What is he best known for?
The fields of study he is best known for:
- Gene
- Enzyme
- Internal medicine
George S. Baillie focuses on Phosphodiesterase, Protein kinase A, Cell biology, Signal transduction and Biochemistry.
His Phosphodiesterase research is multidisciplinary, relying on both Molecular biology, Membrane, Intracellular, Kinase and Gene isoform.
His Protein kinase A study improves the overall literature in Phosphorylation.
His Cell biology research includes elements of Receptor, Internal medicine, PDE4B and Endocrinology.
His Signal transduction research incorporates themes from Plasma protein binding and Computational biology.
In general Biochemistry, his work in Vesicle and Arginine is often linked to Aquaporin 2 and Reabsorption linking many areas of study.
His most cited work include:
- DISC1 and PDE4B are interacting genetic factors in schizophrenia that regulate cAMP signaling. (564 citations)
- Targeting of cyclic AMP degradation to beta 2-adrenergic receptors by beta-arrestins. (444 citations)
- β-Arrestin-mediated PDE4 cAMP phosphodiesterase recruitment regulates β-adrenoceptor switching from Gs to Gi (333 citations)
What are the main themes of his work throughout his whole career to date?
His primary scientific interests are in Cell biology, Phosphodiesterase, Protein kinase A, Biochemistry and Phosphorylation.
George S. Baillie combines topics linked to Receptor with his work on Cell biology.
George S. Baillie has researched Phosphodiesterase in several fields, including Endocrinology, Molecular biology, Internal medicine, Intracellular and Gene isoform.
His work is dedicated to discovering how Gene isoform, Neuroscience are connected with Disease and other disciplines.
His Protein kinase A research incorporates elements of Beta-Arrestins, Signal transduction and Forskolin.
The concepts of his Phosphorylation study are interwoven with issues in Heat shock protein, HEK 293 cells and Kinase.
He most often published in these fields:
- Cell biology (44.79%)
- Phosphodiesterase (33.59%)
- Protein kinase A (27.80%)
What were the highlights of his more recent work (between 2016-2021)?
- Cell biology (44.79%)
- Phosphodiesterase (33.59%)
- Phosphorylation (20.08%)
In recent papers he was focusing on the following fields of study:
His primary areas of investigation include Cell biology, Phosphodiesterase, Phosphorylation, Protein kinase A and Internal medicine.
Cell biology and Receptor are frequently intertwined in his study.
His Phosphodiesterase research is multidisciplinary, relying on both Arrestin, Cyclic nucleotide, Signal transduction, Disease and Gene isoform.
His study on MAPK/ERK pathway is often connected to Soluble adenylyl cyclase as part of broader study in Phosphorylation.
His Protein kinase A research is multidisciplinary, incorporating elements of Cell, LYN, Allosteric regulation and Lipid microdomain.
His biological study spans a wide range of topics, including Endocrinology and Oncology.
Between 2016 and 2021, his most popular works were:
- Therapeutic targeting of 3',5'-cyclic nucleotide phosphodiesterases: inhibition and beyond. (67 citations)
- PDE2A2 regulates mitochondria morphology and apoptotic cell death via local modulation of cAMP/PKA signalling (54 citations)
- TIAM1 Antagonizes TAZ/YAP Both in the Destruction Complex in the Cytoplasm and in the Nucleus to Inhibit Invasion of Intestinal Epithelial Cells (41 citations)
In his most recent research, the most cited papers focused on:
- Gene
- Enzyme
- Internal medicine
His primary areas of study are Cell biology, Phosphodiesterase, Phosphorylation, Protein kinase A and Gene isoform.
His Cell biology study combines topics in areas such as HEK 293 cells and Bioinformatics.
In his study, which falls under the umbrella issue of Phosphodiesterase, Small molecule, Intracellular, Allosteric regulation and Therapeutic targeting is strongly linked to Compartmentalization.
In general Phosphorylation study, his work on SOCS3, Janus kinase and Suppressor of cytokine signalling often relates to the realm of Cavin, thereby connecting several areas of interest.
His Protein kinase A research incorporates themes from SUMO protein, DNA ligase and LYN.
He has included themes like CAMP response element binding, Effective treatment, Disease and Activator in his Gene isoform study.
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