Molecular and cellular pathophysiology of autosomal recessive polycystic kidney disease (ARPKD)
- 10 June 2006
- journal article
- review article
- Published by Springer Science and Business Media LLC in Cell and tissue research
- Vol. 326 (3), 671-685
- https://doi.org/10.1007/s00441-006-0226-0
Abstract
No abstract availableKeywords
This publication has 101 references indexed in Scilit:
- Clinical and Molecular Characterization Defines a Broadened Spectrum of Autosomal Recessive Polycystic Kidney Disease (ARPKD)Medicine, 2006
- Fibrocystin interacts with CAML, a protein involved in Ca2+ signalingBiochemical and Biophysical Research Communications, 2005
- Analysis of missense variants in the PKHD1-gene in patients with autosomal recessive polycystic kidney disease (ARPKD)Human Genetics, 2005
- Activation of the MEK5/ERK5 Cascade Is Responsible for Biliary Dysgenesis in a Rat Model of Caroli's DiseaseThe American Journal of Pathology, 2005
- Cyst fluid composition in human autosomal recessive polycystic kidney diseasePediatric Nephrology, 2004
- Polycystic kidney disease: new understanding in the pathogenesisThe International Journal of Biochemistry & Cell Biology, 2004
- Intraflagellar Transport and Cilia-Dependent Renal DiseaseJournal of the American Society of Nephrology, 2004
- New insights into the molecular pathophysiology of polycystic kidney diseaseKidney International, 1999
- An Inborn Error in Epidermal Growth Factor Prohormone Metabolism in a Mouse Model of Autosomal Recessive Polycystic Kidney DiseaseBiochemical and Biophysical Research Communications, 1993
- Polycystic kidney disease in the first year of lifeThe Journal of Pediatrics, 1987