Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Xuepin Chen"'
Autor:
Rong Luo, Chenqing Zheng, Hao Yang, Xuepin Chen, Panpan Jiang, Xiushan Wu, Zhenglin Yang, Xia Shen, Xiaoping Li
Publikováno v:
Clinical and Translational Medicine, Vol 10, Iss 1, Pp 238-257 (2020)
Abstract Background Atrioventricular nodal reentry tachycardia (AVNRT) is the most common manifestation of paroxysmal supraventricular tachycardia (PSVT). Increasing data have indicated familial clustering and participation of genetic factors in AVNR
Externí odkaz:
https://doaj.org/article/8cafa6a0f0964e3781186123239a3333
Autor:
Tianying Wang, Yujing Qin, Jiansheng Chen, Shuang Chen, Jingqi Wu, Xuepin Chen, Xiaomeng Chen, Shaofei Zhou, Jianhong Zou, Jun Guan
Publikováno v:
BioMed research international. 2022
Coxsackievirus B (CVB) 3C protease (3Cpro) plays a specific cleavage role on AU-rich binding factor (AUF1, also called hnRNP D), which consequently disputes the regulation of AUF1 on downstream molecules. In our study, the iTRAQ approach was first us
Autor:
Xia Shen, Panpan Jiang, Chenqing Zheng, Xuepin Chen, Zhenglin Yang, Xiaoping Li, Hao Yang, Rong Luo, Xiushan Wu
Publikováno v:
Clinical and Translational Medicine, Vol 10, Iss 1, Pp 238-257 (2020)
Clinical and Translational Medicine
Luo, R, Zheng, C, Yang, H, Chen, X, Jiang, P, Wu, X, Yang, Z, Shen, X & Li, X 2020, ' Identification of potential candidate genes and pathways in atrioventricular nodal reentry tachycardia by whole-exome sequencing ', Clinical and Translational Medicine, vol. 10, no. 1, pp. 238-257 . https://doi.org/10.1002/ctm2.25
Clinical and Translational Medicine
Luo, R, Zheng, C, Yang, H, Chen, X, Jiang, P, Wu, X, Yang, Z, Shen, X & Li, X 2020, ' Identification of potential candidate genes and pathways in atrioventricular nodal reentry tachycardia by whole-exome sequencing ', Clinical and Translational Medicine, vol. 10, no. 1, pp. 238-257 . https://doi.org/10.1002/ctm2.25
BACKGROUND: Atrioventricular nodal reentry tachycardia (AVNRT) is the most common manifestation of paroxysmal supraventricular tachycardia (PSVT). Increasing data have indicated familial clustering and participation of genetic factors in AVNRT, and n
Autor:
Xiafei Dai, Huihui Ma, Xiaoping Li, Chenqing Zheng, Yibin Tang, Chao Yan, Xuepin Chen, Hongmei Zhang
Publikováno v:
Human Genome Variation
Human Genome Variation, Vol 6, Iss 1, Pp 1-4 (2019)
Human Genome Variation, Vol 6, Iss 1, Pp 1-4 (2019)
Emery-Dreifuss muscular dystrophy (EDMD) is a rare X-linked recessive disease characterized by the clinical triad of early childhood joint contractures, progressive weakness in muscles and cardiac involvement and can result in sudden death. Targeted
Autor:
Hongmei Zhang, Hui Peng, Chenqing Zheng, Xiafei Dai, Xiaoping Li, Chao Yan, Huihui Ma, Xuepin Chen
Publikováno v:
Human Genome Variation
Human Genome Variation, Vol 6, Iss 1, Pp 1-4 (2019)
Human Genome Variation, Vol 6, Iss 1, Pp 1-4 (2019)
Arrhythmogenic right ventricular cardiomyopathy (ARVC) presents as the progressive fibrofatty replacement of the cardiomyocytes particularly in the right ventricular wall. Here, we report two cases with ARVC. In family A, the proband carries a Desmog