Добірка наукової літератури з теми "Glycotransferase"
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Статті в журналах з теми "Glycotransferase"
Borges, Chad R., Douglas S. Rehder, and Paolo Boffetta. "Multiplexed Surrogate Analysis of Glycotransferase Activity in Whole Biospecimens." Analytical Chemistry 85, no. 5 (February 15, 2013): 2927–36. http://dx.doi.org/10.1021/ac3035579.
Повний текст джерелаZhu, Zhongyu, Boopathy Ramakrishnan, Jinyu Li, Yanping Wang, Yang Feng, Ponraj Prabakaran, Simona Colantonio, Marzena A. Dyba, Pradman K. Qasba, and Dimiter S. Dimitrov. "Site-specific antibody-drug conjugation through an engineered glycotransferase and a chemically reactive sugar." mAbs 6, no. 5 (September 3, 2014): 1190–200. http://dx.doi.org/10.4161/mabs.29889.
Повний текст джерелаRahman, A. K. M. Shofiqur, Naoyasu Sugitani, Masahiro Hatsu та Kazuhiro Takamizawa. "A role of xylanase, α-L-arabinofuranosidase, and xylosidase in xylan degradation". Canadian Journal of Microbiology 49, № 1 (1 січня 2003): 58–64. http://dx.doi.org/10.1139/w02-114.
Повний текст джерелаAlonso, Leocadio, Patrick Fox, María Calvo, and Javier Fontecha. "Effect of Beta Cyclodextrin on the Reduction of Cholesterol in Ewe’s Milk Manchego Cheese." Molecules 23, no. 7 (July 20, 2018): 1789. http://dx.doi.org/10.3390/molecules23071789.
Повний текст джерелаGlickman, J. Fraser, and Doug Auld. "Generic Glycotransferases Assays." Assay and Drug Development Technologies 2, no. 4 (August 1, 2004): 445. http://dx.doi.org/10.1089/1540658041850706.
Повний текст джерелаZHU, Jing, Itaru WATANABE, Amanda POHOLEK, Matthew KOSS, Barbara GOMEZ, Chaowen YAN, Esperanza RECIO-PINTO, and William B. THORNHILL. "Allowed N-glycosylation sites on the Kv1.2 potassium channel S1–S2 linker: implications for linker secondary structure and the glycosylation effect on channel function." Biochemical Journal 375, no. 3 (November 1, 2003): 769–75. http://dx.doi.org/10.1042/bj20030517.
Повний текст джерелаPejenaute-Ochoa, María Dolores, Carlos Santana-Molina, Damien P. Devos, José Ignacio Ibeas, and Alfonso Fernández-Álvarez. "Structural, Evolutionary, and Functional Analysis of the Protein O-Mannosyltransferase Family in Pathogenic Fungi." Journal of Fungi 7, no. 5 (April 23, 2021): 328. http://dx.doi.org/10.3390/jof7050328.
Повний текст джерелаDejgaard, Selma Yilmaz, Ayesha Murshid, Kristina M. Dee, and John F. Presley. "Confocal Microscopy-based Linescan Methodologies for Intra-Golgi Localization of Proteins." Journal of Histochemistry & Cytochemistry 55, no. 7 (March 19, 2007): 709–19. http://dx.doi.org/10.1369/jhc.6a7090.2007.
Повний текст джерелаUrun, Yuksel, Kathryn M. Wilson, Irene M. Shui, Edward L. Giovannucci, Brian M. Wolpin, Paul Linh Nguyen, Lorelei A. Mucci, and Toni K. Choueiri. "ABO blood group and risk of lethal prostate cancer." Journal of Clinical Oncology 32, no. 4_suppl (February 1, 2014): 69. http://dx.doi.org/10.1200/jco.2014.32.4_suppl.69.
Повний текст джерелаTatlow, Dean. "Miglustat: A glycotransferase inhibitor for Covid-19 treatment." Qeios, January 21, 2021. http://dx.doi.org/10.32388/pe4tsq.
Повний текст джерелаДисертації з теми "Glycotransferase"
Azazna, Djamille. "Les bambusurils : molécules-cages pour l'encapsulation d'anions et utilisation comme nouvelles plateformes multivalentes d'intérêt biologique." Thesis, Université Paris-Saclay (ComUE), 2017. http://www.theses.fr/2017SACLS454.
Повний текст джерелаBambusurils, BU[4] and BU[6] are cyclic oligomers that belong to the cucurbiturils family, CBs, assembled respectively by 4 and 6 glycoluril units. Bambusurils are different from cucurbiturils because of their difunctionalized glycolurils. BU[6] are able to encapsulate anions inside their cavity and this property can be useful for the treatment of effluents.A new family of BUs, the allylbambusurils having allyls groups on their macrocyclic portal, has been developed. Their postfunctionalization by oxidation, cross metathesis and thiol-ene coupling has been studied. BU[4] and BU[6] functionalized by respectively 8 and 12 thiols of interest have been prepared.BU[6] are always obtained with an halide inside the cavity. A method using silver hexafluoroantimonate has been developed to remove this halide. Binding constants of these new empty bambusurils have been determined towards severals halide by 1H NMR.Glycobambusurils have been synthesized by thiol- ene coupling with thiosugars. These glycoBUs can lead to multivalent platforms of valency up to 8 for BU[4] and 12 for BU[6]. Inhibition activity of these new platforms has been tested on WaaC enzyme, an heptosyltransferase found in bacterial cell wall. Enzymatic tests show that these glycobambusurils are promising multivalent platforms
Pham, Trang Anh. "Cell wall biosynthesis in barley powdery mildew Blumeria graminis f. sp. hordei." Thesis, 2019. http://hdl.handle.net/2440/120552.
Повний текст джерелаThesis (Ph.D.) -- University of Adelaide, School of Agriculture, Food & Wine, 2019
Частини книг з теми "Glycotransferase"
Schomburg, Dietmar, and Dörte Stephan. "Dolichyl-diphosphooligosaccharide-protein glycotransferase." In Enzyme Handbook 12, 571–75. Berlin, Heidelberg: Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-61117-9_119.
Повний текст джерелаТези доповідей конференцій з теми "Glycotransferase"
Zhu, Zhongyu, Ramakrishnan Boopathy, Jinyu Li, Ponraj Prabakaran, Simona Colantonio, Yang Feng, Yanping Wang, Marzena A. Dyba, and Dimiter S. Dimitrov. "Abstract 2486: Site-specific antibody-drug conjugation through an engineered glycotransferase and a chemically reactive sugar." In Proceedings: AACR 106th Annual Meeting 2015; April 18-22, 2015; Philadelphia, PA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.am2015-2486.
Повний текст джерелаReilly, John P., Nuala J. Meyer, Rui Feng, Scarlett Bellamy, Paul N. Lanken, Robert Gallop, Michael G. S. Shashaty, et al. "Blood Group A And ABO Glycotransferase Genotype Are Associated With Increased Risk Of Acute Lung Injury After Blunt Trauma." In American Thoracic Society 2012 International Conference, May 18-23, 2012 • San Francisco, California. American Thoracic Society, 2012. http://dx.doi.org/10.1164/ajrccm-conference.2012.185.1_meetingabstracts.a1153.
Повний текст джерела