Binding of Aminoglycoside Antibiotics with Modified A-site 16S rRNA Construct Containing Non-Nucleotide Linkers
摘要:
The design and synthesis of synthetically modified cyclic A-site 16S rRNA construct is reported. The binding characteristics of several members of the aminoglycoside antibiotics with this novel class of synthetically modified A-site 16S rRNA constructs were subsequently investigated. (C) 2002 Elsevier Science Ltd. All rights reserved.
Compositions with improved intravitreal half-life and uses thereof
申请人:Vitrisa Therapeutics, Inc.
公开号:US10308943B2
公开(公告)日:2019-06-04
Provided herein are compositions and methods for the treatment of retinal diseases. The compositions and methods include a therapeutic agent conjugated to a vitreous component binding moiety. The vitreous component binding moiety may be an aptamer or a small molecule that binds to a structural component of the vitreous humor (e.g., hyaluronic acid, collagen or vitronectin).
[EN] A SYSTEM FOR DELIVERING THERAPEUTIC AGENTS INTO LIVING CELLS AND CELL NUCLEI<br/>[FR] SYSTEME POUR INTRODUIRE DES AGENTS THERAPEUTIQUES DANS DES CELLULES VIVANTES ET NOYAUX DE CELLULE
申请人:SEGEV DAVID
公开号:WO2006010084A3
公开(公告)日:2006-04-27
BIVALENT ANTISENSE OLIGONUCLEOTIDES
申请人:MIRRX THERAPEUTICS A/S
公开号:US20180127754A1
公开(公告)日:2018-05-10
The present invention provides bivalent molecules comprising a first oligonucleotide linked to a second oligonucleotide. The first and the second oligonucleotide are preferably linked via a linking moiety. Preferably, both the first and/or the second oligonucleotide comprise an antisense sequence complementary to a cellular RNA such as mRNA or microRNA.