Notch3基因变异介导Notch信号通路在非综合征性胎儿颈部淋巴水囊瘤中的作用及机制研究
81873836
2018
H0419.胎儿相关性疾病与胎源性疾病
杨昕
面上项目
副主任医师
广州医科大学
57万元
产前诊断;胎儿发育;淋巴水囊瘤;Notch3基因变异;Notch信号通路
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
查看更多信息请先登录或注册
查看更多信息请先登录或注册
查看更多信息请先登录或注册
| 序号 | 标题 | 类型 | 作者 |
|---|---|---|---|
| 1 | Microarray analysis in fetuses with duodenal obstruction: It is not just trisomy 21 | 期刊论文 | Wenwen Zhang;Tingying Lei;Fang Fu;Qiong Deng;Ru Li;Dan Wang;Xin Yang;Dongzhi Li;Can Liao |
| 2 | Genetic tests aid in counseling of fetuses with cerebellar vermis defects | 期刊论文 | Lushan Li;Fu Fang;Ru Li;Weiqiang Xiao;Qiuxia Yu;Dan Wang;Xiangyi Jing;Yongning Zhang;Xin Yang;Pan Min;Zequn Liu;Can Liao |
| 3 | Prenatal Diagnosis and Outcomes in Fetuses with Hemivertebra | 期刊论文 | Hang Zhou;You Wang;Ruibin Huang;Fang Fu;Ru Li;Ken Cheng;Dan Wang;Qiuxia Yu;Yongling Zhang;Xiangyi Jing;Tingying Lei;Jin Han;Xin Yang;Dongzhi Li;Can Liao |
| 4 | Exome sequencing improves genetic diagnosis of fetal increased nuchal translucency | 期刊论文 | Xin Yang;Lv-Yin Huang;Min Pan;Li-Li Xu;Li Zhen;Jin Han;Dong-Zhi Li |
| 5 | All-trans-retinoid acid induces the differentiation of P19 cells into neurons involved in the PI3K/Akt/GSK3beta signaling pathway | 期刊论文 | Fang Fu;Lu‐Shan Li;Ru Li;Qiong Deng;Qiu‐Xia Yu;Xin Yang;Min Pan;Jin Han;Li Zhen;Li‐Na Zhang;Ting‐Ying Lei;Dong‐Zhi Li;Can Liao |
| 6 | The Genetic and Clinical Outcomes in Fetuses With Isolated Fetal Growth Restriction: A Chinese Single-Center Retrospective Study | 期刊论文 | Hang Zhou;Ken Cheng;Yingsi Li;Fang Fu;Ru Li;Yongling Zhang;Xin Yang;Xiangyi Jing;Fucheng Li;Jin Han;Min Pan;Li Zhen;Dongzhi Li;Can Liao |
| 7 | Whole-exome sequencing in the evaluation of fetal congenital anomalies of the kidney and urinary tract detected by ultrasonography | 期刊论文 | Lei Ting-Ying;Fu Fang;Li Ru;Yu Qiu-Xia;Du Kun;Zhang Wen-Wen;Deng Qiong;Li Lu-Shan;Wang Dan;Yang Xin;Zhen Li;Li Dong-Zhi;Liao Can |
| 8 | Nonimmune hydrops fetalis: genetic analysis and clinical outcome | 期刊论文 | Qiong Deng;Fang Fu;Qiuxia Yu;Ru Li;Fucheng Li;Dan Wang;Tingying Lei;Xin Yang;Can Liao |
| 9 | [Analysis of families with fetal congenital abnormalities but negative prenatal diagnosis by whole exome sequencing]. | 期刊论文 | F Fu;L S Li;K Du;R Li;Q X Yu;D Wang;T Y Lei;Q Deng;Z Q Nie;W W Zhang;X Yang;J Han;L Zhen;M Pan;L N Zhang;F C Li;Y L Zhang;X Y Jing;D Z Li;C Liao |
