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Similar behavior has been observed in monkeys and chimpanzees.
This non-linear numerical mapping of estimates is quite general and depends on no training: it has been observed in monkeys, young children and adults with low training in mathematics and situations where we rely on intuitive estimations rather than learned numeracy.
This behavior has even been observed in monkeys, where, when left with a pile of toys, the females generally prefer stroking and holding baby dolls while the males gravitate to the trucks and toy hammers.
Such a positive bias effect has also been observed in monkeys after amygdala damage [Amaral, 2003].
Furthermore, minimal age-related changes in the HPA axis have been observed in monkeys with average behavior.
It has been observed in monkeys, for example, that abnormalities in ovarian hormone profiles are mirrored by irregularity in menstrual cyclicity [ 184].
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Very crude topography has been observed in monkey LIP [4], corresponding to the low within-field value of ∼10% observed in human MIPS.
This type of extinction has a known neural substrate in animals: A specific deficit of extinction was observed in monkeys with lesions of the posterior medial OFC, but not other parts of the frontal lobes [64].
In contrast to rats (Doerge et al., 2010a), no enterohepatic recirculation was observed in monkeys.
Compared with the wild type virus, the TK-recombinant SPV showed a modest level of attenuation in porcine cells while more attenuation was observed in monkey or human cells.
Interestingly, a similar expression pattern was observed in monkey PG diploid ESCs.
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