ライフサイエンスコーパス: presynaptic cell

1 tsynaptic neuron but only translation in the presynaptic cell.

2 d in response to the stimulation of a single presynaptic cell.

3 gulating transmission at all synapses of the presynaptic cell.

4 o decreased potassium-current density in the presynaptic cell.

5 ion during high-frequency stimulation of the presynaptic cell.

6 rgic suppression of transmitter release from presynaptic cells.

7 the direct inputs, due to the lack of RG in presynaptic cells.

8 required for synaptic growth and function in presynaptic cells.

9 eceptor cells or in GAD1-expressing type III/presynaptic cells.

10 l-cell signalling between receptor cells and presynaptic cells.

11 or cells, glial-like cells or GAD-expressing presynaptic cells.

12 hat receptor cells transmit their signals to presynaptic cells.

13 hese signals serve to adjust the activity of presynaptic cells according to postsynaptic cell outputs

14 Neurexin 1 (NRXN1), a presynaptic cell adhesion molecule, is implicated in sev

15 ssociation between alpha4beta2 AChRs and the presynaptic cell adhesion molecule, neurexin-1beta.

16 Neurexins are essential presynaptic cell adhesion molecules that are linked to s

17 tations of the NRXN1 gene, which encodes the presynaptic cell-adhesion molecule neurexin-1, were repe

18 alpha- and beta-neurexins are presynaptic cell-adhesion molecules implicated in autism

19 eins that form tripartite complexes with the presynaptic cell-adhesion molecules neurexins or 'delete

20 Neurexins are evolutionarily conserved presynaptic cell-adhesion molecules that are essential f

21 Neurexins are presynaptic cell-adhesion molecules that bind to postsyn

22 Neurexins are presynaptic cell-adhesion molecules that form trans-syna

23 alpha- and beta-neurexins are presynaptic cell-adhesion molecules whose general import

24 requires activation of NMDA receptors on the presynaptic cell and postsynaptic calcium-dependent vesi

25 l agents can be directly introduced into the presynaptic cell and that a purely presynaptic perturbat

26 imize the many steps between the firing of a presynaptic cell and the response of its postsynaptic ta

27 eurons looking for synchrony in ensembles of presynaptic cells and allows a low-dimensional descripti

28 Within the taste bud, ChrgA is found only in presynaptic cells and may account for dense-cored vesicl

29 Ca(v)2.1 (a P/Q subunit) is expressed in all presynaptic cells, and underlies depolarization-triggere

30 In contrast, presynaptic cells are broadly tuned: 83% responded to tw

31 uggest that inputs from different classes of presynaptic cells are weighted differently, depending on

32 th these ecto-nucleotidases are expressed by Presynaptic cells, as shown by single-cell RT-PCR, enzym

33 When expressed in the presynaptic cell at synapses between embryonic hippocamp

34 bodies or of MAPK Kinase inhibitors into the presynaptic cell blocks long-term facilitation, without

35 sed a striatum-only preparation in which the presynaptic cell body is cut off, leaving intact only it

36 es synthesis of phospholipids, likely in the presynaptic cell, but not the endocannabinoids 2-arachid

37 4) further expand upon the role of CaMKII in presynaptic cells by demonstrating a role in regulating

38 Here, we report that the presynaptic cell class determines functional properties

39 ell communication between receptor cells and presynaptic cells, consistent with ATP being the transmi

40 We also provide direct evidence that presynaptic cell contact-mediated, clustering of postsyn

41 Also, individual presynaptic cells contact several postsynaptic cell type

42 Three classes of presynaptic cell could be defined, based on their effere

43 ild-type fusl transgene targeted only to the presynaptic cell, demonstrating a strictly presynaptic r

44 pses open to bidirectional current flow when presynaptic cells depolarize relative to their postsynap

45 nt of retrograde signaling through exosomes, presynaptic cells enable retrograde signaling.

46 All presynaptic cells established multiple synaptic junction

47 In contrast, presynaptic cells express the GABA(A) beta3 subunit and

48 ed to synaptic sites and are required within presynaptic cells for structural and functional maturati

49 ingle-cell RT-PCR on functionally identified presynaptic cells from GAD-GFP mice confirmed the pharma

50 with 5-HT and noradrenaline being limited to presynaptic cells, GABA being synthesized in both presyn

51 Because SPNs receive inputs from presynaptic cells in different cortical layers, we inves

52 elease of retrograde signals and the role of presynaptic cells in this signaling event are unknown.

53 -mediated bursts of action potentials in the presynaptic cell increased these PSPs to an average of 4

54 late the inputs generated by a population of presynaptic cells into either the dendrite or the soma o

55 ust be realized with <50% probability if the presynaptic cell is excitatory and >50% probability if t

56 ll is excitatory and >50% probability if the presynaptic cell is inhibitory.

57 tethers connecting synaptic vesicles to the presynaptic cell membrane.

58 s primarily on the excitability of GABAergic presynaptic cells, most likely via alterations of voltag

59 cAMP, triggered Ca(2+) transients in 38% of presynaptic cells (n = 128).

60 providing evidence that transcription in the presynaptic cell nucleus is not necessary for this form

61 be controlled by activity levels in multiple presynaptic cells or by adjusting release probability at

62 tosolic free Ca(2+) either in RGCs, in their presynaptic cells, or in both.

63 ons to the activation of their corresponding presynaptic cell populations.

64 ional differences between receptor cells and presynaptic cells, provide strong evidence for communica

65 Presynaptic cells responded to all taste qualities, incl

66 Physiological patterns of stimulation in the presynaptic cell revealed two populations of postsynapti

67 f neurons, thus indicating connectivity with presynaptic cell(s).

68 alpha1 chain was selectively associated with presynaptic cells (Schwann cells and/or nerve terminals)

69 ors (sensitive to 5-HT and NE), we found all presynaptic cells secrete 5-HT and 33% corelease NE with

70 alpha-Neurexins (alpha-Nrxn) are mostly presynaptic cell surface molecules essential for neurotr

71 In addition, mAChRs showed decreased presynaptic, cell surface, and dendritic distributions a

72 Alpha-neurexins, a family of >1,000 presynaptic cell-surface proteins encoded by three genes

73 , where communication between RGCs and their presynaptic cells takes place.

74 Ca(2+) responses occur only in the subset of presynaptic cells that lack glutamic acid decarboxylase

75 ed by the number of release sites (N) on the presynaptic cell, the probability (p) of transmitter rel

76 of nitric-oxide (NO) formation feeds back to presynaptic cells to S-nitrosylate SR and decrease D-ser

77 wever, neurotrophins can also be released by presynaptic cells to stimulate postsynaptic neurons.

78 dividual postsynaptic cell, but how a single presynaptic cell type diverges to form distinct wiring p

79 individual synapse is unique, a function of presynaptic cell type, postsynaptic cell type, environme

80 Inputs from different presynaptic cell types converge onto a common postsynapt

81 Recent work has focused on how distinct presynaptic cell types form stereotypic connections with

82 To integrate information from different presynaptic cell types, dendrites receive distinct patte

83 e cells, Type II/receptor cells, or Type III/presynaptic cells) undergo taste-evoked changes of cAMP

84 inct expression pattern of GABA receptors in presynaptic cells, we detected no GABAergic suppression

85 nd to consider effects on firing patterns of presynaptic cells, which in turn influence release via u