产品建议,看到了 交易类的投诉是一致的
微信小程序投诉接口接收到的参数与文档不一致这是文档地址 https://developers.weixin.qq.com/miniprogram/dev/platform-capabilities/business-capabilities/complaint.html 消息推动 文档中参数是这样的 [图片] 实际 我获取到的是这样的 : <xml><ToUserName><![CDATA[gh_e0761cd68863]]></ToUserName> <FromUserName><![CDATA[okZzd5QNaIEAAFvAVD3ev74qMIiM]]></FromUserName> <CreateTime>1689746146</CreateTime> <MsgType><![CDATA[text]]></MsgType> <Content><![CDATA[【来源于用户反馈】 反馈类型:产品建议 反馈内容:页面样式建议优化,增加美观性,交互更友好! OpenID:xxxxxxxxxxxxxxxxxxx 联系方式:xxxxxxxxx - - - - - - - - - - - - - - - 更多信息请前往小程序管理后台查看]]></Content> <MsgId>24191347483185108</MsgId> </xml> 不知道怎么做了,请求指导下
2023-07-19我也遇到了类似的问题 在苹果手机上都有这个问题,怎么解决呢
wx.join1v1Chat 视频通话 苹果13 画面变形?roomType :video 设备:安卓(iqooneo5)- 苹果(13) 安卓画面一切正常、苹果画面出现纵向拉伸、该怎么解决
2023-01-17开通了 [图片] appId wx3c1b0a4e64105d92
加入微信小程序 多人视频通话一直反馈签名错误?第一步 签名 [图片] 签名结果 b002b824688dd8593a6079e11d8c5e8734fbcb39a6d5906eb347bfbcad79c617 与https://developers.weixin.qq.com/miniprogram/dev/framework/open-ability/voip-chat.html#%E7%AD%BE%E5%90%8D%E7%AE%97%E6%B3%95 官方文档中结果一直 第二步 调用 wx.joinVoIPChat 返回 {errCode: -1000, errMsg: "joinVoIPChat:fail: -10088, -10, join room failed. …4, errCode: -12020, errMsg: invalid signature, -1"} 参数已经替换为自己小程序对应的参数了,请帮忙分析一下是哪里出了问题?
2022-02-16这是我富文本的内容 <p><span style="color: rgb(51, 51, 51); font-family: arial, 宋体, sans-serif; font-size: 14px; text-indent: 28px; background-color: rgb(255, 255, 255);">上海绿地物业服务有限公司成立于2010年,</span><a target="_blank" href="https://baike.baidu.com/item/%E7%BB%BF%E5%9C%B0%E9%9B%86%E5%9B%A2/2942731" style="color: rgb(19, 110, 194); text-decoration-line: none; font-family: arial, 宋体, sans-serif; font-size: 14px; text-indent: 28px; white-space: normal; background-color: rgb(255, 255, 255);">绿地集团</a><span style="color: rgb(51, 51, 51); font-family: arial, 宋体, sans-serif; font-size: 14px; text-indent: 28px; background-color: rgb(255, 255, 255);">下属全资子公司,中国物业管理协会理事单位,上海市物业行业协会常务理事单位,济南市物业管理协会理事单位,上海市物业管理行业诚信承诺A级企业,国家二级资质物业服务企业,绿地物业在上海、济南、广州等地设立分公司,在管项目及前期签约面积300万平方米。是以绿地集团开发的城市综合体、超高层建筑、超甲级写字楼、购物中心、公寓为主的专业物业公司。</span></p> [图片]
rich-text 组件问题?Parsing failed at charactError: Parsing failed at character position 360 near "H1A1表达增加(p <0.05,n =" Parsing failed at character position 427 near "以克服TMZ诱导的化学抗性的理论基础。" <rich-text nodes="{{Helper.getLanguage(item.Content,values[1])}}" selectable="true" class="articleContent" /> [代码][[代码][代码] [代码][代码]{[代码][代码] [代码][代码]"Title": [[代码][代码] [代码][代码][[代码][代码] [代码][代码]"替莫唑胺通过上调PD-L1促进GBM细胞的免疫逃逸。",[代码][代码] [代码][代码]"Temozolomide promotes immune escape of GBM cells via upregulating PD-L1."