What is he best known for?
The fields of study he is best known for:
- Gene
- Immune system
- Cytokine
His scientific interests lie mostly in Chemokine receptor, Cell biology, Immunology, Chemokine and CCR1.
The concepts of his Chemokine receptor study are interwoven with issues in CXCR4 and Transplantation.
In his research, Compartmentalization and CXCL1 is intimately related to CXCL2, which falls under the overarching field of Cell biology.
His Immunology research integrates issues from Bleomycin and In vivo.
His work carried out in the field of Chemokine brings together such families of science as Endothelium and Plasma protein binding.
His studies in CCR1 integrate themes in fields like CC chemokine receptors, CCR10 and CCL7.
His most cited work include:
- International Union of Pharmacology. LXXXIX. Update on the Extended Family of Chemokine Receptors and Introducing a New Nomenclature for Atypical Chemokine Receptors (504 citations)
- The chemokine receptor D6 limits the inflammatory response in vivo (273 citations)
- CX3CL1/fractalkine is released from apoptotic lymphocytes to stimulate macrophage chemotaxis (265 citations)
What are the main themes of his work throughout his whole career to date?
The scientist’s investigation covers issues in Chemokine receptor, Chemokine, Immunology, Cell biology and Receptor.
His Chemokine research integrates issues from Lymphatic system, Lymphatic Endothelium and Leukocyte migration.
His Immunology research incorporates elements of Cancer research and Stem cell.
His Cell biology study incorporates themes from C-C chemokine receptor type 7, Stromal cell, XCL2 and Chemokine receptor CCR5.
His work on Ligand and Receptor expression is typically connected to Context as part of general Receptor study, connecting several disciplines of science.
His CCL21 research is multidisciplinary, incorporating perspectives in CC chemokine receptors and C-C chemokine receptor type 6.
He most often published in these fields:
- Chemokine receptor (45.73%)
- Chemokine (45.12%)
- Immunology (43.90%)
What were the highlights of his more recent work (between 2017-2021)?
- Chemokine receptor (45.73%)
- Chemokine (45.12%)
- Receptor (23.17%)
In recent papers he was focusing on the following fields of study:
His primary scientific interests are in Chemokine receptor, Chemokine, Receptor, Inflammation and Cell biology.
His work on CCL7 as part of general Chemokine receptor research is often related to Mammary gland, thus linking different fields of science.
In the field of Immune system and Immunology Gerard J. Graham studies Chemokine.
His Immunology research includes elements of Glycosaminoglycan and Function.
His Receptor research is mostly focused on the topic CCR1.
Gerard J. Graham has included themes like CXC chemokine receptors, Transplantation and In vivo in his Cell biology study.
Between 2017 and 2021, his most popular works were:
- Distinct Compartmentalization of the Chemokines CXCL1 and CXCL2 and the Atypical Receptor ACKR1 Determine Discrete Stages of Neutrophil Diapedesis (83 citations)
- Chemokines in depression in health and in inflammatory illness: a systematic review and meta-analysis (83 citations)
- Chemokine receptor redundancy and specificity are context dependent (35 citations)
In his most recent research, the most cited papers focused on:
- Gene
- Immune system
- Cytokine
Gerard J. Graham spends much of his time researching Chemokine, Receptor, Chemokine receptor, Cell biology and T cell.
His Receptor research is multidisciplinary, incorporating elements of Cancer research and Immunology.
His work carried out in the field of Immunology brings together such families of science as Glycosaminoglycan and Function.
The study incorporates disciplines such as CXC chemokine receptors and Immune system, Leukocyte migration in addition to Cell biology.
Gerard J. Graham interconnects Allotransplantation, Umbilical cord, In vivo and Pathology in the investigation of issues within T cell.
His work is dedicated to discovering how CCR1, Stromal cell are connected with CCL7 and other disciplines.
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