Статті в журналах з теми "Sulfate groups"
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Arnoštová, Libuše, Ivan Černý, Vladimír Pouzar та Pavel Drašar. "Synthesis of 5α-Cholestane Type Glycoside Sulfates". Collection of Czechoslovak Chemical Communications 58, № 5 (1993): 1180–90. http://dx.doi.org/10.1135/cccc19931180.
Повний текст джерелаReinehr, Thomas, Alberto Sánchez-Guijo, Nina Lass, and Stefan A. Wudy. "Higher steroid sulfation is linked to successful weight loss in obese children." Endocrine Connections 7, no. 10 (October 2018): 1020–30. http://dx.doi.org/10.1530/ec-18-0233.
Повний текст джерелаHobkirk, R., and Catherine A. Cardy. "The in vitro formation of sulfates and glucuronides of estrogens by adult and fetal ovine tissues." Canadian Journal of Biochemistry and Cell Biology 63, no. 8 (August 1, 1985): 785–91. http://dx.doi.org/10.1139/o85-100.
Повний текст джерелаDrouet, B., S. Matou, P. A. S. Mourão, A. Bros, D. Letourneur, A. M. Fischer, and J. Tapon-Bretaudière. "Modulation of Vascular Human Endothelial and Rat Smooth Muscle Cell Growth by a Fucosylated Chondroitin Sulfate from Echinoderm." Thrombosis and Haemostasis 84, no. 08 (2000): 332–37. http://dx.doi.org/10.1055/s-0037-1614016.
Повний текст джерелаFishbain, Susan, Jesse G. Dillon, Heidi L. Gough, and David A. Stahl. "Linkage of High Rates of Sulfate Reduction in Yellowstone Hot Springs to Unique Sequence Types in the Dissimilatory Sulfate Respiration Pathway." Applied and Environmental Microbiology 69, no. 6 (June 2003): 3663–67. http://dx.doi.org/10.1128/aem.69.6.3663-3667.2003.
Повний текст джерелаKazachenko, Aleksandr S., Natalia Yu Vasilieva, Yaroslava D. Berezhnaya, Olga Yu Fetisova, Valentina S. Borovkova, Yuriy N. Malyar, Irina G. Sudakova, et al. "Sulfation of Birch Wood Microcrystalline Cellulose with Sulfamic Acid Using Ion-Exchange Resins as Catalysts." Polymers 15, no. 5 (February 23, 2023): 1116. http://dx.doi.org/10.3390/polym15051116.
Повний текст джерелаKazachenko, Aleksandr Sergeyevich, Vladimir Aleksandrovich Levdansky, Aleksandr Vladimirovich Levdansky, and Boris Nikolayevich Kuznetsov. "MATHEMATICAL OPTIMIZATION OF THE PROCESS OF BIRCH WOOD XYLAN SULFATION BY SULFAMIC ACID IN N, N-DIMETHYLFORMAMIDE MEDIUM." chemistry of plant raw material, no. 2 (June 10, 2021): 87–94. http://dx.doi.org/10.14258/jcprm.2021027558.
Повний текст джерелаKazachenko, Aleksandr S., Yuriy N. Malyar, and Anna S. Kazachenko. "Synthesis of Galactomannan Sulfate-Citrate." Materials Science Forum 1049 (January 11, 2022): 218–23. http://dx.doi.org/10.4028/www.scientific.net/msf.1049.218.
Повний текст джерелаKim, B. Moon, and K. Barry Sharpless. "Cyclic sulfates containing acid-sensitive groups and chemoselective hydrolysis of sulfate esters." Tetrahedron Letters 30, no. 6 (1989): 655–58. http://dx.doi.org/10.1016/s0040-4039(01)80274-4.
Повний текст джерелаFarzan, Michael, Christine E. Schnitzler, Natalya Vasilieva, Doris Leung, Jens Kuhn, Craig Gerard, Norma P. Gerard, and Hyeryun Choe. "Sulfated Tyrosines Contribute to the Formation of the C5a Docking Site of the Human C5a Anaphylatoxin Receptor." Journal of Experimental Medicine 193, no. 9 (May 7, 2001): 1059–66. http://dx.doi.org/10.1084/jem.193.9.1059.
Повний текст джерелаKowalewski, Björn, Heike Lange, Sabrina Galle, Thomas Dierks, Torben Lübke, and Markus Damme. "Decoding the consecutive lysosomal degradation of 3-O-sulfate containing heparan sulfate by Arylsulfatase G (ARSG)." Biochemical Journal 478, no. 17 (September 7, 2021): 3221–37. http://dx.doi.org/10.1042/bcj20210415.
