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1 b in four squirrel monkeys and one prosimian galago.
2 r primates, suggests the existence of SEF in galagos.
3 posterior parietal cortex (PPC) in prosimian galagos.
4 ose crown clade includes lemurs, lorises and galagos.
5 2, which appear to be less differentiated in galagos.
6 functional connectivity of these modules in galagos, a prosimian primate with relatively simple fron
9 he connections and the architecture of DM of galagos and owl monkeys suggest that the same area has b
10 of both New and Old World monkeys, prosimian galagos, and close relatives of primates, including tree
11 nd posterior parietal cortex of owl monkeys, galagos, and macaques help identify areas that could be
13 striate and extrastriate areas in prosimian galagos are similar to simian primates, with notable exc
15 de that V2 cortical connections in prosimian galagos are similar to those in simian primates, suggest
16 strepsirrhine primates (lemurs, lorises and galagos) arose in Afro-Arabia during the early Palaeogen
18 determined the complete DNA sequence of the galago beta-globin LCR and completed previously unsequen
19 ed poorly to tactile stimuli in anesthetized galagos, but connection patterns with area 3b indicated
20 the organization of the pulvinar complex in galagos by examining superior colliculus (SC) projection
21 posed DM with other cortical visual areas in galagos by placing injections of several different neuro
23 rietal cortex (PPC) of monkeys and prosimian galagos contains a number of subregions where complex, b
26 major simian lineages; thus, the (prosimian) galago gamma gene retains the ancestral embryonic expres
32 ific expression patterns in transgenic mice (galago gamma is expressed exclusively in the embryo, whe
33 human gamma-globin gene and its orthologous galago gamma-globin gene evolved from an ancestral epsil
34 nces required for the down-regulation of the galago gamma-globin gene were localized to the minimal p
35 mma-gene was silenced when controlled by the galago gamma-promoter, but it was expressed at a high le
41 es of the posterior parietal cortex (PPC) in galagos identified by intracortical microstimulation wit
42 ates, PPC likely resembled that of prosimian galagos, in which caudal PPC (PPCc) is visual and rostra
45 AT, and CACCC elements between the human and galago minimal promoters we found that whereas each box
48 ingle cortical hemisphere from two prosimian galagos, one New World owl monkey, one Old World macaque
51 visions of the pulvinar complex of prosimian galagos (Otolemur garnetti) that were revealed in brain
52 es of cortical inputs to the SC in prosimian galagos (Otolemur garnetti) using retrograde anatomical
53 uroanatomical tracers were placed into DM in galagos, owl monkeys, squirrel monkeys, and macaque monk
59 on of the HS5 sequences of mouse, human, and galago revealed two extensively conserved regions, desig
60 Finally, multiunit recording from the two galagos revealed that the deprived portions of S1 were r
63 To complement this analysis, orthologous galago sequences were also used to derive probes and the
64 owl monkeys, Old World macaque monkeys, and galagos share a number of PMV and PMD connections, sugge
65 described in New World monkeys and prosimian galagos support the conclusion that the same visual area
67 owl monkeys, two squirrel monkeys, and three galagos that were processed for cytochrome oxidase, Niss
69 geniculate nucleus of the prosimian primate Galago to better understand the nature and function of t
73 e of Old World macaque monkeys and prosimian galagos, we placed injections of fluorescent tracers and
74 he ipsilateral connections of motor areas of galagos were determined by injecting tracers into primar
75 and premotor fields in the frontal cortex of galagos were examined by placing multiple tracers into t
78 ortex (M1) in three squirrel monkeys and two galagos years after the therapeutic amputation of an inj
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