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1 e symmetric axospinous (57-62%) or symmetric axodendritic (33-35%).
2         The vast majorities of synapses were axodendritic (98%, 580/593), while 2% of them were axoso
3 ditionally, efferent endings may form simple axodendritic and axoaxonal synapses with GAD-negative ve
4            Ultrastructural analyses revealed axodendritic and axosomatic contacts between PRV-labeled
5 anule neurons, were contacted by axosomatic, axodendritic and axospinous synapses.
6 endritic synaptic depression, the balance of axodendritic and dendrodendritic circuitry in external t
7 ent input, and thus the relative strength of axodendritic and dendrodendritic input determines the po
8                             Primary afferent axodendritic and local-circuit dendrodendritic synapses
9 cal microscopy revealed numerous axosomatic, axodendritic, and axoaxonic contacts stained for CCK, PV
10 rofiles were more frequently axospinous than axodendritic, and many axospinous synapses were perforat
11 s such as asymmetric, symmetric, axospinous, axodendritic, and perforated in the patch and matrix of
12 tum radiatum of the CA1 area by its complete axodendritic arborization and characteristic spike timin
13 3beta signaling cascades, and enhancement of axodendritic arborization in rat immortalized hippocampa
14 R/L-M boundary revealed surprisingly modular axodendritic arborizations with consistently uniform loc
15 r the postsynaptic density of axospinous and axodendritic asymmetric synapses and at high levels in d
16 ion of SP-immunoreactive boutons that formed axodendritic asymmetric synapses was observed in the str
17 cases, the ultrastructural analysis revealed axodendritic asymmetric synapses.
18                                       In the axodendritic axis, gold particles coding for PSD-95 lay
19                 Additionally, the excitatory axodendritic boutons of hearing cats were found to be si
20 ophysical properties and localization within axodendritic compartments serve to significantly transfo
21 ve APP gain-of-function that could impact on axodendritic connectivity and contribute to aberrant axo
22  a physiological consequence of increases in axodendritic connectivity and in the magnitude of cAMP-d
23 rowth in transfected neuroblastoma cells and axodendritic connectivity associated with increased spin
24  4 microm/min, and are recruited to sites of axodendritic contact within minutes.
25               To visualize the clustering of axodendritic contacts (potential synapses) within these
26 c and postsynaptic differentiation occurs at axodendritic contacts between CNS neurons.
27                                 To visualize axodendritic contacts between identified cell types, we
28 evealed that CART establishes axosomatic and axodendritic contacts with CRH neurons in the PVN.
29 resynaptic to an afferent terminal also made axodendritic contacts with dendrites postsynaptic to the
30 symmetrical (with small, flattened vesicles) axodendritic contacts, also including multisynaptic spin
31                      Most boutons (95%) made axodendritic contacts, and the mean number of dendrites
32 ajority of the 5-HT-labeled terminals formed axodendritic contacts, but some 5-HT-labeled terminals m
33 I-32-labeled dendrites were primarily simple axodendritic contacts; few triadic arrangements were obs
34 amyloid-beta-induced missorting and that the axodendritic distribution of Tau depends on AIS integrit
35 n channels differentially distributed across axodendritic domains, directly revealing site-dependent
36  are contacted by type I afferents receiving axodendritic efferent contacts; OHCs are contacted by ty
37                    We also demonstrated that axodendritic electrical coupling by projection interneur
38 ar to be transitional between axospinous and axodendritic junctions.
39 ynapses, whereas complexin II is a marker of axodendritic (mainly excitatory) synapses.
40 induction of LTP and are then converted into axodendritic ones during LTP maintenance.
41                     An occasional asymmetric axodendritic or asymmetric axospinous synapse was observ
42 croscopic level IHC revealed the presence of axodendritic or axosomatic synapses between VIP-ir and P
43 afferent boutons received axoaxonic and made axodendritic or axosomatic synaptic contacts.
44               The patterns of axosomatic and axodendritic organization were determined for principal
45  functionally deficient PS1 exhibit enhanced axodendritic outgrowth due to increased levels of APP in
46         Neuronal precursor proliferation and axodendritic outgrowth have been regarded as strictly se
47 which functional synapses form in regions of axodendritic overlap has not been extensively studied.
