Academic literature on the topic 'Transient dimerization'

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Journal articles on the topic "Transient dimerization"

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Lin, C. L., Y. T. Huang, and J. D. Richter. "Transient CPEB dimerization and translational control." RNA 18, no. 5 (2012): 1050–61. http://dx.doi.org/10.1261/rna.031682.111.

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Wendler, Christian, and Hartmut Oehme. "The Synthesis and Dimerization of Transient 1-Silabutadienes." Zeitschrift f�r anorganische und allgemeine Chemie 622, no. 5 (1996): 801–6. http://dx.doi.org/10.1002/zaac.19966220509.

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Hartl, Maximilian J., Kristian Schweimer, Martin H. Reger, et al. "Formation of transient dimers by a retroviral protease." Biochemical Journal 427, no. 2 (2010): 197–203. http://dx.doi.org/10.1042/bj20091451.

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Retroviral proteases have been shown previously to be only active as homodimers. They are essential to form the separate and active proteins from the viral precursors. Spumaretroviruses produce separate precursors for Gag and Pol, rather than a Gag and a Gag–Pol precursor. Nevertheless, processing of Pol into a PR (protease)–RT (reverse transcriptase) and integrase is essential in order to obtain infectious viral particles. We showed recently that the PR–RT from a simian foamy virus, as well as the separate PRshort (protease) domain, exhibit proteolytic activities, although only monomeric form
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Pawar, Aiswarya B., Sneha A. Deshpande, Srinivasa M. Gopal, Tsjerk A. Wassenaar, Chaitanya A. Athale, and Durba Sengupta. "Thermodynamic and kinetic characterization of transmembrane helix association." Physical Chemistry Chemical Physics 17, no. 2 (2015): 1390–98. http://dx.doi.org/10.1039/c4cp03732d.

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The transient dimerization of transmembrane proteins is an important event in several cellular processes and here we use coarse-grain and meso-scale modeling methods to quantify their underlying dynamics.
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Nakasone, Yusuke, Taka-aki Ono, Asako Ishii, Shinji Masuda, and Masahide Terazima. "Transient Dimerization and Conformational Change of a BLUF Protein: YcgF." Journal of the American Chemical Society 129, no. 22 (2007): 7028–35. http://dx.doi.org/10.1021/ja065682q.

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Engelke, Ray, and Normand C. Blais. "Chemical dimerization of crystalline anthracene produced by transient high pressure." Journal of Chemical Physics 101, no. 12 (1994): 10961–72. http://dx.doi.org/10.1063/1.467846.

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Schröder, Jan, Daniel Himmel, Daniel Kratzert, et al. "Isolation of a stable pyridine radical anion." Chemical Communications 55, no. 9 (2019): 1322–25. http://dx.doi.org/10.1039/c8cc09700c.

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For almost 150 years, pyridine radical anions have been described as elusive transient species that cannot be isolated due to dimerization and/or subsequent decomposition reactions. In this work the first example of a stable pyridine radical anion is presented.
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El-Sayed, Ibrahim, Rita Grøbaek Hazell, Jørgen Øgaard Madsen, Per-Ola Norrby, and Alexander Senning. "An Unprecedented [2+3] Cycloadditive Dimerization of a Transient ThiocarbonylS-Ylide." European Journal of Organic Chemistry 2005, no. 2 (2005): 457. http://dx.doi.org/10.1002/ejoc.200400835.

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Cuquerella, M. Consuelo, Virginie Lhiaubet-Vallet, Miguel A. Miranda, and Francisco Bosca. "Drug–DNA complexation as the key factor in photosensitized thymine dimerization." Physical Chemistry Chemical Physics 19, no. 7 (2017): 4951–55. http://dx.doi.org/10.1039/c6cp08485k.

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The crucial role of photosensitizer@DNA complexation in the formation of cyclobutane pyrimidine dimers (CPDs) has been demonstrated using femtosecond and nanosecond transient absorption and emission measurements in combination with in vitro DNA damage assays.
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Li, Zhenzhen, Jianbang Wang, Zhixin Zhou, Michael P. O’Hagan, and Itamar Willner. "Gated Transient Dissipative Dimerization of DNA Tetrahedra Nanostructures for Programmed DNAzymes Catalysis." ACS Nano 16, no. 3 (2022): 3625–36. http://dx.doi.org/10.1021/acsnano.1c06117.

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Dissertations / Theses on the topic "Transient dimerization"

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LIEVENS, Patricia. "Transient dimerization in the early secretory pathway characterizes the FGF-Receptors biosynthesis." Doctoral thesis, 2007. http://hdl.handle.net/11562/337984.

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I recettori per i fattori di crescita dei fibroblasti (FGFR) presentano attività tirosino chinasica (TK) e vengono processati attraverso differenti fasi di maturazione/glicosilazione che avvengono nei compartimenti cellulari della via di secrezione. In questo studio abbiamo determinato due nuovi eventi che caratterizzano la biosintesi dell’FGFR3. Innanzitutto, dimostriamo che una limitata frazione del recettore selvaggio immaturo, ricco in mannosi, è sottoposta a dimerizzazione transeunte nelle fasi precoci della via secretoria. Diversamente, le forme glicosilate mature, proseguono vers
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