Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Fischer, Cornelius Dr. (1) Gerhardt, Holger Prof. Dr. (1) Harabula, Izabela-Cezara (1) Hübner, Norbert Prof. Dr. (1) Janz, Martin Dr. (3) Mathas, Stephan Dr. (4) Patone, Giannino Dr. (1) Scheidereit, Claus Prof. Dr. (2) (-) Altmueller, Janine Dr.med. (27) (-) Lupianez Garcia, Dario Jesus Dr. (1) (-) Potente, Michael Prof. Dr. (5) (-) Rajewsky, Klaus Prof. Dr. (3) (-) 1999 (1) 2002 (1) 2005 (5) 2007 (1) 2008 (4) 2009 (3) 2010 (2) 2011 (2) (-) 2012 (3) 2013 (4) 2014 (1) 2015 (18) (-) 2016 (30) 2017 (35) 2018 (44) 2019 (33) 2020 (28) 2021 (53) 2022 (41) 2023 (24) 2024 (1) (-) Angiogenesis & Metabolism Laboratory (5) (-) Biology of Malignant Lymphomas (2) Cardiac MRI (1) Cellular Neurosciences (2) Computational Regulatory Genomics (2) Experimental Ultrahigh-Field MR (6) Genome Engineering & Disease Models (2) (-) Genomics (27) Immune Regulation and Cancer (17) Integrative Vascular Biology (1) Magnetic Resonance (6) Proteome Dynamics (2) RNA Biology and Posttranscriptional Regulation (3) Transgenics (2) 34 Results: Active Filter: Altmueller, Janine Dr.med.Lupianez Garcia, Dario Jesus Dr.Potente, Michael Prof. Dr.Rajewsky, Klaus Prof. Dr.Angiogenesis & Metabolism LaboratoryBiology of Malignant LymphomasGenomics199920122016 Sort: Result score Newest to oldest Oldest to newest November 01, 2012 / Nat Immunol The cell-cycle regulator c-Myc is essential for the formation and maintenance of germinal centers D.P. Calado Y. Sasaki S.A. Godinho A. Pellerin K. Köchert B.P. Sleckman I.M. de Alboran M. Janz S. Rodig K. Rajewsky May 03, 2016 / Proc Natl Acad Sci U S A Canonical NF-κB signaling is uniquely required for the long-term persistence of functional mature B cells E. Derudder S. Herzog V. Labi T. Yasuda K. Köchert M. Janz A. Villunger M. Schmidt-Supprian K. Rajewsky February 01, 2016 / Genome Res Exome sequencing and CRISPR/Cas genome editing identify mutations of ZAK as a cause of limb defects in humans and mice M. Spielmann N. Kakar N. Tayebi C. Leettola G. Nürnberg N. Sowada D.G. Lupiáñez I. Harabula R. Flöttmann D. Horn W.L. Chan L. Wittler R. Yilmaz J. Altmüller H. Thiele H. van Bokhoven C.E. Schwartz P. Nürnberg J.U. Bowie J. Ahmad C. Kubisch S. Mundlos G. Borck January 14, 2016 / Nature FOXO1 couples metabolic activity and growth state in the vascular endothelium K. Wilhelm K. Happel G. Eelen S. Schoors M.F. Oellerich R. Lim B. Zimmermann I.M. Aspalter C.A. Franco T. Boettger T. Braun M. Fruttiger K. Rajewsky C. Keller J.C. Brüning H. Gerhardt P. Carmeliet M. Potente August 04, 2016 / Am J Hum Genet Exome sequencing identifies biallelic MSH3 germline mutations as a recessive subtype of colorectal adenomatous polyposis R. Adam I. Spier B. Zhao M. Kloth J. Marquez I. Hinrichsen J. Kirfel A. Tafazzoli S. Horpaopan S. Uhlhaas D. Stienen N. Friedrichs J. Altmüller A. Laner S. Holzapfel S. Peters K. Kayser H. Thiele E. Holinski-Feder G. Marra G. Kristiansen M.M. Nöthen R. Büttner G. Möslein R.C. Betz A. Brieger R.P. Lifton S. Aretz August 01, 2016 / Biol Chem A systematic comparison of two new releases of exome sequencing products: the aim of use determines the choice of product J. Altmüller S. Motameny C. Becker H. Thiele S. Chatterjee B. Wollnik P. Nürnberg February 25, 2016 / Blood Mutations in AP3D1 associated with immunodeficiency and seizures define a new type of Hermansky-Pudlak syndrome S. Ammann A. Schulz I. Krägeloh-Mann N.M.G. Dieckmann K. Niethammer S. Fuchs K.M. Eckl R. Plank R. Werner J. Altmüller H. Thiele P. Nürnberg J. Bank A. Strauss H. von Bernuth U. Zur Stadt S. Grieve G.M. Griffiths K. Lehmberg H.C. Hennies S. Ehl March 15, 2016 / Hum Mol Genet Three-layered proteomic characterization of a novel ACTN4 mutation unravels its pathogenic potential in FSGS M.P. Bartram S. Habbig C. Pahmeyer M. Höhne L.T. Weber H. Thiele J. Altmüller N. Kottoor A. Wenzel