Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Fa-xin Ren"'
Autor:
Tian-Yuan Xiong, Yi-Ming Li, Yi-Jun Yao, Yu-Heng Jia, Kai Xu, Zhen-Fei Fang, Jun Jin, Guo-Sheng Fu, Yi-Ning Yang, Lei Jiang, Wei-Dong Li, Yan-Qing Wu, Yan-Song Guo, Ran Guo, Yun-Dai Chen, Yi Li, Yi-Bing Shao, Yi Zhang, Bo-Sen Yang, Yi-Ke Zhang, Jing-Jing He, Kai-Yu Jia, Sheng-Hu He, Fa-Xin Ren, Jian-Cheng Xiu, Xing-Hua Gu, Liang-Long Chen, Ke Han, Yuan Feng, Mao Chen, Ning-Ning Wang
Publikováno v:
Chinese Medical Journal, Vol 134, Iss 22, Pp 2738-2740 (2021)
Externí odkaz:
https://doaj.org/article/bfa56c2b041a431eb5a512d1d28f6de7
Autor:
Guo-hui Yuan, Rong Du, Shou-yan Zhang, Wei Li, Cai-lian Kang, Li Tian, Fa-xin Ren, Le Gui, Jin Li, J. Yang
Publikováno v:
Frontiers of medicine in China. 1(3)
Long QT syndrome (LQTS) is the prototype of the cardiac ion channelopathies, which cause syncope and sudden death. Inherited LQTS is represented by the autosomal dominant Romano-ward syndrome (RWS), which is not accompanied by congenital deafness, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f67859291ec56d758d72b079227499c
https://pubmed.ncbi.nlm.nih.gov/24573873
https://pubmed.ncbi.nlm.nih.gov/24573873
Autor:
Le, Gui, Zhi-Wang, Li, Rong, Du, Guo-Hui, Yuan, Wei, Li, Fa-Xin, Ren, Jing, Li, Jun-Guo, Yang
Publikováno v:
Sheng li xue bao : [Acta physiologica Sinica]. 57(5)
We studied the effects of Chinese traditional medicine rhynchophylline (Rhy) on human ether-a-go-go related gene (HERG) channel and characterized the electrophysiological properties of Rhy's pharmacological effect on HERG channel using Xenopus oocyte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ca827a50f36981a5f5ef04277fee5a00
https://pubmed.ncbi.nlm.nih.gov/16220205
https://pubmed.ncbi.nlm.nih.gov/16220205
Autor:
Rong, Du, Fa-xin, Ren, Jun-guo, Yang, Guo-hui, Yuan, Shou-yan, Zhang, Cai-lian, Kang, Wei, Li, Le, Gui, Jing, Li
Publikováno v:
Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae. 27(3)
To investigate the molecular pathology in families with long QT syndrome (LQTS) including Jervell-Longe-Nielsen syndrome (JLNS) and Romano-ward syndrome (RWS) and Brugada syndrome (BS) in Chinese population.Polymerase chain reaction and DNA sequencin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4168e5376c5189dd8a3562551fe9ba0f
https://pubmed.ncbi.nlm.nih.gov/16038262
https://pubmed.ncbi.nlm.nih.gov/16038262
Autor:
Rong, Du, Jun-guo, Yang, Wei, Li, Le, Gui, Guo-hui, Yuan, Cai-lian, Kang, Fa-xin, Ren, Shou-yan, Zhang
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 22(1)
To identify the mutation of a Chinese family with inherited long QT syndrome(LQTS).The disease-causing gene was tentatively determined in light of the clinical manifestations and electrophysiological properties, and then polymerase chain reaction and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::98ac95d62ab9289cb542171531cde130
https://pubmed.ncbi.nlm.nih.gov/15696484
https://pubmed.ncbi.nlm.nih.gov/15696484
Publikováno v:
Yi chuan = Hereditas. 26(5)
To study PCR site-directed mutagenesis of long QT syndrome KCNQ1 gene in vitro. The site-directed mutagenesis of LQTS gene KCNQ1 was made by PCR. Two sets of primers were designed according to the sequence of KCNQ1 cDNA, and mismatch was introduced i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b95262e1d762912cf23ac6358a886564
https://pubmed.ncbi.nlm.nih.gov/15640067
https://pubmed.ncbi.nlm.nih.gov/15640067
Publikováno v:
Heart. 98:E265.2-E266
Objectives Primary percutaneous coronary intervention (PPCI) is an important therapy for patients with acute ST-segment elevation myocardial infarction (STEMI). However, the restoration of epicardial coronary patency after coronary occlusion does not
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::039005347387f4c4a4c7c88e6ab0bead
https://doi.org/10.1136/heartjnl-2012-302920u.1
https://doi.org/10.1136/heartjnl-2012-302920u.1