Works matching DE "PYRIMIDINE nucleosides"
Results: 85
Serum thymidine kinase 1 and C-reactive protein as biomarkers for screening clinically healthy dogs for occult disease.
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- Veterinary & Comparative Oncology, 2015, v. 13, n. 4, p. 373, doi. 10.1111/vco.12052
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A Shared Prebiotic Formation of Neopterins and Guanine Nucleosides from Pyrimidine Bases.
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- Chemistry - A European Journal, 2022, v. 28, n. 39, p. 1, doi. 10.1002/chem.202201680
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Front Cover: A Shared Prebiotic Formation of Neopterins and Guanine Nucleosides from Pyrimidine Bases (Chem. Eur. J. 39/2022).
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- Chemistry - A European Journal, 2022, v. 28, n. 39, p. 1, doi. 10.1002/chem.202201679
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A Shared Prebiotic Formation of Neopterins and Guanine Nucleosides from Pyrimidine Bases.
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- Chemistry - A European Journal, 2022, v. 28, n. 39, p. 1, doi. 10.1002/chem.202200714
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Synthesis of N‐Glycosides by Silver‐Assisted Gold Catalysis.
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- Angewandte Chemie, 2023, v. 135, n. 6, p. 1, doi. 10.1002/ange.202214167
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Microwave chemistry: Synthesis of purine and pyrimidine nucleosides using microwave radiation.
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- Journal of Carbohydrate Chemistry, 2019, v. 38, n. 1, p. 20, doi. 10.1080/07328303.2018.1543430
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Engineering a Bifunctional Fusion Purine/Pyrimidine Nucleoside Phosphorylase for the Production of Nucleoside Analogs.
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- Biomolecules (2218-273X), 2024, v. 14, n. 9, p. 1196, doi. 10.3390/biom14091196
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Repair and DNA Polymerase Bypass of Clickable Pyrimidine Nucleotides.
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- Biomolecules (2218-273X), 2024, v. 14, n. 6, p. 681, doi. 10.3390/biom14060681
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Nucleoside–AuCl<sub>4</sub><sup>−</sup> interactions as studied by electrospray ionization mass spectrometry.
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- Rapid Communications in Mass Spectrometry: RCM, 2019, v. 33, n. 13, p. 1164, doi. 10.1002/rcm.8452
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A thermostable pyrimidine nucleoside phosphorylase from Brevibacillus borstelensis LK01 for synthesizing halogenated nucleosides.
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- Biotechnology Letters, 2017, v. 39, n. 12, p. 1903, doi. 10.1007/s10529-017-2423-1
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Comparative Proteomic Analysis of Mycoplasma hominis Grown on Media with Different Carbon Sources.
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- Bulletin of Experimental Biology & Medicine, 2021, v. 171, n. 4, p. 449, doi. 10.1007/s10517-021-05247-8
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Thymidine kinases share a conserved function for nucleotide salvage and play an essential role in Arabidopsis thaliana growth and development.
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- New Phytologist, 2015, v. 208, n. 4, p. 1089, doi. 10.1111/nph.13530
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Total Synthesis of Nucleoside Antibiotics Amicetin, Plicacetin, and Cytosaminomycin A—D.
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- Chinese Journal of Chemistry, 2021, v. 39, n. 10, p. 2679, doi. 10.1002/cjoc.202100284
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Arabidopsis thaliana thymidine kinase 1a is ubiquitously expressed during development and contributes to confer tolerance to genotoxic stress.
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- Plant Molecular Biology, 2015, v. 87, n. 3, p. 303, doi. 10.1007/s11103-014-0277-7
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Understanding the Behavior of Thermomyces lanuginosus Lipase in Acylation of Pyrimidine Nucleosides Possessing 2′-Substituent.
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- Applied Biochemistry & Biotechnology, 2014, v. 174, n. 2, p. 556, doi. 10.1007/s12010-014-1096-7
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NMR studies of pyrimidinic nucleosides derived from 2,3‐dideoxy‐d‐ribose with inhibitory activity on LINE‐1 mobility.
