Статті в журналах з теми "Glycan derivatives"
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Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Glycan derivatives".
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Park, Sungjin, Jung-Won Sung, and Injae Shin. "Fluorescent Glycan Derivatives: Their Use for Natural Glycan Microarrays." ACS Chemical Biology 4, no. 9 (September 18, 2009): 699–701. http://dx.doi.org/10.1021/cb9002078.
Повний текст джерелаZhang, Yao Y., Ahmed M. Senan, Ting Wang, Li Liu, and Josef Voglmeir. "1-(2-Aminoethyl)-3-methyl-1H-imidazol-3-ium tetrafluoroborate: synthesis and application in carbohydrate analysis." Pure and Applied Chemistry 91, no. 9 (September 25, 2019): 1441–50. http://dx.doi.org/10.1515/pac-2019-0117.
Повний текст джерелаHung, Wei-Ting, Yi-Ting Chen, Chung-Hsuan Chen, Yuan Chuan Lee, Jim-Min Fang, and Wen-Bin Yang. "Flow Chemistry System for Carbohydrate Analysis by Rapid Labeling of Saccharides after Glycan Hydrolysis." SLAS TECHNOLOGY: Translating Life Sciences Innovation 25, no. 4 (June 19, 2020): 356–66. http://dx.doi.org/10.1177/2472630320924620.
Повний текст джерелаTang, Jo Sing Julia, Sophia Rosencrantz, Lucas Tepper, Sany Chea, Stefanie Klöpzig, Anne Krüger-Genge, Joachim Storsberg, and Ruben R. Rosencrantz. "Functional Glyco-Nanogels for Multivalent Interaction with Lectins." Molecules 24, no. 10 (May 15, 2019): 1865. http://dx.doi.org/10.3390/molecules24101865.
Повний текст джерелаFujikawa, Kohki. "Glycan Derivatives That Possess Chaperone-Like Activity." Trends in Glycoscience and Glycotechnology 30, no. 177 (November 25, 2018): E241—E243. http://dx.doi.org/10.4052/tigg.1831.6e.
Повний текст джерелаFujikawa, Kohki. "Glycan Derivatives That Possess Chaperone-Like Activity." Trends in Glycoscience and Glycotechnology 30, no. 177 (November 25, 2018): J201—J202. http://dx.doi.org/10.4052/tigg.1831.6j.
Повний текст джерелаBrockhausen, Inka, Gabriele Möller, Annette Pollex-Krüger, Volker Rutz, Hans Paulsen та Khushi L. Matta. "Control of O-glycan synthesis: specificity and inhibition of O-glycan core 1 UDP-galactose:N-acetylgalactosamine-α-R β3-galactosyltransferase from rat liver". Biochemistry and Cell Biology 70, № 2 (1 лютого 1992): 99–108. http://dx.doi.org/10.1139/o92-015.
Повний текст джерелаYamada, Keita, Jun Hirabayashi, and Kazuaki Kakehi. "Analysis of O-Glycans as 9-Fluorenylmethyl Derivatives and Its Application to the Studies on Glycan Array." Analytical Chemistry 85, no. 6 (March 2013): 3325–33. http://dx.doi.org/10.1021/ac303771q.
Повний текст джерелаPikora, Cheryl, Christine Wittish, and Ronald C. Desrosiers. "Identification of Two N-Linked Glycosylation Sites within the Core of the Simian Immunodeficiency Virus Glycoprotein Whose Removal Enhances Sensitivity to Soluble CD4." Journal of Virology 79, no. 19 (October 1, 2005): 12575–83. http://dx.doi.org/10.1128/jvi.79.19.12575-12583.2005.
Повний текст джерелаSoriano del Amo, David, Wei Wang, Christen Besanceney, Tianqing Zheng, Yizheng He, Brian Gerwe, Ronald D. Seidel, and Peng Wu. "Chemoenzymatic synthesis of the sialyl Lewis X glycan and its derivatives." Carbohydrate Research 345, no. 9 (June 2010): 1107–13. http://dx.doi.org/10.1016/j.carres.2010.03.032.
