ライフサイエンスコーパス: coincidence detection

1 cause they constitute a feedback circuit for coincidence detection.

2 s are chemical compartments that can perform coincidence detection.

3 from noise is provided by an extreme form of coincidence detection.

4 delay as an intrinsic part of the process of coincidence detection.

5 ium channels in the dendrites modulates such coincidence detection.

6 rce with full three-dimensional electron-ion coincidence detection.

7 threshold and timing variability, as well as coincidence detection.

8 output by neurons, allowing integration and coincidence detection.

9 ents and integrated through Ret using ligand coincidence detection.

10 nductance demonstrated its essential role in coincidence detection.

11 directly counted without employing two-color coincidence detection.

12 ing the operational mode from integration to coincidence detection.

13 g functions of both temporal integration and coincidence detection.

14 lation, providing a second demonstration for coincidence detection.

15 ed signals to nucleus laminaris for binaural coincidence detection.

16 odel and examined how specific parameters of coincidence detection affect monaural and binaural AM co

17 data suggest that KA1 domains contribute to "coincidence detection," allowing kinases to bind other r

18 ts at cortical output layer 5, demonstrating coincidence detection along the apical dendrites.

19 ated, but all proposals include a process of coincidence detection and a separate source of internal

20 t intensities, using an analysis inspired by coincidence detection and by the binaural "latency hypot

21 Coincidence detection and crosstalk between signal trans

22 ate cells achieve temporal precision through coincidence detection and disynaptic inhibition, despite

23 ad gamma camera capable of FDG imaging using coincidence detection and equipped with an integrated x-

24 iation from the RPT radionuclide may disturb coincidence detection and impair image resolution.

25 These mechanisms allow for both coincidence detection and input selection in this integr

26 important computational properties, such as coincidence detection and input specificity, critical fo

27 binaural glutamatergic EPSCs, thus refining coincidence detection and interaural timing differences.

28 spikes from other spikes and thereby permit coincidence detection and rate coding to operate in para

29 calcium (Ca2+) nonlinearities allow neuronal coincidence detection and site-specific plasticity.

30 role in maintaining the temporal fidelity of coincidence detection and suggest a previously unrecogni

31 a mechanism for the lack of desensitization, coincidence detection, and allodynia that characterize p

32 ptors, regulates neuronal firing, influences coincidence detection, and can synchronize the output of

33 speed; the second transformation implements coincidence detection, and it improves speed but not pea

34 egardless of how the images are interpreted, coincidence detection-based (18)F-FDG imaging is less ac

35 is physiological setup to be well suited for coincidence detection between basal and apical tuft inpu

36 abled first ring of detectors, which permits coincidence detection between the 2 systems.

37 e submillisecond time resolution of binaural coincidence detection, but little is known about their i

38 Coincidence detection by coactivation of the specific (V

39 hronization of its output as a framework for coincidence detection by its target, the mushroom body (

40 revealed forms of plasticity that depend on coincidence detection by presynaptic NMDA receptors.

41 l activation, illustrating the potential for coincidence detection by TRP channels.

42 how synaptic plasticity can affect temporal coincidence detection, by experimentally characterizing

43 we show that the time resolution of synaptic coincidence detection can be maintained during trains if

44 n ability, and changes in the time course of coincidence detection can be ruled out as alternative ex

45 External scintillation probes with coincidence detection circuitry were used to measure myo

46 an central nervous system, the mechanisms of coincidence detection described here may be widely used

47 understanding the signalling mechanisms for coincidence detection during associative learning.

48 ecruits l-type Ca(2+) channels to facilitate coincidence detection during t-LTP induction.

49 he number of coincident events and using the coincidence detection efficiency, it is possible to dete

50 This coincidence detection enables crayfish to produce reflex

51 nd that a decoding strategy that is based on coincidence detection enhances both noise tolerance and

52 ial for basic neuronal computations, such as coincidence detection, grouping by synchrony, and spike-

53 ability of Ca2+ to directly mediate Hebbian coincidence detection has been confirmed.

54 in the lateral superior olive (LSO) roles of coincidence detection have remained unclear.

55 The model supports the coincidence detection hypothesis, and suggests that diff

56 chlea could provide the delays necessary for coincidence detection if the ipsilateral and contralater

57 We report our experience with coincidence detection imaging of 18F-fluorodeoxyglucose

58 Had the findings of the coincidence detection imaging study been considered, the

59 embrane, where they act via Ca(2+) to signal coincidence detection in Hebbian plasticity.

60 idence for a novel presynaptic mechanism for coincidence detection in induction of timing-dependent L

61 r olivary nucleus (SON) that greatly improve coincidence detection in mature animals.

