Wissenschaftliche Publikationen Suche Suche Autor/in Forschungsgruppe Veröffentlichungsdatum Suchen Sortieren nach RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Reihenfolge AufsteigendAbsteigend Hübner, Norbert Prof. Dr. (11) Langanki, Reika (1) Lusatis, Simone (1) Maatz, Henrike Dr. (1) Marenholz, Ingo Dr. (1) Saar, Kathrin Dr. (2) Wollert-Wulf, Brigitte (1) (-) Janz, Martin Dr. (1) (-) Lee, Young-Ae Prof. Dr. (1) (-) Mathas, Stephan Dr. (1) (-) Selbach, Matthias Prof. Dr. (2) Biologie maligner Lymphome (5) (-) Genetik und Genomik von Herz- Kreislauferkrankungen (7) Hochschulambulanz für Pädiatrische Allergologie und Neurodermitis (1) Molekulare Genetik allergischer Erkrankungen (1) (-) Proteom Dynamik (2) 1995 (2) 1997 (2) 1999 (3) 2001 (3) 2002 (3) 2003 (2) 2004 (11) 2005 (11) (-) 2006 (9) 2007 (8) 2008 (7) 2009 (18) 2011 (10) 2012 (11) 2013 (8) 2014 (16) 2015 (18) 2016 (10) 2019 (8) 2020 (11) 2021 (14) 2022 (12) 2023 (5) 2024 (3) 9 Ergebnisse: Active Filter: Janz, Martin Dr.Lee, Young-Ae Prof. Dr.Mathas, Stephan Dr.Selbach, Matthias Prof. Dr.Genetik und Genomik von Herz- KreislauferkrankungenProteom Dynamik2006 Sortieren: Treffgenauigkeit Neueste nach älteste Älteste nach neueste 01. Oktober 2006 / Am J Med Genet A Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation A. Rauch J. Hoyer S. Guth C. Zweier C. Kraus C. Becker M. Zenker U. Hueffmeier C. Thiel F. Rueschendorf P. Nuernberg A. Reis U. Trautmann 01. Oktober 2006 / Am J Hum Genet Familial chilblain lupus, a monogenic form of cutaneous lupus erythematosus, maps to chromosome 3p M.A. Lee-Kirsch M. Gong H. Schulz F. Rüschendorf A. Stein C. Pfeiffer A. Ballarini M. Gahr N. Hubner M. Linne 01. Oktober 2006 / J Allergy Clin Immunol Filaggrin loss-of-function mutations predispose to phenotypes involved in the atopic march I. Marenholz R. Nickel F. Rueschendorf F. Schulz J. Esparza-Gordillo T. Kerscher C. Grueber S. Lau M. Worm T. Keil M. Kurek E. Zaluga U. Wahn Y.A. Lee 01. November 2006 / Nat Genet The gene encoding R-spondin 4 (RSPO4), a secreted protein implicated in Wnt signaling, is mutated in inherited anonychia D.C. Blaydon Y. Ishii E.A. O'Toole H.C. Unsworth M.T. Teh F. Rueschendorf C. Sinclair V.K. Hopsu-Havu N. Tidman C. Moss R. Watson D. de Berker M. Wajid A.M. Christiano D.P. Kelsell 01. November 2006 / Diabetes Dysregulation of the peripheral and adipose tissue endocannabinoid system in human abdominal obesity M. Blueher S. Engeli N. Kloeting J. Berndt M. Fasshauer S. Batkai P. Pacher M.R. Schoen J. Jordan M. Stumvoll 16. März 2006 / Nature Robust Salmonella metabolism limits possibilities for new antimicrobials D. Becker M. Selbach C. Rollenhagen M. Ballmaier T.F. Meyer M. Mann D. Bumann 01. Dezember 2006 / Nat Methods Protein interaction screening by quantitative immunoprecipitation combined with knockdown (QUICK) M. Selbach M. Mann 01. Februar 2006 / Hum Genet SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly M. Garshasbi M.M. Motazacker K. Kahrizi F. Behjati S.S. Abedini S.E. Nieh S.G. Firouzabadi C. Becker F. Rueschendorf P. Nuernberg A. Tzschach R. Vazifehmand F. Erdogan R. Ullmann S. Lenzner A.W. Kuss H.H. Ropers H. Najmabadi 01. Februar 2006 / Nat Immunol Intrinsic inhibition of transcription factor E2A by HLH proteins ABF-1 and Id2 mediates reprogramming of neoplastic B cells in Hodgkin lymphoma S. Mathas M. Janz F. Hummel M. Hummel B. Wollert-Wulf S. Lusatis I. Anagnostopoulos A. Lietz M. Sigvardsson F. Jundt K. Joehrens K. Bommert H. Stein B. Doerken
01. Oktober 2006 / Am J Med Genet A Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation A. Rauch J. Hoyer S. Guth C. Zweier C. Kraus C. Becker M. Zenker U. Hueffmeier C. Thiel F. Rueschendorf P. Nuernberg A. Reis U. Trautmann
01. Oktober 2006 / Am J Hum Genet Familial chilblain lupus, a monogenic form of cutaneous lupus erythematosus, maps to chromosome 3p M.A. Lee-Kirsch M. Gong H. Schulz F. Rüschendorf A. Stein C. Pfeiffer A. Ballarini M. Gahr N. Hubner M. Linne
01. Oktober 2006 / J Allergy Clin Immunol Filaggrin loss-of-function mutations predispose to phenotypes involved in the atopic march I. Marenholz R. Nickel F. Rueschendorf F. Schulz J. Esparza-Gordillo T. Kerscher C. Grueber S. Lau M. Worm T. Keil M. Kurek E. Zaluga U. Wahn Y.A. Lee
01. November 2006 / Nat Genet The gene encoding R-spondin 4 (RSPO4), a secreted protein implicated in Wnt signaling, is mutated in inherited anonychia D.C. Blaydon Y. Ishii E.A. O'Toole H.C. Unsworth M.T. Teh F. Rueschendorf C. Sinclair V.K. Hopsu-Havu N. Tidman C. Moss R. Watson D. de Berker M. Wajid A.M. Christiano D.P. Kelsell
01. November 2006 / Diabetes Dysregulation of the peripheral and adipose tissue endocannabinoid system in human abdominal obesity M. Blueher S. Engeli N. Kloeting J. Berndt M. Fasshauer S. Batkai P. Pacher M.R. Schoen J. Jordan M. Stumvoll
16. März 2006 / Nature Robust Salmonella metabolism limits possibilities for new antimicrobials D. Becker M. Selbach C. Rollenhagen M. Ballmaier T.F. Meyer M. Mann D. Bumann
01. Dezember 2006 / Nat Methods Protein interaction screening by quantitative immunoprecipitation combined with knockdown (QUICK) M. Selbach M. Mann
01. Februar 2006 / Hum Genet SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly M. Garshasbi M.M. Motazacker K. Kahrizi F. Behjati S.S. Abedini S.E. Nieh S.G. Firouzabadi C. Becker F. Rueschendorf P. Nuernberg A. Tzschach R. Vazifehmand F. Erdogan R. Ullmann S. Lenzner A.W. Kuss H.H. Ropers H. Najmabadi
01. Februar 2006 / Nat Immunol Intrinsic inhibition of transcription factor E2A by HLH proteins ABF-1 and Id2 mediates reprogramming of neoplastic B cells in Hodgkin lymphoma S. Mathas M. Janz F. Hummel M. Hummel B. Wollert-Wulf S. Lusatis I. Anagnostopoulos A. Lietz M. Sigvardsson F. Jundt K. Joehrens K. Bommert H. Stein B. Doerken