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2. 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]
3. Oligodeoxynucleotides containing C-7 propyne analogs of 7-deaza-2'-deoxyguanosine and 7-deaza-2'-deoxyadenosine. Buhr CA; Wagner RW; Grant D; Froehler BC Nucleic Acids Res; 1996 Aug; 24(15):2974-80. PubMed ID: 8760882 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Specific recognition of CG base pairs by 2-deoxynebularine within the purine.purine.pyrimidine triple-helix motif. Stilz HU; Dervan PB Biochemistry; 1993 Mar; 32(9):2177-85. PubMed ID: 8443159 [TBL] [Abstract][Full Text] [Related]
7. Effect of third strand composition on the triple helix formation: purine versus pyrimidine oligodeoxynucleotides. Faucon B; Mergny JL; Héléne C Nucleic Acids Res; 1996 Aug; 24(16):3181-8. PubMed ID: 8774898 [TBL] [Abstract][Full Text] [Related]
8. Inhibition of gene transcription by purine rich triplex forming oligodeoxyribonucleotides. Roy C Nucleic Acids Res; 1993 Jun; 21(12):2845-52. PubMed ID: 7687346 [TBL] [Abstract][Full Text] [Related]
9. Strand orientation of [alpha]-oligodeoxynucleotides in triple helix structures: dependence on nucleotide sequence. Sun JS; Lavery R J Mol Recognit; 1992 Sep; 5(3):93-8. PubMed ID: 1298305 [TBL] [Abstract][Full Text] [Related]
11. Design of oligonucleotides for sequence-specific triple-helix formation. Properties of oligonucleotides containing 2'-deoxyxanthosine. Shimizu M; Inoue H; Ohtsuka E Nucleic Acids Symp Ser; 1991; (25):141-2. PubMed ID: 1842059 [TBL] [Abstract][Full Text] [Related]
12. Triplex formation at physiological pH by 5-Me-dC-N4-(spermine) [X] oligodeoxynucleotides: non protonation of N3 in X of X*G:C triad and effect of base mismatch/ionic strength on triplex stabilities. Barawkar DA; Rajeev KG; Kumar VA; Ganesh KN Nucleic Acids Res; 1996 Apr; 24(7):1229-37. PubMed ID: 8614624 [TBL] [Abstract][Full Text] [Related]
13. 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]
19. Synthesis of 2'-deoxyoxanosine from 2'-deoxyguanosine, conversion to its phosphoramidite, and incorporation into oxanine-containing oligodeoxynucleotides. Pack SP; Makino K Curr Protoc Nucleic Acid Chem; 2010 Jun; Chapter 4():Unit 4.39. PubMed ID: 20517989 [TBL] [Abstract][Full Text] [Related]
20. Formation of DNA triple helices incorporating blocks of G.GC and T.AT triplets using short acridine-linked oligonucleotides. Fox KR Nucleic Acids Res; 1994 Jun; 22(11):2016-21. PubMed ID: 8029007 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]