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1 ograde endocannabinoid signaling as a second coincidence detector.
2 c42 and phosphoinositides, the hallmark of a coincidence detector.
3 he idea that LITE-1 is a photon and H(2)O(2)-coincidence detector.
4  the mammalian auditory brainstem are superb coincidence detectors.
5 cally, where they cannot act as conventional coincidence detectors.
6 l Mg(2+) ions, thereby making them effective coincidence detectors.
7 nal Mg2+ ions, thereby making them effective coincidence detectors.
8                       Thus NL neurons act as coincidence detectors.
9 nized into networks by molecules that act as coincidence detectors.
10  (N-methyl-D-aspartate) receptor, a synaptic coincidence detector, acts as a graded switch for memory
11 Cs function as a calcium- and cAMP-sensitive coincidence detector and mediate individual and synergis
12 onitoring of FDG accumulation with a pair of coincidence detectors and by cumulative release of 3HOH
13 at rectifying electrical synapses can act as coincidence detectors, and regulation of the strength of
14 hanisms, single-input sensory systems versus coincidence detectors, and tuning of input-output dynami
15  circuit is composed of delay line inputs to coincidence detectors, and we predicted that plastic cha
16 f N-methyl-D-asparate receptor (NMDA-R)--the coincidence detector--and Ca(2+)/calmodulin-dependent pr
17 lipids, the PH domain of Sec3 functions as a coincidence detector at the plasma membrane.
18 es that at cell adhesion sites vinculin is a coincidence detector awaiting simultaneous signals from
19   The Jeffress model consists of an array of coincidence detectors--binaural neurones that respond ma
20        They are considered prime examples of coincidence detectors but are poorly characterized in vi
21           In contrast, PT dendrites acted as coincidence detectors by responding to spatially distrib
22 , Rutabaga (Rut) adenylate cyclase acts as a coincidence detector during associative conditioning to
23  in Aplysia has been proposed as a molecular coincidence detector during conditioning.
24 d-spoke architecture may implement an analog coincidence detector enabling distinct responses to dist
25 observations show how ESCRT-I could act as a coincidence detector for acidic phospholipids and protei
26 hus, the presynaptic NMDAR may function as a coincidence detector for adjacent glutamatergic and GABA
27             Our results establish TRPM2 as a coincidence detector for ADPR and cADPR signaling and pr
28 +)/calmodulin-dependent manner, serving as a coincidence detector for associative learning and likely
29  a single, postsynaptic, NMDA receptor-based coincidence detector for LTP and LTD components of STDP.
30  in the medial superior olive, an ultra-fast coincidence detector for sound source localization, acqu
31 nsitive adenylyl cyclase (AC) as a molecular coincidence detector for temporally paired stimuli durin
32 ed by PIP(3) and Gbetagamma and may act as a coincidence detector for these signaling molecules.
33 amma and Galpha(q) and have been shown to be coincidence detectors for dual stimulation of Galpha(q)
34 e possibility that ASIC channels function as coincidence detectors for extracellular protons and othe
35 rons of the owl's nucleus laminaris serve as coincidence detectors for measurement of interaural time
36  receptors (NMDARs) are classically known as coincidence detectors for the induction of long-term syn
37  NMDA glutamate receptors, GLRs may serve as coincidence detectors gated by the combined requirement
38 utamate receptors that function as molecular coincidence detectors, have critical roles in models of
39 NMDARs suggest that they may be the Hebbian "coincidence detectors" hypothesized to underlie associat
40 se data suggest that rutabaga functions as a coincidence detector in an intact neuronal circuit, with
41 denylyl cyclase RUTABAGA is believed to be a coincidence detector in gamma neurons, one of the three
42 hat Fru(M) functions as a downstream genomic coincidence detector in Or47b ORNs-integrating reproduct
43 ese communication systems act as a three-way coincidence detector in the regulation of a variety of g
44        We show that the QS system works as a coincidence detector in which both autoinducers must be
45 mputed using axonal delay lines and cellular coincidence detectors in nucleus laminaris (NL).
46  rather than uncaging, or by two independent coincidence detectors in series.