Повний текст джерелаZhao, Xuesen, Fang Guo, Mary Ann Comunale, Anand Mehta, Mohit Sehgal, Pooja Jain, Andrea Cuconati, et al. "Inhibition of Endoplasmic Reticulum-Resident Glucosidases Impairs Severe Acute Respiratory Syndrome Coronavirus and Human Coronavirus NL63 Spike Protein-Mediated Entry by Altering the Glycan Processing of Angiotensin I-Converting Enzyme 2." Antimicrobial Agents and Chemotherapy 59, no. 1 (October 27, 2014): 206–16. http://dx.doi.org/10.1128/aac.03999-14.
Повний текст джерелаLe Guennec, Loic, Zoé Virion, Haniaa Bouzinba-Ségard, Catherine Robbe-Masselot, Renaud Léonard, Xavier Nassif, Sandrine Bourdoulous, and Mathieu Coureuil. "Receptor recognition by meningococcal type IV pili relies on a specific complex N-glycan." Proceedings of the National Academy of Sciences 117, no. 5 (January 21, 2020): 2606–12. http://dx.doi.org/10.1073/pnas.1919567117.
Повний текст джерелаCruz, Esteban, Vicki Sifniotis, Zeynep Sumer-Bayraktar, Mouhamad Reslan, Lorna Wilkinson-White, Stuart Cordwell, and Veysel Kayser. "Glycan Profile Analysis of Engineered Trastuzumab with Rationally Added Glycosylation Sequons Presents Significantly Increased Glycan Complexity." Pharmaceutics 13, no. 11 (October 20, 2021): 1747. http://dx.doi.org/10.3390/pharmaceutics13111747.
Повний текст джерелаHitchen, Paul, Joanna Brzostek, Maria Panico, Jonathan A. Butler, Howard R. Morris, Anne Dell, and Dennis Linton. "Modification of the Campylobacter jejuni flagellin glycan by the product of the Cj1295 homopolymeric-tract-containing gene." Microbiology 156, no. 7 (July 1, 2010): 1953–62. http://dx.doi.org/10.1099/mic.0.038091-0.
Повний текст джерелаFarese, R. V., D. R. Cooper, T. S. Konda, G. Nair, M. L. Standaert, and R. J. Pollet. "Insulin provokes co-ordinated increases in the synthesis of phosphatidylinositol, phosphatidylinositol phosphates and the phosphatidylinositol–glycan in BC3H-1 myocytes." Biochemical Journal 256, no. 1 (November 15, 1988): 185–88. http://dx.doi.org/10.1042/bj2560185.
Повний текст джерелаWang, W., T. Hu, P. A. Frantom, T. Zheng, B. Gerwe, D. S. del Amo, S. Garret, R. D. Seidel, and P. Wu. "Chemoenzymatic synthesis of GDP-L-fucose and the Lewis X glycan derivatives." Proceedings of the National Academy of Sciences 106, no. 38 (September 4, 2009): 16096–101. http://dx.doi.org/10.1073/pnas.0908248106.
Повний текст джерелаShao, M. C., C. C. Chin, R. M. Caprioli, and F. Wold. "The regulation of glycan processing in glycoproteins. The effect of avidin on individual steps in the processing of biotinylated glycan derivatives." Journal of Biological Chemistry 262, no. 7 (March 1987): 2973–79. http://dx.doi.org/10.1016/s0021-9258(18)61455-3.
Повний текст джерелаTang, Jo Sing Julia, Kristin Schade, Lucas Tepper, Sany Chea, Gregor Ziegler, and Ruben R. Rosencrantz. "Optimization of the Microwave Assisted Glycosylamines Synthesis Based on a Statistical Design of Experiments Approach." Molecules 25, no. 21 (November 4, 2020): 5121. http://dx.doi.org/10.3390/molecules25215121.
Повний текст джерелаMohammed, Soran, and Natalie Ferry. "Characterization of Sialic Acid Affinity of the Binding Domain of Mistletoe Lectin Isoform One." International Journal of Molecular Sciences 22, no. 15 (July 31, 2021): 8284. http://dx.doi.org/10.3390/ijms22158284.
Повний текст джерелаVirág, Dávid, Tibor Kremmer, Kende Lőrincz, Norbert Kiss, Antal Jobbágy, Szabolcs Bozsányi, Lili Gulyás, et al. "Altered Glycosylation of Human Alpha-1-Acid Glycoprotein as a Biomarker for Malignant Melanoma." Molecules 26, no. 19 (October 3, 2021): 6003. http://dx.doi.org/10.3390/molecules26196003.
