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1  behaviors through the activity of the NPR-1 neuropeptide receptor.
2  regulated by natural variation in the npr-1 neuropeptide receptor.
3 n that is similar to a Phe-Met-Arg-Phe-amide neuropeptide receptor.
4 ell identity for these neuropeptides and the neuropeptide receptors.
5  in identifying novel antagonist ligands for neuropeptide receptors.
6 signaling through multiple G protein-coupled neuropeptide receptors.
7                                              Neuropeptide receptor 1 (NPR-1) is a G-protein coupled r
8 crease in the expression of the CREB targets neuropeptide receptor 1 (NPY1R) and brain-derived neurot
9 e ASH-mediated aversive behavior through the neuropeptide receptor-17 (NPR-17) receptor.
10    We developed a multiscale model to bridge neuropeptide receptor-activated signaling pathway activi
11                  We focused on the mu-opioid neuropeptide receptor and the beta(2)-adrenergic catecho
12 n defined that exhibit broad specificity for neuropeptide receptors and induce apoptosis in SCLC by f
13  complex neurochemical profiles that include neuropeptides, receptors and components of fast neurotra
14 owever, dieldrin had more notable effects on neuropeptide receptors, and overlap between diazinon and
15 ty of these responses was demonstrated using neuropeptide receptor antagonists and nerve growth facto
16 gulate the MCH system, we investigated which neuropeptide receptors are expressed by MCH neurons by u
17 eutic agents for treatment of SCLC and other neuropeptide receptor-bearing cancers.
18             The data provide evidence that a neuropeptide receptor controls gene expression in the CN
19                                              Neuropeptide receptors couple via G-proteins to two prin
20 iations in receptor gene structure can alter neuropeptide receptor distribution and thereby contribut
21              These findings suggest that the neuropeptide receptor EGL-6 regulates the potassium chan
22                   Differential regulation of neuropeptide receptor expression may explain species dif
23 ls, an increased expression of the mitogenic neuropeptide receptors for gastrin-releasing peptide and
24                   We further identified four neuropeptide-receptor functional modules with ten or mor
25     RMG is the central site of action of the neuropeptide receptor gene npr-1, which distinguishes so
26 henotypic variation to a polymorphism in the neuropeptide receptor gene npr-1.
27 phrodites with reduced activity of the npr-1 neuropeptide receptor gene.
28  is inhibited by the npr-1 G protein-coupled neuropeptide receptor gene.
29                 Thus, isoforms of a putative neuropeptide receptor generate natural variation in C. e
30     Similar experiments on midline-expressed neuropeptide receptor genes reveal considerable diversit
31 s express 9 neuropeptide precursor genes, 13 neuropeptide receptor genes, and 31 small-molecule neuro
32 ress in the characterization of invertebrate neuropeptide receptors, has the potential to propel neur
33 approach to de-orphan and study 11 GPCRs for neuropeptide receptors in Drosophila melanogaster.
34 l terminus of a chimeric mutant delta opioid neuropeptide receptor is sufficient to re-route internal
35 hrough Gq and PLCbeta by autocrine-signaling neuropeptide receptors is a dominant pathway involved in
36                                          The neuropeptide receptor Nmur1 was preferentially expressed
37                     Dopamine, serotonin, the neuropeptide receptor NPR-1, and the TGF-beta peptide DA
38 raging is modified by the naturally variable neuropeptide receptor npr-1, providing insights into how
39 voidance behaviour through inhibition of the neuropeptide receptor NPR-1, which we have previously sh
40 CO2 response is regulated by the polymorphic neuropeptide receptor NPR-1: animals with the N2 allele
41  to decrease adaptation on food, whereas the neuropeptide receptors NPR-1 and NPR-2 act to increase a
42 lethargus was abolished in mutants lacking a neuropeptide receptor (NPR-1) and was reduced in mutants
43 ith an array of ASI neuropeptides activating neuropeptide receptors on additional neurons involved in
44             The precise in vivo role of this neuropeptide-receptor pathway has not been fully demonst
45 icular stressors may be mediated by specific neuropeptide receptor patterns in the brain.
46 ence in NPR-1, a predicted G-protein-coupled neuropeptide receptor related to Neuropeptide Y receptor
47                      We found that mu-opioid neuropeptide receptors signal to their enclosing CCPs by
48                     This review focuses on 3 neuropeptide receptor systems (bombesin, neurotensin, an
49                                 Knowledge on neuropeptide receptor systems is integral to understandi
50                            Studies show that neuropeptide-receptor systems in the basolateral amygdal
51 mical characterization of GLB-33, a putative neuropeptide receptor that is exclusively expressed in t
52          We studied the relationship between neuropeptide receptor transcript expression and current
53                                  Overall, 11 neuropeptide receptors were found to exhibit significant
54  gene, npr-1, encodes a previously described neuropeptide receptor whose high activity in N2 promotes

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