Статті в журналах з теми "Synthetic Oligomers"
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Bazaco, Raúl Blanco, José L. Segura, and Carlos Seoane. "Recent advances in the design, synthesis and study of covalent conjugated oligomer–C60 ensembles." Collection of Czechoslovak Chemical Communications 74, no. 6 (2009): 857–86. http://dx.doi.org/10.1135/cccc2008218.
Повний текст джерелаKayama, Kotetsu, Hibiki Hashizume, Gerry Amor Camer, and Daiji Endoh. "An improved gene synthesis method with asymmetric directions of oligonucleotides designed using a simulation program." BioTechniques 69, no. 3 (September 2020): 211–19. http://dx.doi.org/10.2144/btn-2020-0062.
Повний текст джерелаAli, Dildar, Zaheer Ahmed, Peter M. Kazmaier, and Erwin Buncel. "Synthesis and characterization of low-molecular-weight azo-acetoxystyrene and azo-naphthalene oligomers via stable free radical polymerization (SFRP)." Canadian Journal of Chemistry 88, no. 9 (September 2010): 910–21. http://dx.doi.org/10.1139/v10-072.
Повний текст джерелаPils, Marlene, Alexandra Dybala, Fabian Rehn, Lara Blömeke, Tuyen Bujnicki, Victoria Kraemer-Schulien, Wolfgang Hoyer, Detlev Riesner, Dieter Willbold, and Oliver Bannach. "Development and Implementation of an Internal Quality Control Sample to Standardize Oligomer-Based Diagnostics of Alzheimer’s Disease." Diagnostics 13, no. 10 (May 11, 2023): 1702. http://dx.doi.org/10.3390/diagnostics13101702.
Повний текст джерелаOrlov, Y. N. "The impact of the of cationic polyelectrolyte polymerization degree in latexes coagulation dosage of synthetic emulsion rubbers." Proceedings of the Voronezh State University of Engineering Technologies 81, no. 1 (July 18, 2019): 318–24. http://dx.doi.org/10.20914/2310-1202-2019-1-318-324.
Повний текст джерелаMao, Jialin, Wei Zhang, Stephen ZD Cheng, and Chrys Wesdemiotis. "Analysis of monodisperse, sequence-defined, and POSS-functionalized polyester copolymers by MALDI tandem mass spectrometry." European Journal of Mass Spectrometry 25, no. 1 (February 2019): 164–74. http://dx.doi.org/10.1177/1469066719828875.
Повний текст джерелаWalsh, D. M., I. Klyubin, G. M. Shankar, M. Townsend, J. V. Fadeeva, V. Betts, M. B. Podlisny та ін. "The role of cell-derived oligomers of Aβ in Alzheimer's disease and avenues for therapeutic intervention". Biochemical Society Transactions 33, № 5 (26 жовтня 2005): 1087–90. http://dx.doi.org/10.1042/bst0331087.
Повний текст джерелаUrrego-Riveros, Sara, Matthias Bremer, Jonas Hoffmann, Anne Heitmann, Thibault Reynaldo, Janek Buhl, Paul J. Gates, et al. "Conjugated oligomers with alternating heterocycles from a single monomer: synthesis and demonstration of electroluminescence." Organic Chemistry Frontiers 6, no. 21 (2019): 3636–43. http://dx.doi.org/10.1039/c9qo00947g.
Повний текст джерелаNúñez-Villanueva, Diego, and Christopher A. Hunter. "Controlled mutation in the replication of synthetic oligomers." Chemical Science 12, no. 11 (2021): 4063–68. http://dx.doi.org/10.1039/d0sc06770a.
Повний текст джерелаBianco, Alberto. "ChemInform Abstract: Combinatorial Synthetic Oligomers." ChemInform 32, no. 41 (May 24, 2010): no. http://dx.doi.org/10.1002/chin.200141275.
Повний текст джерелаBouchard, Jacob L., Taylor C. Davey та Todd M. Doran. "Aβ(M1–40) and Wild-Type Aβ40 Self-Assemble into Oligomers with Distinct Quaternary Structures". Molecules 24, № 12 (15 червня 2019): 2242. http://dx.doi.org/10.3390/molecules24122242.
Повний текст джерелаDondoni, Alessandro. "Formylation of carbohydrates and the evolution of synthetic routes to artificial oligosaccharides and glycoconjugates." Pure and Applied Chemistry 72, no. 9 (January 1, 2000): 1577–88. http://dx.doi.org/10.1351/pac200072091577.
