ライフサイエンスコーパス: coincidence detector

1 ograde endocannabinoid signaling as a second coincidence detector.

2 c42 and phosphoinositides, the hallmark of a coincidence detector.

3 cally, where they cannot act as conventional coincidence detectors.

4 nal Mg2+ ions, thereby making them effective coincidence detectors.

5 Thus NL neurons act as coincidence detectors.

6 l Mg(2+) ions, thereby making them effective coincidence detectors.

7 nized into networks by molecules that act as coincidence detectors.

8 (N-methyl-D-aspartate) receptor, a synaptic coincidence detector, acts as a graded switch for memory

9 Cs function as a calcium- and cAMP-sensitive coincidence detector and mediate individual and synergis

10 onitoring of FDG accumulation with a pair of coincidence detectors and by cumulative release of 3HOH

11 at rectifying electrical synapses can act as coincidence detectors, and regulation of the strength of

12 f N-methyl-D-asparate receptor (NMDA-R)--the coincidence detector--and Ca(2+)/calmodulin-dependent pr

13 lipids, the PH domain of Sec3 functions as a coincidence detector at the plasma membrane.

14 es that at cell adhesion sites vinculin is a coincidence detector awaiting simultaneous signals from

15 The Jeffress model consists of an array of coincidence detectors--binaural neurones that respond ma

16 In contrast, PT dendrites acted as coincidence detectors by responding to spatially distrib

17 in Aplysia has been proposed as a molecular coincidence detector during conditioning.

18 d-spoke architecture may implement an analog coincidence detector enabling distinct responses to dist

19 observations show how ESCRT-I could act as a coincidence detector for acidic phospholipids and protei

20 hus, the presynaptic NMDAR may function as a coincidence detector for adjacent glutamatergic and GABA

21 Our results establish TRPM2 as a coincidence detector for ADPR and cADPR signaling and pr

22 a single, postsynaptic, NMDA receptor-based coincidence detector for LTP and LTD components of STDP.

23 nsitive adenylyl cyclase (AC) as a molecular coincidence detector for temporally paired stimuli durin

24 ed by PIP(3) and Gbetagamma and may act as a coincidence detector for these signaling molecules.

25 e possibility that ASIC channels function as coincidence detectors for extracellular protons and othe

26 rons of the owl's nucleus laminaris serve as coincidence detectors for measurement of interaural time

27 receptors (NMDARs) are classically known as coincidence detectors for the induction of long-term syn

28 utamate receptors that function as molecular coincidence detectors, have critical roles in models of

29 NMDARs suggest that they may be the Hebbian "coincidence detectors" hypothesized to underlie associat

30 se data suggest that rutabaga functions as a coincidence detector in an intact neuronal circuit, with

31 denylyl cyclase RUTABAGA is believed to be a coincidence detector in gamma neurons, one of the three

32 ese communication systems act as a three-way coincidence detector in the regulation of a variety of g

33 mputed using axonal delay lines and cellular coincidence detectors in nucleus laminaris (NL).

34 rather than uncaging, or by two independent coincidence detectors in series.

35 first in vivo intracellular recordings from coincidence detectors in the nucleus laminaris of barn o

36 l form of the rule is consistent with a dual coincidence detector mechanism that has been suggested b

37 neurons in the avian auditory brainstem are coincidence detectors necessary for the computation of i

38 se responses to construct inputs to binaural coincidence detector neurons in nucleus laminaris (NL).

39 e-timing precision of phase-locked inputs to coincidence detector neurons in nucleus laminaris and th

40 l axonal delay lines innervating an array of coincidence detector neurons that encode external ITDs.

41 The owl's nucleus laminaris contains coincidence detector neurons that receive input from the

42 e segregated dendritic regions of the MSO/NL coincidence detector neurons.

43 n in birds consist of axonal delay lines and coincidence detector neurons.

44 Coincidence-detector neurons in the auditory brainstem o

45 ximal activation within an array of binaural coincidence-detector neurons that are tuned to different

46 Thus, by functioning as a coincidence detector of chemotactic signals from both GP

47 omains, suggesting that this kinase may be a coincidence detector of signaling by Cdc42 and phosphoin

48 a and speculate that ASAP1 may function as a coincidence detector of simultaneous protein association

49 al data, we propose that Opy1 functions as a coincidence detector of the Mss4 PtdIns(4)P 5-kinase and

50 Thus, Cdc15 functions as a coincidence detector of two essential cell cycle oscilla

51 s in Purkinje cells, enabling them to act as coincidence detectors of parallel fibre input.

52 ane can provide the necessary delays, if the coincidence detectors receive input from fibers innervat

53 erspike interval, neurons act essentially as coincidence detectors, relay preferentially synchronized

54 This system functions as a chemical coincidence detector, releasing small molecules only in

55 -aspartate (NMDA) receptors are Hebbian-like coincidence detectors, requiring binding of glycine and

56 o answer whether cross-correlation describes coincidence detector responses and a demonstration that

57 Moreover, we show that a model of coincidence detector responses derived from responses to

58 s of the mushroom bodies, are able to act as coincidence detectors, sensitive to synchronized activit

59 esis were true, the left and right inputs to coincidence detectors should differ in their frequency t

60 de support for a processing of the output of coincidence detectors subserving low-frequency sound loc

61 th sharp frequency tuning act as narrow-band coincidence detectors; such neurons respond equally well

62 hus, a simple gap-junction circuit acts as a coincidence detector that allows primary sensory neurons

63 Sec24 can thus be considered a coincidence detector that binds simultaneously to multip

64 hus indicate that the Bim promoter acts as a coincidence detector that optimally responds to the simu

65 lso find that betaII-spectrin functions as a coincidence detector that requires recognition of both a

66 ns of the medial superior olive (MSO) act as coincidence detectors that fire when inputs from both ea

67 However, the coincidence detectors that link these pathways into netw

68 NL neurons act as coincidence detectors that respond maximally when input

69 nsing circuit may function exclusively as a 'coincidence detector' that discriminates between conditi

70 t has long been assumed that delay lines and coincidence detectors turn these time differences into a

71 nylyl cyclase (Rut-AC), a putative molecular coincidence detector vital for simultaneous conditioning

72 ial superior olive (MSO) are known to act as coincidence detectors, whereas in the lateral superior o

73 LapD appears to act as a coincidence detector, whereby a weak interaction of LapG

74 gulators of Pak1 and suggest that Pak1 is a "coincidence detector" whose activation depends on GTPase

75 wed that high afferent discharge rates cause coincidence detectors with only excitatory input to lose

76 But the firing probability of an ideal coincidence detector would depend on the temporal coinci