O-2(center dot-) and H2O2-Mediated Disruption of Fe Metabolism Causes the Differential Susceptibility of NSCLC and GBM Cancer Cells to Pharmacological Ascorbate (vol 31, pg 487, 2017)

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作者： Schoenfeld, Joshua D. ; Sibenaller, Zita A. ; Mapuskar, Kranti A. ; Wagner, Brett A. ; Cramer-Morales, Kimberly L. ; Furqan, Muhammad ; Sandhu, Sonia ; Carlisle, Thomas L. ; Smith, Mark C. ; Abu Hejleh, Taher ; Berg, Daniel J. ; Zhang, Jun ; Keech, John ; Parekh, Kalpaj R. ; Bhatia, Sudershan ; Monga, Varun ; Bodeker, Kellie L. ; Ahmann, Logan ; Vollstedt, Sandy ; Brown, Heather ; Kauffman, Erin P. Shanahan ; Schall, Mary E. ; Hohl, Ray J. ; Clamon, Gerald H. ; Greenlee, Jeremy D. ; Howard, Matthew A. ; Schultz, Michael K. ; Smith, Brian J. ; Riley, Dennis P. ; Domann, Frederick E. ; Cullen, Joseph J. ; Buettner, Garry R. ; Buatti, John M. ; Spitz, Douglas R. ; Allen, Bryan G.

发布时间 2018-01-30

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Cancer Cell

2017年32卷2期

268-268页

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O-2(center dot-) and H2O2-Mediated Disruption of Fe Metabolism Causes the Differential Susceptibility of NSCLC and GBM Cancer Cells to Pharmacological Ascorbate (vol 31, pg 487, 2017)

Cancer Cell

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O-2(center dot-) and H2O2-Mediated Disruption of Fe Metabolism Causes the Differential Susceptibility of NSCLC and GBM Cancer Cells to Pharmacological Ascorbate (vol 31, pg 487, 2017)

Cancer Cell

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Cancer Cell

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