Relevant bibliographies by topics / Uracil

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Uracil'

Author: Grafiati
Published: 4 June 2021
Last updated: 26 July 2025

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Journal articles on the topic "Uracil"

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Isono, Yohei, Norikazu Sakakibara, Paula Ordonez, et al. "Synthesis of 1-benzyl-3-(3,5-dimethylbenzyl)Uracil Derivatives with Potential Anti-HIV Activity." Antiviral Chemistry and Chemotherapy 22, no. 2 (2011): 57–65. http://dx.doi.org/10.3851/imp1844.

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Background: Nine novel uracil analogues were synthesized and evaluated as inhibitors of HIV-1. Methods: Key structural modifications included replacement of the 6-chloro group of 1-benzyl-6-chloro-3-(3,5-dimethylbenzyl)uracil by other functional groups or N1-alkylation of 3-(3,5-dimethylbenzyl)-5-fluorouracil. Results: These compounds showed only micromolar potency against HIV-1 in MT-4, though two of them; 6-azido-1-benzyl-3-(3,5-dimethylbenzyl) uracil and 6-amino-1-benzyl-3-(3,5-dimethylbenzyl) uracil were highly potent (half maximal effective concentration =0.067 and 0.069 μM) and selective
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Maruyama, Tokumi, Shigetada Kozai, Tetsuo Yamasaki, et al. "Synthesis and Antiviral Activity of 1,3-Disubstituted Uracils against HIV-1 and HCMV." Antiviral Chemistry and Chemotherapy 14, no. 5 (2003): 271–79. http://dx.doi.org/10.1177/095632020301400506.

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The development of new non-nucleoside reverse transcriptase inhibitors (NNRTIs) is an efficient strategy for finding new therapeutic agents against human immunodeficiency virus (HIV). A large number of 6-substituted uracil derivatives have been prepared in order to explore new NNRTIs. However, there are few approaches to anti-HIV agents from 1,3-disubstituted uracil derivatives. Therefore, we tried to prepare several 1,3-disubstituted uracils, which were easily obtainable from uracil by preparation under alkali and Mitsunobu conditions, and examined their antiviral activity against HIV-1 and h
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Focher, F., A. Verri, S. Spadari, R. Manservigi, J. Gambino, and G. E. Wright. "Herpes simplex virus type 1 uracil-DNA glycosylase: isolation and selective inhibition by novel uracil derivatives." Biochemical Journal 292, no. 3 (1993): 883–89. http://dx.doi.org/10.1042/bj2920883.

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We have purified Herpes simplex type 1 (HSV1) uracil-DNA glycosylase from the nuclei of HSV1-infected HeLa cells harvested 8 h post-infection, at which time the induction of the enzyme is a maximum. The enzyme has been shown to be distinct from the host enzyme, isolated from HeLa cells, by its lack of sensitivity to a monoclonal antibody to human uracil-DNA glycosylase. Furthermore, several uracil analogues were synthesized and screened for their capacity to discriminate between the viral and human uracil-DNA glycosylases. Both enzymes were inhibited by 6-(p-alkylanilino)uracils, but the viral
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Girelli Zubani, Giulia, Marija Zivojnovic, Annie De Smet, et al. "Pms2 and uracil-DNA glycosylases act jointly in the mismatch repair pathway to generate Ig gene mutations at A-T base pairs." Journal of Experimental Medicine 214, no. 4 (2017): 1169–80. http://dx.doi.org/10.1084/jem.20161576.

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During somatic hypermutation (SHM) of immunoglobulin genes, uracils introduced by activation-induced cytidine deaminase are processed by uracil-DNA glycosylase (UNG) and mismatch repair (MMR) pathways to generate mutations at G-C and A-T base pairs, respectively. Paradoxically, the MMR-nicking complex Pms2/Mlh1 is apparently dispensable for A-T mutagenesis. Thus, how detection of U:G mismatches is translated into the single-strand nick required for error-prone synthesis is an open question. One model proposed that UNG could cooperate with MMR by excising a second uracil in the vicinity of the
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Colasurdo, Diego D., Matías N. Pila, Dacio A. Iglesias, Sergio L. Laurella, and Danila L. Ruiz. "Tautomerism of uracil and related compounds: A mass spectrometry study." European Journal of Mass Spectrometry 24, no. 2 (2017): 214–24. http://dx.doi.org/10.1177/1469066717712461.

