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Kreutz N. Hübner M.R. James M.T. Bihoreau D. Gauguier G.M. Lathrop D. Ganten K. Lindpaintner January 01, 1995 / Hypertension Altered angiotensinogen amino acid sequence and plasma angiotensin II levels in genetically hypertensive rats: a study on cause and effects N. Huebner R. Kreutz S. Takahashi D. Ganten K. Lindpaintner January 01, 1995 / Mamm Genome The gene encoding endothelial nitric oxide synthase, Nos3, maps to rat chromosome 4 N. Hübner R. Kreutz S. Rubattu Y.A. Lee D. Ganten P.D. Allen K. Lindpaintner November 01, 1995 / Circulation Genetic linkage of the ACE gene to plasma angiotensin-converting enzyme activity but not to blood pressure: a quantitative trait locus confers identical complex phenotypes in human and rat hypertension R. Kreutz N. Hübner D. Ganten K. Lindpaintner January 01, 1995 / Herz Genetics in arterial hypertension - clinical and experimental aspects N. Hübner D. Ganten January 01, 1995 Genetische Analyse des Bluthochdrucks Y.A. Lee N. Hübner D. Ganten September 01, 2008 / Brain Perivascular spaces - MRI marker of inflammatory activity in the brain? J. Wuerfel M. Haertle H. Waiczies E. Tysiak I. Bechmann K.D. Wernecke F. Zipp F. Paul 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 Pagination Current page 1 Page 2 Page 3 Page 4 … Next page Next › Last page Last »
September 12, 1995 / Proc Natl Acad Sci U S A Dissection of a quantitative trait locus for genetic hypertension on rat chromosome 10 R. Kreutz N. Hübner M.R. James M.T. Bihoreau D. Gauguier G.M. Lathrop D. Ganten K. Lindpaintner
January 01, 1995 / Hypertension Altered angiotensinogen amino acid sequence and plasma angiotensin II levels in genetically hypertensive rats: a study on cause and effects N. Huebner R. Kreutz S. Takahashi D. Ganten K. Lindpaintner
January 01, 1995 / Mamm Genome The gene encoding endothelial nitric oxide synthase, Nos3, maps to rat chromosome 4 N. Hübner R. Kreutz S. Rubattu Y.A. Lee D. Ganten P.D. Allen K. Lindpaintner
November 01, 1995 / Circulation Genetic linkage of the ACE gene to plasma angiotensin-converting enzyme activity but not to blood pressure: a quantitative trait locus confers identical complex phenotypes in human and rat hypertension R. Kreutz N. Hübner D. Ganten K. Lindpaintner
January 01, 1995 / Herz Genetics in arterial hypertension - clinical and experimental aspects N. Hübner D. Ganten
September 01, 2008 / Brain Perivascular spaces - MRI marker of inflammatory activity in the brain? J. Wuerfel M. Haertle H. Waiczies E. Tysiak I. Bechmann K.D. Wernecke F. Zipp F. Paul
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