Results 121 to 130 of about 25,601 (192)

T‐2 Toxin‐Mediated β‐Arrestin‐1 O‐GlcNAcylation Exacerbates Glomerular Podocyte Injury via Regulating Histone Acetylation

open access: yesAdvanced Science
T‐2 toxin causes renal dysfunction with proteinuria and glomerular podocyte damage. This work explores the role of metabolic disorder/reprogramming‐mediated epigenetic modification in the progression of T‐2 toxin‐stimulated podocyte injury.
Tushuai Li   +6 more
doaj   +1 more source

ATHENA: A Phase 3, Open-Label Study Of The Safety And Effectiveness Of Oliceridine (TRV130), A G-Protein Selective Agonist At The µ-Opioid Receptor, In Patients With Moderate To Severe Acute Pain Requiring Parenteral Opioid Therapy. [PDF]

open access: yes, 2019
Background:Pain management with conventional opioids can be challenging due to dose-limiting adverse events (AEs), some of which may be related to the simultaneous activation of β-arrestin (a signaling pathway associated with opioid-related AEs) and G ...
Beard, Timothy L   +10 more
core  

Mechanistic insights into the versatile stoichiometry and biased signaling of the apelin receptor-arrestin complex

open access: yesNature Communications
The apelin receptor (APJR) plays a pivotal role in regulating cardiovascular and metabolic health1,2. Understanding the mechanisms of biased agonism at APJR is crucial for drug discovery, as stimulation of the β-arrestin pathway may lead to some adverse ...
Yang Yue   +13 more
doaj   +1 more source

GRK phosphorylation drives β-arrestin-independent internalization of chemokine receptor CXCR5. [PDF]

open access: yesJ Biol Chem
Crecelius JM   +6 more
europepmc   +1 more source

Functional and structural insights into interactions between β-Arrestin 1 and Gαs or Gαi1. [PDF]

open access: yesNat Commun
Duan L   +8 more
europepmc   +1 more source

β-Arrestin 1 Differentially Modulates cAMP and ERK Pathways Downstream of the FSH Receptor. [PDF]

open access: yesCurr Issues Mol Biol
Park SH   +8 more
europepmc   +1 more source

Discovery of a β-arrestin-biased CCKBR agonist that blocks CCKBR-dependent long-term potentiation. [PDF]

open access: yesNat Commun
Shi H   +14 more
europepmc   +1 more source

Carfentanil is a β-arrestin-biased agonist at the μ opioid receptor. [PDF]

open access: yesBr J Pharmacol, 2023
Ramos-Gonzalez N   +7 more
europepmc   +1 more source

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