{"id":6945,"date":"2025-01-22T13:10:46","date_gmt":"2025-01-22T12:10:46","guid":{"rendered":"https:\/\/ern-ithaca.eu\/?post_type=resources&#038;p=6945"},"modified":"2025-01-23T22:06:15","modified_gmt":"2025-01-23T21:06:15","slug":"in-depth-webinar-19-rho-gtpase-in-intellectual-disability-and-neurodevelopmental-disorders","status":"publish","type":"resources","link":"https:\/\/ern-ithaca.eu\/es\/education\/documentation-for-patients\/in-depth-webinar-19-rho-gtpase-in-intellectual-disability-and-neurodevelopmental-disorders\/","title":{"rendered":"Seminario web en profundidad #19: La Rho-GTPasa en la discapacidad intelectual y los trastornos del desarrollo neurol\u00f3gico"},"content":{"rendered":"<p class=\"wp-block-paragraph\"><em>This webinar focused on elucidating neurodevelopmental disorders caused by deleterious variants in the human RAC1 and RAC3 genes, including intellectual disability, autism spectrum disorders and epilepsy. &nbsp;These genes encode proteins that are crucial for brain development by regulating cell signalling pathways involved in neuronal migration, differentiation and synaptic function. <\/em><\/p>\n\n\n\n<div style=\"height:26px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h2 class=\"wp-block-heading\">Program: <\/h2>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Rho family GTPases: key players in neuronal development and synaptic function \u2013&nbsp;<\/strong>Speaker\u202f:&nbsp;Antonio Falace, PhD &nbsp;\u2013 Pediatric Neurology and Muscular Diseases Unit, IRCCS Istituto Giannina Gaslini\u201d, Genoa, Italy.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>RAC3-related disorders of cortical development in human neurodevelopmental phenotypes &nbsp;\u2013&nbsp;<\/strong>Speaker\u202f:&nbsp;Marcello Scala, MD PhD \u201cNeuroRacopathies \u2013 Department of Neurosciences (DINOGMI), University of Genoa, Genoa, Italy; Medical Genetics Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Mechanistic analysis of RAC1-related neurodevelopmental disorders \u2013&nbsp;<\/strong>Speaker\u202f:&nbsp;Tom H. Millard, PhD \u2013 Division of Developmental Biology and Medicine, Faculty of Biology, Medicine and Health, University of Manchester M13 9PL, UK.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Discussion &amp; Conclusion with speakers and moderator<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><a href=\"https:\/\/ern-ithaca.eu\/wp-content\/uploads\/2025\/01\/PPT_FINAL_2025-Webinar-\u202fRho-GTPase-in-ID-NDDv1.pdf\">AQU\u00cd<\/a> to dowload the webinar&#8217;s powerpoint<\/p>\n\n\n\n<div style=\"height:26px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h2 class=\"wp-block-heading\">Grabaci\u00f3n<\/h2>\n\n\n\n<figure class=\"wp-block-embed is-type-video is-provider-youtube wp-block-embed-youtube wp-embed-aspect-16-9 wp-has-aspect-ratio\"><div class=\"wp-block-embed__wrapper\">\nhttps:\/\/youtu.be\/xlxLbfdLyKU\n<\/div><\/figure>","protected":false},"excerpt":{"rendered":"<p>This webinar focused on elucidating neurodevelopmental disorders caused by deleterious variants in the human RAC1 and RAC3 genes, including intellectual disability, autism spectrum disorders and epilepsy. &nbsp;These genes encode proteins that are crucial for brain development by regulating cell signalling pathways involved in neuronal migration, differentiation and synaptic function. Program: Rho family GTPases: key players [&hellip;]<\/p>\n","protected":false},"featured_media":6947,"template":"","tags":[],"resources-type":[17],"class_list":["post-6945","resources","type-resources","status-publish","has-post-thumbnail","hentry","resources-type-webinar"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.7 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>In-Depth Webinar #19\u00a0Rho-GTPase in intellectual disability and neurodevelopmental disorders - ERN ITHACA<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/ern-ithaca.eu\/es\/education\/documentation-for-patients\/in-depth-webinar-19-rho-gtpase-in-intellectual-disability-and-neurodevelopmental-disorders\/\" \/>\n<meta property=\"og:locale\" content=\"es_ES\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"In-Depth Webinar #19\u00a0Rho-GTPase in intellectual disability and neurodevelopmental disorders - ERN ITHACA\" \/>\n<meta property=\"og:description\" content=\"This webinar focused on elucidating neurodevelopmental disorders caused by deleterious variants in the human RAC1 and RAC3 genes, including intellectual disability, autism spectrum disorders and epilepsy. &nbsp;These genes encode proteins that are crucial for brain development by regulating cell signalling pathways involved in neuronal migration, differentiation and synaptic function. 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