ライフサイエンスコーパス: operant conditioning

1 e motor output expression induced by in vivo operant conditioning.

2 ncrease in performance, as often observed in operant conditioning.

3 ol group), for 1 h a day under fixed ratio 1 operant conditioning.

4 arning the distinction of visual cues during operant conditioning.

5 nalog, whereas D1R mediates reinforcement in operant conditioning.

6 s new insights into the neural mechanisms of operant conditioning.

7 ion of cAMP into B51 mimicked the effects of operant conditioning.

8 Thus, both PKA and PKC were necessary for operant conditioning.

9 , and classical conditioning, also undergoes operant conditioning.

10 ol animals during each period, demonstrating operant conditioning.

11 the role of a behavior-initiating neuron in operant conditioning.

12 cellular and molecular processes underlying operant conditioning.

13 motor output by contingent reinforcement in operant conditioning.

14 ion that expressed the essential features of operant conditioning.

15 place preference (CPP) and progressive ratio operant-conditioning.

16 Using operant conditioning and a psychophysical task, budgerig

17 examine the cellular locus and mechanism of operant conditioning and compare them with those for oth

18 Operant conditioning and the magnetic search coil techni

19 ysia has been demonstrated to be modified by operant conditioning, and a neural pathway (esophageal n

20 ate in neuroscience is whether classical and operant conditioning are mechanistically similar or dist

21 Although classical and operant conditioning are operationally distinct, it is u

22 tor coordination, and apparent motivation in operant conditioning, as well as spine morphology and ph

23 his laser tracking system can be used for an operant conditioning assay in which a courting male quic

24 contributions towards a mechanistic model of operant conditioning, because of their special technical

25 activity within various brain areas through operant conditioning, but the relevance of that control

26 nally, a new experimental paradigm utilizing operant conditioning combined with motor tasks is propos

27 nt cortical regions and in A(I) cortex after operant conditioning employing an acoustic cue.

28 al ganglia expressed an essential feature of operant conditioning (i.e., contingent reinforcement mod

29 This analog expressed a key feature of operant conditioning (i.e., selective enhancement of the

30 how these molecules can interact to mediate operant conditioning in an individual neuron important f

31 Previously, an analog of operant conditioning in Aplysia was developed using the

32 To test this hypothesis, we used operant conditioning in male rats to determine whether o

33 rogress to excessive ethanol drinking during operant conditioning in mice lacking ethanol-sensitive a

34 Using a single-cell analog of operant conditioning in neuron B51 of Aplysia, we examin

35 melanogaster implicated the ignorant gene in operant conditioning in the heat-box, research on the se

36 While Pavlovian and operant conditioning influence drug-seeking behavior, th

37 Operant conditioning is a form of associative learning t

38 Operant conditioning is a type of associative learning i

39 Operant conditioning is a ubiquitous but mechanistically

40 designated operant) and that this analog of operant conditioning is accessible to cellular analysis.

41 Operant conditioning is characterized by the contingent

42 In practice, operant conditioning is the study of reversible behavior

43 with the consequences of one's own behavior (operant conditioning) is a simple form of learning that

44 e details that links the decision making and operant conditioning literatures and extends choice prop

45 This analog expressed a key feature of operant conditioning, namely a selective enhancement in

46 In the current experiments, operant conditioning occurred in Context A, extinction i

47 ago, when Joseph Kamiya reported successful operant conditioning of alpha-rhythm in humans, the effe

48 Here we report that classical and operant conditioning of feeding behavior differentially

49 More direct evidence comes from studies on operant conditioning of neural activity using biofeedbac

50 This study asked whether operant conditioning of the H-reflex can modify locomoti

51 Operant conditioning of the primate triceps surae H-refl

52 Operant conditioning of the spinal stretch reflex or its

53 Operant conditioning of the vertebrate H-reflex, which a

54 nal magnetic resonance imaging (fMRI) and an operant conditioning paradigm for the discrete delivery

55 ish both learning and memory formation of an operant conditioning paradigm occur better during the da

56 using amphetamine as a reinforcer and in an operant conditioning paradigm using sucrose reinforcemen

57 Using an operant conditioning paradigm, we demonstrated that rats

58 By using an operant conditioning paradigm, we show that CNGA4-null m

59 d within a single test session in a modified operant conditioning paradigm.

60 behavior for sucrose in a progressive ratio operant-conditioning paradigm when administered peripher

61 research has been dominated by pavlovian and operant conditioning paradigms.

62 tively" framed custom application focused on operant conditioning principles of reinforcement schedul

63 Here, we report an appetitive operant conditioning procedure in Aplysia that induces l

64 We found that in vitro analogs of operant conditioning produced a long-term (24 h) increas

65 Operant conditioning protocols can modify the activity o

66 Operant conditioning protocols in animals and humans can

67 y can also be modified by both classical and operant conditioning protocols.

68 High-throughput operant conditioning systems for rodents provide efficie

69 tem can be incorporated into high-throughput operant conditioning systems.

70 Using an effort-based operant conditioning task for head-fixed mice, we discov

71 nhibitory neurons (INs) during a neuron-pair operant conditioning task using two-photon imaging of IN

72 sual display on a touch screen as part of an operant conditioning task.

73 habit-based responding in a food-reinforced operant conditioning task.

74 during the acquisition and performance of an operant conditioning task.

75 sual display on a touch screen as part of an operant conditioning task.

76 inforcement learning model to simulations of operant conditioning tasks that have been argued to quan

77 rd prediction functions during Pavlovian and operant conditioning tasks, less is understood about the

78 All were trained with operant conditioning techniques to discriminate coherent

79 Operant conditioning techniques were used to demonstrate

80 erigars and zebra finches were tested, using operant conditioning techniques, on their ability to ide

81 Operant-conditioning techniques were used to investigate

82 In sucrose operant conditioning, the photoactivation of these termi

83 neuronal mechanisms that mediate features of operant conditioning, the present study identified a neu

84 ry, rats were trained using olfactometry and operant conditioning to detect and discriminate odors.

85 Rats were trained using olfactometry and operant conditioning to discriminate among homologous fa

86 re eye and ear movements, we trained cats by operant conditioning to look in the direction of light a

87 e an object-discrimination paradigm based on operant conditioning to show, for the first time to our

88 Moreover, a single-cell analog of operant conditioning was developed using neuron B51, a c

89 Previously, an analog of operant conditioning was developed using the buccal gang

90 s a first step toward a cellular analysis of operant conditioning, we developed an in vitro buccal ga

91 Using operant conditioning, we trained mice to detect visual c