Cargando…
Role of endothelial nitric oxide synthase VNTR (intron 4 a/b) polymorphism on the progression of renal disease in autosomal dominant polycystic kidney disease
Introduction: Autosomal dominant polycystic kidney disease (ADPKD) is an inherited disorder, and it is mainly associated with renal cyst formation. Several studies have also shown that these mutations regulate the physiology of epithelial tissues and determine renal cyst formation and growth in poly...
Autores principales: | Elumalai, Ramprasad, Periasamy, Soundararajan, Ramanathan, Gnanasambandan, Lakkakula, Bhaskar VKS |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nickan Research Institute
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4206055/ https://www.ncbi.nlm.nih.gov/pubmed/25340172 http://dx.doi.org/10.12861/jrip.2014.21 |
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) -
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) -
Renin gene rs1464816 polymorphism contributes to chronic kidney disease progression in ADPKD
por: Ramanathan, Gnanasambandan, et al.
Publicado: (2016) -
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)