HIV-1 infection
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
MARCH2 inhibits the production and infection of HIV-1 through ligase activity-dependent envelope protein degradation and/or intracellular retention, a mechanism shared by MARCH8 that also leads to the inhibition of HIV-1 infection.
|
29573664 |
2018 |
HIV-1 infection
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
Antibodies bound to human immunodeficiency virus type 1 (HIV-1) envelope protein expressed by infected cells mobilize antibody-dependent cellular cytotoxicity (ADCC) to eliminate the HIV-1-infected cells and thereby suppress HIV-1 infection and delay disease progression.
|
28794022 |
2017 |
HIV-1 infection
|
0.100 |
Biomarker
|
disease |
BEFREE |
We evaluated the risk factors for intrafamilial transmission of HIV-1 infection through qualitative epidemiology following pol and env gene sequencing and phylogenetic analysis.
|
22918554 |
2013 |
HIV-1 infection
|
0.100 |
Biomarker
|
disease |
BEFREE |
For example, the evolution of Env during the course of HIV-1 infection increases the efficiency of Env-CCR5 interactions, which consequently increases Env-mediated fusogenicity and decreases sensitivity to entry inhibitors.
|
17073614 |
2006 |
HIV-1 infection
|
0.100 |
Biomarker
|
disease |
BEFREE |
Efficient human immunodeficiency virus (HIV)-1 infection depends on multiple interactions between the viral gp41/gp120 envelope (Env) proteins and cell surface receptors.
|
16148047 |
2005 |
HIV-1 infection
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
We analysed three host response and viral characteristics were associated with recent HIV-1 infection: rapidly increasing EIA optical density (OD) values, genetically homogeneous env gene quasispecies, and putative non-syncytium inducing env V3 loop sequences.
|
11741169 |
2002 |
HIV-1 infection
|
0.100 |
Biomarker
|
disease |
BEFREE |
Infection of macaques with chimeric simian/human immunodeficiency virus (SHIV) expressing the envelope protein of HIV-1 provides a model system for studying HIV-1 infection in humans.
|
9705259 |
1998 |
HIV-1 infection
|
0.100 |
Biomarker
|
disease |
BEFREE |
According to the rate of depletion of CD4 cell counts, we grouped 12 cases of human immunodeficiency virus type 1 (HIV-1) infection as 6 rapid (21.0 to 33.8 cells per microl per month) and 6 slow (0.9 to 7.9 cells per microl per month) progressors and determined the individual viral quasispecies patterns by sequencing the genome region encoding the V1, V2, and V3 loops of envelope protein.
|
9188549 |
1997 |
HIV-1 infection
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
To determine HIV-1 genomic RNA and proviral DNA sequences of the third hypervariable region (V3 loop) of the envelope protein in patients with primary HIV-1 infection (PHI), and to compare these sequences with sequences from patients with more advanced HIV-1 infection.
|
7893436 |
1995 |
HIV-1 infection
|
0.100 |
Biomarker
|
disease |
BEFREE |
HIV-1 infection of a human T-cell line transduced with this vector led to induction of sCD4-KDEL synthesis and a block in transport of the HIV envelope protein to the cell surface.
|
8464877 |
1993 |
HIV-1 infection
|
0.100 |
Biomarker
|
disease |
BEFREE |
Our data suggest that antibodies against select epitopes of HIV envelope protein gp120 might play an important role in preventing mother-to-child transmission of HIV-1 infection.
|
2479014 |
1989 |