[代码][代码] [代码][代码]][代码][代码] [代码][代码]],[代码][代码] [代码][代码]"Content": [[代码][代码] [代码][代码][[代码][代码] [代码][代码]"多形性胶质母细胞瘤(GBM)是最常见的恶性原发性脑肿瘤,预后不良,目前有效的治疗策略仍然有限。",[代码][代码] [代码][代码]"Glioblastoma multiforme (GBM) is the most common malignant primary brain tumor with poor prognosis, and currently effective therapeutic strategies are still limited."[代码][代码] [代码][代码]],[代码][代码] [代码][代码][[代码][代码] [代码][代码]"虽然替莫唑胺(TMZ)常用于GBM治疗,其作用机制已得到很好的表征,但其副作用需要全面研究。",[代码][代码] [代码][代码]"Although temozolomide (TMZ) is commonly used for GBM therapy and its mechanism was well characterized, while its side effects were required comprehensive investigation."[代码][代码] [代码][代码]],[代码][代码] [代码][代码][[代码][代码] [代码][代码]"在本研究中,我们发现TMZ攻击的GBM细胞强烈抑制激活的外周血单核细胞(PBMC)中的促炎细胞因子表达,这依赖于增强的CD274转录(编码PD-L1),但不依赖于其他免疫检查点,",[代码][代码] [代码][代码]"In the present study, we revealed that TMZ-challenged GBM cells strongly suppressed pro-inflammatory cytokines expression in activated periphery blood mononuclear cells (PBMC), which depended on enhanced transcription of CD274 (encoding PD-L1), but not other immune checkpoints,"[代码][代码] [代码][代码]],[代码][代码] [代码][代码][[代码][代码] [代码][代码]"例如CD276,HVEM和galectin-9。",[代码][代码] [代码][代码]"such as CD276, HVEM and galectin-9."[代码][代码] [代码][代码]],[代码][代码] [代码][代码][[代码][代码] [代码][代码]"此外,在TMZ处理的GBM细胞中,膜PD-L1的丰度也增加。",[代码][代码] [代码][代码]"Moreover, abundance of membranous PD-L1 was also increased in TMZ-treated GBM cells."[代码][代码] [代码][代码]],[代码][代码] [代码][代码][[代码][代码] [代码][代码]"当短发夹RNA(shRNA)敲低PD-L1表达时,TMZ处理的GBM细胞对PBMC的抑制作用变弱,表明PD-L1对TMZ处理的GBM细胞的免疫抑制能力至关重要。",[代码][代码] [代码][代码]"When PD-L1 expression was knocked down by short hairpin RNA (shRNA), inhibitory effect of TMZ-treated GBM cells on PBMC became weakened, suggesting that PD-L1 was crucial for immune inhibition capacity of TMZ-treated GBM cells."[代码][代码] [代码][代码]],[代码][代码] [代码][代码][[代码][代码] [代码][代码]"另外,放线菌素D在TMZ攻击后降低GBM细胞中的PD-L1表达,表明PD-L1诱导发生在转录水平。",[代码][代码] [代码][代码]"Additionally, actinomycin D reduced PD-L1 expression in GBM cells after TMZ challenge, indicating that PD-L1 induction occurred at transcriptional level."[代码][代码] [代码][代码]],[代码][代码] [代码][代码][[代码][代码] [代码][代码]"免疫印迹结果表明STAT3信号传导参与TMZ介导的PD-L1诱导,并且使用STAT3抑制剂VI或STAT3shRNA观察到PD-L1的减毒表达。",[代码][代码] [代码][代码]"The immunoblotting results demonstrated that STAT3 signaling was involved in TMZ-mediated PD-L1 induction, and attenuated expression of PD-L1 was observed using STAT3 inhibitor VI or STAT3 shRNA."[代码][代码] [代码][代码]],[代码][代码] [代码][代码][[代码][代码] [代码][代码]"最后,动物研究表明,TMZ和PD-1抗体疗法的组合强烈抑制肿瘤生长并实现GBM小鼠的存活率提高。",[代码][代码] [代码][代码]"Finally, the animal study showed that combination of TMZ and PD-1 antibody therapy strongly inhibited tumor growth and achieved the improved survival rate of GBM mice."