Cargando…
Renin gene rs1464816 polymorphism contributes to chronic kidney disease progression in ADPKD
BACKGROUND: Autosomal dominant polycystic kidney disease (ADPKD) is a monogenic disorder and is a common genetic cause of chronic renal failure in children and adults. The enzyme renin plays a key role in the RAAS cascade and an important role in the development of hypertension and progression of re...
Autores principales: | Ramanathan, Gnanasambandan, Elumalai, Ramprasad, Periyasamy, Soundararajan, Lakkakula, Bhaskar V. K. S. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4710007/ https://www.ncbi.nlm.nih.gov/pubmed/26753721 http://dx.doi.org/10.1186/s12929-015-0217-0 |
Ejemplares similares
-
Influence of angiotensin converting enzyme (ACE) gene rs4362 polymorphism on the progression of kidney failure in patients with autosomal dominant polycystic kidney disease (ADPKD)
por: Ramanathan, Gnanasambandan, et al.
Publicado: (2016) -
Role of endothelial nitric oxide synthase VNTR (intron 4 a/b) polymorphism on the progression of renal disease in autosomal dominant polycystic kidney disease
por: Elumalai, Ramprasad, et al.
Publicado: (2014) -
Endothelin 1 gene is not a major modifier of chronic kidney disease advancement among the autosomal dominant polycystic kidney disease patients
por: Annapareddy, Shiva Nagendra Reddy, et al.
Publicado: (2015) -
TRPC6 gene promoter polymorphisms in steroid resistant nephrotic syndrome children
por: Mahesh Kumar, Kempanahalli Basappa, et al.
Publicado: (2015) -
Pathways, perspectives and pursuits in polycystic kidney disease
por: Bhaskar, L. V. K. S., et al.
Publicado: (2015)