Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Shengchuan Dai"'
Autor:
Khalid Abusaada, Fnu Asad-ur-Rahman, Vladimir Pech, Umair Majeed, Shengchuan Dai, Xiang Zhu, Sally A. Litherland
Publikováno v:
Advances in Medicine, Vol 2016 (2016)
Background. Blatchford and AIMS65 scores were developed to risk stratify patients with upper gastrointestinal bleed (UGIB). We sought to assess the performance of Blatchford and AIMS65 scores in predicting outcomes in elderly patients with nonvaricea
Externí odkaz:
https://doaj.org/article/ff450ac696b641e99fb8eb8af908bdc7
Autor:
Shengchuan Dai, Manoucher Manoucheri, Junhong Gui, Xiang Zhu, Divyanshu Malhotra, Shenjing Li, Jason D’souza, Fnu Virkram, Aditya Chada, Haibing Jiang
Publikováno v:
Cardiology Research and Practice, Vol 2016 (2016)
Background. Heart failure (HF) is one of the most common diagnoses associated with hospital readmission. We designed this prospective study to evaluate whether Kansas City Cardiomyopathy Questionnaire (KCCQ) score is associated with 30-day readmissio
Externí odkaz:
https://doaj.org/article/8082d8eec83044b8802d6f79b6dca9d8
Autor:
Divyanshu Malhotra, Manoucher Manoucheri, Aditya Chada, Haibing Jiang, Shengchuan Dai, Jason D’Souza, Shenjing Li, Fnu Virkram, Xiang Zhu, Junhong Gui
Publikováno v:
Cardiology Research and Practice
Cardiology Research and Practice, Vol 2016 (2016)
Cardiology Research and Practice, Vol 2016 (2016)
Background. Heart failure (HF) is one of the most common diagnoses associated with hospital readmission. We designed this prospective study to evaluate whether Kansas City Cardiomyopathy Questionnaire (KCCQ) score is associated with 30-day readmissio
Publikováno v:
Journal of Cardiovascular Disease Research. 7:90-92
Reversible Cerebral Vasoconstriction Syndrome (RCVS) is a rare postpartum angiopathic syndrome which can cause ischemic or hemorrhagic stroke. Peripartum cardiomyopathy (PPCM) is a non-ischemiccardiomyopathy that also occurs postpartum. Here we repor
Autor:
Jing Liu, Barry London, Jin-Young Yoon, Ryan L. Boudreau, Ajay Kumar, Santosh Kumar, Kenneth B. Margulies, Shengchuan Dai, Gina M. Morgan, Vikas Kumar, Haider Mehdi, William J. Kutschke, Julia S. Jacobs, Asma Naqvi, Ajit Vikram, Daniel S. Matasic, Xiaodong Zhu, Kaikobad Irani, Markus Bachschmid, Christopher M. Lewarchik, Xiaoming Zhang, Young-Rae Kim, Saet-Byel Jung, Mohanad Gabani, Modar Kassan, Xiaoqun Guan, Qiuxia Li
The voltage-gated cardiac Na+ channel (Nav1.5), encoded by the SCN5A gene, conducts the inward depolarizing cardiac Na+ current (INa) and is vital for normal cardiac electrical activity. Inherited loss-of-function mutations in SCN5A lead to defects i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13f9a9ea8e08c79c1266209f9ee7fab4
https://europepmc.org/articles/PMC6218171/
https://europepmc.org/articles/PMC6218171/
Autor:
Xiangxiang Shi, Hongyu Wang, Suyun Wang, Xiaoyan Huang, Fengquan Dong, Fang Huang, Shengchuan Dai, Deye Yang, Xi Zhou
Publikováno v:
Journal of Cellular and Molecular Medicine
The microRNAs (miRNAs) can post-transcriptionally regulate gene expression and heart development. The Pax-8 gene knockout mice have apparent heart abnormalities. This study investigated the role of miRNAs in regulation of cardiac apoptosis and develo
Autor:
Yunxiu Yang, Shaoling Zheng, Yong-heng Bai, Bicheng Chen, Mei Sun, Shengchuan Dai, Yirong Yang, Xiao-Jie Ni, Feifei Xu
Publikováno v:
International Urology and Nephrology. 44:301-307
This study aims to determine whether six polymorphisms of the genes involved in drug metabolism are associated with susceptibility to the development and progression of aristolochic acid nephropathy (AAN). In the study, 91 aristolochic acid nephropat
Autor:
Bin Han, Xiaoxia Pan, Nan Chen, Xiaonong Chen, Shengchuan Dai, Hong Ren, John Cijiang He, Zhaohui Wang, Qi Feng, Weiming Wang
Publikováno v:
Nephron Clinical Practice. 111:c87-c94
Aim: To investigate the association between mutations or single nucleotide polymorphisms (SNPs) of the gene ACTN4 in Chinese patients with idiopathic focal segmental glomerulosclerosis (FSGS). Materials and Methods: Genomic DNA of 82 Chinese idiopath
Publikováno v:
Gastrointestinal Endoscopy. 83:AB432-AB433
Autor:
Rebecca Gutmann, Gina Morgan, Jeanne M. Nerbonne, Shengchuan Dai, Alexander Greiner, Haider Mehdi, Anthony J Klappa, Barry London
Publikováno v:
Journal of the American College of Cardiology. 69:332
Background: Mutations in the voltage-gated sodium channel (SCN5A; Nav1.5) and its regulating genes, such as fibroblast growth factor 12 (FGF12), are linked to Brugada syndrome (BrS). The goal of this study is to identify additional FGF12 mutations an