{"id":2253,"date":"2015-03-31T15:21:30","date_gmt":"2015-03-31T15:21:30","guid":{"rendered":"http:\/\/blogs.sld.cu\/oserranob\/?p=2253"},"modified":"2015-03-31T23:52:34","modified_gmt":"2015-03-31T23:52:34","slug":"edicion-del-genoma-corrige-hemoglobinopatia","status":"publish","type":"post","link":"https:\/\/blogs.sld.cu\/oserranob\/2015\/03\/31\/edicion-del-genoma-corrige-hemoglobinopatia\/","title":{"rendered":"Edici\u00f3n del genoma corrige hemoglobinopat\u00eda"},"content":{"rendered":"<p style=\"text-align: justify\"><a href=\"https:\/\/blogs.sld.cu\/oserranob\/files\/2015\/03\/SC-cover-HBB.gif\"><img loading=\"lazy\" class=\"alignleft  wp-image-2333\" style=\"border: 1px solid black;margin: 5px\" src=\"https:\/\/blogs.sld.cu\/oserranob\/files\/2015\/03\/SC-cover-HBB.gif\" alt=\"\" width=\"81\" height=\"105\" \/><\/a>La edici\u00f3n del genoma en c\u00e9lulas madres pluripotenciales humanas inducidas derivadas de pacientes con <a title=\"Informaci\u00f3n sobre la enfermedad\" href=\"http:\/\/omim.org\/entry\/603903\" target=\"_blank\">anemia drepanoc\u00edtica<\/a> permiti\u00f3 corregir uno de los alelos del gen <a title=\"Informaci\u00f3n sobre el gen\" href=\"http:\/\/www.ncbi.nlm.nih.gov\/gene\/3043\" target=\"_blank\">HBB<\/a>, lo que acerca m\u00e1s la posibilidad de resolver el defecto gen\u00e9tico de esta enfermedad. El reporte est\u00e1 disponible en Huang X, Wang Y, Yan W, Smith C, Ye Z, Wang J, <em>et al<\/em>. <a title=\"Resumen con acceso a PDF\" href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/stem.1969\/abstract\" target=\"_blank\">Production of gene-corrected adult beta globin protein in human erythrocytes differentiated from patient iPSCs after genome editing of the sickle point mutation<\/a>. Stem Cells 2015; DOI: 10.1002\/stem.1969.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>La edici\u00f3n del genoma en c\u00e9lulas madres pluripotenciales humanas inducidas derivadas de pacientes con anemia drepanoc\u00edtica permiti\u00f3 corregir uno de los alelos del gen HBB, lo que acerca m\u00e1s la posibilidad de resolver el defecto gen\u00e9tico de esta enfermedad. El reporte est\u00e1 disponible en Huang X, Wang Y, Yan W, Smith C, Ye Z, Wang [&hellip;]<\/p>\n","protected":false},"author":125,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[14,21,23,32],"tags":[],"_links":{"self":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/2253"}],"collection":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/users\/125"}],"replies":[{"embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/comments?post=2253"}],"version-history":[{"count":4,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/2253\/revisions"}],"predecessor-version":[{"id":2338,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/2253\/revisions\/2338"}],"wp:attachment":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/media?parent=2253"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/categories?post=2253"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/tags?post=2253"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}