Повний текст джерелаZhao, Tingting, Xiaoguang Lu, Neal M. Davies, Yuewen Gong, Jingzhen Guo, Haojun Zhang, Zhiguo Li, Jing Hong, Guixiang Fu, and Ping Li. "Diabetes Results in Structural Alteration of Chondroitin Sulfate in the Urine." Journal of Pharmacy & Pharmaceutical Sciences 16, no. 3 (July 30, 2013): 486. http://dx.doi.org/10.18433/j3gs3c.
Повний текст джерелаZhang, Cong, Ding An, Qiong Xiao, Fu-Quan Chen, Yong-Hui Zhang, Hui-Fen Weng, and An-Feng Xiao. "Convenient Agarose Preparation with Hydrogen Peroxide and Desulfation Process Analysis." Marine Drugs 19, no. 6 (May 23, 2021): 297. http://dx.doi.org/10.3390/md19060297.
Повний текст джерелаLevdansky, Alexander V., Natalya Yu Vasilyeva, Yuriy N. Malyar, Alexander A. Kondrasenko, Olga Yu Fetisova, Aleksandr S. Kazachenko, Vladimir A. Levdansky, and Boris N. Kuznetsov. "An Efficient Method of Birch Ethanol Lignin Sulfation with a Sulfaic Acid-Urea Mixture." Molecules 27, no. 19 (September 26, 2022): 6356. http://dx.doi.org/10.3390/molecules27196356.
Повний текст джерелаBar-Ner, M., A. Eldor, L. Wasserman, Y. Matzner, IR Cohen, Z. Fuks, and I. Vlodavsky. "Inhibition of heparanase-mediated degradation of extracellular matrix heparan sulfate by non-anticoagulant heparin species." Blood 70, no. 2 (August 1, 1987): 551–57. http://dx.doi.org/10.1182/blood.v70.2.551.551.
Повний текст джерелаBar-Ner, M., A. Eldor, L. Wasserman, Y. Matzner, IR Cohen, Z. Fuks, and I. Vlodavsky. "Inhibition of heparanase-mediated degradation of extracellular matrix heparan sulfate by non-anticoagulant heparin species." Blood 70, no. 2 (August 1, 1987): 551–57. http://dx.doi.org/10.1182/blood.v70.2.551.bloodjournal702551.
Повний текст джерелаBarron, Denis, and Ragai K. Ibrahim. "Synthesis of Flavonoid Sulfates. III. Synthesis of 3′,4′-ortho Disulfates Using Sulfur Trioxide-trimethylamine Complex, and of 3′-SuIfates Using Aryl Sulfatase." Zeitschrift für Naturforschung C 43, no. 9-10 (October 1, 1988): 631–35. http://dx.doi.org/10.1515/znc-1988-9-1002.
Повний текст джерелаTangelder, GJ, and KE Arfors. "Inhibition of leukocyte rolling in venules by protamine and sulfated polysaccharides." Blood 77, no. 7 (April 1, 1991): 1565–71. http://dx.doi.org/10.1182/blood.v77.7.1565.1565.
Повний текст джерелаTangelder, GJ, and KE Arfors. "Inhibition of leukocyte rolling in venules by protamine and sulfated polysaccharides." Blood 77, no. 7 (April 1, 1991): 1565–71. http://dx.doi.org/10.1182/blood.v77.7.1565.bloodjournal7771565.
Повний текст джерелаSilchenko, Kalinovsky, Avilov, Kalinin, Andrijaschenko, Dmitrenok, Popov, and Chingizova. "Structures and Bioactivities of Psolusosides B1, B2, J, K, L, M, N, O, P, and Q from the Sea Cucumber Psolus fabricii. The First Finding of Tetrasulfated Marine Low Molecular Weight Metabolites." Marine Drugs 17, no. 11 (November 6, 2019): 631. http://dx.doi.org/10.3390/md17110631.
Повний текст джерелаSilchenko, Alexandra S., Sergey A. Avilov, Roman S. Popov, Pavel S. Dmitrenok, Ekaterina A. Chingizova, Boris B. Grebnev, Anton B. Rasin, and Vladimir I. Kalinin. "Chilensosides E, F, and G—New Tetrasulfated Triterpene Glycosides from the Sea Cucumber Paracaudina chilensis (Caudinidae, Molpadida): Structures, Activity, and Biogenesis." Marine Drugs 21, no. 2 (February 5, 2023): 114. http://dx.doi.org/10.3390/md21020114.
