Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Miaoyue Hu"'
Autor:
Jinshuang Wei, Junlin Zhang, Junyu Wei, Miaoyue Hu, Xiuqi Chen, Xuankai Qin, Jie Chen, Fengying Lei, Yuanhan Qin
Publikováno v:
PLoS ONE, Vol 18, Iss 2, p e0281439 (2023)
Acute kidney injury (AKI) is a serious and frequently observed disease associated with high morbidity and mortality. Weighted gene co-expression network analysis (WGCNA) is a research method that converts the relationship between tens of thousands of
Externí odkaz:
https://doaj.org/article/3fee9d1ea7874851bc2854831947c144
Autor:
Jinshuang Wei, Junlin Zhang, Xiuqi Chen, Jiasen Zou, Junyu Wei, Miaoyue Hu, Shiqun Zhu, Yuanhan Qin, Fengying Lei
Publikováno v:
Pharmacological Research - Modern Chinese Medicine, Vol 3, Iss , Pp 100114- (2022)
Objective: To investigate the molecular mechanism underlying the therapeutic effect of resveratrol for nephrotic syndrome using various online network pharmacology databases. Methods: Genes related to resveratrol and nephrotic syndrome were downloade
Externí odkaz:
https://doaj.org/article/82eb9c08c1384e9698ba9aee1250514c
Autor:
Zhihui Yue, Miaoyue Hu, Haiyan Wang, Min Li, Huamu Chen, Liangzhong Sun, Huajuan Tong, Hongrong Lin, Ting Liu
Publikováno v:
Clinica Chimica Acta. 506:136-144
Background Nephronophthisis (NPHP) is the most common genetic cause of end-stage renal disease (ESRD) in children. This study was performed to explore the pathogenic gene mutations and clinical and pathological features of Chinese patients with NPHP.
Autor:
Huamu Chen, Min Li, Xuefei Gao, Dantong Li, Xiaohong Wu, Miaoyue Hu, Liangzhong Sun, Haiyan Wang, Zhihui Yue, Albert C.M. Ong, Xiaoya Wei, Hongrong Lin
Nephronophthisis (NPH) is the most prevalent monogenetic disorder leading to end-stage renal failure (ESRD) in childhood. Mutations in Nphp1, encoding a cilia-localized protein, account for the majority of NPH cases. Despite its identification many y
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f2f1e92a0607c6ac444b064fb785ce5