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It has been demonstrated that uracil has a preponderant tautomeric form, but it is also known that different tautomers co-exist in this equilibrium. In this work, mass spectrometry is used as a helpful tool to analyse the equilibria, using derivative compounds to forbid the presence of some tautomers and ion trap mass spectrometry to follow relevant fragmentation pathways. Theoretical calculations were performed to confirm tautomers abundance by energy minimization in gas phase. Analysis of mass spectra of uracil, three methyl-substituted uracils, 2-thiouracil and three benzouracils suggest th
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Kavli, Bodil, Tobias S. Iveland, Edith Buchinger, et al. "RPA2 winged-helix domain facilitates UNG-mediated removal of uracil from ssDNA; implications for repair of mutagenic uracil at the replication fork." Nucleic Acids Research 49, no. 7 (2021): 3948–66. http://dx.doi.org/10.1093/nar/gkab195.

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Abstract Uracil occurs at replication forks via misincorporation of deoxyuridine monophosphate (dUMP) or via deamination of existing cytosines, which occurs 2–3 orders of magnitude faster in ssDNA than in dsDNA and is 100% miscoding. Tethering of UNG2 to proliferating cell nuclear antigen (PCNA) allows rapid post-replicative removal of misincorporated uracil, but potential ‘pre-replicative’ removal of deaminated cytosines in ssDNA has been questioned since this could mediate mutagenic translesion synthesis and induction of double-strand breaks. Here, we demonstrate that uracil-DNA glycosylase
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Di Noia, Javier M., Gareth T. Williams, Denice T. Y. Chan, Jean-Marie Buerstedde, Geoff S. Baldwin, and Michael S. Neuberger. "Dependence of antibody gene diversification on uracil excision." Journal of Experimental Medicine 204, no. 13 (2007): 3209–19. http://dx.doi.org/10.1084/jem.20071768.

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Activation-induced deaminase (AID) catalyses deamination of deoxycytidine to deoxyuridine within immunoglobulin loci, triggering pathways of antibody diversification that are largely dependent on uracil-DNA glycosylase (uracil-N-glycolase [UNG]). Surprisingly efficient class switch recombination is restored to ung−/− B cells through retroviral delivery of active-site mutants of UNG, stimulating discussion about the need for UNG's uracil-excision activity. In this study, however, we find that even with the overexpression achieved through retroviral delivery, switching is only mediated by UNG mu
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Bojarska, Elżbieta, Jarosław Kamiński, Ryszard Stolarski, and Zygmunt Kazimierczuk. "Novel Electrochemically Derived Dimers of Methylated Uracils." Zeitschrift für Naturforschung B 52, no. 6 (1997): 742–48. http://dx.doi.org/10.1515/znb-1997-0612.

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Abstract Electrolysis of acetic acid/sodium acetate solutions of N-methylated uracils results in the formation of 5-substituted methyl and acethoxy derivatives. Electrolysis of trifluoroacetic acid/potassium trifluoroacetate solutions of N-1-and N-3-methylated uracils provided, be­ sides 5-trifluoromethyl derivatives, novel N-C uracil dimers. In the case of 1,3-dimethyluracil in trifluoroacetic acid. N-l demethylathion was also observed.
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Nicodemos, Rodrigo A. Matus, David Ambrozak, Amy Ransier, Samuel Darko, Daniel C. Douek, and Richard A. Koup. "Identification of a New Lentivirus Restriction Counteracted by Vpr." Journal of Immunology 206, no. 1_Supplement (2021): 20.17. http://dx.doi.org/10.4049/jimmunol.206.supp.20.17.

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Abstract Lentiviruses encode non-structural accessory proteins that function to counteract host restriction factors. The lentivirus protein Vpr is known to block G2 to M transition of the cell cycle and degrades various host DNA repair proteins, including UNG2. The reason why Vpr induces these cellular changes in the infected cell is unknown. We explored this question by direct infection of primary resting and activated CD4 T cells with a CCR5-tropic replication-competent GFP reporter virus. We measured GFP expression by flow cytometry and virus expression by ELISA. We also performed bulk and
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Connolly, B. A., M. J. Fogg, G. Shuttleworth, and B. T. Wilson. "Uracil recognition by archaeal family B DNA polymerases." Biochemical Society Transactions 31, no. 3 (2003): 699–702. http://dx.doi.org/10.1042/bst0310699.

