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1 partially different regions of higher order olfactory centers.
2 a also regulates PN axon targeting in higher olfactory centers.
3 essing of odor strength downstream of higher olfactory centers.
4 ns converge on distinct glomeruli in primary olfactory centers.
5 thin the modules before being sent to higher olfactory centers.
6 ttern that is specific to their second-order olfactory centers.
7 t pathways from the olfactory lobes (primary olfactory centers) and accessory lobes (higher-order int
8 eopteran insects are considered to be higher olfactory centers because their calyces receive abundant
10 tain projection neurons (PNs) in the primary olfactory center in the brain give context-dependent res
15 the paired antennal lobes (ALs; the primary olfactory centers in the insect brain) has one 5HT-immun
16 terspecific transplantation upon the primary olfactory centers in the moth brain were then examined i
17 urons (PNs), reformatted output to secondary olfactory centers, including the mushroom body (MB) caly
20 performed functional imaging in the primary olfactory center of M. sexta females with GLV structural
21 ique type of centrifugal neuron in the brain olfactory center of two heliothine moth species; one in
25 ese patterns defines an "axon map" in higher olfactory centers reflecting which olfactory receptors p
28 ion and comparison of the brains and primary olfactory centers, the antennal lobes, of the different
30 phila antennal lobe is represented in higher olfactory centers, the mushroom body and lateral horn.
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