Wissenschaftliche Publikationen Suche Suche Autor/in Forschungsgruppe Veröffentlichungsdatum Wirkungsfaktor Suchen Sortieren nach RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Reihenfolge AufsteigendAbsteigend Adami, Eleonora Dr. (3) Ahmad, Ata Ul Wakeel (1) Akalin, Altuna Dr. (9) Albrecht, Jan Philipp (2) Alenina, Natalia Dr. (18) Altmueller, Janine Dr.med. (18) Anandakumar, Harithaa (1) Annibale, Paolo Dr. (1) Apaydin, Onur (2) Arnau Soler, Aleix Dr. (2) Bader, Michael Prof. Dr. (73) Badillo Lisakowski, Victor Christian Dr. (2) Bähring, Sylvia Dr. (7) Bartolomaeus, Hendrik (2) Bartolomaeus, Theda (6) Baumann, Elisabeth (1) Begay-Müller, Valerie Dr. (2) Bemmann, Franziska (1) Benlasfer, Nouhad (1) Beule, Dieter Dr. (16) Birchmeier, Walter Prof. Dr. (18) Birchmeier-Kohler, Carmen Prof. Dr. (21) Birkner, Till (3) Birol, Melissa Dr. (2) Blankenstein, Thomas Prof. Dr. (29) Blume, Alexander Dr. (2) Blüthgen, Nils (1) Borodina, Tatiana Dr. (3) Bosco, Bartolomeo Dr. (1) Bunina, Daria Dr. (2) Bunse, Mario Dr. (2) Burkert, Christian Martin (1) Carneiro Raimundo, Sandra Cristina Dr. (1) Cerda Esteban, Nuria Dr. (1) Chekulaeva, Marina Dr. (3) Chen, Chia-Yu (2) Chen, Wei Prof. Dr. (14) Chu, Van Trung Dr. (2) Chu, Xiaofeng (1) Collins, Russell Thomas Dr. (1) Conrad, Thomas Dr. (6) Coscia, Fabian Dr. (4) Costanza, Mariantonia Dr. (2) Crocini, Claudia Dr. (1) Dahlmann, Mathias Dr. (1) Daniel, Peter Prof. Dr. (9) Dartsch, Josephine (1) Daumke, Oliver Prof. Dr. (9) Dechend, Ralf Priv. 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Januar 2013 / ACS Chem Neurosci Postnatal growth defects in mice with constitutive depletion of central serotonin N. Narboux-Neme G. Angenard V. Mosienko F. Klempin P.M. Pitychoutis E. Deneris M. Bader B. Giros N. Alenina P. Gaspar 01. September 2013 / Int J Cardiol Left ventricular non-compaction: prevalence in congenital heart disease B.E. Stähli C. Gebhard P. Biaggi S. Klaassen E. Valsangiacomo Buechel C.H. Attenhofer Jost R. Jenni F.C. Tanner M. Greutmann 01. 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 21. März 2013 / Nature Circular RNAs are a large class of animal RNAs with regulatory potency S. Memczak M. Jens A. Elefsinioti F. Torti J. Krueger A. Rybak L. Maier S.D. Mackowiak L.H. Gregersen M. Munschauer A. Loewer U. Ziebold M. Landthaler C. Kocks F. le Noble N. Rajewsky 08. Mai 2013 / J Neurosci Serotonin is required for exercise-induced adult hippocampal neurogenesis F. Klempin D. Beis V. Mosienko G. Kempermann M. Bader N. Alenina 11. Juli 2013 / Am J Hum Genet Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy A.K. Arndt S. Schaefer J.D. Drenckhahn M.K. Sabeh E.R. Plovie A. Caliebe E. Klopocki G. Musso A.A. Werdich H. Kalwa M. Heinig R.F. Padera K. Wassilew J. Bluhm C. Harnack J. Martitz P.J. Barton M. Greutmann F. Berger N. Huebner R. Siebert H.H. Kramer S.A. Cook C.A. Macrae S. Klaassen 01. August 2013 / Am J Med Genet C Semin Med Genet Ebstein anomaly associated with left ventricular noncompaction: an autosomal dominant condition that can be caused by mutations in MYH7 A.M. Vermeer K. van Engelen A.V. Postma M.J. Baars I. Christiaans S. De Haij S. Klaassen B.J. Mulder B. Keavney 01. März 2013 / Neth Heart J Ebstein's anomaly may be caused by mutations