{"id":9,"date":"2019-09-10T15:25:52","date_gmt":"2019-09-10T19:25:52","guid":{"rendered":"https:\/\/health.uconn.edu\/bae-lab\/?page_id=9"},"modified":"2023-01-06T11:54:27","modified_gmt":"2023-01-06T16:54:27","slug":"research","status":"publish","type":"page","link":"https:\/\/health.uconn.edu\/scanlon-lab\/research\/","title":{"rendered":"Research"},"content":{"rendered":"<div id=\"pl-9\"  class=\"panel-layout\" ><div id=\"pg-9-0\"  class=\"panel-grid panel-no-style\" ><div id=\"pgc-9-0-0\"  class=\"panel-grid-cell\" ><div id=\"panel-9-0-0-0\" class=\"so-panel widget widget_black-studio-tinymce widget_black_studio_tinymce panel-first-child panel-last-child\" data-index=\"0\" ><div class=\"textwidget\"><p>Dr. Scanlon currently works on understanding extrinsic mechanisms that underlie hematopoietic progenitor cell fate decisions. She has developed a novel method for time-lapse microscopy of bipotent progenitors dividing and committing to two potential lineages. She is also interested in developing 3D engineered in vitro cell culture models to further investigate spatial regulation between cells of the bone marrow microenvironment.<\/p>\n<\/div><\/div><\/div><div id=\"pgc-9-0-1\"  class=\"panel-grid-cell\" ><div id=\"panel-9-0-1-0\" class=\"so-panel widget widget_widget_sp_image widget_sp_image panel-first-child panel-last-child\" data-index=\"1\" ><img loading=\"lazy\" decoding=\"async\" width=\"630\" height=\"360\" alt=\"Mixed Mk\/E Colony Grown from Single Human MEP\" class=\"attachment-full aligncenter\" style=\"max-width: 100%;\" srcset=\"https:\/\/health.uconn.edu\/scanlon-lab\/wp-content\/uploads\/sites\/283\/2022\/05\/pastedImage.png 630w, https:\/\/health.uconn.edu\/scanlon-lab\/wp-content\/uploads\/sites\/283\/2022\/05\/pastedImage-300x171.png 300w\" sizes=\"(max-width: 630px) 100vw, 630px\" src=\"https:\/\/health.uconn.edu\/scanlon-lab\/wp-content\/uploads\/sites\/283\/2022\/05\/pastedImage.png\" \/><div class=\"widget_sp_image-description\" ><p>Mixed Mk\/E Colony Grown from Single Human MEP: The entire colony arose from a single human bipotent Megakaryocytic-Erythroid Progenitor (MEP). Megakaryocyte-committed cells are expressing CD41 (green fluorescence) and CD235a (red fluorescence).<\/p>\n<\/div><\/div><\/div><\/div><\/div>","protected":false},"excerpt":{"rendered":"<p>Dr. Scanlon currently works on understanding extrinsic mechanisms that underlie hematopoietic progenitor cell fate decisions. She has developed a novel method for time-lapse microscopy of bipotent progenitors dividing and committing to two potential lineages. She is also interested in developing 3D engineered in vitro cell culture models to further investigate spatial regulation between cells of [&hellip;]<\/p>\n","protected":false},"author":38,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"acf":[],"publishpress_future_action":{"enabled":false,"date":"2026-05-15 18:15:22","action":"change-status","newStatus":"draft","terms":[],"taxonomy":""},"_links":{"self":[{"href":"https:\/\/health.uconn.edu\/scanlon-lab\/wp-json\/wp\/v2\/pages\/9"}],"collection":[{"href":"https:\/\/health.uconn.edu\/scanlon-lab\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/health.uconn.edu\/scanlon-lab\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/health.uconn.edu\/scanlon-lab\/wp-json\/wp\/v2\/users\/38"}],"replies":[{"embeddable":true,"href":"https:\/\/health.uconn.edu\/scanlon-lab\/wp-json\/wp\/v2\/comments?post=9"}],"version-history":[{"count":40,"href":"https:\/\/health.uconn.edu\/scanlon-lab\/wp-json\/wp\/v2\/pages\/9\/revisions"}],"predecessor-version":[{"id":195,"href":"https:\/\/health.uconn.edu\/scanlon-lab\/wp-json\/wp\/v2\/pages\/9\/revisions\/195"}],"wp:attachment":[{"href":"https:\/\/health.uconn.edu\/scanlon-lab\/wp-json\/wp\/v2\/media?parent=9"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}