PTCH1基因调控心脏流出道发育的机制及其在先天性心脏病患者中的突变谱分析

81871717
2018
H2605.分子生物学检验
傅启华
面上项目
教授
上海交通大学
57万元
PTCH1;突变谱;基因;生物标志物;先天性心脏病
2019-01-01到2022-12-31
  • 中英文摘要
  • 结题摘要
  • 结题报告
  • 项目成果
  • 项目参与人
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序号 标题 类型 作者
1 Copy number variation analysis in Chinese children with complete atrioventricular canal and single ventricle 期刊论文 Zhang Xingyu;Wang Bo;You Guoling;Xiang Ying;Fu Qihua;Yu Yongguo;Zhang Xiaoqing
2 FGD5-AS1 Is a Hub lncRNA ceRNA in Hearts With Tetralogy of Fallot Which Regulates Congenital Heart Disease Genes Transcriptionally and Epigenetically 期刊论文 Zhang Xingyu;Gao Yunqian;Zhang Xiaoping;Zhang Xiaoqing;Xiang Ying;Fu Qihua;Wang Bo;Xu Zhuoming
3 15q11.2 deletion is enriched in patients with total anomalous pulmonary venous connection 期刊论文 Li Xiaoliang;Shi Guocheng;Li Yang;Zhang Xiaoqing;Xiang Ying;Wang Teng;Li Yanxin;Chen Huiwen;Fu Qihua;Zhang Hong;Wang Bo
4 Long Noncoding RNA lnc-TSSK2-8 Activates Canonical Wnt/beta-Catenin Signaling Through Small Heat Shock Proteins HSPA6 and CRYAB 期刊论文 Fa Jingjing;Zhang Xiaoqing;Zhang Xiaoping;Qi Ming;Zhang Xingyu;Fu Qihua;Xu Zhuoming;Gao Yunqian;Wang Bo
5 Generation of a homozygous CRISPR/Cas9-mediated knockout human iPSC line for PTCH1 gene 期刊论文 Zu Bailing;Zhang Xiaoqing;You Guoling;Fu Qihua
6 SORBS2 is a genetic factor contributing to cardiac malformation of 4q deletion syndrome patients. 期刊论文 Liang Fei;Wang Bo;Geng Juan;You Guoling;Fa Jingjing;Zhang Min;Sun Hunying;Chen Huiwen;Fu Qihua;Zhang Xiaoqing;Zhang Zhen
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