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One or more keywords matched the following properties of Arac-Ozkan, Demet
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overview PI last name in publications: ARAÇ ARAÇ LAB RESEARCH Cells in multicellular organisms have the extraordinary ability of adhering to each other and exchanging information. Cellular adhesion and communication is essential for the development of all organs such as the brain, and is a key phenomenon that is disrupted in many human diseases. The Araç Lab is interested in understanding cellular communication with a special focus on the cell-surface receptors that mediate intercellular adhesion and communication. Genetic studies revealed critical roles for these surface proteins in embryonic development (especially of the brain and the heart), and in neurobiology (especially in synaptogenesis, axon pathfinding, axon-dendrite partner marching and wiring the brain); and link them to numerous diseases including neurological disorders, developmental impairments, multiple types of cancers (such as glioblastoma and ovarian cancer) and congenital general anosmia (the inability to smell). Considering that many drugs target the extracellular regions of membrane receptors to regulate receptor function, and have excellent therapeutic benefits, these proteins may be promising targets for drugs to treat numerous diseases once mechanistic details about the components that regulate their functions are understood. However, in spite of the recent exciting advances, their mechanisms of action, high-resolution structures in isolation or in complex with their ligands, and how they can mediate such broad range of functions remain majorly unknown. Our lab’s ultimate goal is to understand the mechanisms by which cell-adhesion receptors mediate communication between cells.
One or more keywords matched the following items that are connected to Arac-Ozkan, Demet
Item TypeName
Concept Cell Adhesion
Concept Cell Adhesion Molecules
Concept Cell Adhesion Molecules, Neuronal
Concept Substrate Specificity
Academic Article Understanding the Structural Basis of Adhesion GPCR Functions.
Academic Article Structures of neuroligin-1 and the neuroligin-1/neurexin-1 beta complex reveal specific protein-protein and protein-Ca2+ interactions.
Academic Article Matching structure with function: the GAIN domain of adhesion-GPCR and PKD1-like proteins.
Academic Article Neurexins physically and functionally interact with GABA(A) receptors.
Academic Article Neuroligin-1 performs neurexin-dependent and neurexin-independent functions in synapse validation.
Academic Article Dissecting signaling and functions of adhesion G protein-coupled receptors.
Academic Article Structural Basis of Latrophilin-FLRT-UNC5 Interaction in Cell Adhesion.
Academic Article International Union of Basic and Clinical Pharmacology. XCIV. Adhesion G protein-coupled receptors.
Academic Article New functions and signaling mechanisms for the class of adhesion G protein-coupled receptors.
Academic Article Direct visualization of trans-synaptic neurexin-neuroligin interactions during synapse formation.
Academic Article A novel evolutionarily conserved domain of cell-adhesion GPCRs mediates autoproteolysis.
Academic Article Structural Basis for Teneurin Function in Circuit-Wiring: A Toxin Motif at the Synapse.
Academic Article Mechanism for adhesion G protein-coupled receptor GPR56-mediated RhoA activation induced by collagen III stimulation.
Academic Article A potent peptidomimetic inhibitor of botulinum neurotoxin serotype A has a very different conformation than SNAP-25 substrate.
Academic Article A Comprehensive Mutagenesis Screen of the Adhesion GPCR Latrophilin-1/ADGRL1.
Grant Structural and Functional Studies of Adhesion GPCRs
Grant Structural and Functional Studies of Teneurins: A bacterial toxin homolog in human
Grant Structural and Functional Studies of Brain Angiogenesis Inhibitors (BAIs/ADGRBs)
Search Criteria
  • substrate
  • adhesion