Статті в журналах з теми "Thymidine monophosphate"
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Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Thymidine monophosphate".
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Miyasaki, Taiko, and Katsuhiko Harada. "Effects of specific purine and pyrimidine compounds on the ingestion of test diets by the abalone Haliotis discus and the oriental weatherfish Misgurnus anguillicaudatus." Marine and Freshwater Research 54, no. 3 (2003): 235. http://dx.doi.org/10.1071/mf02066.
Повний текст джерелаGogolin, Lars, Ralf Seidel, Martin Engelhard, Roger S. Goody, and Christian F. W. Becker. "Semisynthesis of human thymidine monophosphate kinase." Biopolymers 94, no. 4 (June 3, 2010): 433–40. http://dx.doi.org/10.1002/bip.21398.
Повний текст джерелаWu, R. R., L. A. Hamlow, C. C. He, Y. w. Nei, G. Berden, J. Oomens, and M. T. Rodgers. "The intrinsic basicity of the phosphate backbone exceeds that of uracil and thymine residues: protonation of the phosphate moiety is preferred over the nucleobase for pdThd and pUrd." Physical Chemistry Chemical Physics 19, no. 45 (2017): 30351–61. http://dx.doi.org/10.1039/c7cp05521h.
Повний текст джерелаThompson, L. F. "Ecto-5'-nucleotidase can provide the total purine requirements of mitogen-stimulated human T cells and rapidly dividing human B lymphoblastoid cells." Journal of Immunology 134, no. 6 (June 1, 1985): 3794–97. http://dx.doi.org/10.4049/jimmunol.134.6.3794.
Повний текст джерелаGul, Sana, Ruqaiya Khalil, Zaheer Ul-Haq, and Mohammad S. Mubarak. "Computational Overview of Mycobacterial Thymidine Monophosphate Kinase." Current Pharmaceutical Design 26, no. 15 (May 18, 2020): 1676–81. http://dx.doi.org/10.2174/1381612826666200403114152.
Повний текст джерелаGustavsson, Thomas, Alexei Sharonov, and Dimitra Markovitsi. "Thymine, thymidine and thymidine 5′-monophosphate studied by femtosecond fluorescence upconversion spectroscopy." Chemical Physics Letters 351, no. 3-4 (January 2002): 195–200. http://dx.doi.org/10.1016/s0009-2614(01)01375-6.
Повний текст джерелаSchlosser, Julika, Julian F. M. Hebborn, Daria V. Berdnikova, and Heiko Ihmels. "Selective Fluorimetric Detection of Pyrimidine Nucleotides in Neutral Aqueous Solution with a Styrylpyridine-Based Cyclophane." Chemistry 5, no. 2 (May 11, 2023): 1220–32. http://dx.doi.org/10.3390/chemistry5020082.
Повний текст джерелаTomasz, Jeno, Barbara Ramsay Shaw, Ken Porter, Bernard F. Spielvogel, and Anup Sood. "5′-P-Borane-Substituted Thymidine Monophosphate and Triphosphate." Angewandte Chemie International Edition in English 31, no. 10 (October 1992): 1373–75. http://dx.doi.org/10.1002/anie.199213731.
Повний текст джерелаVan Poecke, Sara, Hélène Munier-Lehmann, Olivier Helynck, Matheus Froeyen, and Serge Van Calenbergh. "Synthesis and inhibitory activity of thymidine analogues targeting Mycobacterium tuberculosis thymidine monophosphate kinase." Bioorganic & Medicinal Chemistry 19, no. 24 (December 2011): 7603–11. http://dx.doi.org/10.1016/j.bmc.2011.10.021.
Повний текст джерелаKeita, M., A. Kumar, B. Dali, E. Megnassan, M. I. Siddiqi, V. Frecer, and S. Miertus. "Quantitative structure–activity relationships and design of thymine-like inhibitors of thymidine monophosphate kinase of Mycobacterium tuberculosis with favourable pharmacokinetic profiles." RSC Adv. 4, no. 99 (2014): 55853–66. http://dx.doi.org/10.1039/c4ra06917j.
