These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

126 related articles for article (PubMed ID: 11551753)

  • 1. A new reactive nucleoside analogue for highly reactive and selective cross-linking reaction to cytidine under neutral conditions.
    Nagatsugi F; Tokuda N; Maeda M; Sasaki S
    Bioorg Med Chem Lett; 2001 Oct; 11(19):2577-9. PubMed ID: 11551753
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Efficient cross-linking to cytidine under neutral conditions using the 2-amino-6-vinylpurine derivative having an additional activating group.
    Nagatsugi F; Tokuda N; Kawasaki T; Maeda M; Sasaki S
    Nucleic Acids Res Suppl; 2001; (1):87-8. PubMed ID: 12836277
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Site-directed alkylation to cytidine within duplex by the oligonucleotides containing functional nucleobases.
    Nagatsugi F; Kawasaki T; Tokuda N; Maeda M; Sasaki S
    Nucleosides Nucleotides Nucleic Acids; 2001; 20(4-7):915-9. PubMed ID: 11563144
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hybridization-promoted and cytidine-selective activation for cross-linking with the use of 2-amino-6-vinylpurine derivatives.
    Kawasaki T; Nagatsugi F; Ali MM; Maeda M; Sugiyama K; Hori K; Sasaki S
    J Org Chem; 2005 Jan; 70(1):14-23. PubMed ID: 15624902
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Efficient cross-linking to cytidine using substituted phenylsulfide derivatives of 2-amino-6-vinylpurine nucleoside via synchronous activation within duplex.
    Kawasaki T; Nagatsugi F; Maeda M; Sasaki S
    Nucleic Acids Symp Ser; 2000; (44):129-30. PubMed ID: 12903302
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Substituent effects on the in situ activation of the double activated cross-linking reaction.
    Nagatsugi F; Mori S; Ali MM; Ogata Y; Sasaki S
    Nucleic Acids Symp Ser (Oxf); 2005; (49):175-6. PubMed ID: 17150690
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Synthesis of the new nucleoside analogue connecting 2-amino-6-vinylpurine to the 2'-deoxyribose skeleton via the methylene linker.
    Kurose Y; Taniguchi Y; Nagatsugi F; Sasaki S
    Nucleic Acids Symp Ser (Oxf); 2008; (52):43-4. PubMed ID: 18776244
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Active oligonucleotides incorporating alkylating an agent as potential sequence- and base selective modifier of gene expression.
    Sasaki S
    Eur J Pharm Sci; 2001 Apr; 13(1):43-51. PubMed ID: 11292567
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Alteration of cross-linking selectivity with the 2'-OMe analogue of 2-amino-6-vinylpurine and evaluation of antisense effects.
    Imoto S; Hori T; Hagihara S; Taniguchi Y; Sasaki S; Nagatsugi F
    Bioorg Med Chem Lett; 2010 Oct; 20(20):6121-4. PubMed ID: 20817451
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Design and synthesis of the novel cross-linking reagents triggered by the triple helix formation.
    Nagatsugi F; Usui D; Kawasaki T; Maeda M; Sasaki S
    Nucleic Acids Symp Ser; 2000; (44):39-40. PubMed ID: 12903257
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Application of 2-amino-6-vinylpurine as an efficient agent for conjugation of oligonucleotides.
    Ali MM; Nagatsugi F; Sasaki S; Nakahara R; Maeda M
    Nucleosides Nucleotides Nucleic Acids; 2006; 25(2):159-69. PubMed ID: 16541959
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Fast DNA interstrand cross-linking reaction by 6-vinylpurine.
    Imoto S; Chikuni T; Kansui H; Kunieda T; Nagatsugi F
    Nucleosides Nucleotides Nucleic Acids; 2012; 31(10):752-62. PubMed ID: 23067126
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Design and synthesis of the novel cross-linking agent.
    Kusano S; Hattori K; Imoto S; Nagatsugi F
    Nucleic Acids Symp Ser (Oxf); 2009; (53):169-70. PubMed ID: 19749314
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Synthesis of 6-amino-2-vinylpurine derivatives for cross-linking and evaluation of the reactivity.
    Kusano S; Sakuraba T; Hagihara S; Nagatsugi F
    Bioorg Med Chem Lett; 2012 Nov; 22(22):6957-61. PubMed ID: 23044366
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Selective cross-linking to the adenine of the TA interrupting site within the triple helix.
    Nagatsugi F; Matsuyama Y; Maeda M; Sasaki S
    Bioorg Med Chem Lett; 2002 Feb; 12(3):487-9. PubMed ID: 11814825
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel cross-linking reaction of oligonucleotides incorporating new base analogs with selective reactivity toward cytidine.
    Nagatsugi F; Kawasaki T; Maeda M; Sasaki S
    Nucleic Acids Symp Ser; 1997; (37):67-8. PubMed ID: 9586002
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Synthesis of the peptide nucleic acid (PNA) incorporating 2-amino-6-vinylpurine derivative and evaluation of the reactivity.
    Imoto S; Shimotazawa A; Hirohama T; Goto M; Nagatsugi F
    Nucleic Acids Symp Ser (Oxf); 2008; (52):391-2. PubMed ID: 18776418
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Synthesis of RNA Crosslinking Oligonucleotides Modified with 2-Amino-7-Deaza-7-Propynyl-6-Vinylpurine.
    Yamada K; Abe Y; Nagatsugi F
    Curr Protoc Nucleic Acid Chem; 2019 Jun; 77(1):e79. PubMed ID: 30860656
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The alkyl-connected 2-amino-6-vinylpurine (AVP) crosslinking agent for improved selectivity to the cytosine base in RNA.
    Taniguchi Y; Kurose Y; Nishioka T; Nagatsugi F; Sasaki S
    Bioorg Med Chem; 2010 Apr; 18(8):2894-901. PubMed ID: 20346683
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Efficient cross-linking to cytidine by functional nucleobases capable of in situ activation.
    Kawasaki T; Nagatsugi F; Usui D; Maeda M; Sasaki S
    Nucleic Acids Symp Ser; 1999; (42):43-4. PubMed ID: 10780370
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.