戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 s-lacunosum moleculare (O-LMC), basket (BC), axo-axonic (AAC), bistratified (BiC) and oriens-bistrati
2  oscillations and, together with MGE-derived axo-axonic and bistratified cells, provide attractive ca
3 at three distinct interneuron types--basket, axo-axonic and oriens-lacunosum-moleculare cells--visual
4 inct firing dynamics and synaptic targets of axo-axonic and other parvalbumin-expressing cells provid
5   Teevra cells synaptically target GABAergic axo-axonic and some CCK interneurons in restricted septo
6 ast-spiking cells tested (25 of 29 basket, 1 axo-axonic, and 5 of 6 bistratified cells) were PV-IR.
7 we found that parvalbumin-expressing basket, axo-axonic, bistratified, and oriens-lacunosum molecular
8                       2) Both the density of axo-axonic cartridges and the degree of gamma-aminobutyr
9                                       4) The axo-axonic cartridges innervate the majority of excitato
10                           One was a putative axo-axonic cell with an axonal arbour confined to half o
11 ajority of GABAergic cells in the LA and BA: axo-axonic cells (5.5%-6%), basket cells expressing parv
12                                              Axo-axonic cells (AACs) in cortical regions selectively
13                                              Axo-axonic cells (AACs) regulate action potential genera
14                                              Axo-axonic cells (AACs), also called chandelier cells (C
15 der GABAergic control by the "chandelier" or axo-axonic cells (AACs).
16                                Chandelier or axo-axonic cells are the most selective of all cortical
17                                 In addition, axo-axonic cells differ from other GABAergic parvalbumin
18 alient sensory stimuli selectively triggered axo-axonic cells firing and inhibited firing of a discti
19                                 The axons of axo-axonic cells formed "axonal cartridges," with cluste
20 eir privileged location on initial segments, axo-axonic cells have often been assumed to have the ult
21 ine in utero disrupts the development of the axo-axonic cells in the prefrontal cortex and this disru
22 c cortex of anesthetized rats, and show that axo-axonic cells increase their firing during tail pinch
23                                              Axo-axonic cells never establish autapses, and the fast-
24 edly versatile functional effects exerted by axo-axonic cells on their postsynaptic targets.
25                      The spike AHPs of three axo-axonic cells tested showed no sensitivity to etomida
26 ket cells (PVBCs), while PV bistratified and axo-axonic cells were unimpaired.
27 euronal subtypes, including bistratified and axo-axonic cells, are spared.
28 because of their unique anatomical features: axo-axonic cells, neurogliaform cells, and giant cells.
29 valbumin-expressing basket, bistratified, or axo-axonic cells.
30 d in 25 basket, three bistratified and eight axo-axonic cells.
31                               Chandelier (or axo-axonic) cells are a distinct group of GABAergic inte
32 bset of GABAergic interneurons that includes axo-axonic chandelier cells.
33 pal interneurons are classified into basket, axo-axonic (chandelier), and bistratified cells.
34            This variability in the number of axo-axonic ChC synapses is higher than the variability s
35                              This example of axo-axonic conduction block--neurons in one pathway inhi
36       Synaptic depression was studied at the axo-axonic connection between the goldfish Mauthner axon
37 lower degree of OSN lateralization, stronger axo-axonic connections between OSNs, dendro-dendritic co
38               We find that KCs have numerous axo-axonic connections mediated by the muscarinic type-B
39 d optogenetic approaches, we show that these axo-axonic connections suppress both odor-evoked calcium
40 al window result in a reversible decrease in axo-axonic connections.
41 , we find new connectivity motifs, including axo-axonic connectivity between projection neurons, feed
42                         This nonconventional axo-axonic contact extends beyond the perisomatic chemic
43  and a greater proportion of boutons receive axo-axonic contacts and are involved in synaptic triads.
