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1 and 38% were visiting countries endemic for yellow fever.
2 ncluding smallpox, polio, measles, mumps and yellow fever.
3 ored diseases such as bovine tuberculosis or yellow fever.
4 of Aedes aegypti, a mosquito that transmits yellow fever.
5 tuberculosis to 8043 (95% CI 7621-8464) for yellow fever.
6 mopolitan vector of dengue, chikungunya, and yellow fever.
7 there is no specific antiviral treatment for yellow fever.
8 tion during investigations on the ecology of yellow fever.
9 its derivatives as antiviral agents to treat yellow fever.
10 iral therapeutics for clinical management of yellow fever.
12 than candidates based on Langat E5, TBE, and yellow fever 17D backbones, and was found to be highly i
13 tracerebral (i.c.) route, whereas commercial yellow fever 17D vaccine (YF-Vax) caused lethal encephal
15 s for a human vaccine; it appears safer than yellow fever 17D vaccine but has a similar profile of im
18 Viral encephalitis caused by neuroadapted yellow fever 17D virus (PYF) was studied in parental and
21 irus (LGTV), a former live TBEV vaccine; and yellow fever 17D virus vaccine (YF 17D) in rhesus monkey
26 ome of Aedes aegypti, the primary vector for yellow fever and dengue fever, which at approximately 13
29 he acquisition of the genome sequence of the yellow fever and Dengue vector, Aedes aegypti (Aa), has
31 edes aegypti is the principal vector for the yellow fever and dengue viruses, and is also responsible
32 k-borne encephalitis, Japanese encephalitis, yellow fever and dengue viruses, constitute a significan
34 borne infectious diseases such as dengue and yellow fever and emerging diseases such as Zika and chik
43 for other flaviviruses, including West Nile, yellow fever, and dengue viruses, and the critical role
45 e flavivirus methyltransferases from dengue, yellow fever, and West Nile virus (WNV) sequentially gen
46 other Flaviviridae, including dengue, Zika, yellow fever, and West Nile virus, identifies conserved
47 anese encephalitis, tick-borne encephalitis, yellow fever, and West Nile viruses cause substantial mo
49 viral diseases (notably dengue, chikungunya, yellow fever, and Zika virus disease) resulting from the
50 tion serum samples for measles, rubella, and yellow fever; and the post-vaccination antibody titres g
52 nohistochemical assay of liver tissue showed yellow fever antigen in the Kuppfer cells of the liver s
53 the XRX-001 vaccine, containing inactivated yellow fever antigen with an alum adjuvant, induced neut
54 est Nile fever, tick-borne encephalitis, and yellow fever, are endemic in tropical and temperate part
56 uito vectors of diseases such as malaria and yellow fever, but the molecular basis of CO(2) detection
57 ffective vaccine is available, the number of yellow fever cases has increased over the past two decad
60 ka virus, and the threat of global spread of yellow fever, combined with the resurgence of dengue and
61 vaccination coverage for polio, measles, and yellow fever continued to decrease, whereas the trend in
63 urg, Lassa, the South American arenaviruses, yellow fever, Crimean-Congo and Rift Valley fever viruse
64 elicits a protective immune response against yellow fever, dengue, and tick-borne encephalitis flaviv
67 It is closely related to the mosquito-borne yellow fever, dengue, Japanese encephalitis, and West Ni
68 ito-borne or tick-borne flaviviruses such as yellow fever, dengue, West Nile, St Louis encephalitis,
70 14c10 light chain CDRs.IMPORTANCE A chimeric yellow fever-dengue live-attenuated tetravalent vaccine
71 eviously reported construction of a chimeric yellow fever-dengue type 2 virus (YF/DEN2) and determine
78 human diseases such as malaria, dengue, and yellow fever has received much interest due to the abili
80 c diseases, such as cholera, meningitis, and yellow fever, have become common over the past decade, h
82 timate the effective reproductive number for yellow fever in Angola using disease natural history and
83 iseases (Chagas' disease, leishmaniasis, and yellow fever) in Colombia, we show the links between sys
90 s a significant health burden in areas where yellow fever is endemic, but it is preventable through v
91 travelers to and residents of areas in which yellow fever is endemic, but the vaccine can cause serio
92 des aegypti, the global vector of dengue and yellow fever, is inexorably linked to water-filled human
94 West Nile fever (WNF), chikungunya, dengue, yellow fever, Japanese encephalitis virus, GBS, and cont
95 VPDs), including polio, measles and rubella, yellow fever, Japanese encephalitis, rotavirus, and inva
97 s including dengue fever, chikungunya, zika, yellow fever, leishmaniasis, chagas disease, and malaria
98 fection (hepatitis C virus) and vaccination (yellow fever, malaria, influenza), but poor outcome in a
100 by plaque reduction neutralisation (measles, yellow fever), microneutralisation (polio serotypes 1 an
