Cargando…
Magnetic resonance microscopy of renal and biliary abnormalities in excised tissues from a mouse model of autosomal recessive polycystic kidney disease
Polycystic kidney disease (PKD) is transmitted as either an autosomal dominant or recessive trait and is a major cause of renal failure and liver fibrosis. The cpk mouse model of autosomal recessive PKD (ARPKD) has been extensively characterized using standard histopathological techniques after euth...
Autores principales: | Lee, Choong H, O’Connor, Amber K, Yang, Chaozhe, Tate, Joshua M, Schoeb, Trenton R, Flint, Jeremy J, Blackband, Stephen J, Guay-Woodford, Lisa M |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4562597/ https://www.ncbi.nlm.nih.gov/pubmed/26320214 http://dx.doi.org/10.14814/phy2.12517 |
Ejemplares similares
-
Cystin genetic variants cause autosomal recessive polycystic kidney disease associated with altered Myc expression
por: Yang, Chaozhe, et al.
Publicado: (2021) -
Transcription factor Ap2b regulates the mouse autosomal recessive polycystic kidney disease genes, Pkhd1 and Cys1
por: Wu, Maoqing, et al.
Publicado: (2023) -
Design of two ongoing clinical trials of tolvaptan in the treatment of pediatric patients with autosomal recessive polycystic kidney disease
por: Mekahli, Djalila, et al.
Publicado: (2023) -
Autosomal Recessive Polycystic Kidney Disease
por: Salati, Sajad Ahmad
Publicado: (2014) -
Autosomal Recessive Polycystic Kidney Disease
por: Hafer, Ashley S., et al.
Publicado: (2017)