[代码][代码] [代码][代码]],[代码][代码] [代码][代码][[代码][代码] [代码][代码]"因此,本研究揭示了经典化疗药物TMZ促进GBM细胞免疫逃逸,即使TMZ联合PD-1抗体治疗也未进一步提高复发性GBM患者的生存率,与传统治疗方法相比,而我们的动物研究提供了证据表明TMZ的组合",[代码][代码] [代码][代码]"Accordingly, this study revealed the classical chemotherapy drug TMZ promoted GBM cells immune escape, even TMZ combine with PD-1 antibody treatment not further improve survival ratio of recurrent GBM patients compared with traditional therapy methods, while our animal study provided evidence that combination of TMZ"[代码][代码] [代码][代码]],[代码][代码] [代码][代码][[代码][代码] [代码][代码]"和PD-1抗体是治疗GBM的一种有前景的方法,这些相互矛盾的结果表明,提高PD-1抗体的递送效率可以发挥强大的联合治疗效果。",[代码][代码] [代码][代码]"and PD-1 antibody was a promising way to treat GBM, these contradictory results indicate improving the PD-1 antibody delivery efficiency can exert strong combinational therapy outcomes."[代码][代码] [代码][代码]][代码][代码] [代码][代码]],[代码][代码] [代码][代码]"UID": "31285949",[代码][代码] [代码][代码]"Date": "2019-07-11",[代码][代码] [代码][代码]"Links": {[代码][代码] [代码][代码]"pubmed": "31285949",[代码][代码] [代码][代码]"pmc": "PMC6610056"[代码][代码] [代码][代码]},[代码][代码] [代码][代码]"Authors": "Silu.Wang,Fuli.Yao,Xianghe.Lu,Qun.Li,Zhipeng.Su,Jong-Ho.Lee,Chengde.Wang,Linyong.Du",[代码][代码] [代码][代码]"JournalTitle": "American journal of cancer research"[代码][代码] [代码][代码]},[代码][代码] [代码][代码]{[代码][代码] [代码][代码]"Title": [[代码][代码] [代码][代码][[代码][代码] [代码][代码]"对EGFR抑制的抗性机制揭示了人GBM中的代谢脆弱性。",[代码][代码] [代码][代码]"Mechanisms of resistance to EGFR inhibition reveal metabolic vulnerabilities in human GBM."[代码][代码] [代码][代码]][代码][代码] [代码][代码]],[代码][代码] [代码][代码]"Content": [[代码][代码] [代码][代码][[代码][代码] [代码][代码]"表皮生长因子受体基因(EGFR)的扩增代表胶质母细胞瘤(GBM)中最常见的遗传病变之一,然而,靶向该信号传导途径的疗法在临床上失败。",[代码][代码] [代码][代码]"Amplification of the epidermal growth factor receptor gene (EGFR) represents one of the most commonly observed genetic lesions in glioblastoma (GBM), however, therapies targeting this signaling pathway have failed clinically."[代码][代码] [代码][代码]],[代码][代码] [代码][代码][[代码][代码] [代码][代码]"在这里,使用人类肿瘤,原发性患者来源的异种移植物(PDX)和GBM的鼠模型,我们证明EGFR抑制导致肿瘤细胞的侵袭增加。",[代码][代码] [代码][代码]"Here, using human tumors, primary patient-derived xenografts (PDXs), and a murine model for GBM, we demonstrate that EGFR inhibition leads to increased invasion of tumor cells."[代码][代码] [代码][代码]],[代码][代码] [代码][代码][[代码][代码] [代码][代码]"此外,EGFR抑制剂处理的GBM表现出改变的氧化应激,增加的脂质过氧化作用和产生有毒的脂质过氧化产物。",[代码][代码] [代码][代码]"Further, EGFR inhibitor-treated GBM demonstrate altered oxidative stress, with increased lipid peroxidation, and generation of toxic lipid peroxidation products."[代码][代码] [代码][代码]],[代码][代码] [代码][代码][[代码][代码] [代码][代码]"确定具有升高的醛脱氢酶(ALDH)水平的肿瘤细胞亚群包含在EGFR抑制剂处理的GBM中观察到的显着比例的侵袭性细胞。",[代码][代码] [代码][代码]"A tumor cell subpopulation with elevated aldehyde dehydrogenase (ALDH) levels were determined to comprise a significant proportion of the invasive cells observed in EGFR inhibitor-treated GBM."