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1    The majority of afferent boutons received axoaxonic and made axodendritic or axosomatic synaptic c
2                             We also observed axoaxonic appositions between MGE and host terminals.
3 eceptors may ensure the inhibitory effect of axoaxonic cells at the AIS due to activation of Kv7/KCNQ
4 between parvalbumin-containing basket cells, axoaxonic cells, and type 1 cannabinoid receptor (CB1)-e
5                                  Chandelier (axoaxonic) cells (ChCs) are a distinct group of GABAergi
6 vate spinal GABAergic interneurons that have axoaxonic connections onto proprioceptive (Ia) afferents
7                           The mean number of axoaxonic contacts received per afferent terminal in thi
8 ealed numerous axosomatic, axodendritic, and axoaxonic contacts stained for CCK, PV, and the presynap
9 and in large ventral horn synapses receiving axoaxonic contacts.
10 e elements, but no evidence of axosomatic or axoaxonic degeneration in the adjacent granule cell laye
11                              The presence of axoaxonic GABAergic synapses was determined by costainin
12 old labeling, 10 close appositions revealing axoaxonic gap junctions ( approximately 30-70 nm in diam
13 ere, we provide ultrastructural evidence for axoaxonic gap junctions in dentate granule cells.
14 ro electrophysiological data suggesting that axoaxonic gap junctions play an important role in the ge
15  of transmitter from the axons that received axoaxonic inputs.
16 is is in contrast to rats and cats, in which axoaxonic interactions involving GLY-IR terminals have b
17 so noteworthy was the conspicuous absence of axoaxonic interactions involving GLY-IR terminals.
18  molecular underpinnings of this specialized axoaxonic organization remain unclear.
19 BAergic neurons in the spinal cord that sent axoaxonic projections to the terminal endings of sensory
20  that Kenyon cells and dopamine neurons from axoaxonic reciprocal synapses.
21                 Presynaptic boutons at these axoaxonic synapses always contained gamma-aminobutyric a
22 se afferent types innervate iCRs and receive axoaxonic synapses from them, providing feedback inhibit
23 n of these interneurons, and the presence of axoaxonic synapses indicates that their excitatory input
24 th GABAergic interneurons forming last-order axoaxonic synapses onto afferent terminals.
25  II of the spinal cord and receive GABAergic axoaxonic synapses, which mediate presynaptic inhibition
26 h noncatecholamine dendrites, and 20% formed axoaxonic synapses.
27 ons, and collaterals of one cell also formed axoaxonic synapses.
28                                  Inhibitory, axoaxonic, synapses provide a mechanism for this regulat
29      Eighty-nine percent of boutons received axoaxonic synaptic contacts, the mean number of contacts
30        However, until now the source of this axoaxonic synaptic input was not known.