2010 - Distinguished Service Award, Clinical Immunology Society
2007 - Fellow of the American Association for the Advancement of Science (AAAS)
Member of the Association of American Physicians
His primary scientific interests are in Immunology, Molecular biology, T cell, Lupus erythematosus and Immune system. George C. Tsokos has included themes like Systemic lupus erythematosus and Lupus nephritis in his Immunology study. His work carried out in the field of Molecular biology brings together such families of science as Chromatin immunoprecipitation, Interleukin 2, Receptor, Transcription and CAMP-Responsive Element Modulator.
His biological study deals with issues like B cell, which deal with fields such as Immunoglobulin M. George C. Tsokos focuses mostly in the field of Lupus erythematosus, narrowing it down to matters related to Epigenetics and, in some cases, Histone and Regulation of gene expression. He works mostly in the field of Immune system, limiting it down to topics relating to Antigen and, in certain cases, Cell signaling, as a part of the same area of interest.
The scientist’s investigation covers issues in Immunology, Molecular biology, Immune system, T cell and Lupus erythematosus. His study explores the link between Immunology and topics such as Systemic lupus erythematosus that cross with problems in Lupus nephritis. In his research, Tyrosine phosphorylation and CD3 is intimately related to T-cell receptor, which falls under the overarching field of Molecular biology.
His Immune system study integrates concerns from other disciplines, such as Inflammation, Disease, Cytokine and Antigen. The T cell study combines topics in areas such as Cytotoxic T cell, Cancer research, CD8 and Cell biology. His research integrates issues of Internal medicine, Connective tissue disease and Endocrinology in his study of Lupus erythematosus.
Immunology, Autoimmunity, Immune system, T cell and Systemic lupus erythematosus are his primary areas of study. His Immunology research focuses on Disease and how it connects with Diarrhea. His research in Autoimmunity intersects with topics in Cancer research, Spleen, Peripheral blood mononuclear cell, Cell biology and Anti-SSA/Ro autoantibodies.
His work deals with themes such as Inflammation, Lupus nephritis, Signal transduction and Interferon, which intersect with Immune system. His biological study spans a wide range of topics, including Cytokine, CD8, Antigen, Molecular biology and Cytotoxic T cell. His Systemic lupus erythematosus study is focused on Internal medicine in general.
Immunology, Autoimmunity, Immune system, Lupus erythematosus and T cell are his primary areas of study. His is doing research in Autoantibody, Pathogenesis, Immune tolerance, Antigen and Interleukin 17, both of which are found in Immunology. His Autoimmunity study combines topics from a wide range of disciplines, such as Cancer research, Cellular differentiation, Autoimmune disease, Systemic lupus erythematosus and PI3K/AKT/mTOR pathway.
His Immune system research is multidisciplinary, incorporating elements of Inflammation, Signal transduction, Disease and Epigenetics. He interconnects Cytotoxic T cell, Lupus nephritis and Molecular biology in the investigation of issues within T cell. His work in Cytotoxic T cell addresses issues such as CD8, which are connected to fields such as T-cell receptor.
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.
Systemic Lupus Erythematosus
George C. Tsokos.
The New England Journal of Medicine (2011)
Heat Shock Protein 70 kDa ☆: Molecular Biology, Biochemistry, and Physiology
Juliann G. Kiang;George C. Tsokos.
Pharmacology & Therapeutics (1998)
Expanded Double Negative T Cells in Patients with Systemic Lupus Erythematosus Produce IL-17 and Infiltrate the Kidneys
José C. Crispín;Mohammed Oukka;George Bayliss;Robert A. Cohen.
Journal of Immunology (2008)
T cell receptor alpha/beta expressing double-negative (CD4-/CD8-) and CD4+ T helper cells in humans augment the production of pathogenic anti-DNA autoantibodies associated with lupus nephritis.
S Shivakumar;G C Tsokos;S K Datta.
Journal of Immunology (1989)
New insights into the immunopathogenesis of systemic lupus erythematosus
George C. Tsokos;Mindy S. Lo;Patricia Costa Reis;Kathleen E. Sullivan.
Nature Reviews Rheumatology (2016)
Altered pattern of TCR/CD3-mediated protein-tyrosyl phosphorylation in T cells from patients with systemic lupus erythematosus. Deficient expression of the T cell receptor zeta chain.
S.-N. C. Liossis;X. Z. Ding;G. J. Dennis;G. C. Tsokos.
Journal of Clinical Investigation (1998)
Pathogenesis of human systemic lupus erythematosus: recent advances
José C. Crispín;Stamatis-Nick C. Liossis;Katalin Kis-Toth;Linda A. Lieberman.
Trends in Molecular Medicine (2010)
The Role of IL-23/IL-17 Axis in Lupus Nephritis
Zheng Zhang;Vasileios C. Kyttaris;George C. Tsokos.
Journal of Immunology (2009)
Pathogenic anti-DNA autoantibody-inducing T helper cell lines from patients with active lupus nephritis: isolation of CD4-8- T helper cell lines that express the gamma delta T-cell antigen receptor.
Sumati Rajagopalan;Tracy Zordan;George C. Tsokos;Syamal K. Datta.
Proceedings of the National Academy of Sciences of the United States of America (1990)
B CELLS FROM PATIENTS WITH SYSTEMIC LUPUS ERYTHEMATOSUS DISPLAY ABNORMAL ANTIGEN RECEPTOR-MEDIATED EARLY SIGNAL TRANSDUCTION EVENTS
S.-N. C. Liossis;B. Kovacs;G. Dennis;G. M. Kammer.
Journal of Clinical Investigation (1996)
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