M. Krueger B. Schermer T. Benzing M.M. Rinschen B.B. Beck October 01, 2016 / Am J Med Genet A Update on the ACTG1-associated Baraitser–Winter cerebrofrontofacial syndrome N. Di Donato A. Kuechler S. Vergano W. Heinritz J. Bodurtha S.R. Merchant G. Breningstall R. Ladda S. Sell J. Altmüller N. Bögershausen A.E. Timms K. Hackmann E. Schrock S. Collins C. Olds A. Rump W.B. Dobyns August 30, 2016 / Sci Rep Characterization of non-olfactory GPCRs in human sperm with a focus on GPR18 C. Flegel F. Vogel A. Hofreuter S. Wojcik C. Schoeder K. Kieć-Kononowicz N.H. Brockmeyer C.E. Müller C. Becker J. Altmüller H. Hatt G. Gisselmann Pagination Current page 1 Page 2 Page 3 Page 4 Next page Next › Last page Last »
November 01, 2012 / Nat Immunol The cell-cycle regulator c-Myc is essential for the formation and maintenance of germinal centers D.P. Calado Y. Sasaki S.A. Godinho A. Pellerin K. Köchert B.P. Sleckman I.M. de Alboran M. Janz S. Rodig K. Rajewsky
May 03, 2016 / Proc Natl Acad Sci U S A Canonical NF-κB signaling is uniquely required for the long-term persistence of functional mature B cells E. Derudder S. Herzog V. Labi T. Yasuda K. Köchert M. Janz A. Villunger M. Schmidt-Supprian K. Rajewsky
February 01, 2016 / Genome Res Exome sequencing and CRISPR/Cas genome editing identify mutations of ZAK as a cause of limb defects in humans and mice M. Spielmann N. Kakar N. Tayebi C. Leettola G. Nürnberg N. Sowada D.G. Lupiáñez I. Harabula R. Flöttmann D. Horn W.L. Chan L. Wittler R. Yilmaz J. Altmüller H. Thiele H. van Bokhoven C.E. Schwartz P. Nürnberg J.U. Bowie J. Ahmad C. Kubisch S. Mundlos G. Borck
January 14, 2016 / Nature FOXO1 couples metabolic activity and growth state in the vascular endothelium K. Wilhelm K. Happel G. Eelen S. Schoors M.F. Oellerich R. Lim B. Zimmermann I.M. Aspalter C.A. Franco T. Boettger T. Braun M. Fruttiger K. Rajewsky C. Keller J.C. Brüning H. Gerhardt P. Carmeliet M. Potente
August 04, 2016 / Am J Hum Genet Exome sequencing identifies biallelic MSH3 germline mutations as a recessive subtype of colorectal adenomatous polyposis R. Adam I. Spier B. Zhao M. Kloth J. Marquez I. Hinrichsen J. Kirfel A. Tafazzoli S. Horpaopan S. Uhlhaas D. Stienen N. Friedrichs J. Altmüller A. Laner S. Holzapfel S. Peters K. Kayser H. Thiele E. Holinski-Feder G. Marra G. Kristiansen M.M. Nöthen R. Büttner G. Möslein R.C. Betz A. Brieger R.P. Lifton S. Aretz
August 01, 2016 / Biol Chem A systematic comparison of two new releases of exome sequencing products: the aim of use determines the choice of product J. Altmüller S. Motameny C. Becker H. Thiele S. Chatterjee B. Wollnik P. Nürnberg
February 25, 2016 / Blood Mutations in AP3D1 associated with immunodeficiency and seizures define a new type of Hermansky-Pudlak syndrome S. Ammann A. Schulz I. Krägeloh-Mann N.M.G. Dieckmann K. Niethammer S. Fuchs K.M. Eckl R. Plank R. Werner J. Altmüller H. Thiele P. Nürnberg J. Bank A. Strauss H. von Bernuth U. Zur Stadt S. Grieve G.M. Griffiths K. Lehmberg H.C. Hennies S. Ehl
March 15, 2016 / Hum Mol Genet Three-layered proteomic characterization of a novel ACTN4 mutation unravels its pathogenic potential in FSGS M.P. Bartram S. Habbig C. Pahmeyer M. Höhne L.T. Weber H. Thiele J. Altmüller N. Kottoor A. Wenzel M. Krueger B. Schermer T. Benzing M.M. Rinschen B.B. Beck
October 01, 2016 / Am J Med Genet A Update on the ACTG1-associated Baraitser–Winter cerebrofrontofacial syndrome N. Di Donato A. Kuechler S. Vergano W. Heinritz J. Bodurtha S.R. Merchant G. Breningstall R. Ladda S. Sell J. Altmüller N. Bögershausen A.E. Timms K. Hackmann E. Schrock S. Collins C. Olds A. Rump W.B. Dobyns
August 30, 2016 / Sci Rep Characterization of non-olfactory GPCRs in human sperm with a focus on GPR18 C. Flegel F. Vogel A. Hofreuter S. Wojcik C. Schoeder K. Kieć-Kononowicz N.H. Brockmeyer C.E. Müller C. Becker J. Altmüller H. Hatt G. Gisselmann