ライフサイエンスコーパス: owl monkey

1 squirrel monkeys) and one nocturnal primate (owl monkey).

2 ong the same axis as observed in macaque and owl monkey.

3 rtion of a paralogous Alu Sq sequence in the owl monkey.

4 aque monkey hold for the squirrel monkey and owl monkey.

5 f the inferior pulvinar nucleus (IPm) of the owl monkey.

6 Cultured parasites successfully infected an owl monkey.

7 n one hemisphere of each of two anesthetized owl monkeys.

8 ary somatosensory cortex of two anesthetized owl monkeys.

9 al (PMD) and ventral (PMV) premotor areas of owl monkeys.

10 tic tract were also observed in squirrel and owl monkeys.

11 pper visual quadrant) of titi, squirrel, and owl monkeys.

12 ion (MI) to identify ODCs in V1 of New World owl monkeys.

13 ns provided most of the projections to V1 in owl monkeys.

14 he CD4 receptor encoded by permissive Spix's owl monkey alleles.

15 V2 organization in owl monkeys also appears similar to that of other simian

16 Strabismic owl monkeys also showed ocular dominance columns; normal

17 usion with TRIM5 that is unique to New World owl monkeys also targets HIV-1 CA, but this interaction

18 ounts for post-entry restriction of HIV-1 in owl monkeys and blocks HIV-1 infection when transferred

19 al CD4 alleles in a colony of captive Spix's owl monkeys and found that 88% of surveyed individuals a

20 ually evoked activity in MT in two primates, owl monkeys and galagos, where MT is exposed on the brai

21 visual area (MT) was determined in six adult owl monkeys and one adult marmoset 69 d to 10 months aft

22 ggests that, if AVPR1A modulates behavior in owl monkeys and other neotropical primates, it does so i

23 00-electrode array and compared results from owl monkeys and squirrel monkeys 5-10 weeks after lesion

24 In owl monkeys and squirrel monkeys, connections were with

25 resentation in cortical area 3b of New World owl monkeys and squirrel monkeys.

26 connections, and visual topography of DM in owl monkeys and the presumptive DM in squirrel monkeys.

27 previously described in the laboratory rat, owl monkey, and squirrel monkey.

28 of such connections in New World marmosets, owl monkeys, and squirrel monkeys.

29 ion of GB virus A were isolated from mystax, owl monkeys, and tamarins.

30 t of primate taxa, including the Argentinean owl monkey (Aotus azarai).

31 er understand this restriction, we expressed owl monkey (Aotus nancymaae) CD4 and CXCR4 in the owl mo

32 monkey (Saimiri sciureus) and the nocturnal owl monkey (Aotus trivirgatis).

33 oyed a triple-labeling technique in the same owl monkey (Aotus trivirgatus).

34 D4 receptors encoded by two other species of owl monkeys (Aotus azarae and Aotus nancymaae) also serv

35 Sixteen New World owl monkeys (Aotus nancymae [karyotype 1, formerly belie

36 the middle temporal crescent area (MT(C)) in owl monkeys (Aotus trivirgatus), squirrel monkeys (Saimi

37 ross the primary auditory cortex (AI) in six owl monkeys (Aotus trivirgatus).

38 me, but not all, CD4 alleles found in Spix's owl monkeys (Aotus vociferans) encode functional recepto

39 ed free-ranging New World monkeys (nocturnal owl monkeys [Aotus nancymai] and diurnal capuchin monkey

40 The owl monkey, Aotus azarae, has developed a fully nocturna

41 emur griseus, or of platyrrhines such as the owl monkey, Aotus trivirgatus, or the titi monkey, Calli

42 triate area that was originally described in owl monkeys as a complete representation of the visual h

43 (DM) was originally identified in New World owl monkeys as an area rostral to dorsomedial visual are

44 IEGs, we not only revealed apparent ODCs in owl monkeys but also discovered a number of unique featu

45 M, P, and K axons were labeled in adult owl monkeys by means of injections of wheat germ aggluti

46 Paradoxically, the barrier to HIV-1 in owl monkey cells is released by capsid mutants or drugs

47 ction of a wild type HIV-1 reporter virus in owl monkey cells.

48 We conclude that the owl monkey cellular restriction machinery recognizes a p

49 MV) species, squirrel monkey CMV (SMCMV) and owl monkey CMV (OMCMV), that infect New World monkeys.

50 tes, the lateral geniculate nucleus (LGN) of owl monkeys contains three anatomically and physiologica

51 ternatively, the loss of color vision in the owl monkey could impact K pathway circuitry earlier in t

52 Here we show that knockdown of owl monkey CypA by RNA interference (RNAi) correlates wi

53 Chesson strain parasites were passaged from owl monkey erythrocytes to human reticulocytes in McCoy'

54 ic arrangements made by M, P, and K axons in owl monkey exhibit more similarities than differences.