Повний текст джерелаStelzl, Tamara, Kerstin E. Geillinger-Kästle, Jürgen Stolz, and Hannelore Daniel. "Glycans in the intestinal peptide transporter PEPT1 contribute to function and protect from proteolysis." American Journal of Physiology-Gastrointestinal and Liver Physiology 312, no. 6 (June 1, 2017): G580—G591. http://dx.doi.org/10.1152/ajpgi.00343.2016.
Повний текст джерелаLafont, Dominique, Paul Boullanger, Joseph Banoub та Gerard Descotes. "Synthesis of glycan fragments of glycoproteins using peracetylated N-allyloxycarbonyl-β-D-glucosamine and 1,6-anhydro-β-D-mannopyranose derivatives". Canadian Journal of Chemistry 68, № 6 (1 червня 1990): 828–35. http://dx.doi.org/10.1139/v90-131.
Повний текст джерелаOhkawa, Yuki, Yoichiro Harada, and Naoyuki Taniguchi. "Keratan sulfate-based glycomimetics using Langerin as a target for COPD: lessons from studies on Fut8 and core fucose." Biochemical Society Transactions 49, no. 1 (February 22, 2021): 441–53. http://dx.doi.org/10.1042/bst20200780.
Повний текст джерелаShamsi Kazem Abadi, Saeideh, Matthew C. Deen, Jacqueline N. Watson, Fahimeh S. Shidmoossavee, and Andrew J. Bennet. "Directed evolution of a remarkably efficient Kdnase from a bacterial neuraminidase." Glycobiology 30, no. 5 (December 4, 2019): 325–33. http://dx.doi.org/10.1093/glycob/cwz099.
Повний текст джерелаYang, Wen-Bin, Wei-Ting Hung, Yi-Ting Chen, Shwu-Huey Wang, and Yin-Chen Liu. "A new method for aldo-sugar analysis in beverages and dietary foods." Functional Foods in Health and Disease 6, no. 4 (April 27, 2016): 234. http://dx.doi.org/10.31989/ffhd.v6i4.251.
Повний текст джерелаPongracz, Tamas, Aswin Verhoeven, Manfred Wuhrer, and Noortje de Haan. "The structure and role of lactone intermediates in linkage-specific sialic acid derivatization reactions." Glycoconjugate Journal 38, no. 2 (January 18, 2021): 157–66. http://dx.doi.org/10.1007/s10719-020-09971-7.
Повний текст джерелаFaltinek, Lukáš, Eva Fujdiarová, Filip Melicher, Josef Houser, Martina Kašáková, Nikolay Kondakov, Leonid Kononov, Kamil Parkan, Sébastien Vidal та Michaela Wimmerová. "Lectin PLL3, a Novel Monomeric Member of the Seven-Bladed β-Propeller Lectin Family". Molecules 24, № 24 (11 грудня 2019): 4540. http://dx.doi.org/10.3390/molecules24244540.
Повний текст джерелаCollot, Mayeul, Julie Savreux, and Jean-Maurice Mallet. "New thioglycoside derivatives for use in odourless synthesis of MUXF3 N-glycan fragments related to food allergens." Tetrahedron 64, no. 7 (February 2008): 1523–35. http://dx.doi.org/10.1016/j.tet.2007.11.002.
Повний текст джерелаAdamiak, Kathrin, Thorsten Anders, Manja Henze, Helmut Keul, Martin Möller, and Lothar Elling. "Chemo-enzymatic synthesis of functionalized oligomers of N-acetyllactosamine glycan derivatives and their immobilization on biomaterial surfaces." Journal of Molecular Catalysis B: Enzymatic 84 (December 2012): 108–14. http://dx.doi.org/10.1016/j.molcatb.2012.02.002.
Повний текст джерелаLiu, Mingqi, Xiang Luo, Qiujun Qiu, Le Kang, Tang Li, Junqiang Ding, Yan Xiong, et al. "Redox- and pH-Sensitive Glycan (Polysialic Acid) Derivatives and F127 Mixed Micelles for Tumor-Targeted Drug Delivery." Molecular Pharmaceutics 15, no. 12 (November 3, 2018): 5534–45. http://dx.doi.org/10.1021/acs.molpharmaceut.8b00687.