Повний текст джерелаKravchenko, Kateryna, Andreas Kulawik, Maren Hülsemann, Katja Kühbach, Christian Zafiu, Yvonne Herrmann, Christina Linnartz та ін. "Analysis of anticoagulants for blood-based quantitation of amyloid β oligomers in the sFIDA assay". Biological Chemistry 398, № 4 (1 квітня 2017): 465–75. http://dx.doi.org/10.1515/hsz-2016-0153.
Повний текст джерелаZeisig, Bernd B., Colin Kwok, Amanda J. Wilson, Arthur Zelent, Hinrich Gronemeyer, Shuo Dong та Chi Wai Eric So. "Recruitment of RXRα by Homo-Oligomeric RARα Is a Key for RARα-Mediated Transformation." Blood 108, № 11 (16 листопада 2006): 360. http://dx.doi.org/10.1182/blood.v108.11.360.360.
Повний текст джерелаVastl, Julian, Rendy Kartika, Kichul Park, Art E. Cho, and David A. Spiegel. "Peptidines: glycine-amidine-based oligomers for solution- and solid-phase synthesis." Chemical Science 7, no. 5 (2016): 3317–24. http://dx.doi.org/10.1039/c5sc03882k.
Повний текст джерелаCheung, David L. "Aggregation of an Amyloidogenic Peptide on Gold Surfaces." Biomolecules 13, no. 8 (August 18, 2023): 1261. http://dx.doi.org/10.3390/biom13081261.
Повний текст джерелаStross, Alexander E., Giulia Iadevaia, and Christopher A. Hunter. "Cooperative duplex formation by synthetic H-bonding oligomers." Chemical Science 7, no. 1 (2016): 94–101. http://dx.doi.org/10.1039/c5sc03414k.
Повний текст джерелаPugacheva, Inna N., Nadezhda S. Nikulina, and Sergey S. Nikulin. "TECHNOLOGICAL ASPECT OF PRODUCTION AND USE OF OIL-OLIGOMERIC ADDITIVE ON BASIS OF SECONDARY OLIGOMERS IN PRODUCTION OF EMULSION RUBBER." IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENIY KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA 61, no. 4-5 (April 17, 2018): 105. http://dx.doi.org/10.6060/tcct.20186104-05.5688.
Повний текст джерелаSancesario, Giulia M., Marzia Nuccetelli, Andrea Cerri, Joshua Zegeer, Cinzia Severini, Maria T. Ciotti, Massimo Pieri та ін. "Bromelain Degrades Aβ1-42 Monomers and Soluble Aggregates: An In Vitro Study in Cerebrospinal Fluid of Alzheimer’s Disease Patients". Current Alzheimer Research 15, № 7 (9 травня 2018): 628–36. http://dx.doi.org/10.2174/1567205015666180123124851.
Повний текст джерелаGalzitskaya, Oxana. "New Mechanism of Amyloid Fibril Formation." Current Protein & Peptide Science 20, no. 6 (May 20, 2019): 630–40. http://dx.doi.org/10.2174/1389203720666190125160937.
Повний текст джерелаBalducci, Claudia, Marten Beeg, Matteo Stravalaci, Antonio Bastone, Alessandra Sclip, Emiliano Biasini, Laura Tapella та ін. "Synthetic amyloid-β oligomers impair long-term memory independently of cellular prion protein". Proceedings of the National Academy of Sciences 107, № 5 (19 січня 2010): 2295–300. http://dx.doi.org/10.1073/pnas.0911829107.
Повний текст джерелаGabrielli, Luca, and Christopher A. Hunter. "Supramolecular catalysis by recognition-encoded oligomers: discovery of a synthetic imine polymerase." Chemical Science 11, no. 28 (2020): 7408–14. http://dx.doi.org/10.1039/d0sc02234a.
Повний текст джерелаNúñez-Villanueva, Diego, and Christopher A. Hunter. "Replication of Sequence Information in Synthetic Oligomers." Accounts of Chemical Research 54, no. 5 (February 6, 2021): 1298–306. http://dx.doi.org/10.1021/acs.accounts.0c00852.
Повний текст джерелаOhmori, Ken, Tomohiro Shono, Yuki Hatakoshi, Takahisa Yano, and Keisuke Suzuki. "Integrated Synthetic Strategy for Higher Catechin Oligomers." Angewandte Chemie International Edition 50, no. 21 (February 25, 2011): 4862–67. http://dx.doi.org/10.1002/anie.201007473.
Повний текст джерелаOhmori, Ken, Tomohiro Shono, Yuki Hatakoshi, Takahisa Yano, and Keisuke Suzuki. "Integrated Synthetic Strategy for Higher Catechin Oligomers." Angewandte Chemie 123, no. 21 (February 25, 2011): 4964–69. http://dx.doi.org/10.1002/ange.201007473.