47  first in vivo intracellular recordings from coincidence detectors in the nucleus laminaris of barn o
48 l form of the rule is consistent with a dual coincidence detector mechanism that has been suggested b
49  neurons in the avian auditory brainstem are coincidence detectors necessary for the computation of i
50 in contacts for imitating the spatial map of coincidence detector neurons and tunable RC circuits for
51 se responses to construct inputs to binaural coincidence detector neurons in nucleus laminaris (NL).
52 e-timing precision of phase-locked inputs to coincidence detector neurons in nucleus laminaris and th
53 l axonal delay lines innervating an array of coincidence detector neurons that encode external ITDs.
54         The owl's nucleus laminaris contains coincidence detector neurons that receive input from the
55                                              Coincidence detector neurons transmit timing information
56 e segregated dendritic regions of the MSO/NL coincidence detector neurons.
57 n in birds consist of axonal delay lines and coincidence detector neurons.
58                                              Coincidence-detector neurons in the auditory brainstem o
59 ximal activation within an array of binaural coincidence-detector neurons that are tuned to different
60                    Thus, by functioning as a coincidence detector of chemotactic signals from both GP
61 omains, suggesting that this kinase may be a coincidence detector of signaling by Cdc42 and phosphoin
62 a and speculate that ASAP1 may function as a coincidence detector of simultaneous protein association
63 al data, we propose that Opy1 functions as a coincidence detector of the Mss4 PtdIns(4)P 5-kinase and
64                   Thus, Cdc15 functions as a coincidence detector of two essential cell cycle oscilla
65 we show that all three receptors function as coincidence detectors of H(+) and Na(+).
66 s in Purkinje cells, enabling them to act as coincidence detectors of parallel fibre input.
67 ic plasticity due to their ability to act as coincidence detectors of presynaptic and postsynaptic ne
68 hough we consider the particular case of MSO coincidence detectors, our method for creating and explo
69    AC isoforms have been suggested to act as coincidence detectors, promoting cellular responses only
70 ane can provide the necessary delays, if the coincidence detectors receive input from fibers innervat
71 erspike interval, neurons act essentially as coincidence detectors, relay preferentially synchronized
72          This system functions as a chemical coincidence detector, releasing small molecules only in
73 -aspartate (NMDA) receptors are Hebbian-like coincidence detectors, requiring binding of glycine and
74 o answer whether cross-correlation describes coincidence detector responses and a demonstration that
75            Moreover, we show that a model of coincidence detector responses derived from responses to
76 s of the mushroom bodies, are able to act as coincidence detectors, sensitive to synchronized activit
77 esis were true, the left and right inputs to coincidence detectors should differ in their frequency t
78 at selected GABA(A)R arrangements can act as coincidence detectors, simultaneously responding to two
79 de support for a processing of the output of coincidence detectors subserving low-frequency sound loc
80 th sharp frequency tuning act as narrow-band coincidence detectors; such neurons respond equally well
81 hus, a simple gap-junction circuit acts as a coincidence detector that allows primary sensory neurons
82               Sec24 can thus be considered a coincidence detector that binds simultaneously to multip
83 hus indicate that the Bim promoter acts as a coincidence detector that optimally responds to the simu
84 tly controlled and identify TPC2 as a likely coincidence detector that optimizes lysosomal Ca(2+) sig
85 lso find that betaII-spectrin functions as a coincidence detector that requires recognition of both a
86            Here, we show that many GPCRs are coincidence detectors that couple proton (H(+)) binding
87 ns of the medial superior olive (MSO) act as coincidence detectors that fire when inputs from both ea
88                                 However, the coincidence detectors that link these pathways into netw
89                            NL neurons act as coincidence detectors that respond maximally when input
90 nsing circuit may function exclusively as a 'coincidence detector' that discriminates between conditi
91  but not CAI-1, contribute to satisfying the coincidence detector to repress biofilm formation and pr
92 t has long been assumed that delay lines and coincidence detectors turn these time differences into a
93 nylyl cyclase (Rut-AC), a putative molecular coincidence detector vital for simultaneous conditioning
94 ial superior olive (MSO) are known to act as coincidence detectors, whereas in the lateral superior o
95                     LapD appears to act as a coincidence detector, whereby a weak interaction of LapG
96 gulators of Pak1 and suggest that Pak1 is a "coincidence detector" whose activation depends on GTPase
97 wed that high afferent discharge rates cause coincidence detectors with only excitatory input to lose
98       But the firing probability of an ideal coincidence detector would depend on the temporal coinci