ライフサイエンスコーパス: olfactory lobe

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1 lla also have differing connections with the olfactory lobe.

2 rget neuropil of the output pathway from the olfactory lobe.

3 ent ingrowth pioneers the development of the olfactory lobe.

4 uniquely represented in the moth's antennal (olfactory) lobe.

5 oked ensemble patterns in the moth antennal (olfactory) lobe.

6 a, development of glomeruli in the antennal (olfactory) lobes (ALs) follows a precise timetable and i

7 nterneurons were confined to the ipsilateral olfactory lobe and accessory lobe, but only a few branch

8 a previously undescribed pathway linking the olfactory lobe and the ventral nerve cord.

9 recovered at low numbers initially from the olfactory lobe and then from the brain for 3 to 4 days a

10 terminals of receptor neurons in the lobster olfactory lobe and turtle olfactory bulb.

11 of all ganglia, in glomeruli of the brain's olfactory lobes, and in the cytoplasm of a small number

12 recording from living embryos, we show that olfactory lobe development depends sequentially on conta

13 lobe, but only a few branches innervated the olfactory lobe glomeruli.

14 ent study examines glomerular numbers in the olfactory lobes of 17 crustacean species from six of the

15 hroughout development of the adult antennal (olfactory) lobe of the brain of the moth Manduca sexta.

16 Glomerulus development in the antennal (olfactory) lobe of the moth brain, which is initiated by

17 of cells in the lateral cluster (LC) of the olfactory lobe (OL) and in the cluster of the hemiellips

18 s are different from those innervated by the olfactory lobe output pathway.

19 contrast, projection neurons innervating the olfactory lobes primarily target neuropil regions of the

20 Output from the olfactory lobe (primary olfactory center) of eumalacostr

21 The main output pathways from the olfactory lobes (primary olfactory centers) and accessor

22 t whereas projection neurons innervating the olfactory lobe project primarily to the MT, those innerv

23 Although the olfactory lobe seems to receive only primary olfactory i

24 Local field potential recordings on the olfactory lobe showed that administration of SNP or SIN-

25 Counts of axons in tracts leading from the olfactory lobes to the hemiellipsoid bodies resolve 20,0

26 By using dye injections into the olfactory lobe, we demonstrate that the accessory lobe c

27 al PN AL output tract (l-APT) connecting the olfactory lobes with higher-order brain centers.

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