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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 bonobo, gorilla, orangutan, gibbon, macaque, owl monkey, and marmoset.
28  previously described in the laboratory rat, owl monkey, and squirrel monkey.
29 and the dorsolateral posterior area (DLP) in owl monkeys, and represents the entire contralateral hem
30  of such connections in New World marmosets, owl monkeys, and squirrel monkeys.
31 ion of GB virus A were isolated from mystax, owl monkeys, and tamarins.
32 t of primate taxa, including the Argentinean owl monkey (Aotus azarai).
33 er understand this restriction, we expressed owl monkey (Aotus nancymaae) CD4 and CXCR4 in the owl mo
34  monkey (Saimiri sciureus) and the nocturnal owl monkey (Aotus trivirgatis).
35 oyed a triple-labeling technique in the same owl monkey (Aotus trivirgatus).
36 D4 receptors encoded by two other species of owl monkeys (Aotus azarae and Aotus nancymaae) also serv
37                            Sixteen New World owl monkeys (Aotus nancymae [karyotype 1, formerly belie
38 the middle temporal crescent area (MT(C)) in owl monkeys (Aotus trivirgatus), squirrel monkeys (Saimi
39 ross the primary auditory cortex (AI) in six owl monkeys (Aotus trivirgatus).
40 me, but not all, CD4 alleles found in Spix's owl monkeys (Aotus vociferans) encode functional recepto
41 ed free-ranging New World monkeys (nocturnal owl monkeys [Aotus nancymai] and diurnal capuchin monkey
42                                          The owl monkey, Aotus azarae, has developed a fully nocturna
43 emur griseus, or of platyrrhines such as the owl monkey, Aotus trivirgatus, or the titi monkey, Calli
44 triate area that was originally described in owl monkeys as a complete representation of the visual h
45  (DM) was originally identified in New World owl monkeys as an area rostral to dorsomedial visual are
46  IEGs, we not only revealed apparent ODCs in owl monkeys but also discovered a number of unique featu
47      M, P, and K axons were labeled in adult owl monkeys by means of injections of wheat germ aggluti
48       Paradoxically, the barrier to HIV-1 in owl monkey cells is released by capsid mutants or drugs
49 ction of a wild type HIV-1 reporter virus in owl monkey cells.
50                         We conclude that the owl monkey cellular restriction machinery recognizes a p
51 MV) species, squirrel monkey CMV (SMCMV) and owl monkey CMV (OMCMV), that infect New World monkeys.
52 tes, the lateral geniculate nucleus (LGN) of owl monkeys contains three anatomically and physiologica
53 ternatively, the loss of color vision in the owl monkey could impact K pathway circuitry earlier in t
54               Here we show that knockdown of owl monkey CypA by RNA interference (RNAi) correlates wi
55  Chesson strain parasites were passaged from owl monkey erythrocytes to human reticulocytes in McCoy'
56 ic arrangements made by M, P, and K axons in owl monkey exhibit more similarities than differences.
57               Among New World primates, only owl monkeys exhibit post-entry restriction of HIV-1.
58 x and neighboring areas in 14 hemispheres of owl monkeys, focusing on the somatotopic distribution of
59 eral sulcus and posterior parietal cortex of owl monkeys, galagos, and macaques help identify areas t
60 mall genomic regions were recovered from the owl monkey genome, indicating a higher Alu amplification
61                         Other species (e.g., owl monkey) had a similar low density of OMP (+) VSNs as
62               We conclude that the nocturnal owl monkey has a specialized perinasal thermoreceptive t
63          More recently, connections of DM in owl monkeys have been described.
64 ry visual cortex (V1), in nine anaesthetized owl monkeys injected with a neuromuscular blocker.
