BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

196 related articles for article (PubMed ID: 23437864)

  • 1. Stepwise click functionalization of DNA through a bifunctional azide with a chelating and a nonchelating azido group.
    Ingale SA; Seela F
    J Org Chem; 2013 Apr; 78(7):3394-9. PubMed ID: 23437864
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Stepwise "click" chemistry for the template independent construction of a broad variety of cross-linked oligonucleotides: influence of linker length, position, and linking number on DNA duplex stability.
    Xiong H; Seela F
    J Org Chem; 2011 Jul; 76(14):5584-97. PubMed ID: 21591729
    [TBL] [Abstract][Full Text] [Related]  

  • 3. High-density functionalization and cross-linking of DNA: "click" and "bis-click" cycloadditions performed on alkynylated oligonucleotides with fluorogenic anthracene azides.
    Pujari SS; Ingale SA; Seela F
    Bioconjug Chem; 2014 Oct; 25(10):1855-70. PubMed ID: 25154019
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cross-linked DNA: site-selective "click" ligation in duplexes with bis-azides and stability changes caused by internal cross-links.
    Xiong H; Seela F
    Bioconjug Chem; 2012 Jun; 23(6):1230-43. PubMed ID: 22554072
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 8-Aza-7-deazaguanine nucleosides and oligonucleotides with octadiynyl side chains: synthesis, functionalization by the azide-alkyne 'click' reaction and nucleobase specific fluorescence quenching of coumarin dye conjugates.
    Seela F; Xiong H; Leonard P; Budow S
    Org Biomol Chem; 2009 Apr; 7(7):1374-87. PubMed ID: 19300823
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Construction and assembly of branched Y-shaped DNA: "click" chemistry performed on dendronized 8-aza-7-deazaguanine oligonucleotides.
    Xiong H; Leonard P; Seela F
    Bioconjug Chem; 2012 Apr; 23(4):856-70. PubMed ID: 22443223
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Alkynylated and Dendronized 5-Aza-7-deazaguanine Nucleosides: Cross-Coupling with Tripropargylamine and Linear Alkynes, Click Functionalization, and Fluorescence of Pyrene Adducts†.
    Kondhare D; Zhang A; Leonard P; Seela F
    J Org Chem; 2020 Aug; 85(16):10525-10538. PubMed ID: 32700909
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Modification of DNA with octadiynyl side chains: synthesis, base pairing, and formation of fluorescent coumarin dye conjugates of four nucleobases by the alkyne--azide "click" reaction.
    Seela F; Sirivolu VR; Chittepu P
    Bioconjug Chem; 2008 Jan; 19(1):211-24. PubMed ID: 18020404
    [TBL] [Abstract][Full Text] [Related]  

  • 9. "Double click" reaction on 7-deazaguanine DNA: synthesis and excimer fluorescence of nucleosides and oligonucleotides with branched side chains decorated with proximal pyrenes.
    Seela F; Ingale SA
    J Org Chem; 2010 Jan; 75(2):284-95. PubMed ID: 20000692
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Versatile site-specific conjugation of small molecules to siRNA using click chemistry.
    Yamada T; Peng CG; Matsuda S; Addepalli H; Jayaprakash KN; Alam MR; Mills K; Maier MA; Charisse K; Sekine M; Manoharan M; Rajeev KG
    J Org Chem; 2011 Mar; 76(5):1198-211. PubMed ID: 21299239
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cross-linked DNA generated by "bis-click" reactions with bis-functional azides: site independent ligation of oligonucleotides via nucleobase alkynyl chains.
    Pujari SS; Xiong H; Seela F
    J Org Chem; 2010 Dec; 75(24):8693-6. PubMed ID: 21070038
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Azide-Modified Nucleosides as Versatile Tools for Bioorthogonal Labeling and Functionalization.
    Müggenburg F; Müller S
    Chem Rec; 2022 May; 22(5):e202100322. PubMed ID: 35189013
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Nucleosides and oligonucleotides containing 1,2,3-triazole residues with nucleobase tethers: synthesis via the azide-alkyne 'click' reaction.
    Chittepu P; Sirivolu VR; Seela F
    Bioorg Med Chem; 2008 Sep; 16(18):8427-39. PubMed ID: 18774721
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 7-Deazapurine and 8-aza-7-deazapurine nucleoside and oligonucleotide pyrene "click" conjugates: synthesis, nucleobase controlled fluorescence quenching, and duplex stability.
    Ingale SA; Pujari SS; Sirivolu VR; Ding P; Xiong H; Mei H; Seela F
    J Org Chem; 2012 Jan; 77(1):188-99. PubMed ID: 22129276
    [TBL] [Abstract][Full Text] [Related]  

  • 15. An Entry of the Chemoselective Sulfo-Click Reaction into the Sphere of Nucleic Acids.
    Clavé G; Dursun E; Vasseur JJ; Smietana M
    Org Lett; 2020 Mar; 22(5):1914-1918. PubMed ID: 32077293
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Synthesis and Excellent Duplex Stability of Oligonucleotides Containing 2'-Amino-LNA Functionalized with Galactose Units.
    Kumar R; Ries A; Wengel J
    Molecules; 2017 May; 22(5):. PubMed ID: 28531137
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A nucleobase-discriminating pyrrolo-dC click adduct designed for DNA fluorescence mismatch sensing.
    Ming X; Seela F
    Chemistry; 2012 Jul; 18(31):9590-600. PubMed ID: 22767494
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Azide-alkyne "click" conjugation of 8-aza-7-deazaadenine-DNA: synthesis, duplex stability, and fluorogenic dye labeling.
    Seela F; Pujari SS
    Bioconjug Chem; 2010 Sep; 21(9):1629-41. PubMed ID: 20681566
    [TBL] [Abstract][Full Text] [Related]  

  • 19. DNA with branched internal side chains: synthesis of 5-tripropargylamine-dU and conjugation by an azide-alkyne double click reaction.
    Sirivolu VR; Chittepu P; Seela F
    Chembiochem; 2008 Sep; 9(14):2305-16. PubMed ID: 18780386
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Oligonucleotides with "clickable" sugar residues: synthesis, duplex stability, and terminal versus central interstrand cross-linking of 2'-O-propargylated 2-aminoadenosine with a bifunctional azide.
    Pujari SS; Leonard P; Seela F
    J Org Chem; 2014 May; 79(10):4423-37. PubMed ID: 24693949
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.