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1 ector for arboviruses (e.g. dengue, zika and yellow fever).
2 tion during investigations on the ecology of yellow fever.
3 tuberculosis to 8043 (95% CI 7621-8464) for yellow fever.
4 mopolitan vector of dengue, chikungunya, and yellow fever.
5 there is no specific antiviral treatment for yellow fever.
6 its derivatives as antiviral agents to treat yellow fever.
7 iral therapeutics for clinical management of yellow fever.
8 and 38% were visiting countries endemic for yellow fever.
9 ncluding smallpox, polio, measles, mumps and yellow fever.
10 ored diseases such as bovine tuberculosis or yellow fever.
11 of a vaccine to protect the species against yellow fever.
12 first death of a golden lion tamarin due to yellow fever.
13 ctors that may favor the mosquito vectors of yellow fever.
15 rus 2 (SARS-CoV-2) that uses live-attenuated yellow fever 17D (YF17D) vaccine as a vector to express
16 than candidates based on Langat E5, TBE, and yellow fever 17D backbones, and was found to be highly i
19 us serotypes 1 to 4 (DENV1 to DENV4) and the yellow fever 17D vaccine strain (YFV-17D) did not antago
20 ruses, dengue virus serotypes 1 to 4 and the yellow fever 17D vaccine strain, did not antagonize STAT
21 irus (LGTV), a former live TBEV vaccine; and yellow fever 17D virus vaccine (YF 17D) in rhesus monkey
27 edes aegypti is the principal vector for the yellow fever and dengue viruses, and is also responsible
28 k-borne encephalitis, Japanese encephalitis, yellow fever and dengue viruses, constitute a significan
30 borne infectious diseases such as dengue and yellow fever and emerging diseases such as Zika and chik
34 mitigate the spread of chikungunya, dengue, yellow fever and Zika viruses must consider the so far u
38 for other flaviviruses, including West Nile, yellow fever, and dengue viruses, and the critical role
39 other Flaviviridae, including dengue, Zika, yellow fever, and West Nile virus, identifies conserved
41 viral diseases (notably dengue, chikungunya, yellow fever, and Zika virus disease) resulting from the
43 tion serum samples for measles, rubella, and yellow fever; and the post-vaccination antibody titres g
44 g the participants who were seronegative for yellow fever antibody at baseline varied significantly a
47 the XRX-001 vaccine, containing inactivated yellow fever antigen with an alum adjuvant, induced neut
48 est Nile fever, tick-borne encephalitis, and yellow fever, are endemic in tropical and temperate part
50 oduce Bayesian model averaged predictions of yellow fever burden across the African endemic region.
53 ffective vaccine is available, the number of yellow fever cases has increased over the past two decad
54 om mosquito-borne diseases-including dengue, yellow fever, chikungunya and Zika-is expanding in conce
57 ka virus, and the threat of global spread of yellow fever, combined with the resurgence of dengue and
58 vaccination coverage for polio, measles, and yellow fever continued to decrease, whereas the trend in
62 tempt to control the mosquito-borne diseases yellow fever, dengue, chikungunya, and Zika fevers, a st
64 It is closely related to the mosquito-borne yellow fever, dengue, Japanese encephalitis, and West Ni
65 ito-borne or tick-borne flaviviruses such as yellow fever, dengue, West Nile, St Louis encephalitis,
66 egypti mosquitoes transmit pathogens such as yellow fever, dengue, Zika, and chikungunya viruses to m
67 CE Arbovirus infections in Brazil, including yellow fever, dengue, zika, and chikungunya, result in c
68 14c10 light chain CDRs.IMPORTANCE A chimeric yellow fever-dengue live-attenuated tetravalent vaccine
70 igned to explore the effects of the Chimeric Yellow Fever Derived Tetravalent Dengue Vaccine (CYD-TDV
73 theastern Brazil experienced the most severe yellow fever epidemic/epizootic in the country in 80 yea
79 c diseases, such as cholera, meningitis, and yellow fever, have become common over the past decade, h
80 clones in response to primary and secondary yellow fever immunization - the model for acute infectio
84 timate the effective reproductive number for yellow fever in Angola using disease natural history and
85 say to measure protective antibodies against yellow fever in Malian and Ghanaian children vaccinated
86 late 2016 Brazil faced the worst outbreak of Yellow Fever in recent decades, mainly located in southe
93 s a significant health burden in areas where yellow fever is endemic, but it is preventable through v
94 travelers to and residents of areas in which yellow fever is endemic, but the vaccine can cause serio
