His primary scientific interests are in Immunology, T lymphocyte, Cell biology, Cytotoxic T cell and Interleukin 2. His Immunology study combines topics from a wide range of disciplines, such as Haematopoiesis and Stem cell. His T lymphocyte study frequently involves adjacent topics like Molecular biology.
Rhodri Ceredig works mostly in the field of Molecular biology, limiting it down to topics relating to Interleukin and, in certain cases, Monoclonal antibody, as a part of the same area of interest. His work carried out in the field of Cell biology brings together such families of science as Natural killer T cell, Cell, Thymocyte and Cellular differentiation. The study incorporates disciplines such as C57BL/6, T cell, Antigen and Cutaneous leishmaniasis in addition to Cytotoxic T cell.
The scientist’s investigation covers issues in Immunology, Molecular biology, Cell biology, Cellular differentiation and T cell. He has researched Immunology in several fields, including Cytotoxic T cell, In vitro and Haematopoiesis. Rhodri Ceredig has included themes like Endocrinology, T lymphocyte, Antigen, Thymocyte and Interleukin 2 in his Molecular biology study.
The concepts of his Thymocyte study are interwoven with issues in Internal medicine and Lymphocyte. His Interleukin 2 research incorporates themes from Interleukin and Lymphokine. His work in Cell biology addresses issues such as T-cell receptor, which are connected to fields such as Receptor.
Rhodri Ceredig focuses on Haematopoiesis, Progenitor cell, Immunology, Stem cell and Mesenchymal stem cell. His Haematopoiesis research is included under the broader classification of Cell biology. His Progenitor cell research is multidisciplinary, incorporating elements of Myeloid and Bone marrow.
His work on Immunosuppression as part of general Immunology research is frequently linked to INT, thereby connecting diverse disciplines of science. Rhodri Ceredig studied Stem cell and Stromal cell that intersect with Pro-B-Cells, B cell and Transplantation. His Mesenchymal stem cell research includes elements of Molecular biology, Flow cytometry and Potency.
His scientific interests lie mostly in Haematopoiesis, Progenitor cell, Immune system, Cell biology and Bone marrow. His Haematopoiesis study frequently draws connections between adjacent fields such as Molecular biology. His Progenitor cell research is multidisciplinary, relying on both Myeloid, Transcriptome, RNA and CD19.
His studies in Cell biology integrate themes in fields like Phenotype, Immunological synapse, Glycosylation, CD8 and Epigenetics. In Bone marrow, he works on issues like Transcription factor, which are connected to Mesenchymal stem cell. His Mesenchymal stem cell research incorporates elements of Inflammation, Immunosuppression, Chemokine, Immunology and Immunity.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Expression of interleukin-2 receptors as a differentiation marker on intrathymic stem cells.
R Ceredig;J W Lowenthal;M Nabholz;H R MacDonald.
Mesenchymal stem cell effects on T-cell effector pathways
Michelle M Duffy;Thomas Ritter;Rhodri Ceredig;Matthew D Griffin.
Stem Cell Research & Therapy (2011)
Homeostasis of V alpha 14i NKT cells.
Jennifer L. Matsuda;Laurent Gapin;Stéphane Sidobre;William C. Kieper.
Nature Immunology (2002)
Overexpression of Interleukin (IL)-7 Leads to IL-15–independent Generation of Memory Phenotype CD8+ T Cells
William C. Kieper;Joyce T. Tan;Brea Bondi-Boyd;Laurent Gapin.
Journal of Experimental Medicine (2002)
Cells mediating graft rejection in the mouse. I. Lyt-1 cells mediate skin graft rejection.
Bruce Edward Loveland;P. M. Hogarth;R. Ceredig;I. F. C. McKenzie.
Journal of Experimental Medicine (1981)
Precursors of T cell growth factor producing cells in the thymus: ontogeny, frequency, and quantitative recovery in a subpopulation of phenotypically mature thymocytes defined by monoclonal antibody GK-1.5.
R Ceredig;D P Dialynas;F W Fitch;H R MacDonald.
Journal of Experimental Medicine (1983)
Therapeutic effect of anti-L3T4 monoclonal antibody GK1.5 on cutaneous leishmaniasis in genetically-susceptible BALB/c mice.
R G Titus;R Ceredig;J C Cerottini;J A Louis.
Journal of Immunology (1985)
Murine cutaneous leishmaniasis: disease patterns in intact and nude mice of various genotypes and examination of some differences between normal and infected macrophages
Emanuela Handman;Rhodri Ceredig;Graham F Mitchell.
Immunology and Cell Biology (1979)
Bone marrow mesenchymal stromal cells (BM-MSCs) from healthy donors and auto-immune disease patients reduce the proliferation of autologous- and allogeneic-stimulated lymphocytes in vitro
Ciara Bocelli-Tyndall;L. Bracci;G. Spagnoli;A. Braccini.
Mesenchymal stem cell inhibition of T-helper 17 cell- differentiation is triggered by cell-cell contact and mediated by prostaglandin E2 via the EP4 receptor
Michelle M. Duffy;Jana Pindjakova;Shirley A. Hanley;Cathal McCarthy.
European Journal of Immunology (2011)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below: