Gerhard J. Zlabinger mostly deals with Cell biology, T cell, Cytokine, Immunology and Immune system. The concepts of his Cell biology study are interwoven with issues in Jurkat cells, Dendritic cell, Biochemistry and Polyunsaturated fatty acid. His T cell research is multidisciplinary, relying on both Molecular biology, Signal transduction and Cell growth.
His study in Cytokine is interdisciplinary in nature, drawing from both Myeloid, Receptor and MHC class II. Gerhard J. Zlabinger has included themes like Adipose tissue macrophages and Adipose tissue in his Immunology study. As part of the same scientific family, Gerhard J. Zlabinger usually focuses on Immune system, concentrating on Proinflammatory cytokine and intersecting with Microbiology, Interleukin 10, Serum Amyloid A Protein and Uremia.
Immunology, Cell biology, T cell, Immune system and Cytokine are his primary areas of study. The Immunology study combines topics in areas such as In vitro and Transplantation. His biological study spans a wide range of topics, including Antigen-presenting cell, Dendritic cell, CD28, Receptor and T-cell receptor.
His study looks at the intersection of T cell and topics like Molecular biology with Complement system. His study focuses on the intersection of Immune system and fields such as Proinflammatory cytokine with connections in the field of Cancer research. His Cytokine study integrates concerns from other disciplines, such as Tumor necrosis factor alpha and BTLA.
The scientist’s investigation covers issues in Cell biology, Immunology, T cell, Cytokine and Immune system. His Cell biology study combines topics from a wide range of disciplines, such as CD28, Jurkat cells and Transferrin receptor, Receptor. His research combines In vitro and Immunology.
His T cell study combines topics in areas such as Cancer research, Antigen, Fatty acid, Proinflammatory cytokine and Metabolism. His Cytokine study necessitates a more in-depth grasp of Internal medicine. The various areas that Gerhard J. Zlabinger examines in his Immune system study include Endometriosis, Pathogenesis, HMGB1, Interleukin 33 and Disease.
His primary scientific interests are in Immunology, Cell biology, T cell, Viral replication and Anabolism. His research is interdisciplinary, bridging the disciplines of CD80 and Immunology. The study incorporates disciplines such as Regulatory T cell, HEK 293 cells and Metabolic pathway in addition to Cell biology.
His T cell research is included under the broader classification of Immune system. His Viral replication research integrates issues from Reprogramming, Lipogenesis and Glycolysis Inhibition. His Complement system research is multidisciplinary, incorporating elements of Molecular biology and Monocyte.
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Human adipose tissue macrophages are of an anti-inflammatory phenotype but capable of excessive pro-inflammatory mediator production
M Zeyda;D Farmer;J Todoric;O Aszmann.
International Journal of Obesity (2007)
A microplate assay for the detection of oxidative products using 2',7'-dichlorofluorescin-diacetate.
Alexander R. Rosenkranz;Sabine Schmaldienst;Karl M. Stuhlmeier;Wanjun Chen.
Journal of Immunological Methods (1992)
Anti-inflammatory effects of sodium butyrate on human monocytes: potent inhibition of IL-12 and up-regulation of IL-10 production
Marcus D. Säemann;Georg A. Böhmig;Christoph H. Österreicher;Helmut Burtscher.
The FASEB Journal (2000)
CC Chemokine and CC Chemokine Receptor Profiles in Visceral and Subcutaneous Adipose Tissue Are Altered in Human Obesity
Joakim Huber;Florian W. Kiefer;Maximilian Zeyda;Bernhard Ludvik.
The Journal of Clinical Endocrinology and Metabolism (2008)
B7-H1 (Programmed Death-1 Ligand) on Dendritic Cells Is Involved in the Induction and Maintenance of T Cell Anergy
Nicole Selenko-Gebauer;Otto Majdic;Andreas Szekeres;Gerald Höfler.
Journal of Immunology (2003)
Prevention of organ allograft rejection by a specific Janus kinase 3 inhibitor
M. D. Säemann;F. Mühlbacher;G. Zlabinger;T. Wekerle.
European Surgery-acta Chirurgica Austriaca (2004)
Molecular characterization of human 4Ig-B7-H3, a member of the B7 family with four Ig-like domains.
Peter Steinberger;Otto Majdic;Sophia V. Derdak;Sophia V. Derdak;Katharina Pfistershammer.
Journal of Immunology (2004)
Endothelial C4d deposition is associated with inferior kidney allograft outcome independently of cellular rejection
Heinz Regele;Markus Exner;Bruno Watschinger;Christian Wenter.
Nephrology Dialysis Transplantation (2001)
Tamm-Horsfall glycoprotein links innate immune cell activation with adaptive immunity via a Toll-like receptor-4–dependent mechanism
Marcus D. Säemann;Thomas Weichhart;Maximilian Zeyda;Günther Staffler.
Journal of Clinical Investigation (2005)
B7-H3 is a potent inhibitor of human T-cell activation: No evidence for B7-H3 and TREML2 interaction.
Judith Leitner;Christoph Klauser;Winfried F. Pickl;Johannes Stöckl.
European Journal of Immunology (2009)
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