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 available Theropithecus gelada genomes using Papio and Macaca Y chromosome as reference sequences.

5 In addition to assembling a first set of Papio and Theropithecus Y-specific microsatellite marker

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

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

8 of swordtail fish (Xiphophorus) and baboons (Papio) and to inferred Neanderthal introgression in mode

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

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

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

12 Papio anubis baboons underwent PET scans of the brain af

13 0 on LPS-induced inflammatory responses, six Papio anubis baboons were i.v. injected with a sublethal

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

15 Female Papio anubis were evaluated for periodontal health at ba

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

17 olfactory signals in captive olive baboons (Papio anubis) and relate these to the female fertile per

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

19 sing 30 years of data on wild olive baboons (Papio anubis) in Gombe National Park, Tanzania, we found

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

21 6% reduction in the worm burden in a baboon (Papio anubis) model.

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

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

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

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

26 induced endometriosis in non-human primates (Papio Anubis) to test our hypothesis that the growth of

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

28 e sleep patterns of a group of wild baboons (Papio anubis), we found that ecological and social press

29 (totaling 29 individuals) of olive baboons (Papio anubis), who reproduce at approximately 10 years o

30 n and vertical transfer in the olive baboon (Papio anubis).

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

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

33 and the immune response of the olive baboon (Papio anubis).

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

35 e strepsirrhine primates, and olive baboons (Papio anubis).

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

37 ilis), Colobus sp (C.angolensis, C.guereza), Papio anubis, Lophocebus albigena, Mandrillus sphinx, Al

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

39 11C-MMP under its new name, 11C-CUMI-101, in Papio anubis.

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

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

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

43 Baboons (genus Papio) are a morphologically and behaviorally diverse cl

44 Baboons (genus Papio) are broadly studied in the wild and in captivity.

45 have looked to baboons (monkeys of the genus Papio) as a source of hypotheses about the ecology and b

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

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

48 Baboons, members of the genus Papio, comprise six closely related species distributed

49 In yellow and chacma baboons (Papio cynocephalus and P. ursinus), there is a -shaped r

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

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

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

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

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

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

56 We focus on the yellow baboon (Papio cynocephalus) mating system as a case study to pro

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

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

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

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

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

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

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

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

65 very of SPK100.NPY-Y2R to the hippocampus of Papio hamadryas (baboon).

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

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

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

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

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

71 is to show that two New Kingdom specimens of Papio hamadryas originate from the Horn of Africa.

72 0 days gestational age (dGA) female baboons (Papio hamadryas spp.) of similar age and weight were ran

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

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

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

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

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

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

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

80 For example, hamadryas baboons (Papio hamadryas) live in units consisting of one male an

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

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

83 At ~9 months preconception, female baboons (Papio hamadryas) were randomly assigned to either a cont

84 for luxury goods, including sacred baboons (Papio hamadryas), but its location is disputed.

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

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

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

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

89 Herpesvirus papio IgG antibody titers were measured by IFA.

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

91 monstrated serologic evidence of herpesvirus papio infection.

92 wo experiments, we demonstrate that baboons (Papio papio) show a capacity for compositionality.

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

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

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

96 We used fetal liver from a baboon (Papio sp.) model of intrauterine growth restriction due

97 hose measured at high resolution in baboons (Papio spp.) living across a gradient of aridity and mode

98 orium for living animals, including baboons (Papio spp.).

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

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

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

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

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

104 als in a habituated group of chacma baboons (Papio ursinus griseipes) displayed consistent and indivi

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

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

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

108 Baboons (Papio ursinus) plan their foraging journeys to out-of-si

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

110 We investigated this in chacma baboons (Papio ursinus) using over a million camera-trap detectio

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

112 highly hierarchical(8)(,)(9) chacma baboons (Papio ursinus).

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

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

115 ging to different species of baboons (genus: Papio) using Y chromosome references belonging to the sa

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