What is he best known for?
The fields of study he is best known for:
- Gene
- Immune system
- Antibody
His primary areas of investigation include Immunology, Cell biology, Molecular biology, IL-2 receptor and Cytotoxic T cell.
His Immunology research includes elements of Genetically modified mouse and Transgene.
His Cell biology research includes themes of Regulatory T cell, Receptor and MHC class II.
Andrew J. Caton has included themes like Hemagglutinin, B cell, Antibody, Immunoglobulin heavy chain and Polymerase chain reaction in his Molecular biology study.
His studies in Cytotoxic T cell integrate themes in fields like T cell and CD8.
His T-cell receptor course of study focuses on Antigen and Virology.
His most cited work include:
- Thymic selection of CD4+CD25+ regulatory T cells induced by an agonist self-peptide. (1497 citations)
- The antigenic structure of the influenza virus A/PR/8/34 hemagglutinin (H1 subtype). (824 citations)
- Major Histocompatibility Complex Class II–Positive Cortical Epithelium Mediates the Selection of Cd4+25+ Immunoregulatory T Cells (386 citations)
What are the main themes of his work throughout his whole career to date?
His scientific interests lie mostly in Immunology, Cell biology, T-cell receptor, Molecular biology and Antigen.
As a part of the same scientific study, he usually deals with the Immunology, concentrating on Cytotoxic T cell and frequently concerns with CD8.
His studies deal with areas such as Central tolerance and Antigen presentation as well as Cell biology.
The study incorporates disciplines such as Receptor, Thymocyte, Major histocompatibility complex and FOXP3 in addition to T-cell receptor.
His work deals with themes such as Transgene, Immunoglobulin heavy chain, Hemagglutinin, Gene and Antibody, which intersect with Molecular biology.
The concepts of his Antigen study are interwoven with issues in Adoptive cell transfer and Virology.
He most often published in these fields:
- Immunology (52.99%)
- Cell biology (28.21%)
- T-cell receptor (27.35%)
What were the highlights of his more recent work (between 2010-2020)?
- Immunology (52.99%)
- Cell biology (28.21%)
- T-cell receptor (27.35%)
In recent papers he was focusing on the following fields of study:
His primary areas of study are Immunology, Cell biology, T-cell receptor, Immune system and FOXP3.
As part of his studies on Immunology, he often connects relevant subjects like Receptor.
His research investigates the connection between Cell biology and topics such as Antigen presentation that intersect with problems in Cellular differentiation.
Andrew J. Caton interconnects Cytotoxic T cell and Thymocyte in the investigation of issues within T-cell receptor.
His Immune system research is multidisciplinary, incorporating perspectives in Influenza A virus, Antigen and Virology.
His FOXP3 research incorporates themes from Regulatory T cell, IL-2 receptor and Major histocompatibility complex.
Between 2010 and 2020, his most popular works were:
- Viral Antigen Induces Differentiation of Foxp3 + Natural Regulatory T Cells in Influenza Virus–Infected Mice (50 citations)
- Protective antiviral antibody responses in a mouse model of influenza virus infection require TACI (49 citations)
- The role of T-cell receptor recognition of peptide:MHC complexes in the formation and activity of Foxp3⁺ regulatory T cells. (44 citations)
In his most recent research, the most cited papers focused on:
- Gene
- Immune system
- Antibody
Andrew J. Caton focuses on Immunology, T-cell receptor, Immune system, FOXP3 and Virus.
His work carried out in the field of Immunology brings together such families of science as Receptor and Virology.
His Influenza A virus study in the realm of Virology connects with subjects such as Respiratory tract infections.
His work deals with themes such as Cell and Cell biology, which intersect with T-cell receptor.
His work on Effector as part of his general Cell biology study is frequently connected to Repertoire, thereby bridging the divide between different branches of science.
His Virus study combines topics in areas such as CD8, Antigen, Adoptive cell transfer and B cell.
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