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See Latest ArticlesLocus heterogeneity of Dents disease: OCRL1 and TMEM27 genes in patients with no CLCN5 mutations
Pediatric Nephrology, 07/14/09
Tosetto E et al. - OCRL1 is involved in the functional defects characteristic of Dent’s disease and suggest that patients carrying missense mutations in exons where many Lowe mutations are mapped may represent a phenotypic variant of Lowe syndrome.
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
Today in Glomerular/Tubular Dz...keeping you current
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Mycophenolate mofetil and intravenous cyclophosphamide are similar as induction therapy for class V lupus nephritis
Kidney International, 11/05/09
Change in Estimated GFR Associates with Coronary Heart Disease and Mortality
Journal of the American Society of Nephrology, 11/23/09
Biomarkers for Lupus Nephritis: The Quest Continues
Clinical Journal of the American Society of Nephrology, 11/13/09
Today in Pediatric Nephrology...keeping you current
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Results of surgical treatment for renovascular hypertension in children: 30 year single centre experience
Nephrology Dialysis Transplantation, 10/30/09
New aspects in the pathogenesis, prevention, and treatment of hyponatremic encephalopathy in children
Pediatric Nephrology, 11/11/09
Effects of steroid avoidance and novel protocols on growth in paediatric renal transplant patients
Pediatric Nephrology, 11/03/09
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