Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Huanwan Yang"'
Autor:
Tianwen Han, Qun Wang, Huanwan Yang, Shanshan Zhou, Jing Wang, Jing Jing, Tao Zhang, Yuqi Liu, Yundai Chen
Publikováno v:
PeerJ, Vol 7, p e6804 (2019)
Background The incidences of premature coronary heart disease present a rising trend worldwide. The possible risk factors that may predict the incidence of repeat percutaneous coronary intervention (PCI) in premature acute coronary syndrome (ACS) rem
Externí odkaz:
https://doaj.org/article/b8f1a9d537dc48c9ab7c7a32f504e9ce
Publikováno v:
Artificial Intelligence in Medicine. 142:102573
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7084a3938a0766f6f4c88f0889c7d3bb
https://doi.org/10.1016/j.artmed.2023.102573
https://doi.org/10.1016/j.artmed.2023.102573
Publikováno v:
Oxidative Medicine and Cellular Longevity
Oxidative Medicine and Cellular Longevity, Vol 2021 (2021)
Oxidative Medicine and Cellular Longevity, Vol 2021 (2021)
Background. Mitochondrial NADH dehydrogenase subunit 2 (MT-ND2) m. 5178C>A gene mutation has protective effects against various diseases, but the molecular mechanism is still unclear. In previous study, we found a heteroplasmy level of MT-ND2 m. 5178
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d80e4c95fe30ae4d32d1bf7e1fc971b3
Publikováno v:
European Journal of Pharmacology. 865:172622
Mitochondrial DNA mutations promote hypertensive renal dysfunction, but the molecular mechanism remains unclear. This study compared renal damage between spontaneously hypertensive rats (SHR) and SHR with mitochondrial transfer (t)RNA mutations. To i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a4010666ea8d49cb6bf5b53adfb1656
https://doi.org/10.1016/j.ejphar.2019.172622
https://doi.org/10.1016/j.ejphar.2019.172622