What is he best known for?
The fields of study he is best known for:
- Gene
- Immune system
- Cytokine
Michael B. Brenner spends much of his time researching Antigen, Cell biology, T-cell receptor, Molecular biology and T cell.
His studies in Antigen integrate themes in fields like Biochemistry, Antigen presentation and Microbiology.
His Cell biology study incorporates themes from Receptor, Integrin, Autoimmune disease and Cell–cell interaction.
His work deals with themes such as Cell surface receptor, T lymphocyte, Monoclonal antibody and CD3, which intersect with T-cell receptor.
Michael B. Brenner has researched Molecular biology in several fields, including Beta, Protein subunit, CD8 and Virology.
Michael B. Brenner interconnects Cytotoxic T cell and Antibody in the investigation of issues within T cell.
His most cited work include:
- Adhesion between epithelial cells and T lymphocytes mediated by E-cadherin and the α E β 7 integrin (952 citations)
- CD1: antigen presentation and T cell function. (905 citations)
- Recognition of a lipid antigen by CD1-restricted αβ+ T cells (868 citations)
What are the main themes of his work throughout his whole career to date?
His main research concerns Cell biology, Antigen, Molecular biology, Immunology and T cell.
His Cell biology research is multidisciplinary, relying on both Cadherin, Cell, Cell adhesion, Natural killer T cell and Pathology.
His Antigen research incorporates elements of Cell culture, Biochemistry and Virology.
His research in Molecular biology intersects with topics in T lymphocyte, CD3, T-cell receptor and Antibody, Monoclonal antibody.
His studies in T-cell receptor integrate themes in fields like Receptor and Gene.
CD8 is closely connected to Cytotoxic T cell in his research, which is encompassed under the umbrella topic of T cell.
He most often published in these fields:
- Cell biology (38.55%)
- Antigen (31.33%)
- Molecular biology (27.71%)
What were the highlights of his more recent work (between 2013-2021)?
- Cell biology (38.55%)
- Immunology (25.78%)
- Immune system (17.11%)
In recent papers he was focusing on the following fields of study:
Cell biology, Immunology, Immune system, Cell and Inflammation are his primary areas of study.
His Cell biology research is multidisciplinary, relying on both Adipose tissue, T cell, Chemokine and Cytokine.
His research integrates issues of Antigen and CD11c in his study of T cell.
His work deals with themes such as Lupus nephritis and Disease, which intersect with Immunology.
His study looks at the intersection of Immune system and topics like Receptor with T-cell receptor.
His research investigates the connection between Cell and topics such as Mass cytometry that intersect with problems in Flow cytometry, Molecular biology and Effector.
Between 2013 and 2021, his most popular works were:
- Fast, sensitive and accurate integration of single-cell data with Harmony. (439 citations)
- Pathologically expanded peripheral T helper cell subset drives B cells in rheumatoid arthritis (361 citations)
- Defining inflammatory cell states in rheumatoid arthritis joint synovial tissues by integrating single-cell transcriptomics and mass cytometry. (229 citations)
In his most recent research, the most cited papers focused on:
- Gene
- Immune system
- Cytokine
His primary areas of study are Immune system, Immunology, Cell biology, Cancer research and Natural killer T cell.
His studies deal with areas such as Receptor and Cytotoxic T cell as well as Immune system.
His work focuses on many connections between Immunology and other disciplines, such as Lupus nephritis, that overlap with his field of interest in Acquired immune system, Systemic lupus erythematosus, CD11c, B cell and Autoimmunity.
His work carried out in the field of Cell biology brings together such families of science as Adipose tissue, Plasma membrane repair and Antigen.
His Natural killer T cell study combines topics from a wide range of disciplines, such as Interleukin 12, IL-2 receptor, T helper cell and CD40.
Michael B. Brenner has researched CD1D in several fields, including Major histocompatibility complex and Antigen presentation.
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