Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Yao-bin Zhu"'
Autor:
Yu-lin Wu, Guo-kai Yang, Qian Chen, Yi Tang, Jian-hui Zhang, Shao-jie Wu, Sen-lin Cai, Yan-feng Zhou, Yao-Bin Zhu, Jie-wei Luo, Zhu-ting Fang
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
BackgroundDouble inferior vena cava (DIVC) is a rare vascular malformation. With advances in radiological techniques and diagnosis, more and more types of DIVC were identified and diagnosed. Recognition of the variety of DIVC seen on imaging is essen
Externí odkaz:
https://doaj.org/article/57cacb6ebf434730a43a72d82750027f
Autor:
Yu-mian Gan, Yan-ping Zhang, Dan-dan Ruan, Jian-bin Huang, Yao-bin Zhu, Xin-fu Lin, Xiao-ping Xiao, Qiong Cheng, Zhen-bo Geng, Li-sheng Liao, Fa-qiang Tang, Jie-wei Luo
Publikováno v:
Cell Death and Disease, Vol 13, Iss 6, Pp 1-9 (2022)
Abstract X-linked hypophosphatemic rickets (XLH) is characterized by increased circulating fibroblast growth factor 23 (FGF23) concentration caused by PHEX (NM_000444.5) mutations. Renal tubular resorption of phosphate is impaired, resulting in ricke
Externí odkaz:
https://doaj.org/article/0ae6637eaaa247b48cc806435f97fd1b
Autor:
Yao-Bin Zhu, Jian-Hui Zhang, Yuan-Yuan Ji, Ya-Nan Hu, Han-Lu Wang, Dan-Dan Ruan, Xiao-Rong Meng, Xin-Fu Lin, Jie-Wei Luo, Wei Chen
Publikováno v:
Cardiology Research and Practice, Vol 2022 (2022)
Background. Brugada syndrome is a hereditary cardiac disease associated with mutations in ion channel genes. The clinical features include ventricular fibrillation, syncope, and sudden cardiac death. A family with Brugada syndrome with sudden cardiac
Externí odkaz:
https://doaj.org/article/98098a3cd4b24a7484d6b4d863c89fdf
Publikováno v:
Kidney & Blood Pressure Research, Vol 41, Iss 4, Pp 460-470 (2016)
Background/Aims: Renal ischemia/reperfusion injury (IRI) is a very common clinical event and usually leads to ischemic acute renal failure (ARF). In the present study, we investigated the protective role of vitamin C in renal function and renal arter
Externí odkaz:
https://doaj.org/article/21275deed4964afca8818f7d306540a5
Autor:
Hong-Hong Pan, Dan-Dan Ruan, Min Wu, Ting Chen, Tao Lu, Yu-Mian Gan, Chen Wang, Li-Sheng Liao, Xin-Fu Lin, Xin Chen, Yao-Bin Zhu, Zhu-Ting Fang, Qing-Hua Yu, Guo-Kai Yang, Lie-Fu Ye, Jie-Wei Luo
Publikováno v:
Journal of Medical Genetics; Dec2023, Vol. 60 Issue 12, p1210-1214, 24p
Autor:
Wu Chi, Min Wu, Han-lu Wang, Qiu-yan Wu, Yan-ping Zhang, Ya-nan Hu, Yao-bin Zhu, Xin-fu Lin, Ting Chen, Jie-wei Luo, Xing-lin Ruan, Yun-fei Li
Publikováno v:
Neurological Sciences. 44:2003-2015
Autor:
Yao-Bin Zhu, Jian-Hui Zhang, Jie-Wei Luo, Dan-Dan Ruan, Xin-Fu Lin, Jia-Bin Wu, Fa-Qiang Tang, Ya-Nan Hu, Xiao Yang, Xing-Lin Ruan
Publikováno v:
BioMed Research International, Vol 2021 (2021)
BioMed Research International
BioMed Research International
Gitelman syndrome (GS) is an autosomal recessive inherited salt-losing renal tubular disease, which is caused by a pathogenic mutation of SLC12A3 encoding thiazide-sensitive Na-Cl cotransporter, which leads to disturbance of sodium and chlorine reabs
Autor:
Lin-hui Yang, Li-zhen Xu, Zhi-jian Huang, Hong-hong Pan, Min Wu, Qiu-yan Wu, Tao Lu, Yan-ping Zhang, Yao-bin Zhu, Jia-bin Wu, Jie-wei Luo, lie-fu Ye
In this study, immune-ferropotosis-related prognostic differentially expressed genes (IFR-DEGs) were selected from the TCGA database, and a total of 103 differentially expressed genes were found. Fifty-two differentially expressed genes related to im
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2cd099bd33c34b1334cbd2d0c41274b
https://doi.org/10.21203/rs.3.rs-1611057/v1
https://doi.org/10.21203/rs.3.rs-1611057/v1
Autor:
Lin-Hui, Yang, Li-Zhen, Xu, Zhi-Jian, Huang, Hong-Hong, Pan, Min, Wu, Qiu-Yan, Wu, Tao, Lu, Yan-Ping, Zhang, Yao-Bin, Zhu, Jia-Bin, Wu, Jie-Wei, Luo, Guo-Kai, Yang, Lie-Fu, Ye
Publikováno v:
Am J Transl Res
Objective: We conducted an in-depth study of the immune system and ferroptosis to identify prognostic biomarkers and therapeutic targets for renal clear cell carcinoma. Methods: Immune ferroptosis-related differentially expressed genes (IFR-DEGs) wer
Autor:
Qing-Hua Yu, Jie-Wei Luo, Fa-Qiang Tang, Dan-Dan Ruan, Yao-Bin Zhu, Ning Lin, Yu-Mian Gan, Li-Sheng Liao, Xin Qian, Xiao Yang, Tao Lu
Publikováno v:
World Journal of Clinical Cases
BACKGROUND It is not easy to identify the cause of various iron overload diseases because the phenotypes overlap. Therefore, it is important to perform genetic testing to determine the genetic background of patients. AIM To investigate the genetic ba