Synthetic gene transfer vectors II: back to the future.
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[1] Joseph Zabner,et al. Cellular and Molecular Barriers to Gene Transfer by a Cationic Lipid (*) , 1995, The Journal of Biological Chemistry.
[2] D. Scherman,et al. A versatile vector for gene and oligonucleotide transfer into cells in culture and in vivo: polyethylenimine. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[3] Leaf Huang,et al. Nonviral methods for siRNA delivery. , 2009, Molecular pharmaceutics.
[4] C. Lanz,et al. Ligation of cell surface heparan sulfate proteoglycans by antibody-coated beads stimulates phagocytic uptake into epithelial cells: a model for cellular invasion by Neisseria gonorrhoeae. , 1998, Experimental cell research.
[5] Y. George. Receptor-mediated in Vitro Gene Transformation by a Soluble DNA Carrier System , 2022 .
[6] J. Behr. Synthetic Gene‐Transfer Vectors , 1993 .
[7] J. Behr,et al. Monomolecular collapse of plasmid DNA into stable virus-like particles. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[8] D. Papahadjopoulos,et al. Liposomes revisited , 1995, Science.
[9] J. Behr,et al. A model for non‐viral gene delivery: through syndecan adhesion molecules and powered by actin , 2004, The journal of gene medicine.
[10] Daniel G. Anderson,et al. Semi-automated synthesis and screening of a large library of degradable cationic polymers for gene delivery. , 2003, Angewandte Chemie.
[11] Carey Dj. N-syndecan: structure and function of a transmembrane heparan sulfate proteoglycan. , 1996 .
[12] F. Szoka,et al. The influence of polymer structure on the interactions of cationic polymers with DNA and morphology of the resulting complexes , 1997, Gene Therapy.
[13] J. Behr,et al. Optimized galenics improve in vitro gene transfer with cationic molecules up to 1000-fold. , 1996, Gene therapy.
[14] D. Crommelin,et al. An NLS peptide covalently linked to linear DNA does not enhance transfection efficiency of cationic polymer based gene delivery systems , 2005, The journal of gene medicine.
[15] Kathryn A. Whitehead,et al. Lipid-like materials for low-dose, in vivo gene silencing , 2010, Proceedings of the National Academy of Sciences.
[16] S. Fukushima,et al. PEG-based block catiomers possessing DNA anchoring and endosomal escaping functions to form polyplex micelles with improved stability and high transfection efficacy. , 2007, Journal of controlled release : official journal of the Controlled Release Society.
[17] F. Szoka,et al. In vitro gene delivery by degraded polyamidoamine dendrimers. , 1996, Bioconjugate chemistry.
[18] E. Brambilla,et al. An electron microscopy study into the mechanism of gene transfer with lipopolyamines. , 1996, Gene therapy.
[19] J. Behr,et al. Gene delivery: a single nuclear localization signal peptide is sufficient to carry DNA to the cell nucleus. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[20] Matthias John,et al. RNAi-mediated gene silencing in non-human primates , 2006, Nature.
[21] T. Park,et al. Multimeric small interfering ribonucleic acid for highly efficient sequence-specific gene silencing. , 2010, Nature materials.
[22] J. Behr,et al. Cationic siRNAs provide carrier-free gene silencing in animal cells. , 2009, Journal of the American Chemical Society.
[23] J. Behr,et al. Efficient gene transfer into mammalian primary endocrine cells with lipopolyamine-coated DNA. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[24] J. Northrop,et al. Lipofection: a highly efficient, lipid-mediated DNA-transfection procedure. , 1987, Proceedings of the National Academy of Sciences of the United States of America.
[25] Darren H. Wakefield,et al. Dynamic PolyConjugates for targeted in vivo delivery of siRNA to hepatocytes , 2007, Proceedings of the National Academy of Sciences.
[26] M. Manoharan. Oligonucleotide conjugates as potential antisense drugs with improved uptake, biodistribution, targeted delivery, and mechanism of action. , 2002, Antisense & nucleic acid drug development.
[27] D. Escande,et al. Polyethylenimine but Not Cationic Lipids Promotes Transgene Delivery to the Nucleus in Mammalian Cells* , 1998, The Journal of Biological Chemistry.
[28] C. Sheridan,et al. Gene therapy finds its niche , 2011, Nature Biotechnology.
[29] J. Hagstrom,et al. Plasmid DNA entry into postmitotic nuclei of primary rat myotubes. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[30] Jean-Paul Behr,et al. Sticky overhangs enhance siRNA-mediated gene silencing , 2007, Proceedings of the National Academy of Sciences.
[31] J. Behr. DNA strongly binds to micelles and vesicles containing lipopolyamines or lipointercalants. , 1986 .
[32] G. Levi,et al. Size, diffusibility and transfection performance of linear PEI/DNA complexes in the mouse central nervous system , 1998, Gene Therapy.
[33] John Maraganore,et al. A status report on RNAi therapeutics , 2010, Silence.
[34] J. Wolff,et al. A nuclear localization signal can enhance both the nuclear transport and expression of 1 kb DNA. , 1999, Journal of cell science.
[35] M. Cotten,et al. Transferrin-polycation conjugates as carriers for DNA uptake into cells. , 1990, Proceedings of the National Academy of Sciences of the United States of America.
[36] D. Haussecker,et al. The business of RNAi therapeutics. , 2008, Human gene therapy.
[37] G. Zuber,et al. Targeted gene delivery to cancer cells: directed assembly of nanometric DNA particles coated with folic acid. , 2003, Angewandte Chemie.
[38] D. Lamm,et al. Phase I/II marker lesion study of intravesical BC-819 DNA plasmid in H19 over expressing superficial bladder cancer refractory to bacillus Calmette-Guerin. , 2008, The Journal of urology.
[39] F. Szoka,et al. Mechanism of DNA release from cationic liposome/DNA complexes used in cell transfection. , 1996, Biochemistry.
[40] L. Huang,et al. A novel cationic liposome reagent for efficient transfection of mammalian cells. , 1991, Biochemical and biophysical research communications.
[41] S. Tumova,et al. Heparan sulfate proteoglycans on the cell surface: versatile coordinators of cellular functions. , 2000, The international journal of biochemistry & cell biology.
[42] R. Langer,et al. Exploring polyethylenimine‐mediated DNA transfection and the proton sponge hypothesis , 2005, The journal of gene medicine.
[43] Amit Kumar Sharma,et al. Crystal structure of a heparin‐ and integrin‐binding segment of human fibronectin , 1999, The EMBO journal.
[44] A S Verkman,et al. Size-dependent DNA Mobility in Cytoplasm and Nucleus* , 2000, The Journal of Biological Chemistry.
[45] I. Khalil,et al. Uptake Pathways and Subsequent Intracellular Trafficking in Nonviral Gene Delivery , 2006, Pharmacological Reviews.