2009 - Fellow of the American Association for the Advancement of Science (AAAS)
Member of the Association of American Physicians
His scientific interests lie mostly in Biochemistry, Acetylation, Mitochondrion, SIRT3 and Histone. His Biochemistry study frequently links to other fields, such as Calorie restriction. The Acetylation study which covers Lysine that intersects with Metabolic pathway, RNA, Recombinant DNA and Cyclin T1.
His SIRT3 research incorporates themes from Oxidative stress, Internal medicine, Reactive oxygen species, HDAC10 and Insulin resistance. His work deals with themes such as Chromatin, Regulation of gene expression and Transcription, Transcriptional regulation, which intersect with Histone. The study incorporates disciplines such as Regulator, Bacteria and Cell biology in addition to NAD+ kinase.
Eric Verdin mostly deals with Cell biology, Virology, Biochemistry, Molecular biology and Acetylation. His Cell biology study incorporates themes from Proinflammatory cytokine and Cell. His Virology study integrates concerns from other disciplines, such as Chromatin and Immunology.
SIRT3, Sirtuin, Mitochondrion, NAD+ kinase and SIRT5 are the primary areas of interest in his Biochemistry study. His Molecular biology research includes elements of Enhancer, Transcription factor, Transcription, Transactivation and Histone deacetylase. His Acetylation research is multidisciplinary, incorporating perspectives in Histone and Lysine.
Eric Verdin focuses on Cell biology, NAD+ kinase, Virology, CD38 and Inflammation. Eric Verdin interconnects Transcription factor and NFAT in the investigation of issues within Cell biology. His NAD+ kinase research is multidisciplinary, incorporating elements of Reprogramming, Granzyme B production and Memory T cell.
His Virology research incorporates elements of Chromatin, Plasma protein binding and Provirus. His biological study deals with issues like Molecular biology, which deal with fields such as Gene. Within one scientific family, Eric Verdin focuses on topics pertaining to Nuclear protein under Mitochondrion, and may sometimes address concerns connected to SIRT3.
His primary areas of investigation include Cell biology, NAD+ kinase, Mitochondrion, SIRT3 and Inflammation. His research integrates issues of Regulation of gene expression, Fatty acid synthase, Metabolism and Sirtuin in his study of Cell biology. His research in Metabolism intersects with topics in Longevity, Acetylation and Enzyme.
His research in the fields of Nicotinamide adenine dinucleotide overlaps with other disciplines such as CD38. His Mitochondrion study improves the overall literature in Biochemistry. His research investigates the connection with Inflammation and areas like Effector which intersect with concerns in Immune system.
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A SARS-CoV-2 protein interaction map reveals targets for drug repurposing.
David E. Gordon;Gwendolyn M. Jang;Mehdi Bouhaddou;Jiewei Xu.
The human Sir2 ortholog, SIRT2, is an NAD+-dependent tubulin deacetylase
Brian J North;Brett L Marshall;Margie T Borra;John M Denu.
Molecular Cell (2003)
SIRT3 regulates mitochondrial fatty-acid oxidation by reversible enzyme deacetylation
Matthew D. Hirschey;Tadahiro Shimazu;Tadahiro Shimazu;Eric Goetzman;Enxuan Jing.
Duration of nuclear NF-κB action regulated by reversible acetylation
Lin-feng Chen;Wolfgang Fischle;Eric Verdin;Warner C. Greene.
Mammalian Sir2 homolog SIRT3 regulates global mitochondrial lysine acetylation.
David B. Lombard;Frederick W. Alt;Hwei Ling Cheng;Jakob Bunkenborg.
Molecular and Cellular Biology (2007)
A class of hybrid polar inducers of transformed cell differentiation inhibits histone deacetylases
Victoria M. Richon;Stephane Emiliani;Eric Verdin;Yael Webb.
Proceedings of the National Academy of Sciences of the United States of America (1998)
Calorie Restriction Reduces Oxidative Stress by SIRT3-Mediated SOD2 Activation
Xiaolei Qiu;Katharine Brown;Matthew D. Hirschey;Eric Verdin.
Cell Metabolism (2010)
The expression of a small fraction of cellular genes is changed in response to histone hyperacetylation.
Carine Van Lint;Stephane Emiliani;Eric Verdin.
Gene Expression (1996)
Suppression of Oxidative Stress by β-Hydroxybutyrate, an Endogenous Histone Deacetylase Inhibitor
Tadahiro Shimazu;Matthew D. Hirschey;John Newman;Wenjuan He.
The growing landscape of lysine acetylation links metabolism and cell signalling
Chunaram Choudhary;Brian T. Weinert;Yuya Nishida;Eric Verdin.
Nature Reviews Molecular Cell Biology (2014)
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