ライフサイエンスコーパス: accumulator

1 brain regions reflect the whole-animal level accumulator.

2 ormed into a binary decision by a downstream accumulator.

3 ependent updates to the initial state of the accumulator.

4 wer evidence), compatible with a symmetrical accumulator.

5 wer), compatible with an asymmetrical memory accumulator.

6 c transducer followed by a rise-to-threshold accumulator.

7 e constructed from a variety of neural-level accumulators.

8 ingly, the lag between the primary and motor accumulators.

9 s and RT is not governed by the most extreme accumulators.

10 de from a salience map to multiple competing accumulators.

11 in GlyBet levels as high as those in natural accumulators.

12 ion of the Arabidopsis sng2 (sinapoylglucose accumulator 2) mutant has identified another SCPL protei

13 hyperaccumulator A. murale compared with non-accumulator A. montanum.

14 s, and the alleles vis1-hta (high-transcript accumulator; accession no. AY128101) and vis1-lta (low t

15 n no. AY128101) and vis1-lta (low transcript accumulator; accession no. AY128102) are associated with

16 of mutations on the coding region of the non-accumulator AdSMT enzyme to better resemble enzymes that

17 ed nickel hyperaccumulator A. murale and non-accumulator Alyssum montanum.

18 Furthermore, the network acts as an evidence accumulator and maintains its decision even after the in

19 nus exhibited frequent flipping between wall accumulator and wall escaper regimes.

20 )/kg from CRTs, 27.0 kg CO(2)/kg from Li-ion accumulators and 25.9 kg CO(2)/kg from PCBs.

21 Biofilms act as accumulators and biodegraders of hydrophobic compounds.

22 n tested in a defined microbial community of accumulators and non-accumulators, duloxetine markedly a

23 cent lamps, cathode ray tubes (CRTs), Li-ion accumulators and printed circuit boards (PCBs).

24 that jointly depend on the state of multiple accumulators and speed-accuracy trade-offs.

25 Nitrate hyper-accumulators and wide genotypic differences in Na, K and

26 search arrays of different set sizes if the accumulators are mutually inhibitory.

27 ders depend on ion exclusion in roots, Na(+) accumulators are proficient Na(+) managers that can comp

28 (RT) that can be explained by a single model accumulator arise from numerous, redundant accumulator n

29 methyltransferase (SMT) enzyme from the non-accumulator Astragalus drummondii and biochemically comp

30 Peninsula) connect neighboring regions, and accumulators (Australia, India, Palawan, and the Philipp

31 Then a cryptographic accumulator-based data storage scheme is designed which

32 In contrast, both the Se accumulator Brassica juncea and the nonaccumulator Arabi

33 Salt-sensitive plants are Na(+) accumulators, but their inherent tissue tolerance abilit

34 arvense, Thlaspi caerulescens (a heavy metal accumulator) can grow in, tolerate, and accumulate very

35 phasic alertness but only when the evidence accumulators compete with each other through lateral inh

36 nd that the threshold measured on individual accumulators, corresponding to the firing rate of neuron

37 microbial community of accumulators and non-accumulators, duloxetine markedly altered the compositio

38 MT) shows a high degree of homology with the accumulator enzyme (AbSMT) but lacks the selenocysteine

39 The non-accumulator enzyme (AdSMT) shows a high degree of homolo

40 ully gain the activity observed in the AbSMT accumulator enzyme.

41 by the GIADA (Grain Impact Analyser and Dust Accumulator) experiment on the European Space Agency's R

42 of neural mechanisms was reconciled with the accumulator framework through an integrated accumulator

43 Accumulator frameworks of decision-making tacitly acknow

44 ither the roots or shoots of the superior Cd accumulator, Ganges.

45 two ALDH10 isoenzymes: those known to be GB accumulators have a high-BAL-affinity isoenzyme with Ala

46 eine in this critical position, while non GB accumulators have low-BAL-affinity isoenzymes containing

47 arker, he or she was likely to be a reliable accumulator in other biomarkers.

48 constructions identified 10 additional Abeta accumulators in the Abeta- group, resulting in a 22% inc

49 Kelp are main iodine accumulators in the ocean, and their growth and photosyn

50 nsport via NKCC1, the principal neuronal Cl- accumulator, in neonatal CA1 pyramidal neurons.

51 High nitrate accumulators included spinach, purslane, chards, dill, c

52 to TMs but that such high exposure due to TM accumulator items can be " diluted" by diet richness due

53 This strongly suggests that TM accumulator items can lead to a high oral exposure to TM

54 " diluted" by diet richness due to other low accumulator items.

55 ge dynamics of alphabeta(c) KCs thus form an accumulator memory for sequential samples of information

56 ess this limitation, we introduce the visual accumulator model (VAM), in which convolutional neural n

57 An accumulator model applied to these sensory representatio

58 Generalizing existing accumulator model assumptions from stationary to time-va

59 We developed a leaky accumulator model based on the MVT that generates estima

60 accumulator framework through an integrated accumulator model constrained by requirements of the mot

61 We describe a stochastic accumulator model demonstrating that visual search perfo

62 We fitted an accumulator model of RT to 46 female human participants'

63 By fitting an accumulator model of saccadic decision-making, we show t

64 A dual accumulator model recapitulates both mouse and human beh

65 lop a generalization of the leaky stochastic accumulator model using a Langevin equation whose non-li

66 This hysteresis was best explained by an accumulator model, in which individual decisions to join

67 Monkey behavior was well fit by a bounded accumulator model, where choice and confidence are proce

68 re well captured by a bound-adjustable leaky accumulator model.

