Статті в журналах з теми "Serine octamers"
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Nanita, Sergio C., and R. Graham Cooks. "Negatively-Charged Halide Adducts of Homochiral Serine Octamers." Journal of Physical Chemistry B 109, no. 10 (March 2005): 4748–53. http://dx.doi.org/10.1021/jp046653+.
Повний текст джерелаTakats, Zoltan, Sergio C. Nanita, Gitta Schlosser, Karoly Vekey, and R. Graham Cooks. "Atmospheric Pressure Gas-Phase H/D Exchange of Serine Octamers." Analytical Chemistry 75, no. 22 (November 2003): 6147–54. http://dx.doi.org/10.1021/ac034284s.
Повний текст джерелаNanita, Sergio C., and R. Graham Cooks. "Serine Octamers: Cluster Formation, Reactions, and Implications for Biomolecule Homochirality." Angewandte Chemie International Edition 45, no. 4 (January 16, 2006): 554–69. http://dx.doi.org/10.1002/anie.200501328.
Повний текст джерелаLiao, Guanhua, Yijie Yang, and Xianglei Kong. "Chirality effects on proline-substituted serine octamers revealed by infrared photodissociation spectroscopy." Phys. Chem. Chem. Phys. 16, no. 4 (2014): 1554–58. http://dx.doi.org/10.1039/c3cp53469c.
Повний текст джерелаYan, C., and T. Mélèse. "Multiple regions of NSR1 are sufficient for accumulation of a fusion protein within the nucleolus." Journal of Cell Biology 123, no. 5 (December 1, 1993): 1081–91. http://dx.doi.org/10.1083/jcb.123.5.1081.
Повний текст джерелаVandenbussche, Sophie, Guy Vandenbussche, Jacques Reisse, and Kristin Bartik. "Do Serine Octamers Exist in Solution? Relevance of this Question in the Context of the Origin of Homochirality on Earth." European Journal of Organic Chemistry 2006, no. 14 (July 2006): 3069–73. http://dx.doi.org/10.1002/ejoc.200600370.
Повний текст джерелаCriglar, Jeanette M., Ramakrishnan Anish, Liya Hu, Sue E. Crawford, Banumathi Sankaran, B. V. Venkataram Prasad, and Mary K. Estes. "Phosphorylation cascade regulates the formation and maturation of rotaviral replication factories." Proceedings of the National Academy of Sciences 115, no. 51 (December 3, 2018): E12015—E12023. http://dx.doi.org/10.1073/pnas.1717944115.
Повний текст джерелаJordan, Jacob S., and Evan R. Williams. "Dissociation of large gaseous serine clusters produces abundant protonated serine octamer." Analyst 146, no. 8 (2021): 2617–25. http://dx.doi.org/10.1039/d1an00273b.
Повний текст джерелаTakáts, Zoltán, and R. Graham Cooks. "Thermal formation of serine octamer ions." Chem. Commun., no. 4 (2004): 444–45. http://dx.doi.org/10.1039/b316768b.
Повний текст джерелаScutelnic, Valeriu, Marta A. S. Perez, Mateusz Marianski, Stephan Warnke, Aurelien Gregor, Ursula Rothlisberger, Michael T. Bowers, et al. "The Structure of the Protonated Serine Octamer." Journal of the American Chemical Society 140, no. 24 (April 11, 2018): 7554–60. http://dx.doi.org/10.1021/jacs.8b02118.
Повний текст джерелаTakats, Zoltan, Sergio C. Nanita, and R. Graham Cooks. "Serine Octamer Reactions: Indicators of Prebiotic Relevance." Angewandte Chemie International Edition 42, no. 30 (August 4, 2003): 3521–23. http://dx.doi.org/10.1002/anie.200351210.
Повний текст джерелаJordan, Jacob S., and Evan R. Williams. "Homochiral preference of serine octamer in solution and formed by dissociation of large gaseous clusters." Analyst 146, no. 22 (2021): 6822–30. http://dx.doi.org/10.1039/d1an01646f.
Повний текст джерелаJordan, Jacob S., and Evan R. Williams. "Homochiral preference of serine octamer in solution and formed by dissociation of large gaseous clusters." Analyst 146, no. 22 (2021): 6822–30. http://dx.doi.org/10.1039/d1an01646f.
Повний текст джерелаSpencer, Emily A. C., Tony Ly, and Ryan R. Julian. "Formation of the serine octamer: Ion evaporation or charge residue?" International Journal of Mass Spectrometry 270, no. 3 (March 2008): 166–72. http://dx.doi.org/10.1016/j.ijms.2007.12.011.
