Zobrazeno 1 - 10
of 393
pro vyhledávání: '"foot process"'
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
Podocytopathies encompass kidney diseases where direct or indirect podocyte injury leads to proteinuria or nephrotic syndrome. Although Semaphorin3A (Sema3A) is expressed in podocytes and tubular cells in adult mammalian kidneys and has a common effe
Externí odkaz:
https://doaj.org/article/8df48a3a69214fbeb1f85f2c201e24fd
Autor:
Hua Wei, Peng Lan, Chen Xue-mei, Jiang XuShun, Hu JianGuo, Jiang Xian-Hong, Xiang Xu, Wan Jiangmin, Long Yingfei, Xiong Jianqiong, Ma Xueyi, Du Xiaogang
Publikováno v:
Open Medicine, Vol 19, Iss 1, Pp 440-51 (2024)
Lipid metabolism disorders lead to lipotoxicity. The hyperlipidemia-induced early stage of renal injury mainly manifests as podocyte damage. CD36 mediates fatty acid uptake and the subsequent accumulation of toxic lipid metabolites, resulting in podo
Externí odkaz:
https://doaj.org/article/c96a20d25ee64ddfa079325a5269936d
Publikováno v:
Journal of Nephropharmacology, Vol 13, Iss 2, Pp e11657-e11657 (2024)
Membranous nephropathy is an immune complex disease caused by subepithelial deposits. The pathological manifestations of membranous nephropathy are considered by the creation of immune complexes in the epithelial cells of the glomerular basement memb
Externí odkaz:
https://doaj.org/article/e6baddb1199745ec90052403eff22dff
Akademický článek
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Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 11 (2023)
Introduction: The unique architecture of glomerular podocytes is integral to kidney filtration. Interdigitating foot processes extend from the podocyte cell body, wrap around fenestrated capillaries, and form specialized junctional complexes termed s
Externí odkaz:
https://doaj.org/article/8d9aacd26e664a2bb74d69baf6205a26
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
ObjectiveThe present study aimed to explore the relationship between nephrotic syndrome and atopic diseases in childhood.MethodsFrom 2018 to 2019, 234 children with first-onset primary nephrotic syndrome (PNS) were selected for observation and long-t
Externí odkaz:
https://doaj.org/article/c6f9f63e0d704fe987b53c9f1e96f176
Autor:
Guo-min Li, Yi-fan Li, Qiao-qian Zeng, Xiao-mei Zhang, Hai-mei Liu, Jia-yan Feng, Yu Shi, Bing-bing Wu, Hong Xu, Li Sun
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Lupus podocytopathy is a glomerular lesion in systemic lupus erythematosus (SLE) characterized by diffuse podocyte foot process effacement (FPE) without immune complex (IC) deposition or with only mesangial IC deposition. It is rarely seen in childre
Externí odkaz:
https://doaj.org/article/dac9dab191bb4544a69fa2e0db3f47e9
Akademický článek
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Publikováno v:
Kidney Diseases, Pp 1-10 (2020)
Introduction: Long-term exposure to mercury can cause minimal change disease. However, the current understanding of mercury-associated minimal change disease (M-MCD) is inadequate. To improve the understanding of M-MCD, this study retrospectively ana
Externí odkaz:
https://doaj.org/article/f1932a3f397b4bb5b089b9d1ed50857f
Autor:
Peco-Antić Amira, Mulić Bilsana
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 148, Iss 9-10, Pp 631-636 (2020)
Podocytopathies include a wide spectrum of primary or secondary glomerular diseases that are the consequence of the podocyte injuries. The damage of podocytes can occur due to congenital or acquired disorders of podocyte transcriptional regulators, a
Externí odkaz:
https://doaj.org/article/4b46bb550ee64d828da646a973c04d3a