Results 171 to 180 of about 1,660,729 (286)
Dual Blockade of LILRB1 and LILRB2 Enhances Antiviral Immune Responses in SIV Infection
Dual LILRB1/B2 blockade with mac20G10 reshapes myeloid activation during acute SIV infection by targeting LILRB1 and LILRB2 on myeloid cells. This treatment enhances CD80 expression on selected myeloid subsets and increases plasma IFN‐λ, IL‐8, and IL‐1RA.
Florian Meurisse +20 more
wiley +1 more source
Two-Step Ligand-Directed Covalent Fluorescent Labeling of the Adenosine A<sub>1</sub>-Receptor That Maintains Its Orthosteric Binding Site's Availability to Bind Ligands. [PDF]
Lin CY +8 more
europepmc +1 more source
This study introduces β‐glucan‐shielded apremilast laden nanomicelles that withstand gastrointestinal degradation, selectively accumulate in inflamed colon tissue, and modulate the microbiota–gut–brain axis. The formulation restores barrier integrity, reduces systemic and neuroinflammation, and improves anxiety‐ and depression‐like behaviors in colitis
Chandrashekhar Jori +10 more
wiley +1 more source
The Signaling Pathways Involved in the Anticonvulsive Effects of the Adenosine A1 Receptor. [PDF]
Spanoghe J +6 more
europepmc +1 more source
This study revealed that a PEAR1/HIF‐1α/ glycolysis/lactate/H3K18la positive feedback loop in PMVECs that drives the development of S‐ALI. Mechanistically, PEAR1 mediates the binding of HIF‐1α to AARS1, leading to the lactylation of HIF‐1α, the primary lactylation site of which is K172.
Shuai Li +15 more
wiley +1 more source
β-Lapachone Exerts Hypnotic Effects via Adenosine A1 Receptor in Mice. [PDF]
Lee DH, Jee HJ, Jung YS.
europepmc +1 more source
The adenosine A1 receptor agonist WAG 994 suppresses acute kainic acid-induced status epilepticus in vivo. [PDF]
Klaft ZJ +3 more
europepmc +1 more source
Adenosine A<sub>1</sub> receptor is dispensable for hepatocyte glucose metabolism and insulin sensitivity. [PDF]
Jain S +4 more
europepmc +1 more source
Allosteric Modulators of the A1 Adenosine receptor
The present invention provides compounds active as allosteric modulators of the A1 adenosine receptor and, thus, may be employed for the treatment of conditions mediated by the A1 adenosine receptor, such as treatment of pain, in particular chronic pain
ROMAGNOLI, Romeo +2 more
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