D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Biology and Biochemistry D-index 40 Citations 13,267 48 World Ranking 17535 National Ranking 7177

Overview

What is he best known for?

The fields of study he is best known for:

  • Signal transduction
  • G protein-coupled receptor
  • Receptor

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.

His most cited work include:

  • β-Arrestins and Cell Signaling (1132 citations)
  • Independent β-arrestin 2 and G protein-mediated pathways for angiotensin II activation of extracellular signal-regulated kinases 1 and 2 (577 citations)
  • Essential Role for G Protein-coupled Receptor Endocytosis in the Activation of Mitogen-activated Protein Kinase (484 citations)

What are the main themes of his work throughout his whole career to date?

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.

He most often published in these fields:

  • Cell biology (64.15%)
  • Receptor (56.60%)
  • G protein-coupled receptor (47.17%)

What were the highlights of his more recent work (between 2016-2020)?

  • Receptor (56.60%)
  • Allosteric regulation (20.75%)
  • G protein-coupled receptor (47.17%)

In recent papers he was focusing on the following fields of study:

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.

Between 2016 and 2020, his most popular works were:

  • Manifold roles of β-arrestins in GPCR signaling elucidated with siRNA and CRISPR/Cas9 (96 citations)
  • Mechanism of intracellular allosteric β 2 AR antagonist revealed by X-ray crystal structure (74 citations)
  • Allosteric "beta-blocker" isolated from a DNA-encoded small molecule library. (59 citations)

In his most recent research, the most cited papers focused on:

  • Signal transduction
  • G protein-coupled receptor
  • Biochemistry

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.

Best Publications

β-Arrestins and Cell Signaling

Scott M. DeWire;Seungkirl Ahn;Robert J. Lefkowitz;Sudha K. Shenoy.
Annual Review of Physiology (2007)

1815 Citations

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)

870 Citations

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)

702 Citations

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)

663 Citations

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)

648 Citations

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)

581 Citations

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)

515 Citations

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)

506 Citations

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)

493 Citations

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)

460 Citations

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