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X-WR-CALNAME;VALUE=TEXT:2023 Prather Lecture Series: Thomas Südhof
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SUMMARY:2023 Prather Lecture Series: Thomas Südhof
DESCRIPTION:<p>	<a href="https://med.stanford.edu/sudhoflab.html" title=""><drupal-media data-entity-type="media" data-entity-uuid="b6761145-aae0-4d42-a6ff-57fed018a0f0" data-align="left" alt="Thomas Südhof" data-view-mode="hwp_small"></drupal-media>Thomas Südhof</a><br>Avram Goldstein Professor Investigator, Howard Hughes Medical Institute; Professor, Dept. of Molecular &amp; Cellular Physiology and of Neurosurgery; Professor, Dept. of Neurology &amp; Neurological Sciences and of Psychiatry &amp; Behavioral Science</p><p>	<!--break--><a data-url="https://www.mcb.harvard.edu/department/news/thomas-sudhof-to-give-2023-john-m-prather-lectures-april-12-13-and-14/" href="https://www.mcb.harvard.edu/department/news/thomas-sudhof-to-give-2023-john-m-prather-lectures-april-12-13-and-14/" title="">Adhesion-GPCRs in synapse formation</a></p><p>	<strong>Abstract:</strong> In the last decade, two families of postsynaptic adhesion-GPCRs, latrophilins and BAI’s, have emerged as major drivers of synapse formation. However, how these adhesion-GPCRs orchestrate synapse assembly and other processes in brain remains unclear. Current data demonstrate that these adhesion-GPCRs interact with multiple ligands in synapse formation and function as true GPCRs, suggesting that synapse formation involves a classical signal transduction cascade pathway that is rendered specific for synapse assembly via defined extra- and intracellular interactions. In my talk, I will focus on recent results that illustrate facets of the function of these important molecules that constitute central regulators of how neural circuits are assembled and restructured continuously in brain.</p><p>	Co-sponsored by The Departments of Molecular and Cellular Biology and Organismic and Evolutionary Biology</p>
LOCATION:Biological Labs Lecture Hall 1080, 16 Divinity Avenue
STATUS:CONFIRMED
DTSTART:20230414T143000Z
DTEND:20230414T143000Z
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