Wissenschaftliche Publikationen Suche Suche Autor/in Forschungsgruppe Veröffentlichungsdatum Suchen Sortieren nach RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Reihenfolge AufsteigendAbsteigend Bähring, Sylvia Dr. (1) Birchmeier, Walter Prof. Dr. (1) Birchmeier-Kohler, Carmen Prof. Dr. (1) Chen, Wei Prof. Dr. (1) Dechend, Ralf Priv. Doz. (1) Gösele, Claudia Dr. (1) Haucke, Volker Professor (1) Heuser, Arnd Dr. (1) Hübner, Norbert Prof. Dr. (23) Hummel, Oliver (2) Klaus-Bergmann, Alexandra Dr. (1) Lee, Young-Ae Prof. Dr. (2) Lewin, Gary Prof. Dr. (1) Luft, Friedrich Prof. Dr. (2) Maatz, Henrike Dr. (2) Mathas, Stephan Dr. (1) Müller, Dominik Prof. Dr. (1) Müller, Marion (1) Patone, Giannino Dr. (2) Perrot, Andreas (1) Radke, Michael Dr. (2) Scheidereit, Claus Prof. Dr. (1) Schmidt-Krüger, Vanessa Dr. (1) Willnow, Thomas Prof. Dr. (1) (-) Gotthardt, Michael Prof. Dr. (6) (-) Klaassen, Sabine Prof. Dr. med. (7) (-) Marenholz, Ingo Dr. (1) (-) Pilz, Bernhard Dr. (1) (-) Saar, Kathrin Dr. (7) AG Müller/Dechend (ECRC) (7) Animal Phenotyping (1) Entwicklungsbiologie / Signaltransduktion in Nerven und Muskelzellen (1) (-) Genetik und Genomik von Herz- Kreislauferkrankungen (9) (-) Genetik von Angeborenen Herzerkrankungen (7) Hochschulambulanz für Pädiatrische Allergologie und Neurodermitis (1) Hypertonie-vermittelter Endorganschaden (7) Hypertonie bedingte Endorganschäden (7) Molekulare Genetik allergischer Erkrankungen (1) Molekulare Physiologie der somatosensorischen Wahrnehmung (1) (-) Translationale Kardiologie und Funktionelle Genomforschung (6) 1994 (1) 1996 (1) 1997 (1) 1998 (1) 1999 (1) 2000 (4) 2001 (1) (-) 2002 (5) 2003 (4) 2004 (4) 2005 (2) 2006 (8) 2007 (8) 2008 (12) 2009 (11) 2010 (6) 2011 (10) (-) 2012 (9) 2013 (15) 2014 (14) 2015 (12) (-) 2016 (6) 2017 (8) 2018 (12) 2019 (14) 2020 (11) 2021 (18) 2022 (19) 2023 (17) 2024 (3) 20 Ergebnisse: Active Filter: Gotthardt, Michael Prof. Dr.Klaassen, Sabine Prof. Dr. med.Marenholz, Ingo Dr.Pilz, Bernhard Dr.Saar, Kathrin Dr.Genetik und Genomik von Herz- KreislauferkrankungenGenetik von Angeborenen HerzerkrankungenTranslationale Kardiologie und Funktionelle Genomforschung200220122016 Sortieren: Treffgenauigkeit Neueste nach älteste Älteste nach neueste 01. Mai 2002 / J Lipid Res Upregulation of hepatic LDL transport by n-3 fatty acids in LDL receptor knockout mice C. Vasandani A.I. Kafrouni A. Caronna Y. Bashmakov M. Gotthardt J.D. Horton D.K. Spady 14. Mai 2002 / Proc Natl Acad Sci U S A Smooth muscle-selective deletion of guanylyl cyclase-A prevents the acute but not chronic effects of ANP on blood pressure R. Holtwick M. Gotthardt B. Skryabin M. Steinmetz R. Potthast B. Zetsche R.E. Hammer J. Herz M. Kuhn 25. Juni 2002 / Proc Natl Acad Sci U S A Conditional mutation of the ErbB2 (HER2) receptor in cardiomyocytes leads to dilated cardiomyopathy C. Özcelik B. Erdmann B. Pilz N. Wettschureck S. Britsch N. Hübner K.R. Chien