His main research concerns Cell biology, Protein kinase A, Aquaporin 2, Biochemistry and Signal transduction. His work on Phosphorylation as part of general Cell biology research is frequently linked to Clostridium difficile toxin B, bridging the gap between disciplines. The Phosphorylation study combines topics in areas such as Calcium-binding protein, Endoplasmic reticulum and Adrenergic.
His studies deal with areas such as Scaffold protein, Serine and Phosphodiesterase as well as Protein kinase A. His Biochemistry research is multidisciplinary, incorporating elements of Compartmentalization and Antigen. His Signal transduction research is multidisciplinary, relying on both Phosphatase, Protein subunit, Calcium and Cyclic adenosine monophosphate.
Cell biology, Protein kinase A, Biochemistry, Aquaporin 2 and Phosphorylation are his primary areas of study. He usually deals with Cell biology and limits it to topics linked to Cyclic adenosine monophosphate and Signalling and Second messenger system. The study incorporates disciplines such as Scaffold protein, Protein subunit and Phosphodiesterase in addition to Protein kinase A.
His study looks at the intersection of Biochemistry and topics like Biophysics with HEK 293 cells. His research integrates issues of Molecular biology and Endoplasmic reticulum in his study of Phosphorylation. He combines subjects such as Transport protein, Diabetes insipidus and Cell membrane with his study of Reabsorption.
The scientist’s investigation covers issues in Cell biology, Protein kinase A, Aquaporin 2, Phosphodiesterase and Phosphorylation. His study in Compartmentalization, Homeostasis, Small GTPase, RAC1 and Guanine nucleotide exchange factor is carried out as part of his Cell biology studies. Protein kinase A is a subfield of Kinase that Enno Klussmann studies.
His work deals with themes such as Cardiology, Blood pressure, Intracellular, Cardiovascular death and Risk factor, which intersect with Phosphodiesterase. His study in Phosphorylation is interdisciplinary in nature, drawing from both Umbilical vein and Angiogenesis. His biological study spans a wide range of topics, including Diabetes insipidus and Vasopressin.
Enno Klussmann mostly deals with Cell biology, Aquaporin 2, Compartmentalization, Phosphodiesterase and Protein kinase A. His work on GTPase and Transport protein as part of his general Cell biology study is frequently connected to ATG16L1, thereby bridging the divide between different branches of science. His Aquaporin 2 research spans across into subjects like RHOA, RAC1, Guanine nucleotide exchange factor, Small GTPase and CDC42.
His Compartmentalization research is multidisciplinary, incorporating perspectives in Adenosine, Heart failure, Homeostasis, Function and Gene. The concepts of his Phosphodiesterase study are interwoven with issues in Activator, Small molecule, Intracellular, Allosteric regulation and Gene isoform. To a larger extent, Enno Klussmann studies Phosphorylation with the aim of understanding Protein kinase A.
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RNA Silencing Identifies PDE4D5 as the Functionally Relevant cAMP Phosphodiesterase Interacting with βArrestin to Control the Protein Kinase A/AKAP79-mediated Switching of the β2-Adrenergic Receptor to Activation of ERK in HEK293B2 Cells *
Martin J. Lynch;George S. Baillie;Ahmed Mohamed;Xiang Li.
Journal of Biological Chemistry (2005)
Protein Kinase A Anchoring Proteins Are Required for Vasopressin-mediated Translocation of Aquaporin-2 into Cell Membranes of Renal Principal Cells *
Enno Klussmann;Kenan Maric;Burkhard Wiesner;Michael Beyermann.
Journal of Biological Chemistry (1999)
AKAP complex regulates Ca2+ re‐uptake into heart sarcoplasmic reticulum
Birgitte Lygren;Cathrine Rein Carlson;Katja Santamaria;Valentina Lissandron.
EMBO Reports (2007)
Mechanisms of protein kinase A anchoring.
Philipp Skroblin;Solveig Grossmann;Solveig Grossmann;Gesa Schäfer;Walter Rosenthal;Walter Rosenthal.
International Review of Cell and Molecular Biology (2010)
Isoform-Selective Susceptibility of DISC1/Phosphodiesterase-4 Complexes to Dissociation by Elevated Intracellular cAMP Levels
Hannah Murdoch;Shaun Mackie;Daniel M Collins;Elaine V Hill.
The Journal of Neuroscience (2007)
An inhibitory role of Rho in the vasopressin-mediated translocation of aquaporin-2 into cell membranes of renal principal cells.
Enno Klussmann;Grazia Tamma;Dorothea Lorenz;Burkhard Wiesner.
Journal of Biological Chemistry (2001)
Identification of a Novel A-kinase Anchoring Protein 18 Isoform and Evidence for Its Role in the Vasopressin-induced Aquaporin-2 Shuttle in Renal Principal Cells
Volker Henn;Bayram Edemir;Eduard Stefan;Burkhard Wiesner.
Journal of Biological Chemistry (2004)
Scanning peptide array analyses identify overlapping binding sites for the signalling scaffold proteins, β-arrestin and RACK1, in cAMP-specific phosphodiesterase PDE4D5
Graeme B. Bolger;George S. Baillie;Xiang Li;Martin J. Lynch.
Biochemical Journal (2006)
Regulation of Aquaporin-2 Trafficking
Pavel I. Nedvetsky;Grazia Tamma;Sven Beulshausen;Giovanna Valenti.
Handbook of experimental pharmacology (2009)
Expression of MUC2-mucin in colorectal adenomas and carcinomas of different histological types
Monika Blank;Enno Klussmann;Sabine Krüger-Krasagakes;Anette Schmitt-Gräff.
International Journal of Cancer (1994)
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