[代码][代码] [代码][代码]],[代码][代码] [代码][代码][[代码][代码] [代码][代码]"我们对新诊断的GBM中ALDH1A1蛋白的分析显示,在69%(35/51)的病例中可检测到ALDH1A1表达,但肿瘤细胞的百分比相对较低。",[代码][代码] [代码][代码]"Our analysis of ALDH1A1 protein in newly diagnosed GBM revealed detectable ALDH1A1 expression in 69% (35/51) of the cases, but in relatively low percentages of tumor cells."[代码][代码] [代码][代码]],[代码][代码] [代码][代码][[代码][代码] [代码][代码]"对EGFR抑制剂治疗前后配对的人GBM的分析显示EGFR扩增的肿瘤中ALDH1A1表达增加(p <0.05,n = 13个肿瘤对),并且在鼠GBM中ALDH1A1-高克隆比ALDH1A1对EGFR抑制更具抗性。",[代码][代码] [代码][代码]"Analysis of paired human GBM before and after EGFR inhibitor therapy showed an increase in ALDH1A1 expression in EGFR-amplified tumors (p<0.05, n=13 tumor pairs), and in murine GBM ALDH1A1-high clones were more resistant to EGFR inhibition than ALDH1A1"[代码][代码] [代码][代码]],[代码][代码] [代码][代码][[代码][代码] [代码][代码]"低克隆。",[代码][代码] [代码][代码]"-low clones."[代码][代码] [代码][代码]],[代码][代码] [代码][代码][[代码][代码] [代码][代码]"我们的数据将ALDH水平鉴定为具有高侵袭能力,改变的氧化应激和对EGFR抑制的抗性的GBM细胞的生物标志物,并揭示其抑制应限制GBM侵袭的治疗靶标。",[代码][代码] [代码][代码]"Our data identify ALDH levels as a biomarker of GBM cells with high invasive potential, altered oxidative stress, and resistance to EGFR inhibition, and reveal a therapeutic target whose inhibition should limit GBM invasion."[代码][代码] [代码][代码]][代码][代码] [代码][代码]],[代码][代码] [代码][代码]"UID": "31270152",[代码][代码] [代码][代码]"Date": "2019-07-23",[代码][代码] [代码][代码]"Links": {[代码][代码] [代码][代码]"pubmed": "31270152",[代码][代码] [代码][代码]"pii": "1535-7163.MCT-18-1330",[代码][代码] [代码][代码]"doi": "10.1158/1535-7163.MCT-18-1330"[代码][代码] [代码][代码]},[代码][代码] [代码][代码]"Authors": "Andrew.McKinney,Olle R.Lindberg,Jane R.Engler,Katharine Y.Chen,Anupam.Kumar,Henry.Gong,Kan V.Lu,Erin F.Simonds,Timothy F.Cloughesy,Linda M.Liau,Michael.Prados,Andrew W.Bollen,Mitchel S.Berger,Joseph T C.Shieh,C David.James,Theodore P.Nicolaides,William H.Yong,Albert.Lai,Monika E.Hegi,William A.Weiss,Joanna J.Phillips",[代码][代码] [代码][代码]"JournalTitle": "Molecular cancer therapeutics"[代码][代码] [代码][代码]},[代码][代码] [代码][代码]{[代码][代码] [代码][代码]"Title": [[代码][代码] [代码][代码][[代码][代码] [代码][代码]"替莫唑胺抗性原代GBM干细胞样细胞和复发性GBM的比较转录组学分析鉴定碳酸酐酶CA2基因作为抗性因子的上调。",[代码][代码] [代码][代码]"Comparative Transcriptomic Analysis of Temozolomide Resistant Primary GBM Stem-Like Cells and Recurrent GBM Identifies Up-Regulation of the Carbonic Anhydrase <i>CA2</i> Gene as Resistance Factor."[代码][代码] [代码][代码]][代码][代码] [代码][代码]],[代码][代码] [代码][代码]"Content": [[代码][代码] [代码][代码][[代码][代码] [代码][代码]"大约95%的胶质母细胞瘤(GBM)患者显示肿瘤复发,使他们的治疗选择有限,因为复发性肿瘤最常耐受一线化疗标准替莫唑胺(TMZ)。",[代码][代码] [代码][代码]"About 95% of patients with Glioblastoma (GBM) show tumor relapse, leaving them with limited therapeutic options as recurrent tumors are most often resistant to the first line chemotherapy standard Temozolomide (TMZ)."