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1 gellum of the antennule of the spiny lobster Panulirus argus houses more than 1,000 morphologically s
2 e we report, however, that the spiny lobster Panulirus argus oriented reliably towards a capture site
3 eptor neurons of the Caribbean spiny lobster Panulirus argus possesses receptors for L-glutamate that
4 he antennules of the Caribbean spiny lobster Panulirus argus revealed three types of nonaesthetasc ch
5 ated from the hemocytes of the spiny lobster Panulirus argus with regulatory functions on the melaniz
6 ropod predators-the Caribbean spiny lobster (Panulirus argus) and the grunt black margate (Anisotremu
7 ormally gregarious Caribbean spiny lobsters (Panulirus argus) avoid conspecifics that are infected wi
8  larval phases, the Caribbean spiny lobster (Panulirus argus).
9 eurogenic complexes in adult spiny lobsters, Panulirus argus, based on transmission electron microsco
10                 The Caribbean spiny lobster, Panulirus argus, is one of the most valuable fisheries c
11 pheral olfactory system of the spiny lobster Panulirus argus--located on paired antennules--undergoes
12 tive 'bursting' ORNs (bORNs) in the lobster, Panulirus argus.
13 capod crustaceans, including spiny lobsters, Panulirus argus.
14 anglion (STG) of the Caribbean spiny lobster Panulirus argus.
15 ant nursery for the Caribbean spiny lobster, Panulirus argus.
16 on antennules of the Caribbean spiny lobster Panulirus argus.
17 nile habitat for the Caribbean spiny lobster Panulirus argus.
18 ysis of CoG tissues from Cancer borealis and Panulirus interruptus and show that orcokinins in P. int
19 n the stomatogastric ganglion of the lobster Panulirus interruptus is a graded function of membrane p
20 ogastric neuromuscular system of the lobster Panulirus interruptus produce highly deterministic (rang
21 bundance with fishery data of spiny lobster (Panulirus interruptus) landings to evaluate whether: (1)
22 us system of male and female spiny lobsters (Panulirus interruptus), focused on dynamic SUMOylation i
23 ca), which, when attacked by spiny lobsters (Panulirus interruptus), release defensive secretions fro
24 of the pyloric network in the spiny lobster, Panulirus interruptus, and its modulation by dopamine.
25 nal response of the California spiny lobster Panulirus interruptus, foraging on a key ecosystem engin
26  a co-occurring predator, the spiny lobster, Panulirus interruptus, might be a natural sensitizing st
27 tomatogastric ganglion of the spiny lobster, Panulirus interruptus, results not only from the synapti
28 ically active pyloric network of the lobster Panulirus interruptus, synaptic connections from the pac
29 stomatogastric ganglion of the spiny lobster Panulirus interruptus.
30 it and cellular levels in the spiny lobster, Panulirus interruptus.
31 e arthropod receptor from the spiny lobster, Panulirus interruptus.
32 es, Homarus americanus, Cancer borealis, and Panulirus interruptus.
33 ogastric ganglion (STG) of the spiny lobster Panulirus interruptus.
34 neuron pyloric network of the spiny lobster, Panulirus interruptus.
35 otassium channel gene from the spiny lobster Panulirus interruptus.
36 tomatogastric ganglion of the spiny lobster, Panulirus interruptus.
37 assium (K+) channel, from the spiny lobster, Panulirus interruptus.
38  the IAs obtained from oocytes injected with Panulirus shaker and shal cRNA (lobster Ishaker and lobs
39                                  However, in Panulirus shaker, alternative splicing also occurs withi
40 ty, we examined the relationship between the Panulirus shal current, the IAs in the lateral pyloric (
41 , heteromers between the two pore forms, and Panulirus shal were not blocked.
42                    When it was tested in the Panulirus stomatogastric ganglion, the toxin produced no