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 64 Citations 16,997 140 World Ranking 4329 National Ranking 2159

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Enzyme
  • DNA

His scientific interests lie mostly in Biochemistry, High-throughput screening, G protein-coupled receptor kinase, G protein and Drug discovery. James Inglese interconnects Biological activity, Structure–activity relationship and Enzyme in the investigation of issues within High-throughput screening. His G protein-coupled receptor kinase study which covers Protein kinase A that intersects with Protein prenylation and Cell surface receptor.

In G protein, he works on issues like G alpha subunit, which are connected to Binding domain. His Drug discovery study integrates concerns from other disciplines, such as Combinatorial chemistry and Computational biology. His research in Luciferase intersects with topics in Molecular biology and Bioluminescence.

His most cited work include:

  • Role of beta gamma subunits of G proteins in targeting the beta-adrenergic receptor kinase to membrane-bound receptors. (628 citations)
  • Quantitative high-throughput screening: a titration-based approach that efficiently identifies biological activities in large chemical libraries. (623 citations)
  • Protein kinases that phosphorylate activated G protein-coupled receptors. (466 citations)

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

James Inglese mainly investigates Biochemistry, High-throughput screening, Cell biology, Molecular biology and Small molecule. His study in Enzyme, Luciferase, Structure–activity relationship, G protein-coupled receptor kinase and Kinase are all subfields of Biochemistry. The various areas that James Inglese examines in his G protein-coupled receptor kinase study include Mitogen-activated protein kinase kinase and Beta adrenergic receptor kinase.

His High-throughput screening research integrates issues from Receptor, Antibody, Computational biology and Drug discovery. His Drug discovery study combines topics in areas such as Chemical biology and Pharmacology. His work deals with themes such as Identification and Fusion protein, which intersect with Cell biology.

He most often published in these fields:

  • Biochemistry (42.93%)
  • High-throughput screening (21.74%)
  • Cell biology (21.20%)

What were the highlights of his more recent work (between 2014-2021)?

  • Cell biology (21.20%)
  • High-throughput screening (21.74%)
  • Drug discovery (12.50%)

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

His primary scientific interests are in Cell biology, High-throughput screening, Drug discovery, Biochemistry and Cell. His studies examine the connections between Cell biology and genetics, as well as such issues in Nonsense-mediated decay, with regards to Exon junction complex, DNA and Messenger RNA. His studies deal with areas such as Gs alpha subunit, Computational biology, Small molecule and Heterologous expression as well as High-throughput screening.

His Drug discovery study combines topics from a wide range of disciplines, such as Secretory protein, Quantitative proteomics and Pharmacology. He performs integrative Biochemistry and Phosphoglycerate mutase research in his work. His study in Cell is interdisciplinary in nature, drawing from both Neuropeptide, Nuclear localization sequence, Fusion protein and Gene isoform.

Between 2014 and 2021, his most popular works were:

  • Mitigating risk in academic preclinical drug discovery (82 citations)
  • High-throughput matrix screening identifies synergistic and antagonistic antimalarial drug combinations. (64 citations)
  • Chemogenomic profiling of endogenous PARK2 expression using a genome-edited coincidence reporter. (36 citations)

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

  • Gene
  • Enzyme
  • DNA

James Inglese mostly deals with Drug discovery, Cell biology, Pharmacology, Extramural and Gene. His studies in Drug discovery integrate themes in fields like Orphan drug and Preclinical pharmacology. His research in the fields of Transport protein overlaps with other disciplines such as Streptavidin.

His work on Drug development is typically connected to Institutional level as part of general Pharmacology study, connecting several disciplines of science. His Extramural research incorporates elements of Drug resistance, Drug, Inhibitory concentration 50, Drug Antagonism and Drug synergism. When carried out as part of a general Gene research project, his work on RNA splicing and Messenger RNA is frequently linked to work in RNA surveillance and mRNA surveillance, therefore connecting diverse disciplines of study.

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

Role of beta gamma subunits of G proteins in targeting the beta-adrenergic receptor kinase to membrane-bound receptors.

Julie A. Pitcher;James Inglese;Joyce B. Higgins;Jeffery L. Arriza.
Science (1992)

873 Citations

Quantitative high-throughput screening: a titration-based approach that efficiently identifies biological activities in large chemical libraries.

James Inglese;Douglas S. Auld;Ajit Jadhav;Ronald L. Johnson.
Proceedings of the National Academy of Sciences of the United States of America (2006)

758 Citations

High-throughput screening assays for the identification of chemical probes

James Inglese;Ronald L Johnson;Anton Simeonov;Menghang Xia.
Nature Chemical Biology (2007)

634 Citations

Protein kinases that phosphorylate activated G protein-coupled receptors.

Richard T. Premont;James Inglese;Robert J. Lefkowitz.
The FASEB Journal (1995)

633 Citations

Binding of G protein beta gamma-subunits to pleckstrin homology domains.

K. Touhara;J. Inglese;J.A. Pitcher;G. Shaw.
Journal of Biological Chemistry (1994)

592 Citations

Structure and mechanism of the G protein-coupled receptor kinases.

J Inglese;N J Freedman;W J Koch;R J Lefkowitz.
Journal of Biological Chemistry (1993)

591 Citations

Activation of the cloned muscarinic potassium channel by G protein βγ subunits

Eitan Reuveny;Paul A. Slesinger;James Inglese;Janine M. Morales.
Nature (1994)

567 Citations

Pyruvate kinase M2 activators promote tetramer formation and suppress tumorigenesis.

Dimitrios Anastasiou;Yimin Yu;William James Israelsen;Jian-Kang Jiang.
Nature Chemical Biology (2012)

559 Citations

The binding site for the beta gamma subunits of heterotrimeric G proteins on the beta-adrenergic receptor kinase.

W J Koch;J Inglese;W C Stone;R J Lefkowitz.
Journal of Biological Chemistry (1993)

548 Citations

Cellular expression of the carboxyl terminus of a G protein-coupled receptor kinase attenuates G beta gamma-mediated signaling.

W J Koch;B E Hawes;J Inglese;L M Luttrell.
Journal of Biological Chemistry (1994)

483 Citations

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