Повний текст джерелаFerreira da Silva, Filipe, Peter Bartl, Stephan Denifl, Tilmann D. Märk, Andrew M. Ellis, and Paul Scheier. "Formation of the Magic L-Serine Octamer in Helium Nanodroplets." ChemPhysChem 11, no. 1 (January 18, 2010): 90–92. http://dx.doi.org/10.1002/cphc.200900826.
Повний текст джерелаKoch, Kim J., Duxi Zhang, R. Graham Cooks, Fabio C. Gozzo, and Marcos N. Eberlin. "Serine octamer metaclusters: formation, structure elucidation and implications for homochiral polymerization." Chemical Communications, no. 18 (2001): 1854–55. http://dx.doi.org/10.1039/b107148n.
Повний текст джерелаSeo, Jongcheol, Stephan Warnke, Kevin Pagel, Michael T. Bowers, and Gert von Helden. "Infrared spectrum and structure of the homochiral serine octamer–dichloride complex." Nature Chemistry 9, no. 12 (July 10, 2017): 1263–68. http://dx.doi.org/10.1038/nchem.2821.
Повний текст джерелаKong, Xianglei, Cheng Lin, Giuseppe Infusini, Han-Bin Oh, Honghai Jiang, Kathrin Breuker, Chih-Che Wu, Oleg P. Charkin, Huan-Cheng Chang, and Fred W. McLafferty. "Numerous Isomers of Serine Octamer Ions Characterized by Infrared Photodissociation Spectroscopy." ChemPhysChem 10, no. 15 (October 19, 2009): 2603–6. http://dx.doi.org/10.1002/cphc.200900564.
Повний текст джерелаTakats, Zoltan, Sergio C. Nanita, and R. Graham Cooks. "Titelbild: Serine Octamer Reactions: Indicators of Prebiotic Relevance (Angew. Chem. 30/2003)." Angewandte Chemie 115, no. 30 (August 4, 2003): 3565. http://dx.doi.org/10.1002/ange.200390570.
Повний текст джерелаJulian, Ryan R., Robert Hodyss, Brian Kinnear, Martin F. Jarrold, and J. L. Beauchamp. "Nanocrystalline Aggregation of Serine Detected by Electrospray Ionization Mass Spectrometry: Origin of the Stable Homochiral Gas-Phase Serine Octamer." Journal of Physical Chemistry B 106, no. 6 (February 2002): 1219–28. http://dx.doi.org/10.1021/jp012265l.
Повний текст джерелаMazurek, Ulf, Orit Geller, Chava Lifshitz, Melinda A. McFarland, Alan G. Marshall, and Bryan G. Reuben. "Protonated Serine Octamer Cluster: Structure Elucidation by Gas-Phase H/D Exchange Reactions†." Journal of Physical Chemistry A 109, no. 10 (March 2005): 2107–12. http://dx.doi.org/10.1021/jp0451344.
Повний текст джерелаSunahori, Fumie X., Guochun Yang, Elena N. Kitova, John S. Klassen, and Yunjie Xu. "Chirality recognition of the protonated serine dimer and octamer by infrared multiphoton dissociation spectroscopy." Phys. Chem. Chem. Phys. 15, no. 6 (2013): 1873–86. http://dx.doi.org/10.1039/c2cp43296j.
Повний текст джерелаMazurek, Ulf. "Letter: Some More Aspects of Formation and Stability of the Protonated Serine Octamer Cluster." European Journal of Mass Spectrometry 12, no. 1 (February 2006): 63–69. http://dx.doi.org/10.1255/ejms.783.
Повний текст джерелаKasibhatla, Shailaja, Pankaj Tailor, Nathalie Bonefoy-Berard, Tomas Mustelin, Amnon Altman та Arun Fotedar. "Jun Kinase Phosphorylates and Regulates the DNA Binding Activity of an Octamer Binding Protein, T-Cell Factor β1". Molecular and Cellular Biology 19, № 3 (1 березня 1999): 2021–31. http://dx.doi.org/10.1128/mcb.19.3.2021.
Повний текст джерелаTakats, Zoltan, Sergio C. Nanita, and R. Graham Cooks. "Cover Picture: Serine Octamer Reactions: Indicators of Prebiotic Relevance (Angew. Chem. Int. Ed. 30/2003)." Angewandte Chemie International Edition 42, no. 30 (August 4, 2003): 3443. http://dx.doi.org/10.1002/anie.200390541.
Повний текст джерелаZhang, Hong, Zhenwei Wei, Jie Jiang, and R. Graham Cooks. "Nebulization Prior to Isolation, Ionization, and Dissociation of the Neutral Serine Octamer Allows Its Characterization." Angewandte Chemie 130, no. 52 (November 30, 2018): 17387–91. http://dx.doi.org/10.1002/ange.201811098.
