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Schmidtmann C. Lindow S. Villard A. Heuser A. Muegge R. Gessner C. Granier K. Jaquet Dezember 2008 / Nat Clin Pract Cardiovasc Med Variations in DSG2: V56M, V158G and V920G are not pathogenic for arrhythmogenic right ventricular dysplasia/cardiomyopathy M.G. Posch M.J. Posch A. Perrot R. Dietz C. Oezcelik 2008 / Dis Markers Mitochondrial transcription factors TFA, TFB1 and TFB2: A search for DNA variants/haplotypes and the risk of cardiac hypertrophy C. Alonso-Montes M.G. Castro J.R. Reguero A. Perrot C. Oezcelik C. Geier M.G. Posch C. Moris V. Alvarez M. Ruiz-Ortega E. Coto April 2009 / Heart Rhythm Genetic deletion of arginine 14 in phospholamban causes dilated cardiomyopathy with attenuated electrocardiographic R amplitudes M.G. Posch A. Perrot C. Geier L.H. Boldt G. Schmidt H.B. Lehmkuhl R. Hetzer R. Dietz M. Gutberlet W. Haverkamp C. Oezcelik 16. Dezember 2008 / BMC Genomics Differential RelA- and RelB-dependent gene transcription in LTbetaR-stimulated mouse embryonic fibroblasts A. Lovas D. Radke D. Albrecht Z.B. Yilmaz U. Moeller A.J. Habenicht F. Weih Juni 2007 / Mol Genet Metab Mutations in MYOZ1 as well as MYOZ2 encoding the calsarcins are not associated with idiopathic and familial dilated cardiomyopathy M.G. Posch A. Perrot R. Dietz C. Oezcelik S. Pankuweit V. Ruppert A. Richter B. Maisch 01. Juni 2007 / J Invasive Cardiol Recurrent in-stent restenosis is not associated with the angiotensin-converting enzyme D/I, angiotensinogen Thr174Met and Met235Thr, and the angiotensin-II receptor 1 A1166C polymorphism C.M. Gross A. Perrot C. Geier M.G. Posch S. Hassfeld J. Kramer S. Schmidt W. Derer R. Dietz C. Oezcelik Februar 2008 / Hypertension Dietary n-3 polyunsaturated fatty acids and direct renin inhibition improve electrical remodeling in a model of high human renin hypertension R. Fischer R. Dechend F. Qadri M. Markovic S. Feldt F. Herse J.K. Park A. Gapelyuk I. Schwarz U.B. Zacharzowsky R. Plehm E. Safak A. Heuser A. Schirdewan F.C. Luft W.H. Schunck D.N. Mueller 15. Januar 2008 / Am J Med Genet A Mutations in GATA4, NKX2.5, CRELD1, and BMP4 are infrequently found in patients with congenital cardiac septal defects M.G. Posch A. Perrot K. Schmitt S. Mittelhaus E.M. Esenwein B. Stiller C. Geier R. Dietz R. Gessner C. Oezcelik F. Berger März 2013 / Eur J Hum Genet Novel mutations in the sarcomeric protein myopalladin in patients with dilated cardiomyopathy T. Meyer V. Ruppert S. Ackermann A. Richter A. Perrot S.R. Sperling M.G. Posch B. Maisch S. Pankuweit Seitennummerierung Aktuelle Seite 1 Seite 2 Seite 3 Seite 4 … Nächste Seite Next › Letzte Seite Last »
Dezember 2005 / FEBS J Cardiac troponin C-L29Q, related to hypertrophic cardiomyopathy, hinders the transduction of the protein kinase A dependent phosphorylation signal from cardiac troponin I to C A. Schmidtmann C. Lindow S. Villard A. Heuser A. Muegge R. Gessner C. Granier K. Jaquet
Dezember 2008 / Nat Clin Pract Cardiovasc Med Variations in DSG2: V56M, V158G and V920G are not pathogenic for arrhythmogenic right ventricular dysplasia/cardiomyopathy M.G. Posch M.J. Posch A. Perrot R. Dietz C. Oezcelik
2008 / Dis Markers Mitochondrial transcription factors TFA, TFB1 and TFB2: A search for DNA variants/haplotypes and the risk of cardiac hypertrophy C. Alonso-Montes M.G. Castro J.R. Reguero A. Perrot C. Oezcelik C. Geier M.G. Posch C. Moris V. Alvarez M. Ruiz-Ortega E. Coto
April 2009 / Heart Rhythm Genetic deletion of arginine 14 in phospholamban causes dilated cardiomyopathy with attenuated electrocardiographic R amplitudes M.G. Posch A. Perrot C. Geier L.H. Boldt G. Schmidt H.B. Lehmkuhl R. Hetzer R. Dietz M. Gutberlet W. Haverkamp C. Oezcelik
16. Dezember 2008 / BMC Genomics Differential RelA- and RelB-dependent gene transcription in LTbetaR-stimulated mouse embryonic fibroblasts A. Lovas D. Radke D. Albrecht Z.B. Yilmaz U. Moeller A.J. Habenicht F. Weih
Juni 2007 / Mol Genet Metab Mutations in MYOZ1 as well as MYOZ2 encoding the calsarcins are not associated with idiopathic and familial dilated cardiomyopathy M.G. Posch A. Perrot R. Dietz C. Oezcelik S. Pankuweit V. Ruppert A. Richter B. Maisch
01. Juni 2007 / J Invasive Cardiol Recurrent in-stent restenosis is not associated with the angiotensin-converting enzyme D/I, angiotensinogen Thr174Met and Met235Thr, and the angiotensin-II receptor 1 A1166C polymorphism C.M. Gross A. Perrot C. Geier M.G. Posch S. Hassfeld J. Kramer S. Schmidt W. Derer R. Dietz C. Oezcelik
Februar 2008 / Hypertension Dietary n-3 polyunsaturated fatty acids and direct renin inhibition improve electrical remodeling in a model of high human renin hypertension R. Fischer R. Dechend F. Qadri M. Markovic S. Feldt F. Herse J.K. Park A. Gapelyuk I. Schwarz U.B. Zacharzowsky R. Plehm E. Safak A. Heuser A. Schirdewan F.C. Luft W.H. Schunck D.N. Mueller
15. Januar 2008 / Am J Med Genet A Mutations in GATA4, NKX2.5, CRELD1, and BMP4 are infrequently found in patients with congenital cardiac septal defects M.G. Posch A. Perrot K. Schmitt S. Mittelhaus E.M. Esenwein B. Stiller C. Geier R. Dietz R. Gessner C. Oezcelik F. Berger
März 2013 / Eur J Hum Genet Novel mutations in the sarcomeric protein myopalladin in patients with dilated cardiomyopathy T. Meyer V. Ruppert S. Ackermann A. Richter A. Perrot S.R. Sperling M.G. Posch B. Maisch S. Pankuweit