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- Magnetic Resonance in Chemistry, 2020, v. 58, n. 1, p. 118, doi. 10.1002/mrc.4942
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HISTOPATHOLOGICAL EFFECTS OF FAVIPIRAVIR (705) ON THE LIVER AND KIDNEY OF MALE ALBINO RATS.
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- Biochemical & Cellular Archives, 2022, v. 22, n. 1, p. 887
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Biocoordination reactions in copper(II) ions and phosphocholine systems including pyrimidine nucleosides and nucleotides.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-37986-1
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Saliva Metabolomics in Dry Mouth Patients with Head and Neck Cancer or Sjögren's Syndrome.
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- Cells (2073-4409), 2022, v. 11, n. 3, p. 323, doi. 10.3390/cells11030323
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Tracking excited state decay mechanisms of pyrimidine nucleosides in real time.
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- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-27535-7
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Temporal evolution of master regulator Crp identifies pyrimidines as catabolite modulator factors.
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- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-26098-x
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DFT Study of Conformational Flexibilities and Interaction Profiles of New Class of Nucleoside Analogs Having Nucleic Acid Bases Pairs (Pyrimidine Analogues-Adenine) Linked Through a 1,2,3-Triazole Spacer.
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- Orbital: The Electronic Journal of Chemistry, 2013, v. 5, n. 4, p. 218
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Larger laboratory scale synthesis of 5-methyluridine and formal synthesis of its L-enantiomer.
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- ARKIVOC: Online Journal of Organic Chemistry, 2017, v. 2017, p. 249, doi. 10.3998/ark.5550190.0018.400
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Synthesis of 4'-C-alkylated-5-iodo-2'-deoxypyrimidine nucleosides.
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- ARKIVOC: Online Journal of Organic Chemistry, 2013, p. 46
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Synthesis and cytotoxic evaluation of apioarabinofuranosyl pyrimidines.
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- Drug Development Research, 2020, v. 81, n. 3, p. 274, doi. 10.1002/ddr.21613
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Characterization of pyrimidine nucleoside phosphorylase of Mycoplasma hyorhinis: implications for the clinical efficacy of nucleoside analogues.
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- Biochemical Journal, 2012, v. 445, n. 1, p. 113, doi. 10.1042/BJ20112225
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Substrate specificity of pyrimidine nucleoside phosphorylases of NP-II family probed by X-ray crystallography and molecular modeling.
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- Crystallography Reports, 2016, v. 61, n. 5, p. 830, doi. 10.1134/S1063774516050023
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Three-dimensional structure of thymidine phosphorylase from <i>E. coli</i> in complex with 3′-azido-2′-fluoro-2′,3′-dideoxyuridine.
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- Crystallography Reports, 2013, v. 58, n. 6, p. 842, doi. 10.1134/S1063774513060230
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Mycobacterium tuberculosis Infection: Control and Treatment.
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- Microorganisms, 2023, v. 11, n. 4, p. 1057, doi. 10.3390/microorganisms11041057
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Analogues of Pyrimidine Nucleosides as Mycobacteria Growth Inhibitors.
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- Microorganisms, 2022, v. 10, n. 7, p. N.PAG, doi. 10.3390/microorganisms10071299
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ENZYMATIC SYNTHESIS OF NUCLEOSIDES.
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- Journal of Nature Science & Sustainable Technology, 2022, v. 16, n. 4, p. 275
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Investigation of pyrimidine nucleoside analogues as chemical probes to assess compound effects on the proliferation of Trypanosoma cruzi intracellular parasites.
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- PLoS Neglected Tropical Diseases, 2020, v. 14, n. 3, p. 1, doi. 10.1371/journal.pntd.0008068
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Base Modifications of Nucleosides via the Use of Peptide‐Coupling Agents, and Beyond.
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- Chemical Record, 2023, v. 23, n. 1, p. 1, doi. 10.1002/tcr.202200182
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Relative mRNA expression of prostate-derived E-twenty-six factor and E-twenty-six variant 4 transcription factors, and of uridine phosphorylase-1 and thymidine phosphorylase enzymes, in benign and malignant prostatic tissue.
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- Oncology Letters, 2015, v. 9, n. 6, p. 2886, doi. 10.3892/ol.2015.3093
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Potential of Peptide Nucleic Acids in Future Therapeutic Applications.
