Molecular and cellular pathogenesis of autosomal recessive polycystic kidney disease

Author:

Menezes L.F.1,Onuchic L.F.2

Affiliation:

1. Universidade de São Paulo, Brasil; Johns Hopkins University School of Medicine, USA

2. Universidade de São Paulo, Brasil

Publisher

FapUNIFESP (SciELO)

Subject

Cell Biology,General Pharmacology, Toxicology and Pharmaceutics,General Medicine,Immunology,Physiology,Biochemistry,General Neuroscience,Biophysics

Reference60 articles.

1. Autosomal recessive polycystic kidney disease: the clinical experience in North America;Guay-Woodford LM;Pediatrics,2003

2. Autosomal recessive polycystic kidney disease: outcomes from a single-center experience;Capisonda R;Pediatr Nephrol,2003

3. Comprehensive genomic analysis of PKHD1 mutations in ARPKD cohorts;Sharp AM;J Med Genet,2005

4. Clinical consequences of PKHD1 mutations in 164 patients with autosomal-recessive polycystic kidney disease (ARPKD);Bergmann C;Kidney Int,2005

5. Pathogenesis of polycystic kidneys: Type 1 due to hyperplasia of interstitial portions of collecting tubules;Osathanondh V;Arch Pathol,1964

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