Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Hairui Sun"'
Autor:
Jingjing Liu, Yuduo Wu, Hairui Sun, Xiaowei Liu, Xiaoyan Gu, Ying Zhao, Ye Zhang, Jiancheng Han, Yihua He
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Objective: This study aims to characterize the abnormal changes in placental DNA methylation associated with conotruncal heart defects (CTDs) and the level of methylation as epigenetic biomarkers for CTDs detection.Methods: This was a prospective stu
Externí odkaz:
https://doaj.org/article/b9c3f5b54dc540d08794d94d4cb33743
Autor:
Tong Yi, Hairui Sun, Yuwei Fu, Xiaoyan Hao, Lin Sun, Ye Zhang, Jiancheng Han, Xiaoyan Gu, Xiaowei Liu, Yong Guo, Xin Wang, Xiaoxue Zhou, Siyao Zhang, Qi Yang, Jiaqi Fan, Yihua He
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Objectives: Some genetic causes of heterotaxy have been identified in a small number of heterotaxy familial cases or animal models. However, knowledge on the genetic causes of heterotaxy in the fetal population remains scarce. Here, we aimed to inves
Externí odkaz:
https://doaj.org/article/3b575c98110f4450891f1e558d386aed
Autor:
Hairui Sun, Xiaowei Liu, Xiaoyan Hao, Xiaoxue Zhou, Jingyi Wang, Jiancheng Han, Mengmeng Liang, Hongjia Zhang, Yihua He
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Background: Left ventricular noncompaction (LVNC) is a rare cardiomyopathy, long QT syndrome (LQTS) is a rare ion channel disease, and simultaneous occurrence of both is even rarer. Further clinical reports and studies are needed to identify the asso
Externí odkaz:
https://doaj.org/article/00277a11f99246d2b40d8e416a36de65
Autor:
Hairui Sun, Xiaoyan Hao, Xin Wang, Xiaoxue Zhou, Ye Zhang, Xiaowei Liu, Jiancheng Han, Xiaoyan Gu, Lin Sun, Ying Zhao, Tong Yi, Hongjia Zhang, Yihua He
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 7 (2021)
Objectives: Noncompaction Cardiomyopathy (NCCM) has been classified as primary genetic cardiomyopathy and has gained increasing clinical awareness; however, little is known about NCCM in the fetal population. We aimed to investigate the clinical char
Externí odkaz:
https://doaj.org/article/94fe2c7f3fe048efa663ff89812041fd
Autor:
Hairui Sun, Lu Han, Xiaoshan Zhang, Xiaoyan Hao, Xiaoxue Zhou, Ruiqing Pan, Hongjia Zhang, Yihua He
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
BackgroundThe NONO gene is located on chromosome Xq13.1 and encodes a nuclear protein involved in RNA synthesis, transcriptional regulation, and DNA repair. Hemizygous variants in NONO have been reported to cause mental retardation, X-linked, syndrom
Externí odkaz:
https://doaj.org/article/d1cb85431c714f5c8f80218629a71b5a