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 *

134 related articles for article (PubMed ID: 7827035)

  • 1. Incorporation of 2'-deoxy-6-thioguanosine into G-rich oligodeoxyribonucleotides inhibits G-tetrad formation and facilitates triplex formation.
    Rao TS; Durland RH; Seth DM; Myrick MA; Bodepudi V; Revankar GR
    Biochemistry; 1995 Jan; 34(3):765-72. PubMed ID: 7827035
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Triplex formation at the rat neu gene utilizing imidazole and 2'-deoxy-6-thioguanosine base substitutions.
    Gee JE; Revankar GR; Rao TS; Hogan ME
    Biochemistry; 1995 Feb; 34(6):2042-8. PubMed ID: 7849062
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Synthesis of and triplex formation in oligonucleotides containing 2'-deoxy-6-thioxanthosine.
    Inde T; Nishizawa S; Hattori Y; Kanamori T; Yuasa H; Seio K; Sekine M; Ohkubo A
    Bioorg Med Chem; 2018 Jul; 26(13):3785-3790. PubMed ID: 29914771
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A new odorless procedure for the synthesis of 2'-deoxy-6-thioguanosine and its incorporation into oligodeoxynucleotides.
    Onizuka K; Taniguchi Y; Sasaki S
    Nucleosides Nucleotides Nucleic Acids; 2009 Aug; 28(8):752-60. PubMed ID: 20183614
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Oligodeoxynucleotide containing s-functionalized 2'-deoxy-6-thioguanosine: facile tools for base-selective and site-specific internal modification of RNA.
    Sasaki S; Onizuka K; Taniguchi Y
    Curr Protoc Nucleic Acid Chem; 2012 Mar; Chapter 4():Unit 4.49.1-16. PubMed ID: 22395968
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Synthesis of oligonucleotides containing 2'-deoxy-6-thioguanosine at a predetermined site.
    Christopherson MS; Broom AD
    Nucleic Acids Res; 1991 Oct; 19(20):5719-24. PubMed ID: 1945849
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Synthesis and properties of triple helix-forming oligodeoxyribonucleotides containing 7-chloro-7-deaza-2'-deoxyguanosine.
    Aubert Y; Perrouault L; Hélène C; Giovannangeli C; Asseline U
    Bioorg Med Chem; 2001 Jun; 9(6):1617-24. PubMed ID: 11408181
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Strong, specific, monodentate G-C base pair recognition by N7-inosine derivatives in the pyrimidine.purine-pyrimidine triple-helical binding motif.
    Marfurt J; Parel SP; Leumann CJ
    Nucleic Acids Res; 1997 May; 25(10):1875-82. PubMed ID: 9115352
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Sequence and pH effects of LNA-containing triple helix-forming oligonucleotides: physical chemistry, biochemistry, and modeling studies.
    Sun BW; Babu BR; Sørensen MD; Zakrzewska K; Wengel J; Sun JS
    Biochemistry; 2004 Apr; 43(14):4160-9. PubMed ID: 15065859
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Solution conformation of the (+)-cis-anti-[BP]dG adduct in a DNA duplex: intercalation of the covalently attached benzo[a]pyrenyl ring into the helix and displacement of the modified deoxyguanosine.
    Cosman M; de los Santos C; Fiala R; Hingerty BE; Ibanez V; Luna E; Harvey R; Geacintov NE; Broyde S; Patel DJ
    Biochemistry; 1993 Apr; 32(16):4145-55. PubMed ID: 8476845
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Stable and Selective Antiparallel Type Triplex DNA Formation by Targeting a GC Base Pair with the TFO Containing One N
    Taniguchi Y; Miyazaki M; Matsueda N; Wang L; Okamura H; Sasaki S
    Chem Pharm Bull (Tokyo); 2018; 66(6):624-631. PubMed ID: 29863064
    [TBL] [Abstract][Full Text] [Related]  

  • 12. DNA triplex structures are stabilized by the incorporation of 3'-endo blocked pyrimidine nucleosides in the Hoogsteen strand.
    Savy P; Benhida R; Fourrey JL; Maurisse R; Sun JS
    Bioorg Med Chem Lett; 2000 Oct; 10(20):2287-9. PubMed ID: 11055340
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Solution conformation of [AF]dG opposite a -2 deletion site in a DNA duplex: intercalation of the covalently attached aminofluorene ring into the helix with base displacement of the C8-modified syn guanine and adjacent unpaired 3'-adenine into the major groove.
    Mao B; Hingerty BE; Broyde S; Patel DJ
    Biochemistry; 1995 Dec; 34(51):16641-53. PubMed ID: 8527437
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Triple helix formation by (G,A)-containing oligonucleotides: asymmetric sequence effect.
    Arimondo PB; Barcelo F; Sun JS; Maurizot JC; Garestier T; Hélène C
    Biochemistry; 1998 Nov; 37(47):16627-35. PubMed ID: 9843430
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The C(8)-(2'-deoxy-beta-D-ribofuranoside) of 7-deazaguanine: synthesis and base pairing of oligonucleotides with unusually linked nucleobases.
    Seela F; Debelak H
    J Org Chem; 2001 May; 66(10):3303-12. PubMed ID: 11348111
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Single strand targeted triplex formation: targeting purine-pyrimidine mixed sequences using abasic linkers.
    Kandimalla ER; Manning AN; Venkataraman G; Sasisekharan V; Agrawal S
    Nucleic Acids Res; 1995 Nov; 23(21):4510-7. PubMed ID: 7501477
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Solution conformation of the (-)-cis-anti-benzo[a]pyrenyl-dG adduct opposite dC in a DNA duplex: intercalation of the covalently attached BP ring into the helix with base displacement of the modified deoxyguanosine into the major groove.
    Cosman M; Hingerty BE; Luneva N; Amin S; Geacintov NE; Broyde S; Patel DJ
    Biochemistry; 1996 Jul; 35(30):9850-63. PubMed ID: 8703959
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A new, but old, nucleoside analog: the first synthesis of 1-deaza-2'-deoxyguanosine and its properties as a nucleoside and as oligodeoxynucleotides.
    Kojima N; Inoue K; Nakajima-Shibata R; Kawahara S; Ohtsuka E
    Nucleic Acids Res; 2003 Dec; 31(24):7175-88. PubMed ID: 14654693
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Triple-helix formation by oligonucleotides containing the three bases thymine, cytosine, and guanine.
    Giovannangéli C; Rougée M; Garestier T; Thuong NT; Hélène C
    Proc Natl Acad Sci U S A; 1992 Sep; 89(18):8631-5. PubMed ID: 1528873
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Synthesis and properties of triplex-forming oligonucleotides containing 2'-O-(2-methoxyethyl)-5-(3-aminoprop-1-ynyl)-uridine.
    Lou C; Xiao Q; Brennan L; Light ME; Vergara-Irigaray N; Atkinson EM; Holden-Dye LM; Fox KR; Brown T
    Bioorg Med Chem; 2010 Sep; 18(17):6389-97. PubMed ID: 20674370
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.