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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
13 gh affinity agonists or antagonists at other bombesin receptors had an affinity >1000 nM.
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
16                      Upon stimulation of the bombesin receptors, KUZ increases the docking and activa
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
19 the binding affinity of each peptide for the bombesin receptor site was determined.
20 both Galpha(q) and Galpha(13) in response to bombesin receptor stimulation.
21 lso attenuated PKD activation in response to bombesin receptor stimulation.
22 mediates PKD activation in response to acute bombesin receptor stimulation.
23                                The mammalian bombesin receptor subfamily of G protein-coupled recepto
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
26                                        Human bombesin receptor subtype 3 (BRS-3) was cloned based on
27  (GRP-R), the neuromedin B receptor (NMB-R), bombesin receptor subtype 3 (BRS-3), and bombesin recept
28  (GRP-R), neuromedin B receptor (NMB-R), and bombesin receptor subtype 3 (BRS-3).
29 P-R), the neuromedin B receptor (NMB-R), and bombesin receptor subtype 3 (BRS-3).
30 uromedin B receptor (NMB-R, or bb1), and the bombesin receptor subtype 3 (BRS-3, or bb3).
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
33         Neuromedin B (NMB) receptor-null and bombesin receptor subtype 3-null mice had the same respo
34 besin, gastrin-releasing peptide, NMB, and a bombesin receptor subtype 3-specific ligand induced mast
35 receptor (GRP-R), neuromedin B receptor, and bombesin receptor subtype 3.
36 R), bombesin receptor subtype 3 (BRS-3), and bombesin receptor subtype 4 (bb4).
37 ffinity, but they are diverged in BRS-3, the bombesin receptor subtype that binds bombesin with much
38          We cloned the gene and cDNA for rat bombesin receptor subtype-3 (BRS-3) and characterized it
39                                              Bombesin receptor subtype-3 (BRS-3) is an orphan G-prote
40 astrin-releasing peptide-preferring, and the bombesin-receptor subtype 3.
41 t the expression of the previously described bombesin-receptor subtype 4 is limited to amphibians.
42                              Three mammalian bombesin receptor subtypes have been characterized: the
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
46 ombesin, whereas neither NMB nor a synthetic bombesin receptor type 3 ligand had any effect.

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