C. Birchmeier A.N. Garratt 01. Februar 2002 / Nat Genet Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy B. Gerull M. Gramlich J. Atherton M. McNabb K. Trombitas S. Sasse-Klaassen J.G. Seidman C. Seidman H. Granzier S. Labeit M. Frenneaux L. Thierfelder 03. Mai 2002 / J Biol Chem Platelet-derived growth factor mediates tyrosine phosphorylation of the cytoplasmic domain of the low Density lipoprotein receptor-related protein in caveolae P. Boucher P. Liu M. Gotthardt T. Hiesberger R.G. Anderson J. Herz 01. September 2016 / Hum Mol Genet The progressive ankyloses protein ANK facilitates clathrin- and adaptor-mediated membrane traffic at the trans-Golgi network-to-endosome interface W. Seifert Y. Posor P. Schu G. Stenbeck S. Mundlos S. Klaassen P. Nürnberg V. Haucke U. Kornak J. Kühnisch 01. August 2016 / Nat Genet Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing A. Sifrim M.P. Hitz A. Wilsdon J. Breckpot S.H.A. Turki B. Thienpont J. McRae T.W. Fitzgerald T. Singh G.J. Swaminathan E. Prigmore D. Rajan H. Abdul-Khaliq S. Banka U.M.M. Bauer J. Bentham F. Berger S. Bhattacharya F. Bu'Lock N. Canham I.G. Colgiu C. Cosgrove H. Cox I. Daehnert A. Daly J. Danesh A. Fryer M. Gewillig E. Hobson K. Hoff T. Homfray A.K. Kahlert A. Ketley H.H. Kramer K. Lachlan A.K. Lampe J.J. Louw A.K. Manickara D. Manase K.P. McCarthy K. Metcalfe C. Moore R. Newbury-Ecob S.O. Omer W.H. Ouwehand S.M. Park M.J. Parker T. Pickardt M.O. Pollard L. Robert D.J. Roberts J. Sambrook K. Setchfield B. Stiller C. Thornborough O. Toka H. Watkins D. Williams M. Wright S. Mital P.E.F. Daubeney B. Keavney J. Goodship R.M. Abu-Sulaiman S. Klaassen C.F. Wright H.V. Firth J.C. Barrett K. Devriendt D.R. FitzPatrick J.D. Brook M.E. Hurles 01. Dezember 2016 / J Mol Med Reducing RBM20 activity improves diastolic dysfunction and cardiac atrophy F. Hinze C. Dieterich M.H. Radke H. Granzier M. Gotthardt 09. Dezember 2016 / PLoS ONE The Slavic NBN founder mutation: a role for reproductive fitness? E. Seemanova R. Varon J. Vejvalka P. Jarolim P. Seeman K.H. Chrzanowska M. Digweed I. Resnick I. Kremensky K. Saar K. Hoffmann V. Dutrannoy M. Karbasiyan M. Ghani I. Baric M. Tekin P. Kovacs M. Krawczak A. Reis K. Sperling M. Nothnagel 01. März 2016 / Stem Cells Systems genetics analysis of a recombinant inbred mouse cell culture panel reveals Wnt pathway member Lrp6 as a regulator of adult hippocampal precursor cell proliferation S. Kannan Z. Nicola R.W. Overall M. Ichwan G. Ramírez-Rodríguez A. Grzyb G. Patone K. Saar N. Hübner G. Kempermann Seitennummerierung Aktuelle Seite 1 Seite 2 Nächste Seite Next › Letzte Seite Last »
01. Mai 2002 / J Lipid Res Upregulation of hepatic LDL transport by n-3 fatty acids in LDL receptor knockout mice C. Vasandani A.I. Kafrouni A. Caronna Y. Bashmakov M. Gotthardt J.D. Horton D.K. Spady
