What is he best known for?
The fields of study he is best known for:
Apoptosis, Cell biology, Tissue transglutaminase, Programmed cell death and Biochemistry are his primary areas of study.
He has researched Apoptosis in several fields, including Inflammation, Receptor, Cell and Involution.
His work deals with themes such as Kidney and Cell type, which intersect with Cell biology.
László Fésüs has included themes like Cell culture, Autoantibody, Antibody, Pathology and Molecular biology in his Tissue transglutaminase study.
The various areas that László Fésüs examines in his Programmed cell death study include Autophagy, Cancer research and Effector.
His Retinoic acid and Substrate study in the realm of Biochemistry interacts with subjects such as Highly sensitive.
His most cited work include:
- Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (4170 citations)
- Guidelines for the use and interpretation of assays for monitoring autophagy (3242 citations)
- Guidelines for the use and interpretation of assays for monitoring autophagy in higher eukaryotes (1951 citations)
What are the main themes of his work throughout his whole career to date?
His primary scientific interests are in Tissue transglutaminase, Biochemistry, Cell biology, Apoptosis and Molecular biology.
As a part of the same scientific study, László Fésüs usually deals with the Tissue transglutaminase, concentrating on Antibody and frequently concerns with Coeliac disease.
His study in Lysine, Glutamine, Retinoic acid, Protein disulfide-isomerase and Extracellular is done as part of Biochemistry.
His Cell biology study integrates concerns from other disciplines, such as Inflammation, Receptor, Immune system and Autophagy.
His work carried out in the field of Receptor brings together such families of science as Endocrinology and Gene expression.
His research on Apoptosis focuses in particular on Programmed cell death.
He most often published in these fields:
- Tissue transglutaminase (43.34%)
- Biochemistry (35.91%)
- Cell biology (31.27%)
What were the highlights of his more recent work (between 2012-2021)?
- Tissue transglutaminase (43.34%)
- Cell biology (31.27%)
- Biochemistry (35.91%)
In recent papers he was focusing on the following fields of study:
László Fésüs spends much of his time researching Tissue transglutaminase, Cell biology, Biochemistry, Internal medicine and Endocrinology.
His Tissue transglutaminase research incorporates elements of Genetics, Signal transduction, Protein–protein interaction, Plasma protein binding and GTP'.
His Cell biology research includes themes of Autophagy, Inflammation, Cell and Programmed cell death.
His Programmed cell death research includes elements of BECN1, Autophagosome, Autolysosome, Sequestosome 1 and Physiology.
His Internal medicine study incorporates themes from Ex vivo and Gene expression.
László Fésüs combines subjects such as Proinflammatory cytokine and Receptor with his study of Endocrinology.
Between 2012 and 2021, his most popular works were:
- Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (4170 citations)
- Atypical antipsychotics induce both proinflammatory and adipogenic gene expression in human adipocytes in vitro. (63 citations)
- Atypical antipsychotics induce both proinflammatory and adipogenic gene expression in human adipocytes in vitro. (63 citations)
In his most recent research, the most cited papers focused on:
László Fésüs mostly deals with Internal medicine, Endocrinology, Cell biology, Biochemistry and Cell.
His Internal medicine research is multidisciplinary, incorporating elements of Gene expression and Pharmacology.
His study in Cell biology is interdisciplinary in nature, drawing from both Inflammation and Apoptosis, Programmed cell death.
His Programmed cell death research integrates issues from Cell culture, Retinal, Retina, Sequestosome 1 and Autophagosome.
His research related to Enzyme and Tissue transglutaminase might be considered part of Biochemistry.
His research is interdisciplinary, bridging the disciplines of Isopeptidase activity and Tissue transglutaminase.
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