Pharmacology of Antisense Oligonucleotide Inhibitors of Protein Expression

Author:

Cooper Scott R.,Taylor Jennifer K.,Miraglia Loren J.,Dean Nicholas M.

Publisher

Elsevier BV

Subject

Pharmacology (medical),Pharmacology

Reference61 articles.

1. Inhibition of expression of the multidrug resistance-associated P-glycoprotein by phosphorothioate and 5′ cholesterol-conjugated phosphorothioate antisense oligonucleotides;Alahari;Mol. Pharmacol.,1996

2. 2′-O-(2-methoxy)ethyl-modified anti-intercellular adhesion molecule 1 (ICAM-1) oligonucleotides selectively increase the ICAM-1 mRNA level and inhibit formation of the ICAM-1 translation initiation complex in human umbilical vein endothelial cells;Baker;J. Biol. Chem.,1997

3. Intracellular delivery of oligonucleotides with cationic liposomes;Bennett,1995

4. Cationic lipids enhance cellular uptake and activity of phosphorothioate antisense oligonucleotides;Bennett;Mol. Pharmacol.,1992

5. Electroporation enhances c-myc antisense oligodeoxynucleotide efficacy;Bergan;Nucleic Acids Res.,1993

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