Protein structure, Cell biology, Genetics, Biochemistry and RNA are his primary areas of study. His Protein structure research includes themes of Crystallography, SMN Complex Proteins, Biophysics, Ribosome and Binding site. His work focuses on many connections between Cell biology and other disciplines, such as RNA-induced silencing complex, that overlap with his field of interest in 7SK RNA.
His research brings together the fields of Stereochemistry and Biochemistry. His Stereochemistry research is multidisciplinary, relying on both Binding protein, Bcl-2 family, BH3 Mimetic ABT-737, Peptide sequence and Bcl-xL. Michael Sattler is interested in RNA-binding protein, which is a field of RNA.
Michael Sattler mostly deals with Cell biology, Biochemistry, RNA, Biophysics and Nuclear magnetic resonance spectroscopy. In most of his Biochemistry studies, his work intersects topics such as Stereochemistry. His biological study spans a wide range of topics, including Structural biology and Computational biology.
His Biophysics research includes elements of Hsp90, Binding site and Förster resonance energy transfer. The concepts of his Nuclear magnetic resonance spectroscopy study are interwoven with issues in Crystallography and Chemical physics. His biological study deals with issues like Protein structure, which deal with fields such as Molecular biology.
Michael Sattler mainly focuses on Cell biology, Biophysics, Computational biology, RNA and Nuclear magnetic resonance spectroscopy. His Cell biology research integrates issues from Autophagy and Regulation of gene expression. His Biophysics research also works with subjects such as
Michael Sattler has researched Computational biology in several fields, including Splicing factor, RNA splicing and Alternative splicing. His RNA research is multidisciplinary, incorporating elements of Messenger RNA and Function. Nuclear magnetic resonance spectroscopy is a subfield of Stereochemistry that Michael Sattler investigates.
His primary areas of investigation include Cell biology, RNA, Structural biology, Function and RNA-binding protein. As part of his studies on RNA, Michael Sattler often connects relevant areas like Gene silencing. His study looks at the relationship between Structural biology and topics such as Computational biology, which overlap with Dosage compensation.
His research investigates the connection with Function and areas like Biological system which intersect with concerns in Nuclear magnetic resonance spectroscopy and Biomolecule. His RNA-binding protein study combines topics from a wide range of disciplines, such as RRNA processing, Ribosome, Short linear motif, Helicase and Exosome complex. The various areas that Michael Sattler examines in his Gene isoform study include Regulator and Protein structure.
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Heteronuclear multidimensional NMR experiments for the structure determination of proteins in solution employing pulsed field gradients
Michael Sattler;Jürgen Schleucher;Christian Griesinger.
Progress in Nuclear Magnetic Resonance Spectroscopy (1999)
X-ray and NMR structure of human Bcl-xL, an inhibitor of programmed cell death.
Steven W. Muchmore;Michael Sattler;Heng Liang;Robert P. Meadows.
Nature (1996)
Structure of Bcl-xL-Bak peptide complex: recognition between regulators of apoptosis.
Michael Sattler;Heng Liang;David Nettesheim;Robert P. Meadows.
Science (1997)
A general enhancement scheme in heteronuclear multidimensional NMR employing pulsed field gradients.
J. Schleucher;M. Schwendinger;M. Sattler;P. Schmidt.
Journal of Biomolecular NMR (1994)
Structure and nucleic-acid binding of the Drosophila Argonaute 2 PAZ domain
Andreas Lingel;Bernd Simon;Elisa Izaurralde;Michael Sattler.
Nature (2003)
Structure and ligand recognition of the phosphotyrosine binding domain of Shc.
Ming-Ming Zhou;Kodimangalam S. Ravichandran;Edward T. Olejniczak;Andrew M. Petros.
Nature (1995)
Nucleic acid 3′-end recognition by the Argonaute2 PAZ domain
Andreas Lingel;Bernd Simon;Elisa Izaurralde;Michael Sattler.
Nature Structural & Molecular Biology (2004)
SMN tudor domain structure and its interaction with the Sm proteins.
Philipp Selenko;Remco Sprangers;Gunter Stier;Dirk Bühler.
Nature Structural & Molecular Biology (2001)
Endothelin 1 transcription is controlled by nuclear factor-kappaB in AGE-stimulated cultured endothelial cells.
P. Quehenberger;A. Bierhaus;P. Fasching;C. Muellner.
Diabetes (2000)
FSP1 is a glutathione-independent ferroptosis suppressor
Sebastian Doll;Florencio Porto Freitas;Ron Shah;Maceler Aldrovandi.
Nature (2019)
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