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1 ivated transcription factor, greatly reduced arousal responses.
2 d and were not usually associated with other arousal responses.
3 before optical VTA stimulation inhibited the arousal responses and restoration of righting in 6/6 ChR
4 ia, i.e., the heart rate and ventilatory and arousal responses, and abolishes the normal decrease in
5 ripheral theories of emotion was that bodily arousal responses are too undifferentiated to account fo
6 and autonomic function as well as stress and arousal responses attributed to EM-1 in the central nerv
7                  Sound presentations yielded arousal response curves that varied because of sound lev
8 nction, we hypothesized that blunted hypoxic arousal responses during sleep Stage 3/4 would be presen
9                     The amygdala mediates an arousal response in anticipation of rewards, whereas PFo
10                                   The sexual arousal response in healthy women can be monitored at se
11    These results suggest a specific role for arousal responses in loss aversion.
12  models we performed a behavioral screen for arousal responses including emotionality, locomotor, and
13                                   The infant arousal response involves subcortical and cortical respo
14 t appropriately transcoded into somato-motor-arousal responses normally associated with an aversive m
15                              The spontaneous arousal responses occur periodically but with a high lev
16 atory autonomic, respiratory, somatomotor or arousal responses that limit the extent of blood pressur
17 ted the behavioral, but not electrocortical, arousal response to caffeine.
18  neurons mediate the potentially life-saving arousal response to hypercapnia.
19 that Lmx1b(f/f/p) mice completely lacked any arousal response to inhalation of 10% CO(2) (with 21% O(
20  and physiologic evidence points to impaired arousal responses to hypercarbia and hypoxia, which ulti
21 ith 21% O(2) in balance N(2)) but had normal arousal responses to hypoxia, sound, and air puff.
22 ), we evaluated the muscle, ventilatory, and arousal responses to negative-pressure challenges during

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