Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Mei‐Jiao Suo"'
Autor:
Mei‐Jiao Suo, Wei‐Cheng Chen, Zi‐Qing Xu, Gui‐Xiang Tian, Ting Li, Ping Li, Wei Sheng, Guo‐Ying Huang, Xiao‐Jing Ma
Publikováno v:
The journal of gene medicineREFERENCES. 25(1)
Congenital heart disease (CHD) frequently manifests as a complex phenotype and approximately one-third of cases may be caused by genetic factors. BCOR, an X-linked gene encoding the corepressor of BCL6, has been demonstrated to be closely involved in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c2c1e9db937bc2dff5fdb27dd7e0c5c
https://pubmed.ncbi.nlm.nih.gov/36314054
https://pubmed.ncbi.nlm.nih.gov/36314054
Publikováno v:
Journal of clinical laboratory analysis. 36(9)
Congenital heart disease (CHD) is a class of cardiovascular defects that includes septal defects, outflow tract abnormalities, and valve defects. Human homolog of Drosophila headcase (HECA) is a novel cell cycle regulator whose role in CHD has not be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::157391366fe2029a24179b62129b12ec
https://pubmed.ncbi.nlm.nih.gov/35949005
https://pubmed.ncbi.nlm.nih.gov/35949005
Autor:
Zi-qing Xu, Wei-cheng Chen, Yu-jie Li, Mei-jiao Suo, Gui-xiang Tian, Wei Sheng, Guo-ying Huang
Publikováno v:
Disease markers. 2022
Congenital heart disease (CHD) is the most common congenital birth defect, with a prevalence of 8.98‰ of all live births in China. PTPN11 has been known to be closely involved in heart developments. In this research, we carried out whole-exome sequ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae0b6e485a43681d2ef591318aa14be1
https://pubmed.ncbi.nlm.nih.gov/35440950
https://pubmed.ncbi.nlm.nih.gov/35440950