Cargando…
ATP5B and ETFB metabolic markers in children with congenital hydronephrosis
Congenital obstructive nephropathy is the primary cause of chronic renal failure in children. Disorders of mitochondrial energy metabolism may be a primary factor underlying tubular cell apoptosis in hydronephrosis. The β-F1-ATPase (ATP5B) and electron transfer flavoprotein β subunit (ETFB) metaboli...
Autores principales: | Zhao, Qi, Yang, Yi, Wang, Changlin, Hou, Ying, Chen, Hui |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355659/ https://www.ncbi.nlm.nih.gov/pubmed/27840937 http://dx.doi.org/10.3892/mmr.2016.5914 |
Ejemplares similares
-
A novel ETFB mutation in a patient with glutaric aciduria type II
por: Sudo, Yosuke, et al.
Publicado: (2015) -
A Case of Congenital Hydronephrosis
por: Kane, W. V.
Publicado: (1922) -
Case of Double Congenital Hydronephrosis
por: Johnstone, R. W., et al.
Publicado: (1922) -
Congenital megacalyces presenting as neonatal hydronephrosis
por: Bekele, Woseneneh, et al.
Publicado: (2010) -
A Case of Double Congenital Hydronephrosis
por: Johnstone, R. W., et al.
Publicado: (1921)