ライフサイエンスコーパス: Papio

1 nt change on the lineage leading to baboons (Papio).

2 svirus 15 (CeHV-15) (also called herpesvirus papio 15).

3 The epidemiology of herpesvirus papio, a lymphocryptovirus similar to Epstein-Barr virus

4 ed in the genus Cercocebus, whereas baboons (Papio) and geladas (Theropithecus) are most closely rela

5 (cercopithicine herpesvirus 12, herpesvirus papio) and rhesus monkeys (cercopithicine herpesvirus 15

6 s assayed in CD-1 and sEH knock-out mice and Papio anubis (baboon) through pretreatment with an sEH i

7 in a reperfused hemispheric stroke model in Papio anubis (baboon).

8 ovel KSHV homolog in captive baboon species (Papio anubis and other).

9 Papio anubis baboons underwent PET scans of the brain af

10 0 on LPS-induced inflammatory responses, six Papio anubis baboons were i.v. injected with a sublethal

11 line and cytisine-blocking studies of 4 male Papio anubis baboons.

12 Female Papio anubis were evaluated for periodontal health at ba

13 hown significant correlation between baboon (Papio anubis) and human brain.

14 Baboons (Papio anubis) are natural hosts for Entamoeba histolytic

15 Nine adult baboons (Papio anubis) in good health were treated.

16 6% reduction in the worm burden in a baboon (Papio anubis) model.

17 roviding carrier technologies in the baboon (Papio anubis) model.

18 Baboons (Papio anubis) receiving a lethal intravenous infusion wi

19 andomized controlled study using the baboon (Papio anubis) to analyze the effect of chronic schistoso

20 describe class I MHC molecules from baboon (Papio anubis) to gain an understanding of how similariti

21 The ability of 4 olive baboons (Papio anubis) to use human gaze cues during a competitiv

22 adipose tissue in adult, pedigreed baboons (Papio anubis).

23 closely related to HTLV-1, in olive baboons (Papio anubis).

24 n anthropoid primate, the Senegalese baboon (Papio anubis).

25 drills (M. leucophaeus), and olive baboons (Papio anubis)] performed a prominent muzzle-muzzle behav

26 1), a novel 5-HT(1A) agonist radiotracer, in Papio anubis.

27 11C-MMP under its new name, 11C-CUMI-101, in Papio anubis.

28 ced MR angiography was performed in baboons (Papio anubis; n = 4) by using Mn-PyC3A and Gd-DTPA.

29 macaque [Macaca radiate], and olive baboon [Papio anubis]), 3 chimpanzees (Pan troglodytes), 6 membe

30 es from two normal nonhuman-primate species [Papio-anubis/Macaca-fascicularis] to determine the impac

31 Our juvenile nonhuman primate (Papio baboons) models of endotoxin-free Stx challenge ex

32 Here we describe a nonhuman primate (Papio c. cynocephalus) model of B. anthracis infection u

33 Field study of chacma baboons (Papio cynocephalus ursinus) revealed that contact barks

34 es in a population of wild savannah baboons (Papio cynocephalus) and collected data on interventions

35 l multimale primate society (yellow baboons, Papio cynocephalus) discriminate their own offspring fro

36 Blood smear evaluation of two baboons (Papio cynocephalus) experiencing acute hemolytic crises

37 tural history of HIV-2 infection in baboons (Papio cynocephalus) is a slow and chronic disease that g

38 a well-studied population of yellow baboons (Papio cynocephalus) living in Amboseli National Park in

39 tions in five social groups of wild baboons (Papio cynocephalus) over an 11-y period.

40 Seventy yellow baboons (Papio cynocephalus) were anesthetized and injected with

41 Seven uninjured adult baboons (Papio cynocephalus) were anesthetized with ketamine, sed

42 Healthy adult baboons (Papio cynocephalus), anesthetized with ketamine, sedated

43 in a natural population of savannah baboons (Papio cynocephalus), high-ranking males had higher testo

44 Asymptomatic baboons (Papio cynocephalus), previously infected with HIV-2, wer

45 allenge with purified Stx1 or Stx2, baboons (Papio) developed thrombocytopenia, anemia, and acute ren

46 piens (human), Pan troglodytes (chimpanzee), Papio hamadryas (baboon), Macaca fascicularis (macaque),

47 ism in both Papio hamadryas cynocephalus and Papio hamadryas anubis subspecies.

48 The baboon (Papio hamadryas anubis) can be transcervically instrumen

49 to display very limited polymorphism in both Papio hamadryas cynocephalus and Papio hamadryas anubis

50 sed class I repertoire of the yellow baboon (Papio hamadryas cynocephalus) by cDNA library screening.

51 romosome of Saudi-Arabian hamadryas baboons, Papio hamadryas hamadryas.

52 s on the longevity of female chacma baboons (Papio hamadryas ursinus).

53 ace, the authors trained 1 hamadryas baboon (Papio hamadryas) and 1 squirrel monkey (Saimiri sciureus

54 l, which we have now carried out in baboons (Papio hamadryas) and reported here.

55 ets were also found to work well for baboon (Papio hamadryas) and rhesus monkeys (Macaca mulatta).

56 d from lateral cephalographs of 830 baboons (Papio hamadryas) from the pedigreed population housed at

57 eneration genetic linkage map of the baboon (Papio hamadryas) genome was developed for use in biomedi

58 Life tables of female baboons (Papio hamadryas) in two wild populations of East Africa

59 To this end, 52 baboons (Papio hamadryas) underwent partial pancreatectomy, follo

60 In this study, a nonhuman primate model (Papio hamadryas) was used to assess the effect of humani

61 or mandibular defects in non-human primates (Papio hamadryas).

62 mmunology and transplantation in the baboon (papio hamadryas).

63 in the simian lymphocryptovirus herpesvirus papio (HVP) by cloning HVP-3A, the homolog of EBNA-3A en

64 ocryptoviruses found in baboons (herpesvirus papio; HVP) and Rhesus macaques (RhEBV).

65 Herpesvirus papio IgG antibody titers were measured by IFA.

66 The epidemiology of herpesvirus papio infection in baboons closely parallels that of EBV

67 monstrated serologic evidence of herpesvirus papio infection.

68 The authors trained 6 baboons (Papio papio) to make 1 of 2 report responses to 16-icon

69 tic relatedness data of wild Guinea baboons (Papio papio), we show that this species exhibits a multi

70 Earlier, we showed that nonhuman primates (Papio) recapitulated clinical HUS after Stx challenge an

71 pecies in the vaginal microflora of baboons (Papio spp.).

72 MHC class I expression and variation within Papio subspecies and to further investigate the evolutio

73 terization of MHC class I gene expression of Papio subspecies is a prerequisite for studies of immuno

74 ave indicated that the large African monkeys Papio, Theropithecus, and Mandrillus have a diphyletic r

75 hoblastoid cell lines derived by Herpesvirus Papio transformation of peripheral blood cells were virt

76 imes (PRTs) recorded from 54 chacma baboons (Papio ursinus) across two groups in natural (n = 6175 pa

77 cesses by which raiding male chacma baboons (Papio ursinus) exploit the opportunities and mitigate th

78 nt on a wild social primate (chacma baboons, Papio ursinus) in order to gain new insights into despot

79 Retrospective data from 33 septic baboons (Papio ursinus) subjected to Escherichia coli infusion.

80 s as sexual coercion in wild chacma baboons (Papio ursinus).

81 h experimental food patches in wild baboons (Papio ursinus).

82 (SA12), whose natural host is thought to be Papio ursinus, the chacma baboon.

83 d clearly link mandrills with Cercocebus and Papio with Lophocebus.