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1 ions exhibiting unique patterns of processed Env glycoprotein.
2 IV-2 isolates, where it is controlled by the Env glycoprotein.
3 with protein and glycan features of the HIV Env glycoprotein.
4 levels as well as fusogenic activity of the Env glycoprotein.
5 lls mediated by cell surface-expressed HIV-1 Env glycoprotein.
6 bodies reactive with xenotropic or MCF virus env glycoproteins.
7 ASBP-M(4070A) forms particles containing MLV Env glycoproteins.
8 inactivation of sensitive but not resistant Env glycoproteins.
9 r stomatitis virus, or murine leukemia virus Env glycoproteins.
10 ency virus it is a property of the envelope (Env) glycoprotein.
11 or immune recognition of the HIV-1 envelope (Env) glycoprotein.
12 n by expressing a SER5-insensitive envelope (Env) glycoprotein.
13 ease-causing agents, such as HIV-1 envelope (Env) glycoprotein.
14 unodeficiency virus type 1 (HIV-1) envelope (Env) glycoprotein.
15 iciency virus type 1 (HIV-1) gp120 envelope (Env) glycoprotein.
16 ls of genetic diversity in the HIV envelope (Env) glycoprotein.
17 udding even in the presence of the envelope (Env) glycoproteins.
18 ent preparations of oligomeric SIV envelope (Env) glycoproteins.
19 ytoplasmic domains of the relevant envelope (Env) glycoproteins.
20 y and phenotypically diverse SIVsm envelope (Env) glycoproteins.
21 PIV1 from a chimpanzee for the pol, gag, and env glycoprotein 120 (gp120) regions, indicating greater
23 ion deletion of the C-terminal tail of HIV-1 Env glycoprotein 41 (gp41) showed reduced sensitivity to
24 man immunodeficiency virus (HIV-1) envelope (Env) glycoprotein, a (gp120-gp41)(3) trimer, mediates fu
26 HIV-1-infected cells to ADCC by opening the Env glycoprotein and exposing CD4-induced (CD4i) epitope
28 e the human immunodeficiency virus envelope (Env) glycoprotein and intracellular fusion machines, are
29 in the incorporation of the viral envelope (Env) glycoproteins and can influence particle infectivit
30 ld-type levels of the Gag cleavage products, Env glycoproteins, and reverse transcriptase activity wh
31 c antibody responses against HIV-1 envelope (Env) glycoproteins, and little is known about how the ra
32 luble oligomeric form of an avian retroviral Env glycoprotein (API) and soluble forms of its receptor
33 se released virus particles unable to obtain Env glycoproteins are non-infectious and unable to propa
38 tance genes Fv4 and Rmcf in that it produces Env glycoprotein but fails to produce infectious virus;
39 le HIV-1 pseudotyped with an HIV-1 envelope (Env) glycoprotein, but not with vesicular stomatitis vir
40 ring of soluble mimetics of the trimeric HIV Env glycoprotein (commonly termed gp140 immunogens).
42 al production of a clinical HIV vaccine with Env glycoprotein components.IMPORTANCE HIV-1 Env protein
45 IV-1 and simian immunodeficiency virus (SIV) Env glycoproteins, despite no HIV/SIV-related proteins b
46 transmembrane proteins in addition to viral Env glycoprotein during assembly at the plasma membrane.
47 ructurally defined mimics of native trimeric Env glycoproteins (e.g., SOSIP trimers) present multiple
49 biased lambda light chain use during the HIV Env glycoprotein (Env) response in HIV infection and vac
51 se in mice that is largely mediated by viral Env glycoprotein expression within central nervous syste
53 erties that target six epitopes of the HIV-1 Env glycoprotein for their ability to inhibit viruses th
55 construct can restrict the incorporation of Env glycoproteins from an evolutionarily distant HIV-1 p
56 xpressing clade B Gag-Pol fusion protein and Env glycoproteins from clades A, B, and C) was administe
57 brane-spanning domain (MSD) of the envelope (Env) glycoprotein from human (HIV) and simian immunodefi
59 ities of 48 donor and 25 recipient envelope (Env) glycoproteins from five subtype C heterosexual tran
60 deficiency viruses (SHIVs) bearing envelope (Env) glycoproteins from primary HIV-1 strains fail to in
61 attachment and entry properties of envelope (Env) glycoproteins from T/F and chronic control (CC) vir
62 Biologically functional clade C envelope (Env) glycoproteins from the chronically (donor) and newl
64 referentially bind the HIV (HIV-1) envelope (Env) glycoprotein (gp) trimer and broadly neutralize the
65 INC5 is determined by sequences in the viral Env glycoprotein gp120, and the antiviral effect of SERI
66 d many recognize novel epitopes on envelope (Env) glycoprotein gp120, illuminating new targets for va
67 tibodies (bNAbs) against the viral envelope (Env) glycoproteins gp120 and gp41, but no immunogen has
68 r NYVAC vectors alone or in combination with Env glycoprotein (gp120) followed by a co-delivered NYVA
