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Prof. Dr. (87) Schmidt-Krüger, Vanessa Dr. (1) Schmidt-Ullrich, Ruth Dr. (2) Schmitt, Clemens Prof. Dr. (2) Schulz-Menger, Jeanette Prof. Dr. (8) Schütz, Anja Dr. (1) Schwarz, Roland Dr. (3) Selbach, Matthias Prof. Dr. (6) Smith, Janice (1) Sommer, Thomas Prof. Dr. (6) Spagnoli, Francesca Dr. (1) Sperling, Silke Prof. Dr. (5) Sporbert, Anje Dr. (3) Spuler, Simone Prof. (3) Stein, Ulrike Prof. Dr. (14) Taube, Martin (1) Todiras, Mihail (5) Tursun, Baris Dr. (1) Uckert, Wolfgang Prof. Dr. (3) Volkwein, Corinna (1) von Kries, Jens Peter Dr. (1) Waiczies, Helmar Dr. (2) Waiczies, Sonia PD Dr. (7) Wallukat, Gerd Dr. (7) Walther, Wolfgang Prof. Dr. (9) Wanker, Erich Prof. Dr. (11) Wellner, Maren Dr. (8) Wenzel, Katrin Dr. (3) Willimsky, Gerald Dr. (3) Willnow, Thomas Prof. Dr. (13) Woehler, Andrew Dr. (2) Wolf, Susanne Dr. (2) Yilmaz, Zekiye Buket Dr. (1) Zinzen, Robert Patrick Dr. (1) (-) Marenholz, Ingo Dr. (1) (-) Perrot, Andreas (12) (-) Rahn, Hans-Peter Dr. (1) Genetik und Genomik von Herz- Kreislauferkrankungen (1) Molekularbiologie von Hormonen im Herz-Kreislaufssystem (2) Myologie (1) 1997 (1) 1998 (1) 1999 (2) 2000 (1) 2001 (5) (-) 2002 (4) 2003 (2) 2004 (3) 2005 (9) 2006 (10) 2007 (9) (-) 2008 (10) 2009 (9) 2010 (12) 2011 (12) 2012 (5) 2013 (9) 2014 (8) 2015 (11) 2016 (6) 2017 (6) 2018 (9) 2019 (6) 2020 (6) 2021 (6) 2022 (6) 2023 (6) 2024 (1) 14 Ergebnisse: Active Filter: Marenholz, Ingo Dr.Perrot, AndreasRahn, Hans-Peter Dr.20022008 Sortieren: Treffgenauigkeit Neueste nach älteste Älteste nach neueste 01. November 2002 / Eur J Hum Genet Systematic analysis of the regulatory and essential myosin light chain genes: genetic variants and mutations in hypertrophic cardiomyopathy Z.T. Kabaeva A. Perrot B. Wolter R. Dietz N. Cardim J.M. Correia H.D. Schulte A.A. Aldashev M.M. Mirrakhimov K.J. Osterziel 01. Oktober 2002 / Z Kardiol The heart in Anderson Fabry disease C. Kampmann C.M. Wiethoff A. Perrot M. Beck R. Dietz K.J. Osterziel 01. November 2002 / Herz Fabry disease: focus on cardiac manifestations and molecular mechanisms A. Perrot K.J. Osterziel M. Beck R. Dietz C. Kampmann 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 01. 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 01. Januar 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 01. September 2008 / Mol Genet Metab A missense variant in desmoglein-2 predisposes to dilated cardiomyopathy M.G. Posch M.J. Posch C. Geier B. Erdmann W. Mueller A. Richter V. Ruppert S. Pankuweit B. Maisch A. Perrot J. Buttgereit R. Dietz W. Haverkamp C. Oezcelik 01. Oktober 2008 / Nucleic Acids Res Homogeneity and persistence of transgene expression by omitting antibiotic selection in cell line isolation W.L. Kaufman I. Kocman V. Agrawal H.P. Rahn D. Besser M. Gossen 01. Juni 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 01. Mai 2008 / J Med Genet We need a detailed phenome in the phenomenon of genetics and congenital heart disease M.G. Posch F. Berger A. Perrot C. Oezcelik Seitennummerierung Aktuelle Seite 1 Seite 2 Nächste Seite Next › Letzte Seite Last »
01. November 2002 / Eur J Hum Genet Systematic analysis of the regulatory and essential myosin light chain genes: genetic variants and mutations in hypertrophic cardiomyopathy Z.T. Kabaeva A. Perrot B. Wolter R. Dietz N. Cardim J.M. Correia H.D. Schulte A.A. Aldashev M.M. Mirrakhimov K.J. Osterziel
01. Oktober 2002 / Z Kardiol The heart in Anderson Fabry disease C. Kampmann C.M. Wiethoff A. Perrot M. Beck R. Dietz K.J. Osterziel
01. November 2002 / Herz Fabry disease: focus on cardiac manifestations and molecular mechanisms A. Perrot K.J. Osterziel M. Beck R. Dietz C. Kampmann
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
01. 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
01. Januar 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
01. September 2008 / Mol Genet Metab A missense variant in desmoglein-2 predisposes to dilated cardiomyopathy M.G. Posch M.J. Posch C. Geier B. Erdmann W. Mueller A. Richter V. Ruppert S. Pankuweit B. Maisch A. Perrot J. Buttgereit R. Dietz W. Haverkamp C. Oezcelik
01. Oktober 2008 / Nucleic Acids Res Homogeneity and persistence of transgene expression by omitting antibiotic selection in cell line isolation W.L. Kaufman I. Kocman V. Agrawal H.P. Rahn D. Besser M. Gossen
01. Juni 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
01. Mai 2008 / J Med Genet We need a detailed phenome in the phenomenon of genetics and congenital heart disease M.G. Posch F. Berger A. Perrot C. Oezcelik