Recent Advances in Molecular Genetics of Hereditary Magnesium-Losing Disorders
Localization of pendrin in mouse kidney
Osmolality and solute composition are strong regulators of AQP2 expression in renal principal cells

Localization of pendrin in mouse kidney
Osmolality and solute composition are strong regulators of AQP2 expression in renal principal cells
Transfection of CYP4A1 cDNA increases vascular reactivity in renal interlobar arteries
Urinary tract infection in iNOS-deficient mice with focus on bacterial sensitivity to nitric oxide
Urinary tumor necrosis factor contributes to sodium retention and renal hypertrophy during diabetes

Metabolism of Cisplatin to a Nephrotoxin in Proximal Tubule Cells
Signaling: Focus on Rho in Renal Disease
Transitioning to Therapy in Ischemic Acute Renal Failure

Kidney Transplantation in the Elderly: A Decision Analysis
Rho-Kinase Inhibition Blunts Renal Vasoconstriction Induced by Distinct Signaling Pathways In Vivo

Membrane Expression of Proteinase 3 Is Genetically Determined
p38 Mitogen-Activated Protein Kinase Contributes to Autoimmune Renal Injury in MRL-Faslpr Mice
Spectrum of Mutations in the Gene for Autosomal Recessive Polycystic Kidney Disease (ARPKD/PKHD1)

Recent Advances in Molecular Genetics of Hereditary Magnesium-Losing Disorders
Loop diuretics: from the Na-K-2Cl transporter to clinical use
