Sasaki S - Search Results

1

Modification of the aromatic ring of the WNA analogues for expansion of the triplex recognition codes.

Taniguchi Y, Nakamura A, Aoki E, Sasaki S. Taniguchi Y, et al. Among authors: sasaki s. Nucleic Acids Symp Ser (Oxf). 2005;(49):173-4. doi: 10.1093/nass/49.1.173. Nucleic Acids Symp Ser (Oxf). 2005. PMID: 17150689

2

[Creation of functional recognition molecules for chemical modification of gene expression].

Sasaki S. Sasaki S. Yakugaku Zasshi. 2002 Dec;122(12):1081-93. doi: 10.1248/yakushi.122.1081. Yakugaku Zasshi. 2002. PMID: 12510386 Free article. Review. Japanese.

3

Site-specific mutagenesis by triple helix-forming oligonucleotides containing a reactive nucleoside analog.

Nagatsugi F, Sasaki S, Miller PS, Seidman MM. Nagatsugi F, et al. Among authors: sasaki s. Nucleic Acids Res. 2003 Mar 15;31(6):e31. doi: 10.1093/nar/gng031. Nucleic Acids Res. 2003. PMID: 12626730 Free PMC article.

4

Mutagenesis targeted by triple-helix forming oligonucleotides containing a reactive nucleoside analogue.

Nagatsugi F, Sasaki S, Seidmen MM, Miller PS. Nagatsugi F, et al. Among authors: sasaki s. Nucleic Acids Res Suppl. 2002;(2):31-2. doi: 10.1093/nass/2.1.31. Nucleic Acids Res Suppl. 2002. PMID: 12903090

5

Selective formation of non-natural type triplexes containing TA interrupting sites with the TFO incorporating W-shape nucleic acid (WNA) analogs.

Taniguchi Y, Takahashi R, Kodama K, Senko Y, Maeda M, Sasaki S. Taniguchi Y, et al. Among authors: sasaki s. Nucleic Acids Res Suppl. 2002;(2):35-6. doi: 10.1093/nass/2.1.35. Nucleic Acids Res Suppl. 2002. PMID: 12903092

6

Design and evaluation of novel nucleoside analogs (WNA) for specific formation of non-natural type triplexes containing a TA or CG interrupting site.

Taniguchi Y, Senko Y, Kodama K, Nakamura A, Sasaki S. Taniguchi Y, et al. Among authors: sasaki s. Nucleic Acids Res Suppl. 2003;(3):113-4. doi: 10.1093/nass/3.1.113. Nucleic Acids Res Suppl. 2003. PMID: 14510406

7

Efficient cross-linking reactions by functional nucleobases capable of in situ activation under neutral conditions.

Nagatsugi F, Suenaga Y, Sasaki S. Nagatsugi F, et al. Among authors: sasaki s. Nucleic Acids Res Suppl. 2003;(3):155-6. doi: 10.1093/nass/3.1.155. Nucleic Acids Res Suppl. 2003. PMID: 14510427

8

Selective formation of stable triplexes including a TA or a CG interrupting site with new bicyclic nucleoside analogues (WNA).

Sasaki S, Taniguchi Y, Takahashi R, Senko Y, Kodama K, Nagatsugi F, Maeda M. Sasaki S, et al. J Am Chem Soc. 2004 Jan 21;126(2):516-28. doi: 10.1021/ja037211z. J Am Chem Soc. 2004. PMID: 14719949

9

Expansion of triplex recognition codes by the use of novel bicyclic nucleoside derivatives (WNA).

Taniguchi Y, Nakamura A, Senko Y, Kodama K, Nagatsugi F, Sasaki S. Taniguchi Y, et al. Among authors: sasaki s. Nucleosides Nucleotides Nucleic Acids. 2005;24(5-7):823-7. doi: 10.1081/ncn-200060309. Nucleosides Nucleotides Nucleic Acids. 2005. PMID: 16250103

10

Effects of halogenated WNA derivatives on sequence dependency for expansion of recognition sequences in non-natural-type triplexes.

Taniguchi Y, Nakamura A, Senko Y, Nagatsugi F, Sasaki S. Taniguchi Y, et al. Among authors: sasaki s. J Org Chem. 2006 Mar 3;71(5):2115-22. doi: 10.1021/jo052413u. J Org Chem. 2006. PMID: 16497000

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