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Archaeal family-B DNA polymerases possess a novel uracil-sensing mechanism. A specialized pocket scans the template, ahead of the replication fork, for the presence of uracil; on encountering this base, DNA synthesis is stalled. The structural basis for uracil recognition by polymerases is described and compared with other uracil-recognizing enzymes (uridine-triphosphate pyrophophatases and uracil-DNA glycosylases). Remarkably, protein–protein interactions between all three archaeal uracil sensors are observed; possibly the enzymes co-operate to efficiently eliminate uracil from archaeal genom
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Dissertations / Theses on the topic "Uracil"

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Studebaker, Adam W. "Targeting uracil exclusion mechanisms for development of anti-viral and anti-cancer therapies." Connect to this title online, 2003. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1056034774.

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Thesis (Ph. D.)--Ohio State University, 2003.<br>Title from first page of PDF file. Document formatted into pages; contains xiii, 210 p.; also includes graphics (some col.). Includes bibliographical references (p. 174-210). Available online via OhioLINK's ETD Center
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Kemmerich, Kristin. "Studies of genomic uracil and its excision." Thesis, University of Cambridge, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.610133.

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Kandasamy, Dineshkumar. "Study on yeast enzymes Urc1p and Urc4p in a novel uracil catabolism pathway (URC)." Thesis, Uppsala universitet, Institutionen för biologisk grundutbildning, 2012. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-185013.

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Purine and pyrimidine bases are the central precursors of DNA and RNA and theirintracellular concentration is balanced by three pathways- de novo, salvage and catabolicpathways. Uracil catabolism pathway has been found in several bacteria and in some fungi(including yeast). Seven genes, URC1-7 have been found to be involved in this novelpathway. There are two “unknown genes” in the yeast Lachancea (Saccharomyces) kluyveri,namelyURC1 and URC4, which play a central role in this pathway and their exact functionremains a mystery.In this project, two S. kluyveri genes, URC1&amp;URC4, were over-expr
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Dworkin, Jason P. "Alternatives to uracil in the pre-RNA world /." Diss., Connect to a 24 p. preview or request complete full text in PDF format. Access restricted to UC campuses, 1997. http://wwwlib.umi.com/cr/ucsd/fullcit?p9804027.

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Hendrix, Alicia M. "Adenine Uracil Guanine: An Exploration of Certainty in Science." Scholarship @ Claremont, 2012. http://scholarship.claremont.edu/scripps_theses/157.

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Collaboration and communication between conventionally diverse fields can allow for deeper understanding and clearer analysis of the concepts within each. Two fields traditionally seen as dichotomous are those of art and science. Historically they approach problems in opposite ways. However, I would argue that they in fact investigate very similar questions, hoping to discover the ways that the world works. It makes sense, then, that historically these fields have sometimes been able to interact. Artists have engaged with science by creating work through scientific processes including crossbre
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Shuttleworth, Gillian. "Uracil recognition by the DNA polymerase from Pyrococcus furiosus." Thesis, University of Newcastle Upon Tyne, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.289269.

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Fituri, Hisham Saleh. "Synthesis of uracil containing precursors and analogues of cylindrospermopsin." Thesis, Bangor University, 2015. https://research.bangor.ac.uk/portal/en/theses/synthesis-of-uracil-containing-precursors-and-analogues-of-cylindrospermopsin(3d8eff07-e38b-4988-b4d6-b7942a797035).html.

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The thesis covers three topics: i) Synthesis of the uracil D-ring precursor of the cylindrospermopsin alkaloids: this study entailed the preparation of compounds I and II which were shown to be a RHS D-ring precursor in the synthesis of the cylindrospermopsin alkaloids. Compound I was prepared in 3 steps and in 24% overall yield from dibenzylurea whilst II was prepared from either diethyl 1,3-acetonedicarboxylate in 5 steps and 9% overall yield or barbituric acid in 5 steps and 16% overall yield. ii) Preparation of analogues of cylindrospermopsin: the synthesis of the cylindrospermopsin analog
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Dingler, Felix. "Investigations into origin and fate of uracil in the mouse genome." Thesis, University of Cambridge, 2015. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.708713.

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Galarza, Andrés Fernando Andrade. "Avaliação genotípica e fenotípica da enzima diidropirimidina desidrogenase (DPD) e risco de toxicidade com o uso de fluoropirimidinas." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2016. http://hdl.handle.net/10183/143351.

