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1 l model of HIV-1 infection, SIV infection of pigtailed macaques.
2 mutation K165R in HAART-treated SIV-infected pigtailed macaques.
3 d AIDS following experimental inoculation of pigtailed macaques.
4 ivity with NK cells from rhesus macaques and pigtailed macaques.
5 roducibly induced a rapidly fatal disease in pigtailed macaques.
6 gative (< 1:25) were infused i.v. into naive pigtailed macaques (ages 3-6 months).
7 ned, expressed, and analyzed rhesus macaque, pigtailed macaque, and murine DC-SIGN and made a panel o
8 udy defines sites of immune escape in SIV in pigtailed macaques, and this enables a more refined leve
9             We have recently discovered that pigtailed macaques are naturally infected with viral hom
10                                              Pigtailed macaques became persistently infected by STLV-
11                  We conclude that rhesus and pigtailed macaque DC-SIGN proteins are structurally and
12                                   Rhesus and pigtailed macaque DC-SIGN proteins were highly similar t
13      Most MAbs cross-reacted with rhesus and pigtailed macaque DC-SIGN, although none recognized muri
14  transcriptase inhibitor tenofovir protected pigtailed macaques depending on the timing of viral chal
15                   Sixteen Macaca nemestrina (pigtailed macaques) from 18 to 29 years of age were age-
16 elay viral infection in rotavirus-challenged pigtailed macaques has important implications for the de
17 the C-C chemokine receptor 5 (CCR5) locus in pigtailed macaque HSPCs by zinc finger nucleases (ZFNs)
18                                              Pigtailed macaques infected with a virulent human immuno
19 on in vivo, was enhanced in lymph nodes from pigtailed macaques infected with simian immunodeficiency
20  macrophage infection in vivo, we inoculated pigtailed macaques intravenously or intrarectally with t
21 hed conditions for efficient transduction of pigtailed macaque (Macaca nemestrina) long-term repopula
22 pic virus type I/II (STLV-I/II) seronegative pigtailed macaque (Macaca nemestrina) with a cutaneous T
23 iency virus (SIV) model in which over 90% of pigtailed macaques (Macaca nemestrina) coinoculated with
24 escribe a comprehensive analysis of two male pigtailed macaques (Macaca nemestrina) experimentally in
25                                              Pigtailed macaques (Macaca nemestrina) were coinoculated
26            We conducted a study by infecting pigtailed macaques (Macaca nemestrina) with a geneticall
27          For these purposes, we infected six pigtailed macaques (Macaca nemestrina) with reconstructe
28 lyzed the renal pathology and function of 27 pigtailed macaques (Macaca nemestrina), infected intrave
29 ut' experiments on a large, captive group of pigtailed macaques (Macaca nemestrina), we show that a p
30  characterization of KIR-MHC interactions in pigtailed macaques (Macaca nemestrina).
31 ee dominance-related signal used by monkeys (pigtailed macaques: Macaca nemestrina) means submission
32            We used a rapidly progressing SIV/pigtailed macaque model of HIV to examine enteropathy an
33 sing the simian immunodeficiency virus (SIV)/pigtailed macaque model of HIV-1 disease.
34      Using an accelerated and consistent SIV pigtailed macaque model of HIV-associated neurologic dis
35 ociated neurologic disorders, we used an SIV pigtailed macaque model to study innate immune responses
36 cterization of NKG2A and NKp80 in rhesus and pigtailed macaque NK cells provides a new approach in th
37 pheral blood were isolated from SIV-infected pigtailed macaques on days 4, 14, and 114 postinoculatio
38 of TRIMCyp has, in fact, occurred twice, and pigtailed macaques (pgt) express an independently genera
39  Among nonhuman primates, SIV-infected Asian pigtailed macaques (PM) are relatively more susceptible
40  XMRV replication and spread were limited in pigtailed macaques, predominantly by APOBEC-mediated hyp
41 rican green monkey (AGM), to a new host, the pigtailed macaque (PTM), viral adaptation and increased
42 d, lymph nodes, and intestine collected from pigtailed macaques (PTMs) and African green monkeys (AGM
43 n in pathogenic SIV infections of rhesus and pigtailed macaques (PTMs) and in nonpathogenic SIV infec
44  exposed adult and juvenile AGMs, as well as pigtailed macaques (PTMs) as a nonnatural host control,
45                                         Four pigtailed macaques (PTMs) were infected with SIVrcm, and
46 s species of African green monkeys (AGMs) to pigtailed macaques (PTMs).
47 ve neuropathologic review of 30 SIV-infected pigtailed macaques receiving combination antiretroviral
48 zed the unique genome of an uncultured novel pigtailed macaque roseolovirus.
49  from simian immunodeficiency virus-infected pigtailed macaques showed an increase in YKL-40 concentr
50                            A recent study of pigtailed macaques shows that most effective policing in
51 D169 was observed in lymph nodes of infected pigtailed macaques, suggesting productive infection of C
52 ophage infection in blood and lymph nodes of pigtailed macaques that did or did not develop simian im
53 ransmission, we passaged a modified HIV-1 in pigtailed macaques that were transiently depleted of CD8
54 ferred by blood transfusion from an infected pigtailed macaque to a rhesus macaque.
55                                         Four pigtailed macaques were inoculated with an infectious, a
56                                              Pigtailed macaques were inoculated with human cells harb
57 p CNS disease by 3 months after inoculation, pigtailed macaques were treated with a regimen of tenofo
58 ive immune response following vaccination of pigtailed macaques with envelope protein(s) derived from
59 rated that treatment of acutely SIV-infected pigtailed macaques with the drug sevelamer, which binds

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