Frederick E. Domann mainly investigates Molecular biology, Biochemistry, Reactive oxygen species, Superoxide dismutase and DNA methylation. His studies deal with areas such as Oxidative stress, Catalase, Cancer cell, Mutation and Binding site as well as Molecular biology. His Biochemistry study frequently draws connections between related disciplines such as Cell biology.
His study in Reactive oxygen species is interdisciplinary in nature, drawing from both Cell cycle, Cyclin D1, Cyclin and Signal transduction. His research integrates issues of Dicoumarol, NADH Dehydrogenase and Superoxide in his study of Superoxide dismutase. His work deals with themes such as Chromatin, Cancer research and Epigenetics, which intersect with DNA methylation.
His primary scientific interests are in Cancer research, Molecular biology, DNA methylation, Cell biology and Epigenetics. His biological study spans a wide range of topics, including Cancer cell, Cancer, Metastasis, Carcinogenesis and Pathology. His studies in Molecular biology integrate themes in fields like Cell culture, Transcription factor, Gene expression, Gene and Cell growth.
The concepts of his DNA methylation study are interwoven with issues in Chromatin, Regulation of gene expression and Methylation. His Epigenetics research incorporates elements of Histone, Maspin, Gene silencing and Epigenome. His Reactive oxygen species research is multidisciplinary, incorporating elements of Oxidative stress and Mitochondrion.
His primary areas of investigation include Cancer research, Cell biology, Epigenetics, Molecular biology and Oxidative stress. The study incorporates disciplines such as Cancer cell, Cancer, Metastasis, Carcinogenesis and Pathology in addition to Cancer research. His Cell biology study incorporates themes from Reprogramming, Transcription factor and SOD2.
The various areas that Frederick E. Domann examines in his Epigenetics study include Histone and DNA methylation. Frederick E. Domann has included themes like Chromatin and Gene silencing in his DNA methylation study. His Molecular biology research is multidisciplinary, relying on both Cell culture, Mitochondrial matrix and Extracellular superoxide dismutase.
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Role for DNA methylation in the control of cell type specific maspin expression.
Bernard W. Futscher;Marc M. Oshiro;Ryan J. Wozniak;Nicholas Holtan.
Nature Genetics (2002)
Disruption of an AP-2 alpha binding site in an IRF6 enhancer is associated with cleft lip
Fedik Rahimov;Mary L Marazita;Axel Visel;Margaret E Cooper.
Nature Genetics (2008)
O2⋅− and H2O2-Mediated Disruption of Fe Metabolism Causes the Differential Susceptibility of NSCLC and GBM Cancer Cells to Pharmacological Ascorbate
Joshua D. Schoenfeld;Zita A. Sibenaller;Kranti A. Mapuskar;Brett A. Wagner.
Cancer Cell (2017)
α-Tocopheryl succinate induces apoptosis by targeting ubiquinone-binding sites in mitochondrial respiratory complex II
Lan-Feng Dong;Pauline Low;Jeffrey C. Dyason;Xiu-Fang Wang.
Identification of a Functional Peroxisome Proliferator-Activated Receptor Response Element in the Rat Catalase Promoter
Geoffrey D. Girnun;Frederick E. Domann;Steven A. Moore;Mike E. C. Robbins.
Molecular Endocrinology (2002)
An epigenetic perspective on the free radical theory of development
Michael J Hitchler;Frederick E Domann.
Free Radical Biology and Medicine (2007)
The role of manganese superoxide dismutase in the growth of pancreatic adenocarcinoma.
Joseph J. Cullen;Christine Weydert;Marilyn M. Hinkhouse;Justine Ritchie.
Cancer Research (2003)
Epigenetic silencing of maspin gene expression in human breast cancers.
Frederick E. Domann;Judd C. Rice;Mary J.C. Hendrix;Bernard W. Futscher.
International Journal of Cancer (2000)
The redox basis of epigenetic modifications: from mechanisms to functional consequences.
Anthony R. Cyr;Frederick E. Domann.
Antioxidants & Redox Signaling (2011)
Mitochondria, energetics, epigenetics, and cellular responses to stress.
Daniel T. Shaughnessy;Kimberly McAllister;Leroy Worth;Astrid C. Haugen.
Environmental Health Perspectives (2014)
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