ライフサイエンスコーパス: conjunctive

1 computations in other PC types by detecting conjunctive activation of different afferent input pathw

2 at these transformations are implemented via conjunctive activations in "conjunction hubs"-brain regi

3 llyl-desoxyhumulones followed by dearomative conjunctive allylic alkylation (DCAA).

4 w differential responses to probabilities of conjunctive and disjunctive reward deliveries in the ven

5 Conjunctive and parallel coding of multiple actions and

6 at include pronouns, articles, prepositions, conjunctives, and auxiliary verbs.

7 We developed a computational method based on conjunctive Bayesian networks (CBNs) to quantify the pre

8 in different HIV-1 subtypes, based on Hidden Conjunctive Bayesian Networks (H-CBN), a probabilistic m

9 on on the response of a CO-tuned or MO-tuned conjunctive cell is weaker when the contextual inputs di

10 to be independent of head direction, whereas conjunctive cells generate grid representations that are

11 grid cells integrate inputs from co-aligned conjunctive cells with firing rates that differ between

12 ibit the predicted egocentric-by-allocentric conjunctive characteristics and anticipate orienting tow

13 r (PF)-Purkinje cell (PC) synapse induced by conjunctive climbing fiber and PF stimulation in vivo.

14 Rate remapping is a conjunctive code that potentially enables hippocampal pl

15 ements of an episode, while another posits a conjunctive code, where index neurons code the entire ep

16 g the spatial context, which combine to form conjunctive codes in the hippocampus that form the basis

17 hich is thought to bind cortical inputs into conjunctive codes.

18 Furthermore, this conjunctive coding evolves in the form of enhanced item-

19 A generalized linear model revealed enhanced conjunctive coding in dHPC(->NAc) neurons which improved

20 ing and perturbations demonstrated that this conjunctive coding occurs by means of convergent disinhi

21 Some neurons demonstrated conjunctive coding of both classic place field propertie

22 Here, we show that the conjunctive coding of multiple stimulus features, common

23 opulation geometry supports the emergence of conjunctive coding subspaces that integrate prior inform

24 RNNs were presented with two inputs denoting conjunctive colour-location stimuli, followed by a pre-c

25 ortex and cingulum fiber bundle are tuned to conjunctive combinations of azimuth and tilt, i.e. pitch

26 Conjunctive consolidation was used to create a predictiv

27 Sequential sequestration and conjunctive consolidation was used to develop a composit

28 Using conjunctive consolidation, a 4-stage clinical severity s

29 information from multiple variables through conjunctive consolidation, the group with the highest ra

30 lyses, multivariable logistic regression and conjunctive consolidation.

31 the hippocampus result from the loss of this conjunctive contribution.

32 ls, border cells, head-directions cells, and conjunctive correlates found in the Medial Entorhinal Co

33 The catalytic enantioselective conjunctive coupling of C(sp(3)) electrophiles can be ac

34 results in enhanced chemoselectivity for the conjunctive coupling product relative to the Suzuki-Miya

35 eospecific Zweifel-type reactions, catalytic conjunctive coupling reactions, and transition metal-fre

36 Catalytic enantioselective conjunctive cross-coupling between 9-BBN borate complexe

37 A nickel-catalyzed conjunctive cross-coupling between non-conjugated alkene

38 Palladium-catalyzed conjunctive cross-coupling can be accomplished with the

39 cific 1,2-metallate shift that occurs during conjunctive cross-coupling is shown to enable a practica

40 Palladium-catalyzed conjunctive cross-coupling is used for the synthesis of

41 A nickel-catalyzed conjunctive cross-coupling of alkenyl carboxylic acids,

42 le beta tert-boryl amides is accomplished by conjunctive cross-coupling of alpha-substituted alkenyl

43 Enantioselective conjunctive cross-coupling of enyne-derived boronate com

44 esis of complex alkyl boronic esters through conjunctive cross-coupling of vinyl boronic esters with

45 ronic esters is accomplished by performing a conjunctive cross-coupling reaction on preformed cyclic

46 Allylation and conjunctive cross-coupling represent two useful, yet lar

47 The decarboxylative conjunctive cross-coupling was also applied to the synth

48 e of allyl electrophiles in nickel-catalyzed conjunctive cross-coupling with a non-conjugated alkene

49 Catalytic enantioselective conjunctive cross-couplings that employ Grignard reagent

50 The conjunctive effects, where neurons respond only if sever

51 These representations differed from conjunctive emotion-action goal representations found in

52 We found that FPl contained conjunctive emotion-action goal representations that wer

53 Surprisingly, the conjunctive encoding of these variables in single neuron

54 Whole-baton selectivity arose from a form of conjunctive encoding whereby two parts together exerted

55 d to be discriminated as viewpoint-invariant conjunctive entities.

56 mportant operations such as gain control and conjunctive feature detection.

57 enced task domain, favoring compositional or conjunctive generalization when the task statistics are

58 lation by movement direction associated with conjunctive grid cell firing [7].

59 rising theta-modulated head-direction cells, conjunctive grid x direction cells, and pure grid cells,

60 rnal direction, via an intermediate layer of conjunctive grid x direction cells, producing left-right

61 Conjunctive grid-by-head-direction cells lost grid cell

62 ilarly, state-invariant correlations between conjunctive grid-head direction and pure head direction

63 n in the encoding of allocentric location by conjunctive HD/egocentric cells.

