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of 5
pro vyhledávání: '"Cai-Jie Shen"'
Publikováno v:
Yi chuan = Hereditas. 44(3)
Hypertrophic cardiomyopathy (HCM) is an autosomal dominant genetic disease characterized by left ventricular hypertrophy with prevalence of 1/500-1/200. Up to now, 1500 mutations in more than 30 genes have been found to be related to the disease. Pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a0342d5474e001e30ed80e862c8b7454
https://pubmed.ncbi.nlm.nih.gov/35307643
https://pubmed.ncbi.nlm.nih.gov/35307643
Autor:
Hui‑Min Chu, Bin He, Xiao‑Min Chen, Cai‑Jie Shen, Xian‑Feng Du, Jing Liu, Yi‑Bo Yu, Ming‑Jun Feng
Publikováno v:
Molecular Medicine Reports
The present study was designed to develop a novel method for identifying significant pathways associated with human hypertrophic cardiomyopathy (HCM), based on gene co-expression analysis. The microarray dataset associated with HCM (E-GEOD-36961) was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf225cf1f2e2d3abfd5450357faa002b
https://doi.org/10.3892/mmr.2017.6667
https://doi.org/10.3892/mmr.2017.6667
Publikováno v:
Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association. 28(11)
The CHADSA total of 763 consecutive patients with LS (mean age: 66 ± 12 years; 464 male) were enrolled in this study between January 2013 and December 2014. Patients were divided into LS without AF (LS; n = 679) and LS with AF (LS-AF; n = 84) groups
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::157cdf58236aa204e009d781995bd0d0
https://pubmed.ncbi.nlm.nih.gov/31477449
https://pubmed.ncbi.nlm.nih.gov/31477449
Autor:
Ming-jun, Feng, Hui-min, Chu, Han-bin, Cui, Bin, He, Jing, Liu, Yi-bo, Yu, Cai-jie, Shen, Xiao-Min, Chen
Publikováno v:
Zhonghua xin xue guan bing za zhi. 41(1)
Recent studies suggest that mutation of the slow delayed rectifier potassium channel [I(Ks)] contributes to familial atrial fibrillation (FAF). In the current study, we explored the potential association between KCNQ1 polymorphism with lone AF (LAF).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5a154c8dcbcfd896b376cbc4f3615f12
https://pubmed.ncbi.nlm.nih.gov/23651960
https://pubmed.ncbi.nlm.nih.gov/23651960
Autor:
Xiao-Min Chen, Ming-Jun Feng, Cai-Jie Shen, Bin He, Xian-Feng Du, Yi-Bo Yu, Jing Liu, Hui-Min Chu
Publikováno v:
Molecular Medicine Reports; Jul2017, Vol. 16 Issue 1, p773-777, 5p