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Collectively, this work highlights the potential of ultrashort pulsed electric fields to disrupt the dense structure of glioma (78)

FDA approval requires formal clinical trials, safety and efficacy review, labeling approval, and manufacturing validation under a New Drug Application (NDA) or Biologics License Application (BLA)

Although much work has been done since the discovery of the c- MET oncogene to map out the details of c-MET signaling, this suggests that our understanding of the greater c-MET network remains incomplete