Повний текст джерелаSable, Ganesh A., Kang Ju Lee та Hyun-Suk Lim. "Solid-Phase Synthesis and Circular Dichroism Study of β-ABpeptoids". Molecules 24, № 1 (5 січня 2019): 178. http://dx.doi.org/10.3390/molecules24010178.
Повний текст джерелаWuttke, André, Sebastian Nils Fischer, Annika Nebel, Michael Marsch та Armin Geyer. "Improved δ-valerolactam templates for the assembly of Aβ-miniamyloids by boronic ester formation". Organic & Biomolecular Chemistry 14, № 22 (2016): 5032–48. http://dx.doi.org/10.1039/c6ob00565a.
Повний текст джерелаHoyas Pérez, Nadia, and James E. M. Lewis. "Synthetic strategies towards mechanically interlocked oligomers and polymers." Organic & Biomolecular Chemistry 18, no. 35 (2020): 6757–80. http://dx.doi.org/10.1039/d0ob01583k.
Повний текст джерелаKim, DaWon, Jeong Hwa Lee, Hye Yun Kim, Jisu Shin, Kyeonghwan Kim, Sejin Lee, Jinwoo Park, JinIkyon Kim та YoungSoo Kim. "Fluorescent indolizine derivative YI-13 detects amyloid-β monomers, dimers, and plaques in the brain of 5XFAD Alzheimer transgenic mouse model". PLOS ONE 15, № 12 (23 грудня 2020): e0243041. http://dx.doi.org/10.1371/journal.pone.0243041.
Повний текст джерелаLi, Jie, Maxime Leclercq, Mathieu Fossepré, Mathieu Surin, Karine Glinel, Alain M. Jonas, and Antony E. Fernandes. "Discrete multifunctional sequence-defined oligomers with controlled chirality." Polymer Chemistry 11, no. 24 (2020): 4040–46. http://dx.doi.org/10.1039/d0py00537a.
Повний текст джерелаOta, Yusuke, Toshiki Murayama, and Kyoko Nozaki. "One-step catalytic asymmetric synthesis of all-syn deoxypropionate motif from propylene: Total synthesis of (2R,4R,6R,8R)-2,4,6,8-tetramethyldecanoic acid." Proceedings of the National Academy of Sciences 113, no. 11 (February 23, 2016): 2857–61. http://dx.doi.org/10.1073/pnas.1518898113.
Повний текст джерелаRosa-Gastaldo, Daniele, Vytautas Pečiukėnas, Christopher A. Hunter, and Luca Gabrielli. "Duplex vs. folding: tuning the self-assembly of synthetic recognition-encoded aniline oligomers." Organic & Biomolecular Chemistry 19, no. 41 (2021): 8947–54. http://dx.doi.org/10.1039/d1ob01882e.
Повний текст джерелаXu, Zhanjie, Peng Du, Peter Meiser, and Claus Jacob. "Proanthocyanidins: Oligomeric Structures with Unique Biochemical Properties and Great Therapeutic Promise." Natural Product Communications 7, no. 3 (March 2012): 1934578X1200700. http://dx.doi.org/10.1177/1934578x1200700321.
Повний текст джерелаVyas, Sandip B., and Lawrence K. Duffy. "Equilibration of a Synthetic Alzheimer 6-Protein Analog, 622-35, During RP-HPLC." Protein & Peptide Letters 3, no. 2 (April 1996): 89–94. http://dx.doi.org/10.2174/092986650302220614093454.
Повний текст джерелаStriepe, Laura, Marcus Vespa, and Thomas Baumgartner. "Synthesis and properties of electron accepting star-shaped phosphaviologen oligomers." Organic Chemistry Frontiers 4, no. 5 (2017): 717–23. http://dx.doi.org/10.1039/c6qo00872k.
Повний текст джерелаFurusho, Yoshio, and Eiji Yashima. "Development of synthetic double helical polymers and oligomers." Journal of Polymer Science Part A: Polymer Chemistry 47, no. 20 (October 15, 2009): 5195–207. http://dx.doi.org/10.1002/pola.23596.
Повний текст джерелаLehnherr, Dan, and Rik R. Tykwinski. "Conjugated Oligomers and Polymers Based on Anthracene, Tetracene, Pentacene, Naphthodithiophene, and Anthradithiophene Building Blocks." Australian Journal of Chemistry 64, no. 7 (2011): 919. http://dx.doi.org/10.1071/ch11169.
Повний текст джерелаde la Torre, Beatriz G., and Ramon Eritja. "Synthesis of labelled PNA oligomers by a post-synthetic modification approach." Bioorganic & Medicinal Chemistry Letters 13, no. 3 (February 2003): 391–93. http://dx.doi.org/10.1016/s0960-894x(02)00994-0.