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- Advanced Pharmaceutical Bulletin, 2018, v. 8, n. 4, p. 551, doi. 10.15171/apb.2018.064
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The Influence of pH on Complexation Process of Copper(II) Phosphoethanolamine to Pyrimidine Nucleosides.
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- Materials (1996-1944), 2021, v. 14, n. 15, p. 4309, doi. 10.3390/ma14154309
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Direct Access to Unique C‐5'‐Acyl Modified Nucleosides through Liebeskind–Srogl Cross‐Coupling Reaction.
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- European Journal of Organic Chemistry, 2022, v. 2022, n. 21, p. 1, doi. 10.1002/ejoc.202101061
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2'‐Derivatisation of 3'‐C‐Methyl Pyrimidine Nucleosides.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 29, p. 4007, doi. 10.1002/ejoc.202100236
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Effect of 5-Fluorouracil on Thymidine Phosphorylase Activity in Model Experiment.
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- Bulletin of Experimental Biology & Medicine, 2016, v. 160, n. 5, p. 646, doi. 10.1007/s10517-016-3239-z
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Nucleosides 11: synthesis of new derivatives of pyrido[2,3-d]pyrimidines and their nucleosides.
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- Nucleosides, Nucleotides & Nucleic Acids, 2021, v. 40, n. 2, p. 222, doi. 10.1080/15257770.2020.1862869
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Synthesis of 1′- C -Cyano Pyrimidine Nucleosides and Characterization as HCV Polymerase Inhibitors.
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- Nucleosides, Nucleotides & Nucleic Acids, 2015, v. 34, n. 11, p. 763, doi. 10.1080/15257770.2015.1075550
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The Pyrimidine Nucleoside Phosphorylase of Mycoplasma hyorhinis and How It May Affect Nucleoside-Based Therapy.
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- Nucleosides, Nucleotides & Nucleic Acids, 2014, v. 33, n. 4-6, p. 394, doi. 10.1080/15257770.2013.851394
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Phosphorylation of Nucleoside-Metallacarborane and Carborane Conjugates by Nucleoside Kinases.
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- Nucleosides, Nucleotides & Nucleic Acids, 2013, v. 32, n. 10, p. 571, doi. 10.1080/15257770.2013.838259
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Disaccharide Pyrimidine Nucleosides and Their Derivatives: A Novel Group of Cell-Penetrating Inhibitors of Poly(ADP-Ribose) Polymerase 1.
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- Nucleosides, Nucleotides & Nucleic Acids, 2013, v. 32, n. 9, p. 510, doi. 10.1080/15257770.2013.827793
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Synthesis of Novel Nucleoside Analogue Phosphorothioamidate Prodrugs and in vitro Anticancer Evaluation Against RKO Human Colon Carcinoma Cells.
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- Nucleosides, Nucleotides & Nucleic Acids, 2013, v. 32, n. 4, p. 161, doi. 10.1080/15257770.2013.770523
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Synthesis and Cytotoxic Activity of Novel 5-Substituted-1-(β-L-Arabinofuranosyl) Pyrimidine Nucleosides.
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- Nucleosides, Nucleotides & Nucleic Acids, 2012, v. 31, n. 6, p. 482, doi. 10.1080/15257770.2012.689410
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Novel C-5 Hydroxypropyl Pyrimidine Nucleosides: Synthesis and Structural Characterization.
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- Bulletin of the Chemists & Technologists of Bosnia & Herzegovina / Glasnik Hemičara i Tehnologa Bosne i Hercegovine, 2016, p. 121
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Increased renal elimination of endogenous and synthetic pyrimidine nucleosides in concentrative nucleoside transporter 1 deficient mice.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-38789-8
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Derivatives of Pyrimidine Nucleosides Affect Artificial Membranes Enriched with Mycobacterial Lipids.
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- Pharmaceutics, 2024, v. 16, n. 9, p. 1110, doi. 10.3390/pharmaceutics16091110
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Direct labeling of nucleosides with 3-thiazolylcoumarin fluorescent dyes.
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- Biopolymers & Cell, 2020, v. 36, n. 1, p. 36, doi. 10.7124/bc.000A1F
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