Results 171 to 180 of about 6,662 (210)
Engineering MSC Migration: Roles of Nanoparticles in Activating Migratory Pathways and Functions. [PDF]
Batsaikhan T, Lee HS, Seo YJ.
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CXCR7 promotes pulmonary vascular remodeling via targeting p38/MMP2 pathway in pulmonary arterial hypertension. [PDF]
Xu J +5 more
europepmc +1 more source
The effect of CXCL12 on survival outcomes of patients with viral hepatitis-associated hepatocellular carcinoma after hepatectomy. [PDF]
Lu Y, Xing F, Peng S.
europepmc +1 more source
The Use of Biologics for Targeting GPCRs in Metastatic Cancers. [PDF]
McBrien C, O'Connell DJ.
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CXCR7 heterodimerizes with CXCR4, leading to preferential activation of β-arrestin–mediated signaling pathways.
Elizabeth M. Adler
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Resonating with the signaling bias of CXCR7
Molecular Cell, 2022Kleist et al. combine NMR spectroscopy and residue contact network analysis to identify a potential allosteric network in CXCR7, a β-arrestin-biased chemokine receptor, which links the extracellular ligand-binding pocket and the intracellular transducer-coupling region through the receptor transmembrane core.
Parishmita, Sarma, Arun K, Shukla
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CXCR7, CXCR4 and CXCL12: An eccentric trio?
Journal of Neuroimmunology, 2008CXCR7, formerly called RDC1 is a recently deorphanized G-protein coupled receptor which binds with high affinity the inflammatory and homing chemokines CXCL11/ITAC and CXCL12/SDF-1. Despite its phylogenetic relation and ligand binding properties CXCR7 does not mediate typical chemokine receptor responses such as leukocyte trafficking.
Marcus, Thelen, Sylvia, Thelen
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Differential Expression of RDC1/CXCR7 in the Human Placenta
Journal of Clinical Immunology, 2008Chemokine receptor expression by human trophoblast and other placental cells have important implications for understanding the regulation of placental growth, development, and their role in maternofetal HIV transmission. CXCR7, now a deorphanized G protein coupled receptor that has been recently shown to bind to the ligands ITAC and CXCL12 has been ...
Vishwas, Tripathi +5 more
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AMD3100 Is a CXCR7 Ligand with Allosteric Agonist Properties
Molecular Pharmacology, 2009The bicyclam AMD3100 is known as a small synthetic inhibitor of the CXCL12-binding chemokine receptor CXCR4. Here, we show that AMD3100 also binds to the alternative CXCL12 receptor CXCR7. CXCL12 or AMD3100 alone activate beta-arrestin recruitment to CXCR7, which we identify as a previously unreported signaling pathway of CXCR7.
Irina, Kalatskaya +5 more
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