96 des aegypti, the global vector of dengue and yellow fever, is inexorably linked to water-filled human
98 West Nile fever (WNF), chikungunya, dengue, yellow fever, Japanese encephalitis virus, GBS, and cont
99 VPDs), including polio, measles and rubella, yellow fever, Japanese encephalitis, rotavirus, and inva
100 s including dengue fever, chikungunya, zika, yellow fever, leishmaniasis, chagas disease, and malaria
101 fection (hepatitis C virus) and vaccination (yellow fever, malaria, influenza), but poor outcome in a
103 by plaque reduction neutralisation (measles, yellow fever), microneutralisation (polio serotypes 1 an
105 fficking, we disrupted COPI functions in the Yellow Fever mosquito Aedes aegypti to interfere with bl
111 gand selectivity and in vivo function of the yellow fever mosquito sterol carrier protein-2 protein (
112 apidly displaced resident populations of the yellow fever mosquito, Aedes aegypti in the southeastern
114 locus) establishes the male sex (M/m) in the yellow fever mosquito, Aedes aegypti Nix, a gene in the
115 ed neuropeptides in the antennal lobe of the yellow fever mosquito, Aedes aegypti, a major vector of
118 colactone may be an interkingdom cue for the yellow fever mosquito, Aedes aegypti, seeking blood-meal
124 no-acid transporter Slimfast (Slif) from the yellow-fever mosquito Aedes aegypti using codon-optimize
125 ET-elicited protection against ZIKV-infected yellow fever mosquitoes from old and recent laboratory c
126 evious estimates on the basis of more recent yellow fever occurrence data and improved estimation met
127 are coupled to a generalised linear model of yellow fever occurrence which uses environmental covaria
128 ion kinetics, innate gene activation by live yellow-fever or varicella-zoster virus (YFV/VZV) vaccine
129 graphic factors to the ongoing spread of the yellow fever outbreak and provide estimates of the areas
130 graphic factors to the ongoing spread of the yellow fever outbreak and provide estimates of the areas
133 were fitted to a dataset of the locations of yellow fever outbreaks within the last 25 years to estim
135 doses and the lack of therapeutic agents for yellow fever put global health at risk, should this viru
136 complete follow-up history, and no record of yellow fever revaccination were included; children serop
137 between 43% and 52% of the population within yellow fever risk zones, compared with between 66% and 7
139 rus seroprevalence and measles, rubella, and yellow fever seroconversion, and (1/3) log2 for log2-tra
140 t human pathogens such as dengue, West Nile, yellow fever, tick-borne encephalitis and Japanese encep
141 tavirus, measles, meningitis A, rubella, and yellow fever to approximate the future deaths averted be
143 model which suggests a higher proportion of yellow fever transmission occurs as a result of infectio
146 h-service-provider registeries) reporting on yellow fever vaccination activities between May 1, 1939,
147 e aims of this study were to estimate global yellow fever vaccination coverage from 1970 through to 2
148 ION: Our results highlight important gaps in yellow fever vaccination coverage, can contribute to imp
151 As a result, a fractional dose of the 17DD yellow fever vaccine (containing one fifth [0.1 ml] of t
154 Burkina Faso immunization schedule includes yellow fever vaccine (YFV) at 9 months and meningococcal
156 dividuals immunized with the live attenuated yellow fever vaccine (YFV-17D) by sampling peripheral bl
157 t transcriptomic gene expression profiles in Yellow Fever vaccine 17D (YF-17D) immunized human subjec
158 oenvironment to the response to the licensed yellow fever vaccine 17D (YF-17D) in an African cohort.
161 ology contain the nonstructural genes of the yellow fever vaccine and the premembrane and envelope ge
163 on of the population who had ever received a yellow fever vaccine for each second level administrativ
167 whole-virus, beta-propiolactone-inactivated yellow fever vaccine produced in Vero cell cultures and
168 2)-expressing plasmid (EP rDNA plus pIL-12), yellow fever vaccine virus 17D (rYF17D), and recombinant
181 IPV given alongside the measles-rubella and yellow fever vaccines at 9 months and when given as a fu
182 serum in the 1918 flu epidemic, contaminated yellow fever vaccines in World War II, and unethical hum
183 -administration of IPV, measles-rubella, and yellow fever vaccines within the Expanded Programme on I
184 ned to receive the IPV, measles-rubella, and yellow fever vaccines, singularly or in combination.