44 X also led to malformation of GABApre neuron axo-axonic contacts on Ia afferents and of the recurrent
45 alized GABAergic neurons (GAD2(+)) that form axo-axonic contacts onto myelinated proprioceptive senso
46                           The mean number of axo-axonic contacts received per terminal was 2.7, and t
47 d set of spinal GABAergic interneurons forms axo-axonic contacts with the central terminals of sensor
48 cal GABAergic interneurons which make direct axo-axonic contacts with the dual glutamatergic/GABAergi
49 e boutons formed the presynaptic elements at axo-axonic contacts: none of these were found to contain
50 sporter GAT-1, which project axo-somatic and axo-axonic GABAergic inhibitory terminals to granule cel
51 imulations show that the observed pattern of axo-axonic inhibition is particularly effective in contr
52 ss of interneurons providing axo-somatic and axo-axonic inhibition may regulate spike output to pyram
53 ergic interneurons providing axo-somatic and axo-axonic inhibition, may be important in the developme
54  However, quantitative information regarding axo-axonic inhibitory synapses mediated by chandelier ce
55  AIS extracellular matrix, and regulates AIS axo-axonic innervation by inhibitory basket cells in the
56                                              Axo-axonic interneurons, innervating exclusively axon in
57                 The ionic coupling resembles axo-axonic junction and hence we refer to this framework
58 c synaptic transmission at axo-dendritic and axo-axonic junctions and that NO may be generated indepe
59               However, IPSC decays evoked by axo-axonic, parvalbumin- or cholecystokinin-expressing b
60 inhibitory GABA transporter-1 immunoreactive axo-axonic structures commonly called "candles" or "cart
61 d membrane transporter 1 innervation in each axo-axonic synapse are significantly higher in the pirif
62                 Here, we review evidence for axo-axonic synapse contributions to neural signaling in
63  this, the cellular mechanisms governing ChC axo-axonic synapse formation remain poorly understood.
64 ns including action potential initiation and axo-axonic synapse formation.
65 served to form the presynaptic element in an axo-axonic synapse with a CSN afferent.
66 investigated the physiological properties of axo-axonic synapses (AASs) in brain slices from the piri
67 lation of chandelier cells mediates abundant axo-axonic synapses across the entire piriform cortex.
68 hyrin is required for the proper assembly of axo-axonic synapses at the AIS.
69 alyses revealed axo-dendritic and occasional axo-axonic synapses between graft and host.
70  the pre- and postsynaptic components of the axo-axonic synapses did not change position after AIS re
71 ique type of GABAergic interneuron that form axo-axonic synapses exclusively on the axon initial segm
72 on, our results highlight a critical role of axo-axonic synapses in regulating information flow and o
73 ue of Neuron, Mende et al. (2016) report how axo-axonic synapses of interneurons balance the strength
74             Chandelier cells form inhibitory axo-axonic synapses on pyramidal neurons with their char
75 ticulospinal axons and the neurons that make axo-axonic synapses onto those axons.
76 ive analysis of structural plasticity across axo-axonic synapses revealed that ChCs redistributed inh
77 n that control pyramidal cell output through axo-axonic synapses that target the axon initial segment
78 t the axon initial segment (AIS) showed that axo-axonic synapses were depolarizing during this period
79                                Five types of axo-axonic synapses were observed in the dlNTS.
80 structural features of interneurons and form axo-axonic synapses with putative cortical-like glutamat
81                          Among these are the axo-axonic synapses, which consist of an axon terminatin
82 hibitory, resulted instead in an increase in axo-axonic synapses.
83 ostatic rules that depend on the polarity of axo-axonic synapses.
84 y be used to identify and functionally assay axo-axonic synapses.
85 t apposition to one another, without forming axo-axonic synapses.
86  afferent boutons (94%) were postsynaptic at axo-axonic synapses: 67% of presynaptic boutons presynap
87 s elemental circuit architecture includes an axo-axonic synaptic connection from the glutamatergic mo
88 s at the axon initial segment (AIS), altered axo-axonic synaptic inhibition, disrupted action potenti
89 r organizing neural coding through selective axo-axonic synaptic plasticity.
90 cked PV, which was shown previously to label axo-axonic terminals provided by chandelier cells.
91 nal pathway from the eye to the LoC involves axo-axonic transfer of NGF with receptor switching (p75