ライフサイエンスコーパス: periglomerular

1 biopsy samples and were distributed as broad periglomerular aggregates or intermixed with CD8+ T cell

2 Labeled periglomerular and granular neurons with extensive dendr

3 Bulbar interneurons such as periglomerular and granule cells are thought to influenc

4 Nurr1 expression was confined to periglomerular and midbrain dopaminergic neurons.

5 nto the OB but fail to generate dopaminergic periglomerular and superficial granule cells.

6 ssion is the same in simultaneously recorded periglomerular and tufted neurons, and that this form of

7 ates or intermixed with CD8+ T cells forming periglomerular caps.

8 axodendritic synapses with mitral/tufted and periglomerular cell dendrites, whereas the dendrites of

9 spikes, whereas in the GL, DHPG facilitates periglomerular cell GABA release via both spike-dependen

10 or antagonists, indicating the engagement of periglomerular cells (PGCs) and/or short axon cells (SAC

11 ion in the overall number of adult-generated periglomerular cells (PGCs), but not of granule cells (G

12 trongest expression was found in a subset of periglomerular cells (PGCs).

13 rom the glomerular layer reflect activity in periglomerular cells and that Cl- efflux through non-GAB

14 Ca(2+) spikes in periglomerular cells are evoked by powerful excitatory i

15 granule cells at six to seven months and OB periglomerular cells at 12-14 months, respectively, both

16 iate into phenotypically diverse granule and periglomerular cells by as yet undefined mechanisms.

17 t feedforward inhibition from olfactory bulb periglomerular cells can mediate this signal normalizati

18 PSCs in mitral cells by 50%, suggesting that periglomerular cells exert strong tonic GABAergic inhibi

19 Granule and periglomerular cells in the main olfactory bulb express

20 The robust expression of TH in some periglomerular cells in the OCNC1-null mice suggests tha

21 s and olfactory tubercle, and to granule and periglomerular cells in the olfactory bulb.

22 lude neurons in the caudate and putamen, and periglomerular cells in the olfactory bulb.

23 ith activity-dependent protein expression in periglomerular cells innervated by olfactory receptor ce

24 Er81, which is also expressed in granule and periglomerular cells of the developing and adult olfacto

25 laureatum neurons that resemble dopaminergic periglomerular cells of the OB.

26 Interglomerular excitation of these periglomerular cells potently inhibits mitral cells and

27 reflect correlated feedback inhibition from periglomerular cells that are driven by ET cell spike bu

28 OB and differentiate into granule cells and periglomerular cells that are presumed to integrate into

29 find that L-type dendritic Ca(2+) spikes in periglomerular cells underlie dendrodendritic transmissi

30 rus moved down the olfactory nerve, first to periglomerular cells, then past the mitral cell layer to

31 reased expression of tyrosine hydroxylase in periglomerular cells, vesicular glutamate transporter 1,

32 ecursors that differentiate into granule and periglomerular cells.

33 ulb and differentiate into granule cells and periglomerular cells.

34 granule interneurons and calbindin-positive periglomerular cells.

35 ncipal neurons activates a large ensemble of periglomerular cells.

36 input and lateral signaling onto neighboring periglomerular cells.

37 TH protein in adults was further limited to periglomerular cells.

38 ansgenes in neonatal superficial granule and periglomerular cells.

39 th granule cells more severely affected than periglomerular cells.

40 ergic granule cells but not in the GABAergic periglomerular cells.

41 dendrodendritic transmission by depolarizing periglomerular dendrites and activating P/Q type channel

42 To visualize spatiotemporal aspects of periglomerular dopamine (DA) neuron differentiation, two

43 mokines were expressed only on the immediate periglomerular epithelium and that these events coincide

44 art disease present with glomerulosclerosis, periglomerular fibrosis and albuminuria.

45 dhesion, interstitial foam cells, deflation, periglomerular fibrosis, mononuclear white blood cells,

46 f glomerular capillaries, tuft collapse, and periglomerular fibrosis.

47 formation of typical cellular crescents with periglomerular infiltrate, albeit without accompanying p

48 eas the dendrites of mitral/tufted cells and periglomerular interneurons form dendrodendritic synapse

49 lial-derived cells generate granule cell and periglomerular interneurons in the olfactory bulb and co

50 on of granular interneurons and Calbindin(+) periglomerular interneurons seemed unaffected by the los

51 B interneurons, including TH+ and calbindin+ periglomerular interneurons.

52 y differentiate into granule cells (GCs) and periglomerular interneurons.

53 that reached the OB and integrated into the periglomerular layer, revealing a crucial role for EphA4

54 ps of mice had migrated into the granule and periglomerular layers of the olfactory bulb.

