Quantitative relationship between the chemical structure of antisense nucleosides and their capacity to interact with cyclomalto-octaose-Reference-Cited by-同舟云学术

Quantitative relationship between the chemical structure of antisense nucleosides and their capacity to interact with cyclomalto-octaose

Published:2001-01 Issue:1 Volume:51 Page:39-44
ISSN:0939-6411
Container-title:European Journal of Pharmaceutics and Biopharmaceutics
language:en
Short-container-title:European Journal of Pharmaceutics and Biopharmaceutics

Author:

Cserháti Tibor,Forgács Esther

Publisher

Elsevier BV

Subject

Pharmaceutical Science,General Medicine,Biotechnology

Reference30 articles.

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1. Interest of designed cyclodextrin-tools in gene delivery;Annales Pharmaceutiques Françaises;2012-11

2. Synthesis and Complexation Ability of a Novel Bis- (guanidinium)-tetrakis-(β-cyclodextrin) Dendrimeric Tetrapod as a Potential Gene Delivery (DNA and siRNA) System. Study of Cellular siRNA Transfection;Bioconjugate Chemistry;2008-11-18

3. Effect of pH and sodium chloride on the strength and selectivity of the interaction of τ-cyclodextrin with some antisense nucleosides;International Journal of Pharmaceutics;2003-03