in the sarcomere protein gene MYH7 K. van Engelen A.V. Postma J.B.A. van de Meerakker J.W. Roos-Hesselink A.T.J.M. Helderman-van den Enden H.W. Vliegen T. Rahman M.J.H. Baars J.W. Sels U. Bauer T. Pickardt S.R. Sperling A.F.M. Moorman B. Keavney J. Goodship S. Klaassen B.J. Mulder 01. Februar 2001 / Hum Mol Genet Triple A syndrome is caused by mutations in AAAS, a new WD-repeat protein gene K. Handschug S. Sperling S.J. Yoon S. Hennig A.J. Clark A. Huebner 24. September 1997 / J Immunol Methods Generation of Cre recombinase-specific monoclonal antibodies, able to characterize the pattern of Cre expression in cre-transgenic mouse strains F. Schwenk B. Sauer N. Kukoč R. Hoess W. Müller C. Kocks R. Kühn K. Rajewsky Seitennummerierung Aktuelle Seite 1 Seite 2 Seite 3 Seite 4 Nächste Seite Next › Letzte Seite Last »
16. Januar 2013 / ACS Chem Neurosci Postnatal growth defects in mice with constitutive depletion of central serotonin N. Narboux-Neme G. Angenard V. Mosienko F. Klempin P.M. Pitychoutis E. Deneris M. Bader B. Giros N. Alenina P. Gaspar
01. September 2013 / Int J Cardiol Left ventricular non-compaction: prevalence in congenital heart disease B.E. Stähli C. Gebhard P. Biaggi S. Klaassen E. Valsangiacomo Buechel C.H. Attenhofer Jost R. Jenni F.C. Tanner M. Greutmann
01. 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
21. März 2013 / Nature Circular RNAs are a large class of animal RNAs with regulatory potency S. Memczak M. Jens A. Elefsinioti F. Torti J. Krueger A. Rybak L. Maier S.D. Mackowiak L.H. Gregersen M. Munschauer A. Loewer U. Ziebold M. Landthaler C. Kocks F. le Noble N. Rajewsky
08. Mai 2013 / J Neurosci Serotonin is required for exercise-induced adult hippocampal neurogenesis F. Klempin D. Beis V. Mosienko G. Kempermann M. Bader N. Alenina
11. Juli 2013 / Am J Hum Genet Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy A.K. Arndt S. Schaefer J.D. Drenckhahn M.K. Sabeh E.R. Plovie A. Caliebe E. Klopocki G. Musso A.A. Werdich H. Kalwa M. Heinig R.F. Padera K. Wassilew J. Bluhm C. Harnack J. Martitz P.J. Barton M. Greutmann F. Berger N. Huebner R. Siebert H.H. Kramer S.A. Cook C.A. Macrae S. Klaassen
01. August 2013 / Am J Med Genet C Semin Med Genet Ebstein anomaly associated with left ventricular noncompaction: an autosomal dominant condition that can be caused by mutations in MYH7 A.M. Vermeer K. van Engelen A.V. Postma M.J. Baars I. Christiaans S. De Haij S. Klaassen B.J. Mulder B. Keavney
01. März 2013 / Neth Heart J Ebstein's anomaly may be caused by mutations in the sarcomere protein gene MYH7 K. van Engelen A.V. Postma J.B.A. van de Meerakker J.W. Roos-Hesselink A.T.J.M. Helderman-van den Enden H.W. Vliegen T. Rahman M.J.H. Baars J.W. Sels U. Bauer T. Pickardt S.R. Sperling A.F.M. Moorman B. Keavney J. Goodship S. Klaassen B.J. Mulder
01. Februar 2001 / Hum Mol Genet Triple A syndrome is caused by mutations in AAAS, a new WD-repeat protein gene K. Handschug S. Sperling S.J. Yoon S. Hennig A.J. Clark A. Huebner
24. September 1997 / J Immunol Methods Generation of Cre recombinase-specific monoclonal antibodies, able to characterize the pattern of Cre expression in cre-transgenic mouse strains F. Schwenk B. Sauer N. Kukoč R. Hoess W. Müller C. Kocks R. Kühn K. Rajewsky