Wissenschaftliche Publikationen Suche Suche Autor/in Forschungsgruppe Veröffentlichungsdatum Suchen Sortieren nach RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Reihenfolge AufsteigendAbsteigend Bähring, Sylvia Dr. (1) Chen, Wei Prof. Dr. (1) Dechend, Ralf Priv. Doz. (2) Fielitz, Jens Dr. (1) Gösele, Claudia Dr. (1) Haase, Nadine Dr. (1) Hammes-Lewin, Annette Dr. (2) Herse, Florian PD Dr. (2) Hübner, Norbert Prof. Dr. (28) Hummel, Oliver (4) Ivics, Zoltan Dr. (1) Izsvak, Zsuzsanna Dr. (1) Janz, Martin Dr. (2) Lee, Young-Ae Prof. Dr. (1) Luft, Friedrich Prof. Dr. (3) Maatz, Henrike Dr. (2) Mathas, Stephan Dr. (5) Müller, Dominik Prof. Dr. (3) Qadri, Fatimunnisa Dr. (1) Rajewsky, Klaus Prof. Dr. (1) Saar, Kathrin Dr. (6) Scheidereit, Claus Prof. Dr. (1) Schmidt, Sabine (1) Schmidt-Krüger, Vanessa Dr. (1) Sommer, Thomas Prof. Dr. (1) Wallukat, Gerd Dr. (1) Wenzel, Katrin Dr. (1) Willnow, Thomas Prof. Dr. (1) (-) Heuser, Arnd Dr. (6) (-) Morano, Ingo Prof. Dr. (1) (-) Patone, Giannino Dr. (3) Advanced Light Microscopy (1) AG Müller/Dechend (ECRC) (3) (-) Animal Phenotyping (6) (-) Biologie maligner Lymphome (1) (-) Genetik und Genomik von Herz- Kreislauferkrankungen (11) Hypertonie-vermittelter Endorganschaden (3) Hypertonie bedingte Endorganschäden (3) Intrazelluläre Proteolyse (1) Molekularbiologie von Hormonen im Herz-Kreislaufssystem (4) 2003 (2) 2004 (8) 2005 (8) 2006 (9) 2007 (6) 2008 (9) 2009 (13) (-) 2010 (7) 2011 (1) 2012 (6) 2013 (5) 2014 (6) 2015 (7) (-) 2016 (8) 2017 (8) 2018 (11) 2019 (6) 2020 (13) 2021 (11) 2022 (7) 2023 (6) 2024 (3) 15 Ergebnisse: Active Filter: Heuser, Arnd Dr.Morano, Ingo Prof. Dr.Patone, Giannino Dr.Animal PhenotypingBiologie maligner LymphomeGenetik und Genomik von Herz- Kreislauferkrankungen20102016 Sortieren: Treffgenauigkeit Neueste nach älteste Älteste nach neueste 01. September 2010 / Birth Defects Res A Clin Mol Teratol Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous iranian family H. Reutter F. Rueschendorf M. Mattheisen M. Draaken E. Bartels N. Huebner P. Hoffmann S. Payabvash K. Saar M.M. Noethen A.M. Kajbafzadeh M. Ludwig 01. November 2010 / Hypertension Childhood hypertension in autosomal-dominant hypertension with brachydactyly O. Toka P.G. Maass A. Aydin H. Toka N. Huebner F. Rueschendorf M. Gong F.C. Luft S. Bähring 01. August 2010 / J Neurol Clinical and genetic features in a family with CADASIL and high lipoprotein (a) values M. Gong F. Rueschendorf P. Marx H. Schulz H.G. Kraft N. Huebner H.C. Koennecke 01. Januar 2010 / J Orofac Orthop Die primaere Durchbruchsstoerung (PFE) - klinische und molekulargenetische Analyse [Primary failure of eruption (PFE) - clinical and molecular genetics analysis] A. Stellzig-Eisenhauer E. Decker P. Meyer-Marcotty C. Rau B.S. Fiebig W. Kress K. Saar F. Rueschendorf N. Huebner T. Grimm E. Witt B.H. Weber 24. Februar 2010 / PLoS ONE alpha(1A)-adrenergic receptor-directed autoimmunity induces left ventricular damage and diastolic dysfunction in rats K. Wenzel G. Wallukat F. Qadri N. Huebner H. Schulz O. Hummel F. Herse A. Heuser R. Fischer H. Heidecke F.C. Luft D.N. Mueller R. Dietz R. Dechend 01. Juni 2010 / Genome Res The genome sequence of the spontaneously hypertensive rat: analysis and functional significance S.S. Atanur I. Birol V. Guryev M. Hirst O. Hummel C. Morrissey J. Behmoaras X.M. Fernandez-Suarez M.D. Johnson W.M. McLaren G. Patone E. Petretto C. Plessy K.S. Rockland C. Rockland K. Saar Y. Zhao P. Carninci P. Flicek T. Kurtz E. Cuppen M. Pravenec N. Huebner