Повний текст джерелаMukhina, T. M. "The effect of chlorination of nucleotide bases on the conformational properties of thymidine monophosphate." Ukrainian Biochemical Journal 87, no. 2 (April 27, 2015): 141–55. http://dx.doi.org/10.15407/ubj87.02.141.
Повний текст джерелаVanheusden, Veerle, Philippe Van Rompaey, Hélène Munier-Lehmann, Sylvie Pochet, Piet Herdewijn, and Serge Van Calenbergh. "Thymidine and thymidine-5′-O-monophosphate analogues as inhibitors of Mycobacterium tuberculosis thymidylate kinase." Bioorganic & Medicinal Chemistry Letters 13, no. 18 (September 2003): 3045–48. http://dx.doi.org/10.1016/s0960-894x(03)00643-7.
Повний текст джерелаHellendahl, Katja F., Sarah Kamel, Albane Wetterwald, Peter Neubauer, and Anke Wagner. "Human Deoxycytidine Kinase Is a Valuable Biocatalyst for the Synthesis of Nucleotide Analogues." Catalysts 9, no. 12 (November 27, 2019): 997. http://dx.doi.org/10.3390/catal9120997.
Повний текст джерелаSusan-Resiga, Delia, Alice T. Bentley, Matthew D. Lynx, Darcy D. LaClair, and Edward E. McKee. "Zidovudine Inhibits Thymidine Phosphorylation in the Isolated Perfused Rat Heart." Antimicrobial Agents and Chemotherapy 51, no. 4 (January 12, 2007): 1142–49. http://dx.doi.org/10.1128/aac.01227-06.
Повний текст джерелаChen, Bi-Xing, Karen Hubbard, Hiroshi Ide, Susan S. Wallace, and Bernard F. Erlanger. "Characterization of a Monoclonal Antibody to Thymidine Glycol Monophosphate." Radiation Research 124, no. 2 (November 1990): 131. http://dx.doi.org/10.2307/3577856.
Повний текст джерелаGarone, Caterina, Beatriz Garcia‐Diaz, Valentina Emmanuele, Luis C. Lopez, Saba Tadesse, Hasan O. Akman, Kurenai Tanji, Catarina M. Quinzii, and Michio Hirano. "Deoxypyrimidine monophosphate bypass therapy for thymidine kinase 2 deficiency." EMBO Molecular Medicine 6, no. 8 (June 26, 2014): 1016–27. http://dx.doi.org/10.15252/emmm.201404092.
Повний текст джерелаGabryel-Skrodzka, Malwina, Martyna Nowak, Anna Teubert, and Renata Jastrzab. "Coordination Chemistry of Phosphate Groups in Systems Including Copper(II) Ions, Phosphoethanolamine and Pyrimidine Nucleotides." International Journal of Molecular Sciences 23, no. 22 (November 8, 2022): 13718. http://dx.doi.org/10.3390/ijms232213718.
Повний текст джерелаBusam, Robert D. "Structure ofEscherichia coliexonuclease I in complex with thymidine 5′-monophosphate." Acta Crystallographica Section D Biological Crystallography 64, no. 2 (January 16, 2008): 206–10. http://dx.doi.org/10.1107/s090744490706012x.
Повний текст джерелаLee, Hyeon Cheol, Jung Mi Ahn, Sang Nam Lee, and Jung Hoe Kim. "Overproduction of thymidine by recombinant Brevibacterium helvolum amplified with thymidine monophosphate phosphohydrolase gene from bacteriophage PBS2." Biotechnology Letters 26, no. 4 (February 2004): 265–68. http://dx.doi.org/10.1023/b:bile.0000015423.83278.e2.
Повний текст джерелаFrecer, Vladimir, Pierfausto Seneci, and Stanislav Miertus. "Computer-assisted combinatorial design of bicyclic thymidine analogs as inhibitors of Mycobacterium tuberculosis thymidine monophosphate kinase." Journal of Computer-Aided Molecular Design 25, no. 1 (November 17, 2010): 31–49. http://dx.doi.org/10.1007/s10822-010-9399-4.
