Member of the European Molecular Biology Organization (EMBO)
Andreas G. Ladurner mainly investigates Biochemistry, Chromatin, Cell biology, Histone and Enzyme. His study on DNA damage, NAD+ kinase, Plasma protein binding and DNA supercoil is often connected to DNA clamp as part of broader study in Biochemistry. The Chromatin study combines topics in areas such as Poly ADP ribose polymerase and Macro domain.
His work carried out in the field of Cell biology brings together such families of science as Genetics, Histone code, Transcription Factor TFIID, HMG-box and Histone H2A. His work deals with themes such as Biomarker, Lung cancer, Epigenetics and Immunology, which intersect with Histone. Andreas G. Ladurner works mostly in the field of Enzyme, limiting it down to concerns involving Peptide sequence and, occasionally, PARG, DNA repair and Mutation.
Andreas G. Ladurner focuses on Cell biology, Chromatin, Histone, Biochemistry and Genetics. His Cell biology research incorporates themes from DNA, DNA damage, PARP1, Nucleosome and NAD+ kinase. His Nucleosome research focuses on Molecular biology and how it relates to Transcription factor II D, TAF1 and RNA polymerase II.
His study in Chromatin is interdisciplinary in nature, drawing from both Regulation of gene expression, CHD1L and Poly ADP ribose polymerase. The study incorporates disciplines such as Gene expression, Acetylation, Epigenetics and DNA-binding protein in addition to Histone. His Biochemistry study frequently draws connections to other fields, such as Biophysics.
His main research concerns Cell biology, Chromatin, PARP1, Histone and DNA damage. Andreas G. Ladurner studied Cell biology and DNA repair that intersect with NAD+ kinase and Poly ADP ribose polymerase. His Poly ADP ribose polymerase study results in a more complete grasp of Biochemistry.
Andreas G. Ladurner interconnects RNA polymerase II and Active site in the investigation of issues within Chromatin. His studies deal with areas such as Pharmacology toxicology, Schizosaccharomyces pombe and Chaperone as well as Histone. His biological study spans a wide range of topics, including Heterochromatin, Serine, DNA-binding protein and Gene isoform.
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Structure and function of a human TAFII250 double bromodomain module.
Raymond H. Jacobson;Andreas G. Ladurner;David S. King;Robert Tjian.
Science (2000)
The macro domain is an ADP-ribose binding module
Georgios I Karras;Georg Kustatscher;Heeran R Buhecha;Mark D Allen.
The EMBO Journal (2004)
The transcriptional cofactor complex CRSP is required for activity of the enhancer-binding protein Sp1.
Soojin Ryu;Sharleen Zhou;Andreas G. Ladurner;Robert Tjian.
Nature (1999)
A macrodomain-containing histone rearranges chromatin upon sensing PARP1 activation.
Gyula Timinszky;Susanne Till;Paul O Hassa;Michael Hothorn.
Nature Structural & Molecular Biology (2009)
Poly(ADP-ribosyl)ation directs recruitment and activation of an ATP-dependent chromatin remodeler.
Aaron J. Gottschalk;Gyula Timinszky;Stephanie E. Kong;Jingji Jin.
Proceedings of the National Academy of Sciences of the United States of America (2009)
Splicing regulates NAD metabolite binding to histone macroH2A.
Georg Kustatscher;Michael Hothorn;Céline Pugieux;Klaus Scheffzek.
Nature Structural & Molecular Biology (2005)
A unified phylogeny-based nomenclature for histone variants
Paul B Talbert;Kami Ahmad;Geneviève Almouzni;Juan Ausió.
Epigenetics & Chromatin (2012)
Bromodomains mediate an acetyl-histone encoded antisilencing function at heterochromatin boundaries.
Andreas G. Ladurner;Carla Inouye;Rajan Jain;Robert Tjian.
Molecular Cell (2003)
A conserved motif in Argonaute-interacting proteins mediates functional interactions through the Argonaute PIWI domain.
Susanne Till;Erwan Lejeune;Rolf Thermann;Miriam Bortfeld.
Nature Structural & Molecular Biology (2007)
A family of macrodomain proteins reverses cellular mono-ADP-ribosylation
Gytis Jankevicius;Markus Hassler;Barbara Golia;Vladimir Rybin.
Nature Structural & Molecular Biology (2013)
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