S.J. Jones E. Birney T.J. Aitman 01. August 2010 / Psychiatr Genet Haplotypes of dopamine and serotonin transporter genes are associated with antisocial personality disorder in alcoholics J. Reese A. Kraschewski I. Anghelescu G. Winterer L.G. Schmidt J. Gallinat F. Rueschendorf H. Rommelspacher C. Wernicke 15. April 2016 / Toxicology Inhibition of chymotryptic-like standard proteasome activity exacerbates doxorubicin-induced cytotoxicity in primary cardiomyocytes E.M. Spur N. Althof D. Respondek K. Klingel A. Heuser H.S. Overkleeft A. Voigt 01. September 2016 / JAMA Otolaryngol Head Neck Surg Association of TMTC2 with human nonsyndromic sensorineural hearing loss C.L. Runge A. Indap Y. Zhou J.W. Kent E. King C.B. Erbe R. Cole J. Littrell K. Merath R. James F. Rüschendorf J.E. Kerschner G. Marth N. Hübner H.H.H. Göring D.R. Friedland W.M. Kwok M. Olivier 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. September 2010 / Birth Defects Res A Clin Mol Teratol Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous iranian family H. Reutter F. Rueschendorf M. Mattheisen M. Draaken E. Bartels N. Huebner P. Hoffmann S. Payabvash K. Saar M.M. Noethen A.M. Kajbafzadeh M. Ludwig
01. November 2010 / Hypertension Childhood hypertension in autosomal-dominant hypertension with brachydactyly O. Toka P.G. Maass A. Aydin H. Toka N. Huebner F. Rueschendorf M. Gong F.C. Luft S. Bähring
01. August 2010 / J Neurol Clinical and genetic features in a family with CADASIL and high lipoprotein (a) values M. Gong F. Rueschendorf P. Marx H. Schulz H.G. Kraft N. Huebner H.C. Koennecke
01. Januar 2010 / J Orofac Orthop Die primaere Durchbruchsstoerung (PFE) - klinische und molekulargenetische Analyse [Primary failure of eruption (PFE) - clinical and molecular genetics analysis] A. Stellzig-Eisenhauer E. Decker P. Meyer-Marcotty C. Rau B.S. Fiebig W. Kress K. Saar F. Rueschendorf N. Huebner T. Grimm E. Witt B.H. Weber
24. Februar 2010 / PLoS ONE alpha(1A)-adrenergic receptor-directed autoimmunity induces left ventricular damage and diastolic dysfunction in rats K. Wenzel G. Wallukat F. Qadri N. Huebner H. Schulz O. Hummel F. Herse A. Heuser R. Fischer H. Heidecke F.C. Luft D.N. Mueller R. Dietz R. Dechend
01. Juni 2010 / Genome Res The genome sequence of the spontaneously hypertensive rat: analysis and functional significance S.S. Atanur I. Birol V. Guryev M. Hirst O. Hummel C. Morrissey J. Behmoaras X.M. Fernandez-Suarez M.D. Johnson W.M. McLaren G. Patone E. Petretto C. Plessy K.S. Rockland C. Rockland K. Saar Y. Zhao P. Carninci P. Flicek T. Kurtz E. Cuppen M. Pravenec N. Huebner S.J. Jones E. Birney T.J. Aitman
01. August 2010 / Psychiatr Genet Haplotypes of dopamine and serotonin transporter genes are associated with antisocial personality disorder in alcoholics J. Reese A. Kraschewski I. Anghelescu G. Winterer L.G. Schmidt J. Gallinat F. Rueschendorf H. Rommelspacher C. Wernicke
15. April 2016 / Toxicology Inhibition of chymotryptic-like standard proteasome activity exacerbates doxorubicin-induced cytotoxicity in primary cardiomyocytes E.M. Spur N. Althof D. Respondek K. Klingel A. Heuser H.S. Overkleeft A. Voigt
01. September 2016 / JAMA Otolaryngol Head Neck Surg Association of TMTC2 with human nonsyndromic sensorineural hearing loss C.L. Runge A. Indap Y. Zhou J.W. Kent E. King C.B. Erbe R. Cole J. Littrell K. Merath R. James F. Rüschendorf J.E. Kerschner G. Marth N. Hübner H.H.H. Göring D.R. Friedland W.M. Kwok M. Olivier
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