2015 - Fellow of the Australian Academy of Health and Medical Science
Ross L. Coppel spends much of his time researching Primary biliary cirrhosis, Immunology, Antibody, Molecular biology and Plasmodium falciparum. The concepts of his Primary biliary cirrhosis study are interwoven with issues in Autoantibody, Biliary cirrhosis, Pyruvate dehydrogenase complex, Epitope and Autoimmunity. In most of his Immunology studies, his work intersects topics such as Cytotoxic T cell.
In his work, Mitochondrion is strongly intertwined with Recombinant DNA, which is a subfield of Antibody. Ross L. Coppel has included themes like Amino acid, Genetics, Gene, Protein primary structure and Dihydrolipoyllysine-Residue Acetyltransferase in his Molecular biology study. Ross L. Coppel combines subjects such as Peptide sequence, Cell biology, Antigen and Virology with his study of Plasmodium falciparum.
His primary scientific interests are in Plasmodium falciparum, Immunology, Antigen, Primary biliary cirrhosis and Antibody. The Plasmodium falciparum study combines topics in areas such as Genetics, Peptide sequence, Gene, Virology and Molecular biology. His research integrates issues of DNA, Antigenicity and Recombinant DNA in his study of Molecular biology.
The study incorporates disciplines such as Complementary DNA, Rhoptry, Membrane protein and Cell biology in addition to Antigen. His Primary biliary cirrhosis research includes themes of Autoantibody, Autoimmune disease, Biliary cirrhosis and Pyruvate dehydrogenase complex. His biological study spans a wide range of topics, including Immune system and Pathology.
Immunology, Primary biliary cirrhosis, Biochemistry, Plasmodium falciparum and Antibody are his primary areas of study. His Primary biliary cirrhosis study combines topics from a wide range of disciplines, such as Immunohistochemistry, Pathology, Liver disease, Pyruvate dehydrogenase complex and Interleukin. His Biochemistry study integrates concerns from other disciplines, such as Lipoarabinomannan and Mycobacterium smegmatis.
His study in Plasmodium falciparum is interdisciplinary in nature, drawing from both Red blood cell and Cell biology. His study in Antibody focuses on Isotype in particular. His research in Antigen intersects with topics in Malaria vaccine and CD40.
His primary areas of study are Immunology, Primary biliary cirrhosis, Antibody, Cytokine and Biochemistry. His Immunology research is multidisciplinary, relying on both Receptor and CD40. His Primary biliary cirrhosis study incorporates themes from Asymptomatic, Pathology, Autoimmunity and Pyruvate dehydrogenase complex.
Ross L. Coppel has researched Antibody in several fields, including Cleavage and Antigen. His studies in Biochemistry integrate themes in fields like Plasmodium falciparum and Apicomplexa. He is involved in the study of Plasmodium falciparum that focuses on KAHRP in particular.
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Identification and specificity of a cDNA encoding the 70 KD mitochondrial antigen recognized in primary biliary cirrhosis
M E Gershwin;I R Mackay;A Sturgess;R L Coppel.
Journal of Immunology (1987)
Targeted Gene Disruption Shows That Knobs Enable Malaria-Infected Red Cells to Cytoadhere under Physiological Shear Stress
Brendan S. Crabb;Brian M. Cooke;John C. Reeder;Ross F. Waller.
Exported Proteins Required for Virulence and Rigidity of Plasmodium falciparum-Infected Human Erythrocytes
Alexander G Maier;Melanie Rug;Matthew T O'Neill;Monica Brown.
Genome reduction in Leptospira borgpetersenii reflects limited transmission potential.
Dieter Mark Bulach;Richard L Zuerner;Peter Wilson;Torsten Seemann.
Proceedings of the National Academy of Sciences of the United States of America (2006)
Contribution of parasite proteins to altered mechanical properties of malaria-infected red blood cells.
Fiona K. Glenister;Ross L. Coppel;Alan F. Cowman;Narla Mohandas.
Identification of HLA-A2-restricted CD8(+) cytotoxic T cell responses in primary biliary cirrhosis: T cell activation is augmented by immune complexes cross-presented by dendritic cells.
Hiroto Kita;Zhe-Xiong Lian;Judy Van de Water;Xiao-Song He.
Journal of Experimental Medicine (2002)
Genome Sequence of the Saprophyte Leptospira biflexa Provides Insights into the Evolution of Leptospira and the Pathogenesis of Leptospirosis
Mathieu Picardeau;Dieter Mark Bulach;Dieter Mark Bulach;Christiane Bouchier;Richard L Zuerner.
PLOS ONE (2008)
Primary structure of the human M2 mitochondrial autoantigen of primary biliary cirrhosis: dihydrolipoamide acetyltransferase
R L Coppel;L J McNeilage;C D Surh;J Van de Water.
Proceedings of the National Academy of Sciences of the United States of America (1988)
The autoepitope of the 74-kD mitochondrial autoantigen of primary biliary cirrhosis corresponds to the functional site of dihydrolipoamide acetyltransferase.
J. Van De Water;M. E. Gershwin;P. Leung;Aftab Ansari.
Journal of Experimental Medicine (1988)
Liver‐targeted and peripheral blood alterations of regulatory T cells in primary biliary cirrhosis
Ruth Y. Lan;Chunmei Cheng;Zhe Xiong Lian;Koichi Tsuneyama.
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