Повний текст джерелаKiso, Makoto, Masayuki Kitagawa, Hideharu Ishida, and Akira Hasegawa. "Studies on Glycan Processing Inhibitors: Synthesis of N-Acetylhexosamine Analogs and Cyclic Carbamate Derivatives of 1-Deoxynojirimycin." Journal of Carbohydrate Chemistry 10, no. 1 (January 1991): 25–45. http://dx.doi.org/10.1080/07328309108543888.
Повний текст джерелаHoagland, Luke F. M., Michael J. Campa, Elizabeth B. Gottlin, James E. Herndon, and Edward F. Patz. "Haptoglobin and posttranslational glycan-modified derivatives as serum biomarkers for the diagnosis of nonsmall cell lung cancer." Cancer 110, no. 10 (2007): 2260–68. http://dx.doi.org/10.1002/cncr.23049.
Повний текст джерелаQu, Xiaowang, Xiaoben Pan, Jessica Weidner, Wenquan Yu, Dominic Alonzi, Xiaodong Xu, Terry Butters, Timothy Block, Ju-Tao Guo та Jinhong Chang. "Inhibitors of Endoplasmic Reticulum α-Glucosidases Potently Suppress Hepatitis C Virus Virion Assembly and Release". Antimicrobial Agents and Chemotherapy 55, № 3 (20 грудня 2010): 1036–44. http://dx.doi.org/10.1128/aac.01319-10.
Повний текст джерелаReihill, Mark, Lorenzo Guazzelli, Han Remaut, and Stefan Oscarson. "Synthesis of Fucose Derivatives with Thiol Motifs towards Suicide Inhibition of Helicobacter pylori." Molecules 25, no. 18 (September 18, 2020): 4281. http://dx.doi.org/10.3390/molecules25184281.
Повний текст джерелаTanaka, Katsunori, and Koichi Fukase. "Development of Azaelectrocyclization-Based Labeling and Application to Noninvasive Imaging and Targeting Using N-Glycan Derivatives—In Pursuit of N-Glycan Functions on Proteins, Dendrimers, and Living Cells—." Trends in Glycoscience and Glycotechnology 24, no. 136 (2012): 47–64. http://dx.doi.org/10.4052/tigg.24.47.
Повний текст джерелаNakano, M., D. Higo, E. Arai, T. Nakagawa, K. Kakehi, N. Taniguchi, and A. Kondo. "Capillary electrophoresis-electrospray ionization mass spectrometry for rapid and sensitive N-glycan analysis of glycoproteins as 9-fluorenylmethyl derivatives." Glycobiology 19, no. 2 (October 24, 2008): 135–43. http://dx.doi.org/10.1093/glycob/cwn115.
Повний текст джерелаKISO, M., M. KITAGAWA, H. ISHIDA, and A. HASEGAWA. "ChemInform Abstract: Studies on Glycan Processing Inhibitors: Synthesis of N- Acetylhexosamine Analogs and Cyclic Carbamate Derivatives of 1- Deoxynojirimycin." ChemInform 23, no. 3 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199203310.
Повний текст джерелаWU, Albert M., June H. WU, Anthony HERP, and Jia-Hau LIU. "Effect of polyvalencies of glycotopes on the binding of a lectin from the edible mushroom, Agaricus bisporus." Biochemical Journal 371, no. 2 (April 15, 2003): 311–20. http://dx.doi.org/10.1042/bj20021361.
Повний текст джерелаTkachuk, Zenoviy, Nataliia Melnichuk, Roman O. Nikolaiev, Kosma Szutkowski, and Igor Zhukov. "The Natural Oligoribonucleotides Functionalized by D-Mannitol Affected Interactions of Hemagglutinin with Glycan Receptor Indicating Anti-Influenza Activity." Membranes 11, no. 10 (September 30, 2021): 757. http://dx.doi.org/10.3390/membranes11100757.
Повний текст джерелаHorník, Štěpán, Lucie Červenková Šťastná, Petra Cuřínová, Jan Sýkora, Kateřina Káňová, Roman Hrstka, Ivana Císařová, Martin Dračínský, and Jindřich Karban. "Synthesis and in vitro cytotoxicity of acetylated 3-fluoro, 4-fluoro and 3,4-difluoro analogs of D-glucosamine and D-galactosamine." Beilstein Journal of Organic Chemistry 12 (April 20, 2016): 750–59. http://dx.doi.org/10.3762/bjoc.12.75.
