ライフサイエンスコーパス: pigtailed macaque

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 membrane and envelope proteins (VSV-KFDV) in pigtailed macaques.

7 gative (< 1:25) were infused i.v. into naive pigtailed macaques (ages 3-6 months).

8 ned, expressed, and analyzed rhesus macaque, pigtailed macaque, and murine DC-SIGN and made a panel o

9 udy defines sites of immune escape in SIV in pigtailed macaques, and this enables a more refined leve

10 We have recently discovered that pigtailed macaques are naturally infected with viral hom

11 Pigtailed macaques became persistently infected by STLV-

12 We conclude that rhesus and pigtailed macaque DC-SIGN proteins are structurally and

13 Rhesus and pigtailed macaque DC-SIGN proteins were highly similar t

14 Most MAbs cross-reacted with rhesus and pigtailed macaque DC-SIGN, although none recognized muri

15 transcriptase inhibitor tenofovir protected pigtailed macaques depending on the timing of viral chal

16 Sixteen Macaca nemestrina (pigtailed macaques) from 18 to 29 years of age were age-

17 In contrast to our prediction, pigtailed macaques had higher serotonergic innervation t

18 elay viral infection in rotavirus-challenged pigtailed macaques has important implications for the de

19 the C-C chemokine receptor 5 (CCR5) locus in pigtailed macaque HSPCs by zinc finger nucleases (ZFNs)

20 Pigtailed macaques infected with a virulent human immuno

21 on in vivo, was enhanced in lymph nodes from pigtailed macaques infected with simian immunodeficiency

22 macrophage infection in vivo, we inoculated pigtailed macaques intravenously or intrarectally with t

23 hed conditions for efficient transduction of pigtailed macaque (Macaca nemestrina) long-term repopula

24 pic virus type I/II (STLV-I/II) seronegative pigtailed macaque (Macaca nemestrina) with a cutaneous T

25 iency virus (SIV) model in which over 90% of pigtailed macaques (Macaca nemestrina) coinoculated with

26 escribe a comprehensive analysis of two male pigtailed macaques (Macaca nemestrina) experimentally in

27 Pigtailed macaques (Macaca nemestrina) were coinoculated

28 We conducted a study by infecting pigtailed macaques (Macaca nemestrina) with a geneticall

29 For these purposes, we infected six pigtailed macaques (Macaca nemestrina) with reconstructe

30 lyzed the renal pathology and function of 27 pigtailed macaques (Macaca nemestrina), infected intrave

31 ut' experiments on a large, captive group of pigtailed macaques (Macaca nemestrina), we show that a p

32 characterization of KIR-MHC interactions in pigtailed macaques (Macaca nemestrina).

33 ee dominance-related signal used by monkeys (pigtailed macaques: Macaca nemestrina) means submission

34 We used a rapidly progressing SIV/pigtailed macaque model of HIV to examine enteropathy an

35 sing the simian immunodeficiency virus (SIV)/pigtailed macaque model of HIV-1 disease.

36 Using an accelerated and consistent SIV pigtailed macaque model of HIV-associated neurologic dis

37 ociated neurologic disorders, we used an SIV pigtailed macaque model to study innate immune responses

38 cterization of NKG2A and NKp80 in rhesus and pigtailed macaque NK cells provides a new approach in th

39 pheral blood were isolated from SIV-infected pigtailed macaques on days 4, 14, and 114 postinoculatio

40 of TRIMCyp has, in fact, occurred twice, and pigtailed macaques (pgt) express an independently genera

41 Among nonhuman primates, SIV-infected Asian pigtailed macaques (PM) are relatively more susceptible

42 XMRV replication and spread were limited in pigtailed macaques, predominantly by APOBEC-mediated hyp

43 rican green monkey (AGM), to a new host, the pigtailed macaque (PTM), viral adaptation and increased

44 d, lymph nodes, and intestine collected from pigtailed macaques (PTMs) and African green monkeys (AGM

45 n in pathogenic SIV infections of rhesus and pigtailed macaques (PTMs) and in nonpathogenic SIV infec

46 exposed adult and juvenile AGMs, as well as pigtailed macaques (PTMs) as a nonnatural host control,

47 Four pigtailed macaques (PTMs) were infected with SIVrcm, and

48 s species of African green monkeys (AGMs) to pigtailed macaques (PTMs).

49 ve neuropathologic review of 30 SIV-infected pigtailed macaques receiving combination antiretroviral

50 zed the unique genome of an uncultured novel pigtailed macaque roseolovirus.

51 from simian immunodeficiency virus-infected pigtailed macaques showed an increase in YKL-40 concentr

52 A recent study of pigtailed macaques shows that most effective policing in

53 enic (African green monkeys) and pathogenic (pigtailed macaques) SIV hosts.

54 D169 was observed in lymph nodes of infected pigtailed macaques, suggesting productive infection of C

55 ophage infection in blood and lymph nodes of pigtailed macaques that did or did not develop simian im

56 ransmission, we passaged a modified HIV-1 in pigtailed macaques that were transiently depleted of CD8

57 ferred by blood transfusion from an infected pigtailed macaque to a rhesus macaque.

58 Four pigtailed macaques were inoculated with an infectious, a

59 Pigtailed macaques were inoculated with human cells harb

60 p CNS disease by 3 months after inoculation, pigtailed macaques were treated with a regimen of tenofo

61 ive immune response following vaccination of pigtailed macaques with envelope protein(s) derived from

62 rated that treatment of acutely SIV-infected pigtailed macaques with the drug sevelamer, which binds