ライフサイエンスコーパス: freely behaving

1 orded in neonatally isolated and non-handled freely behaving adult male rats.

2 inhibits LTP, but not LTD at MF synapses of freely behaving adult rats.

3 uditory cortex (areas Te1, Te1v, and Te3) of freely behaving, amygdalectomized rats using a movable b

4 l integration may be reliably estimated in a freely behaving animal in its natural habitat and that w

5 nd neuropharmacological information from the freely behaving animal shows great promise for further i

6 ar manipulation of membrane potential in the freely behaving animal to perturb the dynamics within a

7 d behavior, but tools to modulate neurons in freely behaving animals are limited.

8 genetic reduction of cholinergic activity in freely behaving animals disrupted odor discrimination of

9 on of estradiol in the auditory forebrain of freely behaving animals disrupts behavioral responses to

10 the superior colliculus and barrel cortex of freely behaving animals during active exploration, awake

11 Hippocampal pyramidal neurons in freely behaving animals exhibit spatially selective firi

12 e soft implants extracted cortical states in freely behaving animals for brain-machine interface and

13 sonance translates into spiking resonance in freely behaving animals is unknown.

14 anization of dopamine (DA) release events in freely behaving animals relies on a set of characteristi

15 h correlates reasonably well with the period freely behaving animals were found to crawl after they s

16 We hypothesized that SC activity in freely behaving animals would reveal dynamic shifts in n

17 ojections at particular times, either within freely behaving animals, or in reduced preparations such

18 veloped a novel methodology that enabled, in freely behaving animals, simultaneous unit recording and

19 elemetry system to simultaneously record, in freely behaving animals, the activity of the DCMD and of

20 In freely behaving animals, we find that the DA signal from

21 mpal correlates of space ("place fields") in freely behaving animals.

22 h patterns of activity that were recorded in freely behaving animals.

23 motor control, and sensorimotor learning in freely behaving animals.

24 s of the somatic and dendritic potentials in freely behaving animals.

25 mounted miniature microscopes for imaging in freely behaving animals.

26 or minimally invasive, untethered studies on freely behaving animals.

27 of targeted sets of neurons in the brains of freely behaving animals.

28 respond to a given odorant ligand in awake, freely behaving animals.

29 rocorticographic recordings were acquired in freely behaving animals.

30 f fluids and light into the brains of awake, freely behaving animals.

31 lows effective recording of brain signals in freely behaving animals.

32 deoxyglucose (2DG) method was carried out in freely behaving animals.

33 dy sensory-induced gene expression in awake, freely behaving animals.

34 nucleus (CN) have not been studied in awake, freely behaving animals.

35 monitored jumps evoked by looming stimuli in freely behaving animals.

36 's effects on hippocampal function in awake, freely-behaving animals.

37 Injection of CP2 into freely behaving Aplysia increases the rate of respirator

38 We show that freely behaving bats constantly control their biosonar f

39 rom the majority of neurons in the head of a freely behaving Caenorhabditis elegans with cellular res

40 tive principal (i.e., excitatory) neurons in freely behaving cats across periods of waking MD and pos

41 In vivo microdialysis measurements in freely behaving cats showed that adenosine extracellular

42 posterior suprasylvian gyrus (vPS cortex) of freely behaving cats was reversibly deactivated with coo

43 their activity patterns, particularly under freely behaving conditions.

44 In conscious, freely behaving females, three infusions of an excitator

45 of electric signaling patterns recorded from freely behaving fish revealed that the IPI and direction

46 s into or out of a phasic firing mode in two freely behaving genetic rodent models of absence epileps

47 y rhythm in the output of 5-HT in the SCN of freely behaving hamsters.

48 e obtained between 2 and 12 months of age in freely behaving HI-treated and sham control rats.

49 ble aspects of vestibular function in intact freely behaving human subjects.

50 aneous neocortical local field potentials in freely behaving infant rats during natural interactions

51 s measured at the individual neuron level in freely behaving male rats change as a function of vigila

52 urons with appropriate temporal precision in freely behaving mammals, the causal role of these action

53 paminergic neuron action potential firing in freely behaving mammals.

54 d calcium activity using fiber photometry in freely behaving mice and found arousal-state-dependent a

55 anges in neuronal activity of ACC neurons in freely behaving mice during early learning.

56 ry mouse neurons, as well as in the brain of freely behaving mice in vivo to mediate reversible modul

57 activation of Mrgprb4-expressing neurons in freely behaving mice promoted conditioned place preferen

58 corded neural activity in the hippocampus of freely behaving mice that had a forebrain-specific knock

59 Using Ca(2+) imaging in freely behaving mice that repeatedly explored a familiar

60 here a variety of optogenetic approaches in freely behaving mice to evaluate the role of the arcuate

61 Employing in vivo calcium imaging in freely behaving mice to record activity dynamics from hu

62 of glutamatergic MnPO neuron stimulation in freely behaving mice while monitoring drinking behaviour

63 d multiple electrode recording techniques to freely behaving mice with a CA1 pyramidal cell-specific

64 In freely behaving mice, activation of these neurons in the

65 For freely behaving mice, our results show that information

66 for normal odor sensation and adaptation of freely behaving mice, preventing saturation of the olfac

67 the role of nociceptive sensory afferents in freely behaving mice, we developed a fully implantable,

68 neurons for 1 min generated pulses of LH in freely behaving mice, whereas inhibition with archaerhod

69 dopsin channels by performing stimulation in freely behaving mice.

70 e of minutes in specific brain subregions of freely behaving mice.

71 sed to validate stable chronic recordings in freely behaving mice.

