Gerd Krause mainly investigates Biochemistry, Cell biology, Receptor, Transmembrane domain and Tight junction. His Biochemistry research includes elements of Biophysics and Stereochemistry. His Cell biology study combines topics from a wide range of disciplines, such as Tyrosine, Cadherin, Binding protein and Ubiquitin.
The study incorporates disciplines such as Thyrotropin receptor and Endocrinology in addition to Receptor. His Tight junction research integrates issues from Extracellular and Transmembrane protein. His Claudin study integrates concerns from other disciplines, such as Endothelial stem cell and Paracellular transport.
His primary areas of investigation include Biochemistry, Receptor, Cell biology, Transmembrane domain and Amino acid. Many of his studies on Biochemistry involve topics that are commonly interrelated, such as Biophysics. He combines subjects such as Thyrotropin receptor, Endocrinology and Mutant with his study of Receptor.
His is involved in several facets of Cell biology study, as is seen by his studies on Tight junction, Extracellular, Claudin and Protein–protein interaction. His studies in Tight junction integrate themes in fields like Paracellular transport and Transmembrane protein. As part of the same scientific family, Gerd Krause usually focuses on Transmembrane domain, concentrating on Ectodomain and intersecting with Epitope.
Gerd Krause mainly focuses on Claudin, Cell biology, Tight junction, Biochemistry and Receptor. His work on CLDN3 as part of general Claudin research is frequently linked to Clostridium perfringens, bridging the gap between disciplines. Gerd Krause has included themes like Endothelial stem cell, Aryl hydrocarbon receptor, Mutant, Zebrafish and Neural plate in his Cell biology study.
The various areas that Gerd Krause examines in his Tight junction study include Biophysics, Cell junction and Cell polarity. His study on Amino acid is often connected to A-kinase-anchoring protein as part of broader study in Biochemistry. His research integrates issues of Thyrotropin receptor, Endocrinology and Signal transduction in his study of Receptor.
Gerd Krause mainly focuses on Tight junction, Claudin, Cell biology, Clostridium perfringens and Enterotoxin. Gerd Krause regularly links together related areas like Paracellular transport in his Tight junction studies. His studies deal with areas such as Endothelial stem cell, Downregulation and upregulation, Cell type and Anatomy as well as Paracellular transport.
His Cell biology study combines topics from a wide range of disciplines, such as Receptor and Zebrafish. The concepts of his Zebrafish study are interwoven with issues in Quorum sensing, Cell signaling, Mutant and Aryl hydrocarbon receptor. His biological study spans a wide range of topics, including Small intestine and Virulence.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Hakai, a c-Cbl-like protein, ubiquitinates and induces endocytosis of the E-cadherin complex
Yasuyuki Fujita;Gerd Krause;Martin Scheffner;Dietmar Zechner.
Nature Cell Biology (2002)
Structure and function of claudins.
Gerd Krause;Lars Winkler;Sebastian L. Mueller;Reiner F. Haseloff.
Biochimica et Biophysica Acta (2008)
Formation of tight junction: determinants of homophilic interaction between classic claudins
Jörg Piontek;Lars Winkler;Hartwig Wolburg;Sebastian L. Müller.
The FASEB Journal (2008)
Specific interactions between the syntrophin PDZ domain and voltage-gated sodium channels.
Johan Schultz;Ulrich Hoffmuüller;Gerd Krause;Jennifer Ashurst.
Nature Structural & Molecular Biology (1998)
AhR sensing of bacterial pigments regulates antibacterial defence
Pedro Moura-Alves;Kellen Faé;Erica Houthuys;Anca Dorhoi.
Nature (2014)
A Dileucine Sequence and an Upstream Glutamate Residue in the Intracellular Carboxyl Terminus of the Vasopressin V2Receptor Are Essential for Cell Surface Transport in COS.M6 Cells
Ralf Schülein;Ricardo Hermosilla;Alexander Oksche;Marcel Dehe.
Molecular Pharmacology (1998)
Pharmacochaperones post-translationally enhance cell surface expression by increasing conformational stability of wild-type and mutant vasopressin V2 receptors.
Stefan Wüller;Burkhard Wiesner;Anja Löffler;Jens Furkert.
Journal of Biological Chemistry (2004)
General structural motifs of amyloid protofilaments
Neil Ferguson;Johanna Becker;Henning Tidow;Sandra Tremmel.
Proceedings of the National Academy of Sciences of the United States of America (2006)
Quantification of PDZ domain specificity, prediction of ligand affinity and rational design of super-binding peptides.
Urs Wiedemann;Prisca Boisguerin;Prisca Boisguerin;Rainer Leben;Dietmar Leitner.
Journal of Molecular Biology (2004)
The Tight Junction Protein Occludin and the Adherens Junction Protein α-Catenin Share a Common Interaction Mechanism with ZO-1
Sebastian L. Müller;Michael Portwich;Anke Schmidt;Darkhan I. Utepbergenov.
Journal of Biological Chemistry (2005)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:
University of Calgary
Freie Universität Berlin
Leibniz Institute for Neurobiology
Max Planck Institute for Infection Biology
Leibniz Institute for Neurobiology
Freie Universität Berlin
Max Delbrück Center for Molecular Medicine
University of Bonn
Charité - University Medicine Berlin
Charité - University Medicine Berlin
Technical University of Berlin
École Polytechnique Fédérale de Lausanne
London School of Economics and Political Science
Applied Materials (United States)
University of Colorado Boulder
Linköping University
Landcare Research
Xiamen University
German Cancer Research Center
United States Geological Survey
Chinese Academy of Sciences
University of Massachusetts Lowell
Leiden University Medical Center
University of Pavia
Yale University
Duke University