What is he best known for?
The fields of study he is best known for:
His primary areas of study are Cell biology, Immunology, Innate immune system, Biochemistry and Receptor.
Felix Randow interconnects Xenophagy, Ubiquitin and Binding site in the investigation of issues within Cell biology.
His work carried out in the field of Immunology brings together such families of science as IL-2 receptor, CD40 and Antigen-presenting cell.
The various areas that he examines in his Innate immune system study include Cell surface receptor, Endoplasmic reticulum, Chaperone and Transfection.
Felix Randow has included themes like Mediator and BAG3 in his Biochemistry study.
His work in the fields of Receptor, such as CD36, intersects with other areas such as Scavenger receptor.
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 (3rd edition) (4170 citations)
- Monocyte deactivation in septic patients: restoration by IFN-gamma treatment. (995 citations)
What are the main themes of his work throughout his whole career to date?
His primary areas of investigation include Cell biology, Ubiquitin, Biochemistry, Cytosol and Receptor.
Felix Randow has researched Cell biology in several fields, including Innate immune system and BAG3.
His BAG3 research integrates issues from ATG8, Plasma protein binding and ATG16L1.
His studies deal with areas such as Effector and Bacteria as well as Ubiquitin.
His Stable isotope labeling by amino acids in cell culture and Signal transduction study in the realm of Biochemistry interacts with subjects such as Membrane protein.
His work deals with themes such as Selective autophagy and Dead cell, which intersect with Receptor.
He most often published in these fields:
- Cell biology (95.06%)
- Ubiquitin (35.80%)
- Biochemistry (34.57%)
What were the highlights of his more recent work (between 2017-2021)?
- Cell biology (95.06%)
- Cytosol (33.33%)
- Receptor (22.22%)
In recent papers he was focusing on the following fields of study:
Felix Randow mainly investigates Cell biology, Cytosol, Receptor, Vacuole and Bacteria.
His work in the fields of Cell biology, such as PI3K/AKT/mTOR pathway, overlaps with other areas such as ULK1.
His ULK1 investigation overlaps with other areas such as Mitophagy, Lysosome, Autophagosome, Autophagy-related protein 13 and PINK1.
His study in Receptor is interdisciplinary in nature, drawing from both Immunology, Galectin-8, Kinase and Dead cell.
His Bacteria study combines topics in areas such as Lipopolysaccharide and Ubiquitin.
The Ubiquitin study which covers Colony-forming unit that intersects with Galectin.
Between 2017 and 2021, his most popular works were:
- Spatiotemporal Control of ULK1 Activation by NDP52 and TBK1 during Selective Autophagy (131 citations)
- Spatiotemporal Control of ULK1 Activation by NDP52 and TBK1 during Selective Autophagy (131 citations)
- The Cargo Receptor NDP52 Initiates Selective Autophagy by Recruiting the ULK Complex to Cytosol-Invading Bacteria (105 citations)
In his most recent research, the most cited papers focused on:
Felix Randow spends much of his time researching Cell biology, Cytosol, ULK1, Binding site and Kinase.
His studies link Pyroptosis with Cell biology.
His Pyroptosis study integrates concerns from other disciplines, such as Intracellular parasite, Bacteria, Lipopolysaccharide and Caspase, Caspase 4.
Felix Randow incorporates Intracellular parasite and Shigella flexneri in his studies.
ULK1 is connected with Mitophagy, Autophagosome, PI3K/AKT/mTOR pathway, PINK1 and Autophagy-related protein 13 in his study.
The Binding site study combines topics in areas such as Receptor, Galectin-8 and Xenophagy.
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