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Synaptopathies SymposiumFriday 20 September 2019UCL Institute of Neurology33 Queen Square lecture theatreProgramme8.25Registration, coffee9.00Dimitri Kullmann (UCL): Introduction(Chair: Sanjay Sisodiya)9.05Matt Hurles (Sanger) Deciphering the genetics of neurodevelopmental diseases9.40Lucia Sivilotti (UCL) Glycine receptor function in startle disease (hyperekplexia)10.15Stephen Tucker (Oxford): New Insights into K2P channel structure, function and pharmacology10.50Coffee break(Chair: Peter Goadsby)11.15Mark Farrant (UCL) Calcium-permeable AMPARs and their modulation by auxiliary subunits11.50Radu Ariescu (LMB): Molecular mechanisms of human GABAA receptor modulation by pharmacological agents12.25Trevor Smart (UCL) Variant GABA-A receptor assembly and epilepsy13.00Lunch & Posters(Chair: Henry Houlden)14.00Fabio Benfenati (IIT Genoa) Synapsin genes: from bathing epilepsy to autoimmune synaptopathies14.35Sarosh Irani (Oxford): Clinical and laboratory observations inform molecular mechanisms of autoantibodies affecting the CNS15.10Stephen Brickley (Imperial College): Changes in synaptic function in age-related cognitive decline15.45Tea break(Chair: Kirill Volynski)16.10Matt Jones (Bristol) Thalamocortical dysfunction in neurodevelopmental disorders.16.45Emily Osterweil (Edinburgh) TRAP-seq identifies novel signatures of translation dysregulation in mouse models of autism17.20Karl Friston (UCL) Dynamic causal modelling of synaptopathy17.55Closing Comments18.00ReceptionSupported by a Wellcome Strategic Award – Synaptopathies: genetics, biophysics and circuit mechanisms of paroxysmal neurological disordersTo attend please register through the UCL Eventbrite page, accessible via:ucl.ac.uk/ion/synaptopathies/meetings ................
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