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2 eedback objective, participants successfully learned to activate the target perceptual representation
3 strongly suppressed but recovered as animals learned to adapt the previously learned task to the new
5 CLIS without reliable means of communication-learned to answer personal questions with known answers
8 imultaneously in six limbic areas as rabbits learned to approach a spout for water reinforcement afte
9 ring the same task, rats with fornix lesions learned to approach a visible platform but did not learn
10 al neuronal activity was recorded while rats learned to approach different reward locations in two co
14 e mid-lateral cerebellum when 2 male monkeys learned to associate a right or left-hand movement with
15 jects (N = 14) and healthy controls (N = 14) learned to associate a visual cue with a juice reward.
16 hanges in brain activation when participants learned to associate an arbitrarily located visual cue w
19 mulation results of a forward model that had learned to associate motor commands with new sensory con
22 ains recorded during a task in which monkeys learned to associate novel images with rewarding and ave
23 in the mid-lateral cerebellum as the monkey learned to associate one arbitrary symbol with the movem
25 ing encoding, male and female human subjects learned to associate spatial locations of visual objects
26 ess for sucrose pellets, and they separately learned to associate sucrose pellets with Pavlovian cues
28 ce; these neurons were found as soon as mice learned to associate the rewarded sequence with licking.
29 ich mice avoid an environment that they have learned to associate with inflammation-induced discomfor
30 esults suggest that sympatric predators have learned to attack and consume mountain katydids despite
33 ton-top tamarins (Saguinus oedipus) socially learned to avoid a preferred food when it was made unpal
35 , predicted the degree to which participants learned to avoid choices that had been probabilistically
39 nisms and their neural basis as participants learned to avoid painful electric shocks for themselves
40 this fMRI study, 96 male human participants learned to avoid painful stimuli either for themselves o
42 patients and 33 healthy comparison subjects learned to avoid shocks while undergoing a functional MR
48 We discovered that, after C. elegans have learned to avoid the pathogenic bacteria Pseudomonas aer
56 ere reinitialized to new values as the model learned to categorize 10 different classes of objects.
58 agnetic resonance imaging while participants learned to categorize visual stimuli as predicting "rain
59 ral activity in the substantia nigra as mice learned to change their action duration to earn food rew
60 hort-term memory, honeybees (Apis mellifera) learned to choose between 2 colors on the basis of immed
61 tional magnetic resonance imaging while they learned to choose instrumental actions that were associa
64 d psychophysical experiments in which people learned to classify binary sequences according to determ
69 ast 150+ years, these 'microbe hunters' have learned to combine epidemiological information with know
74 sured patterns of generalization as children learned to control a novel tool and found that the autis
79 and once cooperation was initiated, rapidly learned to coordinate in more complex conditions as well
80 A recent study found that marmoset monkeys learned to coordinate their actions to successfully comp
82 mic." In this article, they describe lessons learned to counteract misleading information and nudge t
83 rying pattern of disturbing forces, subjects learned to counteract the disturbance by producing force
84 Here, we wish to shed light on what has been learned to date about the 1918 virus with regard to path
85 ncluding report takes stock of what has been learned to date about the successes and challenges in pa
87 myriad of contexts and repetitions, we have learned to deploy certain exploratory movements in order
90 s in the motor cortex over weeks, while mice learned to detect objects with their whiskers and report
91 ver, like the other groups, IMA participants learned to differentiate fingertip forces with repeated
93 .1 mg/kg nicotine discrimination but readily learned to discriminate 0.001 mg/kg of the nicotinic ful
96 task, rhesus macaques and human participants learned to discriminate between sequences of trial-uniqu
101 n gradient, two groups of participants first learned to discriminate between two color stimuli, one p
112 s subsequent periods of a task in which rats learned to discriminate two odors associated with positi
113 same layer 2/3 neuronal populations as mice learned to discriminate two visual patterns while runnin
115 LA) neural ensembles as awake, behaving rats learned to dislike the taste of saccharin [via condition
117 r discrimination tasks, the mice effectively learned to distinguish the cues, which indicates that re
118 the CA1 region of the hippocampus while mice learned to efficiently collect rewards from two subtly d
119 in a near-optimal manner, meaning that they learned to efficiently use all available information to
124 ificantly decreased indicating that crayfish learned to escape from the maze more rapidly and efficie
128 of either 1 or 3 juice drops so that animals learned to expect 2 juice drops on average even though i
129 he human immune system, these organisms have learned to exploit immunoregulatory pathways, resulting
131 , we show using fMRI that while participants learned to find rewards in multiple different Y-maze env
134 only a small number of variables need to be learned to greatly improve on the accuracy of MC mean.
135 ction selectivity is removed after mice have learned to hunt, and despite abolishing the gaze-stabili
138 pipeline demonstrated that Mirai implicitly learned to identify mammographic lesion features, partic
141 s differ from those of novices; experts have learned to ignore features that are visually salient but
142 gest that black rats preexposed to prey odor learned to ignore the unrewarding cue, leading to a sign
143 senescence is limited and much remains to be learned to improve the effectiveness of next generation
148 addition, this review summarizes the lessons learned to inform the scientific community about ways to
149 mpared two groups of participants who either learned to insert a real or virtual tool into a fixture.
