ライフサイエンスコーパス: axodendritic

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 We also demonstrated that axodendritic electrical coupling by projection interneur

37 ar to be transitional between axospinous and axodendritic junctions.

38 ynapses, whereas complexin II is a marker of axodendritic (mainly excitatory) synapses.

39 induction of LTP and are then converted into axodendritic ones during LTP maintenance.

40 An occasional asymmetric axodendritic or asymmetric axospinous synapse was observ

41 croscopic level IHC revealed the presence of axodendritic or axosomatic synapses between VIP-ir and P

42 afferent boutons received axoaxonic and made axodendritic or axosomatic synaptic contacts.

43 The patterns of axosomatic and axodendritic organization were determined for principal

44 functionally deficient PS1 exhibit enhanced axodendritic outgrowth due to increased levels of APP in

45 Neuronal precursor proliferation and axodendritic outgrowth have been regarded as strictly se

46 f local and long-range excitatory axons, but axodendritic overlap is not always a good predictor of a

47 Moreover, we found that the average axodendritic overlap of the presynaptic and postsynaptic

48 computed the geometric circuit predicted by axodendritic overlap.

49 ed D1 receptor binding in nucleus accumbens; axodendritic pathology and altered hippocampal cytoarchi

50 In mature neurons, TBB reduces the axodendritic polarity of FGF14.

51 rn of ERK activation was seen in superficial axodendritic processes of epileptic neocortex that coloc

52 es and postsynaptic structures, being either axodendritic (PV(+)) or axospinous (SOM(+)).

53 the human and rodent Tau isoforms differ in axodendritic sorting and amyloid-beta-induced missorting

54 ber of axosomatic and one-half the number of axodendritic spine synapses as females.

55 , the majority of SP-containing axons formed axodendritic symmetric synapses.

56 This was linked with greater axodendritic synapse density and ultrastructural charact

57 t significantly different from the length of axodendritic synapses (0.523 micron) or the area of term

58 rating CT terminal boutons formed asymmetric axodendritic synapses and contained small, clear, spheri

59 ority of labelled terminals formed symmetric axodendritic synapses and displayed gamma-aminobutyric a

60 These axodendritic synapses are anatomically separated from de

61 ere located in white matter and did not form axodendritic synapses but expressed presynaptic markers

62 The axospinous synapses outnumbered the axodendritic synapses by more than two to one.

63 egenerating into the nucleus gracilis formed axodendritic synapses containing rounded vesicles, refle

64 The number of axodendritic synapses in the glomeruli of OMP-null mice

65 nputs that could account for the increase in axodendritic synapses in the matrix, we undertook an ele

66 The number of asymmetrical axodendritic synapses increased (by 28%) during LTP main

67 newborn neurons do not receive axosomatic or axodendritic synapses indicating the absence of basket c

68 ber (AF) system in piriform cortex (PC) make axodendritic synapses on granule cells within the granul

69 labeled M72 glomeruli showed no evidence of axodendritic synapses other than those with GFP-labeled

70 linear rise in the number of axospinous and axodendritic synapses present in the neuropil.

71 ately 35-50% of all symmetric axospinous and axodendritic synapses were formed by TH-i boutons.

72 These afferents form axodendritic synapses with mitral/tufted and periglomeru

73 logical analyses, we found that densities of axodendritic synapses, especially axo-spinous synapses,

74 except for a few that established asymmetric axodendritic synapses.

75 occasionally were observed to form symmetric axodendritic synapses.

76 fferents through a complex of axosomatic and axodendritic synapses.

77 , with a small percentage forming asymmetric axodendritic synapses.

78 ly suggested to mediate the formation of new axodendritic synaptic contacts.

79 Our results suggest that despite strong axodendritic synaptic depression, the balance of axodend

80 e have previously found that thalamostriatal axodendritic terminals are reduced as early as 1 month o

81 0 striata, as was the abundance of VGLUT2(+) axodendritic terminals making synaptic contact with ChAT

82 interneurons are a major target of thalamic axodendritic terminals, we examined the VGLUT2-immunolab

83 hat the PF is the sole source of significant axodendritic thalamic inputs to striatal projection neur

84 e reduction in the areal striatal density of axodendritic thalamic terminals on cholinergic neurons w

85 The ratio of labeled axodendritic to axosomatic synapses encountered was roug

86 evealed septal boutons forming axosomatic or axodendritic type II synapses.

87 Most of the terminals are axodendritic, with multiple asymmetric synapses, and con