What is he best known for?
The fields of study he is best known for:
His main research concerns Biochemistry, Mucosal associated invariant T cell, Peptide, Antigen and Immunology.
Proteases, Protease, In vitro, Enzyme and Receptor are subfields of Biochemistry in which his conducts study.
His Peptide study integrates concerns from other disciplines, such as Protein structure, Helix and Stereochemistry.
His Stereochemistry study combines topics from a wide range of disciplines, such as Cyclic peptide, Amyloid beta and Protein secondary structure.
He has researched Antigen in several fields, including T cell and Immune system.
His research integrates issues of Cancer research, Pharmacology and Ischemia in his study of Immunology.
His most cited work include:
- The Future of Peptide‐based Drugs (966 citations)
- MR1 presents microbial vitamin B metabolites to MAIT cells (790 citations)
- Protease inhibitors: current status and future prospects. (671 citations)
What are the main themes of his work throughout his whole career to date?
His primary areas of study are Stereochemistry, Biochemistry, Peptide, Receptor and Pharmacology.
His studies in Stereochemistry integrate themes in fields like Cyclic peptide, Peptidomimetic and Amide.
His work is connected to Protease, Enzyme, Proteases, Small molecule and Histone deacetylase, as a part of Biochemistry.
His Peptide study combines topics in areas such as Amino acid, Crystallography, Alpha helix, Helix and Turn.
His Receptor study frequently intersects with other fields, such as C5a receptor.
The study incorporates disciplines such as Antagonist and Immunology in addition to Pharmacology.
He most often published in these fields:
- Stereochemistry (23.68%)
- Biochemistry (22.85%)
- Peptide (15.40%)
What were the highlights of his more recent work (between 2014-2021)?
- Cell biology (9.77%)
- Mucosal associated invariant T cell (6.79%)
- Immunology (10.93%)
In recent papers he was focusing on the following fields of study:
David P. Fairlie focuses on Cell biology, Mucosal associated invariant T cell, Immunology, Antigen and Biochemistry.
Proteases, Kidney and Endocrinology is closely connected to Protease-activated receptor 2 in his research, which is encompassed under the umbrella topic of Cell biology.
His Mucosal associated invariant T cell research focuses on subjects like Cell activation, which are linked to Interleukin 23.
His study looks at the relationship between Antigen and fields such as T cell, as well as how they intersect with chemical problems.
His Biochemistry and Agonist, Peptide, Amino acid, Receptor and Virtual screening investigations all form part of his Biochemistry research activities.
His Peptide study incorporates themes from Alpha helix, Plasma protein binding and Stereochemistry.
Between 2014 and 2021, his most popular works were:
- Identification of phenotypically and functionally heterogeneous mouse mucosal-associated invariant t cells using MR1 tetramers (201 citations)
- A three-stage intrathymic development pathway for the mucosal-associated invariant T cell lineage (169 citations)
- Human mucosal-associated invariant T cells contribute to antiviral influenza immunity via IL-18-dependent activation. (151 citations)
In his most recent research, the most cited papers focused on:
David P. Fairlie mostly deals with Mucosal associated invariant T cell, Antigen, Immunology, Cell biology and T cell.
His Mucosal associated invariant T cell research incorporates themes from Cell activation, Cell, Interleukin 17, Interferon gamma and Interleukin 12.
The Antigen study combines topics in areas such as Receptor, Biochemistry and T-cell receptor.
His studies deal with areas such as Histone deacetylase, Histone and In vivo as well as Immunology.
His Cell biology research includes themes of Minor histocompatibility antigen, Antigen processing, Antigen presentation and Jurkat cells.
His work in T cell covers topics such as Molecular biology which are related to areas like Pulmonary fibrosis, Western blot and CD8.
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