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1 n that is similar to a Phe-Met-Arg-Phe-amide neuropeptide receptor.
2  behaviors through the activity of the NPR-1 neuropeptide receptor.
3  regulated by natural variation in the npr-1 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  changes in gene expression, notably of many neuropeptide receptors.
8 le downstream neurons that express different neuropeptide receptors.
9 urotransmitter receptors, neuropeptides, and neuropeptide receptors.
10                                              Neuropeptide receptor 1 (NPR-1) is a G-protein coupled r
11 crease in the expression of the CREB targets neuropeptide receptor 1 (NPY1R) and brain-derived neurot
12 e ASH-mediated aversive behavior through the neuropeptide receptor-17 (NPR-17) receptor.
13 we identified the G-protein-coupled receptor neuropeptide receptor 36 (NPR-36) as an NLP-3 neuropepti
14    We developed a multiscale model to bridge neuropeptide receptor-activated signaling pathway activi
15                  We focused on the mu-opioid neuropeptide receptor and the beta(2)-adrenergic catecho
16 n defined that exhibit broad specificity for neuropeptide receptors and induce apoptosis in SCLC by f
17  complex neurochemical profiles that include neuropeptides, receptors and components of fast neurotra
18 be an array of genes encoding neuropeptides, neuropeptide receptors, and other nerve-related proteins
19 owever, dieldrin had more notable effects on neuropeptide receptors, and overlap between diazinon and
20 cules, transcription factors, neuropeptides, neuropeptide receptors, and Wnts have unique patterns of
21 ty of these responses was demonstrated using neuropeptide receptor antagonists and nerve growth facto
22                                     Numerous neuropeptide receptors are expressed by DCs but only a f
23 gulate the MCH system, we investigated which neuropeptide receptors are expressed by MCH neurons by u
24 eutic agents for treatment of SCLC and other neuropeptide receptor-bearing cancers.
25 nsmitter (ACh, GABA, glutamate), and various neuropeptide receptor-coding genes showed differential e
26             The data provide evidence that a neuropeptide receptor controls gene expression in the CN
27                                              Neuropeptide receptors couple via G-proteins to two prin
28 inct codes of ~23 neuropeptide genes and ~36 neuropeptide receptors, delineating a complex and expans
29 iations in receptor gene structure can alter neuropeptide receptor distribution and thereby contribut
30              These findings suggest that the neuropeptide receptor EGL-6 regulates the potassium chan
31 n orchestrated by differential post-synaptic neuropeptide receptor expression at the GnRH neuron dend
32                 We surveyed neuropeptide and neuropeptide receptor expression in the central brain us
33                   Differential regulation of neuropeptide receptor expression may explain species dif
34 dge gap, we conducted a screen of mutants in neuropeptide receptor family genes.
35 ls, an increased expression of the mitogenic neuropeptide receptors for gastrin-releasing peptide and
36 e diverse pharmacological characteristics of neuropeptide receptors form the basis of unique neuromod
37                   We further identified four neuropeptide-receptor functional modules with ten or mor
38     RMG is the central site of action of the neuropeptide receptor gene npr-1, which distinguishes so
39 henotypic variation to a polymorphism in the neuropeptide receptor gene npr-1.
40 phrodites with reduced activity of the npr-1 neuropeptide receptor gene.
41  is inhibited by the npr-1 G protein-coupled neuropeptide receptor gene.
42                 Thus, isoforms of a putative neuropeptide receptor generate natural variation in C. e
43     Similar experiments on midline-expressed neuropeptide receptor genes reveal considerable diversit
44 s express 9 neuropeptide precursor genes, 13 neuropeptide receptor genes, and 31 small-molecule neuro
45 ress in the characterization of invertebrate neuropeptide receptors, has the potential to propel neur
46                                     Specific neuropeptide receptors have been identified as possible
47 tected expression of 60 neuropeptides and 60 neuropeptide receptors in at least one of the hPFC subre
48               The differential expression of neuropeptide receptors in disinhibitory, inhibitory, and
49 approach to de-orphan and study 11 GPCRs for neuropeptide receptors in Drosophila melanogaster.