158 cumbens (NAS) increased locomotion, and rats learned to lever-press for injections of Delta9THC into
161 nectivity that would have occurred as humans learned to light fires in the dry season and to transfor
165 lly led to dissonant or consonant music, and learned to make choices associated with the consonance,
166 that in a context where a non-human primate learned to make novel visuomotor associations, classifyi
170 Human participants wore a data glove and learned to manipulate a computer cursor by moving their
174 When moving in the channel, participants learned to modulate grip force in synchrony with load fo
175 neuron-to-movement mapping, the participant learned to modulate the activity of the recorded neurons
177 e recorded EMG from four muscles as subjects learned to move a manipulandum that created systematic f
178 Consistent with our hypothesis, subjects learned to move the simulated linkage along geodesic lin
181 n auditory discrimination task in which rats learned to navigate to goal locations based on the frequ
182 gic inputs was found when the Thy1-ChR2 mice learned to nose-poke to self-stimulate these inputs, ind
184 ld pointing when beneficial, whereas the 3rd learned to obtain the hidden food by pointing deceptivel
185 However, a third of naive observer bees learned to open the two-step box from these demonstrator
186 analysis, we found that 14 naive chimpanzees learned to operate a puzzle box that they failed to oper
189 cumbens while rats licked for taste cues and learned to perform a taste discrimination go/no-go task.
195 hythms are modulated differently as the rats learned to perform the T-maze task but nevertheless beco
196 lthough both lesioned rats and sham controls learned to perform the task, we found that they relied o
200 r associated with 3 food items, the tamarins learned to pick the color associated with 1 food item.
201 uring the following motor task, participants learned to play target notes of the melodies on a keyboa
206 en received avoidance training in which they learned to prevent a foot-shock by stepping in an activi
208 However, in the gain-up paradigm, the brain learned to produce a larger amplitude saccade with traje
209 d that, in the gain-down paradigm, the brain learned to produce a smaller amplitude saccade by alteri
210 attentively to the sound sequences they had learned to produce and to two control sequences, which w
212 ed the detailed structure of learning: birds learned to produce the average of the behavioral traject
215 hese results indicate that the visual system learned to rapidly adjust to the reddish environment, sw
216 Squirrel monkeys (Saimiri sciureus) that had learned to reach toward 1 piece of food instead of 4 in
217 Three squirrel monkeys (Saimiri sciureus) learned to reach toward a container that covered food if
221 and functional imaging at age 5, before they learned to read, and at age 8, after they learned to rea
226 dentity paradigm, undergraduate participants learned to recognize and name varying views of 22 unknow
228 nse patterns, while native English listeners learned to recognize unfamiliar vocal pitch patterns in
230 d a closed-loop brain-machine interface that learned to reduce participants' pain by decoding pain-re
231 NF and 61.9% of participants in the fNIRS-NF learned to regulate the respective NF target parameter.
232 reness, sensitivity, and language; graduates learned to relate more meaningfully to patients/families
240 ptual-motor learning using monkeys that have learned to search for a visual target among distractors.
241 hey had cached them 4 hr earlier but rapidly learned to search for peanuts and avoid decayed wax worm
244 ance imaging (fMRI) experiment, participants learned to select between two response options by trial-
254 ever discrimination procedure, in which rats learned to selectively respond between active and inacti
255 tion, which was assessed by how rapidly rats learned to self-administer a threshold dose of cocaine,
256 to determine their role in extinction, rats learned to self-administer cocaine before receiving inje
260 We found that, with practice, human subjects learned to shape patterns of covariation between arbitra
261 t phases of the task, chimpanzees eventually learned to shift their analogical reasoning strategy to
263 rk with chimpanzees, most children who first learned to solve a puzzlebox in an inefficient way switc
266 Born with tuberous sclerosis, Deborah never learned to speak and lived in a group home for the last
267 ine percent suffered hearing loss, 58% never learned to speak, and nearly all had significant intelle
269 nd 53 years; for every month earlier a child learned to stand, there was, on average, a gain of one h
271 e monitored hippocampal ensembles while rats learned to switch from two familiar trajectories to a ne
273 ccine-level concentrations and apply what we learned to the components of the SHINGRIX(TM) vaccine.
275 of these efforts by focusing on what we have learned to this point on non-nucleoside inhibitors and o
278 oncept study, eight patients with depression learned to upregulate brain areas involved in the genera
280 ound-to-word learning paradigm in which they learned to use a foreign phonetic contrast for signaling
284 t years, however, many Chinese children have learned to use electronic communication devices based on
287 ular, as predicted by the ideal actors, they learned to use smaller control signals when forces were
292 With experience, members of both species learned to use the switch strategy at above chance level
298 cerebral cortex of captive chimpanzees that learned to voluntarily produce sounds to attract the att