2012 - Fellow of the American Association for the Advancement of Science (AAAS)
1985 - Fellow of John Simon Guggenheim Memorial Foundation
His main research concerns Primary biliary cirrhosis, Immunology, Antibody, Autoantibody and Epitope. His Primary biliary cirrhosis research incorporates elements of T cell, Autoimmune disease, Biliary cirrhosis and Cell. In general Immunology study, his work on Autoimmunity, Immune system and T lymphocyte often relates to the realm of Spirulina, thereby connecting several areas of interest.
M. E. Gershwin has included themes like Immunohistochemistry, Molecular biology and Recombinant DNA in his Antibody study. In his study, which falls under the umbrella issue of Autoantibody, Framingham Risk Score, Disease and Immunopathology is strongly linked to Antigen. His Epitope study incorporates themes from Biochemistry, Pyruvate dehydrogenase complex and Lipoic acid binding.
Immunology, Primary biliary cirrhosis, Antibody, Autoantibody and Internal medicine are his primary areas of study. His works in Autoimmunity, Autoimmune disease, T cell, Antigen and Immune system are all subjects of inquiry into Immunology. M. E. Gershwin interconnects CD8, Biliary cirrhosis, Disease, Pathology and Pyruvate dehydrogenase complex in the investigation of issues within Primary biliary cirrhosis.
His Antibody research is multidisciplinary, relying on both Molecular biology and Recombinant DNA. His Autoantibody research integrates issues from Cytokine, Proinflammatory cytokine, Autoimmune hepatitis, Serology and Polyclonal antibodies. His Internal medicine study integrates concerns from other disciplines, such as Gastroenterology and Endocrinology.
The scientist’s investigation covers issues in Immunology, Primary biliary cirrhosis, Autoimmunity, Autoantibody and Internal medicine. His is involved in several facets of Immunology study, as is seen by his studies on Antibody, T cell, CD8, Immune system and Immune tolerance. Specifically, his work in Antibody is concerned with the study of Immunoglobulin G.
His Primary biliary cirrhosis research is multidisciplinary, incorporating elements of Genetics, Cytokine, Genome-wide association study and Immunopathology. His research integrates issues of Acquired immune system, CD40, Virology, Neurogenesis and Autoimmune hepatitis in his study of Autoimmunity. His study in Internal medicine is interdisciplinary in nature, drawing from both Gastroenterology and Oncology.
M. E. Gershwin mainly investigates Immunology, Primary biliary cirrhosis, Autoimmunity, Autoantibody and Antibody. His work in the fields of Immunology, such as Molecular mimicry, Immune system, Gut flora and Gut microbiome, intersects with other areas such as Discordant Twin. His work investigates the relationship between Molecular mimicry and topics such as Immune tolerance that intersect with problems in Nod, Natural killer T cell, Escherichia coli infection, Epitope and Dysbiosis.
The study incorporates disciplines such as T cell, Autoimmune disease, CD8 and Genetics in addition to Primary biliary cirrhosis. M. E. Gershwin has included themes like Acquired immune system, Gut dysbiosis, Cytokine and Disease activity in his Autoimmunity study. His Autoantibody study deals with Proinflammatory cytokine intersecting with Cirrhosis.
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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)
Nutrition and immunity
Gershwin Me;Keen Cl;Fletcher Mp;Hurley Ls.
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)
The Immunobiology and Pathophysiology of Primary Biliary Cirrhosis
Hirschfield Gm;Gershwin Me.
Annual Review of Pathology-mechanisms of Disease (2013)
Autoantibodies of primary biliary cirrhosis recognize dihydrolipoamide acetyltransferase and inhibit enzyme function.
J Van de Water;D Fregeau;P Davis;A Ansari.
Journal of Immunology (1988)
Molecular mimicry in primary biliary cirrhosis. Evidence for biliary epithelial expression of a molecule cross-reactive with pyruvate dehydrogenase complex-E2
J. Van De Water;J. Turchany;P. S. C. Leung;J. Lake.
Journal of Clinical Investigation (1993)
Generation of biliary lesions after transfer of human lymphocytes into severe combined immunodeficient (SCID) mice.
S M Krams;K Dorshkind;M E Gershwin.
Journal of Experimental Medicine (1989)
Structural requirement for autoreactivity on human pyruvate dehydrogenase-E2, the major autoantigen of primary biliary cirrhosis. Implication for a conformational autoepitope.
C D Surh;R Coppel;M E Gershwin.
Journal of Immunology (1990)
In situ nucleic acid hybridization of cytokines in primary biliary cirrhosis: Predominance of the Th1 subset
K. Harada;J. Van De Water;P. S. C. Leung;R. L. Coppel.
Treatment of irritable bowel syndrome with Lacteol Fort: a randomized, double-blind, cross-over trial.
Halpern Gm;Prindiville T;Blankenburg M;Hsia T.
The American Journal of Gastroenterology (1996)
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