65  The middle temporal visual area (MT) of the owl monkey is anatomically organized with respect to bot
66 areas, and they also suggest that MST of the owl monkey is, like MST of the macaque, functionally org
67          The dorsomedial visual area (DM) of owl monkeys is a cortical area that has been described r
68  Our data indicate that HIV-1 replication in owl monkeys is not restricted at entry but can be limite
69 ving branches (e.g. humans, macaque monkeys, owl monkeys) is difficult for several reasons.
70                              We also used an owl monkey kidney (OMK) cell assay that is based on time
71 onkey (Aotus nancymaae) CD4 and CXCR4 in the owl monkey kidney cell line, OMK.
72                                        Adult owl monkeys learned to discriminate tones higher than a
73 n in the cat, corticogeniculate axons in the owl monkey maintained topographic innervation in the LGN
74 al orientations than oblique orientations in owl monkey middle temporal visual area (MT), a visual ar
75 stages of naturally acquired immunity in the owl monkey model.
76                                    New World owl monkeys, Old World macaque monkeys, and galagos shar
77 stitutions render HIV-1 capable of infecting Owl monkey (OMK) cells that highly restrict HIV-1.
78                               Remarkably, in Owl monkeys (omk), a cyclophilin A (CypA) cDNA has been
79 re from two prosimian galagos, one New World owl monkey, one Old World macaque monkey, and one baboon
80 , we report a series of experiments in which owl monkeys performed reaching movements guided by spati
81 in the diurnal monkeys than in the nocturnal owl monkey, perhaps reflecting the importance of color w
82  we found that some individuals from captive owl monkey populations harbor CD4 alleles that are compa
83             A similar MRI experiment with an owl monkey produced parallel, though smaller, signal enh
84  to visual stimuli in extrastriate cortex of owl monkeys provided evidence for the dorsal half of the
85                       In squirrel monkey and owl monkey, receptive fields of magnocellular neurones w
86 ndicating a higher Alu amplification rate in owl monkeys relative to many other primates.
87       An HIV-1 variant modified to evade the owl monkey restriction factor TRIM-cyp replicated effici
88 also showed ocular dominance columns; normal owl monkeys showed variable expression.
89                               Finally, V3 of owl monkeys shows a compartmental organization for orien
90                              TRIM-CypA is an owl monkey-specific variant of the retrovirus restrictio
91 ical tracers were placed into DM in galagos, owl monkeys, squirrel monkeys, and macaque monkeys.
92 ns and the architecture of DM of galagos and owl monkeys suggest that the same area has been identifi
93 trigeminal nucleus caudalis of the New World owl monkey that is not immunoreactive for substance P or
94  similar analysis of restriction mediated by owl monkey TRIM-cyclophilin A (CypA) or human TRIM5alpha
95 n TRIM5alpha, rhesus macaque TRIM5alpha, and owl monkey TRIM-Cyp remained potent in cells depleted of
96 restriction, proteasome inhibition prevented owl monkey TRIM-CypA restriction of HIV-1 reverse transc
97 M5 (TRIM5alpha(rh)) or by the product of the owl monkey TRIM5-cyclophilin A gene fusion (TRIMCyp).
98 re, we demonstrate that heat shock perturbed owl monkey TRIMCyp and rhesus TRIM5alpha-mediated restri
99 brain sections from two macaque monkeys, two owl monkeys, two squirrel monkeys, and three galagos tha
100 s in the representation of central vision in owl monkey V1 was relatively small and inconsistent.
101 tions of biotinylated dextran were made into owl monkey V1, and the resulting labeled axons were reco
102 VPR1A on the evolution of social behavior in owl monkeys, we sequenced this locus in a wild populatio
103             Although visual responses in the owl monkey were significantly slower than in the squirre
104         In the present study, splenectomized owl monkeys were infected with P. falciparum in order to
105                                        Adult owl monkeys were trained to detect an increase in the en
106 rons in two primate species, bush babies and owl monkeys, were retrogradely labeled, then charted in
107 well developed in nocturnal primates such as owl monkeys, which are likely to be color blind.

 
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