{"id":4444,"date":"2019-07-02T21:43:07","date_gmt":"2019-07-02T21:43:07","guid":{"rendered":"http:\/\/blogs.sld.cu\/oserranob\/?p=4444"},"modified":"2019-07-04T19:30:35","modified_gmt":"2019-07-04T19:30:35","slug":"nuevas-variantes-y-asociaciones-de-riesgo","status":"publish","type":"post","link":"https:\/\/blogs.sld.cu\/oserranob\/2019\/07\/02\/nuevas-variantes-y-asociaciones-de-riesgo\/","title":{"rendered":"Nuevas variantes y asociaciones de riesgo"},"content":{"rendered":"<p><a href=\"https:\/\/blogs.sld.cu\/oserranob\/files\/2019\/07\/2019-07-03-CTCF.png\"><img loading=\"lazy\" class=\"alignleft wp-image-4480 size-full\" style=\"border-width: 1px;margin: 5px\" title=\"(c) Konrad EDH, et al. Genetics in Medicine, 2019\" src=\"https:\/\/blogs.sld.cu\/oserranob\/files\/2019\/07\/2019-07-03-CTCF.png\" alt=\"2019 07 03 CTCF\" width=\"85\" height=\"111\" \/><\/a>&#8211; <a title=\"PLOS Genetics, 2019;15(6):e1008107 \" href=\"https:\/\/journals.plos.org\/plosgenetics\/article?id=10.1371\/journal.pgen.1008107\" target=\"_blank\">Risk of spontaneous preterm birth and fetal growth associates with fetal SLIT2<\/a>.<br \/>\n&#8211; <a href=\"https:\/\/www.cell.com\/ajhg\/fulltext\/S0002-9297(19)30203-4\" target=\"_blank\">Bioinformatics-Based Identification of Expanded Repeats: A Non-reference Intronic Pentamer Expansion in RFC1 Causes CANVAS<\/a>.<br \/>\n&#8211; <a href=\"https:\/\/www.nature.com\/articles\/s41436-019-0585-z\" target=\"_blank\">CTCF variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum<\/a>.<br \/>\n&#8211; <a href=\"https:\/\/www.nature.com\/articles\/s41467-019-10591-5\" target=\"_blank\">Pathologic gene network rewiring implicates PPP1R3A as a central regulator in pressure overload heart failure<\/a>.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>&#8211; Risk of spontaneous preterm birth and fetal growth associates with fetal SLIT2. &#8211; Bioinformatics-Based Identification of Expanded Repeats: A Non-reference Intronic Pentamer Expansion in RFC1 Causes CANVAS. &#8211; CTCF variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum. &#8211; Pathologic gene network rewiring implicates PPP1R3A as a central [&hellip;]<\/p>\n","protected":false},"author":125,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[8,13,14,15,25,29],"tags":[],"_links":{"self":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/4444"}],"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=4444"}],"version-history":[{"count":3,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/4444\/revisions"}],"predecessor-version":[{"id":4482,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/4444\/revisions\/4482"}],"wp:attachment":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/media?parent=4444"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/categories?post=4444"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/tags?post=4444"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}