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Connection

Demet Arac-Ozkan to Receptors, G-Protein-Coupled

This is a "connection" page, showing publications Demet Arac-Ozkan has written about Receptors, G-Protein-Coupled.
  1. The far extracellular CUB domain of the adhesion GPCR ADGRG6/GPR126 is a key regulator of receptor signaling. Proc Natl Acad Sci U S A. 2025 Dec 02; 122(48):e2409184122.
    View in: PubMed
    Score: 0.854
  2. Structural basis for regulation of CELSR1 by a compact module in its extracellular region. Nat Commun. 2025 Apr 28; 16(1):3972.
    View in: PubMed
    Score: 0.821
  3. Conformational coupling between extracellular and transmembrane domains modulates holo-adhesion GPCR function. Nat Commun. 2024 12 04; 15(1):10545.
    View in: PubMed
    Score: 0.798
  4. Isoform- and ligand-specific modulation of the adhesion GPCR ADGRL3/Latrophilin3 by a synthetic binder. Nat Commun. 2023 02 06; 14(1):635.
    View in: PubMed
    Score: 0.703
  5. Alternative splicing controls teneurin-latrophilin interaction and synapse specificity by a shape-shifting mechanism. Nat Commun. 2020 05 01; 11(1):2140.
    View in: PubMed
    Score: 0.581
  6. Structural basis for adhesion G protein-coupled receptor Gpr126 function. Nat Commun. 2020 01 10; 11(1):194.
    View in: PubMed
    Score: 0.568
  7. Teneurins and latrophilins: two giants meet at the synapse. Curr Opin Struct Biol. 2019 02; 54:141-151.
    View in: PubMed
    Score: 0.539
  8. Stachel-independent modulation of GPR56/ADGRG1 signaling by synthetic ligands directed to its extracellular region. Proc Natl Acad Sci U S A. 2017 09 19; 114(38):10095-10100.
    View in: PubMed
    Score: 0.483
  9. Structural Basis for Regulation of GPR56/ADGRG1 by Its Alternatively Spliced Extracellular Domains. Neuron. 2016 Sep 21; 91(6):1292-1304.
    View in: PubMed
    Score: 0.452
  10. Structural Basis of Latrophilin-FLRT-UNC5 Interaction in Cell Adhesion. Structure. 2015 Sep 01; 23(9):1678-1691.
    View in: PubMed
    Score: 0.418
  11. Mechanism for adhesion G protein-coupled receptor GPR56-mediated RhoA activation induced by collagen III stimulation. PLoS One. 2014; 9(6):e100043.
    View in: PubMed
    Score: 0.387
  12. Matching structure with function: the GAIN domain of adhesion-GPCR and PKD1-like proteins. Trends Pharmacol Sci. 2013 Aug; 34(8):470-8.
    View in: PubMed
    Score: 0.362
  13. Dissecting signaling and functions of adhesion G protein-coupled receptors. Ann N Y Acad Sci. 2012 Dec; 1276:1-25.
    View in: PubMed
    Score: 0.348
  14. The adhesion GPCRs CELSR1-3 and LPHN3 engage G proteins via distinct activation mechanisms. Cell Rep. 2023 06 27; 42(6):112552.
    View in: PubMed
    Score: 0.179
  15. Specific and direct modulation of the interaction between adhesion GPCR GPR56/ADGRG1 and tissue transglutaminase 2 using synthetic ligands. Sci Rep. 2020 10 09; 10(1):16912.
    View in: PubMed
    Score: 0.150
  16. The expanding functional roles and signaling mechanisms of adhesion G protein-coupled receptors. Ann N Y Acad Sci. 2019 11; 1456(1):5-25.
    View in: PubMed
    Score: 0.136
  17. Structural Basis for Teneurin Function in Circuit-Wiring: A Toxin Motif at the Synapse. Cell. 2018 04 19; 173(3):735-748.e15.
    View in: PubMed
    Score: 0.126
  18. Understanding the Structural Basis of Adhesion GPCR Functions. Handb Exp Pharmacol. 2016; 234:67-82.
    View in: PubMed
    Score: 0.108
  19. International Union of Basic and Clinical Pharmacology. XCIV. Adhesion G protein-coupled receptors. Pharmacol Rev. 2015; 67(2):338-67.
    View in: PubMed
    Score: 0.100
  20. New functions and signaling mechanisms for the class of adhesion G protein-coupled receptors. Ann N Y Acad Sci. 2014 Dec; 1333:43-64.
    View in: PubMed
    Score: 0.100
  21. A novel evolutionarily conserved domain of cell-adhesion GPCRs mediates autoproteolysis. EMBO J. 2012 Mar 21; 31(6):1364-78.
    View in: PubMed
    Score: 0.082
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.