ライフサイエンスコーパス: accumulator

1 wer evidence), compatible with a symmetrical accumulator.

2 wer), compatible with an asymmetrical memory accumulator.

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

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

5 de from a salience map to multiple competing accumulators.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

35 Stochastic accumulator models commonly explain this speed-accuracy

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

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

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

39 Stochastic accumulator models provide a comprehensive framework for

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

41 Although stochastic accumulator models relate SRT increases to reduced rates

42 Accumulator models that integrate incoming sensory infor

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

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

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

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

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

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

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

50 Charophytes are therefore very efficient accumulators of hydrophobic compounds.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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