Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Guang-rong Qiu"'
Publikováno v:
Chinese Medical Journal, Iss 6, Pp 738-740 (2020)
Externí odkaz:
https://doaj.org/article/78540542ff8b42a38bc01716affa0caa
Autor:
Tao Zhang, Xiao Bing Tang, Li Li Wang, Yu Zuo Bai, Guang Rong Qiu, Zheng Wei Yuan, Wei Lin Wang
Publikováno v:
International Journal of Medical Sciences, Vol 10, Iss 2, Pp 191-197 (2013)
Background: Anorectal malformations (ARMs) represent a variety of congenital disorders that involve abnormal termination of the anorectum. This study was to reveal relation between CDX1 and human ARMs phenotypes.Methods: 108 Chinese patients and 120
Externí odkaz:
https://doaj.org/article/336c51a1a83f44229608d653dc7cbd00
Publikováno v:
Cytogenetic and Genome Research. 159:190-200
It is currently believed that the TBX1 gene is one of the core genes of congenital heart disease (CHD). However, there are few studies on the abnormal regulation of TBX1 gene expression. The purpose of this work was to investigate the role of miR-144
Autor:
Yuan Lv, Yue-Ling Sun, Yue Zhao, Pei-Yan Liu, Tian-xing Gong, Jing-Shu Zhang, Guang-Rong Qiu, Jun-Xia Ruan, Nan Wan
Publikováno v:
Gene. 626:426-432
MicroRNAs (miRNAs) are a class of endogenous, non-coding small RNAs that regulate the expression of target genes. Previous studies have suggested that miRNAs are key regulators in cardiovascular systems. This study investigated the role of miR-873 in
Publikováno v:
Cytogenetic and genome research. 159(4)
It is currently believed that the TBX1 gene is one of the core genes of congenital heart disease (CHD). However, there are few studies on the abnormal regulation of TBX1 gene expression. The purpose of this work was to investigate the role of miR-144
Publikováno v:
Molecular Medicine Reports
Congenital heart diseases (CHDs) are the most common birth defects due to abnormal cardiac development. The T-box 20 (TBX20) gene is a member of the T‑box family of transcription factors and encodes TBX20, which is essential for early heart develop
Autor:
Guang Rong Qiu, Tao Zhang, Lili Wang, Wei Lin Wang, Zheng Wei Yuan, Yu Zuo Bai, Xiao Bing Tang
Publikováno v:
International Journal of Medical Sciences
Background: Anorectal malformations (ARMs) represent a variety of congenital disorders that involve abnormal termination of the anorectum. This study was to reveal relation between CDX1 and human ARMs phenotypes. Methods: 108 Chinese patients and 120
Autor:
Xiao-Ming Li, Chun-Yi Li, Yan-Yan Zhao, Cai-Xia Liu, Hong Liu, Gui-Yuan Sun, Kai-Lai Sun, Chun-lian Jin, Guang-rong Qiu, Fangjie Chen, Fu-Cai Li
Publikováno v:
Hereditas (Beijing). 32:397-403
Establishment of integrated course system in human development and genetics is an important part of course reformation, and the improvement of this system is achieved by integrating the content of course, stabilizing teaching force, building teaching
Publikováno v:
Steroids. 75:368-372
Fhl1 (Four and a Half LIM domain 1) regulates muscle growth and development. In addition, skeletal myoblast growth is significantly affected by gender differences, implicating estrogen in the regulation of muscle development. We sought to determine i
Publikováno v:
Hereditas (Beijing). 31:374-380
To explore the mechanism of TBX5 abnormal expression in simple congenital heart disease (CHD), 100 CHD venous blood, 50 CHD heart tissues, and 5 non-CHD heart tissues were involved in this study. The mutation and methylation in the 1 200 bp region up