50                                      Mapping neuropeptide receptors in these nontraditional species q
51 uped Clytia MIHR with a subset of bilaterian neuropeptide receptors, including neuropeptide Y, gonado
52 l terminus of a chimeric mutant delta opioid neuropeptide receptor is sufficient to re-route internal
53 hrough Gq and PLCbeta by autocrine-signaling neuropeptide receptors is a dominant pathway involved in
54 rformed a comprehensive functional screen of neuropeptide receptor mutants for pheromone-induced diap
55                                          The neuropeptide receptor neuropeptide Y receptor type 1 (Np
56                                          The neuropeptide receptor Nmur1 was preferentially expressed
57                     Dopamine, serotonin, the neuropeptide receptor NPR-1, and the TGF-beta peptide DA
58 raging is modified by the naturally variable neuropeptide receptor npr-1, providing insights into how
59 voidance behaviour through inhibition of the neuropeptide receptor NPR-1, which we have previously sh
60 CO2 response is regulated by the polymorphic neuropeptide receptor NPR-1: animals with the N2 allele
61 hat elevated ADL expression of the conserved neuropeptide receptor NPR-22 is necessary for enhanced A
62  to decrease adaptation on food, whereas the neuropeptide receptors NPR-1 and NPR-2 act to increase a
63 lethargus was abolished in mutants lacking a neuropeptide receptor (NPR-1) and was reduced in mutants
64 ith an array of ASI neuropeptides activating neuropeptide receptors on additional neurons involved in
65 trin-releasing peptide receptor (GRP-R) is a neuropeptide receptor overexpressed by low-risk prostate
66                                            A neuropeptide-receptor pair promotes the differentiation
67             The precise in vivo role of this neuropeptide-receptor pathway has not been fully demonst
68 icular stressors may be mediated by specific neuropeptide receptor patterns in the brain.
69 and pheromone signals requires the conserved neuropeptide receptor PDFR-1, as pdfr-1 mutant hermaphro
70 ence in NPR-1, a predicted G-protein-coupled neuropeptide receptor related to Neuropeptide Y receptor
71 ermore, most neuron classes expressed unique neuropeptide receptor repertoires that have opposing eff
72 ral circuit signals through peripheral NPR-4/neuropeptide receptor, SGK-1/serum- and glucocorticoid-i
73                      We found that mu-opioid neuropeptide receptors signal to their enclosing CCPs by
74  conducting a systems-level investigation of neuropeptide receptor signaling function and cell-type-s
75               Here, we identify two opposing neuropeptide/receptor signaling pathways: NLP-22 promote
76                                 Further, the neuropeptide receptor somatostatin receptor 3 (SSTR3) is
77 ion of individual neuron classes by distinct neuropeptide receptor subsets could serve as a strategy
78                     This review focuses on 3 neuropeptide receptor systems (bombesin, neurotensin, an
79                                 Knowledge on neuropeptide receptor systems is integral to understandi
80                            Studies show that neuropeptide-receptor systems in the basolateral amygdal
81 novel neuropeptides, it is likely that other neuropeptide-receptor systems may also utilize changes i
82 mical characterization of GLB-33, a putative neuropeptide receptor that is exclusively expressed in t
83                                Surprisingly, neuropeptide receptors that influence breathing (e.g., u
84          We studied the relationship between neuropeptide receptor transcript expression and current
85 europeptide receptor 36 (NPR-36) as an NLP-3 neuropeptide receptor using genetic and molecular experi
86 licated WBS phenotypes by downregulating the neuropeptide receptor VIPR1.
87                                              Neuropeptide receptors were expressed more broadly and a
88                                  Overall, 11 neuropeptide receptors were found to exhibit significant
89  gene, npr-1, encodes a previously described neuropeptide receptor whose high activity in N2 promotes