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1 b in four squirrel monkeys and one prosimian galago.
2  directly or indirectly to cortex in newborn galagos.
3 posterior parietal cortex (PPC) in prosimian galagos.
4 ose crown clade includes lemurs, lorises and galagos.
5 r primates, suggests the existence of SEF in galagos.
6 2, which appear to be less differentiated in galagos.
7  functional connectivity of these modules in galagos, a prosimian primate with relatively simple fron
8                             This analysis of galago and human gamma genes in transgenic mice demonstr
9       In a previous study, it was shown that galago and human gamma genes retain their characteristic
10 he connections and the architecture of DM of galagos and owl monkeys suggest that the same area has b
11 of both New and Old World monkeys, prosimian galagos, and close relatives of primates, including tree
12 nd posterior parietal cortex of owl monkeys, galagos, and macaques help identify areas that could be
13                                              Galagos appear to have retained an ancestral preprimate
14                                              Galagos are representative of the large strepsirrhine br
15  striate and extrastriate areas in prosimian galagos are similar to simian primates, with notable exc
16             Although most FEF connections in galagos are similar to those in monkeys, the FEF-SC conn
17 de that V2 cortical connections in prosimian galagos are similar to those in simian primates, suggest
18  strepsirrhine primates (lemurs, lorises and galagos) arose in Afro-Arabia during the early Palaeogen
19 limb is largely from the contralateral M1 in galagos, as in other primates.
20  determined the complete DNA sequence of the galago beta-globin LCR and completed previously unsequen
21 ed poorly to tactile stimuli in anesthetized galagos, but connection patterns with area 3b indicated
22  the organization of the pulvinar complex in galagos by examining superior colliculus (SC) projection
23 posed DM with other cortical visual areas in galagos by placing injections of several different neuro
24       Posterior parietal cortex of prosimian galagos consists of a caudal half characterized by conne
25 rietal cortex (PPC) of monkeys and prosimian galagos contains a number of subregions where complex, b
26             The evidence suggests that PL of galagos contains a single, large nucleus, as in monkeys,
27                                           In galago, expression of the gamma-gene remained restricted
28 major simian lineages; thus, the (prosimian) galago gamma gene retains the ancestral embryonic expres
29                              Once again, the galago gamma gene was embryonic and the human gamma gene
30 he 4-kb fragments that contain the human and galago gamma genes proper.
31 ansgenic lines were tested in which human or galago gamma genes were linked to HS2.
32                In that experiment, human and galago gamma genes were linked to hypersensitive site 3
33 ssion patterns shown by the two gamma genes (galago gamma is embryonic; human gamma is fetal).
34 ific expression patterns in transgenic mice (galago gamma is expressed exclusively in the embryo, whe
35  human gamma-globin gene and its orthologous galago gamma-globin gene evolved from an ancestral epsil
36 nces required for the down-regulation of the galago gamma-globin gene were localized to the minimal p
37 mma-gene was silenced when controlled by the galago gamma-promoter, but it was expressed at a high le
38 gamma-gene driven by either the human or the galago gamma-promoters in transgenic mice.
39  examined in a lorisiform prosimian primate (Galago garnetti).
40  results obtained from an African prosimian, Galago garnetti.
41 nd cingulate cortex of the prosimian primate Galago garnetti.
42        These results indicate that prosimian galagos have a complex of motor areas that closely resem
43 es of the posterior parietal cortex (PPC) in galagos identified by intracortical microstimulation wit
44 ates, PPC likely resembled that of prosimian galagos, in which caudal PPC (PPCc) is visual and rostra
45 osensory cortex of adult macaque monkeys and galagos, including giant Betz cells in area 4.
46 rons contained in the separate layers of the Galago lateral geniculate nucleus.
47  cortical connections of these two nuclei in galagos, members of the stepsirrhine primate radiation,
48 AT, and CACCC elements between the human and galago minimal promoters we found that whereas each box
49  parts of the hindlimb and tail of prosimian galagos, New World monkeys, and Old World monkeys.
50  DM homologue has been proposed in prosimian galagos on the basis of physiological mapping.
51 ingle cortical hemisphere from two prosimian galagos, one New World owl monkey, one Old World macaque
52 re, belt, and parabelt) in Garnett's greater galago (Otolemur garnetti).
53  to investigate this region in the prosimian galago (Otolemur garnettii).
54 visions of the pulvinar complex of prosimian galagos (Otolemur garnetti) that were revealed in brain
55 es of cortical inputs to the SC in prosimian galagos (Otolemur garnetti) using retrograde anatomical
56 uroanatomical tracers were placed into DM in galagos, owl monkeys, squirrel monkeys, and macaque monk
57 the pattern of proteins binding to human and galago probes was compared.
58       Using a five-species alignment (human, galago, rabbit, goat, and mouse) that represents 370 mil
59 bcortical components of the visual system in galagos ranging from newborns to adults.
60          The superficial layers of the SC in galagos received the majority of their inputs from early
61                                              Galagos represent the prosimian radiation of surviving p
62                              While prosimian galagos resemble other primates in having early visual a
63 on of the HS5 sequences of mouse, human, and galago revealed two extensively conserved regions, desig
64    Finally, multiunit recording from the two galagos revealed that the deprived portions of S1 were r
65 t gene of two of these nocturnal prosimians: Galago senegalensis and Otolemur garnettii.
66  was isolated from human DNA as well as from Galago senegalis DNA.
67     To complement this analysis, orthologous galago sequences were also used to derive probes and the
68  owl monkeys, Old World macaque monkeys, and galagos share a number of PMV and PMD connections, sugge
69 described in New World monkeys and prosimian galagos support the conclusion that the same visual area
70 ries less across cortical areas in prosimian galagos than in the Old World monkeys.
71 owl monkeys, two squirrel monkeys, and three galagos that were processed for cytochrome oxidase, Niss
72                            This circuitry in galagos, therefore, is more complex than in nonprimates,
73  geniculate nucleus of the prosimian primate Galago to better understand the nature and function of t
74                       The present results in galagos, together with those obtained from macaque monke
75 eys (macaque and marmoset), and a prosimian (galago), tracking key changes.
76               In one squirrel monkey and one galago we demonstrated that these five groups of cells r
77 e of Old World macaque monkeys and prosimian galagos, we placed injections of fluorescent tracers and
78 he ipsilateral connections of motor areas of galagos were determined by injecting tracers into primar
79 and premotor fields in the frontal cortex of galagos were examined by placing multiple tracers into t
80 ivity in MT in two primates, owl monkeys and galagos, where MT is exposed on the brain surface.
81 , but an altered arrangement was seen in the galagos, with a ventrolateral location for toe 1.
82 ortex (M1) in three squirrel monkeys and two galagos years after the therapeutic amputation of an inj