function getval(val){ var a1=val.replace(/<\/?.+?>/g,""); var a2=a1.replace(/ /g,""); return a2; } //document.write('http://wxzl.cogonline.com/html/CeShiZhuanLanYi/WenZhang/YiShiBaoDao/797.html'); wx.config({ debug: false, appId: 'wx85d01b1d7184c45d', timestamp: 1714507359, nonceStr: 'hY6lrZmcGJelIURY', signature: '91388227799c8e501804f308eccefb66211c0403', jsApiList: [ 'checkJsApi', 'onMenuShareTimeline', 'onMenuShareAppMessage', 'onMenuShareQQ', 'onMenuShareWeibo' ] }); wx.ready(function () { wx.onMenuShareTimeline({ title: '低级别浆液性卵巢癌MAPK 通路改变与总生存期的关系', link: 'http://wxzl.cogonline.com/html/CeShiZhuanLanYi/WenZhang/YiShiBaoDao/797.html', imgUrl: 'http://wxzl.cogonline.com/wp/logo.jpg', success: function () { //alert('fx-ok'); }, cancel: function () { //alert('fx-no'); } }); wx.onMenuShareAppMessage({ title: '低级别浆液性卵巢癌MAPK 通路改变与总生存期的关系', link: 'http://wxzl.cogonline.com/html/CeShiZhuanLanYi/WenZhang/YiShiBaoDao/797.html', imgUrl: 'http://wxzl.cogonline.com/wp/logo.jpg', desc: getval('有假说认为,LGSOC是浆液性囊腺瘤或腺纤维瘤进展为SBOT和(或)浸润性癌的中间型病理学改变,而LGSOC的组织形态、分子通路与SBOT的相关度达到75%以上,有力支持了这一假说。Kurman等提出LGSOC的另一种发病机制,即输卵管上皮乳头状增生(papillary tubal hyperplasia,PTH)来源学说。认为LGSOC原发部位并非源于卵巢,证据为91%的LGSOC患者输卵管上皮存在乳头状增生性病变,由此推论PTH是浆液性肿瘤的癌前病变。通过慢性炎症诱导输卵管黏膜上皮增生,进而'), success: function () { //alert('fx-ok'); }, cancel: function () { //alert('fx-no'); } }); }); wx.error(function (res) { //alert(location.href.split('#')[0]); //alert('err:'+res.errMsg); }); if(location.href.indexOf("?") >= 1 ){ location.href=location.href.substring(0,location.href.indexOf("?")); }