What is he best known for?
The fields of study he is best known for:
His primary areas of study are Biochemistry, Glutathione, Kinase, Cell biology and Glutathione S-transferase.
His Oxidative stress, Reactive oxygen species, Antioxidant, Signal transduction and Programmed cell death study are his primary interests in Biochemistry.
His Reactive oxygen species research integrates issues from Cell, Endogeny and Intracellular.
His biological study spans a wide range of topics, including Isozyme and Cysteine.
The various areas that he examines in his Glutathione S-transferase study include Molecular biology and Protein–protein interaction.
The concepts of his Enzyme study are interwoven with issues in Homeostasis and Mechanism of action.
His most cited work include:
- The importance of glutathione in human disease. (1333 citations)
- Regulation of JNK signaling by GSTp (977 citations)
- Trace elements in human physiology and pathology: zinc and metallothioneins. (902 citations)
What are the main themes of his work throughout his whole career to date?
His main research concerns Biochemistry, Glutathione, Molecular biology, Cell biology and Pharmacology.
His work on Biochemistry is being expanded to include thematically relevant topics such as Cell culture.
Kenneth D. Tew works mostly in the field of Glutathione, limiting it down to concerns involving Kinase and, occasionally, Signal transduction and Glutathione S-Transferase pi.
His research in Molecular biology intersects with topics in Gene expression, Gene, Blot, Transfection and Nuclear protein.
His work in Cell biology addresses subjects such as Cancer cell, which are connected to disciplines such as Cancer research.
His Pharmacology research includes themes of Cancer and Cell.
He most often published in these fields:
- Biochemistry (44.44%)
- Glutathione (38.15%)
- Molecular biology (20.37%)
What were the highlights of his more recent work (between 2012-2021)?
- Glutathione (38.15%)
- Biochemistry (44.44%)
- Cell biology (18.15%)
In recent papers he was focusing on the following fields of study:
The scientist’s investigation covers issues in Glutathione, Biochemistry, Cell biology, Cancer research and Reactive oxygen species.
His study of Glutathione S-transferase is a part of Glutathione.
As part of one scientific family, Kenneth D. Tew deals mainly with the area of Glutathione S-transferase, narrowing it down to issues related to the Molecular biology, and often Protein kinase B.
His study looks at the relationship between Cell biology and fields such as Zebrafish, as well as how they intersect with chemical problems.
His Cancer research research incorporates elements of Cancer cell, Cancer, Cancer stem cell, Lung and In vivo.
His work carried out in the field of Reactive oxygen species brings together such families of science as Apoptosis, Transcription factor, Pharmacology and Cytotoxicity.
Between 2012 and 2021, his most popular works were:
- Glutathione-Associated Enzymes In Anticancer Drug Resistance. (711 citations)
- Causes and Consequences of Cysteine S-Glutathionylation * (214 citations)
- Oxidative stress, redox regulation and diseases of cellular differentiation. (135 citations)
In his most recent research, the most cited papers focused on:
Kenneth D. Tew focuses on Biochemistry, Glutathione, Oxidative stress, Glutathione S-transferase and Cell biology.
His study involves Chaperone, Glutathione S-Transferase pi and Signal transduction, a branch of Biochemistry.
Kenneth D. Tew interconnects Lipid peroxidation, Isozyme, Cysteine and Transfection in the investigation of issues within Glutathione.
His study in Oxidative stress is interdisciplinary in nature, drawing from both Gastroenterology, Reactive oxygen species, Cerebrospinal fluid and Antioxidant.
As a part of the same scientific family, he mostly works in the field of Glutathione S-transferase, focusing on S-Glutathionylation and, on occasion, Mitochondrion, Glutaredoxin, Proteolysis and Peroxiredoxin.
His Cell biology research focuses on Cancer cell and how it relates to Carcinogenesis, AMPK and Cell cycle checkpoint.
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