Theory and Practice of Using Polycationic Amphiphiles and polymers for In Vitro and In Vivo Gene Transfer
暂无分享,去创建一个
C. Benoist | J. Behr | B. Demeneix | J. Rémy | D. Goula | J. Remy
[1] Abdallah,et al. Gene transfer with lipospermines and polyethylenimines. , 1998, Advanced drug delivery reviews.
[2] B. Demeneix,et al. Adenovirus enhancement of polyethylenimine-mediated transfer of regulated genes in differentiated cells , 1997, Gene Therapy.
[3] M. Monsigny,et al. Enhanced biological activity of antisense oligonucleotides complexed with glycosylated poly-L-lysine. , 1996, Molecular pharmacology.
[4] F. Szoka,et al. In vitro gene delivery by degraded polyamidoamine dendrimers. , 1996, Bioconjugate chemistry.
[5] E. Brambilla,et al. An electron microscopy study into the mechanism of gene transfer with lipopolyamines. , 1996, Gene therapy.
[6] K. Mislick,et al. Evidence for the role of proteoglycans in cation-mediated gene transfer. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[7] C. Benoist,et al. A powerful nonviral vector for in vivo gene transfer into the adult mammalian brain: polyethylenimine. , 1996, Human gene therapy.
[8] J. Hagstrom,et al. Complexes of non-cationic liposomes and histone H1 mediate efficient transfection of DNA without encapsulation. , 1996, Biochimica et biophysica acta.
[9] K. Mechtler,et al. Activation of the complement system by synthetic DNA complexes: a potential barrier for intravenous gene delivery. , 1996, Human gene therapy.
[10] P. Felgner,et al. Converting an alcohol to an amine in a cationic lipid dramatically alters the co-lipid requirement, cellular transfection activity and the ultrastructure of DNA-cytofectin complexes. , 1996, Biochimica et biophysica acta.
[11] R. Lambert,et al. Polyethylenimine-Mediated DNA Transfection of Peripheral and Central Neurons in Primary Culture: Probing Ca2+Channel Structure and Function with Antisense Oligonucleotides , 1996, Molecular and Cellular Neuroscience.
[12] D. Scherman,et al. Lipospermine-based gene transfer into the newborn mouse brain is optimized by a low lipospermine/DNA charge ratio. , 1995, Human gene therapy.
[13] L. Mahan,et al. Systemic gene therapy: biodistribution and long-term expression of a transgene in mice. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[14] 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.
[15] T. Ochiya,et al. Gene transfer and expression in progeny after intravenous DNA injection into pregnant mice , 1995, Nature Genetics.
[16] J. Behr,et al. Targeted gene transfer into hepatoma cells with lipopolyamine-condensed DNA particles presenting galactose ligands: a stage toward artificial viruses. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[17] C. Sirlin,et al. Gene transfer with a series of lipophilic DNA-binding molecules. , 1994, Bioconjugate chemistry.
[18] H. Paik,et al. Ionization of Poly(ethylenimine) and Poly(allylamine) at Various pH′s , 1994 .
[19] J. Behr,et al. Gene transfer with synthetic cationic amphiphiles: prospects for gene therapy. , 1994, Bioconjugate chemistry.
[20] C. Benoist,et al. Temporal and spatial expression of lipospermine-compacted genes transferred into chick embryos in vivo. , 1994, BioTechniques.
[21] F. Szoka,et al. Polyamidoamine cascade polymers mediate efficient transfection of cells in culture. , 1993, Bioconjugate chemistry.
[22] K. Zatloukal,et al. Influenza virus hemagglutinin HA-2 N-terminal fusogenic peptides augment gene transfer by transferrin-polylysine-DNA complexes: toward a synthetic virus-like gene-transfer vehicle. , 1992, Proceedings of the National Academy of Sciences of the United States of America.
[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] F. Vogel,et al. Condensation of vector DNA by the chromosomal protein HMG1 results in efficient transfection. , 1988, Biochimica et biophysica acta.
[25] M. Heller,et al. Artificial self-assembling systems for gene delivery , 1996 .
[26] N. Nelson. Structure and pharmacology of the proton-ATPases. , 1991, Trends in pharmacological sciences.
[27] J. Behr. DNA strongly binds to micelles and vesicles containing lipopolyamines or lipointercalants. , 1986 .
[28] T. Curiel,et al. Editorial: Cancer Research: Does It Deliver for the Patient? Phase I Study of Interleukin-2 Combined with Interferon-a and 5-fluorouracil in Patients with Metastatic Renal Cell Cancer. Effect of Liposome-muramyl Tripeptide Combined with Recombinant Canine Granulocyte Colony-stimulating Factor on Can , 2022 .