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Base teórica: As fluoropirimidinas possuem significativa variabilidade na resposta terapêutica e na ocorrência de toxicidade, o que tem sido relacionado à deficiência na depuração metabólica mediada pela enzima diidropirimidina desidrogenase (DPD). Mutações nos genes codificadores da enzima, bem como fatores ambientais podem levar à baixa ou nula expressão enzimática, provocando efeitos adversos graves devido ao acúmulo destes fármacos. Até o presente, nenhum teste reconhecidamente valido para a identificação de indivíduos em risco de toxicidade severa está estabelecido na prática oncológica.
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Krusong, Kuakarun. "Recognition and repair of DNA damage by uracil DNA glycosylase." Thesis, Imperial College London, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.417133.

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Books on the topic "Uracil"

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McKinnell, Denise. Phototransformation of 5-[inferior t]-butyl uracil derivatives. University of Birmingham, 1997.

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Bouzid, Bachir. Electrochemical behaviour and flow injection determination of uracil derivatives. University of Birmingham, 1987.

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Mutikainen, Ilpo. X-ray structural studies on metal complexes of uracil and orotic acid: A survey of coordination induced changes in the uracil fragment. Suomalainen Tiedeakatemia, 1988.

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Mori, Keita. Metal-Responsive Base Pair Switching of Ligand-type Uracil Nucleobases. Springer Nature Singapore, 2024. http://dx.doi.org/10.1007/978-981-99-9400-7.

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Koistinen, Pirjo. Uracil-DNA glycosylase activity in human benign and malignant hematopoiesis. University of Oulu, 1987.

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National Institute for Clinical Excellence. Guidance on the use of capecitabine and tegafur with uracil for metastatic colorectal cancer. National Institute for Clinical Excellence, 2003.

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Sue, Ward, and National Co-ordinating Centre for HTA (Great Britain), eds. Clinical and cost-effectiveness of capecitabine and tegafur with uracil for the treatment of metastatic colorectal cancer: Systematic review and economic evaluation. Core Research on behalf of the NCCHTA, 2003.

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Pavittiran̲. Uracal ōcaikaḷ. Tēciya Kalai Ilakkiyap Pēravai, 2002.

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Valeria, Finucci, ed. Urania. Bulzoni, 2002.

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Giulia, Bigolina. Urania. Bulzoni, 2002.

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Book chapters on the topic "Uracil"

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Miyakawa, Shin. "Uracil (Ura)." In Encyclopedia of Astrobiology. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-11274-4_1631.

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Schomburg, Dietmar, and Dörte Stephan. "Uracil dehydrogenase." In Enzyme Handbook 10. Springer Berlin Heidelberg, 1995. http://dx.doi.org/10.1007/978-3-642-57756-7_148.

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Miyakawa, Shin. "Uracil (Ura)." In Encyclopedia of Astrobiology. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-44185-5_1631.

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Schomburg, Dietmar, and Dörte Stephan. "Uracil phosphoribosyltransferase." In Enzyme Handbook 12. Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-61117-9_215.

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Miyakawa, Shin. "Uracil (Ura)." In Encyclopedia of Astrobiology. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65093-6_1631.

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Miyakawa, Shin. "Uracil (Ura)." In Encyclopedia of Astrobiology. Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-642-27833-4_1631-4.

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Miyakawa, Shin. "Uracil (Ura)." In Encyclopedia of Astrobiology. Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-27833-4_1631-3.

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Schomburg, Dietmar, and Ida Schomburg. "uracil-DNA glycosylase 3.2.2.27." In Class 2–3.2 Transferases, Hydrolases. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-36240-8_123.

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Schomburg, Dietmar, and Margit Salzmann. "Uracil-5-carboxylate decarboxylase." In Enzyme Handbook 1. Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-86605-0_62.

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Arnemann, J. "UNG (Uracil-DNA-Glycosidase)." In Springer Reference Medizin. Springer Berlin Heidelberg, 2019. http://dx.doi.org/10.1007/978-3-662-48986-4_3628.

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Conference papers on the topic "Uracil"

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Zamiri, Athena, Neaman Sohrabi, Kylie Raasch, Mina Sumita, and Mohammad Shavezipur. "Monitoring a Pseudouridine 5’-Monophosphate Synthesis Process Using an Interdigitated MEMS Sensor and Electrochemical Impedance Spectroscopy (EIS)." In ASME 2024 International Design Engineering Technical Conferences and Computers and Information in Engineering Conference. American Society of Mechanical Engineers, 2024. http://dx.doi.org/10.1115/detc2024-143474.

