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Viral vectors transcriptional sequences

As described above, improved and durable transcription from exogenous DNAs in the nucleus is also important in developing non-viral vector systems for clinical applications. To this end, the disposition of transcriptionally active DNA (molecules in the active DNA compartment) need to be regulated properly. This "controlled intranuclear disposition of exogenous DNA can possibly be achieved by altering the structure of the DNA and the addition of functional sequences. [Pg.1534]

See other pages where Viral vectors transcriptional sequences is mentioned: [Pg.85]    [Pg.36]    [Pg.270]    [Pg.48]    [Pg.419]    [Pg.652]    [Pg.265]    [Pg.182]    [Pg.902]    [Pg.244]    [Pg.347]    [Pg.358]    [Pg.58]    [Pg.117]    [Pg.264]    [Pg.248]    [Pg.16]    [Pg.7]    [Pg.101]    [Pg.249]    [Pg.266]    [Pg.58]    [Pg.47]    [Pg.47]    [Pg.248]    [Pg.205]    [Pg.776]    [Pg.776]    [Pg.420]    [Pg.421]    [Pg.424]    [Pg.811]    [Pg.378]    [Pg.219]    [Pg.244]    [Pg.608]    [Pg.210]    [Pg.66]    [Pg.441]    [Pg.157]    [Pg.330]    [Pg.580]   
See also in sourсe #XX -- [ Pg.265 ]



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