RGSZ1 interacts with protein kinase C interacting protein PKCI-1 and modulates mu opioid receptor signaling.
about
Duration of action of a broad range of selective κ-opioid receptor antagonists is positively correlated with c-Jun N-terminal kinase-1 activationRGS17, an overexpressed gene in human lung and prostate cancer, induces tumor cell proliferation through the cyclic AMP-PKA-CREB pathwayThe HINT1 tumor suppressor regulates both gamma-H2AX and ATM in response to DNA damageAxonal neuropathy with neuromyotonia: there is a HINT.Mu-opioid receptors transiently activate the Akt-nNOS pathway to produce sustained potentiation of PKC-mediated NMDAR-CaMKII signaling.SUMO-SIM interactions regulate the activity of RGSZ2 proteins.Regulation of neurite outgrowth by G(i/o) signaling pathways.Fine mapping of chromosome 6q23-25 region in familial lung cancer families reveals RGS17 as a likely candidate gene.Regulation of Smad-mediated gene transcription by RGS3.Variation in regulator of G-protein signaling 17 gene (RGS17) is associated with multiple substance dependence diagnoses.HINT1 protein cooperates with cannabinoid 1 receptor to negatively regulate glutamate NMDA receptor activity.Regulator of G Protein Signaling 17 as a Negative Modulator of GPCR Signaling in Multiple Human Cancers.Nitric oxide and zinc-mediated protein assemblies involved in mu opioid receptor signaling.Histidine triad nucleotide-binding protein 1 up-regulates cellular levels of p27KIP1 by targeting ScfSKP2 ubiquitin ligase and Src.PsHint1, associated with the G-protein α subunit PsGPA1, is required for the chemotaxis and pathogenicity of Phytophthora sojae.Functional cooperation of of IL-1β and RGS4 in the brachial plexus avulsion mediated brain reorganization.Kinetic mechanism of human histidine triad nucleotide binding protein 1.Gz mediates the long-lasting desensitization of brain CB1 receptors and is essential for cross-tolerance with morphine.Endocannabinoid control of glutamate NMDA receptors: the therapeutic potential and consequences of dysfunction.Cannabinoid receptors couple to NMDA receptors to reduce the production of NO and the mobilization of zinc induced by glutamate.The σ1 receptor engages the redox-regulated HINT1 protein to bring opioid analgesia under NMDA receptor negative control.The histidine triad nucleotide-binding protein 1 supports mu-opioid receptor-glutamate NMDA receptor cross-regulation.HINT1 in Neuropsychiatric Diseases: A Potential Neuroplastic Mediator.Suppression of RGSz1 function optimizes the actions of opioid analgesics by mechanisms that involve the Wnt/β-catenin pathway.
P2860
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P2860
RGSZ1 interacts with protein kinase C interacting protein PKCI-1 and modulates mu opioid receptor signaling.
description
2006 nî lūn-bûn
@nan
2006 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
RGSZ1 interacts with protein k ...... mu opioid receptor signaling.
@ast
RGSZ1 interacts with protein k ...... mu opioid receptor signaling.
@en
RGSZ1 interacts with protein k ...... mu opioid receptor signaling.
@nl
type
label
RGSZ1 interacts with protein k ...... mu opioid receptor signaling.
@ast
RGSZ1 interacts with protein k ...... mu opioid receptor signaling.
@en
RGSZ1 interacts with protein k ...... mu opioid receptor signaling.
@nl
prefLabel
RGSZ1 interacts with protein k ...... mu opioid receptor signaling.
@ast
RGSZ1 interacts with protein k ...... mu opioid receptor signaling.
@en
RGSZ1 interacts with protein k ...... mu opioid receptor signaling.
@nl
P2093
P1433
P1476
RGSZ1 interacts with protein k ...... mu opioid receptor signaling.
@en
P2093
John R Hepler
Kathleen H Young
Rachel A Hunt
Seena K Ajit
Suneela Ramineni
Wade Edris
Wah-Tung Hum
P304
P356
10.1016/J.CELLSIG.2006.09.008
P577
2006-10-07T00:00:00Z