Selective Chemical Modification to the Higher‐Order Structures of Nucleic Acids-Reference-Cited by-同舟云学术

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Selective Chemical Modification to the Higher‐Order Structures of Nucleic Acids

Published:2022-09-16 Issue:2 Volume:23 Page:
ISSN:1527-8999
Container-title:The Chemical Record
language:en
Short-container-title:The Chemical Record

Author:

Nagatsugi Fumi¹²^ORCID,Onizuka Kazumitsu¹²³

Affiliation:

1. Institute of Multidisciplinary Research for Advanced Materials Tohoku University 2-1-1 Katahira Aoba-ku Sendai, Miyagi 980-8577 Japan

2. Department of Chemistry Graduate School of Science Tohoku University Aoba-ku Sendai 980-8578 Japan

3. Division for the Establishment of Frontier Sciences of Organization for Advanced Studies Tohoku University Aoba-ku Sendai, Miyagi 980-8577 Japan

Funder

Japan Society for the Promotion of Science

Japan Science and Technology Agency

TOBE MAKI Scholarship Foundation

Publisher

Wiley

Subject

Materials Chemistry,General Chemical Engineering,Biochemistry,General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/tcr.202200194

Reference95 articles.

1. Regulatory role of Non-canonical DNA Polymorphisms in human genome and their relevance in Cancer

2. Functional Studies of Potential Intrastrand Triplex Elements in the Escherichia coli Genome

3. Left-handed Z-DNA and intramolecular triplex formation at the site of an unequal sister chromatid exchange.

4. Cruciform DNA Sequences in Gene Promoters Can Impact Transcription upon Oxidative Modification of 2′-Deoxyguanosine

5. Chemical profiling of DNA G-quadruplex-interacting proteins in live cells

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1. Michael addition-activated alkylation of G-quadruplex DNA with methylamine-protected vinyl-quinazolinone derivatives;Bioorganic & Medicinal Chemistry Letters;2024-09

2. Construction and Enhancement of an RNA-Based Knowledge Graph for Discovering New RNA Drugs;2024 IEEE 40th International Conference on Data Engineering (ICDE);2024-05-13

3. Photocontrolled Binding of Styrylnaphthyridine Ligands to Abasic Site‐Containing DNA by Reversible [2+2] Cycloaddition and Cycloreversion;Chemistry – A European Journal;2024-04-23

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