Повний текст джерелаSato, Toyohiro, Yoshiaki Ohi, Daisuke Kato, Masayuki Mizuno, Hiroshi Takase, Tetsuko Kanamori, Cesar V. Borlongan, Akira Haji, and Noriyuki Matsukawa. "Hippocampal Cholinergic Neurostimulating Peptide as a Possible Modulating Factor against Glutamatergic Neuronal Disability by Amyloid Oligomers." Cell Transplantation 26, no. 9 (September 2017): 1542–50. http://dx.doi.org/10.1177/0963689717721232.
Повний текст джерелаFujiwara, Yoshiki, and Hitoshi Tamiaki. "Stereoselective self-aggregation of synthetic zinc 31-epimeric bacteriochlorophyll-d analogs possessing a methylene group at the 132-position as models of green photosynthetic bacterial chlorosomes." Photochemical & Photobiological Sciences 18, no. 5 (2019): 1218–27. http://dx.doi.org/10.1039/c8pp00535d.
Повний текст джерелаBlovský, Tomáš, Karel Šindelka, Zuzana Limpouchová, and Karel Procházka. "Changes in Ion Concentrations upon the Binding of Short Polyelectrolytes on Phospholipid Bilayers: Computer Study Addressing Interesting Physiological Consequences." Polymers 14, no. 17 (September 2, 2022): 3634. http://dx.doi.org/10.3390/polym14173634.
Повний текст джерелаZhang, Lei, Ling-Yan Jiang, Ke Zheng, Hua Duan, Min Li, and Yuan-Chen Cui. "Enzymatic Synthesis of p-Cresol Oligomers and Evaluation of their Free Radical Scavenging Activity." Australian Journal of Chemistry 68, no. 2 (2015): 282. http://dx.doi.org/10.1071/ch13734.
Повний текст джерелаWang, Peng, Filippa Lo Cascio, Jia Gao, Rakez Kayed, and Xuefei Huang. "Binding and neurotoxicity mitigation of toxic tau oligomers by synthetic heparin like oligosaccharides." Chemical Communications 54, no. 72 (2018): 10120–23. http://dx.doi.org/10.1039/c8cc05072d.
Повний текст джерелаMatos, Ana M., Joana S. Cristóvão, Dmitry V. Yashunsky, Nikolay E. Nifantiev, Ana S. Viana, Cláudio M. Gomes та Amélia P. Rauter. "Synthesis and effects of flavonoid structure variation on amyloid-β aggregation". Pure and Applied Chemistry 89, № 9 (28 серпня 2017): 1305–20. http://dx.doi.org/10.1515/pac-2017-0201.
Повний текст джерелаDuan, Chaofeng, Lu Shen, Yuqing Guo, Xiaogang Wang, Xiaohua Wang, and Zhixian Hao. "SERRS Detection on Silver Nanoparticles Supported on Acid-Treated Melamine-Resin Microspheres." Nanomaterials 11, no. 5 (May 19, 2021): 1337. http://dx.doi.org/10.3390/nano11051337.
Повний текст джерелаSouthcott, Mark, Mike Amone, James Senger, Andy Wang, Amy Polio, and C. H. Sheppard. "The development of processable, fully imidized, polyimides for high-temperature applications." High Performance Polymers 6, no. 1 (February 1994): 1–12. http://dx.doi.org/10.1088/0954-0083/6/1/001.
Повний текст джерелаDossi, Eleftheria, Jacob Earnshaw, Laurence Ellison, Gabriella Rabello dos Santos, Hamish Cavaye, and Douglas J. Cleaver. "Understanding and controlling the glass transition of HTPB oligomers." Polymer Chemistry 12, no. 17 (2021): 2606–17. http://dx.doi.org/10.1039/d1py00233c.
Повний текст джерелаSchwarzacher, Trude, and J. S. Heslop-Harrison. "In situ hybridization to plant telomeres using synthetic oligomers." Genome 34, no. 3 (June 1, 1991): 317–23. http://dx.doi.org/10.1139/g91-052.
Повний текст джерелаJohn, E., and F. Jähnig. "A synthetic analogue of melittin aggregates in large oligomers." Biophysical Journal 63, no. 6 (December 1992): 1536–43. http://dx.doi.org/10.1016/s0006-3495(92)81737-x.
Повний текст джерелаAdamus, Grazyna, Piotr Kurcok, Iza Radecka, and Marek Kowalczuk. "Bioactive oligomers from natural polyhydroxyalkanoates and their synthetic analogues." Polimery 62, no. 04 (April 2017): 317–22. http://dx.doi.org/10.14314/polimery.2017.317.
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