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PKD1 Haploinsufficiency Causes a Syndrome of Inappropriate Antidiuresis in Mice
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- Variable Cyst Development in Autosomal Dominant Polycystic Kidney Disease: The Biologic Context
- Aberrant Glycosylation and Localization of Polycystin-1 Cause Polycystic Kidney in an AQP11 Knockout Model
- A Protein Kinase A-Independent Pathway Controlling Aquaporin 2 Trafficking as a Possible Cause for the Syndrome of Inappropriate Antidiuresis Associated with Polycystic Kidney Disease 1 Haploinsufficiency
- Vasopressin-2 Receptor Signaling and Autosomal Dominant Polycystic Kidney Disease: From Bench to Bedside and Back Again
- Strategies Targeting cAMP Signaling in the Treatment of Polycystic Kidney Disease
- Bully Renal Cysts Knock Down Urine-Concentrating Capacity in the Early Rounds
- Polycystin-1 Interacts with Inositol 1,4,5-Trisphosphate Receptor to Modulate Intracellular Ca2+ Signaling with Implications for Polycystic Kidney Disease
- Pkd1 Haploinsufficiency Increases Renal Damage and Induces Microcyst Formation following Ischemia/Reperfusion
- A Case for Water in the Treatment of Polycystic Kidney Disease
- Role of Vasopressin Antagonists