Beta-Arrestins, Cell biology, G protein-coupled receptor kinase, Arrestin and G protein-coupled receptor are his primary areas of study. In his study, Protein kinase C is strongly linked to G protein, which falls under the umbrella field of Beta-Arrestins. With his scientific publications, his incorporates both Cell biology and MAP2K7.
The Arrestin study combines topics in areas such as Endocrinology and MAPK/ERK pathway. His Beta adrenergic receptor kinase study in the realm of G protein-coupled receptor interacts with subjects such as Rhodopsin-like receptors. His work on Signal transduction is being expanded to include thematically relevant topics such as Phosphorylation.
The scientist’s investigation covers issues in Cell biology, Receptor, G protein-coupled receptor, Signal transduction and Beta-Arrestins. His Cell biology study incorporates themes from Internalization and Endocytosis. His research integrates issues of Protein structure, Computational biology and MAPK/ERK pathway in his study of Receptor.
His study of G protein-coupled receptor kinase is a part of G protein-coupled receptor. His work in the fields of Signal transduction, such as Functional selectivity, intersects with other areas such as Ubiquitin-conjugating enzyme. His work deals with themes such as Protein kinase B and Signal transducing adaptor protein, which intersect with Beta-Arrestins.
Seungkirl Ahn mostly deals with Receptor, Allosteric regulation, G protein-coupled receptor, Cell biology and G protein. His research in Allosteric regulation intersects with topics in Small molecule and Adrenergic receptor. His G protein-coupled receptor study combines topics from a wide range of disciplines, such as Cooperative binding, Phosphorylation and Stereochemistry.
His Phosphorylation research is multidisciplinary, incorporating elements of G protein-coupled receptor kinase and Receptor complex. His study in Arrestin and Signal transduction falls under the purview of Cell biology. His Signal transduction research incorporates elements of HEK 293 cells and Internalization.
Seungkirl Ahn focuses on Receptor, G protein-coupled receptor, Inverse agonist, Allosteric modulator and Allosteric regulation. The various areas that Seungkirl Ahn examines in his Receptor study include Stereochemistry and Binding site. The concepts of his Stereochemistry study are interwoven with issues in Agonist and Cooperative binding.
His Binding site study deals with the bigger picture of Biochemistry. Inverse agonist is frequently linked to Allosteric enzyme in his study. A majority of his CRISPR research is a blend of other scientific areas, such as HEK 293 cells, Signal transduction, G protein, Cell biology and Internalization.
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.
β-Arrestins and Cell Signaling
Scott M. DeWire;Seungkirl Ahn;Robert J. Lefkowitz;Sudha K. Shenoy.
Annual Review of Physiology (2007)
Independent β-arrestin 2 and G protein-mediated pathways for angiotensin II activation of extracellular signal-regulated kinases 1 and 2
Huijun Wei;Seungkirl Ahn;Sudha K. Shenoy;Sadashiva S. Karnik.
Proceedings of the National Academy of Sciences of the United States of America (2003)
A unique mechanism of β-blocker action: Carvedilol stimulates β-arrestin signaling
James W. Wisler;Scott M. DeWire;Erin J. Whalen;Jonathan D. Violin.
Proceedings of the National Academy of Sciences of the United States of America (2007)
Differential Kinetic and Spatial Patterns of β-Arrestin and G Protein-mediated ERK Activation by the Angiotensin II Receptor
Seungkirl Ahn;Sudha K. Shenoy;Huijun Wei;Robert J. Lefkowitz;Robert J. Lefkowitz.
Journal of Biological Chemistry (2004)
Essential Role for G Protein-coupled Receptor Endocytosis in the Activation of Mitogen-activated Protein Kinase
Yehia Daaka;Louis M. Luttrell;Seungkirl Ahn;Gregory J. Della Rocca.
Journal of Biological Chemistry (1998)
Molecular Mechanism of β-Arrestin-Biased Agonism at Seven-Transmembrane Receptors
Eric Reiter;Seungkirl Ahn;Arun K. Shukla;Robert J. Lefkowitz.
Annual Review of Pharmacology and Toxicology (2012)
Distinct phosphorylation sites on the β(2)-adrenergic receptor establish a barcode that encodes differential functions of β-arrestin.
Kelly N. Nobles;Kunhong Xiao;Seungkirl Ahn;Arun K. Shukla;Arun K. Shukla.
Science Signaling (2011)
β-arrestin- but not G protein-mediated signaling by the “decoy” receptor CXCR7
Sudarshan Rajagopal;Jihee Kim;Seungkirl Ahn;Stewart Craig.
Proceedings of the National Academy of Sciences of the United States of America (2010)
The β2-Adrenergic Receptor Mediates Extracellular Signal-regulated Kinase Activation via Assembly of a Multi-receptor Complex with the Epidermal Growth Factor Receptor
Stuart Maudsley;Kristen L. Pierce;A.Musa Zamah;William E. Miller.
Journal of Biological Chemistry (2000)
Distinct β-arrestin- and G protein-dependent pathways for parathyroid hormone receptor-stimulated ERK1/2 activation
Diane Gesty-Palmer;Minyong Chen;Eric Reiter;Seungkirl Ahn.
Journal of Biological Chemistry (2006)
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