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10.1038/s41467-017-01222-y

http://scihub22266oqcxt.onion/10.1038/s41467-017-01222-y
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C5662744!5662744!29084946
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suck abstract from ncbi


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pmid29084946      Nat+Commun 2017 ; 8 (ä): ä
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  • Drug-tunable multidimensional synthetic gene control using inducible degron-tagged dCas9 effectors #MMPMID29084946
  • Kleinjan DA; Wardrope C; Nga Sou S; Rosser SJ
  • Nat Commun 2017[]; 8 (ä): ä PMID29084946show ga
  • The nuclease-deactivated variant of CRISPR-Cas9 proteins (dCas9) fused to heterologous transactivation domains can act as a potent guide RNA sequence-directed inducer or repressor of gene expression in mammalian cells. In such a system the long-term presence of a stable dCas9 effector can be a draw-back precluding the ability to switch rapidly between repressed and activated target gene expression states, imposing a static environment on the synthetic regulatory circuits in the cell. To address this issue we have generated a toolkit of conditionally degradable or stabilisable orthologous dCas9 or Cpf1 effector proteins, thus opening options for multidimensional control of functional activities through combinations of orthogonal, drug-tunable artificial transcription factors.
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