186 ent oral poliovirus (OPV), rubella, measles, yellow fever, varicella-zoster, multivalent measles/mump
187 ry gland anticoagulant from the mosquito and yellow fever vector Aedes albopictus, has been character
188 ified Wolbachia in Kenyan populations of the yellow fever vector Aedes bromeliae and its relative Aed
189 analysed datasets describing the epidemic of yellow fever, vector suitability, human demography, and
191 e a high mosquito infectivity phenotype, the yellow fever virus (YFV) 17D backbone of the ChimeriVax-
193 phosphorylation sites of the NS5 proteins of yellow fever virus (YFV) and dengue virus (DENV), two fl
194 tricts two medically important flaviviruses, yellow fever virus (YFV) and dengue virus serotype 2 (DE
196 out metagenomic sequencing which implicated yellow fever virus (YFV) as the etiology of this outbrea
197 In the present study we characterize the Yellow Fever Virus (YFV) associated with this outbreak i
200 etime recommendation for vaccination against yellow fever virus (YFV) has been controversial, leading
202 e previously demonstrated to be required for yellow fever virus (YFV) infection and others subsequent
205 sequencing is presented using as a model the yellow fever virus (YFV) live vaccine strain 17D-204 and
206 It was previously reported that mutations in yellow fever virus (YFV) nonstructural protein NS2A bloc
207 gue virus (DENV), West Nile virus (WNV), and yellow fever virus (YFV) NS1 attenuate classical and lec
208 verexpressed DNAJC14 is targeted to sites of yellow fever virus (YFV) replication complex (RC) format
210 safety and immunogenicity of live attenuated yellow fever virus (YFV) vaccination of nonatopic subjec
211 In this study, we used the live attenuated yellow fever virus (YFV) vaccine 17D as a human in vivo
212 Here we address this issue using the live yellow fever virus (YFV) vaccine, which induces long-ter
214 of many important human pathogens including yellow fever virus (YFV), dengue virus (DENV), and Zika
215 that TRIM56 poses a barrier to infections by yellow fever virus (YFV), dengue virus serotype 2 (DENV2
216 low Fever (YF) is a severe disease caused by Yellow Fever Virus (YFV), endemic in some parts of Afric
217 importance, such as dengue virus (DENV) and yellow fever virus (YFV), originated in sylvatic transmi
219 + T cells specific for a single epitope from Yellow Fever Virus (YFV), we show that the recently desc
220 flaviviruses.IMPORTANCE Flaviviruses such as yellow fever virus (YFV), Zika virus (ZIKV), and dengue
224 e insights into how a prototypic flavivirus, yellow fever virus (YFV-17D), differentially interacts w
226 DV, hepatitis C virus, West Nile virus, and yellow fever virus (YFV; vaccine strain 17D) were expres
227 he related mosquito-transmitted flaviviruses yellow fever virus 17D (YFV) and dengue virus type 2 (DE
229 wing ex vivo exposure to the live attenuated yellow fever virus 17D strain vaccine, a virus that we s
230 s of the flavivirus dengue virus (DV) and by yellow fever virus 17D were cholesterol independent, and
232 sis of CD8(+) T cells responding to the live yellow fever virus and smallpox vaccines--two highly suc
233 include the 2 flaviviruses dengue virus and yellow fever virus and the alphavirus chikungunya virus,
234 revaccination or natural infection with wild yellow fever virus during a 2011-12 outbreak in northern
235 rm persistence of neutralising antibodies to yellow fever virus following routine vaccination in infa
236 s such as Zika virus, chikungunya virus, and yellow fever virus have drawn attention toward other coc
237 ssessed neutralizing antibody titers against yellow fever virus in blood samples obtained before vacc
239 eplication of infectious West Nile virus and yellow fever virus in cell culture with low toxicity.
240 ogistic model to infer the district-specific yellow fever virus infection risk during the course of t
244 timated timing, source, and likely routes of yellow fever virus transmission and dispersion during on
246 till require vaccination in areas at risk of yellow fever virus transmission to achieve the 80% popul
249 ax-II), rotavirus (Rotateq and Rotarix), and yellow fever virus were negative for XMRV and highly rel
250 ift Valley fever virus, West Nile virus, and yellow fever virus), 8 bacteria (Bartonella spp., Brucel
253 ae family, including dengue virus (DENV) and yellow fever virus, cause serious disease in humans, whi
254 ing three members of the family Flaviviridae(yellow fever virus, dengue virus, and bovine viral diarr
256 ephalitis virus, norovirus, metapneumovirus, yellow fever virus, Japanese encephalitis virus, parainf
257 d mosquito-borne flaviviruses, which include yellow fever virus, Sepik virus, Saboya virus, and other
258 wide range of viruses, including DENV, WNV, yellow fever virus, Sindbis virus, Venezuelan equine enc
259 animal viruses, including hepatitis C virus, yellow fever virus, West Nile virus, chikungunya virus,
260 sed analyses of mass cytometry data, we show yellow fever virus-specific cCXCR5 T cells elicited by v
271 tion of Zika, Ebola, dengue, chikungunya and yellow fever viruses in plasma samples from infected pat
273 vectors of African malaria, dengue fever and yellow fever viruses, and lymphatic filariasis, respecti
274 aviviruses, including West Nile, dengue, and yellow fever viruses, is capable of inducing variable de
275 o many flavivirus types including Dengue and yellow fever viruses, the nonstructural NS3 multifunctio
279 r medically-important flaviviruses including yellow fever, West Nile and Japanese encephalitis viruse
280 aks, including those caused by dengue, Zika, yellow fever, West Nile, and chikungunya viruses, to dem
281 transmits two major arboviruses, dengue and yellow fever, which cause significant global morbidity a
283 g the most prevalent transmission routes for yellow fever will be limited by the sparsity of data whi
284 d Japanese encephalitis vaccination enhanced yellow fever (YF) immunogenicity upon YF vaccination.
290 ing in 2016, Brazil faced one of the largest Yellow Fever (YF) outbreaks in recent decades, mainly in
295 gainst measles, mumps, and rubella (MMR) and yellow fever (YF) with live attenuated viruses can rarel
296 y-transplanted patient, unvaccinated against yellow fever (YF), developed high fever, progressed rapi
298 s repeated outbreaks of Chikungunya (CHIKV), Yellow fever (YFV) and Japanese encephalitis (JEV) virus
299 ese encephalitis (JEV), West Nile (WNV), and yellow fever (YFV) viruses by intracellular cytokine sta