| 10 | Prenatal diagnosis of Williams-Beuren syndrome by ultrasound and chromosomal microarray analysis | 期刊论文 | Ruibin Huang;Hang Zhou;Fang Fu;Ru Li;Tingying Lei;Yingsi Li;Ken Cheng;You Wang;Xin Yang;Lushan Li;Xiangyi Jing;Yongling Zhang;Fucheng Li;Dongzhi Li;Can Liao |
| 11 | Prenatal exome sequencing in fetuses with callosal anomalies | 期刊论文 | Ting‐ying Lei;Qin She;Fang Fu;Li Zhen;Ru Li;Qiu‐xia Yu;Dan Wang;Ying‐si Li;Ken Cheng;Hang Zhou;Xin Yang;Min Pan;Dong‐zhi Li;Can Liao |
| 12 | 突变的HoxA10基因及应用 | 专利 | 廖灿;符芳;李东至;李茹;党孝;黎璐珊;杨昕;韩瑾;潘敏;甄理;李坚;王丹;黎福成 |
| 13 | Case Report: Two Novel L1CAM Mutations in Two Unrelated Chinese Families With X-Linked Hydrocephalus | 期刊论文 | Hang Zhou;Qiuxia Yu;Yingsi Li;Fang Fu;Ru Li;Guilan Chen;Dan Wang;Yan Lu;Xin Yang;Dongzhi Li;Can Liao |
| 14 | A novel splicing mutation of ARHGAP29 is associated with nonsyndromic cleft lip with or without cleft palate | 期刊论文 | Qiuxia Yu;Qiong Deng;Fang Fu;Ru Li;Wenwen Zhang;Junhui Wan;Xin Yang;Dan Wang;Fucheng Li;Shaoqing Wu;Jian Li;Dong-Zhi Li;Can Liao |
| 15 | Prenatal Diagnosis of Talipes Equinovarus by Ultrasound and Chromosomal Microarray Analysis: A Chinese Single-Center Retrospective Study | 期刊论文 | Ruibin Huang;Xin Yang;Hang Zhou;Fang Fu;Ken Cheng;You Wang;Chunling Ma;Ru Li;Xiangyi Jing;Jin Han;Li Zhen;Min Pan;Dongzhi Li;Can Liao |
| 16 | 高通量测序和基因芯片技术在染色体病产前筛查及诊断中的应用研究 | 奖励 | 廖灿;李东至;符芳;李茹;杨昕;韩瑾;李发涛;张永玲;万均辉;景象一 |
| 17 | Should prenatal chromosomal microarray analysis be offered for isolated ventricular septal defect? A single-center retrospective study from China | 期刊论文 | Ken Cheng;Hang Zhou;Fang Fu;Tingying Lei;Fucheng Li;Ruibin Huang;You Wang;Xin Yang;Ru Li;Dongzhi Li;Can Liao |
| 18 | 早孕期颈项透明层增厚胎儿染色体异常的临床研究 | 期刊论文 | 杨昕;易翠兴;袁思敏;甄理;潘敏;李东至;廖灿 |
| 19 | Application of exome sequencing for prenatal diagnosis of fetal structural anomalies: clinical experience and lessons learned from a cohort of 1618 fetuses | 期刊论文 | Fang Fu;Ru Li;Qiuxia Yu;Dan Wang;Qiong Deng;Lushan Li;Tingying Lei;Guilan Chen;Zhiqiang Nie;Xin Yang;Jin Han;Min Pan;Li Zhen;Yongling Zhang;Xiangyi Jing;Fucheng Li;Fatao Li;Lina Zhang;Cuixing Yi;Yingsi Li;Yan Lu;Hang Zhou;Ken Cheng;Jian Li;Lina Xiang;Jing Zhang;Sha Tang;Ping Fang;Dongzhi Li;Can Liao |
| 20 | 产前诊断致病性拷贝数变异的56例家系分析 | 期刊论文 | 杨昕;李茹;黎福成;景象一;黄锐斌;李东至;廖灿 |
查看更多信息请先登录或注册
