Sequence, Stability, and Structure of G‐Quadruplexes and Their Interactions with Drugs-Reference-Cited by-同舟云学术

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Sequence, Stability, and Structure of G‐Quadruplexes and Their Interactions with Drugs

Published:2012-09 Issue:1 Volume:50 Page:
ISSN:1934-9270
Container-title:Current Protocols in Nucleic Acid Chemistry
language:en
Short-container-title:Current Protocols in Nucleic Acid Chemistry

Author:

Chen Yuwei¹,Yang Danzhou¹²³⁴

Affiliation:

1. Department of Chemistry and Biochemistry, The University of Arizona Tucson Arizona

2. College of Pharmacy, The University of Arizona Tucson Arizona

3. BIO5 Institute, The University of Arizona Tucson Arizona

4. Arizona Cancer Center Tucson Arizona

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/0471142700.nc1705s50

Reference84 articles.

1. Solution Structure of the Biologically Relevant G-Quadruplex Element in the Human c-MYC Promoter. Implications for G-Quadruplex Stabilization

2. Human telomeric sequence forms a hybrid-type intramolecular G-quadruplex structure with mixed parallel/antiparallel strands in potassium solution

3. Puf/Nm23‐H2/Ndpk‐B transactivates a human c‐myc promoter‐CAT gene via a functional nuclease hypersensitive element;Berberich S.J.;Oncogene,1995

4. The role of supercoiling in transcriptional control of MYC and its importance in molecular therapeutics

5. Structural Basis of DNA Quadruplex Recognition by an Acridine Drug

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