His primary areas of investigation include Biochemistry, Sirtuin, SIRT3, SIRT5 and Mitochondrion. His Acetylation and NAD+ kinase study are his primary interests in Biochemistry. His NAD+ kinase study incorporates themes from Histone, Transcriptional regulation and Kidney metabolism.
His Sirtuin study integrates concerns from other disciplines, such as Lysine and Metabolism. His studies in SIRT3 integrate themes in fields like Calorie restriction, Oxidative stress, Reactive oxygen species, Cell biology and Insulin resistance. His studies deal with areas such as Apoptosis and Model organism as well as Cell biology.
His main research concerns Biochemistry, Mitochondrion, Sirtuin, SIRT3 and Cell biology. His research in NAD+ kinase, Acetylation, SIRT5, Lysine and Metabolism are components of Biochemistry. His work in Mitochondrion addresses subjects such as Oxidative phosphorylation, which are connected to disciplines such as Metabolite.
He works mostly in the field of Sirtuin, limiting it down to concerns involving Pharmacology and, occasionally, Nicotinamide mononucleotide. His SIRT3 research integrates issues from Calorie restriction, Internal medicine, Endocrinology, Frataxin and Deacetylase activity. His biological study spans a wide range of topics, including Beta oxidation, Caenorhabditis elegans, Metabolic pathway and Longevity.
The scientist’s investigation covers issues in Cell biology, Breast cancer, Cancer research, Caenorhabditis elegans and Context. Matthew D. Hirschey interconnects Amino acid, Cell, Saccharomyces cerevisiae and Longevity in the investigation of issues within Cell biology. His Breast cancer research includes themes of Oxidative stress, In vitro and Downregulation and upregulation.
The study incorporates disciplines such as Transcription factor, In vitro toxicology, Mammary tumor and Oncogene in addition to Cancer research. His research in Caenorhabditis elegans intersects with topics in Reactive oxygen species, Nuclear DNA, Mitochondrial DNA, Metabolic pathway and Mitochondrion. Reactive oxygen species and Bioenergetics are commonly linked in his work.
Cell biology, Longevity, Yeast, Growth medium and Saccharomyces cerevisiae are his primary areas of study. Matthew D. Hirschey integrates Cell biology and Mechanism in his research. As part of his studies on Longevity, Matthew D. Hirschey often connects relevant subjects like AMP-activated protein kinase.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
SIRT3 regulates mitochondrial fatty-acid oxidation by reversible enzyme deacetylation
Matthew D. Hirschey;Tadahiro Shimazu;Tadahiro Shimazu;Eric Goetzman;Enxuan Jing.
Nature (2010)
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)
Calorie Restriction Reduces Oxidative Stress by SIRT3-Mediated SOD2 Activation
Xiaolei Qiu;Katharine Brown;Matthew D. Hirschey;Eric Verdin.
Cell Metabolism (2010)
Suppression of Oxidative Stress by β-Hydroxybutyrate, an Endogenous Histone Deacetylase Inhibitor
Tadahiro Shimazu;Matthew D. Hirschey;John Newman;Wenjuan He.
Science (2013)
SIRT3 deficiency and mitochondrial protein hyperacetylation accelerate the development of the metabolic syndrome.
Matthew D. Hirschey;Tadahiro Shimazu;Enxuan Jing;Carrie A. Grueter.
Molecular Cell (2011)
Lysine Glutarylation Is a Protein Posttranslational Modification Regulated by SIRT5
Minjia Tan;Chao Peng;Kristin A. Anderson;Peter Chhoy.
Cell Metabolism (2014)
Sirtuin regulation of mitochondria: energy production, apoptosis, and signaling.
Eric Verdin;Matthew D. Hirschey;Lydia W.S. Finley;Marcia C. Haigis.
Trends in Biochemical Sciences (2010)
SIRT3 deacetylates mitochondrial 3-hydroxy-3-methylglutaryl CoA synthase 2 and regulates ketone body production.
Tadahiro Shimazu;Matthew D. Hirschey;Lan Hua;Kristin E. Dittenhafer-Reed.
Cell Metabolism (2010)
Sirtuin-3 (Sirt3) regulates skeletal muscle metabolism and insulin signaling via altered mitochondrial oxidation and reactive oxygen species production
Enxuan Jing;Brice Emanuelli;Matthew D. Hirschey;Jeremie Boucher.
Proceedings of the National Academy of Sciences of the United States of America (2011)
Designing a broad-spectrum integrative approach for cancer prevention and treatment
Keith I. Block;Charlotte Gyllenhaal;Leroy Lowe;Amedeo Amedei.
Seminars in Cancer Biology (2015)
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