In VivoTransfer Efficiency of Antisense Oligonucleotides into the Myocardium Using HVJ–Liposome Method-Reference-Cited by-同舟云学术

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In VivoTransfer Efficiency of Antisense Oligonucleotides into the Myocardium Using HVJ–Liposome Method

Published:1997-02 Issue:3 Volume:231 Page:540-545
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Aoki Motokuni,Morishita Ryuichi,Higaki Jitsuo,Moriguchi Atsushi,Kida Iwao,Hayashi Shin-ichiro,Matsushita Hidetsugu,Kaneda Yasufumi,Ogihara Toshio

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference22 articles.

1. Human gene therapy

2. Human gene therapy comes of age

3. Single intraluminal delivery of antisense cdc2 kinase and proliferating-cell nuclear antigen oligonucleotides results in chronic inhibition of neointimal hyperplasia.

4. Intimal hyperplasia after vascular injury is inhibited by antisense cdk 2 kinase oligonucleotides.

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1. Versatility of Liposomes for Antisense Oligonucleotide Delivery: A Special Focus on Various Therapeutic Areas;Pharmaceutics;2023-05-08

2. Injectable, rapid gelling and highly flexible hydrogel composites as growth factor and cell carriers;Acta Biomaterialia;2010-06

3. Nonviral gene transfer to skeletal, smooth, and cardiac muscle in living animals;American Journal of Physiology-Cell Physiology;2005-08

4. Synthetic, self-assembly ABCD nanoparticles; a structural paradigm for viable synthetic non-viral vectors;Chemical Society Reviews;2005

5. What Role Can Chemistry Play in Cationic Liposome‐Based Gene Therapy Research Today?;Non-Viral Vectors for Gene Therapy, Second Edition: Part 1;2005

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