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November 2011 / Eur J Heart Fail Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: results from the German Competence Network Heart Failure S. Waldmueller J. Erdmann P. Binner G. Gelbrich S. Pankuweit C. Geier B. Timmermann J. Haremza A. Perrot S. Scheer R. Wachter N. Schulze-Waltrup A. Dermintzoglou J. Schoenberger W. Zeh B. Jurmann T. Brodherr J. Boergel M. Farr H. Milting W. Blankenfeldt R. Reinhardt C. Oezcelik K.J. Osterziel M. Loeffler B. Maisch V. Regitz-Zagrosek H. Schunkert T. Scheffold 11. August 2011 / PLoS ONE An RNA interference phenotypic screen identifies a role for FGF signals in colon cancer progression M. Leushacke R. Spoerle C. Bernemann A. Brouwer-Lehmitz J. Fritzmann M. Theis F. Buchholz B.G. Herrmann M. Morkel 01. August 2011 / J Med Genet Rapid detection of genetic variants in hypertrophic cardiomyopathy by custom DNA resequencing array in clinical practice S. Fokstuen A. Munoz P. Melacini S. Iliceto A. Perrot C. Ozcelik X. Jeanrenaud C. Rieubland M. Farr L. Faber U. Sigwart F. Mach R. Lerch S.E. Antonarakis J.L. Blouin 14. Dezember 2011 / PLoS ONE Cardiac alpha-myosin (MYH6) is the predominant sarcomeric disease gene for familial atrial septal defects M.G. Posch S. Waldmuller M. Mueller T. Scheffold D. Fournier M.A. Andrade-Navarro B. De Geeter S. Guillaumont C. Dauphin D. Yousseff K.R. Schmitt A. Perrot F. Berger R. Hetzer P. Bouvagnet C. Ozcelik 01. November 2011 / Basic Res Cardiol Unequal allelic expression of wild-type and mutated beta-myosin in familial hypertrophic cardiomyopathy S. Tripathi I. Schultz E. Becker J. Montag B. Borchert A. Francino F. Navarro-Lopez A. Perrot C. Oezcelik K.J. Osterziel W.J. McKenna B. Brenner T. Kraft 01. Juli 2011 / PLoS Genet Pathologic and phenotypic alterations in a mouse expressing a connexin47 missense mutation that causes pelizaeus-merzbacher-like disease in humans O. Tress M. Maglione A. Zlomuzica D. May N. Dicke J. Degen E. Dere H. Kettenmann D. Hartmann K. Willecke 18. Februar 2011 / Biochem Biophys Res Commun A myomesin mutation associated with hypertrophic cardiomyopathy deteriorates dimerisation properties R. Siegert A. Perrot S. Keller J. Behlke A. Michalewska-Wludarczyk A. Wycisk M. Tendera I. Morano C. Oezcelik 01. Juni 2011 / Cardiovasc Res Human essential myosin light chain isoforms revealed distinct myosin binding, sarcomeric sorting, and inotropic activity D. Petzhold J. Lossie S. Keller S. Werner H. Haase I. Morano
01. November 2011 / Eur J Heart Fail Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: results from the German Competence Network Heart Failure S. Waldmueller J. Erdmann P. Binner G. Gelbrich S. Pankuweit C. Geier B. Timmermann J. Haremza A. Perrot S. Scheer R. Wachter N. Schulze-Waltrup A. Dermintzoglou J. Schoenberger W. Zeh B. Jurmann T. Brodherr J. Boergel M. Farr H. Milting W. Blankenfeldt R. Reinhardt C. Oezcelik K.J. Osterziel M. Loeffler B. Maisch V. Regitz-Zagrosek H. Schunkert T. Scheffold
11. August 2011 / PLoS ONE An RNA interference phenotypic screen identifies a role for FGF signals in colon cancer progression M. Leushacke R. Spoerle C. Bernemann A. Brouwer-Lehmitz J. Fritzmann M. Theis F. Buchholz B.G. Herrmann M. Morkel
01. August 2011 / J Med Genet Rapid detection of genetic variants in hypertrophic cardiomyopathy by custom DNA resequencing array in clinical practice S. Fokstuen A. Munoz P. Melacini S. Iliceto A. Perrot C. Ozcelik X. Jeanrenaud C. Rieubland M. Farr L. Faber U. Sigwart F. Mach R. Lerch S.E. Antonarakis J.L. Blouin
14. Dezember 2011 / PLoS ONE Cardiac alpha-myosin (MYH6) is the predominant sarcomeric disease gene for familial atrial septal defects M.G. Posch S. Waldmuller M. Mueller T. Scheffold D. Fournier M.A. Andrade-Navarro B. De Geeter S. Guillaumont C. Dauphin D. Yousseff K.R. Schmitt A. Perrot F. Berger R. Hetzer P. Bouvagnet C. Ozcelik
01. November 2011 / Basic Res Cardiol Unequal allelic expression of wild-type and mutated beta-myosin in familial hypertrophic cardiomyopathy S. Tripathi I. Schultz E. Becker J. Montag B. Borchert A. Francino F. Navarro-Lopez A. Perrot C. Oezcelik K.J. Osterziel W.J. McKenna B. Brenner T. Kraft
01. Juli 2011 / PLoS Genet Pathologic and phenotypic alterations in a mouse expressing a connexin47 missense mutation that causes pelizaeus-merzbacher-like disease in humans O. Tress M. Maglione A. Zlomuzica D. May N. Dicke J. Degen E. Dere H. Kettenmann D. Hartmann K. Willecke
18. Februar 2011 / Biochem Biophys Res Commun A myomesin mutation associated with hypertrophic cardiomyopathy deteriorates dimerisation properties R. Siegert A. Perrot S. Keller J. Behlke A. Michalewska-Wludarczyk A. Wycisk M. Tendera I. Morano C. Oezcelik
01. Juni 2011 / Cardiovasc Res Human essential myosin light chain isoforms revealed distinct myosin binding, sarcomeric sorting, and inotropic activity D. Petzhold J. Lossie S. Keller S. Werner H. Haase I. Morano