[代码][代码] [代码][代码]],[代码][代码] [代码][代码][[代码][代码] [代码][代码]"为了鉴定涉及TMZ抗性的分子途径,分离,表征和选择原代GBM干细胞样细胞(GSC)用于体外TMZ抗性。",[代码][代码] [代码][代码]"To identify molecular pathways involved in TMZ resistance, primary GBM Stem-like Cells (GSCs) were isolated, characterized, and selected for TMZ resistance in vitro."[代码][代码] [代码][代码]],[代码][代码] [代码][代码][[代码][代码] [代码][代码]"随后,进行RNA测序分析并显示在TMZ抗性干细胞样细胞中总共49个差异表达的基因(| log2倍变化|> 0.5并且调整的<p> - 值<0.1)。",[代码][代码] [代码][代码]"Subsequently, RNA sequencing analysis was performed and revealed a total of 49 differentially expressed genes (|log2-fold change| > 0.5 and adjusted <i>p</i>-value < 0.1) in TMZ resistant stem-like cells compared"[代码][代码] [代码][代码]],[代码][代码] [代码][代码][[代码][代码] [代码][代码]"到他们匹配的DMSO对照细胞。",[代码][代码] [代码][代码]"to their matched DMSO control cells."[代码][代码] [代码][代码]],[代码][代码] [代码][代码][[代码][代码] [代码][代码]"在上调基因中,我们将碳酸酐酶2(CA2)鉴定为与胶质瘤恶性肿瘤和患者存活相关的候选基因。",[代码][代码] [代码][代码]"Among up-regulated genes, we identified carbonic anhydrase 2 (CA2) as a candidate gene correlated with glioma malignancy and patient survival."[代码][代码] [代码][代码]],[代码][代码] [代码][代码][[代码][代码] [代码][代码]"值得注意的是,我们描述了CA2不仅在TMZ抗性GSC中对mRNA和蛋白质水平的一致上调,而且在患者匹配的第一次出现和复发肿瘤的临床样本中也是如此。",[代码][代码] [代码][代码]"Notably, we describe consistent up-regulation of CA2 not only in TMZ resistant GSCs on mRNA and protein level, but also in patient-matched clinical samples of first manifest and recurrent tumors."[代码][代码] [代码][代码]],[代码][代码] [代码][代码][[代码][代码] [代码][代码]"与碳酸酐酶抑制剂乙酰唑胺(ACZ)共处理使细胞对TMZ诱导的细胞死亡敏感。",[代码][代码] [代码][代码]"Co-treatment with the carbonic anhydrase inhibitor Acetazolamid (ACZ) sensitized cells to TMZ induced cell death."[代码][代码] [代码][代码]],[代码][代码] [代码][代码][[代码][代码] [代码][代码]"累积地,我们的发现说明了CA2作为复发性GBM中的化学增敏靶标的潜力,并提供了治疗相关的抑制CA2以克服TMZ诱导的化学抗性的理论基础。",[代码][代码] [代码][代码]"Cumulatively, our findings illustrate the potential of CA2 as a chemosensitizing target in recurrent GBM and provide a rationale for a therapy associated inhibition of CA2 to overcome TMZ induced chemoresistance."[代码][代码] [代码][代码]][代码][代码] [代码][代码]],[代码][代码] [代码][代码]"UID": "31262047",[代码][代码] [代码][代码]"Date": "2019-07-02",[代码][代码] [代码][代码]"Links": {[代码][代码] [代码][代码]"pubmed": "31262047",[代码][代码] [代码][代码]"pii": "cancers11070921",[代码][代码] [代码][代码]"doi": "10.3390/cancers11070921"[代码][代码] [代码][代码]},[代码][代码] [代码][代码]"Authors": "Ricarda.Hannen,Martin.Selmansberger,Maria.Hauswald,Axel.Pagenstecher,Andrea.Nist,Thorsten.Stiewe,Till.Acker,Barbara.Carl,Christopher.Nimsky,Jörg Walter.Bartsch",[代码][代码] [代码][代码]"JournalTitle": "Cancers"[代码][代码] [代码][代码]}[代码][代码] [代码][代码]][代码]
2020-01-01这个问题修复了吗?
wx.openDocument 打开文件报错fail no third apps supported[图片] 同样的问题,很多用户都打不开已下载的xls文件;好多机型都不支持文件打开功能,api:wx.openDocument; 下载功能是没有问题,望提供可以直接转发文件的接口,即小程序下载文件后可以直接转发功能的api,例如转发给文件传输助手。
2019-12-31[图片][图片] 在登录页面会出现白屏 是什么原因呢?页面开始只是静态的页面 没有引用组件
微信小程序白屏有时候打开小程序出现空白页面,加载了很久,没有任何信息,有时候又显示正常,调试未发现错误信息。 [图片]
2019-12-30