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Development of Digital Fetal Heart Models with Virtual Ultrasound Function Based on Cardiovascular Casting and Computed Tomography Scan
期刊论文
BIOENGINEERING-BASEL, 2022, 卷号: 9, 期号: 10, 页码: 9
作者:
Yang, Qi
;
Han, Jiancheng
;
Wang, Rui
;
Zhang, Tong
;
Zhang, Yingying
收藏
  |  
浏览/下载:16/0
  |  
提交时间:2022/11/21
congenital heart disease
fetal echocardiography
digital twin
cardiovascular casting
virtual ultrasound
Smyd1 is essential for myosin expression and sarcomere organization in craniofacial, extraocular, and cardiac muscles
期刊论文
JOURNAL OF GENETICS AND GENOMICS, 2021, 卷号: 48, 期号: 3, 页码: 208-218
作者:
Jiao, Shuang
;
Xu, Rui
;
Du, Shaojun
收藏
  |  
浏览/下载:16/0
  |  
提交时间:2021/09/18
Smyd1
Myosin
Sarcomere
Craniofacial muscle
Cardiac muscle
Analysis of NKX2-5 in 439 Chinese Patients with Sporadic Atrial Septal Defect
期刊论文
MEDICAL SCIENCE MONITOR, 2019, 卷号: 25
作者:
Wang, Hongshu
;
Liu, Yong
;
Li, Yaxiong
;
Wang, Wenju
;
Li, Lin
收藏
  |  
浏览/下载:28/0
  |  
提交时间:2019/12/04
Genetic Variation
Heart Diseases
Heart Septal Defects, Atrial
Polymorphism, Single Nucleotide
Bilateral absence of the superior vena cava presenting with superior vena cava syndrome: A case report
期刊论文
ECHOCARDIOGRAPHY-A JOURNAL OF CARDIOVASCULAR ULTRASOUND AND ALLIED TECHNIQUES, 2019, 卷号: 36, 期号: 8
作者:
Zhang, Luni
;
Zhang, Li
;
Wang, Hui
;
Chen, Libo
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  |  
浏览/下载:24/0
  |  
提交时间:2019/12/05
congenital heart defects
superior vena cava
ultrasonography
Insights Figure for "Susceptibility to congenital heart defects associated with a polymorphism in TBX2 3 ' untranslated region in the Han Chinese population''
期刊论文
PEDIATRIC RESEARCH, 2019, 卷号: 85, 期号: 3
作者:
Wang, Feng
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  |  
浏览/下载:12/0
  |  
提交时间:2019/12/05
Susceptibility to congenital heart defects associated with a polymorphism in TBX2 3 ' untranslated region in the Han Chinese population
期刊论文
PEDIATRIC RESEARCH, 2019, 卷号: 85, 期号: 3
作者:
Wang, Jie
;
Zhang, Ran-ran
;
Ca, Ke
;
Yang, Qian
;
Duan, Wen-yuan
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/05
ISL1 loss-of-function mutation contributes to congenital heart defects
期刊论文
HEART AND VESSELS, 2019, 卷号: 34, 期号: 4
作者:
Ma, Lan
;
Wang, Juan
;
Li, Li
;
Qiao, Qi
;
Di, Ruo-Min
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  |  
浏览/下载:25/0
  |  
提交时间:2019/12/05
Congenital heart defect
Patent ductus arteriosus
Molecular genetics
Transcription factor
ISL1
Reporter gene assay
Intracardiac echogenic focus and its location: association with congenital heart defects.
期刊论文
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians, 2019, 页码: 1-5
作者:
Chiu Gin
;
Zhao Andi
;
Zhang Bo
;
Zhang Tianxiao
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  |  
浏览/下载:116/0
  |  
提交时间:2019/11/19
Intracardiac echogenic focus
echocardiography
low-risk pregnant women
fetal heart structure defects
retrospective cohort study
Deficiency of NONO is associated with impaired cardiac function and fibrosis in mice
期刊论文
Journal of Molecular and Cellular Cardiology, 2019, 卷号: 137, 页码: 46-58
作者:
Xu X.
;
Jiang H.
;
Lu Y.
;
Zhang M.
;
Cheng C.
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2019/12/11
Cardiac collagen metabolism
Cardiac fibroblasts
Heart defects
NONO
RNA-seq
Detection of copy number variants using chromosomal microarray analysis for the prenatal diagnosis of congenital heart defects with normal karyotype
期刊论文
JOURNAL OF CLINICAL LABORATORY ANALYSIS, 2019, 卷号: Vol.33 No.1
作者:
Song, Tingting
;
Wan, Shanning
;
Li, Yu
;
Xu, Ying
;
Dang, Yinghui
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  |  
浏览/下载:40/0
  |  
提交时间:2019/12/17
chromosomal microarray analysis
congenital heart defects
prenatal diagnosis
variants of unknown significance
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