What is he best known for?
The fields of study he is best known for:
- Gene
- Immune system
- Antibody
John J. Miles spends much of his time researching T-cell receptor, Antigen, Immunology, T cell and Major histocompatibility complex.
In most of his Antigen studies, his work intersects topics such as Receptor.
His Immune system, Vaccination and Adjuvant study in the realm of Immunology interacts with subjects such as Repertoire.
Mucosal associated invariant T cell is the focus of his T cell research.
His work carried out in the field of Major histocompatibility complex brings together such families of science as CD8 and Cell biology.
His CD8 research focuses on Epitope and how it relates to Human leukocyte antigen, Molecular biology, Mononucleosis, Seroconversion and Tetanus.
His most cited work include:
- Immune self-reactivity triggered by drug-modified HLA-peptide repertoire (469 citations)
- Immune self-reactivity triggered by drug-modified HLA-peptide repertoire (469 citations)
- T Cell Antigen Receptor Recognition of Antigen-Presenting Molecules (367 citations)
What are the main themes of his work throughout his whole career to date?
John J. Miles mostly deals with T-cell receptor, T cell, Immunology, Antigen and Major histocompatibility complex.
His T-cell receptor study combines topics in areas such as Molecular biology, Human leukocyte antigen, CD8 and Cell biology.
His T cell research includes elements of MHC class I, Gene and Stem cell.
The Antigen study combines topics in areas such as Receptor and Computational biology.
His studies in Major histocompatibility complex integrate themes in fields like T-Cell Antigen Receptor Specificity, Acquired immune system and Plasma protein binding.
His Epitope research focuses on subjects like Virology, which are linked to Mutation.
He most often published in these fields:
- T-cell receptor (96.96%)
- T cell (78.26%)
- Immunology (69.57%)
What were the highlights of his more recent work (between 2017-2021)?
- Immune system (53.91%)
- Cancer research (15.22%)
- T-cell receptor (96.96%)
In recent papers he was focusing on the following fields of study:
The scientist’s investigation covers issues in Immune system, Cancer research, T-cell receptor, T cell and Immunology.
His research in Immune system intersects with topics in Epitope, Antigen, Ex vivo and Cytokine.
His T-cell receptor research is multidisciplinary, incorporating elements of Receptor, Ligand, Cell biology, Computational biology and Major histocompatibility complex.
The concepts of his Major histocompatibility complex study are interwoven with issues in Amino acid and Peptide.
His study in T cell is interdisciplinary in nature, drawing from both UniProt, Proteomics, Quantitative proteomics, Genomics and PeptideAtlas.
His research integrates issues of Phenotype, Hypoestrogenism and Pectus excavatum in his study of Immunology.
Between 2017 and 2021, his most popular works were:
- T cell autoreactivity directed toward CD1c itself rather than toward carried self lipids. (28 citations)
- The Rise of Non-Tuberculosis Mycobacterial Lung Disease (23 citations)
- The Rise of Non-Tuberculosis Mycobacterial Lung Disease (23 citations)
In his most recent research, the most cited papers focused on:
- Gene
- Immune system
- Antibody
His primary areas of study are Cancer research, Cell cycle, Major histocompatibility complex, Immune system and Programmed cell death.
His Cancer research research includes themes of Foreskin, Infectious disease, Immune checkpoint, Phenotype and CD8.
John J. Miles has researched Major histocompatibility complex in several fields, including Epitope, T cell and Influenza A virus.
John J. Miles combines subjects such as Priming, Autologous transplantation, Multiple myeloma and Immunotherapy with his study of T cell.
The study incorporates disciplines such as Ex vivo, Colitis, Inflammatory bowel disease, Ancylostoma caninum and Ancylostoma in addition to Immune system.
The various areas that John J. Miles examines in his Antigen study include Receptor, Cell biology, Antigen presentation and T-cell receptor.
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