Повний текст джерелаZhang, Hong, Zhenwei Wei, Jie Jiang, and R. Graham Cooks. "Nebulization Prior to Isolation, Ionization, and Dissociation of the Neutral Serine Octamer Allows Its Characterization." Angewandte Chemie International Edition 57, no. 52 (November 30, 2018): 17141–45. http://dx.doi.org/10.1002/anie.201811098.
Повний текст джерелаLansky, Shifra, Onit Alalouf, Hodaya Vered Solomon, Anat Alhassid, Lata Govada, Naomi E. Chayen, Hassan Belrhali, Yuval Shoham, and Gil Shoham. "A unique octameric structure of Axe2, an intracellular acetyl-xylooligosaccharide esterase fromGeobacillus stearothermophilus." Acta Crystallographica Section D Biological Crystallography 70, no. 2 (January 17, 2014): 261–78. http://dx.doi.org/10.1107/s139900471302840x.
Повний текст джерелаNanita, Sergio C., Zoltan Takats, R. Graham Cooks, Sunnie Myung, and David E. Clemmer. "Chiral enrichment of serine via formation, dissociation, and soft-landing of octameric cluster ions." Journal of the American Society for Mass Spectrometry 15, no. 9 (September 2004): 1360–65. http://dx.doi.org/10.1016/j.jasms.2004.06.010.
Повний текст джерелаRen, Juan, Yi-Yun Wang, Ru-Xia Feng, and Xiang-Lei Kong. "Investigation of l / d -threonine substituted l -serine octamer ions by mass spectrometry and infrared photodissociation spectroscopy." Chinese Chemical Letters 28, no. 3 (March 2017): 537–40. http://dx.doi.org/10.1016/j.cclet.2016.10.032.
Повний текст джерелаNebl, Gabriele, Stefan C. Meuer, and Yvonne Samstag. "Cyclosporin A-Resistant Transactivation of the IL-2 Promoter Requires Activity of Okadaic Acid-Sensitive Serine/Threonine Phosphatases." Journal of Immunology 161, no. 4 (August 15, 1998): 1803–10. http://dx.doi.org/10.4049/jimmunol.161.4.1803.
Повний текст джерелаGronert, Scott, Richard A. J. O'Hair, and Adelaide E. Fagin. "Ion/molecule reactions of the protonated serine octamerGas Phase Ion Chemistry of Biomolecules. Part 42.20." Chemical Communications, no. 17 (2004): 1944. http://dx.doi.org/10.1039/b407721k.
Повний текст джерелаKim, Dong Keon, Bomin Song, Suji Han, Hansol Jang, Seung-Hyun Bae, Hee Yeon Kim, Seon-Hyeong Lee, et al. "Phosphorylation of OCT4 Serine 236 Inhibits Germ Cell Tumor Growth by Inducing Differentiation." Cancers 12, no. 9 (September 11, 2020): 2601. http://dx.doi.org/10.3390/cancers12092601.
Повний текст джерелаHornemann, Thorsten, Yu Wei, and Arnold von Eckardstein. "Is the mammalian serine palmitoyltransferase a high-molecular-mass complex?" Biochemical Journal 405, no. 1 (June 13, 2007): 157–64. http://dx.doi.org/10.1042/bj20070025.
Повний текст джерелаMazurek, Ulf, Marianne Engeser, and Chava Lifshitz. "Gas-phase H/D exchange of the protonated serine octamer cluster: “Ion ping pong” of populations A and B." International Journal of Mass Spectrometry 249-250 (March 2006): 473–76. http://dx.doi.org/10.1016/j.ijms.2005.11.006.
Повний текст джерелаHernáez, M. J., E. Andújar, J. L. Ríos, S. R. Kaschabek, W. Reineke, and E. Santero. "Identification of a Serine Hydrolase Which Cleaves the Alicyclic Ring of Tetralin." Journal of Bacteriology 182, no. 19 (October 1, 2000): 5448–53. http://dx.doi.org/10.1128/jb.182.19.5448-5453.2000.
Повний текст джерелаKoch, Kim J., Fabio C. Gozzo, Sergio C. Nanita, Z. Takats, Marcos N. Eberlin, and R. Graham Cooks. "Chiral Transmission between Amino Acids: Chirally Selective Amino Acid Substitution in the Serine Octamer as a Possible Step in Homochirogenesis." Angewandte Chemie International Edition 41, no. 10 (May 17, 2002): 1721–24. http://dx.doi.org/10.1002/1521-3773(20020517)41:10<1721::aid-anie1721>3.0.co;2-5.