48 f local and long-range excitatory axons, but axodendritic overlap is not always a good predictor of a
49          Moreover, we found that the average axodendritic overlap of the presynaptic and postsynaptic
50  computed the geometric circuit predicted by axodendritic overlap.
51 ed D1 receptor binding in nucleus accumbens; axodendritic pathology and altered hippocampal cytoarchi
52           In mature neurons, TBB reduces the axodendritic polarity of FGF14.
53      Neuronal function is intimately tied to axodendritic polarity.
54 e fascinating cellular processes involved in axodendritic polarization.
55 rn of ERK activation was seen in superficial axodendritic processes of epileptic neocortex that coloc
56 neuronal cell death, neuronal cell position, axodendritic projection patterns, and synaptic connectiv
57 es and postsynaptic structures, being either axodendritic (PV(+)) or axospinous (SOM(+)).
58  the human and rodent Tau isoforms differ in axodendritic sorting and amyloid-beta-induced missorting
59 ber of axosomatic and one-half the number of axodendritic spine synapses as females.
60 , the majority of SP-containing axons formed axodendritic symmetric synapses.
61                 This was linked with greater axodendritic synapse density and ultrastructural charact
62 t significantly different from the length of axodendritic synapses (0.523 micron) or the area of term
63 rating CT terminal boutons formed asymmetric axodendritic synapses and contained small, clear, spheri
64 ority of labelled terminals formed symmetric axodendritic synapses and displayed gamma-aminobutyric a
65                                        These axodendritic synapses are anatomically separated from de
66 ere located in white matter and did not form axodendritic synapses but expressed presynaptic markers
67      The axospinous synapses outnumbered the axodendritic synapses by more than two to one.
68 egenerating into the nucleus gracilis formed axodendritic synapses containing rounded vesicles, refle
69                                The number of axodendritic synapses in the glomeruli of OMP-null mice
70 nputs that could account for the increase in axodendritic synapses in the matrix, we undertook an ele
71                   The number of asymmetrical axodendritic synapses increased (by 28%) during LTP main
72 newborn neurons do not receive axosomatic or axodendritic synapses indicating the absence of basket c
73 ber (AF) system in piriform cortex (PC) make axodendritic synapses on granule cells within the granul
74 erficial external plexiform layer (EPL); (2) axodendritic synapses onto GC proximal dendrites via the
75  labeled M72 glomeruli showed no evidence of axodendritic synapses other than those with GFP-labeled
76  linear rise in the number of axospinous and axodendritic synapses present in the neuropil.
77 ately 35-50% of all symmetric axospinous and axodendritic synapses were formed by TH-i boutons.
78                         These afferents form axodendritic synapses with mitral/tufted and periglomeru
79                           The iCRs also form axodendritic synapses, and their targets include cells t
80 logical analyses, we found that densities of axodendritic synapses, especially axo-spinous synapses,
81 rodendritic synapses but facilitation of the axodendritic synapses.
82 except for a few that established asymmetric axodendritic synapses.
83 occasionally were observed to form symmetric axodendritic synapses.
84 fferents through a complex of axosomatic and axodendritic synapses.
85 , with a small percentage forming asymmetric axodendritic synapses.
86 ly suggested to mediate the formation of new axodendritic synaptic contacts.
87      Our results suggest that despite strong axodendritic synaptic depression, the balance of axodend
88 e have previously found that thalamostriatal axodendritic terminals are reduced as early as 1 month o
89 0 striata, as was the abundance of VGLUT2(+) axodendritic terminals making synaptic contact with ChAT
90  interneurons are a major target of thalamic axodendritic terminals, we examined the VGLUT2-immunolab
91 hat the PF is the sole source of significant axodendritic thalamic inputs to striatal projection neur
92 e reduction in the areal striatal density of axodendritic thalamic terminals on cholinergic neurons w
93                         The ratio of labeled axodendritic to axosomatic synapses encountered was roug
94 evealed septal boutons forming axosomatic or axodendritic type II synapses.
95                    Most of the terminals are axodendritic, with multiple asymmetric synapses, and con