Year |
Citation |
Score |
2022 |
Honcharenko D, Rocha CSJ, Lundin KE, Maity J, Milton S, Tedebark U, Murtola M, Honcharenko M, Slaitas A, Smith CIE, Zain R, Strömberg R. 2'--(-(Aminoethyl)carbamoyl)methyl Modification Allows for Lower Phosphorothioate Content in Splice-Switching Oligonucleotides with Retained Activity. Nucleic Acid Therapeutics. PMID 35238623 DOI: 10.1089/nat.2021.0086 |
0.492 |
|
2019 |
Lundin KE, Gissberg O, Smith CIE, Zain R. Chemical Development of Therapeutic Oligonucleotides. Methods in Molecular Biology (Clifton, N.J.). 2036: 3-16. PMID 31410788 DOI: 10.1007/978-1-4939-9670-4_1 |
0.39 |
|
2019 |
Zain R, Smith CIE. Targeted Oligonucleotides for Treating Neurodegenerative Tandem Repeat Diseases. Neurotherapeutics : the Journal of the American Society For Experimental Neurotherapeutics. PMID 31098852 DOI: 10.1007/S13311-019-00712-9 |
0.311 |
|
2019 |
Umek T, Sollander K, Bergquist H, Wengel J, Lundin KE, Smith CIE, Zain R. Oligonucleotide Binding to Non-B-DNA in . Molecules (Basel, Switzerland). 24. PMID 30871121 DOI: 10.3390/Molecules24051000 |
0.321 |
|
2018 |
Smith CIE, Zain R. Therapeutic Oligonucleotides: State of the Art. Annual Review of Pharmacology and Toxicology. PMID 30285540 DOI: 10.1146/Annurev-Pharmtox-010818-021050 |
0.338 |
|
2017 |
Pabon-Martinez YV, Xu Y, Villa A, Lundin KE, Geny S, Nguyen CH, Pedersen EB, Jørgensen PT, Wengel J, Nilsson L, Smith CIE, Zain R. LNA effects on DNA binding and conformation: from single strand to duplex and triplex structures. Scientific Reports. 7: 11043. PMID 28887512 DOI: 10.1038/S41598-017-09147-8 |
0.313 |
|
2016 |
Bergquist H, Rocha CS, Álvarez-Asencio R, Nguyen CH, Rutland MW, Smith CI, Good L, Nielsen PE, Zain R. Disruption of Higher Order DNA Structures in Friedreich's Ataxia (GAA)n Repeats by PNA or LNA Targeting. Plos One. 11: e0165788. PMID 27846236 DOI: 10.1371/Journal.Pone.0165788 |
0.328 |
|
2016 |
Ghidini A, Bergquist H, Murtola M, Punga T, Zain R, Strömberg R. Clamping of RNA with PNA enables targeting of microRNA. Organic & Biomolecular Chemistry. 14: 5210-3. PMID 27203783 DOI: 10.1039/C6Ob00516K |
0.533 |
|
2010 |
BOLLMARK M, KERS A, KERS I, SZABO T, ZAIN R, STAWINSKI J, CIESLAK J, JANKOWSKA J, KRASZEWSKI A. ChemInform Abstract: Studies on Nucleoside Phosphonates and Their Derivatives. A Progress Report Cheminform. 28: no-no. DOI: 10.1002/CHIN.199748298 |
0.739 |
|
2010 |
KERS A, KERS I, KRASZEWSKI A, SOBKOWSKI M, SZABO T, THELIN M, ZAIN R, STAWINSKI J. ChemInform Abstract: Nucleoside Phosphonates. Development of Synthetic Methods and Reagents Cheminform. 27: no-no. DOI: 10.1002/chin.199625321 |
0.505 |
|
2010 |
STAWINSKI J, STROEMBERG R, ZAIN R. ChemInform Abstract: Stereospecific Oxidation and Oxidative Coupling of H-Phosphonate and H- Phosphonothioate Diesters. Cheminform. 23: no-no. DOI: 10.1002/chin.199247254 |
0.557 |
|
2009 |
Bergquist H, Nikravesh A, Fernández RD, Larsson V, Nguyen CH, Good L, Zain R. Structure-specific recognition of Friedreich's ataxia (GAA)n repeats by benzoquinoquinoxaline derivatives. Chembiochem : a European Journal of Chemical Biology. 10: 2629-37. PMID 19746387 DOI: 10.1002/Cbic.200900263 |
0.358 |
|
2005 |
Amiri H, Nekhotiaeva N, Sun JS, Nguyen CH, Grierson DS, Good L, Zain R. Benzoquinoquinoxaline derivatives stabilize and cleave H-DNA and repress transcription downstream of a triplex-forming sequence. Journal of Molecular Biology. 351: 776-83. PMID 16045927 DOI: 10.1016/J.Jmb.2005.03.044 |
0.423 |
|
2004 |
Zaid A, Sun JS, Nguyen CH, Bisagni E, Garestier T, Grierson DS, Zain R. Triple-helix directed cleavage of double-stranded DNA by benzoquinoquinoxaline-1,10-phenanthroline conjugates. Chembiochem : a European Journal of Chemical Biology. 5: 1550-7. PMID 15515089 DOI: 10.1002/Cbic.200400074 |
0.323 |
|
2003 |
Zain R, Polverari D, Nguyen CH, Blouquit Y, Bisagni E, Garestier T, Grierson DS, Sun JS. Optimization of triple-helix-directed DNA cleavage by benzoquinoquinoxaline-ethylenediaminetetraacetic acid conjugates. Chembiochem : a European Journal of Chemical Biology. 4: 856-62. PMID 12964160 DOI: 10.1002/Cbic.200300621 |
0.329 |
|
1999 |