72 apidly suppresses BLAPCs and BLA activity in freely behaving mice.

73 the real-time activity of individual DGCs in freely behaving mice.

74 ls from many brain regions simultaneously in freely behaving mice.

75 gs performed in in vitro preparations and in freely behaving mice.

76 dynamics of genetically specified neurons in freely behaving mice.

77 y out longitudinal studies of brain aging in freely behaving mice.

78 or in one set of experiments using awake and freely behaving mice.

79 fic phases of the endogenous theta rhythm in freely behaving mice.

80 es susceptibility to social-defeat stress in freely behaving mice.

81 ly identified VTA-projecting BNST neurons in freely behaving mice.

82 manual annotations of thousands of clips of freely behaving mice.

83 cence microscopes now allow brain imaging in freely behaving mice.

84 ly representative of spontaneous grooming in freely-behaving mice.

85 paws during spontaneous grooming in multiple freely-behaving mice.

86 ositron emission tomography (FDG-PET) in 238 freely behaving monkeys identified brain regions where m

87 acellular spike activity in two symptomatic, freely behaving mouse models: R6/2 transgenics, which ar

88 ehavioral elements and their patterns in the freely behaving mouse.

89 so noted during locomotion video tracking of freely behaving mutants.

90 we monitored cortical neuron populations in freely behaving nonhuman primates during natural locomot

91 single or multiple electrodes implanted in a freely behaving primate.

92 ion between two sites in the motor cortex of freely behaving primates.

93 elates could drive naturalistic behaviors in freely behaving primates.

94 ion (V E) in 5-d, 10-d, and 15-d-old intact, freely behaving rat pups, using whole-body plethysmograp

95 We used bilateral microdialysis in freely behaving rats (n = 32), instrumented for electroe

96 Here we show that in freely behaving rats after a long period in an awake sta

97 nucleus (LMN) and anterior thalamus (ATN) of freely behaving rats and also made bilateral lesions of

98 f neurons in the medial prefrontal cortex of freely behaving rats are phase locked to the hippocampal

99 sis in individual visual cortical neurons in freely behaving rats as they cycled between sleep and wa

100 (TRN) and medial prefrontal cortex (mPFC) of freely behaving rats at rest to investigate thalamocorti

101 microstimulation within the motor cortex of freely behaving rats before and after striatal disinhibi

102 In this study, we investigated whether freely behaving rats can discriminate fine tactile patte

103 We recorded neurons from the hippocampus of freely behaving rats during an auditory fear conditionin

104 to monitor firing rates in visual cortex of freely behaving rats during chronic monocular visual dep

105 Single neurons were recorded in freely behaving rats during fear conditioning from areas

106 subnucleus of the lateral amygdala (LAd) of freely behaving rats during Pavlovian fear conditioning,

107 tive distal-most dendrites using tetrodes in freely behaving rats over multiple days with a high degr

108 vity and sensory evoked field potential from freely behaving rats previously implanted with permanent

109 d potentials recorded from the PFC and CN in freely behaving rats previously implanted with permanent

110 Freely behaving rats previously implanted with semi-micr

111 To test this hypothesis, freely behaving rats received bilateral intrastriatal in

112 n the dentate gyrus (DG) of anesthetized and freely behaving rats that both acute as well as chronic

113 ialysis in the dorsal raphe nucleus (DRN) of freely behaving rats to study the effect of GABA and glu

114 dings were obtained in the basal amygdala of freely behaving rats undergoing simultaneous reward, fea

115 rahippocampal microdialysis was performed in freely behaving rats, and the firing of single neurons i

116 In contrast, here we show that in freely behaving rats, theta oscillations in area CA1 are

117 In freely behaving rats, VTA GABA neurons were relatively f

118 Using multisite recordings in freely behaving rats, we examined gamma oscillations wit

119 When we used multi-site recordings in freely behaving rats, we observed ripples throughout the

120 lar serotonin in the dorsal raphe nucleus of freely behaving rats.

121 ections of TTX into RPO and SubC on sleep in freely behaving rats.

122 sis and measurement of locomotor activity in freely behaving rats.

123 cholinergic region of the basal forebrain of freely behaving rats.

124 heir cardiorespiratory effects in conscious, freely behaving rats.

125 HD cells were recorded from AD in freely behaving rats.

126 cellular identification of single neurons in freely behaving rats.

127 identification of single layer 3 neurons in freely behaving rats.

128 pus, medial septum, and anterior thalamus of freely behaving rats.

129 eptors in the PF-LHA on sleep-wakefulness in freely behaving rats.

130 cortex using fixed-potential amperometry in freely behaving rats.

131 ampal place-cell and interneuron activity in freely-behaving rats.

132 stributed across multiple cortical areas, in freely behaving rhesus monkeys.

133 Using multisite optogenetic manipulations in freely behaving rodents, we found that depolarization of

134 firing rate homeostasis in the neocortex of freely behaving rodents.

135 ons (PV) in the hippocampus and neocortex of freely behaving rodents.

136 y GABA dose; and the method can be used with freely behaving subjects.

137 ound that individual sensorimotor neurons in freely behaving swamp sparrows expressed categorical aud

138 hippocampus, we have recorded place cells in freely behaving, transgenic mice that express a mutated

139 rrelates, during a seizure on unanesthetized freely behaving unrestrained animals.

140 ues for monitoring neural activity in awake, freely behaving vertebrates are invasive and difficult t

141 ion, we recorded neural firing in the LHb of freely behaving, water-deprived rats before and after an

142 ciplinary approach to map neural circuits in freely behaving worms by integrating functional imaging,

143 activity of genetically specified neurons in freely behaving zebrafish.