ライフサイエンスコーパス: siphon withdrawal

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1 cellular analog of classical conditioning of siphon withdrawal.

2 he CS and US produces greater enhancement of siphon withdrawal and evoked firing of LFS neurons, grea

3 elates significantly with the enhancement of siphon withdrawal and evoked firing of the LFS neurons.

4 The threshold required to elicit siphon withdrawal and the duration of siphon withdrawal

5 ex behaviors in Aplysia, tail withdrawal and siphon withdrawal, both elicited by threshold-level tail

6 , identical to that producing habituation in siphon withdrawal in freely moving animals, also produce

7 ubstantial contribution to the reflex in the siphon withdrawal preparation.

8 mplified gill-withdrawal preparation, in the siphon-withdrawal preparation we found no qualitative di

9 Furthermore, in the siphon-withdrawal preparation, all of the various cellul

10 e recorded evoked firing of LFS neurons, the siphon withdrawal produced by stimulation of an LFS neur

11 ambient environment can regulate the Aplysia siphon withdrawal reflex (SWR) by changing the environme

12 examined the modulation of the tail-induced siphon withdrawal reflex by repeated noxious stimuli app

13 The neural circuit mediating the siphon withdrawal reflex in Aplysia provides a useful ne

14 k-induced sensitization of the tail-elicited siphon withdrawal reflex in Aplysia to examine the role

15 of short- and long-term sensitization of the siphon withdrawal reflex in Aplysia.

16 Using the tail-elicited siphon withdrawal reflex of Aplysia, which is mediated i

17 oped a simplified preparation of the Aplysia siphon withdrawal reflex that allows one to examine beha

18 dies of habituation, such as in the gill and siphon withdrawal reflex to tactile stimulation of the s

19 ucture of sensory neurons mediating the tail-siphon withdrawal reflex.

20 te to classical conditioning of the gill and siphon withdrawal reflex.

21 ch contribute to dynamic gain control in the siphon withdrawal reflex.

22 es a stable reduction in the duration of the siphon-withdrawal reflex (SWR) and the responsiveness of

23 ory for long-term sensitization (LTS) of the siphon-withdrawal reflex (SWR) as late as 7 d after trai

24 ral adaptation and sensory adaptation in the siphon-withdrawal reflex (SWR) of Aplysia californica.

25 involved in simple forms of learning of the siphon-withdrawal reflex in a semiintact preparation.

26 ory for long-term sensitization (LTS) of the siphon-withdrawal reflex in the marine snail Aplysia cal

27 ituation and dishabituation of the gill- and siphon-withdrawal reflex in this preparation.

28 Classical conditioning of Aplysia's siphon-withdrawal reflex is thought to be due to a presy

29 new simplified preparation for studying the siphon-withdrawal reflex of Aplysia in which it is relat

30 nts that induce long-term enhancement of the siphon-withdrawal reflex, or long-term synaptic facilita

31 sing a simplified preparation of the Aplysia siphon-withdrawal reflex, we previously found that assoc

32 in a semi-intact preparation of the Aplysia siphon-withdrawal reflex.

33 n in a simplified preparation of the Aplysia siphon-withdrawal reflex.

34 iphon motor neurons on dishabituation of the siphon-withdrawal reflex.

35 s well as the duration of both the gill- and siphon-withdrawal reflexes were measured after either ta

36 roduces behavioral adaptation in the Aplysia siphon-withdrawal response (SWR).

37 elicit siphon withdrawal and the duration of siphon withdrawal were not regulated by the circadian cl

38 (<30 min) for sensitization of tail-elicited siphon withdrawal, whereas repeated spaced shocks induce

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