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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.
6 compared the preclinical performance of the gastrin-releasing peptide receptor antagonists RM2 (DOTA
7 rostate-specific membrane antigen (PSMA) and gastrin-releasing peptide receptors are both overexpress
8 rostate-specific membrane antigen (PSMA) and gastrin-releasing peptide receptors are both overexpress
11 lls transfected with the Gq-coupled bombesin/gastrin releasing peptide receptor, bombesin stimulated
12 is and to use bombesin analogs to target the gastrin-releasing peptide receptor for the diagnosis and
14 ed by cells expressing the G-protein-coupled gastrin-releasing peptide receptor (GRP-R) and is curren
17 imilar rationale, radioligands targeting the gastrin-releasing peptide receptor (GRP-R) might offer a
18 ll lines were made that stably expressed the gastrin-releasing peptide receptor (GRP-R) with receptor
20 s by the bombesin receptor family, including gastrin-releasing peptide receptor (GRP-R), neuromedin B
21 -coupled receptors currently consists of the gastrin-releasing peptide receptor (GRP-R), neuromedin B
22 udy we demonstrate that for the G(q)-coupled gastrin-releasing peptide receptor (GRP-R), phosphorylat
23 ceptor subtypes have been characterized: the gastrin-releasing peptide receptor (GRP-R), the neuromed
24 of G-protein-coupled receptors includes the gastrin-releasing peptide receptor (GRP-R), the neuromed
26 al, G-protein coupled receptors includes the gastrin-releasing peptide receptor (GRP-R, or bb2), neur
27 ly reported that a gastrin-releasing peptide/gastrin-releasing peptide receptor (GRP/GRPR) autocrine
32 , we show that the spinal neurons expressing gastrin releasing peptide receptor (GRPR) primarily comp
33 into tumor cells, their affinity toward the gastrin releasing peptide receptor (GRPr), metabolic sta
34 e been proposed for diagnosis and therapy of gastrin releasing peptide receptor (GRPR)-expressing tum
38 e treatment of prostate cancer, radiolabeled gastrin-releasing peptide receptor (GRPr) antagonists ha
39 e spinal cord to establish that NK1R and the gastrin-releasing peptide receptor (GRPR) are coexpresse
40 romosome occurred in the first intron of the gastrin-releasing peptide receptor (GRPR) gene and that
43 eraction between u-opioid receptor (MOR) and gastrin-releasing peptide receptor (GRPR) in spinal GRPR
49 Although our previous study suggested that gastrin-releasing peptide receptor (GRPR) is an itch-spe
60 A growing body of evidence suggests that gastrin-releasing peptide receptor (GRPR) might be a val
65 he Trpv1-Cre population, depends on CGRP and gastrin-releasing peptide receptor (GRPR) transmission b
66 ckbones to generate bivalent ligands for the gastrin-releasing peptide receptor (GRPR) with a fixed d
69 BBN) is a peptide with high affinity for the gastrin-releasing peptide receptor (GRPr), a receptor th
70 tion of the mammalian bombesin (Bn) peptide, gastrin-releasing peptide receptor (GRPR), is an excepti
73 peptide that binds with high affinity to the gastrin-releasing peptide receptor (GRPR), which is over
74 isplay very high selectivity/specificity for gastrin-releasing peptide receptor (GRPR)-/prostate-spec
81 the spinal dorsal horn (SDH) that expresses gastrin-releasing peptide receptors (GRPR) is critical f
82 specificity of coupling interactions between gastrin-releasing peptide receptors (GRPrs) and their co
83 rostate-specific membrane antigen (PSMA) and gastrin-releasing peptide receptors (GRPRs) are both ove
90 kinase is dependent on the expression of the gastrin-releasing peptide receptor in rat 1A fibroblasts
91 ded to understand the expression of PSMA and gastrin-releasing peptide receptors in different types o
93 icals, such as prostate-specific membrane or gastrin-releasing peptide receptor ligands for the imagi
96 different neuropeptides for itch, including gastrin-releasing peptide receptor, natriuretic peptide
97 FITC-labeled bombesin-like peptide with the gastrin-releasing peptide receptor on PC-3 and HT-29 cel
102 BON cells or BON cells stably expressing the gastrin-releasing peptide receptor treated with either p
103 between an agonist and an antagonist for the gastrin-releasing peptide receptor were found to have ex
104 ceptors (m3 muscarinic, V1a vasopressin, and gastrin-releasing peptide receptor) were coexpressed (in