What is he best known for?
The fields of study he is best known for:
- Gene
- Immune system
- Cytokine
Reinhold Förster mostly deals with Immunology, Cell biology, C-C chemokine receptor type 7, Antigen and Immune system.
His research is interdisciplinary, bridging the disciplines of Cytotoxic T cell and Immunology.
His Cell biology research incorporates themes from CXCL13, CXCL16, CXCR5, CC chemokine receptors and Chemokine receptor.
His studies in C-C chemokine receptor type 7 integrate themes in fields like Molecular biology, Dendritic cell migration, CCL19 and CCL21.
His study in Antigen is interdisciplinary in nature, drawing from both Mesenteric lymph nodes and CD11c.
In Immune system, Reinhold Förster works on issues like Lymph, which are connected to Lymphocyte homing receptor.
His most cited work include:
- Two subsets of memory T lymphocytes with distinct homing potentials and effector functions (4882 citations)
- CCR7 coordinates the primary immune response by establishing functional microenvironments in secondary lymphoid organs. (2023 citations)
- CD40 ligand on activated platelets triggers an inflammatory reaction of endothelial cells (1760 citations)
What are the main themes of his work throughout his whole career to date?
Reinhold Förster focuses on Immunology, Cell biology, Immune system, C-C chemokine receptor type 7 and Chemokine receptor.
His Immunology study frequently draws connections between related disciplines such as Receptor.
His biological study spans a wide range of topics, including T cell, Cytotoxic T cell, CD40, Antigen-presenting cell and CC chemokine receptors.
His CC chemokine receptors research focuses on subjects like CXCL16, which are linked to CXCL13.
His Immune system research incorporates elements of Inflammation, Transplantation, Lymphocyte and Lymph.
Reinhold Förster has included themes like Cancer research, CCL19 and CCL21 in his C-C chemokine receptor type 7 study.
He most often published in these fields:
- Immunology (59.39%)
- Cell biology (37.55%)
- Immune system (26.05%)
What were the highlights of his more recent work (between 2015-2021)?
- Immunology (59.39%)
- Immune system (26.05%)
- Cell biology (37.55%)
In recent papers he was focusing on the following fields of study:
Immunology, Immune system, Cell biology, Chemokine receptor and T cell are his primary areas of study.
His research in Immunology is mostly focused on Antibody.
His Immune system research is multidisciplinary, incorporating perspectives in Inflammation, Receptor, Stromal cell and Cytokine.
His Cell biology study combines topics in areas such as Cell, C-C chemokine receptor type 7 and Lymph.
The concepts of his C-C chemokine receptor type 7 study are interwoven with issues in Dendritic cell and Lymphatic system.
The T cell study combines topics in areas such as RAR-related orphan receptor gamma, Germinal center and Antigen.
Between 2015 and 2021, his most popular works were:
- Dendritic cell migration in health and disease. (278 citations)
- Human γδ T cells are quickly reconstituted after stem-cell transplantation and show adaptive clonal expansion in response to viral infection. (131 citations)
- In Vivo Killing Capacity of Cytotoxic T Cells Is Limited and Involves Dynamic Interactions and T Cell Cooperativity (125 citations)
In his most recent research, the most cited papers focused on:
- Gene
- Immune system
- Cytokine
His main research concerns Immunology, Immune system, T cell, Cell biology and Antigen.
As part of his studies on Immunology, Reinhold Förster often connects relevant areas like Function.
His work carried out in the field of Immune system brings together such families of science as Young adult, Lymphatic system, Biomarker and Lymph.
His work in T cell tackles topics such as Inflammation which are related to areas like RAR-related orphan receptor gamma, Molecular biology and CD3.
His Cell biology research is multidisciplinary, relying on both Receptor, Cell, INKT Cells and Candidate gene.
His Antigen study combines topics from a wide range of disciplines, such as Gene rearrangement, Interleukin 17, Stem cell and T-cell receptor.
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