Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Sensen Su"'
Autor:
Li Zhang, Hongrui Zhang, Sensen Su, Ye Jia, Chenyang Liang, Yuan Fang, Dengwei Hong, Tianyu Li, Fuzhe Ma
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
BackgroundPeritoneal dialysis-related peritonitis (PDRP) is one of the most common complications of peritoneal dialysis (PD). Understanding the risk factors and etiological characteristics is indispensable for infection prevention and improving the o
Externí odkaz:
https://doaj.org/article/7a2403f3ff384e46b04f99d43de7e7b5
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
BackgroundThe relationship between selenium and renal function has always attracted widespread attention. Increased selenium level has been found to cause impaired renal function in our previous study, but the mechanism is not clear. In this study, w
Externí odkaz:
https://doaj.org/article/316120c545294edcb497cff30effb985
Autor:
Shaojie Fu, Meiyan Wu, Yanli Cheng, Yan Guan, Jinyu Yu, Xueyao Wang, Sensen Su, Hao Wu, Fuzhe Ma, Yan Zou, Shan Wu, Hongzhao Xu, Zhonggao Xu
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
IntroductionIgA nephropathy (IgAN), a prevalent form of glomerulonephritis globally, exhibits complex pathogenesis. Cathepsins, cysteine proteases within lysosomes, are implicated in various physiological and pathological processes, including renal c
Externí odkaz:
https://doaj.org/article/16ec20b1febc459e821c6a01c6afa459
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
ObjectiveDiabetic kidney disease (DKD) is the leading cause of chronic kidney disease and end-stage renal disease worldwide. Early diagnosis is critical to prevent its progression. The aim of this study was to identify potential diagnostic biomarkers
Externí odkaz:
https://doaj.org/article/7d2a03ff5d1440af89423a2bcd958a55
Kimura’s disease with membranoproliferative glomerulonephritis: a case report with literature review
Publikováno v:
Renal Failure, Vol 41, Iss 1, Pp 126-130 (2019)
Background: Kimura's disease is a rare disease and its etiology is still unclear. Here we reported a case with lymphadenopathy complicated with secondary membranoproliferative glomerulonephritis. Case presentation: A 46-year-old Chinese man presented
Externí odkaz:
https://doaj.org/article/1addfd9b54014b75994e9a9aed3c3dd2
Publikováno v:
Life Sciences. 322:121661
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9bdbb784e5830f2b6f47d06eb8595f64
https://doi.org/10.1016/j.lfs.2023.121661
https://doi.org/10.1016/j.lfs.2023.121661
Publikováno v:
Aging (Albany NY)
Background: Anemia is a common complication of chronic kidney disease (CKD). Treating renal anemia with erythropoiesis-stimulating agents (ESAs) or erythropoietin analogs is effective but has side effects. Therefore, we performed a meta-analysis to a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c16d021321af4d906b0702848b0b554c
http://europepmc.org/articles/PMC8312415
http://europepmc.org/articles/PMC8312415
Publikováno v:
Biomedicine & Pharmacotherapy, Vol 111, Iss, Pp 359-366 (2019)
The cholinergic anti-inflammatory pathway modulates cytokine release by activating alpha-7 nicotinic acetylcholine receptors (α7nAChR) in monocytes/macrophages. We aimed to determine the role of α7nAChR in lupus nephritis (LN). We enrolled 36 inact
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5df878fcb13c0f058ee78f03a8105771
http://www.sciencedirect.com/science/article/pii/S0753332218376157
http://www.sciencedirect.com/science/article/pii/S0753332218376157
Autor:
Hao Wu, Yanli Cheng, Sensen Su, Bin Chen, Zhonggao Xu, Weixia Sun, Wanning Wang, Yuan-yuan Zhang
Publikováno v:
Nephron. 142:61-70
Background: 12-Lipoxygenase (12-LO) and angiotensin II (Ang II) are involved in the development of diabetic renal hypertrophy, in which cyclin-kinase inhibitors, p21 and p27 play pivotal roles. Here, we study the effects of 12-LO and its interaction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6429cfc40eaf7a417fcbe3c6ca31951
https://doi.org/10.1159/000496440
https://doi.org/10.1159/000496440
Publikováno v:
Medicine. 100:e25069
RATIONALE Atypical hemolytic uremic syndrome (aHUS) is an uncommon and serious disease that manifests hemolytic anemia, thrombocytopenia, and acute kidney injury. Genetic complement abnormalities have been shown to be responsible. Compared with the a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb4bd93514db51b52c361d8f88d45787
https://doi.org/10.1097/md.0000000000025069
https://doi.org/10.1097/md.0000000000025069