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1 IV-2 isolates, where it is controlled by the Env glycoprotein.
2 with protein and glycan features of the HIV Env glycoprotein.
3 levels as well as fusogenic activity of the Env glycoprotein.
4 lls mediated by cell surface-expressed HIV-1 Env glycoprotein.
5 ions exhibiting unique patterns of processed Env glycoprotein.
6 inactivation of sensitive but not resistant Env glycoproteins.
7 bodies reactive with xenotropic or MCF virus env glycoproteins.
8 ASBP-M(4070A) forms particles containing MLV Env glycoproteins.
9 r stomatitis virus, or murine leukemia virus Env glycoproteins.
10 or immune recognition of the HIV-1 envelope (Env) glycoprotein.
11 unodeficiency virus type 1 (HIV-1) envelope (Env) glycoprotein.
12 iciency virus type 1 (HIV-1) gp120 envelope (Env) glycoprotein.
13 ency virus it is a property of the envelope (Env) glycoprotein.
14 ytoplasmic domains of the relevant envelope (Env) glycoproteins.
15 y and phenotypically diverse SIVsm envelope (Env) glycoproteins.
16 udding even in the presence of the envelope (Env) glycoproteins.
17 ent preparations of oligomeric SIV envelope (Env) glycoproteins.
18 PIV1 from a chimpanzee for the pol, gag, and env glycoprotein 120 (gp120) regions, indicating greater
22 e the human immunodeficiency virus envelope (Env) glycoprotein and intracellular fusion machines, are
23 in the incorporation of the viral envelope (Env) glycoproteins and can influence particle infectivit
24 ld-type levels of the Gag cleavage products, Env glycoproteins, and reverse transcriptase activity wh
25 c antibody responses against HIV-1 envelope (Env) glycoproteins, and little is known about how the ra
26 luble oligomeric form of an avian retroviral Env glycoprotein (API) and soluble forms of its receptor
31 tance genes Fv4 and Rmcf in that it produces Env glycoprotein but fails to produce infectious virus;
32 ring of soluble mimetics of the trimeric HIV Env glycoprotein (commonly termed gp140 immunogens).
36 IV-1 and simian immunodeficiency virus (SIV) Env glycoproteins, despite no HIV/SIV-related proteins b
37 biased lambda light chain use during the HIV Env glycoprotein (Env) response in HIV infection and vac
39 se in mice that is largely mediated by viral Env glycoprotein expression within central nervous syste
41 xpressing clade B Gag-Pol fusion protein and Env glycoproteins from clades A, B, and C) was administe
42 brane-spanning domain (MSD) of the envelope (Env) glycoprotein from human (HIV) and simian immunodefi
44 ities of 48 donor and 25 recipient envelope (Env) glycoproteins from five subtype C heterosexual tran
45 deficiency viruses (SHIVs) bearing envelope (Env) glycoproteins from primary HIV-1 strains fail to in
46 attachment and entry properties of envelope (Env) glycoproteins from T/F and chronic control (CC) vir
47 Biologically functional clade C envelope (Env) glycoproteins from the chronically (donor) and newl
49 referentially bind the HIV (HIV-1) envelope (Env) glycoprotein (gp) trimer and broadly neutralize the
50 d many recognize novel epitopes on envelope (Env) glycoprotein gp120, illuminating new targets for va
51 tibodies (bNAbs) against the viral envelope (Env) glycoproteins gp120 and gp41, but no immunogen has
52 an immunodeficiency type 1 (HIV-1) envelope (Env) glycoprotein (gp120) to CD4 triggers the induction
56 smid-based and recombinant protein envelope (Env) glycoprotein immunogens were derived from a primary
57 activities against conserved epitopes of the env glycoprotein in cultures induced with the AV3 mutant
63 in this domain disrupt the incorporation of Env glycoproteins into virions and markedly impair virus
65 eting of Gag, the incorporation of envelope (Env) glycoproteins into nascent particles, and the nucle
67 n of the human immunodeficiency virus type 1 Env glycoprotein is important for endocytosis from the p
71 unodeficiency virus type 1 (HIV-1) envelope (Env) glycoprotein is oligomeric, with the major points o
73 he high-mannose patch on the HIV-1 envelope (Env) glycoprotein is the epicenter for binding of the po
74 n immunodeficiency virus type 1 (HIV-1) gp41 Env glycoprotein, is a potent inhibitor of virus infecti
76 mation by selectively inactivating sensitive Env glycoproteins, likely through altering their conform
77 e env segments, that distinct regions of the Env glycoprotein may be important for utilization of dif
80 lymphotropic virus type 1 (HTLV-1) envelope (Env) glycoprotein mediates binding of the virus to its r
82 has been associated with expression of viral Env glycoprotein; Northern blotting with specific hybrid
83 ane subunit (TM), the fusion subunit, of the Env glycoprotein of the subtype A avian sarcoma and leuk
84 lizable strategy for constructing SHIVs with Env glycoproteins of interest, including those that in h
93 omains of the strikingly conserved envelope (Env) glycoproteins of bovine leukemia virus (BLV) and it
94 ic Env proteins do not resemble the trimeric Env glycoprotein on HIV-1 viruses, which has implication
98 unodeficiency virus type 1 (HIV-1) envelope (Env) glycoprotein poses a major challenge for the develo
99 bodies (nnAbs) specific to the HIV envelope (Env) glycoproteins present at the surface of virus sensi
100 ibody (NAb) response against viral envelope (Env) glycoproteins present during acute and early infect
102 on SIVMAC but expressing the HIV-1 envelope (Env) glycoproteins (SHIVs) remains the most powerful mod
105 uman immunodeficiency virus type 1 envelope (Env) glycoprotein structure and function is based on stu
106 tly visualize trilobed presumptive envelope (env) glycoprotein structures on the surface of negativel
107 tance genes control expression of xenotropic env glycoprotein that interferes with exogenous virus in
108 s have identified targets on HIV-1 envelope (Env) glycoprotein that are vulnerable to antibody neutra
110 Ps) bear nonnative "junk" forms of envelope (Env) glycoprotein that may undermine the development of
111 we review our current understanding of HIV-1 Env glycoprotein trafficking and incorporation into viri
112 Much is currently known about the HIV-1 Env glycoprotein trafficking pathway and the structure o
113 ration nickel-based liposomes captured HIV-1 Env glycoprotein trimers via a noncovalent linkage with
114 a recombinant vaccinia virus expressing 89.6 Env glycoprotein (vBD3) in a mouse challenge model, we o
116 owever, the stability of the cell-associated Env glycoprotein was decreased and Env incorporation int
118 A retroviral vector that does not encode any Env glycoprotein was packaged into retroviral particles
122 aCFI(HXB2/89.6) vector expressing a modified Env glycoprotein with C-terminal mutations intended to m
123 s dispensable for the incorporation of HIV-1 Env glycoproteins with a shortened cytoplasmic domain.
124 mmunodeficiency virus type 1 (HIV-1), encode Env glycoproteins with unusually long cytoplasmic tails,
125 ncluding HIV-1, have transmembrane envelope (Env) glycoproteins with cytoplasmic tails that are quite
126 with murine leukemia virus (MuLV) envelope (Env) glycoproteins without affecting infectivity conferr
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