{"id":1465,"date":"2018-12-04T16:06:00","date_gmt":"2018-12-04T16:06:00","guid":{"rendered":"https:\/\/cias.uc.pt\/?p=1465"},"modified":"2024-01-03T10:17:16","modified_gmt":"2024-01-03T10:17:16","slug":"genetic-basis-of-haematological-conditions","status":"publish","type":"post","link":"https:\/\/cias.uc.pt\/pt-pt\/projects\/genetic-basis-of-haematological-conditions\/","title":{"rendered":"Genetic basis of haematological conditions (Duration:\u00a02018\u20132025)"},"content":{"rendered":"\n<p class=\"wp-block-paragraph\"><strong>Duration:<\/strong>\u00a02018 \u2013 2025<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Abstract: <\/strong>The aim of the project is the molecular characterization of genetic blood disorders in patients with haemoglobinopathies, red blood cell enzyme defects, venous and arterial thrombosis, haemorragic diseases, congenital erythrocytosis and increased percentages of HbF, searching for genetic variants associated or potentially involved in these clinical phenotypes. This project is conducted in collaboration with the Haematology Service of Centro Hospitalar e Universit\u00e1rio de Coimbra (CHUC).<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Coordinator (PI):&nbsp;<\/strong>Lic\u00ednio Manco (CIAS), Celeste Bento (CIAS), Teresa Fidalgo (CIAS)<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Participants:<\/strong>&nbsp;Lic\u00ednio Manco (CIAS), Celeste Bento (CIAS), Teresa Fidalgo (CIAS), Janet Pereira, Lu\u00eds Relvas, Maria Let\u00edcia Ribeiro (CIAS)<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Financial support:&nbsp;<\/strong><em>Forum hematologico<\/em>&nbsp;(Servi\u00e7o de Hematologia Cl\u00ednica \u2013 CHUC); FCT-CIAS: UID\/ANT\/00283\/2019 (Portugal)<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Duration:\u00a02018 \u2013 2025 Abstract: The aim of the project is the molecular characterization of genetic blood disorders in patients with haemoglobinopathies, red blood cell enzyme defects, venous and arterial thrombosis, haemorragic diseases, congenital erythrocytosis and increased percentages of HbF, searching for genetic variants associated or potentially involved in these clinical phenotypes. This project is conducted [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_et_pb_use_builder":"","_et_pb_old_content":"","_et_gb_content_width":"","footnotes":"","_links_to":"","_links_to_target":""},"categories":[53,3],"tags":[],"clusters":[19],"researcher":[],"class_list":["post-1465","post","type-post","status-publish","format-standard","hentry","category-on-going","category-projects","clusters-genes-populations-and-diseases"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.1 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Genetic basis of haematological conditions (Duration:\u00a02018\u20132025) - CIAS<\/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:\/\/cias.uc.pt\/pt-pt\/projects\/genetic-basis-of-haematological-conditions\/\" \/>\n<meta property=\"og:locale\" content=\"pt_PT\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Genetic basis of haematological conditions (Duration:\u00a02018\u20132025) - CIAS\" \/>\n<meta property=\"og:description\" content=\"Duration:\u00a02018 \u2013 2025 Abstract: The aim of the project is the molecular characterization of genetic blood disorders in patients with haemoglobinopathies, red blood cell enzyme defects, venous and arterial thrombosis, haemorragic diseases, congenital erythrocytosis and increased percentages of HbF, searching for genetic variants associated or potentially involved in these clinical phenotypes. 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