{"version":"1.0","provider_name":"Research for Rare","provider_url":"https:\/\/www.research4rare.de\/en\/","author_name":"mroesele","author_url":"https:\/\/www.research4rare.de\/en\/author\/mroesele\/","title":"GALENUS - Research for Rare","type":"rich","width":600,"height":338,"html":"<blockquote class=\"wp-embedded-content\" data-secret=\"hJMzAA1mbr\"><a href=\"https:\/\/www.research4rare.de\/en\/alumni\/galenus\/\">GALENUS<\/a><\/blockquote><iframe sandbox=\"allow-scripts\" security=\"restricted\" src=\"https:\/\/www.research4rare.de\/en\/alumni\/galenus\/embed\/#?secret=hJMzAA1mbr\" width=\"600\" height=\"338\" title=\"&#8220;GALENUS&#8221; &#8212; Research for Rare\" data-secret=\"hJMzAA1mbr\" frameborder=\"0\" marginwidth=\"0\" marginheight=\"0\" scrolling=\"no\" class=\"wp-embedded-content\"><\/iframe><script>\n\/*! This file is auto-generated *\/\n!function(d,l){\"use strict\";l.querySelector&&d.addEventListener&&\"undefined\"!=typeof URL&&(d.wp=d.wp||{},d.wp.receiveEmbedMessage||(d.wp.receiveEmbedMessage=function(e){var t=e.data;if((t||t.secret||t.message||t.value)&&!\/[^a-zA-Z0-9]\/.test(t.secret)){for(var s,r,n,a=l.querySelectorAll('iframe[data-secret=\"'+t.secret+'\"]'),o=l.querySelectorAll('blockquote[data-secret=\"'+t.secret+'\"]'),c=new RegExp(\"^https?:$\",\"i\"),i=0;i<o.length;i++)o[i].style.display=\"none\";for(i=0;i<a.length;i++)s=a[i],e.source===s.contentWindow&&(s.removeAttribute(\"style\"),\"height\"===t.message?(1e3<(r=parseInt(t.value,10))?r=1e3:~~r<200&&(r=200),s.height=r):\"link\"===t.message&&(r=new URL(s.getAttribute(\"src\")),n=new URL(t.value),c.test(n.protocol))&&n.host===r.host&&l.activeElement===s&&(d.top.location.href=t.value))}},d.addEventListener(\"message\",d.wp.receiveEmbedMessage,!1),l.addEventListener(\"DOMContentLoaded\",function(){for(var e,t,s=l.querySelectorAll(\"iframe.wp-embedded-content\"),r=0;r<s.length;r++)(t=(e=s[r]).getAttribute(\"data-secret\"))||(t=Math.random().toString(36).substring(2,12),e.src+=\"#?secret=\"+t,e.setAttribute(\"data-secret\",t)),e.contentWindow.postMessage({message:\"ready\",secret:t},\"*\")},!1)))}(window,document);\n\/\/# sourceURL=https:\/\/www.research4rare.de\/wp-includes\/js\/wp-embed.min.js\n<\/script>\n","description":"Cystic fibrosis is an autosomal recessive genetic disease caused by mutations of the cystic fibrosis transmembrane conductance regulator gene (CFTR). CFTR is an anion channel located at the apical membrane of epithelia and seems to be of importance for the ion- and watery content of secretions from exocrine glands. Novel genetic tools, like the use [&hellip;]"}