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Abstract This work presents a new method to monitor a biochemical enzymatic reaction, the synthesis of pseudouridine 5’-monophosphate (ΨMP) from uracil and ribose 5’-phosphate (R5P). Pseudouridine is a precursor of an important component, N1-methyl pseudouridine in mRNA-based vaccines. Conventional methods of monitoring the process such as thin-layered chromatography (TLC) and high-performance liquid chromatography (HPLC) are expensive and cumbersome. Here, we propose the use of an interdigitated MEMS sensor and electrochemical impedance spectroscopy (EIS) to monitor the progression of the syn
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Fritz, Hans-Joachim. "Mechanistic and evolutionary aspects of DNA-uracil glycosylases." In XIIth Symposium on Chemistry of Nucleic Acid Components. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2002. http://dx.doi.org/10.1135/css200205230.

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Shih, Yu-Chiao, Ying-Shun Liao, Chun-Chi Lin, et al. "Synthesis of 6-substituted uracil and uridine derivatives." In XVIth Symposium on Chemistry of Nucleic Acid Components. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2014. http://dx.doi.org/10.1135/css201414129.

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Lin, Xiumei, Tanja Deckert-Gaudig, Regina Treffer, Volker Deckert, P. M. Champion, and L. D. Ziegler. "Tip-Enhanced Raman Scattering (TERS) Of Uracil Strands." In XXII INTERNATIONAL CONFERENCE ON RAMAN SPECTROSCOPY. AIP, 2010. http://dx.doi.org/10.1063/1.3482412.

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Elkin, P. M., M. A. Erman, and O. V. Pulin. "Anharmonic analysis of vibrational spectra of substituted uracil." In SPIE Proceedings, edited by Vladimir L. Derbov, Leonid A. Melnikov, and Lev M. Babkov. SPIE, 2006. http://dx.doi.org/10.1117/12.696923.

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Grof, P., S. Gaspar, and A. Berces. "Uracil thin layers in dosimetry of UV-radiation." In Europto Biomedical Optics '93, edited by Kazuhiko Atsumi, Cornelius Borst, Frank W. Cross, et al. SPIE, 1994. http://dx.doi.org/10.1117/12.169152.

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ARSENE, Ion, and Viorica PURCEL. "Theoretical study of proton transfer in the uracil molecule." In "Instruire prin cercetare pentru o societate prosperă", conferinţă ştiinţifico-practică internaţională. Ion Creangă Pedagogical State University, 2024. https://doi.org/10.46727/c.v1.16-17-05-2024.p51-56.

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In this work, the possible mechanisms of proton migration in the process of tautomerization of the nitrogenous base uracil were studied. 3 possibilities for proton transfer initiation were identified and studied, with the stabilization anergy of 5 isomers studied. Using DFT calculations it was demonstrated that it is possible to control the tautomerization energy and the reaction barrier of each individual mechanism. The activation energy for all proton transfer mechanisms varies between 42.86 and 56.48 kcal/mol. The molecular structure with greater stability is the canonical form, present in
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Stewart, Jessica, Shanqiao Wei, Madhurima Datta, Umesh Varshney, and Ashok Bhagwat. "Abstract 3802: A novel uracil-DNA glycosylase, UdgX, as a new biochemical tool to directly detect uracils in DNA." In Proceedings: AACR Annual Meeting 2017; April 1-5, 2017; Washington, DC. American Association for Cancer Research, 2017. http://dx.doi.org/10.1158/1538-7445.am2017-3802.

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Bulgar, Alina, Lachelle D. Weeks, Yanling Miao, et al. "Abstract A104: Removal of uracil by uracil DNA glycosylase limits pemetrexed cytotoxicity: Overriding the limit with methoxyamine (TRC102) to inhibit base excision repair." In Abstracts: AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics--Nov 12-16, 2011; San Francisco, CA. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1535-7163.targ-11-a104.

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Fujita, Marta Akemi, Carla Marisa Brito Carvalho, Timothy John Brocksom та Kleber Thiago de Oliveira. "Synthesis and photophysical evaluations of β-fused Uracil- Porphyrin derivatives". У 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013912183035.

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Reports on the topic "Uracil"

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Niedenzu, K., and L. Komorowski. New Boron-Nitrogen Analogues of Uracil Derivatives. Defense Technical Information Center, 1989. http://dx.doi.org/10.21236/ada210164.