101 This study tested this assumption using the yellow fever mosquito Aedes aegypti and malaria parasite
102 major downstream targets, S6 kinase, of the yellow fever mosquito Aedes aegypti during egg developme
105 fficking, we disrupted COPI functions in the Yellow Fever mosquito Aedes aegypti to interfere with bl
106 e malaria mosquito Anopheles gambiae and the yellow fever mosquito Aedes aegypti were searched by Bla
112 gand selectivity and in vivo function of the yellow fever mosquito sterol carrier protein-2 protein (
113 apidly displaced resident populations of the yellow fever mosquito, Aedes aegypti in the southeastern
114 ed neuropeptides in the antennal lobe of the yellow fever mosquito, Aedes aegypti, a major vector of
115 ivation of the vitellogenin (Vg) gene in the yellow fever mosquito, Aedes aegypti, by EcR/USP and E74
118 colactone may be an interkingdom cue for the yellow fever mosquito, Aedes aegypti, seeking blood-meal
119 site of ferritin expression and that, in the yellow fever mosquito, Aedes aegypti, the expression of
121 from the nanos (nos) orthologous gene of the yellow fever mosquito, Aedes aegypti, to control sex- an
131 no-acid transporter Slimfast (Slif) from the yellow-fever mosquito Aedes aegypti using codon-optimize
133 ET-elicited protection against ZIKV-infected yellow fever mosquitoes from old and recent laboratory c
135 evious estimates on the basis of more recent yellow fever occurrence data and improved estimation met
137 graphic factors to the ongoing spread of the yellow fever outbreak and provide estimates of the areas
138 graphic factors to the ongoing spread of the yellow fever outbreak and provide estimates of the areas
139 were fitted to a dataset of the locations of yellow fever outbreaks within the last 25 years to estim
141 between 43% and 52% of the population within yellow fever risk zones, compared with between 66% and 7
143 rus seroprevalence and measles, rubella, and yellow fever seroconversion, and (1/3) log2 for log2-tra
144 t human pathogens such as dengue, West Nile, yellow fever, tick-borne encephalitis and Japanese encep
147 h-service-provider registeries) reporting on yellow fever vaccination activities between May 1, 1939,
148 e aims of this study were to estimate global yellow fever vaccination coverage from 1970 through to 2
149 ION: Our results highlight important gaps in yellow fever vaccination coverage, can contribute to imp
155 dividuals immunized with the live attenuated yellow fever vaccine (YFV-17D) by sampling peripheral bl
157 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
166 whole-virus, beta-propiolactone-inactivated yellow fever vaccine produced in Vero cell cultures and
167 2)-expressing plasmid (EP rDNA plus pIL-12), yellow fever vaccine virus 17D (rYF17D), and recombinant
177 patients found to be WNV IgM positive and no yellow fever vaccinees found to be WNV IgM positive.
178 IPV given alongside the measles-rubella and yellow fever vaccines at 9 months and when given as a fu
179 -administration of IPV, measles-rubella, and yellow fever vaccines within the Expanded Programme on I
180 ned to receive the IPV, measles-rubella, and yellow fever vaccines, singularly or in combination.
181 ent oral poliovirus (OPV), rubella, measles, yellow fever, varicella-zoster, multivalent measles/mump
182 ry gland anticoagulant from the mosquito and yellow fever vector Aedes albopictus, has been character
183 ified Wolbachia in Kenyan populations of the yellow fever vector Aedes bromeliae and its relative Aed
184 NAT subfamily from the larval midgut of the Yellow Fever vector mosquito, Aedes aegypti (aeAAT1, AAR
185 analysed datasets describing the epidemic of yellow fever, vector suitability, human demography, and
188 e a high mosquito infectivity phenotype, the yellow fever virus (YFV) 17D backbone of the ChimeriVax-
191 phosphorylation sites of the NS5 proteins of yellow fever virus (YFV) and dengue virus (DENV), two fl
193 tricts two medically important flaviviruses, yellow fever virus (YFV) and dengue virus serotype 2 (DE
198 sequencing is presented using as a model the yellow fever virus (YFV) live vaccine strain 17D-204 and
199 It was previously reported that mutations in yellow fever virus (YFV) nonstructural protein NS2A bloc
200 gue virus (DENV), West Nile virus (WNV), and yellow fever virus (YFV) NS1 attenuate classical and lec
201 verexpressed DNAJC14 is targeted to sites of yellow fever virus (YFV) replication complex (RC) format
202 Here we describe a two-component genome yellow fever virus (YFV) replication system in which eac
203 s-packaging system that involved packaging a yellow fever virus (YFV) replicon into pseudo-infectious
205 safety and immunogenicity of live attenuated yellow fever virus (YFV) vaccination of nonatopic subjec
206 In this study, we used the live attenuated yellow fever virus (YFV) vaccine 17D as a human in vivo
