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1  with glutamatergic synaptic transmission at axo-dendritic and axo-axonic junctions and that NO may b
2         All three classes of terminal formed axo-dendritic and axo-somatic contacts onto retrogradely
3 synaptic dendrites or somata, giving rise to axo-dendritic and axo-somatic synapses, respectively.
4  and perisynaptic GluD1 labeling at putative axo-dendritic and axo-spinous glutamatergic synapses, an
5 th had diminished by 50%-75% through loss of axo-dendritic and axo-spinous synapses, was incapable of
6       Electron microscopic analyses revealed axo-dendritic and occasional axo-axonic synapses between
7 rges via differential synaptic maturation of axo-dendritic appositions and is shaped by neurotransmis
8 rough selective changes in the conversion of axo-dendritic appositions to synapses.
9 close correlation between the small angle of axo-dendritic approach and the formation of synaptic clu
10                  Most of these contacts were axo-dendritic (approximately 80%), while approximately 2
11      However, if electrical synapses were in axo-dendritic connections, where chemical synapses occur
12 urites and explore their surroundings before axo-dendritic contact and synaptogenesis.
13 how synaptogenic signals (e.g., adhesion) at axo-dendritic contact sites promote axonal transport of
14 ENT Whether and how synaptogenic adhesion at axo-dendritic contact sites regulates axonal transport o
15 n molecule mediates specific interactions at axo-dendritic contact sites, which is required for upreg
16 nsible for synaptic transmission at sites of axo-dendritic contact.
17  rapid induction of synapses at new sites of axo-dendritic contact.
18 r light microscopy, putative axo-somatic and axo-dendritic contacts were observed between serotonin-p
19 ity, with synapses found at only a subset of axo-dendritic contacts.
20 s the adhesive clustering of SynCAM 1 at new axo-dendritic contacts.
21 tes to the adhesive differentiation of their axo-dendritic contacts.
22 affected whereby the ratio of axo-spinous to axo-dendritic corticostriatal synaptic contacts was redu
23  not labeled, consistent with the absence of axo-dendritic efferent innervation in birds.
24 pport a model in which Bdl mediates specific axo-dendritic interactions in a homophilic manner, which
25       On the basis of spatial constraints on axo-dendritic interactions, we propose positional strate
26 s of isoforms, which may engage in selective axo-dendritic interactions.
27 , but not intracortical, excitation leads to axo-dendritic morphological defects in these interneuron
28 s distinct neurodegenerative programs in the axo-dendritic network and in the cell bodies.
29 ging studies revealed that neurons and their axo-dendritic network are fairly motile under standard c
30 itatory neurons in the cerebral cortex, such axo-dendritic oppositions, termed potential synapses, mu
31                         First, the degree of axo-dendritic overlap reduces the number of potential po
32  Neuronal connectivity is established by the axo-dendritic polarity, correct guidance and targeting o
33 iched protein FOXO6, play a critical role in axo-dendritic polarization of undifferentiated neurites,
34 ocampus as proving grounds to determine when axo-dendritic proximities predict synapses.
35 ck-out mice, but result instead in increased axo-dendritic shaft synapses.
36 the mechanisms that modulate their polarized axo-dendritic sorting and synaptic delivery.
37 s that organize neurogenesis, migration, and axo-dendritic specification in post-mitotic neurons.
38 alian brain, the vast majority of excitatory axo-dendritic synapses occur on dendritic specialization
39 y terminals are in close apposition and make axo-dendritic synapses onto granule cells.
40                    TH nerve terminals formed axo-dendritic synapses upon negative inotropic vagal mot
41                              Axo-somatic and axo-dendritic synapses were detected between terminals l
42 associated with an increase in the number of axo-dendritic synapses, and it appeared to represent a s
43             A similar effect was observed at axo-dendritic synapses, where GABAergic innervation also
44                                              Axo-dendritic synaptogenesis was examined in live hippoc
45                                   Second, an axo-dendritic touch did not predict a synapse; neverthel
46 astructural details that distinguish between axo-dendritic touches and bona fide synapses.