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1 ision in brown, or tufted, capuchin monkeys (Cebus apella).
2  from adults to infants in tufted capuchins (Cebus apella).
3 ational behavior in tufted capuchin monkeys (Cebus apella).
4 rosocial behavior in brown capuchin monkeys (Cebus apella).
5 d globus pallidus in brown capuchin monkeys (Cebus apella).
6 s compared with the diurnal New World monkey Cebus apella.
7 another primate species-the New World monkey Cebus apella.
8 xamined in brown or tufted capuchin monkeys (Cebus apella), a New World primate, by letting subjects
9   We tested brown capuchin monkeys (Sapajus [Cebus] apella), a highly cooperative species, on a compu
10 e for a bimanual task in 45 tufted capuchin (Cebus apella) and 55 rhesus macaque (Macaca mulatta) mon
11 series of experiments four capuchin monkeys (Cebus apella) and four squirrel monkeys (Saimiri sciureu
12 arning was investigated in capuchin monkeys (Cebus apella) and rhesus monkeys (Macaca mulatta).
13  monkeys (Macaca mulatta), capuchin monkeys (Cebus apella), and pigeons (Columba livia) learning a sa
14 tes from three species of New World monkeys (Cebus apella, Aotus azarae, and Callithrix jacchus) repr
15                      Brown capuchin monkeys (Cebus apella apella) in Suriname forage on larvae enclos
16 ng development using brown capuchin monkeys (Cebus apella) as models.
17 ans suggests that the rotational behavior of Cebus apella can be used to model an asymmetric response
18 study investigated whether capuchin monkeys (Cebus apella) can use analogical reasoning to solve a 3-
19    The authors assessed 20 capuchin monkeys (Cebus apella) for the ability to delay gratification in
20 or development to manipulation in capuchins (Cebus apella) from birth to 2 years.
21 ch sensory cues are used by brown capuchins (Cebus apella) in embedded invertebrate foraging.
22                              Four capuchins (Cebus apella) learned categories of circular sine-wave g
23                           In the iron-loaded Cebus apella monkey, a single SC injection of HBED, 150
24                           In the iron-loaded Cebus apella monkey, whereas the PO administration of DF
25  amounts of NaHBED and deferoxamine (DFO) to Cebus apella monkeys as either a subcutaneous (SC) bolus
26 b) tracer into nine sites in area V4 in five Cebus apella monkeys.
27 r) cells within the brain and spinal cord of Cebus apella monkeys.
28 ng in age from 2 weeks to 35 years (Sapajus [Cebus] apella, n = 8).
29 ron-clearing efficacy in the iron-overloaded Cebus apella primate is further underscored by a compari
30 antially augment iron clearing efficiency in Cebus apella primates as well as alter the mode of iron
31 diethylnorspermine (DENSPM) are evaluated in Cebus apella primates, and the results are compared with
32                                Four monkeys (Cebus apella) received injections of HSV1 into three dif
33 nonhuman primate, the brown capuchin monkey (Cebus apella), responds negatively to unequal reward dis
34 bers and volumes in five New World primates (Cebus apella, Saguinus midas niger, Alouatta caraya, Aot
35 -pulvinar complex of six New World primates (Cebus apella, Saimiri ustius, Saguinus midas niger, Alou
36                            Capuchin monkeys (Cebus apella) share food even if their partner is behind
37 an primate species, tufted capuchin monkeys (Cebus apella), socially evaluates humans after witnessin
38  with hand preference in a New World monkey (Cebus apella) that does not display population-level han
39 eys (Ateles geoffroyi) and capuchin monkeys (Cebus apella) to follow the gaze of a human around barri
40 equential movements, we trained two monkeys (Cebus apella) to perform two sequential reaching tasks.
41  of acquired skills, we trained two monkeys (Cebus apella) to perform two sequential reaching tasks.
42 otus nancymai] and diurnal capuchin monkeys [Cebus apella]) to determine the extent to which they use
43 y (ICE) in rodents and iron-loaded primates (Cebus apella), toxicity in rodents, and organ distributi
44 imates, eight female brown capuchin monkeys (Cebus apella) underwent testing in a simple choice parad
45 an troglodytes and P. paniscus) and monkeys (Cebus apella) using a protocol reported in P. M. Greenfi
46                Memory of 3 capuchin monkeys, Cebus apella, was tested with lists of 4 travel-slide pi
47 e and six adult male brown capuchin monkeys (Cebus apella) were exposed twice to three conditions: (i
48                            Tufted capuchins (Cebus apella) were provided with a task that facilitated
49                      Three capuchin monkeys (Cebus apella) were tested on a 2-choice discrimination t
50                            Capuchin monkeys (Cebus apella) were tested on a reverse-reward task invol
51 icating social learning in capuchin monkeys (Cebus apella), which exhibit traditions, is sparse.