ライフサイエンスコーパス: temporal difference

1 Using a temporal difference algorithm to model learning, we foun

2 complicated approval processes, high costs, temporal differences among the registries, and registry

3 The temporal differences and the evidence of repression indi

4 ork has been done to determine whether these temporal differences are actually used in discriminating

5 These temporal differences are greater than expected from neur

6 owever, in early visual pathways, well known temporal differences are present between center and surr

7 ssed but how this variability relates to the temporal differences at central synapses is incompletely

8 resentation at that site may account for the temporal difference between retinal and anterior segment

9 The temporal difference between the tethered and swimming ce

10 The temporal differences between each of these inputs sugges

11 e models is experiential and reports ongoing temporal differences between expected and experienced re

12 ng changes are generally consistent with the temporal differences between spatiotemporal receptive fi

13 This study of the geochemical and temporal differences between the NW and SE Elysium lava

14 We interpret the geochemical and temporal differences between the SE and NW lava fields t

15 Temporal differences between well types were also observ

16 des a biologically predictive alternative to temporal difference conditioning models and explains sub

17 inhibitors (TIMPs), was selective and showed temporal differences during the development of fibrosis.

18 een grass and mite allergen components, with temporal differences (early vs late onset) dominant in g

19 was received as learned, withheld (negative temporal difference error (NTDE)), or received unexpecte

20 (NTDE)), or received unexpectedly (positive temporal difference error (PTDE)).

21 mediated by brain regions that also support temporal difference error (TDE) processing; yet, the imp

22 o 4 degrees C suggests that quantitative and temporal differences exist between these molecular respo

23 Moreover, a temporal difference exists with respect to the timing of

24 operator head radiation exposure (mean left temporal difference [external-internal] radiation dose w

25 differences (i.e., water depth) rather than temporal differences (i.e., day versus night) better-exp

26 The temporal difference in expression of homeostatic changes

27 we have identified cDNA PCR products with a temporal difference in expression.

28 We have previously shown that there is a temporal difference in human CRX: gene expression compar

29 This temporal difference in receptor-activation that was nece

30 s in underestimation of the rates but little temporal difference in the trends.

31 Spatial and temporal differences in ADCs may provide insight into me

32 Spatial and temporal differences in BDNF and NT4 expression can regu

33 In vitro kinase assays demonstrated temporal differences in CDK2 and CDK6 activities which w

34 used compound annual growth rates to assess temporal differences in consumption for each country and

35 e ability of auditory cortex to exploit fine temporal differences in cortical activity is unique to a

36 l reporter from P(sulA) revealed spatial and temporal differences in expression within IBCs, and it w

37 gnaling mechanisms may underlie the reported temporal differences in gene expression during leukotoxi

38 cifically address the research interest: the temporal differences in gene expression profiles between

39 Quantitative and temporal differences in growth hormone secretion are kno

40 Temporal differences in habitat use and foraging special

41 because they do not consider the spatial and temporal differences in health and environmental damages

42 Our studies show that spatial and temporal differences in Hh signaling within a common pop

43 sceptibility at the KCNQ1 locus and identify temporal differences in imprinting status and methylatio

44 These temporal differences in low and high gamma suggest diffe

45 ng the core molecular circadian clock, these temporal differences in MHb activity were absent, indica

46 exclusion by a membrane system causes spatio-temporal differences in molecular crowding states that a

47 These results suggest that spatial and temporal differences in nicotinic receptor activity on b

48 uli in the A(I) cortex, disclose significant temporal differences in primary, secondary and tertiary

49 s across all PVH compartments, clear spatial-temporal differences in recruitment profiles were noted

50 Understanding sex and temporal differences in response to early-life stress mi

51 rveillance data, we evaluated geographic and temporal differences in serotype distribution and within

52 uptake and protein synthesis is explained by temporal differences in signaling induced by these 2 cyt