64 rapidly strengthen synaptic inputs carrying conjunctive information about position and choice.

65 preparatory activity in hotspot regions with conjunctive input-output connectivity to the ALM.

66 reduced activity in regions associated with conjunctive memory encoding.

67 In contrast, conjunctive memory for specific object-location associat

68 ditioning by supporting the acquisition of a conjunctive memory representation of context, which asso

69 ting methodologies, using a compensatory and conjunctive model.

70 tal inputs, leading to a correspondence with conjunctive neural representations observed in dorsal CA

71 held that these computations are governed by conjunctive neural representations of the features.

72 signments of an arbitrary Boolean formula in conjunctive normal form can be computed efficiently, vio

73 ble-light-mediated and transition metal-free conjunctive olefination that uses an alkene 'linchpin' w

74 timization model is proposed for the optimal conjunctive operation of surface and groundwater resourc

75 resumed within a distinct temporal window of conjunctive pairing with PF1.

76 learning is required for the formation of a conjunctive population code, upstream of CA1, while plat

77 ttractor network model that accounts for the conjunctive position-by-velocity selectivity of grid cel

78 Potentiation was dependent on (a) conjunctive presentations of scallop and light, (b) numb

79 used to calculate the mathematically correct conjunctive probability.

80 ng and synaptic plasticity are controlled by conjunctive processing of these separately integrated in

81 ransformations employ [B(pin)]2-methane as a conjunctive reagent, resulting in the formation of two C

82 opment of silyl glyoxylates, a new family of conjunctive reagents for use in multicomponent coupling

83 anchored in tongue-centred, head-centred or conjunctive reference frames.

84 directly proportional to the strength of the conjunctive representation formed during the most recent

85 role for hippocampal pattern separation and conjunctive representation in reinforcement learning.

86 They support the view that a conjunctive representation of context plays an important

87 ts contextual fear conditioning by storing a conjunctive representation of context.

88 exclusively proximal cues by making use of a conjunctive representation of head direction and locatio

89 associated to head directions by virtue of a conjunctive representation of place and head directions

90 ice is thought to require the formation of a conjunctive representation of the conditioning chamber.

91 ocampus has been attributed to the loss of a conjunctive representation of the features of the contex

92 epends on 2 processes: (a) construction of a conjunctive representation of the features that make up

93 dressed this issue and found support for the conjunctive representation view.

94 l fear conditioning: (1) conditioning to the conjunctive representation, which depends on the hippoca

95 that can be flexibly reused across tasks) to conjunctive representations (task-specific activity patt

96 These results provide direct evidence for conjunctive representations as critical precursors of ac

97 atic formation, and later retrieval, of such conjunctive representations can substantially facilitate

98 There is, however, no direct evidence that conjunctive representations contribute to contextual fea

99 ck pairs were bound together into contiguous conjunctive representations during sleep.

100 We decoded conjunctive representations from electroencephalographic

101 The strengthening of conjunctive representations hence serves as a computatio

102 These findings support the view that conjunctive representations in the hippocampus underlie

103 eals with ambiguous discriminations in which conjunctive representations of events are learned as bei

104 Many neuron classes have conjunctive representations of multiple behaviors.

105 This confirms that the formation of conjunctive representations of specific task contexts, s

106 Indeed, stronger initial conjunctive representations predicted significant future

107 nctional MRI data show the hippocampus forms conjunctive representations that are dissociable from fe

108 , we test if the hippocampus forms separable conjunctive representations that enables the learning of

109 dly form and retrieve so-called event files, conjunctive representations that link context-specific i

110 During complex tasks, the brain forms conjunctive representations that link individual task fe

111 tive bias) enables models with fixed, partly conjunctive representations to generalize transitively.

112 In two experiments, we found that conjunctive representations were active throughout the e

113 ation ultimately has to be reintegrated into conjunctive representations, and this is unlikely to be

114 trol point to the role of highly integrated, conjunctive representations, sometimes referred to as ev

115 ated to an important behavioral indicator of conjunctive representations, the so-called partial-overl

116 ted this dynamic shift from compositional to conjunctive representations, which was associated with r

117 olution is to assign value to multi-featural conjunctive representations.

118 h redundant (respond-to-either-modality) and conjunctive (respond-only-to-both) audio-visual detectio

119 ocampal neurons, in both bat species, showed conjunctive sensitivity to the animal's spatial position

120 s of item and sequence position information (conjunctive sequence cells) or for specific probe types

121 These conjunctive signals positively modulated the firing of p

122 We found that individual PFL3 cells show conjunctive, spike-rate tuning to both the heading angle

123 tions developed progressively over 20 min of conjunctive stimulation and were persistent (up to 84 mi

124 Conjunctive stimulation of climbing fiber and parallel f

125 The results thus show that conjunctive stimulation of climbing fibres with other in

126 In cerebellar long-term depression (LTD), conjunctive stimulation of parallel and climbing fiber i

127 Conjunctive stimulation of parallel fibers and climbing

128 llar cortex, we have examined the effects of conjunctive stimulation of peripheral afferents and clim

129 nger latency depressions of firing and after conjunctive stimulation with climbing fibres these were

130 Showing that the formation of conjunctive task representations can have negative futur

131 Healthy conjunctive tissue samples were taken during cataract su

132 controllable multipath interference through conjunctive use of linear wave mixing with active phase