207 Here we address this issue using the live yellow fever virus (YFV) vaccine, which induces long-ter
209 ose of tick-borne encephalitis virus (TBEV), yellow fever virus (YFV), and Japanese encephalitis viru
211 of many important human pathogens including yellow fever virus (YFV), dengue virus (DENV), and Zika
212 that TRIM56 poses a barrier to infections by yellow fever virus (YFV), dengue virus serotype 2 (DENV2
213 involves the gene-specific amplification of yellow fever virus (YFV), Japanese encephalitis virus (J
215 + T cells specific for a single epitope from Yellow Fever Virus (YFV), we show that the recently desc
220 e insights into how a prototypic flavivirus, yellow fever virus (YFV-17D), differentially interacts w
222 DV, hepatitis C virus, West Nile virus, and yellow fever virus (YFV; vaccine strain 17D) were expres
223 wing ex vivo exposure to the live attenuated yellow fever virus 17D strain vaccine, a virus that we s
224 s of the flavivirus dengue virus (DV) and by yellow fever virus 17D were cholesterol independent, and
225 The capsid proteins of two flaviviruses, yellow fever virus and dengue virus, were expressed in E
227 sis of CD8(+) T cells responding to the live yellow fever virus and smallpox vaccines--two highly suc
228 include the 2 flaviviruses dengue virus and yellow fever virus and the alphavirus chikungunya virus,
230 f 18 nucleotides (residues 146 to 163 of the yellow fever virus genome, which encode amino acids 9 to
231 ucleotide sequence found in the 5' region of yellow fever virus genomic RNA that is required for RNA
232 eplication of infectious West Nile virus and yellow fever virus in cell culture with low toxicity.
234 ogistic model to infer the district-specific yellow fever virus infection risk during the course of t
235 that the E protein is a critical factor for yellow fever virus neuropathogenesis in the SCID mouse m
238 Structures of prM-containing dengue and yellow fever virus particles were determined to 16 and 2
239 protein) is essential for replication of the yellow fever virus replicon and that a slightly longer s
240 30451, specifically blocked translation of a yellow fever virus replicon but not a Sindbis virus repl
241 ed nucleotide and that the error rate of the yellow fever virus RNA polymerase employed by the chimer
244 till require vaccination in areas at risk of yellow fever virus transmission to achieve the 80% popul
248 ax-II), rotavirus (Rotateq and Rotarix), and yellow fever virus were negative for XMRV and highly rel
249 ift Valley fever virus, West Nile virus, and yellow fever virus), 8 bacteria (Bartonella spp., Brucel
251 ding vesicular stomatitis virus, poliovirus, yellow fever virus, and herpes simplex virus type 1, rep
254 curred in NS2B-NS3 recombinant proteins from yellow fever virus, dengue virus types 2 and 4, and Japa
255 ing three members of the family Flaviviridae(yellow fever virus, dengue virus, and bovine viral diarr
258 ephalitis virus, norovirus, metapneumovirus, yellow fever virus, Japanese encephalitis virus, parainf
259 d mosquito-borne flaviviruses, which include yellow fever virus, Sepik virus, Saboya virus, and other
260 wide range of viruses, including DENV, WNV, yellow fever virus, Sindbis virus, Venezuelan equine enc
261 animal viruses, including hepatitis C virus, yellow fever virus, West Nile virus, chikungunya virus,
262 cutive plaque purifications of four chimeric yellow fever virus-dengue virus (ChimeriVax-DEN) vaccine
271 vectors of African malaria, dengue fever and yellow fever viruses, and lymphatic filariasis, respecti
272 nd other flaviviruses, such as West Nile and yellow fever viruses, contain a 5' m7GpppN-capped positi
273 o many flavivirus types including Dengue and yellow fever viruses, the nonstructural NS3 multifunctio
278 r medically-important flaviviruses including yellow fever, West Nile and Japanese encephalitis viruse
279 transmits two major arboviruses, dengue and yellow fever, which cause significant global morbidity a
282 cine constructed from an infectious clone of yellow fever (YF) 17D virus in which the premembrane and
283 premembrane (prM) and envelope (E) genes of yellow fever (YF) 17D virus were replaced with those of
284 d Japanese encephalitis vaccination enhanced yellow fever (YF) immunogenicity upon YF vaccination.
285 te the availability of an effective vaccine, yellow fever (YF) is considered a reemerging disease owi
291 relationships among flaviviruses within the yellow fever (YF) virus genetic group were investigated
293 ve indicated that there are two genotypes of yellow fever (YF) virus in Africa, one in west Africa an
295 We have genetically engineered an attenuated yellow fever (YF) virus to carry and express foreign ant
298 (TBE), dengue fever (DF), West Nile (WN) and yellow fever (YF), can aid in the design of antiviral dr
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