Повний текст джерелаRhaman, Md Mhahabubur, Douglas R. Powell, and Md Alamgir Hossain. "Supramolecular Assembly of Uridine Monophosphate (UMP) and Thymidine Monophosphate (TMP) with a Dinuclear Copper(II) Receptor." ACS Omega 2, no. 11 (November 10, 2017): 7803–11. http://dx.doi.org/10.1021/acsomega.7b01293.
Повний текст джерелаOwono Owono, Luc Calvin, Melalie Keita, Eugene Megnassan, Vladimir Frecer, and Stanislav Miertus. "Design of Thymidine Analogues Targeting Thymidilate Kinase ofMycobacterium tuberculosis." Tuberculosis Research and Treatment 2013 (2013): 1–13. http://dx.doi.org/10.1155/2013/670836.
Повний текст джерелаKira, Toshihiko, Susan P. Grill, Ginger E. Dutschman, Ju-Sheng Lin, Fucheng Qu, Yongseok Choi, Chung K. Chu та Yung-Chi Cheng. "Anti-Epstein-Barr Virus (EBV) Activity of β-l-5-Iododioxolane Uracil Is Dependent on EBV Thymidine Kinase". Antimicrobial Agents and Chemotherapy 44, № 12 (1 грудня 2000): 3278–84. http://dx.doi.org/10.1128/aac.44.12.3278-3284.2000.
Повний текст джерелаErickson, Blake A., Zachary N. Heim, Elisa Pieri, Erica Liu, Todd J. Martinez, and Daniel M. Neumark. "Relaxation Dynamics of Hydrated Thymine, Thymidine, and Thymidine Monophosphate Probed by Liquid Jet Time-Resolved Photoelectron Spectroscopy." Journal of Physical Chemistry A 123, no. 50 (November 22, 2019): 10676–84. http://dx.doi.org/10.1021/acs.jpca.9b08258.
Повний текст джерелаGasse, C., V. Huteau, D. Douguet, H. Munier-Lehmann, and S. Pochet. "A New Family of Inhibitors of Mycobacterium Tuberculosis Thymidine Monophosphate Kinase." Nucleosides, Nucleotides & Nucleic Acids 26, no. 8-9 (November 26, 2007): 1057–61. http://dx.doi.org/10.1080/15257770701513349.
Повний текст джерелаAhmad, Rizwan, Khurshid Alam, and Rashid Ali. "Antigen binding characteristics of antibodies against hydroxyl radical modified thymidine monophosphate." Immunology Letters 71, no. 2 (February 2000): 111–15. http://dx.doi.org/10.1016/s0165-2478(99)00177-7.
Повний текст джерелаGrachev, S. A., E. V. Kropachev, and G. I. Litvyakova. "Addition of cysteamine to thymine and thymidine monophosphate, initiated by ?-irradiation." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 34, no. 10 (October 1985): 2178–84. http://dx.doi.org/10.1007/bf00963257.
Повний текст джерелаMondal, Dibyendu, Eric M. Koehn, Jiajun Yao, David F. Wiemer, and Amnon Kohen. "Chemo-enzymatic synthesis of the exocyclic olefin isomer of thymidine monophosphate." Bioorganic & Medicinal Chemistry 26, no. 9 (May 2018): 2365–71. http://dx.doi.org/10.1016/j.bmc.2018.03.032.
Повний текст джерелаAvvakumova, Svetlana, Giorgio Scari, and Francesca Porta. "Au–thymine, thymidine and thymidine 5′-monophosphate nanoparticles: chemical characterisation and cellular uptake studies into U87 cancer cells." RSC Advances 2, no. 9 (2012): 3658. http://dx.doi.org/10.1039/c2ra20386c.
Повний текст джерелаVan Rompaey, Philippe, Koen Nauwelaerts, Veerle Vanheusden, Jef Rozenski, Hélène Munier-Lehmann, Piet Herdewijn, and Serge Van Calenbergh. "Mycobacterium tuberculosis Thymidine Monophosphate Kinase Inhibitors: Biological Evaluation and Conformational Analysis of 2′- and 3′-Modified Thymidine Analogues." European Journal of Organic Chemistry 2003, no. 15 (August 2003): 2911–18. http://dx.doi.org/10.1002/ejoc.200300177.