53 In addition, temporal differences in tear protein expression between

54 ve qualitative, quantitative, positional and temporal differences in TGF-beta-related signals, Msx2 e

55 Our findings suggest that regional and temporal differences in the availability of endogenous H

56 Temporal differences in the conformation of a given subu

57 These temporal differences in the formation of histone locus b

58 Understanding temporal differences in the incidence and outcomes of ou

59 put to inhibitory neurons in M1 may indicate temporal differences in the inhibitory gating in L4 of M

60 We observed temporal differences in the onset of immunoreactivity be

61 Temporal differences in the onset of trbeta2 expression

62 their degree of differentiation, suggesting temporal differences in the origin of each inverted regi

63 The spatial and temporal differences in the patterns of calcium elevatio

64 Our study reveals spatial and temporal differences in the rate of apical constriction

65 a/M1 ATM balance is generated by spatial and temporal differences in the recruitment of distinct ATM

66 We discovered considerable spatial and temporal differences in the requirement for AP3/PI activ

67 Our investigations revealed temporal differences in the responses of S. sclarea to M

68 rons in male rats, and reveal that there are temporal differences in the responsiveness of discrete s

69 This study examines the regional and temporal differences in the statistical relationship bet

70 The temporal differences in the way in which cortical activi

71 Despite marked temporal differences in their accumulation profiles, s36

72 eward and learning is closely related to the temporal difference learning algorithm TD(lambda).

73 tive conditioning, computations described by temporal difference learning are expressed in the human

74 Temporal difference learning has been proposed as a mode

75 r, this behavior is naturally explained by a temporal difference learning model which includes ETs pe

76 e higher order prediction error described by temporal difference learning models, is compatible with

77 Q-learning as a model-free implementation of Temporal difference learning motivated by growing eviden

78 Temporal difference learning solves this problem, but it

79 have inspired computational theories such as temporal difference learning.

80 We hypothesized that temporal differences may also play a role, with tumor ph

81 for discriminating smaller, but not larger, temporal differences (measured in log units), consistent

82 Thus, in mice, amygdala activity conforms to temporal difference models of aversive learning.

83 ly learned values (e.g., prediction error or temporal difference models).

84 signals for sequential learning predicted by temporal difference models.

85 e mechanism to counteract location-dependent temporal differences of dendritic inputs at the soma.

86 y, during three different months showed that temporal differences of taxonomic and functional diversi

87 Despite this temporal difference, our data indicate that the expansio

88 icular type of instructive signal known as a temporal difference prediction error.

89 neurons represents reinforcement learning's temporal difference prediction error.

90 free reinforcement learning theories such as temporal difference reinforcement learning (TDRL), which

91 signals emitted by dopaminergic neurons and temporal difference reinforcement learning algorithms.

92 ural learning systems can be modeled through temporal-difference reinforcement learning (TDRL), which

93 nforced preceding action choices by encoding temporal-difference reward prediction errors.

94 s of rules for each age group to capture the temporal differences seen in the immune responses of the

95 -guided choice in the brain, the predominant temporal difference (TD) algorithm cannot explain many f

96 for understanding this capacity has been the temporal difference (TD) algorithm for reinforcement lea

97 ignal reward prediction errors as defined in temporal difference (TD) learning algorithms.

98 The temporal difference (TD) learning model has been a corne

99 Temporal difference (TD) learning models posit that thes

100 g with those thought to carry out model-free temporal difference (TD) learning.

101 ration) reward-learning signal, described by temporal difference (TD) theory.

102 pamine (DA) neurons as an alternative to the temporal-differences (TD) algorithm.

103 ionally dependent magnitude differences, not temporal differences, underlie PSP directionality.

104 es of associative learning (Rescorla-Wagner, temporal difference vs. Pearce-Hall, Mackintosh).

105 The majority of these spatio-temporal differences were detected before birth, with su

106 increased through the night, while no strong temporal differences were observed at inland sites.