Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Lv-ya Wang"'
Publikováno v:
PLoS ONE, Vol 9, Iss 4, p e94697 (2014)
Familial hypercholesterolemia is an autosomal dominant inherited disease characterized by elevated plasma low-density lipoprotein cholesterol (LDL-C). It is mainly caused by mutations of the low-density lipoprotein receptor (LDLR) gene. Currently, th
Externí odkaz:
https://doaj.org/article/8de0aae24b2b4312b7b5fc0170d32fe1
Autor:
Hai-dong Liu, Jing Zhao, Wen-li Cheng, Ning Li, Jie-wen Zhao, Lv-ya Wang, Ming-yin Man, Kai-jiang Yu
Background Qishen Yiqi Pills (QSYQP) is a traditional Chinese compound recipe. However, our understanding of its mechanism has been hindered due to the complexity of its components and targets. In this work, the network pharmacology-based approaches
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20f580243ee159cf4ee451471e346305
https://doi.org/10.21203/rs.3.rs-889464/v1
https://doi.org/10.21203/rs.3.rs-889464/v1
Publikováno v:
Medical Science Monitor; 2/13/2022, Vol. 28, p1-11, 11p
Autor:
Lv-Ya Wang, Ying-Jie Xu
Publikováno v:
Hereditas (Beijing). 30:671-676
Recent research has demonstrated a strong genetic linkage between premature coronary artery disease (pCAD) and dyslipidemia. Genetic variation in lipid metabolism can lead to impediment of lipid anabolism and catabolism, which promotes vascular arter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03f289f8253c51f13679a17e8495e4c5
https://doi.org/10.3724/sp.j.1005.2008.00671
https://doi.org/10.3724/sp.j.1005.2008.00671
Publikováno v:
PLoS ONE, Vol 9, Iss 4, p e94697 (2014)
PLoS ONE
PLoS ONE
Familial hypercholesterolemia is an autosomal dominant inherited disease characterized by elevated plasma low-density lipoprotein cholesterol (LDL-C). It is mainly caused by mutations of the low-density lipoprotein receptor (LDLR) gene. Currently, th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d35e28b80da9db5a5cea84dda2e95efd
http://europepmc.org/articles/PMC3983231?pdf=render
http://europepmc.org/articles/PMC3983231?pdf=render
Autor:
Ying-Jie, Xu, Lv-Ya, Wang
Publikováno v:
Yi chuan = Hereditas. 30(6)
Recent research has demonstrated a strong genetic linkage between premature coronary artery disease (pCAD) and dyslipidemia. Genetic variation in lipid metabolism can lead to impediment of lipid anabolism and catabolism, which promotes vascular arter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3b6e58790c4b9bb75496bd3dad372dba
https://pubmed.ncbi.nlm.nih.gov/18550487
https://pubmed.ncbi.nlm.nih.gov/18550487