69 an immunodeficiency type 1 (HIV-1) envelope (Env) glycoprotein (gp120) to CD4 triggers the induction
71 NCE The incorporation of the HIV-1 envelope (Env) glycoproteins, gp120 and gp41, into virus particles
73 of risk, such as vaccine-elicited anti-HIV-1 Env glycoprotein IgG3 antibodies and antibody-dependent
75 smid-based and recombinant protein envelope (Env) glycoprotein immunogens were derived from a primary
76 activities against conserved epitopes of the env glycoprotein in cultures induced with the AV3 mutant
82 get cells is mediated by the HIV-1 envelope (Env) glycoprotein interacting with host receptor CD4, wh
83 in this domain disrupt the incorporation of Env glycoproteins into virions and markedly impair virus
86 eting of Gag, the incorporation of envelope (Env) glycoproteins into nascent particles, and the nucle
88 n of the human immunodeficiency virus type 1 Env glycoprotein is important for endocytosis from the p
92 unodeficiency virus type 1 (HIV-1) envelope (Env) glycoprotein is oligomeric, with the major points o
94 he high-mannose patch on the HIV-1 envelope (Env) glycoprotein is the epicenter for binding of the po
97 n immunodeficiency virus type 1 (HIV-1) gp41 Env glycoprotein, is a potent inhibitor of virus infecti
99 mation by selectively inactivating sensitive Env glycoproteins, likely through altering their conform
100 natural polymorphism in the HIV-1 envelope (Env) glycoprotein, lysine at position 425 was selected a
101 e env segments, that distinct regions of the Env glycoprotein may be important for utilization of dif
104 lymphotropic virus type 1 (HTLV-1) envelope (Env) glycoprotein mediates binding of the virus to its r
105 man immunodeficiency virus (HIV-1) envelope (Env) glycoprotein mediates viral entry and is the sole t
107 has been associated with expression of viral Env glycoprotein; Northern blotting with specific hybrid
108 ane subunit (TM), the fusion subunit, of the Env glycoprotein of the subtype A avian sarcoma and leuk
109 lizable strategy for constructing SHIVs with Env glycoproteins of interest, including those that in h
119 omains of the strikingly conserved envelope (Env) glycoproteins of bovine leukemia virus (BLV) and it
121 ic Env proteins do not resemble the trimeric Env glycoprotein on HIV-1 viruses, which has implication
122 generation of a library of Cys mutations in Env glycoprotein on the viral surface, covalent labeling
127 unodeficiency virus type 1 (HIV-1) envelope (Env) glycoprotein poses a major challenge for the develo
128 man immunodeficiency virus (HIV-1) envelope (Env) glycoprotein precursor (gp160) trimerizes, is modif
129 bodies (nnAbs) specific to the HIV envelope (Env) glycoproteins present at the surface of virus sensi
130 ibody (NAb) response against viral envelope (Env) glycoproteins present during acute and early infect
132 on SIVMAC but expressing the HIV-1 envelope (Env) glycoproteins (SHIVs) remains the most powerful mod
135 uman immunodeficiency virus type 1 envelope (Env) glycoprotein structure and function is based on stu
136 tly visualize trilobed presumptive envelope (env) glycoprotein structures on the surface of negativel
138 tance genes control expression of xenotropic env glycoprotein that interferes with exogenous virus in
139 s have identified targets on HIV-1 envelope (Env) glycoprotein that are vulnerable to antibody neutra
141 Ps) bear nonnative "junk" forms of envelope (Env) glycoprotein that may undermine the development of
142 we review our current understanding of HIV-1 Env glycoprotein trafficking and incorporation into viri
143 Much is currently known about the HIV-1 Env glycoprotein trafficking pathway and the structure o
144 ration nickel-based liposomes captured HIV-1 Env glycoprotein trimers via a noncovalent linkage with
145 a recombinant vaccinia virus expressing 89.6 Env glycoprotein (vBD3) in a mouse challenge model, we o
147 owever, the stability of the cell-associated Env glycoprotein was decreased and Env incorporation int
149 A retroviral vector that does not encode any Env glycoprotein was packaged into retroviral particles
153 aCFI(HXB2/89.6) vector expressing a modified Env glycoprotein with C-terminal mutations intended to m
154 s dispensable for the incorporation of HIV-1 Env glycoproteins with a shortened cytoplasmic domain.
155 mmunodeficiency virus type 1 (HIV-1), encode Env glycoproteins with unusually long cytoplasmic tails,
156 ncluding HIV-1, have transmembrane envelope (Env) glycoproteins with cytoplasmic tails that are quite
157 with murine leukemia virus (MuLV) envelope (Env) glycoproteins without affecting infectivity conferr