Cargando…
The ciliary flow sensor and polycystic kidney disease
Since the discovery that proteins mutated in different forms of polycystic kidney disease (PKD) are tightly associated with primary cilia, strong efforts have been made to define the role of this organelle in the pathogenesis of cyst formation. Cilia are filiform microtubular structures, anchored in...
Autores principales: | Kotsis, Fruzsina, Boehlke, Christopher, Kuehn, E. Wolfgang |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588856/ https://www.ncbi.nlm.nih.gov/pubmed/23314319 http://dx.doi.org/10.1093/ndt/gfs524 |
Ejemplares similares
-
Recommendations for the use of tolvaptan in autosomal dominant polycystic kidney disease: a position statement on behalf of the ERA-EDTA Working Groups on Inherited Kidney Disorders and European Renal Best Practice
por: Gansevoort, Ron T., et al.
Publicado: (2016) -
Neprilysin inhibition in chronic kidney disease
por: Judge, Parminder, et al.
Publicado: (2015) -
The French Chronic Kidney Disease-Renal Epidemiology and Information Network (CKD-REIN) cohort study
por: Stengel, Bénédicte, et al.
Publicado: (2014) -
Planar cell polarity and the kidney
por: Papakrivopoulou, Eugenia, et al.
Publicado: (2014) -
A European Renal Best Practice (ERBP) position statement on the Kidney Disease Improving Global Outcomes (KDIGO) Clinical Practice Guidelines on Acute Kidney Injury: Part 1: definitions, conservative management and contrast-induced nephropathy(†)
por: Fliser, Danilo, et al.
Publicado: (2012)