What is he best known for?
The fields of study he is best known for:
His primary areas of investigation include Receptor, Cell biology, G protein-coupled receptor, G protein and Genetics.
Receptor is a subfield of Biochemistry that Torsten Schöneberg studies.
Many of his research projects under Biochemistry are closely connected to Ethylenediamine with Ethylenediamine, tying the diverse disciplines of science together.
His study looks at the relationship between Cell biology and fields such as Membrane protein, as well as how they intersect with chemical problems.
His G protein-coupled receptor research incorporates elements of Protein domain and Nephrogenic diabetes insipidus.
His G protein research is multidisciplinary, relying on both Cell activation, Stimulation and Immunology.
His most cited work include:
- Claudin-2 expression induces cation-selective channels in tight junctions of epithelial cells. (627 citations)
- FUNCTIONAL AND STRUCTURAL COMPLEXITY OF SIGNAL TRANSDUCTION VIA G-PROTEIN-COUPLED RECEPTORS (292 citations)
- Extracellular Ca2+ is a danger signal activating the NLRP3 inflammasome through G protein-coupled calcium sensing receptors. (255 citations)
What are the main themes of his work throughout his whole career to date?
His primary scientific interests are in Receptor, G protein-coupled receptor, Cell biology, Biochemistry and Endocrinology.
His work in Receptor addresses subjects such as Mutant, which are connected to disciplines such as Molecular biology.
His G protein-coupled receptor research is within the category of Genetics.
His Cell biology research integrates issues from Immune system, Inverse agonist and Membrane protein.
The concepts of his Endocrinology study are interwoven with issues in Internal medicine and Exon.
His research on G protein frequently connects to adjacent areas such as 5-HT5A receptor.
He most often published in these fields:
- Receptor (46.39%)
- G protein-coupled receptor (39.18%)
- Cell biology (29.38%)
What were the highlights of his more recent work (between 2015-2021)?
- G protein-coupled receptor (39.18%)
- Receptor (46.39%)
- Cell biology (29.38%)
In recent papers he was focusing on the following fields of study:
Torsten Schöneberg mostly deals with G protein-coupled receptor, Receptor, Cell biology, Signal transduction and Agonist.
Torsten Schöneberg has researched G protein-coupled receptor in several fields, including Extracellular, Biophysics, Function, Transmembrane domain and Computational biology.
His Receptor research is classified as research in Biochemistry.
His biological study spans a wide range of topics, including HEK 293 cells, Membrane and Immune system.
The Signal transduction study combines topics in areas such as Inflammation, Inflammasome and Inflammatory arthritis, Arthritis.
His work carried out in the field of Agonist brings together such families of science as Peptide sequence, COS cells and Ectodomain.
Between 2015 and 2021, his most popular works were:
- The constitutive activity of the adhesion GPCR GPR114/ADGRG5 is mediated by its tethered agonist (54 citations)
- Update of P2Y receptor pharmacology: IUPHAR Review 27. (37 citations)
- Activation of Adhesion G Protein-coupled Receptors AGONIST SPECIFICITY OF STACHEL SEQUENCE-DERIVED PEPTIDES (37 citations)
In his most recent research, the most cited papers focused on:
Receptor, G protein-coupled receptor, Cell biology, Signal transduction and Agonist are his primary areas of study.
His Receptor study is related to the wider topic of Biochemistry.
His research on G protein-coupled receptor often connects related areas such as Prostaglandin E2.
His study on Cell biology also encompasses disciplines like
- Ectodomain and related Conserved sequence, Hormone and G protein,
- Inflammation together with Arthritis and Inflammatory arthritis.
His Signal transduction research includes elements of Function, Metabolite, Transmembrane domain, Systemic inflammation and Energy homeostasis.
The various areas that Torsten Schöneberg examines in his Agonist study include Extracellular, Peptide sequence, COS cells and Pharmacology.
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