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(31) Annibale, Paolo Dr. (3) Araragi, Naozumi Dr. (1) Bader, Michael Prof. Dr. (48) Bähring, Sylvia Dr. (3) Bartolomaeus, Hendrik (3) Baumann, Elisabeth (1) Begay-Müller, Valerie Dr. (1) Bernert, Carola (1) Beule, Dieter Dr. (7) Birchmeier, Walter Prof. Dr. (12) Birchmeier-Kohler, Carmen Prof. Dr. (10) Birol, Melissa Dr. (1) Blachut, Susanne (2) Blankenstein, Thomas Prof. Dr. (11) Blume, Alexander Dr. (1) Bock-Bierbaum, Tobias Dr. (2) Braeuning, Caroline (1) Cakmak-Görür, Nese Dr. (1) Cano Rincon, Elena Dr. (1) Chekulaeva, Marina Dr. (3) Chen, Wei Prof. Dr. (10) Chu, Van Trung Dr. (6) Conrad, Thomas Dr. (1) Coralluzzo, Violeta (1) Coscia, Fabian Dr. (3) Dahlmann, Mathias Dr. (2) Daniel, Peter Prof. Dr. (7) Dartsch, Josephine (3) Daumke, Oliver Prof. Dr. (10) Dechend, Ralf Priv. Doz. 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(6) Luft, Friedrich Prof. Dr. (71) Lupianez Garcia, Dario Jesus Dr. (2) Maatz, Henrike Dr. (1) Maglione, Marta (3) Mais, Lisa (1) Malchin, Victoria (1) Marenholz, Ingo Dr. (1) Marg, Andreas Dr. (1) Marko, Lajos Dr. (10) Mastrobuoni, Guido Dr. (2) Mathas, Stephan Dr. (7) Meier, Katja (1) Merks, Anne Margarete Dr. (1) Mertins, Philipp Dr. (7) Metzger, Jakob Johannes Dr. (2) Meyer, Irmtraud Margret Prof. Dr. (4) Migueles Lozano, Oscar Arturo Dr. (1) Millward, Jason Dr. (2) Mittnenzweig, Markus Dr. (1) Morano, Ingo Prof. Dr. (4) Mücke, Michael Benedikt (2) Müller, Dominik Prof. Dr. (24) Müller, Gerd Dr. (1) Müller, Marion (1) Müller, Thomas Dr. (1) Müthel, Stefanie (2) Na, Il-Kang Dr. (5) Nazare, Marc (5) Neubert, Wilhelm (1) Neuendorf, Nancy (1) Niendorf, Thoralf Prof. Dr. (17) Nimptsch, Katharina Dr. (5) Noel, Jeffrey Dr. (4) Nolte, Christiane Dr. (1) Obermayer-Wasserscheid, Benedikt Dr. (1) Oertel, Frederike Cosima MD/PhD (5) Ofenbauer, Andreas Dr. (3) Ohler, Uwe Prof. Dr. (6) Panakova, Daniela Dr. (3) Patone, Giannino Dr. (3) Paul, Friedemann Prof. Dr. med. 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(6) (-) Mahmoodzadeh, Shokoufeh PD Dr. (2) (-) Sommer, Thomas Prof. Dr. (4) (-) Treier, Mathias Prof. Dr. (2) Epigenetische Regulation und Chromatinstruktur (1) Genetik metabolischer und reproduktiver Störungen (2) Genetik von Angeborenen Herzerkrankungen (6) Genomdiversifikation & Integrität (2) Intrazelluläre Proteolyse (4) Proteomforschung und molekulare Mechanismen bei neurodegenerativen Erkrankungen (1) Strukturbiologie Membran-assoziierter Prozesse (1) Translational Bioinformatics (1) 1998 (1) 2001 (1) (-) 2002 (5) 2003 (2) 2004 (8) 2005 (8) 2006 (9) 2007 (1) 2008 (6) 2009 (7) 2010 (3) 2011 (10) 2012 (11) 2013 (11) 2014 (15) 2015 (17) 2016 (17) 2017 (9) 2018 (10) (-) 2019 (13) 2020 (8) 2021 (13) 2022 (17) 18 Ergebnisse: Active Filter: Di Virgilio, Michela Prof. Dr.Klaassen, Sabine Prof. Dr. med.Mahmoodzadeh, Shokoufeh PD Dr.Sommer, Thomas Prof. Dr.Treier, Mathias Prof. Dr.20022019 Sortieren: Treffgenauigkeit Neueste nach älteste Älteste nach neueste 01. Januar 2002 / J Biol Chem A lack of SUMO conjugation affects cNLS-dependent nuclear protein import in yeast K. Stade F. Vogel I. Schwienhorst B. Meusser C. Volkwein B. Nentwig R.J. Dohmen T. Sommer 01. Januar 2002 / Traffic Protein dislocation from the endoplasmic reticulum - Pulling out the suspect E. Jarosch R. Geiss-Friedlander B. Meusser J. Walter T. Sommer 11. Juli 2002 / Dev Cell BiP binding keeps ATF6 at bay T. Sommer E. Jarosch 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 22. Februar 2002 / J Biol Chem Novel pathogenic mechanisms of congenital insensitivity to pain with anhidrosis genetic disorder unveiled by functional analysis of neurotrophic tyrosine receptor kinase type 