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Cell-targeted gene modification by delivery of CRISPR-Cas9 ribonucleoprotein complexes in pseudotyped lentivirus-derived nanoparticles
by
Nielsen, Ian Helstrup
,
Rovsing, Anne Bruun
,
Janns, Jacob Hørlück
,
Thomsen, Emil Aagaard
,
Ruzo, Albert
,
Bøggild, Andreas
,
Nedergaard, Frederikke
,
Møller, Charlotte Thornild
,
Boesen, Thomas
,
Degn, Søren Egedal
,
Shah, Jagesh V.
,
Mikkelsen, Jacob Giehm
Published in
Molecular therapy. Nucleic acids
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Molecular Therapy. Nucleic Acids
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Cell-Targeted Gene Modification
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Crispr-Cas9
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Lvnp
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Mt: Delivery Strategies
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Primary B Cells
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Pseudotyping
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