Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Hidenori Okamura"'
Publikováno v:
Molecules, Vol 28, Iss 4, p 1766 (2023)
Synthetic unnatural base pairs have been proven to be attractive tools for the development of DNA-based biotechnology. Our group has very recently reported on alkynylated purine–pyridazine pairs, which exhibit selective and stable base-pairing via
Externí odkaz:
https://doaj.org/article/e8138495f98d4e649aa9a5fb46e38520
Autor:
Sidney Becker, Christina Schneider, Hidenori Okamura, Antony Crisp, Tynchtyk Amatov, Milan Dejmek, Thomas Carell
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-9 (2018)
How RNA building blocks have formed on an early Earth by a continuous process is still a mystery awaiting its solution. Here, the authors report that fluctuations of physical parameters like temperature and pH could have been enough to facilitate nuc
Externí odkaz:
https://doaj.org/article/f30b47cab3884e568cef79fb2ecc6324
Publikováno v:
Applied Sciences, Vol 10, Iss 21, p 7709 (2020)
Selective chemical reactions of biomolecules are some of the important tools for investigations by biological studies. We have developed the selective crosslinking reactions to form covalent bonds to DNA or RNA using crosslinking oligonucleotides (CF
Externí odkaz:
https://doaj.org/article/2d6dd9ef7e3c4475bcb8b363b61b32ce
Publikováno v:
Organic Letters. 25:466-470
In this paper, we describe a novel N–O photolysis of o-nitrobenzyl oxime ethers that enables the synthesis of phenanthridines via intramolecular cyclization reactions. Without the use of additional photocatalysts or photosensitizers, the process pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d99cc6cc215e9e7ad007acbb954be2bb
https://doi.org/10.26434/chemrxiv-2022-gjn1v
https://doi.org/10.26434/chemrxiv-2022-gjn1v
Autor:
Ahmed Mostafa, Abdelhady, Yu, Hirano, Kazumitsu, Onizuka, Hidenori, Okamura, Yasuo, Komatsu, Fumi, Nagatsugi
Publikováno v:
Current Protocols. 2
Crosslinking reactions to nucleic acids are an effective way to prepare stable complexes formed by covalent bonding. We demonstrated that fully 2'-O-methylated (2'-OMe) RNAs having a 2-amino-6-vinylpurine (AVP) exhibited an efficient crosslinking to
Publikováno v:
Chemical Communications. 56:9731-9734
We recently found the translocation of double-stranded DNA into the nucleus. We herein describe the concept of novel booster oligodeoxynucleotides including 2'-deoxy uridine, which release antigene oligonucleotides in the nucleus by enzymatic digesti
Autor:
Yosuke Taniguchi, Shigeki Sasaki, Ryotaro Notomi, Takayuki Osuki, Yuya Magata, Lei Wang, Hidenori Okamura
Publikováno v:
Organic & Biomolecular Chemistry. 18:2845-2851
Expansion of the triplex DNA forming sequence is required in the genomic targeting fields. Basically, triplex DNA is formed by the interaction between the triplex-forming oligonucleotides and homo-purine region with the target duplex DNA. The presenc
Autor:
Hidenori Okamura, Giang Hoang Trinh, Zhuoxin Dong, Yoshiaki Masaki, Kohji Seio, Fumi Nagatsugi
Publikováno v:
Nucleic acids research. 50(6)
Unnatural base pairs (UBPs) which exhibit a selectivity against pairing with canonical nucleobases provide a powerful tool for the development of nucleic acid-based technologies. As an alternative strategy to the conventional UBP designs, which invol
Autor:
David Jan Drexler, Samuele Stazzoni, Gregor Witte, Hidenori Okamura, Felix Müller, Alexander Pichler, Thomas Carell, Karl-Peter Hopfner, Clemens Reto Dialer, Simon Veth
Publikováno v:
Chemistry – A European Journal
2'3'-cGAMP is an uncanonical cyclic dinucleotide where one A and one G base are connected via a 3'-5' and a unique 2'-5' linkage. The molecule is produced by the cyclase cGAS in response to cytosolic DNA binding. cGAMP activates STING and hence one o