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CRISPR/Cas9-mediated Targeted Integration In Vivo Using a Homology-mediated End Joining-based Strategy
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优先事项和资金. "知识创新"和中国科学院合作

Richard P Suttmeier1, Cong Cao, Denis Fred Simon

  • 1University of Oregon, Eugene, OR 97403, USA. petesutt@uoregon.edu

Science (New York, N.Y.)
|April 8, 2006
PubMed
概括

No abstract available in PubMed .

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The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
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