Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Xunna Bao"'
Autor:
Jingzhou Chen, Hu Ding, Kai Sun, Jizheng Wang, Xunna Bao, Weili Zhang, Weiwei Ma, Wenlong Li, Hui Yu, Rutai Hui, Changxin Wang, Hu Wang, Weihua Song, Jing Xu, Xiaojian Wang, Lin Zhang, Dao Wen Wang
Publikováno v:
Clinical Science. 119:353-359
uPA (urokinase-plasminogen activator) and its receptor (uPAR) have been implicated in a broad spectrum of pathophysiological processes, including fibrinolysis, proteolysis, inflammation, atherogenesis and plaque destabilization, all of which are invo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e1b98299c3900c343ec1f04c16dee6b
https://doi.org/10.1042/cs20100151
https://doi.org/10.1042/cs20100151
Autor:
Wei Wang, Darryl C. Zeldin, Yujun Xu, Guanglin Cui, Lan Zhang, Bin Wu, Dao Wen Wang, Xunna Bao, Ryan T. Dackor, Qi Wang, Yuanchao Tu, Grace E. Kissling, Rutai Hui, Hu Ding
Publikováno v:
Pharmacogenetics and Genomics. 20:187-194
20-Hydroxyeicosatetraenoic acid has been shown to play an important role in cerebral vascular function. We hypothesized that polymorphisms in genes encoding 20-Hydroxyeicosatetraenoic acid synthesizing enzymes might confer susceptibility to stroke.To
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e621d6613babed1506b328ada7fdf3f9
https://doi.org/10.1097/fpc.0b013e328336eefe
https://doi.org/10.1097/fpc.0b013e328336eefe
Publikováno v:
Pharmacogenetics and genomics. 21(3)
Objective The renin-angiotensin-aldosterone system is important for cerebrovascular research because it influences blood pressure, vasoconstriction, thrombosis, and vessel wall damage. We hypothesized that genetic variations in CYP11B2 gene might con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b14e16220ac6bdbc29351492c50be27b
https://pubmed.ncbi.nlm.nih.gov/21228735
https://pubmed.ncbi.nlm.nih.gov/21228735
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 412(13-14)
Background Congenital adrenal hyperplasia owing to 17α-hydroxylase/17, 20-lyase deficiency is caused by genetic mutations in the CYP17A1 gene. To date, more than 80 different genetic lesions have been described in patients suffering from this disord
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20426f109ccecbda251968e055e032bb
https://pubmed.ncbi.nlm.nih.gov/21420394
https://pubmed.ncbi.nlm.nih.gov/21420394
Publikováno v:
Stroke. 41(1)
Background and Purpose— The first genomewide association study of ischemic stroke in whites has identified multiple susceptibility loci. We confirmed this study by examining associations with ischemic stroke in a Chinese Han population. Methods—
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3f97942e026a6114bd2a4a1fd7293ab
https://pubmed.ncbi.nlm.nih.gov/19910543
https://pubmed.ncbi.nlm.nih.gov/19910543
Autor:
Yujun Xu, Qing Kenneth Wang, Chenqi Xu, Guanglin Cui, Rutai Hui, Hu Ding, Xunna Bao, Xin Tu, Dao Wen Wang, Xiaojing Wang
Publikováno v:
Atherosclerosis. 216:381-382
Recent genome-wide association (GWA) studies have identified two intergenic single nucleotide polymorphisms (SNPs) (rs11833579 and rs12425791) on chromosome 12p13 and within 11 kb of the NINJ2 gene that were significantly associated with stroke in Ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::875fcb3962a56e80fb2ccdb424ba755d
https://doi.org/10.1016/j.atherosclerosis.2011.02.005
https://doi.org/10.1016/j.atherosclerosis.2011.02.005
Autor:
Jing Xu, Wenlong Li, Xunna Bao, Hu Ding, Jingzhou Chen, Weili Zhang, Kai Sun, Jizheng Wang, Xiaojian Wang, Hu Wang, Hui Yu, Weiwei Ma, Lin Zhang, Changxin Wang, Daowen Wang
Publikováno v:
Clinical Science; 2010, Vol. 119 Issue 8, p353-359, 7p