
138 dies have demonstrated prolonged presence of yellow fever virus (YFV) RNA in saliva and urine as an a
140 safety and immunogenicity of live attenuated yellow fever virus (YFV) vaccination of nonatopic subjec
141 previously demonstrated that live attenuated yellow fever virus (YFV) vaccine (LA-YF-Vax) dampens T-c
142 In this study, we used the live attenuated yellow fever virus (YFV) vaccine 17D as a human in vivo
143 Here we address this issue using the live yellow fever virus (YFV) vaccine, which induces long-ter
147 ose of tick-borne encephalitis virus (TBEV), yellow fever virus (YFV), and Japanese encephalitis viru
148 viridae family, such as Dengue virus (DENV), Yellow fever virus (YFV), and Zika virus (ZIKV) are noto
150 of many important human pathogens including yellow fever virus (YFV), dengue virus (DENV), and Zika
151 that TRIM56 poses a barrier to infections by yellow fever virus (YFV), dengue virus serotype 2 (DENV2
152 low Fever (YF) is a severe disease caused by Yellow Fever Virus (YFV), endemic in some parts of Afric
153 involves the gene-specific amplification of yellow fever virus (YFV), Japanese encephalitis virus (J
154 importance, such as dengue virus (DENV) and yellow fever virus (YFV), originated in sylvatic transmi
157 + T cells specific for a single epitope from Yellow Fever Virus (YFV), we show that the recently desc
158 flaviviruses.IMPORTANCE Flaviviruses such as yellow fever virus (YFV), Zika virus (ZIKV), and dengue
167 e insights into how a prototypic flavivirus, yellow fever virus (YFV-17D), differentially interacts w
169 DV, hepatitis C virus, West Nile virus, and yellow fever virus (YFV; vaccine strain 17D) were expres