ライフサイエンスコーパス: autapse

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1 neurons that had formed recurrent synapses (autapses).

2 Some neurons have long collaterals that form autapses.

3 R) and release probability (Pr), compared to autapses.

4 ts modulation by BDNF in mouse glutamatergic autapses.

5 o acid-activated currents in neurons lacking autapses.

6 d 1 of 2 close appositions were confirmed as autapses.

7 ransmission at inhibitory but not excitatory autapses.

8 entials are produced by GABAergic excitatory autapses.

9 was evoked in the axon of a POMC neuron with autapses, a short-latency synaptic current was recorded

10 ll class determines functional properties of autapses and cannabinoid-mediated modulation of synaptic

11 compared synaptic transmission in excitatory autapses and in two-neuron micronetworks consisting of t

12 Axo-axonic cells never establish autapses, and the fast-spiking variety showed narrow (HW

13 sion of transmission in cultured hippocampal autapses; and we perform whole-cell recording, FM imagin

14 Autapses are connections between a neuron and itself.

15 However, autapses are deficient in several aspects of synaptic pl

16 These results show that autapses are not rudimentary nonfunctional structures, b

17 Autapses are synapses made by a neuron onto itself.

18 1 and -2, largely carried out in hippocampal autapses, did not detect changes in the RRP size or in s

19 and morphological experiments in cholinergic autapses established by superior cervical ganglion neuro

20 ptic transmission at more mature synapses or autapses formed in this culture system and are reminisce

21 Autapses from GAD67-gfp-positive neurons were uniformly

22 In contrast, autapses from the GAD67-gfp-negative POMC neurons exclus

23 ough morphological evidence for existence of autapses has been reported in several brain areas, it is

24 mossy fiber long-term potentiation (LTP) at autapses in single-cell cultures of guinea pig hippocamp

25 the optically estimated distribution of p at autapses in single-neuron microislands predicts, with no

26 Autapses, in which the same cell is both presynaptic and

27 oreover, dynamic clamp experiments that show autapse-induced firing in entorhinal cortical interneuro

28 ere much more likely to display both PIR and autapse-induced firing than GAD2(+) cells, supporting th

29 These autapses influence neuronal firing and responses to GABA

30 In hippocampal autapses, PACAP treatment uncoupled postsynaptic mGluR5

31 The number of autapses required to induce bursting was lowered by addi

32 ons, realistic dynamic-clamp hyperpolarizing autapses restored precision of spike timing, even in the

33 In autapses (self-synapses) formed by cultured hippocampal

34 activated after each spike, suggesting that autapses strongly regulate FS-cell spike timing.

35 rticular, Dm9 and Mi1, form >/= 20-fold more autapses than do other neurons.

36 In hippocampal autapses, this eNMDAR activity is followed by reduction

37 red to induce bursting was lowered by adding autapses to high degree excitatory neurons.

38 neurons that had formed recurrent synapses (autapses) to detect the release of neurotransmitter.

39 ampal cells in culture form onto themselves (autapses) to determine if some synapses lack functional

40 g in rat sympathetic neurons and hippocampal autapses using pituitary adenylate cyclase activating pe

41 One 'autapse' was demonstrated.

42 SACs form autapses when self-avoidance is disrupted and fail to fo

43 We examine the role of structural autapses, when a neuron synapses onto itself, in driving

44 eurons, ES neurons had strong and depressing autapses, which enhanced spike-timing precision.

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