ライフサイエンスコーパス: conjunctive

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

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

3 Conjunctive and parallel coding of multiple actions and

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

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

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

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

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

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

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

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

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

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

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

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

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

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

18 Catalytic enantioselective conjunctive cross-couplings that employ Grignard reagent

19 The conjunctive effects, where neurons respond only if sever

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

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

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

23 reduced activity in regions associated with conjunctive memory encoding.

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

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

26 ting methodologies, using a compensatory and conjunctive model.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

49 These conjunctive signals positively modulated the firing of p

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

51 Conjunctive stimulation of climbing fiber and parallel f

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

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

54 Conjunctive stimulation of parallel fibers and climbing

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

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

57 Healthy conjunctive tissue samples were taken during cataract su