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- W2059322023 endingPage "1404" @default.
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- W2059322023 abstract "A recombinant histone (NLS-H1) containing both the SV40 large T antigen nuclear localization signal and the carboxy-terminal domain of human histone H1(0) was produced in bacteria. NLS-H1-plasmid DNA complexes, in the presence of chloroquine, mediated reporter gene transfer into cultured cells with similar efficiencies as plasmid DNA-cationic lipid (lipofectin) complexes. NIH-3T3 or COS-7 cells transfected with NLS-H1-plasmid DNA-lipofectin complexes expressed at least 20 times more luciferase or had at least 2.5 times more beta-galactosidase-positive cells than those transfected with plasmid DNA-lipofectin complexes. Foreign gene expression was also improved by other DNA-binding proteins and cationic lipid formulations, yet the greatest enhancement was obtained with complexes containing either NLS-H1 or calf thymus histone H1. Histone H1-plasmid DNA-lipofectin complexes were internalized by a greater number of cells than plasmid DNA-lipofectin complexes." @default.
- W2059322023 created "2016-06-24" @default.
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- W2059322023 date "1996-08-01" @default.
- W2059322023 modified "2023-10-01" @default.
- W2059322023 title "Gene Transfer into Mammalian Cells Using Histone-Condensed Plasmid DNA" @default.
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- W2059322023 doi "https://doi.org/10.1089/hum.1996.7.12-1395" @default.
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