What is he best known for?
The fields of study he is best known for:
Shiro Bannai mainly focuses on Biochemistry, Cystine, Glutathione, Cysteine and Glutamate receptor.
His study of Complementary DNA is a part of Biochemistry.
The concepts of his Cystine study are interwoven with issues in Amino acid and Cell biology.
His work carried out in the field of Glutathione brings together such families of science as Oxidative stress, Cell culture, Transfection, SLC7A11 and Intracellular.
His Oxidative stress research includes elements of Reactive oxygen species, Peroxiredoxin, Transcription factor and Oxidative phosphorylation.
His Cysteine study combines topics from a wide range of disciplines, such as Serine, Lipopolysaccharide, Alanine, Neutral amino acid transport and Stimulation.
His most cited work include:
- Transcription Factor Nrf2 Coordinately Regulates a Group of Oxidative Stress-inducible Genes in Macrophages (1184 citations)
- Cloning and Expression of a Plasma Membrane Cystine/Glutamate Exchange Transporter Composed of Two Distinct Proteins (656 citations)
- Maintenance of neuronal glutathione by glial cells. (376 citations)
What are the main themes of his work throughout his whole career to date?
His primary areas of investigation include Biochemistry, Cystine, Glutathione, Oxidative stress and Molecular biology.
His study in the field of Cysteine, Amino acid and Antioxidant is also linked to topics like Membrane transport.
The Cystine study combines topics in areas such as In vitro, Glutamate receptor, Intracellular, Cell biology and Glutamic acid.
His Glutathione research is multidisciplinary, incorporating elements of Endocrinology, Extracellular, Internal medicine, Hydrogen peroxide and Vitamin E.
His research integrates issues of In vivo, Peroxiredoxin and Heme oxygenase in his study of Oxidative stress.
He has included themes like Tumor necrosis factor alpha, Signal transduction and Ploidy in his Molecular biology study.
He most often published in these fields:
- Biochemistry (74.49%)
- Cystine (44.90%)
- Glutathione (36.73%)
What were the highlights of his more recent work (between 2000-2010)?
- Biochemistry (74.49%)
- Cystine (44.90%)
- Glutathione (36.73%)
In recent papers he was focusing on the following fields of study:
His primary scientific interests are in Biochemistry, Cystine, Glutathione, Cell biology and Oxidative stress.
His work on Molecular biology expands to the thematically related Biochemistry.
His Cystine research is included under the broader classification of Cysteine.
His work in Cysteine addresses issues such as Glutamate receptor, which are connected to fields such as In situ hybridization, Area postrema and Neurotransmitter.
Within one scientific family, Shiro Bannai focuses on topics pertaining to Transfection under Glutathione, and may sometimes address concerns connected to Cytotoxicity.
His work carried out in the field of Oxidative stress brings together such families of science as Lipopolysaccharide, Antioxidant and In vivo.
Between 2000 and 2010, his most popular works were:
- Electrophile response element-mediated induction of the cystine/glutamate exchange transporter gene expression. (348 citations)
- Redox Imbalance in Cystine/Glutamate Transporter-deficient Mice (273 citations)
- The cystine/cysteine cycle: a redox cycle regulating susceptibility versus resistance to cell death. (160 citations)
In his most recent research, the most cited papers focused on:
Shiro Bannai mainly investigates Biochemistry, Cystine, Cell biology, Glutathione and Cysteine.
His Glutathione research includes elements of SLC7A11, Intracellular and Transfection.
The various areas that he examines in his SLC7A11 study include Luciferase, Mutant, Sequence analysis and Transcriptional regulation.
His biological study spans a wide range of topics, including Oxidative stress, Efflux and Hydrogen peroxide.
The concepts of his Cysteine study are interwoven with issues in Glutamate receptor, Molecular biology and Programmed cell death.
His study in Glutamate receptor is interdisciplinary in nature, drawing from both Area postrema, Circumventricular organs, In situ hybridization and System X.
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