{"id":1470,"date":"2025-02-14T21:25:00","date_gmt":"2025-02-14T20:25:00","guid":{"rendered":"https:\/\/emanuelabottanilab.it\/nuovo-finanziamento-per-testare-una-terapia-per-la-sindrome-di-allan-herndon-dudley\/"},"modified":"2025-11-18T17:32:21","modified_gmt":"2025-11-18T16:32:21","slug":"nuovo-finanziamento-per-testare-una-terapia-per-la-sindrome-di-allan-herndon-dudley","status":"publish","type":"post","link":"https:\/\/emanuelabottanilab.it\/en\/nuovo-finanziamento-per-testare-una-terapia-per-la-sindrome-di-allan-herndon-dudley\/","title":{"rendered":"FIS2 funding of \u20ac1.32 million for research into mitochondria and rare diseases"},"content":{"rendered":"\n<p>We are thrilled to announce that our team has obtained \u20ac1.32 million in funding from the Ministry of University and Research (MUR) as part of the FIS2 initiative!<\/p>\n\n\n\n<p>This new project will allow us to investigate the role of mitochondrial dysfunction in neurogenesis and rare neurodevelopmental disorders, with the aim of clarifying the cellular and molecular mechanisms underlying these conditions.<\/p>\n\n\n\n<p>This is a significant achievement, marking a new phase for our laboratory and paving the way for new perspectives in the development of targeted therapeutic strategies.<\/p>\n\n\n\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>We are thrilled to announce that our team has obtained \u20ac1.32 million in funding from the Ministry of University and Research (MUR) as part of the FIS2 initiative! This new project will allow us to investigate the role of mitochondrial dysfunction in neurogenesis and rare neurodevelopmental disorders, with the aim of clarifying the cellular and [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":1471,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_gspb_post_css":"","footnotes":""},"categories":[22],"tags":[],"class_list":["post-1470","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-events"],"blocksy_meta":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.6 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>FIS2 funding of \u20ac1.32 million for research into mitochondria and rare diseases - Emanuela Bottani Lab<\/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:\/\/emanuelabottanilab.it\/en\/nuovo-finanziamento-per-testare-una-terapia-per-la-sindrome-di-allan-herndon-dudley\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"FIS2 funding of \u20ac1.32 million for research into mitochondria and rare diseases - Emanuela Bottani Lab\" \/>\n<meta property=\"og:description\" content=\"We are thrilled to announce that our team has obtained \u20ac1.32 million in funding from the Ministry of University and Research (MUR) as part of the FIS2 initiative! This new project will allow us to investigate the role of mitochondrial dysfunction in neurogenesis and rare neurodevelopmental disorders, with the aim of clarifying the cellular and [&hellip;]\" \/>\n<meta property=\"og:url\" content=\"https:\/\/emanuelabottanilab.it\/en\/nuovo-finanziamento-per-testare-una-terapia-per-la-sindrome-di-allan-herndon-dudley\/\" \/>\n<meta property=\"og:site_name\" content=\"Emanuela Bottani Lab\" \/>\n<meta property=\"article:published_time\" content=\"2025-02-14T20:25:00+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2025-11-18T16:32:21+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/emanuelabottanilab.it\/cms\/wp-content\/uploads\/2025\/02\/mitogen_5.png\" \/>\n\t<meta property=\"og:image:width\" content=\"1240\" \/>\n\t<meta property=\"og:image:height\" content=\"698\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/png\" \/>\n<meta name=\"author\" content=\"Staff\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Staff\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"1 minute\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/emanuelabottanilab.it\\\/en\\\/nuovo-finanziamento-per-testare-una-terapia-per-la-sindrome-di-allan-herndon-dudley\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/emanuelabottanilab.it\\\/en\\\/nuovo-finanziamento-per-testare-una-terapia-per-la-sindrome-di-allan-herndon-dudley\\\/\"},\"author\":{\"name\":\"Staff\",\"@id\":\"https:\\\/\\\/emanuelabottanilab.it\\\/en\\\/#\\\/schema\\\/person\\\/164f91c3f3cb31655e654fcedb87603a\"},\"headline\":\"FIS2 funding of \u20ac1.32 million for research into mitochondria and rare diseases\",\"datePublished\":\"2025-02-14T20:25:00+00:00\",\"dateModified\":\"2025-11-18T16:32:21+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/emanuelabottanilab.it\\\/en\\\/nuovo-finanziamento-per-testare-una-terapia-per-la-sindrome-di-allan-herndon-dudley\\\/\"},\"wordCount\":96,\"publisher\":{\"@id\":\"https:\\\/\\\/emanuelabottanilab.it\\\/en\\\/#organization\"},\"image\":{\"@id\":\"https:\\\/\\\/emanuelabottanilab.it\\\/en\\\/nuovo-finanziamento-per-testare-una-terapia-per-la-sindrome-di-allan-herndon-dudley\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/emanuelabottanilab.it\\\/cms\\\/wp-content\\\/uploads\\\/2025\\\/02\\\/mitogen_5.png\",\"articleSection\":[\"Events\"],\"inLanguage\":\"en-US\"},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/emanuelabottanilab.it\\\/en\\\/nuovo-finanziamento-per-testare-una-terapia-per-la-sindrome-di-allan-herndon-dudley\\\/\",\"url\":\"https:\\\/\\\/emanuelabottanilab.it\\\/en\\\/nuovo-finanziamento-per-testare-una-terapia-per-la-sindrome-di-allan-herndon-dudley\\\/\",\"name\":\"FIS2 funding of \u20ac1.32 million for research into mitochondria and rare diseases - 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