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1 ncipal neurons activates a large ensemble of periglomerular cells.
2 input and lateral signaling onto neighboring periglomerular cells.
3  TH protein in adults was further limited to periglomerular cells.
4 ansgenes in neonatal superficial granule and periglomerular cells.
5 th granule cells more severely affected than periglomerular cells.
6 ergic granule cells but not in the GABAergic periglomerular cells.
7 ecursors that differentiate into granule and periglomerular cells.
8 ulb and differentiate into granule cells and periglomerular cells.
9  granule interneurons and calbindin-positive periglomerular cells.
10 rom the glomerular layer reflect activity in periglomerular cells and that Cl- efflux through non-GAB
11                             Ca(2+) spikes in periglomerular cells are evoked by powerful excitatory i
12  granule cells at six to seven months and OB periglomerular cells at 12-14 months, respectively, both
13 iate into phenotypically diverse granule and periglomerular cells by as yet undefined mechanisms.
14 t feedforward inhibition from olfactory bulb periglomerular cells can mediate this signal normalizati
15 axodendritic synapses with mitral/tufted and periglomerular cell dendrites, whereas the dendrites of
16 PSCs in mitral cells by 50%, suggesting that periglomerular cells exert strong tonic GABAergic inhibi
17  spikes, whereas in the GL, DHPG facilitates periglomerular cell GABA release via both spike-dependen
18                                  Granule and periglomerular cells in the main olfactory bulb express
19          The robust expression of TH in some periglomerular cells in the OCNC1-null mice suggests tha
20 s and olfactory tubercle, and to granule and periglomerular cells in the olfactory bulb.
21 lude neurons in the caudate and putamen, and periglomerular cells in the olfactory bulb.
22 ith activity-dependent protein expression in periglomerular cells innervated by olfactory receptor ce
23 Er81, which is also expressed in granule and periglomerular cells of the developing and adult olfacto
24 laureatum neurons that resemble dopaminergic periglomerular cells of the OB.
25 or antagonists, indicating the engagement of periglomerular cells (PGCs) and/or short axon cells (SAC
26 ion in the overall number of adult-generated periglomerular cells (PGCs), but not of granule cells (G
27 trongest expression was found in a subset of periglomerular cells (PGCs).
28          Interglomerular excitation of these periglomerular cells potently inhibits mitral cells and
29  reflect correlated feedback inhibition from periglomerular cells that are driven by ET cell spike bu
30  OB and differentiate into granule cells and periglomerular cells that are presumed to integrate into
31 rus moved down the olfactory nerve, first to periglomerular cells, then past the mitral cell layer to
32  find that L-type dendritic Ca(2+) spikes in periglomerular cells underlie dendrodendritic transmissi
33 reased expression of tyrosine hydroxylase in periglomerular cells, vesicular glutamate transporter 1,