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1 the neurosecretory neurons that also express crustacean cardioactive peptide.
2  beta-pigment-dispersing hormone (beta-PDH), crustacean cardioactive peptide, and red pigment-concent
3 ykinin-related peptide, cholecystokinin, and crustacean cardioactive peptide are present in the POs b
4               Previous findings suggest that crustacean cardioactive peptide (CCAP) activates the ecd
5 otic defect is circuit-specific by examining crustacean cardioactive peptide (CCAP) and bursicon circ
6 in ecdysis, including Eclosion hormone (EH), Crustacean cardioactive peptide (CCAP) and Bursicon.
7                                              Crustacean cardioactive peptide (CCAP) and related pepti
8 examine the integrated action of the hormone crustacean cardioactive peptide (CCAP) and the gastropyl
9 eptides ecdysis-triggering hormone (ETH) and crustacean cardioactive peptide (CCAP) elicit the first
10                                              Crustacean cardioactive peptide (CCAP) elicited expressi
11 whereas ecdysis-triggering hormone (ETH) and crustacean cardioactive peptide (CCAP) evolved in the bi
12  subset of Drosophila neurons that expresses crustacean cardioactive peptide (CCAP) has been shown pr
13 ic ganglion of the crab, Cancer borealis, by crustacean cardioactive peptide (CCAP) is described.
14                                              Crustacean cardioactive peptide (CCAP) neurons and the p
15 s, including insulin producing cells (IPCs), crustacean cardioactive peptide (CCAP) neurons, and CCHa
16 t neonicotinoids may disrupt the function of crustacean cardioactive peptide (CCAP) neurons, either b
17 s effect is distinct from that of peripheral crustacean cardioactive peptide (CCAP) neurons, which po
18 y by modulating the release of peptides from crustacean cardioactive peptide (CCAP) neurons.
19 it has been postulated that the neuropeptide Crustacean cardioactive peptide (CCAP) plays a key role
20  transcript with high sequence similarity to crustacean cardioactive peptide (CCAP) receptors in inse
21 ale crabs, Cancer borealis Proctolin (PROC), crustacean cardioactive peptide (CCAP), and red pigment
22        These peptides include allatostatins, crustacean cardioactive peptide (CCAP), calcitonin-like
23 in the vasopressin receptor group respond to crustacean cardioactive peptide (CCAP), corazonin, or ad
24 ng the mechanism by which a peptide hormone, crustacean cardioactive peptide (CCAP), modulates the bi
25 ng kinin, FMRFamides, eclosion hormone (EH), crustacean cardioactive peptide (CCAP), myoinhibitory pe
26 ncer borealis tachykinin-related peptide Ia, crustacean cardioactive peptide (CCAP), red pigment-conc
27 s but also water uptake during moulting; and crustacean cardioactive peptide (CCAP), which is involve
28                         We discovered that 2 crustacean cardioactive peptide (CCAP)-expressing neuron
29                                              Crustacean cardioactive peptide (CCAP)-expressing neuron
30 including the gene encoding the neuropeptide crustacean cardioactive peptide (CCAP).
31  revealed that bursicon is co-expressed with crustacean cardioactive peptide (CCAP).
32 ng hormone (ETH), eclosion hormone (EH), and crustacean cardioactive peptide (CCAP).
33  at ecdysis, and all were immunopositive for crustacean cardioactive peptide (CCAP).
34 ced wing expansion defects when crossed to a crustacean cardioactive peptide (CCAP)/bursicon neuron-s
35                                 In addition, crustacean cardioactive peptide-immunoreactive fibers or
36 rotein labeling of burs and pburs as well as crustacean cardioactive peptide in neurons of the ventra
37      In the PNS, MasITPL is coexpressed with crustacean cardioactive peptide in type II link nerve ne
38 s tachykinin-related peptide Ia (CabTRP Ia), crustacean cardioactive peptide, red pigment-concentrati
39 short neuropeptides F, extended FMRFamides], crustacean cardioactive peptide, tachykinin-related pept
40 se of peptidergic neurons that produce CCAP (crustacean cardioactive peptide), which are key targets