Повний текст джерелаJohnson, Welkin E., Hannah Sanford, Linda Schwall, Dennis R. Burton, Paul W. H. I. Parren, James E. Robinson, and Ronald C. Desrosiers. "Assorted Mutations in the Envelope Gene of Simian Immunodeficiency Virus Lead to Loss of Neutralization Resistance against Antibodies Representing a Broad Spectrum of Specificities." Journal of Virology 77, no. 18 (September 15, 2003): 9993–10003. http://dx.doi.org/10.1128/jvi.77.18.9993-10003.2003.
Повний текст джерелаPARODI, Armando J. "Role of N-oligosaccharide endoplasmic reticulum processing reactions in glycoprotein folding and degradation." Biochemical Journal 348, no. 1 (May 9, 2000): 1–13. http://dx.doi.org/10.1042/bj3480001.
Повний текст джерелаDeng, Lingquan, Xin Wang, Suji Uppalapati, Oscar Norberg, Hai Dong, Adrien Joliton, Mingdi Yan, and Olof Ramström. "Stereocontrolled 1-S-glycosylation and comparative binding studies of photoprobe-thiosaccharide conjugates with their O-linked analogs." Pure and Applied Chemistry 85, no. 9 (September 1, 2013): 1789–801. http://dx.doi.org/10.1351/pac-con-12-08-13.
Повний текст джерелаHattori, Kazuyuki, та Takashi Yoshida. "Synthesis of a new 2-amino-glycan, poly-(1→6)-α-D -mannosamine, by ring-opening polymerization of 1,6-anhydro-mannosamine derivatives". Journal of Polymer Science Part A: Polymer Chemistry 50, № 21 (3 серпня 2012): 4524–31. http://dx.doi.org/10.1002/pola.26262.
Повний текст джерелаAstronomo, Rena D., Hing-Ken Lee, Christopher N. Scanlan, Ralph Pantophlet, Cheng-Yuan Huang, Ian A. Wilson, Ola Blixt, Raymond A. Dwek, Chi-Huey Wong, and Dennis R. Burton. "A Glycoconjugate Antigen Based on the Recognition Motif of a Broadly Neutralizing Human Immunodeficiency Virus Antibody, 2G12, Is Immunogenic but Elicits Antibodies Unable To Bind to the Self Glycans of gp120." Journal of Virology 82, no. 13 (April 23, 2008): 6359–68. http://dx.doi.org/10.1128/jvi.00293-08.
Повний текст джерелаEaston, CJ, та SC Peters. "Reactions of α-Substituted Glycine Derivatives With Stannanes in the Presence of Disulfides". Australian Journal of Chemistry 47, № 5 (1994): 859. http://dx.doi.org/10.1071/ch9940859.
Повний текст джерелаJankowska, Ewa, and John Cipollo. "Platform for analysis of anthranilic acidN-glycan derivatives utilizing multipolarity mode LC–MS with hydrophilic interaction chromatography separation and ion trap MS/MS." Bioanalysis 3, no. 21 (November 2011): 2401–17. http://dx.doi.org/10.4155/bio.11.247.
Повний текст джерелаCao, Benjamin, Jonathan M. White, and Spencer J. Williams. "Synthesis of glycoconjugate fragments of mycobacterial phosphatidylinositol mannosides and lipomannan." Beilstein Journal of Organic Chemistry 7 (March 28, 2011): 369–77. http://dx.doi.org/10.3762/bjoc.7.47.
Повний текст джерелаMistry, Rakesh N., and K. R. Desai. "Studies on Synthesis of Some Novel Heterocyclic Azlactone Derivatives and Imidazolinone Derivatives and their Antimicrobial Activity." E-Journal of Chemistry 2, no. 1 (2005): 42–51. http://dx.doi.org/10.1155/2005/542938.
Повний текст джерелаPföstl, Andreas, Sonja Zayni, Andreas Hofinger, Paul Kosma, Christina Schäffer та Paul Messner. "Biosynthesis of dTDP-3-acetamido-3,6-dideoxy-α-D-glucose". Biochemical Journal 410, № 1 (29 січня 2008): 187–94. http://dx.doi.org/10.1042/bj20071044.
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