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https://www.ncbi.nlm.nih.gov/pubmed/9930332
Polyethylenimine-based intravenous delivery of transgenes to mouse lung. Goula D(1), Benoist C, Mantero S, Merlo G, Levi G, Demeneix BA. Author information: (1)Laboratoire de Physiologie Générale et Comparée, URA 90 CNRS, Muséum National d'Histoire Naturelle, Paris, France.Author: D Goula, C Benoist, S Mantero, G Merlo, G Levi, G Levi, BA Demeneix
https://www.researchgate.net/publication/13359573_Polyethylenimine-based_intravenous_delivery_of_transgenes_to_mouse_lung
Generally, cationic vector-based intravenous delivery of DNA is hindered by interactions of positively charged complexes with serum proteins. However, if optimally formulated, cationic vectors can ...
https://www.nature.com/articles/3301464
Jun 22, 2001 · Inhibition of hepadnaviral replication by polyethylenimine-based intravenous delivery of antisense phosphodiester oligodeoxynucleotides to the liver. M Robaczewska 1,2, S Guerret 3,Author: Robaczewska M, Robaczewska M, Guerret S, Remy Js, Chemin I, Offensperger Wb, Chevallier M, Behr Jp, ...
https://moh-it.pure.elsevier.com/en/publications/polyethylenimine-based-intravenous-delivery-of-transgenes-to-mous
Generally, cationic vector-based intravenous delivery of DNA is hindered by interactions of positively charged complexes with serum proteins. However, if optimally formulated, cationic vectors can provide reasonable levels of transfection in the lung either by intravenous or intrapulmonary routes.Author: D Goula, C Benoist, S Mantero, G Merlo, G Levi, G Levi, BA Demeneix
https://www.ncbi.nlm.nih.gov/pubmed/11423935
Inhibition of hepadnaviral replication by polyethylenimine-based intravenous delivery of antisense phosphodiester oligodeoxynucleotides to the liver. Robaczewska M(1), Guerret S, Remy JS, Chemin I, Offensperger WB, Chevallier M, Behr JP, Podhajska AJ, Blum HE, Trepo C, Cova L.Author: Robaczewska M, Robaczewska M, Guerret S, Remy Js, Chemin I, Offensperger Wb, Chevallier M, Behr Jp, ...
https://www.researchgate.net/publication/11916475_Inhibition_of_hepadnaviral_replication_by_polyethylenimine-based_intravenous_delivery_of_antisense_phosphodiester_oligodeoxynucleotides_to_the_liver
Inhibition of hepadnaviral replication by polyethylenimine-based intravenous delivery of antisense phosphodiester oligodeoxynucleotides to the liver Article in Gene Therapy 8(11):874-81 · July ...
https://www.sciencedirect.com/science/article/pii/S1549963413001895
However, in our gene delivery system with linear 22-kD PEI, we found so far that intravenous injection was the most efficient for gene expression in mice lungs, while intratracheal administration was insufficient (data not shown). The successful aerosol delivery of PEI/DNA found in literatures thus far depends on the use of branched PEI.Author: Erh Hsuan Lin, Hsiang Yi Chang, Shauh Der Yeh, Kuang Yao Yang, Kuang Yao Yang, Huei Sin Hu, Cheng We...
https://www.liebertpub.com/doi/abs/10.1089/10430349950017662
Jul 06, 2004 · Inhibition of hepadnaviral replication by polyethylenimine-based intravenous delivery of antisense phosphodiester oligodeoxynucleotides to the liver. 22 June 2001 Gene Therapy, Vol. 8, No. 11. Sequential Injection of Cationic Liposome and Plasmid DNA Effectively Transfects the Lung with Minimal Inflammatory Toxicity.Author: Jean-Luc Coll, Patrice Chollet, Elisabeth Brambilla, Dominique Desplanques, Jean-Paul Behr, Marie Fa...
https://link.springer.com/content/pdf/10.1023%2FA%3A1014861900478.pdf
Purpose. Low molecular weight branched polyethylenimine (LMW-PEI) was synthesized and studied as a DNA carrier for gene delivery with regard to physico-chemical properties, cytotoxicity, and transfection efficiency. Methods. The architecture of LMW-PEI, synthesized by acid catalyzed ring-opening polymerization of aziridine was characterized by size exclusion chromatography in combination with ...Author: Dagmar Fischer, Thorsten Bieber, Youxin Li, Hans-Peter Elsässer, Thomas Kissel
https://www.academia.edu/14203157/Polyethylenimine-based_intravenous_delivery_of_transgenes_to_mouse_lung
Polyethylenimine-based intravenous delivery of transgenes to mouse lung
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