Повний текст джерелаKoch, Kim J., Fabio C. Gozzo, Sergio C. Nanita, Z. Takats, Marcos N. Eberlin, and R. Graham Cooks. "Chiral Transmission between Amino Acids: Chirally Selective Amino Acid Substitution in the Serine Octamer as a Possible Step in Homochirogenesis." Angewandte Chemie 114, no. 10 (May 17, 2002): 1797–800. http://dx.doi.org/10.1002/1521-3757(20020517)114:10<1797::aid-ange1797>3.0.co;2-v.
Повний текст джерелаCHEN, H., M. LI, W. JIN, Q. JIN, and J. ZHENG. "Detection of Serine Octamer by Desorption Electrospray Ionization Mass Spectrometry in Resultant Mixture of Aspartic Acid Exposed to Sunshine Under Natural Conditions." Chemical Research in Chinese Universities 23, no. 6 (November 2007): 650–53. http://dx.doi.org/10.1016/s1005-9040(07)60141-x.
Повний текст джерелаUmezurike, G. M. "The octameric structure of β-glucosidase from Botryodiplodia theobromae Pat". Biochemical Journal 275, № 3 (1 травня 1991): 721–25. http://dx.doi.org/10.1042/bj2750721.
Повний текст джерелаJameson, S. C., F. R. Carbone, and M. J. Bevan. "Clone-specific T cell receptor antagonists of major histocompatibility complex class I-restricted cytotoxic T cells." Journal of Experimental Medicine 177, no. 6 (June 1, 1993): 1541–50. http://dx.doi.org/10.1084/jem.177.6.1541.
Повний текст джерелаYe, Peng, Xiaoxia Chi, Xiuwen Yan, Fangqin Wu, Zhigang Liang, and Wen-Hao Yang. "Alanine–Glyoxylate Aminotransferase Sustains Cancer Stemness Properties through the Upregulation of SOX2 and OCT4 in Hepatocellular Carcinoma Cells." Biomolecules 12, no. 5 (May 5, 2022): 668. http://dx.doi.org/10.3390/biom12050668.
Повний текст джерелаNoone, David, Alistair Howell, and Kevin M. Devine. "Expression of ykdA, Encoding a Bacillus subtilis Homologue of HtrA, Is Heat Shock Inducible and Negatively Autoregulated." Journal of Bacteriology 182, no. 6 (March 15, 2000): 1592–99. http://dx.doi.org/10.1128/jb.182.6.1592-1599.2000.
Повний текст джерелаTrapp, Stefan, Peter Proks, Stephen J. Tucker, and Frances M. Ashcroft. "Molecular Analysis of ATP-sensitive K Channel Gating and Implications for Channel Inhibition by ATP." Journal of General Physiology 112, no. 3 (September 1, 1998): 333–49. http://dx.doi.org/10.1085/jgp.112.3.333.
Повний текст джерелаO'Leary, Brendan, Joonho Park, and William C. Plaxton. "The remarkable diversity of plant PEPC (phosphoenolpyruvate carboxylase): recent insights into the physiological functions and post-translational controls of non-photosynthetic PEPCs." Biochemical Journal 436, no. 1 (April 27, 2011): 15–34. http://dx.doi.org/10.1042/bj20110078.
Повний текст джерелаRimm, D. L., D. A. Kaiser, D. Bhandari, P. Maupin, D. P. Kiehart, and T. D. Pollard. "Identification of functional regions on the tail of Acanthamoeba myosin-II using recombinant fusion proteins. I. High resolution epitope mapping and characterization of monoclonal antibody binding sites." Journal of Cell Biology 111, no. 6 (December 1, 1990): 2405–16. http://dx.doi.org/10.1083/jcb.111.6.2405.
Повний текст джерелаNanita, Sergio C., and R. Graham Cooks. "Serine Octamers: Cluster Formation, Reactions, and Implications for Biomolecule Homochirality." ChemInform 37, no. 20 (May 16, 2006). http://dx.doi.org/10.1002/chin.200620232.
Повний текст джерела"Serine octamer reveals its structure." C&EN Global Enterprise 96, no. 19 (May 7, 2018): 9. http://dx.doi.org/10.1021/cen-09619-scicon6.
Повний текст джерелаChen, Rong, Zhenwei Wei, and R. Graham Cooks. "Collection and Characterization by Mass Spectrometry of the Neutral Serine Octamer Generated upon Sublimation." Analytical Chemistry, December 10, 2020. http://dx.doi.org/10.1021/acs.analchem.0c04107.
Повний текст джерелаJordan, Jacob S., and Evan R. Williams. "Effects of Electrospray Droplet Size on Analyte Aggregation: Evidence for Serine Octamer in Solution." Analytical Chemistry, December 28, 2020. http://dx.doi.org/10.1021/acs.analchem.0c04343.
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