1/nerve growth factor receptor mutations C. Miranda M. Di Virgilio S. Selleri G. Zanotti S. Pagliardini M.A. Pierotti A. Greco 01. August 2019 / Hum Mutat Biallelic mutation in MYH7 and MYBPC3 leads to severe cardiomyopathy with left ventricular noncompaction phenotype K. Kolokotronis J. Kühnisch E. Klopocki J. Dartsch S. Rost C. Huculak G. Mearini S. Störk L. Carrier S. Klaassen B. Gerull 01. Februar 2019 / Cardiovasc Res Sex-specific regulation of collagen I and III expression by 17β-estradiol in cardiac fibroblasts: role of estrogen receptors E. Dworatzek S. Mahmoodzadeh C. Schriever K. Kusumoto L. Kramer G. Santos D. Fliegner Y.K. Leung S.M. Ho W.H. Zimmermann S. Lutz V. Regitz-Zagrosek 01. September 2019 / Nat Methods BigStitcher: reconstructing high-resolution image datasets of cleared and expanded samples D. Hörl F. Rojas Rusak F. Preusser P. Tillberg N. Randel R.K. Chhetri A. Cardona P.J. Keller H. Harz H. Leonhardt M. Treier S. Preibisch 06. September 2019 / J Cell Sci DCAF8, a novel MuRF1 interaction partner, promotes muscle atrophy M. Nowak B. Suenkel P. Porras R. Migotti F. Schmidt M. Kny X. Zhu E.E. Wanker G. Dittmar J. Fielitz T. Sommer 01. Dezember 2019 / Clin Genet Targeted panel sequencing in pediatric primary cardiomyopathy supports a critical role of TNNI3 J. Kühnisch C. Herbst N. Al-Wakeel-Marquard J. Dartsch M. Holtgrewe A. Baban G. Mearini J. Hardt K. Kolokotronis B. Gerull L. Carrier D. Beule S. Schubert D. Messroghli F. Degener F. Berger S. Klaassen Seitennummerierung Aktuelle Seite 1 Seite 2 Nächste Seite Next › Letzte Seite Last »
01. Januar 2002 / J Biol Chem A lack of SUMO conjugation affects cNLS-dependent nuclear protein import in yeast K. Stade F. Vogel I. Schwienhorst B. Meusser C. Volkwein B. Nentwig R.J. Dohmen T. Sommer
01. Januar 2002 / Traffic Protein dislocation from the endoplasmic reticulum - Pulling out the suspect E. Jarosch R. Geiss-Friedlander B. Meusser J. Walter T. Sommer
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
22. Februar 2002 / J Biol Chem Novel pathogenic mechanisms of congenital insensitivity to pain with anhidrosis genetic disorder unveiled by functional analysis of neurotrophic tyrosine receptor kinase type 1/nerve growth factor receptor mutations C. Miranda M. Di Virgilio S. Selleri G. Zanotti S. Pagliardini M.A. Pierotti A. Greco
01. August 2019 / Hum Mutat Biallelic mutation in MYH7 and MYBPC3 leads to severe cardiomyopathy with left ventricular noncompaction phenotype K. Kolokotronis J. Kühnisch E. Klopocki J. Dartsch S. Rost C. Huculak G. Mearini S. Störk L. Carrier S. Klaassen B. Gerull
01. Februar 2019 / Cardiovasc Res Sex-specific regulation of collagen I and III expression by 17β-estradiol in cardiac fibroblasts: role of estrogen receptors E. Dworatzek S. Mahmoodzadeh C. Schriever K. Kusumoto L. Kramer G. Santos D. Fliegner Y.K. Leung S.M. Ho W.H. Zimmermann S. Lutz V. Regitz-Zagrosek
01. September 2019 / Nat Methods BigStitcher: reconstructing high-resolution image datasets of cleared and expanded samples D. Hörl F. Rojas Rusak F. Preusser P. Tillberg N. Randel R.K. Chhetri A. Cardona P.J. Keller H. Harz H. Leonhardt M. Treier S. Preibisch
06. September 2019 / J Cell Sci DCAF8, a novel MuRF1 interaction partner, promotes muscle atrophy M. Nowak B. Suenkel P. Porras R. Migotti F. Schmidt M. Kny X. Zhu E.E. Wanker G. Dittmar J. Fielitz T. Sommer
01. Dezember 2019 / Clin Genet Targeted panel sequencing in pediatric primary cardiomyopathy supports a critical role of TNNI3 J. Kühnisch C. Herbst N. Al-Wakeel-Marquard J. Dartsch M. Holtgrewe A. Baban G. Mearini J. Hardt K. Kolokotronis B. Gerull L. Carrier D. Beule S. Schubert D. Messroghli F. Degener F. Berger S. Klaassen