Zain R, Marchand C, Sun J, Nguyen CH, Bisagni E, Garestier T, Hélène C. Design of a triple-helix-specific cleaving reagent. Chemistry & Biology. 6: 771-7. PMID 10574778 DOI: 10.1016/S1074-5521(99)80124-0 |
0.364 |
|
1997 |
Zain R, Bollmark M, Stawinski J. Studies on Nucleoside H-Phosphonothioates as Synthons in the Synthesis of Oligonucleotide Analogues Nucleosides and Nucleotides. 16: 1661-1662. DOI: 10.1080/07328319708006250 |
0.8 |
|
1997 |
Bollmark M, Kers A, Kers I, Szabó T, Zain R, Stawiński J, Cieślak J, Jankowska J, Kraszewski A. Studies on Nucleoside Phosphonates and Their Derivatives. a Progress Report Nucleosides and Nucleotides. 16: 679-684. DOI: 10.1080/07328319708002934 |
0.684 |
|
1996 |
Zain R, Stawinski J. Nucleoside H-Phosphonates. 17. Synthetic and (31)P NMR Studies on the Preparation of Dinucleoside H-Phosphonothioates. The Journal of Organic Chemistry. 61: 6617-6622. PMID 11667530 DOI: 10.1021/Jo960810M |
0.647 |
|
1996 |
Bollmark M, Zain R, Stawinski J. Efficient method for the preparation of nucleoside phosphorofluoridates and nucleoside phosphorofluoridothioates Collection of Czechoslovak Chemical Communications. 61: 68-71. DOI: 10.1135/Cccc1996S068 |
0.726 |
|
1996 |
Kers A, Kers I, Kraszewski A, Sobkowski M, Szabó T, Thelin M, Zain R, Stawinski J. Nucleoside Phosphonates. Development of Synthetic Methods and Reagents Nucleosides and Nucleotides. 15: 361-378. DOI: 10.1080/07328319608002390 |
0.703 |
|
1996 |
Zain R, Stawiński J. Nucleoside H-phosphonates. Part 16. 31P NMR studies on the transformation of nucleoside H-phosphonate monoesters into a monofunctional tervalent intermediate, nucleoside acyl silyl phosphite Journal of the Chemical Society-Perkin Transactions 1. 795-799. DOI: 10.1039/P29960000795 |
0.638 |
|
1996 |
Bollmark M, Zain R, Stawiński J. A new entry to nucleoside phosphorofluoridate and nucleoside phosphorofluoridothioate diesters Tetrahedron Letters. 37: 3537-3540. DOI: 10.1016/0040-4039(96)00606-5 |
0.791 |
|
1995 |
Stawinski J, Zain R. Conversion of Nucleoside H-Phosphonate Monoesters to the Corresponding H-Phosphonothioates. 31P NMR Studies Nucleosides, Nucleotides and Nucleic Acids. 14: 711-714. DOI: 10.1080/15257779508012455 |
0.664 |
|
1995 |
Zain R, Stroemberg R, Stawinski J. Nucleoside H-Phosphonates. 15. Preparation of Nucleoside H-Phosphonothioate Monoesters from the Corresponding Nucleoside H-Phosphonates The Journal of Organic Chemistry. 60: 8241-8244. DOI: 10.1021/Jo00130A025 |
0.67 |
|
1993 |
Stawinski J, Strömberg R, Zain R. Hydrolytic stability of nucleoside H-phosphonate and H-phosphonothioate diesters Collection of Czechoslovak Chemical Communications. 58: 79-81. DOI: 10.1135/Cccc1993S079 |
0.737 |
|
1992 |
Stawiński J, Strömberg R, Zain R. Stereospecific oxidation and oxidative coupling of H-phosphonate and H-phosphonothioate diesters Tetrahedron Letters. 33: 3185-3188. DOI: 10.1016/S0040-4039(00)79847-9 |
0.713 |
|
1991 |
Stawinski J, Stromberg R, Zain R. Studies on the Conversion of Nucleoside H-Phosphonate Monoesters into the Corresponding H-Phosphonothioates Nucleosides and Nucleotides. 10: 515-516. DOI: 10.1080/07328319108046512 |
0.74 |
|
1990 |
Stawinski J, Szabó T, Thelin M, Westman E, Zain R. Studies on the preparation of nucleoside H-phosphonothioates Collection of Czechoslovak Chemical Communications. 55: 141-144. DOI: 10.1135/Cccc1990S141 |
0.732 |
|
1990 |
Stawinski J, Thelin M, Westman E, Zain R. Nucleoside H-phosphonates. 12. Synthesis of nucleoside 3'-(hydrogen phosphonothioate) monoesters via phosphinate intermediates The Journal of Organic Chemistry. 55: 3503-3506. DOI: 10.1021/Jo00298A023 |
0.763 |
|
1990 |
STAWINSKI J, THELIN M, WESTMAN E, ZAIN R. ChemInform Abstract: Nucleoside H-Phosphonates. Part 12. Synthesis of Nucleoside 3′-(Hydrogen Phosphonothioate) Monoesters via Phosphinate Intermediates. Cheminform. 21. DOI: 10.1002/chin.199043282 |
0.636 |
|
1989 |
Stawiński J, Thelin M, Zain R. Nucleoside H-phosphonates. X. Studies on nucleoside hydrogenphosphonothioate diester synthesis Tetrahedron Letters. 30: 2157-2160. DOI: 10.1016/S0040-4039(01)93737-2 |
0.81 |
|
Show low-probability matches. |