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อำนวยผล, สุรัตนา, ชัยโย ชัยชาญทิพยุทธ, สมบูรณ์ ธนาศุภวัฒน์ та จุฬาลงกรณ์มหาวิทยาลัย ภาควิชาเภสัชเวท. การศึกษาสารปฏิชีวนะของเชื้อ Micromonospora : รายงานผลการวิจัย. จุฬาลงกรณ์มหาวิทยาลัย, 2000. https://doi.org/10.58837/chula.res.2000.20.

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จากการเก็บตัวอย่างดินจากหลายบริเวณจำนวน 25 ตัวอย่าง พบว่า แยกเชื้อที่มีลักษณะโคโลนีชื้น สีค้ำด้วย 38 สายพันธุ์ นำเชื้อที่แยกได้มาทดสอบความสามารถในการสร้างสารปฏิชีวนะด้วยวิธี agar disc diffusion พบว่าเชื้อทั้ง 38 สายพันธุ์มความสามารถในการยับยั้งเชื้อแบคทีเรียแกรมบวก คือ S. aureus ATCC 25923 และ B. subtilis ATCC 6633 แต่มีผลเพียงเล็กน้อยในการยับยั้งเชื้อแบคทีเรียแกรมลบ คือ E. coli ATCC 25922 จากการศึกษาลักษณะทางสัณฐานวิทยาพบว่าเชื้อทั้งหมด จัดอยู่ในสกุล Micromonospora นำเชื้อคัดเลือกที่ให้ผลดีต่อการยับยั้งเชื้อทดสอบ ได้แก่ สายพันธุ์ JSM 5-1, JSM 1-3 และ A-25 มาศึกษาการสร้างสารปฏิชีวินะในอาหารเหล
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Su, Ning, Jerald S. Bradshaw, Xian X. Zhang, Paul B. Savage, and Krzystof E. Krakowiak. Syntheses of Diaza-18-Crown-6 Ligands Containing Two Units Each of 4-Hydroxyazobenzene, Benzimidazole, Uracil, Anthraquinone, or Ferrocene Groups. Defense Technical Information Center, 1999. http://dx.doi.org/10.21236/ada361715.

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Galán Párraga, Francisco José, and Antonio Ángel Moya Molina. EFECTO DEL VOLTAJE SOBRE LA CARGA ALMACENADA POR UN SUPERCONDENSADOR MEDIANTE LA PLATAFORMA ARDUINO. Fundación Avanza, 2025. https://doi.org/10.60096/fundacionavanza/11302025.

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El actual desarrollo de nuevas fuentes de energía renovable viene motivado por el fuerte aumento en el consumo de energía por parte de la sociedad, y la escasez de recursos naturales como el uranio, el carbón, el gas natural o el petróleo...
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K. Kubatko, K. Helean, A. Navrotsky, and P.C. Burns. Thermodynamics of Uranyl Minerals: Enthalpies of Formation of Uranyl Oxide Hydrates. Office of Scientific and Technical Information (OSTI), 2005. http://dx.doi.org/10.2172/859066.

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Ladd-Lively, Jennifer L. Uranyl Nitrate Flow Loop. Office of Scientific and Technical Information (OSTI), 2008. http://dx.doi.org/10.2172/939393.

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Duerksen, W. K. Photochemical reduction of uranyl nitrate. Office of Scientific and Technical Information (OSTI), 1993. http://dx.doi.org/10.2172/10193761.

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Youker, Amanda J., Michael Kalensky, Kevin J. Quigley, Thomas Brossard, Sergey D. Chemerisov, and George F. Vandegrift. Uranyl sulfate irradiations at the Van de Graaff: A means to combat uranyl peroxide precipitation. Office of Scientific and Technical Information (OSTI), 2017. http://dx.doi.org/10.2172/1409214.

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Bowers, D., and G. F. Vandegrift. Use of Uranyl Peroxide Precipitation as a Means to Clean up Irradiated Uranyl Sulfate Target Solutions. Office of Scientific and Technical Information (OSTI), 2013. http://dx.doi.org/10.2172/1131390.

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Kalensky, Michael, Thomas Brossard, Peter Tkac, and Sergey Chemerisov. Fission Induced Radiolysis of Uranyl Sulfate Solutions. Office of Scientific and Technical Information (OSTI), 2021. http://dx.doi.org/10.2172/1824778.

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