Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Ruyuan Wei"'
Publikováno v:
Cell Death Discovery, Vol 10, Iss 1, Pp 1-11 (2024)
Abstract The role of Basic leucine zipper and W2 domains 2 (BZW2) in the advancement of different types of tumors is noteworthy, but its involvement and molecular mechanisms in lung adenocarcinoma (LUAD) remain uncertain. Through this investigation,
Externí odkaz:
https://doaj.org/article/4fd6087fae344eea8b5f7f20f6c155a8
Autor:
Xin Lv, Jianhua Li, Chuanzhen Liu, Ruyuan Wei, Lingwei Meng, Xiangjin Kong, Kaiming Wei, Guangqing Cao, Kai Liu
Publikováno v:
Journal of Cardiothoracic Surgery, Vol 17, Iss 1, Pp 1-7 (2022)
Abstract Background Hypertrophic cardiomyopathy is a commonly inherited heart disease. In addition, single coronary artery (SCA) is a rare congenital anomaly of the coronary arteries. And SCA concomitant with severe hypertrophic obstructive cardiomyo
Externí odkaz:
https://doaj.org/article/409b340e7d5d40d695deacb0e5ec9001
Publikováno v:
Oxidative medicine and cellular longevity. 2022
Pulmonary arterial hypertension (PAH) is an extremely malignant cardiovascular disease which mainly involves the uncontrollable proliferation of the pulmonary arterial smooth muscular cells (PASMCs). Recent studies have confirmed that mitochondria pl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::119bcdc97403c1aca0901fbb4178ae9f
https://pubmed.ncbi.nlm.nih.gov/35936222
https://pubmed.ncbi.nlm.nih.gov/35936222
Autor:
Xin Lv, Jianhua Li, Chuanzhen Liu, Ruyuan Wei, Lingwei Meng, Xiangjin Kong, Kaiming Wei, Guangqing Cao, Kai Liu
BackgroundHypertrophic cardiomyopathy (HCM) is the monogenic inherited cardiovascular disorder. In addition, single coronary artery (SCA) is a rare congenital anomaly of the coronary arteries. However, single coronary artery concomitant with severe o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9110f1ae81d73251e4a29b106835ee0
https://doi.org/10.21203/rs.3.rs-1532770/v1
https://doi.org/10.21203/rs.3.rs-1532770/v1
