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Tang T. Sander K.B. Craven A. Hempelmann A. Escayg July 15, 2008 / Physiol Genomics Localization of genetic loci controlling hydronephrosis in the Brown Norway rat and its association with hematuria L.T. Kota H. Schulz S. Falak N. Huebner M. Osborne-Pellegrin August 01, 2008 / Nat Genet Identification of renal Cd36 as a determinant of blood pressure and risk for hypertension M. Pravenec P.C. Churchill M.C. Churchill O. Viklicky L. Kazdova T.J. Aitman E. Petretto N. Huebner C.A. Wallace H. Zimdahl V. Zidek V. Landa J. Dunbar A. Bidani K. Griffin N. Qi M. Maxova V. Kren P. Mlejnek J. Wang T.W. Kurtz October 09, 2008 / Am J Physiol Renal Physiol Magnesium stimulates renal phosphate reabsorption J. Thumfart S. Jung S. Amasheh S. Kraemer H. Peters K. Sommer J. Biber H. Murer I.C. Meij U. Querfeld C.A. Wagner D. Mueller November 02, 2008 / Kidney Int Megalin contributes to the early injury of proximal tubule cells during nonselective proteinuria Y. Motoyoshi T. Matsusaka A. Saito I. Pastan T.E. Willnow S. Mizutani I. Ichikawa October 01, 2008 / Hepatology A mutation in the canalicular phospholipid transporter gene, ABCB4, is associated with cholestasis, ductopenia, and cirrhosis in adults D. Gotthardt H. Runz V. Keitel C. Fischer C. Flechtenmacher M. Wirtenberger K.H. Weiss S. Imparato A. Braun K. Hemminki W. Stremmel F. Rueschendorf A. Stiehl R. Kubitz B. Burwinkel P. Schirmacher A.S. Knisely J. Zschocke P. Sauer June 01, 2008 / Gen Physiol Biophys S100A1 deficiency results in prolonged ventricular repolarization in response to sympathetic activation G.E. Ackermann A.A. Domenighetti A. Deten I. Bonath I. Marenholz T. Pedrazzini P. Erne C.W. Heizmann April 01, 2008 / Invest Ophthalmol Vis Sci Mutation in a novel connexin-like gene (Gjf1) in the mouse affects early lens development and causes a variable small-eye phenotype O. Puk J. Loester C. Dalke D. Soewarto H. Fuchs B. Budde P. Nuernberg E. Wolf M.H. de Angelis J. Graw March 21, 2008 / Neurosci Lett Association between variation in the vesicular monoamine transporter 1 gene on chromosome 8p and anxiety-related personality traits F.W. Lohoff M. Lautenschlager J. Mohr T.N. Ferraro T. Sander J. Gallinat January 10, 2008 / Am J Hum Genet Genome-wide analysis indicates more Asian than Melanesian ancestry of Polynesians M. Kayser O. Lao K. Saar S. Brauer X. Wang P. Nuernberg R.J. Trent M. Stoneking Pagination Current page 1 Page 2 Page 3 Page 4 … Next page Next › Last page Last »
January 01, 2008 / Neurobiol Dis Mutation analysis of the hyperpolarization-activated cyclic nucleotide-gated channels HCN1 and HCN2 in idiopathic generalized epilepsy B. Tang T. Sander K.B. Craven A. Hempelmann A. Escayg
July 15, 2008 / Physiol Genomics Localization of genetic loci controlling hydronephrosis in the Brown Norway rat and its association with hematuria L.T. Kota H. Schulz S. Falak N. Huebner M. Osborne-Pellegrin
August 01, 2008 / Nat Genet Identification of renal Cd36 as a determinant of blood pressure and risk for hypertension M. Pravenec P.C. Churchill M.C. Churchill O. Viklicky L. Kazdova T.J. Aitman E. Petretto N. Huebner C.A. Wallace H. Zimdahl V. Zidek V. Landa J. Dunbar A. Bidani K. Griffin N. Qi M. Maxova V. Kren P. Mlejnek J. Wang T.W. Kurtz
October 09, 2008 / Am J Physiol Renal Physiol Magnesium stimulates renal phosphate reabsorption J. Thumfart S. Jung S. Amasheh S. Kraemer H. Peters K. Sommer J. Biber H. Murer I.C. Meij U. Querfeld C.A. Wagner D. Mueller
November 02, 2008 / Kidney Int Megalin contributes to the early injury of proximal tubule cells during nonselective proteinuria Y. Motoyoshi T. Matsusaka A. Saito I. Pastan T.E. Willnow S. Mizutani I. Ichikawa
October 01, 2008 / Hepatology A mutation in the canalicular phospholipid transporter gene, ABCB4, is associated with cholestasis, ductopenia, and cirrhosis in adults D. Gotthardt H. Runz V. Keitel C. Fischer C. Flechtenmacher M. Wirtenberger K.H. Weiss S. Imparato A. Braun K. Hemminki W. Stremmel F. Rueschendorf A. Stiehl R. Kubitz B. Burwinkel P. Schirmacher A.S. Knisely J. Zschocke P. Sauer
June 01, 2008 / Gen Physiol Biophys S100A1 deficiency results in prolonged ventricular repolarization in response to sympathetic activation G.E. Ackermann A.A. Domenighetti A. Deten I. Bonath I. Marenholz T. Pedrazzini P. Erne C.W. Heizmann
April 01, 2008 / Invest Ophthalmol Vis Sci Mutation in a novel connexin-like gene (Gjf1) in the mouse affects early lens development and causes a variable small-eye phenotype O. Puk J. Loester C. Dalke D. Soewarto H. Fuchs B. Budde P. Nuernberg E. Wolf M.H. de Angelis J. Graw
March 21, 2008 / Neurosci Lett Association between variation in the vesicular monoamine transporter 1 gene on chromosome 8p and anxiety-related personality traits F.W. Lohoff M. Lautenschlager J. Mohr T.N. Ferraro T. Sander J. Gallinat
January 10, 2008 / Am J Hum Genet Genome-wide analysis indicates more Asian than Melanesian ancestry of Polynesians M. Kayser O. Lao K. Saar S. Brauer X. Wang P. Nuernberg R.J. Trent M. Stoneking