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1 the distal end of domain II of the West Nile virus envelope protein.
2 ed to domain III of the neuroadapted SPYF-MN virus envelope protein.
3 o sites within domains I and II of West Nile virus envelope protein.
4 ectors by pseudotyping with modified Sindbis virus envelope proteins.
5 in 'tail' formation mediated by the vaccinia virus envelope protein A36R, which utilizes two similarl
6 nant vaccinia virus vector expressing Friend virus envelope protein and a live attenuated Friend viru
8 that both human and simian immunodeficiency virus envelope proteins can undergo endocytosis, the gE
10 nally, the MMTV- and Moloney murine leukemia virus envelope proteins coimmunoprecipitated with TLR4 w
13 protomeric units of Moloney murine leukemia virus envelope protein (Env) are activated in relation t
15 that contains truncated, recombinant, Dengue virus envelope protein from all four Dengue virus seroty
16 he 18-kDa leader peptide (LP18) of the foamy virus envelope protein (FVenv) as a new substrate for in
17 ctor in the presence of vesicular stomatitis virus envelope protein G (VSV-G) produced an insignifica
21 brane-spanning domain of the murine leukemia virus envelope protein in membrane fusion and its regula
22 han 142 in ecotropic Moloney murine leukemia virus envelope protein is essential to virus binding and
26 odies specific to the human immunodeficiency virus envelope protein, neutralizing activities, numbers
28 ional homologies between the Zika and Dengue viruses' envelope proteins raise the possibility that cr
30 stallized soluble mutant forms of the dengue virus envelope protein (sE) that include portions of the
32 f the NCI chemical database using the dengue virus envelope protein structure revealed several hypoth
33 in are structurally homologous to eukaryotic virus envelope proteins, suggesting that Archaea and vir
34 ns and conformational changes of specialized virus envelope proteins termed membrane fusion proteins.
35 tophan 142 being an essential residue on the virus envelope protein that interacts directly with the
36 for activity in preventing binding of dengue virus envelope protein to immobilized heparin; compounds
38 on virions pseudotyped with murine leukemia virus envelope protein was similar to that on particles
39 a recombinant chimeric form of dengue type 2 virus envelope protein was used as a probe to investigat
40 pseudovirions displaying distinct influenza virus envelope proteins were tested for fusion activity.
41 ined the function of Moloney murine leukemia virus envelope proteins with substitutions in the membra
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