62 f NM neurons, which is essential to binaural coincidence detection in nucleus laminaris.

63 ditional electronic collimation achieved via coincidence detection in PET.

64 riphosphate receptor type 1), that underlies coincidence detection in Purkinje cells and could play a

65 process sound-localization cues via binaural coincidence detection, in which excitatory synaptic inpu

66 We show here that extremely precise coincidence detection is a natural consequence of the no

67 Two-color coincidence detection is a single-molecule fluorescence

68 Coincidence detection is important for functions as dive

69 ect do not have to be detected at all and no coincidence detection is necessary.

70 unted for by existing models and reveal that coincidence detection is not an instantaneous process, b

71 mation and integration to the submillisecond coincidence detection known to be required for transmiss

72 This novel form of coincidence detection may explain the temporal window of

73 Thus, we show that a coincidence detection mechanism coordinates inputs from

74 Our results reveal how a fundamental coincidence-detection mechanism in a neural circuit func

75 cortex involves separate calcium sources and coincidence detection mechanisms for LTP and LTD.

76 t the entire N terminus of mDia2 serves as a coincidence detection module, directing mDia2 to the pla

77 n birds) projecting to binaurally innervated coincidence detection neurons in the medial superior oli

78 n neurons in the nucleus magnocellularis and coincidence detection neurons in the nucleus laminaris i

79 rm depression in Purkinje neurons depends on coincidence detection of climbing fiber stimulus evoking

80 These modeling results suggest that coincidence detection of excitatory and inhibitory synap

81 Instead, coincidence detection of inputs from two converging endb

82 asmonate coreceptor complex and suggest that coincidence detection of jasmonate and InsP8 by COI1-JAZ

83 cted intracellular targeting, which requires coincidence detection of multiple signals (Ca2+ and one

84 ical model of interval timing based upon the coincidence detection of oscillatory processes in cortic

85 gnostic applications, we show that two-color coincidence detection of single-stranded DNA molecules,

86 We propose that second messenger coincidence detection of this type may explain how GLP-1

87 -TCR induced metabolic activation to enforce coincidence-detection of pre-TCR expression and Notch-en

88 Recent genetic experiments that enhanced coincidence-detection of the NMDA receptor (a molecular

89 lls, we show here that dendrites improve the coincidence-detection properties of the cells.

90 Here, we argue that coincidence detection, rather than temporal integration,

91 This phenomenon, generally termed "coincidence detection," requires a downstream signaling

92 tum dot (QD)-mediated two-color fluorescence coincidence detection scheme.

93 emory mechanism that requires high-precision coincidence detection suitable for high-fidelity circuit

94 lucose and amino acids represents a nutrient coincidence detection system shared in other pathogenic

95 re to investigate (18)F-FDG imaging, using a coincidence detection system, for diagnosing prosthetic

96 ple microfluidic device to perform two-color coincidence detection (TCCD) and single pair Forster res

97 d of single-molecule fluorescence, two-color coincidence detection (TCCD) to detect coincident events

98 een able to employ single-molecule two-color coincidence detection (TCCD) to observe directly the for

99 anism opens a discriminatory time window for coincidence detection that enables selective facilitatio

100 and subthreshold inputs results in molecular coincidence detection that gives rise to a novel form of

101 s also indicate the existence of presynaptic coincidence detection that is independent of NMDA recept

102 Here, we elucidate the structural basis of coincidence detection that relies on both c-di-GMP and L

103 the ability of pyramidal neurons to perform coincidence detection, that is, to represent input timin

104 ls can combine two functions-integration and coincidence detection-that are normally considered mutua

105 In addition to promoting coincidence detection, the threshold dynamics associated

106 As dendritic complex spikes can serve coincidence detection, these cortical interneuronal circ

107 Such temporal filtering imparts coincidence detection to Ca(2+)-dependent gene activatio

108 We have used two-color fluorescence coincidence detection to directly count individual prote

109 The auditory system uses delay lines and coincidence detection to measure the interaural time dif

110 od should allow the application of two-color coincidence detection to more complex biological systems

111 piking responses to whisker stimulation from coincidence detection to temporal integration.

112 PSP amplification may regulate the impact of coincidence detection versus temporal integration mechan

113 ls with lower fidelity, and the precision of coincidence detection was degraded.

114 ayer 4 circuits are better suited to perform coincidence detection, whereas supra and infragranular c

115 in beta cells a process of second messenger coincidence detection, whereby intracellular Ca2+ releas

116 -simultaneous synaptic inputs, the window of coincidence detection widened significantly with increas

117 a key neuromodulation pathway, modifies the coincidence detection window during Hebbian plasticity t

118 This implies that enhanced synaptic coincidence detection would lead to better learning and