2008 - Gottschalk Medal, Australian Academy of Science
Gabrielle T. Belz mostly deals with Immunology, Cytotoxic T cell, Cell biology, Antigen and Cellular differentiation. Her T cell, Immune system, Antigen presentation, Innate lymphoid cell and Immunity investigations are all subjects of Immunology research. Her Antigen presentation research is multidisciplinary, incorporating perspectives in Dendritic cell, MHC class I and Antigen-presenting cell.
The study incorporates disciplines such as Virus, Virology, CD8 and Molecular biology in addition to Cytotoxic T cell. Her Cell biology study combines topics from a wide range of disciplines, such as Natural killer T cell, Transcription factor and Cytokine. Her studies examine the connections between Cellular differentiation and genetics, as well as such issues in Immunophenotyping, with regards to CD1D, Lymphoid Progenitor Cells, Mucosal associated invariant T cell, Cell and BCL6.
Her primary areas of study are Immunology, Cell biology, Immune system, Innate lymphoid cell and Cytotoxic T cell. Her Antigen presentation, Antigen, T cell, Antigen-presenting cell and Dendritic cell study are her primary interests in Immunology. Her work carried out in the field of Cell biology brings together such families of science as Transcription factor and Cellular differentiation.
The concepts of her Immune system study are interwoven with issues in Interleukin 22, Neuroscience, Cytokine and Cell type. Her study in Innate lymphoid cell is interdisciplinary in nature, drawing from both Inflammation, Natural killer cell and Cancer research. Her Cytotoxic T cell research incorporates themes from CD8 and Virology.
Gabrielle T. Belz spends much of her time researching Cell biology, Innate lymphoid cell, Immune system, Immunology and Innate immune system. The various areas that Gabrielle T. Belz examines in her Cell biology study include T cell, Transcriptome, Transcription factor, Receptor and VIPR2. Gabrielle T. Belz has included themes like Inflammation, Interleukin 13, Homeostasis and Interleukin 5 in her Innate lymphoid cell study.
Organism, Rhythm and Lymphatic system is closely connected to Neuroscience in her research, which is encompassed under the umbrella topic of Immune system. Her studies deal with areas such as Neuropeptide, Irritable bowel syndrome and Lung as well as Immunology. Her Innate immune system research is multidisciplinary, relying on both Sendai virus, Cancer research and Influenza A virus.
Gabrielle T. Belz mainly investigates Cell biology, Innate lymphoid cell, Immune system, Cellular differentiation and Innate immune system. Her Cell biology research incorporates elements of Type I interferon production, Transcription factor, CD8, Receptor and VIPR2. Her CD8 research is multidisciplinary, incorporating elements of Interferon, Interleukin 17 and T cell.
Her work in Immune system covers topics such as Homeostasis which are related to areas like Lung, Hormone and Immunology. Her Cellular differentiation research integrates issues from Immunoglobulin G, BCL6 and Immunoglobulin class switching. Her studies in Innate immune system integrate themes in fields like Acquired immune system, Cancer research, Intestinal mucosa, Tissue homeostasis and Interleukin 22.
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Cross-presentation, dendritic cell subsets, and the generation of immunity to cellular antigens
William R. Heath;Gabrielle T. Belz;Georg M. N. Behrens;Christopher M. Smith.
Immunological Reviews (2004)
Virus-Specific CD8+ T Cells in Primary and Secondary Influenza Pneumonia
Kirsten J Flynn;Gabrielle T Belz;John D Altman;Rafi Ahmed.
Epidermal Viral Immunity Induced by CD8α+ Dendritic Cells But Not by Langerhans Cells
Rhys S. Allan;Chris M. Smith;Gabrielle T. Belz;Allison L. van Lint.
The CD8α+ Dendritic Cell Is Responsible for Inducing Peripheral Self-Tolerance to Tissue-associated Antigens
Gabrielle T. Belz;Georg M.N. Behrens;Chris M. Smith;Jacques F.A.P. Miller.
Journal of Experimental Medicine (2002)
Cognate CD4+ T cell licensing of dendritic cells in CD8+ T cell immunity
Christopher M Smith;Nicholas S Wilson;Jason Waithman;Jose A Villadangos.
Nature Immunology (2004)
Blimp-1 Transcription Factor Is Required for the Differentiation of Effector CD8+ T Cells and Memory Responses
Axel Kallies;Annie Xin;Annie Xin;Gabrielle T. Belz;Stephen L. Nutt.
The transcription factors Blimp-1 and IRF4 jointly control the differentiation and function of effector regulatory T cells
Erika Cretney;Annie Xin;Annie Xin;Wei Shi;Wei Shi;Martina Minnich.
Nature Immunology (2011)
The dominant role of CD8+ dendritic cells in cross-presentation is not dictated by antigen capture
Petra Schnorrer;Georg M N Behrens;Nicholas S Wilson;Joanne L Pooley.
Proceedings of the National Academy of Sciences of the United States of America (2006)
Cutting Edge: Conventional CD8α+ Dendritic Cells Are Generally Involved in Priming CTL Immunity to Viruses
Gabrielle T. Belz;Christopher M. Smith;Daniel Eichner;Ken Shortman.
Journal of Immunology (2004)
Most lymphoid organ dendritic cell types are phenotypically and functionally immature
Nicholas S. Wilson;Dima El-Sukkari;Gabrielle T. Belz;Christopher M. Smith.
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