{"id":4769,"date":"2020-09-11T03:45:59","date_gmt":"2020-09-11T03:45:59","guid":{"rendered":"http:\/\/blogs.sld.cu\/oserranob\/?p=4769"},"modified":"2020-09-11T03:45:59","modified_gmt":"2020-09-11T03:45:59","slug":"polimorfismos-mutaciones-y-variantes-canales-ionicos-sueno-mortinatos-anencefalia-infarto-cardiaco-cancer","status":"publish","type":"post","link":"https:\/\/blogs.sld.cu\/oserranob\/2020\/09\/11\/polimorfismos-mutaciones-y-variantes-canales-ionicos-sueno-mortinatos-anencefalia-infarto-cardiaco-cancer\/","title":{"rendered":"Polimorfismos, mutaciones y variantes: canales i\u00f3nicos, sue\u00f1o, mortinatos, anencefalia, infarto cardiaco, c\u00e1ncer"},"content":{"rendered":"<p style=\"text-align: justify\">&#8211; <a title=\"Texto completo en ingl\u00e9s\" href=\"https:\/\/www.nature.com\/articles\/s41467-020-17558-x\" target=\"_blank\">Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction<\/a><br \/>\n&#8211; <a title=\"Texto completo en ingl\u00e9s\" href=\"https:\/\/www.nature.com\/articles\/s41467-020-18246-6\" target=\"_blank\">Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts<\/a><br \/>\n&#8211; <a title=\"Texto completo en ingl\u00e9s\" href=\"https:\/\/stm.sciencemag.org\/content\/12\/556\/eaay6848\" target=\"_blank\">Predicting functional effects of missense variants in voltage-gated sodium and calcium channels<\/a><br \/>\n&#8211; <a title=\"Texto completo en ingl\u00e9s\" href=\"https:\/\/advances.sciencemag.org\/content\/6\/33\/eabb3567\" target=\"_blank\">Forward genetics identifies a novel sleep mutant with sleep state inertia and REM sleep deficits<\/a><br \/>\n&#8211; <a title=\"Texto completo en ingl\u00e9s\" href=\"https:\/\/www.nejm.org\/doi\/full\/10.1056\/NEJMoa1908753\" target=\"_blank\">Causal Genetic Variants in Stillbirth<\/a><br \/>\n&#8211; <a title=\"Texto completo en ingl\u00e9s\" href=\"https:\/\/rupress.org\/jem\/article\/217\/12\/e20191561\/152044\/A-loss-of-function-NUAK2-mutation-in-humans-causes\" target=\"_blank\">A loss-of-function NUAK2 mutation in humans causes anencephaly due to impaired Hippo-YAP signaling<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>&#8211; Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction &#8211; Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts &#8211; Predicting functional effects of missense variants in voltage-gated sodium and calcium channels &#8211; Forward genetics identifies a novel sleep mutant with sleep state [&hellip;]<\/p>\n","protected":false},"author":125,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[11,13,14,15,26,29],"tags":[],"_links":{"self":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/4769"}],"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=4769"}],"version-history":[{"count":1,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/4769\/revisions"}],"predecessor-version":[{"id":4770,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/4769\/revisions\/4770"}],"wp:attachment":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/media?parent=4769"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/categories?post=4769"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/tags?post=4769"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}