55 Among New World primates, only owl monkeys exhibit post-entry restriction of HIV-1.

56 x and neighboring areas in 14 hemispheres of owl monkeys, focusing on the somatotopic distribution of

57 eral sulcus and posterior parietal cortex of owl monkeys, galagos, and macaques help identify areas t

58 mall genomic regions were recovered from the owl monkey genome, indicating a higher Alu amplification

59 Other species (e.g., owl monkey) had a similar low density of OMP (+) VSNs as

60 We conclude that the nocturnal owl monkey has a specialized perinasal thermoreceptive t

61 More recently, connections of DM in owl monkeys have been described.

62 ry visual cortex (V1), in nine anaesthetized owl monkeys injected with a neuromuscular blocker.

63 The middle temporal visual area (MT) of the owl monkey is anatomically organized with respect to bot

64 areas, and they also suggest that MST of the owl monkey is, like MST of the macaque, functionally org

65 The dorsomedial visual area (DM) of owl monkeys is a cortical area that has been described r

66 Our data indicate that HIV-1 replication in owl monkeys is not restricted at entry but can be limite

67 ving branches (e.g. humans, macaque monkeys, owl monkeys) is difficult for several reasons.

68 We also used an owl monkey kidney (OMK) cell assay that is based on time

69 onkey (Aotus nancymaae) CD4 and CXCR4 in the owl monkey kidney cell line, OMK.

70 Adult owl monkeys learned to discriminate tones higher than a

71 n in the cat, corticogeniculate axons in the owl monkey maintained topographic innervation in the LGN

72 al orientations than oblique orientations in owl monkey middle temporal visual area (MT), a visual ar

73 stages of naturally acquired immunity in the owl monkey model.

74 New World owl monkeys, Old World macaque monkeys, and galagos shar

75 stitutions render HIV-1 capable of infecting Owl monkey (OMK) cells that highly restrict HIV-1.

76 Remarkably, in Owl monkeys (omk), a cyclophilin A (CypA) cDNA has been

77 re from two prosimian galagos, one New World owl monkey, one Old World macaque monkey, and one baboon

78 , we report a series of experiments in which owl monkeys performed reaching movements guided by spati

79 in the diurnal monkeys than in the nocturnal owl monkey, perhaps reflecting the importance of color w

80 we found that some individuals from captive owl monkey populations harbor CD4 alleles that are compa

81 A similar MRI experiment with an owl monkey produced parallel, though smaller, signal enh

82 to visual stimuli in extrastriate cortex of owl monkeys provided evidence for the dorsal half of the

83 In squirrel monkey and owl monkey, receptive fields of magnocellular neurones w

84 ndicating a higher Alu amplification rate in owl monkeys relative to many other primates.

85 An HIV-1 variant modified to evade the owl monkey restriction factor TRIM-cyp replicated effici

86 also showed ocular dominance columns; normal owl monkeys showed variable expression.

87 Finally, V3 of owl monkeys shows a compartmental organization for orien

88 TRIM-CypA is an owl monkey-specific variant of the retrovirus restrictio

89 ical tracers were placed into DM in galagos, owl monkeys, squirrel monkeys, and macaque monkeys.

90 ns and the architecture of DM of galagos and owl monkeys suggest that the same area has been identifi

91 trigeminal nucleus caudalis of the New World owl monkey that is not immunoreactive for substance P or

92 similar analysis of restriction mediated by owl monkey TRIM-cyclophilin A (CypA) or human TRIM5alpha

93 n TRIM5alpha, rhesus macaque TRIM5alpha, and owl monkey TRIM-Cyp remained potent in cells depleted of

94 restriction, proteasome inhibition prevented owl monkey TRIM-CypA restriction of HIV-1 reverse transc

95 M5 (TRIM5alpha(rh)) or by the product of the owl monkey TRIM5-cyclophilin A gene fusion (TRIMCyp).

96 re, we demonstrate that heat shock perturbed owl monkey TRIMCyp and rhesus TRIM5alpha-mediated restri

97 brain sections from two macaque monkeys, two owl monkeys, two squirrel monkeys, and three galagos tha

98 s in the representation of central vision in owl monkey V1 was relatively small and inconsistent.

99 tions of biotinylated dextran were made into owl monkey V1, and the resulting labeled axons were reco

100 VPR1A on the evolution of social behavior in owl monkeys, we sequenced this locus in a wild populatio

101 Although visual responses in the owl monkey were significantly slower than in the squirre

102 In the present study, splenectomized owl monkeys were infected with P. falciparum in order to

103 Adult owl monkeys were trained to detect an increase in the en

104 rons in two primate species, bush babies and owl monkeys, were retrogradely labeled, then charted in

105 well developed in nocturnal primates such as owl monkeys, which are likely to be color blind.