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1 ed vaccines against viral infections such as tick-borne encephalitis.
2 siosis, human granulocytic anaplasmosis, and tick-borne encephalitis.
4 se, continue to increase, or, in the case of tick-borne encephalitis and Crimean-Congo haemorrhagic f
5 ch is consistent with X-ray crystal data for tick-borne encephalitis and dengue viruses, these result
6 ens such as dengue, West Nile, yellow fever, tick-borne encephalitis and Japanese encephalitis virus
7 for yellow fever, Japanese encephalitis and tick-borne encephalitis and several vaccines are in clin
8 sponsible for dengue fever, West Nile fever, tick-borne encephalitis, and yellow fever, are endemic i
9 ses that affect humans and animals including tick-borne encephalitis, borreliosis, tick-borne fever a
10 dification, we used a neurovirulent chimeric tick-borne encephalitis/dengue virus (TBEV/DEN4) that co
11 e response against yellow fever, dengue, and tick-borne encephalitis flaviviruses through poorly defi
12 irus (WNV), and related flaviviruses such as tick-borne encephalitis, Japanese encephalitis, yellow f
13 t Louis encephalitis, Japanese encephalitis, tick-borne encephalitis, Kyasanur Forest disease, and Om
14 against the LGT virus M protein neutralizes tick-borne encephalitis serocomplex flaviviruses but not
18 aviviruses, but not among the members of the tick-borne encephalitis (TBE) serocomplex of flaviviruse
19 rus vaccine particles at different stages in tick-borne encephalitis (TBE) vaccines formulation were
22 flaviviruses, which cause diseases, such as tick-borne encephalitis (TBE), dengue fever (DF), West N
23 uch as West Nile, Japanese encephalitis, and tick-borne encephalitis (TBEV) viruses are important neu
24 ferent types of CpG oligodeoxynucleotides or tick-borne encephalitis vaccine, which occurred in an S1
25 cinated (measles, mumps, and rubella vaccine/tick-borne encephalitis vaccine/BCG vaccine: adjusted ha
26 ngat virus (LGTV), one of the members of the tick-borne encephalitis virus (TBEV) complex, was firstl
27 LGT), the naturally attenuated member of the tick-borne encephalitis virus (TBEV) complex, was tested
30 from a highly virulent Far Eastern strain of tick-borne encephalitis virus (TBEV) on the backbone of
32 mice, albeit less than that associated with tick-borne encephalitis virus (TBEV), the most virulent
33 ing subgenomic RNAs (replicons) derived from tick-borne encephalitis virus (TBEV), West Nile virus (W
34 a dengue virus (strain 16681) with those of tick-borne encephalitis virus (TBEV), yellow fever virus
36 ncer element (REE) within the capsid gene of tick-borne encephalitis virus (TBEV, genus Flavivirus).
37 rt that encephalitic flaviviruses, including tick-borne encephalitis virus and West Nile virus, antag
40 istidine residues in the envelope protein of tick-borne encephalitis virus led Fritz et al. to identi
41 Both Langat virus (LGTV; a member of the tick-borne encephalitis virus serogroup) and Japanese en
43 is potential (influenza virus, Dengue virus, tick-borne encephalitis virus, rabies virus, severe acut
45 n (3'NCR) of the flavivirus genome (chimeric tick-borne encephalitis virus/dengue virus) abolished vi
47 is shared by the E proteins from dengue and tick-borne encephalitis viruses and forms a rod-shaped c
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