Повний текст джерелаLomozik, Lechoslaw, and Renata Jastrzab. "Noncovalent Interaction of Uridine 5′-Monophosphate with Adenosine, Cytidine, and Thymidine, as well as Adenosine 5′-Monophosphate and Cytidine 5′-Monophosphate in Aqueous Solution." Journal of Solution Chemistry 35, no. 2 (February 2006): 161–77. http://dx.doi.org/10.1007/s10953-006-9376-7.
Повний текст джерелаNavé, Jean-François, Bernhard Neises, and Anne Eschbach. "Study of Analogues of Thymidine-5′-Monophosphate and Thymidine as Substrates or Inhibitors of Chick Embryo Liver Thymidylate Kinase." Nucleosides and Nucleotides 15, no. 9 (September 1996): 1469–79. http://dx.doi.org/10.1080/07328319608002448.
Повний текст джерелаVan Daele, Ineke, Hélène Munier-Lehmann, Matheus Froeyen, Jan Balzarini та Serge Van Calenbergh. "Rational Design of 5‘-Thiourea-Substituted α-Thymidine Analogues as Thymidine Monophosphate Kinase Inhibitors Capable of Inhibiting Mycobacterial Growth". Journal of Medicinal Chemistry 50, № 22 (листопад 2007): 5281–92. http://dx.doi.org/10.1021/jm0706158.
Повний текст джерелаNAVE, J. F., B. NEISES, and A. ESCHBACH. "ChemInform Abstract: Analogues of Thymidine-5′-monophosphate and Thymidine as Substrates or Inhibitors of Chick Embryo Liver Thymidylate Kinase." ChemInform 28, no. 2 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199702189.
Повний текст джерелаBrickute, D., A. Beckley, L. Allott, M. Braga, C. Barnes, K. J. Thorley, and E. O. Aboagye. "Synthesis and evaluation of 3′-[18F]fluorothymidine-5′-squaryl as a bioisostere of 3′-[18F]fluorothymidine-5′-monophosphate." RSC Advances 11, no. 20 (2021): 12423–33. http://dx.doi.org/10.1039/d1ra00205h.
Повний текст джерелаZhou, Ping, Qiong Xiao, Zhao-Ting Su, Lin Zhu, Fang-Xia Jin, and Xuan-Yi Du. "Effect of parathyroid hormone-related protein on intracellular calcium ion and cyclic adenosine monophosphate concentrations in cardiac fibroblasts." Journal of International Medical Research 48, no. 9 (September 2020): 030006052093124. http://dx.doi.org/10.1177/0300060520931245.
Повний текст джерелаMaruno, K., A. Absood, and S. I. Said. "VIP inhibits basal and histamine-stimulated proliferation of human airway smooth muscle cells." American Journal of Physiology-Lung Cellular and Molecular Physiology 268, no. 6 (June 1, 1995): L1047—L1051. http://dx.doi.org/10.1152/ajplung.1995.268.6.l1047.
Повний текст джерелаRiegel, J. A., S. H. P. Maddrell, R. W. Farndale, and F. M. Caldwell. "Stimulation of fluid secretion of malpighian tubules of drosophila melanogaster meig. by cyclic nucleotides of inosine, cytidine, thymidine and uridine." Journal of Experimental Biology 201, no. 24 (December 15, 1998): 3411–18. http://dx.doi.org/10.1242/jeb.201.24.3411.
Повний текст джерелаAldritt, S. M., P. Tien, and C. C. Wang. "Pyrimidine salvage in Giardia lamblia." Journal of Experimental Medicine 161, no. 3 (March 1, 1985): 437–45. http://dx.doi.org/10.1084/jem.161.3.437.
Повний текст джерелаKitten, A. M., J. C. Lee, and M. S. Olson. "Osteogenic protein-1 enhances phenotypic expression in ROS 17/2.8 cells." American Journal of Physiology-Endocrinology and Metabolism 269, no. 5 (November 1, 1995): E918—E926. http://dx.doi.org/10.1152/ajpendo.1995.269.5.e918.
Повний текст джерелаIkeda, U., K. Okada, S. Ishikawa, T. Saito, T. Kasahara, and K. Shimada. "Monocyte chemoattractant protein 1 inhibits growth of rat vascular smooth muscle cells." American Journal of Physiology-Heart and Circulatory Physiology 268, no. 3 (March 1, 1995): H1021—H1026. http://dx.doi.org/10.1152/ajpheart.1995.268.3.h1021.
