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Synthesis of Benzene-Glycol Nucleic Acids and Their Biophysical and Biological Properties.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 14, p. 2435, doi. 10.1002/ejoc.201600189
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- Article
4′‐C‐Aminoethoxy‐Modified DNAs Exhibit Increased Nuclease Resistance, Sustained RNase H Activity, and Inhibition of KRAS Gene Expression.
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- Chemistry & Biodiversity, 2022, v. 19, n. 8, p. 1, doi. 10.1002/cbdv.202200125
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Development of synthetic microRNA‐214 showing enhanced cytotoxicity and RNase resistance for treatment of canine hemangiosarcoma.
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- Veterinary & Comparative Oncology, 2020, v. 18, n. 4, p. 570, doi. 10.1111/vco.12580
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Antisense Gapmers with LNA-Wings and (S)-5′- C -Aminopropyl-2′-arabinofluoro-nucleosides Could Efficiently Suppress the Expression of KNTC2.
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- Molecules, 2022, v. 27, n. 21, p. 7384, doi. 10.3390/molecules27217384
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- Article
Intraperitoneal administration of synthetic microRNA-214 elicits tumor suppression in an intraperitoneal dissemination mouse model of canine hemangiosarcoma.
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- Veterinary Research Communications, 2022, v. 46, n. 2, p. 447, doi. 10.1007/s11259-021-09869-1
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- Article
Synthesis of 4′‐C‐(Aminoethyl)thymidine and 4′‐C‐[(N‐Methyl)aminoethyl] Thymidine Nucleosides to Enhance DNA Stability.
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- Current Protocols, 2022, v. 2, n. 9, p. 1, doi. 10.1002/cpz1.501
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IIAEK Targets Intestinal Alkaline Phosphatase (IAP) to Improve Cholesterol Metabolism with a Specific Activation of IAP and Downregulation of ABCA1.
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- Nutrients, 2020, v. 12, n. 9, p. 2859, doi. 10.3390/nu12092859
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Synthesis and Evaluation of 4′‐C‐(S) and 4′‐C‐(R)‐2‐Aminopropoxy−Thymidine‐Modified DNAs for Thermal Stability, RNase H Digestion, and Nuclease Resistance.
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- ChemistrySelect, 2024, v. 9, n. 23, p. 1, doi. 10.1002/slct.202305090
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- Article
A potent 2′-O-methylated RNA-based microRNA inhibitor with unique secondary structures.
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- Nucleic Acids Research, 2012, v. 40, n. 8, p. e58, doi. 10.1093/nar/gkr1317
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- Article
Crystal structures of DNA:DNA and DNA:RNA duplexes containing 5-(N-aminohexyl)carbamoyl-modified uracils reveal the basis for properties as antigene and antisense molecules.
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- Nucleic Acids Research, 2007, v. 35, n. 6, p. 1969, doi. 10.1093/nar/gkl821
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- Article
Synthesis, thermal stability and resistance to enzymatic hydrolysis of the oligonucleotides containing 5‐(N‐aminohexyl)carbamoyl‐2′‐O‐methyluridines.
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- Nucleic Acids Research, 2003, v. 31, n. 10, p. 2514, doi. 10.1093/nar/gkg374
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Crystallographic studies on damaged DNAs IV. N4-methoxycytosine shows a second face for Watson–Crick base-pairing, leading to purine transition mutagenesis.
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- Nucleic Acids Research, 2001, v. 29, n. 19, p. 3949, doi. 10.1093/nar/29.19.3949
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Synthesis and properties of oligonucleotides containing 5-formyl-2′-deoxycytidine: in vitro DNA polymerase reactions on DNA templates containing 5-formyl-2′-deoxycytidine.
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- Nucleic Acids Research, 2001, v. 29, n. 12, p. 2456, doi. 10.1093/nar/29.12.2456
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Insights into the Structures of DNA Damaged by Hydroxyl Radical: Crystal Structures of DNA Duplexes Containing 5-Formyluracil.
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- Journal of Nucleic Acids, 2010, p. 1, doi. 10.4061/2010/107289
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Depolarization-induced differentiation of PC12 cells is mediated by phospholipase D2 through the transcription factor CREB pathway.
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- Journal of Neurochemistry, 2008, v. 104, n. 5, p. 1372, doi. 10.1111/j.1471-4159.2007.05085.x
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- Article
Formation of 5-formyl-2′-deoxycytidine from 5-methyl-2′-deoxycytidine in duplex DNA by Fenton-type reactions and γ-irradiation.
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- Nucleic Acids Research, 1999, v. 27, n. 22, p. 4385, doi. 10.1093/nar/27.22.4385
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Effects of 2′‐O‐(trifluoromethyl)adenosine on oligodeoxynucleotide hybridization andnuclease stability.
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- Nucleic Acids Research, 1998, v. 26, n. 22, p. 5067, doi. 10.1093/nar/26.22.5067
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Effects of 5-(N-aminohexyl)carbamoyl-2'-deoxyuridine on endonuclease stability and the ability of oligodeoxynucleotide to activate RNase H.
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- Nucleic Acids Research, 1997, v. 25, n. 19, p. 3777, doi. 10.1093/nar/25.19.3777
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Site-specific introduction of functional groups into phosphodiester oligodeoxynucleotides and their thermal stability and nuclease-resistance properties.
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- Nucleic Acids Research, 1997, v. 25, n. 14, p. 2784, doi. 10.1093/nar/25.14.2784
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Mutagenicity of 5-Formylcytosine, an Oxidation Product of 5-Methylcytosine, in DNA in Mammalian Cells1.
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- Journal of Biochemistry, 2002, v. 132, n. 4, p. 551, doi. 10.1093/oxfordjournals.jbchem.a003256
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Crystallographic Studies on Damaged DNAs: III. N4-Methoxycytosine Can Form Both Watson-Crick Type and Wobbled Base Pairs in a B-Form Duplex1.
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- Journal of Biochemistry, 2001, v. 130, n. 1, p. 9, doi. 10.1093/oxfordjournals.jbchem.a002967
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- Article