Zobrazeno 1 - 5
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pro vyhledávání: '"Amber E. Boyatzis"'
Autor:
Marisa N. Duong, Peter G. Arthur, Zi Xiang Lim, Alice Vrielink, Emily Golden, Amber E. Boyatzis, Paul A. Fournier
Publikováno v:
Free Radical Research. 54:91-103
Introduction: In order to better understand the physiological and pathophysiological roles of reactive oxygen species (ROS), multiple blood and urine biomarkers of oxidative stress have been develo...
Autor:
Matthew J. Piggott, Mark C. Walkey, Marisa N. Duong, Peter G. Arthur, Adam P. Wdowiak, Rohan D. Joyce, Gareth L. Nealon, Amber E. Boyatzis
Publikováno v:
Bioconjugate chemistry. 32(8)
Isotope-coded affinity tags (ICATs) are valuable tools for mass spectrometry-based quantitative proteomics, in particular, for comparison of protein (cysteine-residue) thiol oxidation state in normal, stressed, and diseased tissue. However, the iodoa
Autor:
Scott Bringans, Amber E. Boyatzis, Peter G. Arthur, Marisa N. Duong, Matthew J. Piggott, Richard J. Lipscombe
Publikováno v:
Journal of Proteome Research. 16:2004-2015
Oxidative stress, caused by reactive oxygen and nitrogen species (RONS), is important in the pathophysiology of many diseases. A key target of RONS is the thiol group of protein cysteine residues. Because thiol oxidation can affect protein function,
Autor:
Peter G. Arthur, Miranda D. Grounds, Amber E. Boyatzis, Jessica R. Terrill, Marisa N. Duong, Rufus Turner, Anthony J. Kettle, Caroline Le Guiner
Publikováno v:
Redox Biology, Vol 9, Iss C, Pp 276-286 (2016)
Redox Biology
Redox Biology
Duchenne Muscular Dystrophy (DMD) is a fatal skeletal muscle wasting disease presenting with excessive myofibre necrosis and increased inflammation and oxidative stress. In the mdx mouse model of DMD, homeostasis of the amino acid taurine is altered,
Publikováno v:
The international journal of biochemistrycell biology. 45(9)
Oxidative stress has been implicated in the pathology of the lethal skeletal muscle disease Duchenne muscular dystrophy (DMD), and various antioxidants have been investigated as a potential therapy. Recently, treatment of the mdx mouse model for DMD