A microfluidic platform for systems pathology: multiparameter single-cell signaling measurements of clinical brain tumor specimens.

@article{Sun2010AMP,
  title={A microfluidic platform for systems pathology: multiparameter single-cell signaling measurements of clinical brain tumor specimens.},
  author={Jing Sun and Michael Masterman-Smith and Nicholas Alexander Graham and Jing Jiao and Jack Mottahedeh and Dan R. Laks and Minori Ohashi and Jason DeJesus and Ken-ichiro Kamei and Ki-Bum Lee and Hao Wang and Zeta Tak For Yu and Yi-Tsung Lu and Shuang Hou and Keyu Li and Max Liu and Nangang Zhang and Shutao Wang and Brigitte Ang{\'e}nieux and Eduard H. Panosyan and Eric R. Samuels and Jun K Park and Dirk Williams and Vera Konkankit and David Nathanson and R. Michael van Dam and Michael E. Phelps and Hong Wu and Linda M. Liau and Paul S. Mischel and Jorge A. Lazareff and Harley I. Kornblum and William H. Yong and Thomas G. Graeber and Hsian‐Rong Tseng},
  journal={Cancer research},
  year={2010},
  volume={70 15},
  pages={
          6128-38
        }
}
The clinical practice of oncology is being transformed by molecular diagnostics that will enable predictive and personalized medicine. Current technologies for quantitation of the cancer proteome are either qualitative (e.g., immunohistochemistry) or require large sample sizes (e.g., flow cytometry). Here, we report a microfluidic platform-microfluidic image cytometry (MIC)-capable of quantitative, single-cell proteomic analysis of multiple signaling molecules using only 1,000 to 2,800 cells… 

Figures from this paper

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