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1 host sooty mangabey and the non-natural host pig-tailed macaque.
2 d Hepatocystis sp. in one long-tailed and 12 pig-tailed macaques.
3 ion of iNKT cells in the peripheral blood of pig-tailed macaques.
4 es in vivo, HIV(NL-DT5R) was inoculated into pig-tailed macaques.
5 e and elicits autoantibodies against CCR5 in pig-tailed macaques.
6 cytes are not a major reservoir for virus in pig-tailed macaques.
7 veloped preferentially in rhesus compared to pig-tailed macaques.
8 eric viruses encoding IIIB env in rhesus and pig-tailed macaques.
9 s, and used this for passive immunization of pig-tailed macaques.
10 acute PBj-like disease when inoculated into pig-tailed macaques.
11 lted in vaginal infection in rhesus, but not pig-tailed, macaques.
12 characterized classical MHC class I genes of pig-tailed macaques and have identified 19 MHC class I a
13 SHIV that caused CD4+ cell loss and AIDS in pig-tailed macaques and used a cell-free stock of this v
14 white colobus), Macaca nemestrina (southern pig-tailed macaque), and Mandrillus leucophaeus (the dri
16 r previous experiments using a single female pig-tailed macaque as a model for M. genitalium infectio
18 This study supports the use of MneRV2 in pig-tailed macaques as an important model for studying r
20 ypeptide comprising the N-terminal domain of pig-tailed macaque CCR5 fused to streptavidin that, when
21 ns, with viruses growing to higher titers in pig-tailed macaque cells than in rhesus macaque cells.
23 marked contrast to rhesus macaques, 19 of 21 pig-tailed macaques controlled DeltaGY replication with
24 We demonstrate that, like human DC-SIGN, pig-tailed macaque DC-SIGN (ptDC-SIGN) is expressed on D
25 n HIV infection, we cloned and characterized pig-tailed macaque DC-SIGN and generated monoclonal anti
29 e, virus was isolated from a lymph node of a pig-tailed macaque (designated PGm) and the cerebrospina
30 carried out serially in three groups of two pig-tailed macaques each, via intravenous blood-bone mar
31 ased on these findings, we conclude that the pig-tailed macaques exhibit potential as a non-human ani
32 , we describe such a system that uses female pig-tailed macaques exposed vaginally to a CCR5-using si
34 and 1015 blood samples from long-tailed and pig-tailed macaques from 3 locations were examined for P
35 herpesvirus Macaca nemestrina (RFHVMn), the pig-tailed macaque homolog of Kaposi's sarcoma-associate
36 the sequence characterization of MneRV2, the pig-tailed macaque homolog of rhesus rhadinovirus (RRV).
38 munoglobulin G (IgG) were administered to 15 pig-tailed macaques in order to obtain a statistically v
39 (TADS) in three long-tailed macaques and 20 pig-tailed macaques in two districts of Narathiwat Provi
40 genomes were amplified from the plasma of 44 pig-tailed macaques infected with SIV(mac251) at 4 to 10
46 DNA extracted from unpassaged LN tissue of a pig-tailed macaque (Macaca nemestrina) infected with SIV
48 simian immunodeficiency virus (SIV)-infected pig-tailed macaque (Macaca nemestrina) model, but this i
49 nothing is known of this interaction in the pig-tailed macaque (Macaca nemestrina), which is used in
50 (AF) was used to test for social learning in pig-tailed macaques (Macaca nemestrina) and adult humans
51 uences in primary SFV isolates obtained from pig-tailed macaques (Macaca nemestrina) and rhesus macaq
54 simian immunodeficiency virus (SIV)-infected pig-tailed macaques (Macaca nemestrina) were treated wit
55 In this model, treatment of SIV-infected pig-tailed macaques (Macaca nemestrina) with the combina
57 ute infection phase (12 hours to 28 days) in pig-tailed macaques (Macaca nemestrina), challenged intr
65 gside previously developed human, mouse, and pig-tailed macaque MR1-Ag tetramers to characterize cros
66 uence-based typing of rhesus, cynomolgus and pig-tailed macaques, nearly half of which have not been
69 ) CD3(+) iNKT cells make up 0.13% to 0.4% of pig-tailed macaque PBMCs, which are comparable to the pe
70 (HIV-1) variant with enhanced replication in pig-tailed macaque peripheral blood mononuclear cells (p
71 replicated efficiently in human, rhesus, and pig-tailed macaque peripheral blood mononuclear cells (P
72 However, in phytohemagglutinin-stimulated pig-tailed macaque peripheral blood mononuclear cells (P
77 SIV-vif-NL4-3) could infect and replicate in pig-tailed macaques (PTM), indicating that APOBEC3 prote
78 We compared and contrasted pathogenic (in pig-tailed macaques [PTMs]) and nonpathogenic (in Africa
79 ooty mangabey (designated FGb) to rhesus and pig-tailed macaques resulted in the development of neuro
82 and F peptide-binding pockets in rhesus and pig-tailed macaques suggests that their MHC-B molecules
83 ipheral blood mononuclear cells (PBMCs) of a pig-tailed macaque that was inoculated with a slow-low/N
84 followed the evolution of coreceptor use in pig-tailed macaques that developed severe CD4 T-cell los
85 SHIV) dynamics from SHIV-1157ipd3N4-infected pig-tailed macaques that underwent autologous transplant
87 less, our data suggest the potential for the pig-tailed macaque to be developed as an animal model of
88 elope glycoprotein cytoplasmic tail leads in pig-tailed macaques to a unique phenotype in which high
90 liferation was blocked in vitro with FK-506, pig-tailed macaques treated preinoculation with FK-506 w
92 o high titers and causes immunodeficiency in pig-tailed macaques, virus loads measured in SHIV(DH12)-
93 oural modifications in sociality of southern pig-tailed macaques visiting Malaysian oil palm plantati
94 imian/human immunodeficiency virus (SHIV) in pig-tailed macaques, we have developed a macaque model o
95 V-I or -II) accelerates progression to AIDS, pig-tailed macaques were inoculated with the simian coun
96 nsity ( <= 1,050 parasites/uL) occurred in 7 pig-tailed macaques, while PCR and TADS diagnosed infect
98 cted, the virus replicated preferentially in pig-tailed macaques with an earlier plasma viral peak an
99 e immunogenicity of mutant Env, we immunized pig-tailed macaques with recombinant vaccinia viruses, o
100 noculation of rhesus macaques with PRV or of pig-tailed macaques with RRV, whether the animals were a