Synthesis of 1′-phenyl-2′-OMe ribose analogues connecting the thymine base at the 1′ position through a flexible linker for the formation of a stable anti-parallel triplex DNA-Reference-Cited by-同舟云学术

Synthesis of 1′-phenyl-2′-OMe ribose analogues connecting the thymine base at the 1′ position through a flexible linker for the formation of a stable anti-parallel triplex DNA

Published:2013-01 Issue:2 Volume:69 Page:600-606
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Taniguchi Yosuke,Okamura Hidenori,Fujino Norihiko,Sasaki Shigeki

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference24 articles.

1. Regulation of Transcription through Light-Activation and Light-Deactivation of Triplex-Forming Oligonucleotides in Mammalian Cells

2. The triple helix: 50 years later, the outcome

3. Mechanisms of triplex DNA-mediated inhibition of transcription initiation in cells

4. DNA triple helices: Biological consequences and therapeutic potential

5. Using Triplex-Forming Oligonucleotide Probes for the Reagentless, Electrochemical Detection of Double-Stranded DNA

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