A carregar...
Pkd1 Inactivation Induced in Adulthood Produces Focal Cystic Disease
Autosomal dominant polycystic kidney disease, the most common monogenetic disorder, is characterized by gradual replacement of normal renal parenchyma by fluid-filled cysts. Mutations in either PKD1 or PKD2 cause autosomal dominant polycystic kidney disease. Pkd1(−/−) or Pkd2(−/−) mice develop rapid...
Na minha lista:
| Main Authors: | , , , |
|---|---|
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society of Nephrology
2008
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2588099/ https://ncbi.nlm.nih.gov/pubmed/18776127 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1681/ASN.2007101139 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|