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1 vation in response to agonist stimulation of bombesin receptor.
2 vation in response to agonist stimulation of bombesin receptor.
3 osphorylation emanate from a single class of bombesin receptor.
4 g to their specific, high-affinity mammalian bombesin receptors.
5 nist with differing affinities for the known bombesin receptors.
6 -His-Sta-Leu-NH2 ((68)Ga-RM2) is a synthetic bombesin receptor antagonist that targets gastrin-releas
7 -His-Sta-Leu-NH2 ((68)Ga-RM2) is a synthetic bombesin receptor antagonist that targets gastrin-releas
8 l endopeptidase, which degrades bombesin, or bombesin receptor antagonists blocked bombesin-induced p
9 in and carbocyanine dyes to somatostatin and bombesin receptor-avid peptides and examined their recep
10 nase (MAPK) by a Gq/11-coupled receptor, the bombesin receptor (BR), and a Gi-coupled receptor, the D
11 ecipitated 60% of the solubilized [125I-Tyr4]bombesin/receptor complex prepared from either Swiss 3T3
12 to purified G protein alpha subunits by the bombesin receptor family, including gastrin-releasing pe
14 as inhibited almost completely by a specific bombesin receptor inhibitor, [Tyr4, D-Phe12]-bombesin (1
15 a selective agonist for the BB(2) subtype of bombesin receptor, is reported to depolarise GABAergic i
17 subtype 3 (BRS-3), shares high homology with bombesin receptors (neuromedin B receptor (NMB-R) and ga
18 4, encoding a receptor related to vertebrate bombesin receptors, responds specifically to allatostati
24 ed that U-87MG xenografts expressed mRNA for bombesin receptor subtype (BRS)-1 (GRP receptor) and BRS
25 rphan receptor discovered in 1993 was called bombesin receptor subtype 3 (BRS-3) because of 47-51% am
27 (GRP-R), the neuromedin B receptor (NMB-R), bombesin receptor subtype 3 (BRS-3), and bombesin recept
31 astrin-releasing peptide [GRP] receptor, and bombesin receptor subtype 3 [BRS-3]) in human non-small
32 ne expression, and identified mRNAs encoding bombesin receptor subtype 3 and neuromedin-B receptor (N
34 besin, gastrin-releasing peptide, NMB, and a bombesin receptor subtype 3-specific ligand induced mast
37 ffinity, but they are diverged in BRS-3, the bombesin receptor subtype that binds bombesin with much
41 t the expression of the previously described bombesin-receptor subtype 4 is limited to amphibians.
43 studies reveal that the structurally similar bombesin receptor subtypes, in particular BRS-3, possess
44 lish a contiguous signaling pathway from the bombesin receptor to ROCK in PC cells, and they implicat
45 and leukemia-associated RhoGEF (LARG), link bombesin receptors to RhoA in a non-redundant manner in
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