Cargando…
Urinary extracellular vesicles signature for diagnosis of kidney disease
Congenital disorders characterized by the quantitative and qualitative reduction in the number of functional nephrons are the primary cause of chronic kidney disease (CKD) in children. We aimed to describe the alteration of urinary extracellular vesicles (uEVs) associated with decreased renal functi...
Autores principales: | Takizawa, Keiichi, Ueda, Koji, Sekiguchi, Masahiro, Nakano, Eiji, Nishimura, Tatsuya, Kajiho, Yuko, Kanda, Shoichiro, Miura, Kenichiro, Hattori, Motoshi, Hashimoto, Junya, Hamasaki, Yuko, Hisano, Masataka, Omori, Tae, Okamoto, Takayuki, Kitayama, Hirotsugu, Fujita, Naoya, Kuramochi, Hiromi, Ichiki, Takanori, Oka, Akira, Harita, Yutaka |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9684058/ https://www.ncbi.nlm.nih.gov/pubmed/36439984 http://dx.doi.org/10.1016/j.isci.2022.105416 |
Ejemplares similares
-
Predominant but silent C1q deposits in mesangium on transplanted kidneys - long-term observational study
por: Kanai, Takahiro, et al.
Publicado: (2018) -
Laminin β(2) variants associated with isolated nephropathy that impact matrix regulation
por: Kikkawa, Yamato, et al.
Publicado: (2021) -
Degree of foot process effacement in patients with genetic focal segmental glomerulosclerosis: a single-center analysis and review of the literature
por: Ishizuka, Kiyonobu, et al.
Publicado: (2021) -
Amnionless-mediated glycosylation is crucial for cell surface targeting of cubilin in renal and intestinal cells
por: Udagawa, Tomohiro, et al.
Publicado: (2018) -
A novel de novo truncating TRIM8 variant associated with childhood-onset focal segmental glomerulosclerosis without epileptic encephalopathy: a case report
por: Shirai, Yoko, et al.
Publicado: (2021)