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1 vity in the CNS compared to previous work on Hermissenda.
2 ane potential in both photoreceptor types of Hermissenda.
3 t may be required for neuronal plasticity in Hermissenda.
4 at are involved in classical conditioning in Hermissenda.
5 havior produced by Pavlovian conditioning of Hermissenda.
6 tage of memory for one-trial conditioning in Hermissenda.
7 ry, detected after one-trial conditioning of Hermissenda.
8 has been studied extensively in conditioned Hermissenda.
9 ay is activated in Pavlovian conditioning of Hermissenda.
10 in Tritonia and Pleurobranchaea, but not in Hermissenda.
11 were examined in isolated photoreceptors of Hermissenda.
12 oked spike frequency) of B photoreceptors in Hermissenda accompanied successive pairings of light and
16 us system, indicating a homology between the Hermissenda channels and their mammalian counterparts.
18 frondosus, and Melibe leonina), Aeolidoidea (Hermissenda crassicornis and Flabellina trophina), Armin
21 ses of CI, we exposed the nudibranch mollusc Hermissenda crassicornis to explicitly unpaired (EU) pre
22 mologs of these neurons also can be found in Hermissenda crassicornis where they are named CPT and C2
28 r photoreceptor responses were recorded from Hermissenda exposed to compound conditioning, light cond
29 ical or biochemical effects were observed in Hermissenda exposed to unpaired light and rotation or in
31 rdings from the type B photoreceptors of the Hermissenda eye reveal a learning specific increase of i
32 light and rotation, B photoreceptors in the Hermissenda eye undergo an increase in excitability that
33 cell types are correlates of conditioning in Hermissenda, modulation of these underlying currents may
34 -type (alpha1(A)) channels in lysates of the Hermissenda nervous system, indicating a homology betwee
35 Although CSP24 is widely distributed in the Hermissenda nervous system, its regulation by one-trial
40 Analysis of protein kinase C (PKC) in the Hermissenda's photoreceptors indicated a training-induce
42 ptions of conditioned response generation in Hermissenda stipulate that the synaptic interaction betw
45 synapse in the nervous system of the mollusc Hermissenda, the influence of somatic calcium accumulati
46 In Tritonia and Pleurobranchaea, but not in Hermissenda, the serotonergic DSI homologs modulated the
47 ntensity influence classical conditioning in Hermissenda through their effects on the light-induced c
48 ence, but not unpaired presentations, causes Hermissenda to contract its foot in response to light al
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