ライフサイエンスコーパス: coincidence detection

1 control the effect of extracellular GABA on coincidence detection.

2 g functions of both temporal integration and coincidence detection.

3 lation, providing a second demonstration for coincidence detection.

4 ed signals to nucleus laminaris for binaural coincidence detection.

5 cause they constitute a feedback circuit for coincidence detection.

6 s are chemical compartments that can perform coincidence detection.

7 tivation and is, therefore, advantageous for coincidence detection.

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

9 rapid recovery that enhances high-frequency coincidence detection.

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

11 ium channels in the dendrites modulates such coincidence detection.

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

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

14 output by neurons, allowing integration and coincidence detection.

15 ents and integrated through Ret using ligand coincidence detection.

16 nductance demonstrated its essential role in coincidence detection.

17 directly counted without employing two-color coincidence detection.

18 ing the operational mode from integration to coincidence detection.

19 s required for PKA activation resulting from coincidence detection, a mechanism by which the MB integ

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

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

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

23 e were developed to establish the additional coincidence detection among the outserts and the scanner

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

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

26 Coincidence detection and crosstalk between signal trans

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

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

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

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

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

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

33 erent functional processing tasks, including coincidence detection and pattern recognition, at ultraf

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

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

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

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

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

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

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

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

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

43 tivity does not derive from across-frequency coincidence detection but hinges on the amplitudes and a

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

45 Coincidence detection by coactivation of the specific (V

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

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

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

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

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

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

52 the Siah2 E3 ubiquitin ligase functions in a coincidence detection circuit linking responses to the S

53 adhesion and Netrin-1 signaling comprises a coincidence detection circuit repelling maturing neurons

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

55 ARF6 in neutrophil polarization as being the coincidence-detection code with PM PtdIns4P.

56 Both effects improve binaural coincidence detection compared with single large synapse

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

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

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

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

61 This coincidence detection enables crayfish to produce reflex

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

63 This leads us to propose a protein-lipid coincidence detection framework for kinesin-1-mediated o

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

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

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

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

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

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

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

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

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

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

74 (axon and axon initial segment) can enhance coincidence detection in MSO neurons.

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

76 ditional electronic collimation achieved via coincidence detection in PET.

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

78 different GABAergic mechanism might control coincidence detection in such cases.

79 eir dendrites that enhance opportunities for coincidence detection in the cell body, thereby allowing

80 the PKA activation process that results from coincidence detection in the MB.

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

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

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

84 Coincidence detection is important for functions as dive

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

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

87 ga-encoded adenylate cyclase, which mediates coincidence detection, is required for learning and shor

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

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

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

91 CFAP36 uses a coincidence detection mechanism to simultaneously bind t

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

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

94 by all endbulbs onto a GBC are subthreshold (coincidence detection mode), or one or two inputs are su

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

96 tegration in this blue light-low temperature coincidence detection module.

97 -to-soma coupling, IKLT in the axon enhances coincidence detection more effectively than IKLT in the

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

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

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

101 d functional assays, reveals how GOLPH3 uses coincidence detection of COPI and lipids to engage Golgi

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

103 Coincidence detection of excitatory inputs by principal

104 Instead, coincidence detection of inputs from two converging endb

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

106 Therefore, coincidence detection of local and global signals follow

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

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

109 Thus, coincidence detection of poly-lysine in the exit tunnel

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

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

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

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

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

115 Here, we show that the coincidence detection property of a spiking-based feed-f

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

117 at the strong effect of membrane shunting on coincidence detection relies on nonlinear amplification

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

119 5 is enhanced in starved cells and occurs by coincidence detection, requiring both phosphatidylinosit

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

121 nt neuron model and characterize extensively coincidence detection sensitivity throughout a parameter

122 We find that IKLT further enhances coincidence detection sensitivity, but with effects that

123 the computation capacity of neurons through coincidence detection, signal amplification, and additio

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

140 ve (MSO), these refinements generate precise coincidence detection to localize sounds in the azimutha

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

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

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

144 Two-color coincidence detection using the fluorescent capsid as th

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

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

147 ers in individual aggregates using two-color coincidence detection, we derived compositional profiles

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

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

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

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

152 Elevations of extracellular GABA narrow the coincidence detection window for excitatory inputs to CA

153 ing GABAergic signalling strongly widens the coincidence detection window of direct excitatory inputs

154 c neuromodulation arises from action-outcome coincidence detection within the raphe.

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