14. Mai 2002 / Proc Natl Acad Sci U S A Smooth muscle-selective deletion of guanylyl cyclase-A prevents the acute but not chronic effects of ANP on blood pressure R. Holtwick M. Gotthardt B. Skryabin M. Steinmetz R. Potthast B. Zetsche R.E. Hammer J. Herz M. Kuhn
25. Juni 2002 / Proc Natl Acad Sci U S A Conditional mutation of the ErbB2 (HER2) receptor in cardiomyocytes leads to dilated cardiomyopathy C. Özcelik B. Erdmann B. Pilz N. Wettschureck S. Britsch N. Hübner K.R. Chien C. Birchmeier A.N. Garratt
01. Februar 2002 / Nat Genet Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy B. Gerull M. Gramlich J. Atherton M. McNabb K. Trombitas S. Sasse-Klaassen J.G. Seidman C. Seidman H. Granzier S. Labeit M. Frenneaux L. Thierfelder
03. Mai 2002 / J Biol Chem Platelet-derived growth factor mediates tyrosine phosphorylation of the cytoplasmic domain of the low Density lipoprotein receptor-related protein in caveolae P. Boucher P. Liu M. Gotthardt T. Hiesberger R.G. Anderson J. Herz
01. September 2016 / Hum Mol Genet The progressive ankyloses protein ANK facilitates clathrin- and adaptor-mediated membrane traffic at the trans-Golgi network-to-endosome interface W. Seifert Y. Posor P. Schu G. Stenbeck S. Mundlos S. Klaassen P. Nürnberg V. Haucke U. Kornak J. Kühnisch
01. August 2016 / Nat Genet Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing A. Sifrim M.P. Hitz A. Wilsdon J. Breckpot S.H.A. Turki B. Thienpont J. McRae T.W. Fitzgerald T. Singh G.J. Swaminathan E. Prigmore D. Rajan H. Abdul-Khaliq S. Banka U.M.M. Bauer J. Bentham F. Berger S. Bhattacharya F. Bu'Lock N. Canham I.G. Colgiu C. Cosgrove H. Cox I. Daehnert A. Daly J. Danesh A. Fryer M. Gewillig E. Hobson K. Hoff T. Homfray A.K. Kahlert A. Ketley H.H. Kramer K. Lachlan A.K. Lampe J.J. Louw A.K. Manickara D. Manase K.P. McCarthy K. Metcalfe C. Moore R. Newbury-Ecob S.O. Omer W.H. Ouwehand S.M. Park M.J. Parker T. Pickardt M.O. Pollard L. Robert D.J. Roberts J. Sambrook K. Setchfield B. Stiller C. Thornborough O. Toka H. Watkins D. Williams M. Wright S. Mital P.E.F. Daubeney B. Keavney J. Goodship R.M. Abu-Sulaiman S. Klaassen C.F. Wright H.V. Firth J.C. Barrett K. Devriendt D.R. FitzPatrick J.D. Brook M.E. Hurles
01. Dezember 2016 / J Mol Med Reducing RBM20 activity improves diastolic dysfunction and cardiac atrophy F. Hinze C. Dieterich M.H. Radke H. Granzier M. Gotthardt
09. Dezember 2016 / PLoS ONE The Slavic NBN founder mutation: a role for reproductive fitness? E. Seemanova R. Varon J. Vejvalka P. Jarolim P. Seeman K.H. Chrzanowska M. Digweed I. Resnick I. Kremensky K. Saar K. Hoffmann V. Dutrannoy M. Karbasiyan M. Ghani I. Baric M. Tekin P. Kovacs M. Krawczak A. Reis K. Sperling M. Nothnagel
01. März 2016 / Stem Cells Systems genetics analysis of a recombinant inbred mouse cell culture panel reveals Wnt pathway member Lrp6 as a regulator of adult hippocampal precursor cell proliferation S. Kannan Z. Nicola R.W. Overall M. Ichwan G. Ramírez-Rodríguez A. Grzyb G. Patone K. Saar N. Hübner G. Kempermann