What is he best known for?
The fields of study he is best known for:
- G protein-coupled receptor
- Signal transduction
- Receptor
Larry S. Barak focuses on G protein-coupled receptor, Cell biology, Arrestin, Beta-Arrestins and Receptor.
His G protein-coupled receptor research focuses on G protein-coupled receptor kinase in particular.
The Cell biology study combines topics in areas such as Internalization and Actin remodeling.
His Arrestin study is associated with Signal transduction.
His research integrates issues of Arrestin beta 2, G-protein coupled receptor internalization, Signal transducing adaptor protein and Endocytosis, Clathrin in his study of Beta-Arrestins.
His Receptor research is under the purview of Biochemistry.
His most cited work include:
- Role of β-Arrestin in Mediating Agonist-Promoted G Protein-Coupled Receptor Internalization (847 citations)
- Differential Affinities of Visual Arrestin, βArrestin1, and βArrestin2 for G Protein-coupled Receptors Delineate Two Major Classes of Receptors (701 citations)
- The beta2-adrenergic receptor interacts with the Na+/H+-exchanger regulatory factor to control Na+/H+ exchange. (557 citations)
What are the main themes of his work throughout his whole career to date?
His main research concerns Cell biology, G protein-coupled receptor, Receptor, Arrestin and Pharmacology.
His work deals with themes such as Enzyme-linked receptor, Internalization and Endocytosis, which intersect with Cell biology.
His work on Arrestin beta 2 is typically connected to Rhodopsin-like receptors as part of general G protein-coupled receptor study, connecting several disciplines of science.
His work carried out in the field of Receptor brings together such families of science as Molecular biology, Kinase and Phosphorylation.
Larry S. Barak has included themes like Endocytic cycle, Neuroscience and Ghrelin in his Arrestin study.
In Pharmacology, Larry S. Barak works on issues like In vivo, which are connected to In vitro.
He most often published in these fields:
- Cell biology (55.33%)
- G protein-coupled receptor (44.67%)
- Receptor (40.00%)
What were the highlights of his more recent work (between 2011-2021)?
- Cell biology (55.33%)
- Pharmacology (21.33%)
- G protein-coupled receptor (44.67%)
In recent papers he was focusing on the following fields of study:
His primary areas of study are Cell biology, Pharmacology, G protein-coupled receptor, Signal transduction and Receptor.
He combines topics linked to Tissue homeostasis with his work on Cell biology.
His study in Pharmacology is interdisciplinary in nature, drawing from both Wnt signaling pathway, In vitro, Structure–activity relationship and In vivo.
His research in the fields of Functional selectivity overlaps with other disciplines such as Transducer.
His Signal transduction research includes themes of Ex vivo, Cancer research, Cell growth and Internalization.
Receptor is the subject of his research, which falls under Biochemistry.
Between 2011 and 2021, his most popular works were:
- IL-6/STAT3 promotes regeneration of airway ciliated cells from basal stem cells (147 citations)
- BRET biosensors to study GPCR biology, pharmacology, and signal transduction (74 citations)
- G Protein and β-Arrestin Signaling Bias at the Ghrelin Receptor (49 citations)
In his most recent research, the most cited papers focused on:
- G protein-coupled receptor
- Biochemistry
- Signal transduction
The scientist’s investigation covers issues in Pharmacology, Cell biology, Signal transduction, G protein-coupled receptor and Wnt signaling pathway.
In his study, which falls under the umbrella issue of Pharmacology, Internalization, Perhexiline, Breast cancer and Biological activity is strongly linked to In vivo.
Larry S. Barak has researched Cell biology in several fields, including Cell Surface Extension and Tissue homeostasis.
His studies in Signal transduction integrate themes in fields like Cell growth and Trace amine-associated receptor.
His G protein-coupled receptor research incorporates themes from Agonist, Inverse agonist, Partial agonist, Intracellular signal transduction and Compound 32.
His FZD1 and Beta-catenin study in the realm of Wnt signaling pathway connects with subjects such as Niclosamide.
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