Ability of various bombesin receptor agonists and antagonists to alter intracellular signaling of the human orphan receptor BRS-3.
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International Union of Pharmacology. LXVIII. Mammalian bombesin receptors: nomenclature, distribution, pharmacology, signaling, and functions in normal and disease statesThe Nutrient-Responsive Hormone CCHamide-2 Controls Growth by Regulating Insulin-like Peptides in the Brain of Drosophila melanogasterInsights into bombesin receptors and ligands: Highlighting recent advancesSystematic optimization of a lead-structure identities for a selective short peptide agonist for the human orphan receptor BRS-3.Rational design of a peptide agonist that interacts selectively with the orphan receptor, bombesin receptor subtype 3.Bombesin receptor subtype 3 as a potential target for obesity and diabetes.Novel chiral-diazepines function as specific, selective receptor agonists with variable coupling and species variability in human, mouse and rat BRS-3 receptor cells.Pharmacology of putative selective hBRS-3 receptor agonists for human bombesin receptors (BnR): affinities, potencies and selectivity in multiple native and BnR transfected cells.Bombesin receptor-mediated imaging and cytotoxicity: review and current statusPharmacology and selectivity of various natural and synthetic bombesin related peptide agonists for human and rat bombesin receptors differs.Peptides with anticancer use or potential.The molecular basis for high affinity of a universal ligand for human bombesin receptor (BnR) family members.Molecular basis for agonist selectivity and activation of the orphan bombesin receptor subtype 3 receptor.Comparative pharmacology of bombesin receptor subtype-3, nonpeptide agonist MK-5046, a universal peptide agonist, and peptide antagonist Bantag-1 for human bombesin receptorsGastrin-releasing peptide (GRP) in the ovine uterus: regulation by interferon tau and progesteroneCharacterization of putative GRP- and NMB-receptor antagonist's interaction with human receptors.A selective human bombesin receptor subtype-3 peptide agonist mediates CREB phosphorylation and transactivation.Developmental expression and biological activity of gastrin-releasing peptide and its receptors in the kidney.Identification and functional characterization of hemorphins VV-H-7 and LVV-H-7 as low-affinity agonists for the orphan bombesin receptor subtype 3.Discovery of potent and selective peptide agonists at the GRP-preferring bombesin receptor (BB2).Molecular basis for high affinity and selectivity of peptide antagonist, Bantag-1, for the orphan BB3 receptor.A possible new target in lung-cancer cells: The orphan receptor, bombesin receptor subtype-3.
P2860
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P2860
Ability of various bombesin receptor agonists and antagonists to alter intracellular signaling of the human orphan receptor BRS-3.
description
1998 nî lūn-bûn
@nan
1998 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Ability of various bombesin re ...... e human orphan receptor BRS-3.
@ast
Ability of various bombesin re ...... e human orphan receptor BRS-3.
@en
Ability of various bombesin re ...... e human orphan receptor BRS-3.
@nl
type
label
Ability of various bombesin re ...... e human orphan receptor BRS-3.
@ast
Ability of various bombesin re ...... e human orphan receptor BRS-3.
@en
Ability of various bombesin re ...... e human orphan receptor BRS-3.
@nl
prefLabel
Ability of various bombesin re ...... e human orphan receptor BRS-3.
@ast
Ability of various bombesin re ...... e human orphan receptor BRS-3.
@en
Ability of various bombesin re ...... e human orphan receptor BRS-3.
@nl
P2093
P2860
P356
P1476
Ability of various bombesin re ...... e human orphan receptor BRS-3.
@en
P2093
P2860
P304
13613-13624
P356
10.1074/JBC.273.22.13613
P407
P577
1998-05-01T00:00:00Z