What is she best known for?
The fields of study she is best known for:
Biochemistry, Peroxiredoxin, Sulfiredoxin, Peroxidase and Tyrosine phosphorylation are her primary areas of study.
Her work on Biochemistry is being expanded to include thematically relevant topics such as Cell biology.
Her research investigates the connection between Peroxiredoxin and topics such as Molecular biology that intersect with problems in Phosphatidylinositol and Peptide sequence.
Her studies deal with areas such as Peroxiredoxin III and Cysteine as well as Sulfiredoxin.
Her Tyrosine phosphorylation research includes themes of Epidermal growth factor and Receptor tyrosine kinase.
Her work carried out in the field of Phospholipase C brings together such families of science as Isozyme and Inositol.
Her most cited work include:
- Peroxiredoxins: a historical overview and speculative preview of novel mechanisms and emerging concepts in cell signaling. (1163 citations)
- Epidermal Growth Factor (EGF)-induced Generation of Hydrogen Peroxide ROLE IN EGF RECEPTOR-MEDIATED TYROSINE PHOSPHORYLATION (1054 citations)
- Reversible Inactivation of Protein-tyrosine Phosphatase 1B in A431 Cells Stimulated with Epidermal Growth Factor (855 citations)
What are the main themes of her work throughout her whole career to date?
Her primary areas of study are Biochemistry, Molecular biology, Phospholipase C, Cell biology and Peroxiredoxin.
Her Cysteine, Enzyme, Sulfiredoxin, Thioredoxin and Peroxidase investigations are all subjects of Biochemistry research.
She studied Sulfiredoxin and Peroxiredoxin III that intersect with PRDX3.
She works mostly in the field of Molecular biology, limiting it down to concerns involving Peptide sequence and, occasionally, Amino acid.
Her study focuses on the intersection of Phospholipase C and fields such as Inositol with connections in the field of Endocrinology.
The various areas that Sue Goo Rhee examines in her Peroxiredoxin study include Binding site and Cytosol.
She most often published in these fields:
- Biochemistry (66.19%)
- Molecular biology (34.76%)
- Phospholipase C (34.29%)
What were the highlights of her more recent work (between 2004-2020)?
- Biochemistry (66.19%)
- Sulfiredoxin (17.14%)
- Peroxiredoxin (21.43%)
In recent papers she was focusing on the following fields of study:
Sue Goo Rhee mainly focuses on Biochemistry, Sulfiredoxin, Peroxiredoxin, Cell biology and Cysteine.
Her Biochemistry study frequently links to related topics such as Stereochemistry.
Her biological study spans a wide range of topics, including Combinatorial chemistry, Peroxiredoxin III, In vitro and Cysteine sulfinic acid.
Her Peroxiredoxin research is multidisciplinary, incorporating elements of NADPH oxidase, Catalase, Cytosol, Molecular biology and Phosphorylation.
Her Phosphorylation study combines topics from a wide range of disciplines, such as Phospholipase C and Binding site.
Sue Goo Rhee interconnects Oxidative stress and Downregulation and upregulation in the investigation of issues within Cell biology.
Between 2004 and 2020, her most popular works were:
- Peroxiredoxins: a historical overview and speculative preview of novel mechanisms and emerging concepts in cell signaling. (1163 citations)
- Intracellular messenger function of hydrogen peroxide and its regulation by peroxiredoxins (607 citations)
- Regulation of PDGF signalling and vascular remodelling by peroxiredoxin II (356 citations)
In her most recent research, the most cited papers focused on:
Sue Goo Rhee spends much of her time researching Biochemistry, Sulfiredoxin, Peroxiredoxin, Cysteine and Cysteine sulfinic acid.
In most of her Biochemistry studies, her work intersects topics such as Stereochemistry.
While the research belongs to areas of Peroxiredoxin, Sue Goo Rhee spends her time largely on the problem of Protein tyrosine phosphatase, intersecting her research to questions surrounding Cytosol, Hydrogen peroxide, Platelet-derived growth factor and Endocrinology.
As a part of the same scientific study, Sue Goo Rhee usually deals with the Cysteine, concentrating on Intracellular and frequently concerns with Active site, Centrosome, Mitochondrion, Effector and Phosphatase.
Her work is dedicated to discovering how Cysteine sulfinic acid, Thioredoxin are connected with Dithiothreitol, Glutathione, PRDX3 and Peroxiredoxin 1 and other disciplines.
Her study in Phosphorylation is interdisciplinary in nature, drawing from both Phospholipase and Binding site.
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