55 rons are seen in the mature granule cell and periglomerular layers, as well as in cells in the subven

56 n interneurons in the external plexiform and periglomerular layers, whereas VPAC2R is expressed in mi

57 ctural features of FSGS, marked albuminuria, periglomerular monocytic and T cell inflammation, and en

58 B cells were often organized into large periglomerular neighborhoods with Tfh cells, while CD4-

59 Strikingly, decreasing activity of periglomerular neuron precursors (PGN-Ps) did not impact

60 ons during their migration: granule cell and periglomerular neuron precursors (PGN-Ps).

61 ent activity, was reduced in the majority of periglomerular neurons but retained in atypical or "neck

62 dressed if a reduced demand specifically for periglomerular neurons impacts on NPC-traits in the rost

63 e hydroxylase-positive GFP (TH(+)-GFP) mouse periglomerular neurons in vitro.

64 droxylase (TH), expressed in a population of periglomerular neurons intrinsic to the olfactory bulb,

65 gamma-aminobutyric acid (GABA) release from periglomerular neurons mediates inhibition of principal

66 pes of neural progenitors, granule cells and periglomerular neurons that migrate tangentially in the

67 to form excitatory synapses with inhibitory periglomerular neurons up to 20-30 glomeruli away.

68 restingly, calbindin+ and calretinin (CalR)+ periglomerular neurons were decreased in both Snca-/-, a

69 ed by the loss of TrkB, whereas dopaminergic periglomerular neurons were reduced.

70 b containing reduced numbers of granular and periglomerular neurons with a distinct paucity of dopami

71 TIMP3 is present in periglomerular neurons, where it could restrict ADAM21-m

72 fficient to produce feedback inhibition from periglomerular neurons.

73 rons with a distinct paucity of dopaminergic periglomerular neurons.

74 ished source for newly generated granule and periglomerular neurons.

75 ynapse with dendrites of mitral, tufted, and periglomerular neurons.

76 are colocalized with TH in the dopaminergic periglomerular neurons.

77 ynapse with dendrites of mitral, tufted, and periglomerular neurons.

78 retinin+, calbindin+, and dopaminergic (TH+) periglomerular OB interneurons correspond to distinct su

79 and SNCA-A30P mice but tyrosine hydroxylase+ periglomerular OB neurons were only decreased in Snca-/-

80 ic neurons of the mouse OB glomerular layer, periglomerular (PG) and short axon (SA) cells, as well a

81 Among them, diverse periglomerular (PG) cell types interact with the apical

82 rcuit consisting of external tufted (ET) and periglomerular (PG) cells and an interglomerular circuit

83 n the adult its expression was restricted to periglomerular (PG) cells in the olfactory bulb (OB).

84 GABAergic periglomerular (PG) cells in the olfactory bulb are prop

85 GABAergic periglomerular (PG) cells in the olfactory bulb are prop

86 ateral dendrites whereas diverse subtypes of periglomerular (PG) cells mediate intraglomerular latera

87 The periglomerular (PG) cells of the accessory olfactory bul

88 use olfactory bulb glomerulus, the GABAergic periglomerular (PG) cells provide a major inhibitory dri

89 he GABA (gamma-aminobutyric-acid)-containing periglomerular (PG) cells provide the first level of inh

90 dition, evidence was obtained that GABAergic periglomerular (PG) cells that surround a glomerulus can

91 rular inhibitory interneurons: (1) GABAergic periglomerular (PG) cells, whose processes are limited t

92 y selectively innervate specific subtypes of periglomerular (PG) cells.

93 ory bulb interneurons: the granule cells and periglomerular (PG) cells.

94 uts modulate activity in diverse subtypes of periglomerular (PG) interneurons using optogenetic stimu

95 glomerular (JG) cells: external tufted (ET), periglomerular (PG), and short axon (SA) cells.

96 uli contain at least three types of neurons: periglomerular (PG), external tufted (ET), and short-axo

97 cluding two types of GABAergic interneurons (periglomerular [PG] and short axon [SA] cells) and OB ou

98 ayers before these cells reached their final periglomerular position.

99 roduce subthreshold modulation of the mitral-periglomerular reciprocal circuit.

100 oliferative regions after 2 hours and in the periglomerular region of the bulb after 7 days following

101 , expression of HGF/SF was restricted to the periglomerular region of the glomerular layer, whereas c

102 d in accumulation of ZBTB46 (+) cells in the periglomerular region.

103 ells, possibly external tufted cells, in the periglomerular region.

104 Sequencing of the TCR from periglomerular regions showed a predominance of clonally

105 particularly in and around perivascular and periglomerular regions, while tubular epithelial cells w

106 iform and glomerular layers and localized to periglomerular somata and dendrites, mitral cell somata,

107 e external plexiform layer, and localized to periglomerular somata and dendrites, short axon somata a