69 xplained by psychologists through stochastic accumulator models and by neurophysiologists through the

70 into the neural instantiation of stochastic accumulator models and the mechanisms through which exec

71 Stochastic accumulator models commonly explain this speed-accuracy

72 fically consider neurobiologically-plausible accumulator models of decision-making, in which decision

73 y uncertainty and provide substantiation for accumulator models of human perceptual decision-making.

74 tiation have been identified with stochastic accumulator models of response time performance.

75 Stochastic accumulator models provide a comprehensive framework for

76 Thus, current stochastic accumulator models provide an incomplete description of

77 Although stochastic accumulator models relate SRT increases to reduced rates

78 Accumulator models that integrate incoming sensory infor

79 Previous work has shown that accumulator models, such as the drift-diffusion model, c

80 Comparing three plausible evidence accumulator models, we found that multisensory RT distri

81 K+-Cl- cotransporter, and NKCC, the chloride accumulator Na+-K+-Cl- cotransporter.

82 l accumulator arise from numerous, redundant accumulator neurons, each of which individually appears

83 rowing season, proving that foliage is a net accumulator of MeHg while foliar gain of biomass did not

84 hich was primarily due to boar meat (a known accumulator of radiocesium).

85 to play as a conductive holder as well as an accumulator of redox active centers on the surface of th

86 ective in jasmonic acid production and hyper-accumulator of SA), and mutants ics1 (depleted in SA acc

87 ammals, including humans, are indiscriminate accumulators of carotenoids but inefficiently distribute

88 Charophytes are therefore very efficient accumulators of hydrophobic compounds.

89 f the Laminariales (kelps) are the strongest accumulators of iodine among living organisms.

90 uggest that northern deltas may be important accumulators of river Hg in their floodplains before exp

91 Grasses are hyper-accumulators of silicon, which play a crucial function i

92 lerance, and salt-tolerant plants may (Na(+) accumulators) or may not (Na(+) excluders) allow sodium

93 nteractions between these material bits; and accumulator pathways which leverage these interactions t

94 nterestingly, gametophytes of the related As accumulator Pityrogramma calomelanos appear to tolerate

95 re we investigated a CysRS from the selenium accumulator plant Astragalus bisulcatus that is reported

96 d that consuming Salicaceae, a known cadmium accumulator plant family, significantly increased exposu

97 MeSeCys accumulation are observed in the non-accumulator plant.

98 lism of Se and may lead to ways to modify Se-accumulator plants with increased efficiency for phytore

99 y appears to restrict GB synthesis in non-GB-accumulator plants.

100 djustment of the leak in the secondary motor accumulator provides the better description of behavior

101 The dynamics of the stochastic accumulators quantitatively predict the activity of pres

102 dapts the "memory" with which this secondary accumulator reintegrates the primary accumulated sensory

103 c inhibitory process, in addition to the two accumulators representing the preparatory processes of i

104 specifying the goal, and compare it with the accumulator's current state [4].

105 In our tasks, the accumulator's memory was noiseless, for both rats and hu

106 measurement of the magnitude of noise in the accumulator's memory, separately from noise associated w

107 re largely invariant to ensemble size if the accumulators share at least modestly correlated accumula

108 These results suggest that in addition to accumulator signals, population responses on the scalp r

109 , MTP1 from various hyperaccumulator and non-accumulator species also confer similar resistance to Zn

110 tter resemble enzymes that originate from Se accumulator species results in increased selenocysteine

111 shoot tissue from T. goesingense and the non-accumulator species Thlaspi arvense revealed no major di

112 forager must recall a previous state of the accumulator specifying the goal, and compare it with the

113 y comparing it with the related secondary Se accumulator Stanleya albescens using a combination of ph

114 h a sun compass and an odometer to update an accumulator that records their current position [1].

115 ers, the best-connected traders, the hubs or accumulators, the modulators, the main flow routes, and

116 t, Thlaspi caerulescens, and the related non-accumulator Thlaspi arvense.

117 also amplifies competition between evidence accumulators, thus slowing down decision-making and impa

118 We used a leaky stochastic accumulator to model the neural decision of "when" to mo

119 and whether activity in the putative memory accumulator tracks the amount of evidence for only previ

120 mbles of redundant, idiosyncratic stochastic accumulators under various termination mechanisms and ac

121 el is that the level of inhibition that each accumulator unit receives from units with the opposite t

122 e demonstrate that a simple model with three accumulator units, two 'Go' and one 'Stop', can then acc

123 pare this framework against different single accumulator variants using formal model comparison, fitt

124 at Tempranillo blanco behaved as an arginine accumulator variety.

125 The number of Abeta accumulators was also used to compare the sensitivity of

126 regimes the termination times of individual accumulators was predictive of ensemble RT.

127 FOF activity was consistent with an accumulator where early evidence was favored while the A

128 ls that forms decisions by acting as a leaky accumulator with non-absorbing bounds.

129 f an individual was classified as a reliable accumulator with one biomarker, he or she was likely to

130 is designed which connects the cryptographic accumulator with the sharding nodes to save storage over