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See Latest ArticlesCompound mutations in human anion exchanger 1 are associated with complete distal renal tubular acidosis and hereditary spherocytosis
Kidney International, 07/23/09
Chang Y–H et al. – The compound E522K/G701D mutation of human anion exchanger 1 causes a trafficking defect in kidney cells, and this may explain the complete distal renal tubular acidosis of the patient.
Today in Acid-Base...keeping you current
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Lactic Acidosis Associated With Metformin in a Patient With Type 2 Diabetes With No Contraindication
The Endocrinologist, 11/13/09
Acid-Base Balance in Peritoneal Dialysis Patients: A Stewart-Fencl Analysis
Renal Failure, 10/29/09
Effect of high-normal compared with low-normal arterial pH on protein balances in automated peritoneal dialysis patients
American Journal of Clinical Nutrition, 10/29/09
Today in Basic Science/Genetics...keeping you current
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Simultaneous Infiltration of Polyfunctional Effector and Suppressor T Cells into Renal Cell Carcinomas
Cancer Research, 11/03/09
Loss of Tsc1, but not Pten, in renal tubular cells causes polycystic kidney disease by activating mTORC1
Human Molecular Genetics, 11/03/09
Mesenchymal Stem Cell Homing Capacity
Transplantation, 10/29/09
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