Повний текст джерелаGustafson, Erik A., Raymond F. Schinazi, and Joyce D. Fingeroth. "Human Herpesvirus 8 Open Reading Frame 21 Is a Thymidine and Thymidylate Kinase of Narrow Substrate Specificity That Efficiently Phosphorylates Zidovudine but Not Ganciclovir." Journal of Virology 74, no. 2 (January 15, 2000): 684–92. http://dx.doi.org/10.1128/jvi.74.2.684-692.2000.
Повний текст джерелаSameer Chitre, Trupti, Kalyani Dhirendra Asgaonkar, Shital Manoj Patil, Muthu Kumaradoss Kathiravan, and Subhash Balkrishna Padhye. "Exploring Pyrimidine Pharmacophore as Thymidine Monophosphate Kinase Inhibitors for Antitubercular Activity: A Review." Current Topics in Medicinal Chemistry 16, no. 28 (September 26, 2016): 3211–23. http://dx.doi.org/10.2174/1568026616666160506130914.
Повний текст джерелаVan Calenbergh, S., S. Pochet, and H. Munier-Lehmann. "Drug Design and Identification of Potent Leads Against Mycobacterium tuberculosis Thymidine Monophosphate Kinase." Current Topics in Medicinal Chemistry 12, no. 7 (March 1, 2012): 694–705. http://dx.doi.org/10.2174/156802612799984580.
Повний текст джерелаByun, Youngjoo, Susan R. Vogel, Andrew J. Phipps, Cecilia Carnrot, Staffan Eriksson, Rohit Tiwari, and Werner Tjarks. "Synthesis and Biological Evaluation of Inhibitors of Thymidine Monophosphate Kinase from Bacillus Anthracis." Nucleosides, Nucleotides and Nucleic Acids 27, no. 3 (February 8, 2008): 244–60. http://dx.doi.org/10.1080/15257770701845238.
Повний текст джерелаOgawa, Aoba, Gen-ichi Sampei, and Gota Kawai. "Crystal structure of the flavin-dependent thymidylate synthase Thy1 from Thermus thermophilus with an extra C-terminal domain." Acta Crystallographica Section F Structural Biology Communications 75, no. 6 (June 1, 2019): 450–54. http://dx.doi.org/10.1107/s2053230x19007192.
Повний текст джерелаWeinfeld, Michael, Norman E. Gentner, Lyle D. Johnson, and Malcolm C. Paterson. "Photoreversal: dependent release of thymidine and thymidine monophosphate from pyrimidine dimer containing DNA excision fragments isolated from ultraviolet-damaged human fibroblasts." Biochemistry 25, no. 9 (May 1986): 2656–64. http://dx.doi.org/10.1021/bi00357a055.
Повний текст джерелаZheng, Yuxiang, and Lewis C. Cantley. "Toward a better understanding of folate metabolism in health and disease." Journal of Experimental Medicine 216, no. 2 (December 26, 2018): 253–66. http://dx.doi.org/10.1084/jem.20181965.
Повний текст джерелаXue, Ying, Wei Jin, Xian-Shun Xu, Li Yong, Bin Hu, Jing Xiong, Xue-Mei Hu, Lin-Sen Qing, and Jing Xie. "Quality Evaluation of Tricholoma matsutake based on the Nucleic Acid Compounds by UPLC-TOF/MS and UPLC-QqQ/MS." Molecules 24, no. 1 (December 21, 2018): 34. http://dx.doi.org/10.3390/molecules24010034.
Повний текст джерелаKo, In Ok, Ki-Hye Jung, Mi Hyun Kim, Kyeung Jun Kang, Kyo Chul Lee, Kyeong Min Kim, Insup Noh, et al. "Preliminary19F-MRS Study of Tumor Cell Proliferation with 3′-deoxy-3′-fluorothymidine and Its Metabolite (FLT-MP)." Contrast Media & Molecular Imaging 2017 (2017): 1–7. http://dx.doi.org/10.1155/2017/3981358.
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