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1 ed independently of neurons that express the gastrin-releasing peptide receptor.
2 3 and neuromedin-B receptor (NMB-R), but not gastrin-releasing peptide receptor.
3 ic bombesin receptor antagonist that targets gastrin-releasing peptide receptors.
5 lls transfected with the Gq-coupled bombesin/gastrin releasing peptide receptor, bombesin stimulated
6 is and to use bombesin analogs to target the gastrin-releasing peptide receptor for the diagnosis and
8 ed by cells expressing the G-protein-coupled gastrin-releasing peptide receptor (GRP-R) and is curren
10 imilar rationale, radioligands targeting the gastrin-releasing peptide receptor (GRP-R) might offer a
11 ll lines were made that stably expressed the gastrin-releasing peptide receptor (GRP-R) with receptor
13 s by the bombesin receptor family, including gastrin-releasing peptide receptor (GRP-R), neuromedin B
14 -coupled receptors currently consists of the gastrin-releasing peptide receptor (GRP-R), neuromedin B
15 udy we demonstrate that for the G(q)-coupled gastrin-releasing peptide receptor (GRP-R), phosphorylat
16 ceptor subtypes have been characterized: the gastrin-releasing peptide receptor (GRP-R), the neuromed
17 of G-protein-coupled receptors includes the gastrin-releasing peptide receptor (GRP-R), the neuromed
19 al, G-protein coupled receptors includes the gastrin-releasing peptide receptor (GRP-R, or bb2), neur
20 ly reported that a gastrin-releasing peptide/gastrin-releasing peptide receptor (GRP/GRPR) autocrine
21 ly reported that a gastrin-releasing peptide/gastrin-releasing peptide receptor (GRP/GRPR) autocrine
25 into tumor cells, their affinity toward the gastrin releasing peptide receptor (GRPr), metabolic sta
26 e been proposed for diagnosis and therapy of gastrin releasing peptide receptor (GRPR)-expressing tum
29 e treatment of prostate cancer, radiolabeled gastrin-releasing peptide receptor (GRPr) antagonists ha
30 romosome occurred in the first intron of the gastrin-releasing peptide receptor (GRPR) gene and that
34 Although our previous study suggested that gastrin-releasing peptide receptor (GRPR) is an itch-spe
40 A growing body of evidence suggests that gastrin-releasing peptide receptor (GRPR) might be a val
44 he Trpv1-Cre population, depends on CGRP and gastrin-releasing peptide receptor (GRPR) transmission b
47 BBN) is a peptide with high affinity for the gastrin-releasing peptide receptor (GRPr), a receptor th
48 tion of the mammalian bombesin (Bn) peptide, gastrin-releasing peptide receptor (GRPR), is an excepti
51 peptide that binds with high affinity to the gastrin-releasing peptide receptor (GRPR), which is over
55 specificity of coupling interactions between gastrin-releasing peptide receptors (GRPrs) and their co
60 kinase is dependent on the expression of the gastrin-releasing peptide receptor in rat 1A fibroblasts
61 ded to understand the expression of PSMA and gastrin-releasing peptide receptors in different types o
62 icals, such as prostate-specific membrane or gastrin-releasing peptide receptor ligands for the imagi
65 FITC-labeled bombesin-like peptide with the gastrin-releasing peptide receptor on PC-3 and HT-29 cel
66 BON cells or BON cells stably expressing the gastrin-releasing peptide receptor treated with either p
67 between an agonist and an antagonist for the gastrin-releasing peptide receptor were found to have ex
68 ceptors (m3 muscarinic, V1a vasopressin, and gastrin-releasing peptide receptor) were coexpressed (in
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