ライフサイエンスコーパス: protocerebral

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1 stage), arise from the central domain of the protocerebral and deuterocerebral neurectoderm, respecti

2 pattern of brain neuroblast segregation, the protocerebral and deuterocerebral neuromeres can be furt

3 ic neurons in Drosophila, referred to as the protocerebral anterior medial (PAM) cluster.

4 usly undescribed paired neurons, the primary protocerebral anterior medial (pPAM) neurons.

5 arbon-fiber microelectrode was placed in the protocerebral anterior medial brain area where dopamine

6 In both of the protocerebral areas in which axonal branches terminated,

7 on about odorants is distributed to multiple protocerebral areas.

8 sts of four midline structures including the protocerebral bridge (PB), fan-shaped body (FB), ellipso

9 in possessing a central complex comprising a protocerebral bridge and central body.

10 e is dense octopaminergic innervation in the protocerebral bridge and ellipsoid body of the central c

11 res to appear in their immature form are the protocerebral bridge and fan-shaped body, which are pres

12 puts from the optic lobes invades the entire protocerebral bridge and was driven by visual motion.

13 Most strikingly, we found that the protocerebral bridge contains 18 glomeruli, not 16, as p

14 the structure of a brain region known as the protocerebral bridge fail to aim their movements correct

15 TB-neurons connect the protocerebral bridge with two adjacent brain areas, the

16 itive tangential neurons (TB-neurons) of the protocerebral bridge, a part of the central complex, giv

17 ith the ellipsoid body, fan-shaped body, and protocerebral bridge, all of which receive both visual a

18 the noduli, 12-15 tangential neurons of the protocerebral bridge, and about 17 neurons that supplied

19 on one structure of the central complex, the protocerebral bridge, and identifies just 17 morphologic

20 um and the central complex, particularly the protocerebral bridge, fan-shaped body, and ellipsoid bod

21 of small-field neurons that interconnect the protocerebral bridge, fan-shaped body, noduli, and ellip

22 A putative output neuron connecting the protocerebral bridge, the fan-shaped body, and one of th

23 Corresponding to ramification domains in the protocerebral bridge, the neurons invaded distinct but o

24 ramen that gave rise to arborizations in the protocerebral bridge.

25 e immunoreactivities were colocalized in the protocerebral cells and their projections terminating on

26 h visual and mechanosensory information from protocerebral centers.

27 neer a medial and a lateral component of the protocerebral connective, respectively.

28 ntal component for which we propose the term protocerebral connective.

29 s individual cells, cells of the dorsomedial protocerebral domain are internalized during stage 12 as

30 on-rich areas in the head resolve paired pre-protocerebral ganglia at the origin of paired frontal ap

31 The position of the protocerebral ganglia in exceptionally preserved Cambria

32 anomalocaridids and Onychophora resolve pre-protocerebral ganglia, associated with pre-ocular fronta

33 ria with an emphasis on the mushroom bodies, protocerebral integration centers implicated in memory f

34 ree main domains: the head midline ectoderm, protocerebral neurectoderm and visual primordium.

35 f tll function results in the absence of all protocerebral neuroblasts, otd functions in a domain tha

36 NB identities in the Drosophila dorsomedial protocerebral neuroectoderm.

37 erm into tritocerebral, deuterocerebral, and protocerebral neuromeres.

38 lso examined the connectivity of the lateral protocerebral neuropils of embryonic lobsters.

39 dy examines the morphogenesis of the lateral protocerebral neuropils of the lobster, Homarus american

40 le systems of perikarya and arborizations in protocerebral neuropils of two species of Diptera, Droso

41 The terminals of these efferents target protocerebral neuropils that are distinct from those rec

42 4) multimodal interneurons that originate in protocerebral neuropils.

43 lied by the antennular nerves, and a lateral protocerebral olfactory neuropil corresponds to the mala

44 al projection-neuron (PN) antennal lobe (AL) protocerebral output tract (m-APT) and a lateral PN AL o

45 . converge on the same set of neurons in the protocerebral posterior lateral 1 (PPL1) cluster in Dros

46 n insects suggest a segmental status for the protocerebral region.

47 Mass-fills of antennal-lobe connections with protocerebral regions showed that the centrifugal neuron

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