Characterization, cell uptake, and subcellular distribution of DNA complexes with lipoglutamides having tetraethylene glycol tails-Reference-Cited by-同舟云学术

Characterization, cell uptake, and subcellular distribution of DNA complexes with lipoglutamides having tetraethylene glycol tails

Published:1998-01 Issue:1 Volume:9 Page:31-42
ISSN:0920-5063
Container-title:Journal of Biomaterials Science, Polymer Edition
language:en
Short-container-title:Journal of Biomaterials Science, Polymer Edition

Author:

Sato Toshinori¹,Akino Hiroyuki²,Shoji Yoko³,Shimada Jingoro⁴,Okahata Yoshio⁵

Affiliation:

1. a Department of Biomolecular Engineering, Tokyo Institute of Technology, Nagatsuta, Midori-ku, Yokohama 226, Japan

2. b Department of Biomolecular Engineering, Tokyo Institute of Technology, Nagatsuta, Midori-ku, Yokohama 226, Japan

3. c Division of Clinical Pharmacology, Institute of Medical Science, St. Marianna University School of Medicine, 2-16-1, Sugao, Miyamae-ku, Kawasaki 216, Japan

4. d Division of Clinical Pharmacology, Institute of Medical Science, St. Marianna University School of Medicine, 2-16-1, Sugao, Miyamae-ku, Kawasaki 216, Japan

5. e Department of Biomolecular Engineering, Tokyo Institute of Technology, Nagatsuta, Midori-ku, Yokohama 226, Japan

Publisher

Informa UK Limited

Subject

Biomedical Engineering,Biomaterials,Bioengineering,Biophysics

Link

https://www.tandfonline.com/doi/pdf/10.1163/156856297X00245

Reference33 articles.

1. A new class of antivirals: antisense oligonucleotides combined with a hydrophobic substituent effectively inhibit influenza virus reproduction and synthesis of virus-specific proteins in MDCK cells

2. Short modified antisense oligonucleotides directed against Ha-ras point mutation induce selective cleavage of the mRNA and inhibit T24 cells proliferation.

3. Synthesis, hybridization properties and antiviral activity of lipid-oligodeoxynucleotide conjugates

4. Synthesis and physical properties ofanti-HIV antisense oligonucleotides bearing terminal lipophilic groups

5. Receptor-mediated gene delivery and expression in vivo.

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