Повний текст джерелаVoronova, M. I., O. V. Surov, and A. G. Zakharov. "Nanocrystalline cellulose with various contents of sulfate groups." Carbohydrate Polymers 98, no. 1 (October 2013): 465–69. http://dx.doi.org/10.1016/j.carbpol.2013.06.004.
Повний текст джерелаDing, Kan, Staffan Sandgren, Katrin Mani, Mattias Belting, and Lars-Åke Fransson. "Modulations of Glypican-1 Heparan Sulfate Structure by Inhibition of Endogenous Polyamine Synthesis." Journal of Biological Chemistry 276, no. 50 (September 27, 2001): 46779–91. http://dx.doi.org/10.1074/jbc.m105419200.
Повний текст джерелаZsiška, Marianne, and Bernd Meyer. "Influence of sulfate and carboxylate groups on the conformation of chondroitin sulfate related disaccharides." Carbohydrate Research 243, no. 2 (May 1993): 225–58. http://dx.doi.org/10.1016/0008-6215(93)87031-m.
Повний текст джерелаЛевданский (Levdanskii), Владимир (Vladimir) Александрович (Aleksandrovich), Александр (Aleksandr) Александрович (Aleksandrovich) Кондрасенко (Kondrasenko), Александр (Aleksandr) Владимирович (Vladimirovich) Левданский (Levdanskii), and Борис (Boris) Николаевич (Nikolaevich) Кузнецов (Kuznetsov). "SYLFATION OF XYLAN WITH SULFAMIC ACID IN N,N-DIMETHYLFORMAMIDE." chemistry of plant raw material, no. 1 (December 6, 2017): 29–36. http://dx.doi.org/10.14258/jcprm.2018012268.
Повний текст джерелаMinh Ly, Bui, Ngo Quoc Buu, Nguyen Duy Nhut, Pham Duc Thinh, and Tran Thi Thanh Van. "STUDIES ON FUCOIDAN AND ITS PRODUCTION FROM VIETNAMESE BROWN SEAWEEDS." ASEAN Journal on Science and Technology for Development 22, no. 4 (November 11, 2017): 371. http://dx.doi.org/10.29037/ajstd.173.
Повний текст джерелаQi, Yihui, Lilong Wang, Ying You, Xiaona Sun, Chengrong Wen, Yinghuan Fu, and Shuang Song. "Preparation of Low-Molecular-Weight Fucoidan with Anticoagulant Activity by Photocatalytic Degradation Method." Foods 11, no. 6 (March 13, 2022): 822. http://dx.doi.org/10.3390/foods11060822.
Повний текст джерелаHolmborn, Katarina, Johan Ledin, Emanuel Smeds, Inger Eriksson, Marion Kusche-Gullberg, and Lena Kjellén. "Heparan Sulfate Synthesized by Mouse Embryonic Stem Cells Deficient in NDST1 and NDST2 Is 6-O-Sulfated but Contains NoN-Sulfate Groups." Journal of Biological Chemistry 279, no. 41 (August 19, 2004): 42355–58. http://dx.doi.org/10.1074/jbc.c400373200.
Повний текст джерелаСherednichenko, D. V., P. D. Vorobiev, V. V. Shevchuk, A. D. Vorobiev, T. N. Potkina, and E. V. Layevskaya. "Influence of polymer and inorganic modifiers on the process of phase formation in potassium sulfate saturated solutions." Proceedings of the National Academy of Sciences of Belarus, Chemical Series 59, no. 1 (March 5, 2023): 18–25. http://dx.doi.org/10.29235/1561-8331-2023-59-1-18-25.
Повний текст джерелаBurkov, V. I., Yu V. Denisov, and Z. B. Perekalina. "Circular dichroism of uniaxial sulfate crystals in the range of electronic transitions of sulfate groups." Crystallography Reports 47, no. 2 (March 2002): 313–17. http://dx.doi.org/10.1134/1.1466509.
Повний текст джерелаZhang, Kai, Dieter Peschel, Thomas Klinger, Kathrin Gebauer, Thomas Groth, and Steffen Fischer. "Synthesis of carboxyl cellulose sulfate with various contents of regioselectively introduced sulfate and carboxyl groups." Carbohydrate Polymers 82, no. 1 (August 2010): 92–99. http://dx.doi.org/10.1016/j.carbpol.2010.04.027.
Повний текст джерелаStoeckli-Evans, Helen, Olha Sereda, Antonia Neels, Sebastien Oguey, Catherine Ionescu та Yvan Jacquier. "In situsingle-crystal to single-crystal (SCSC) transformation of the one-dimensional polymercatena-poly[[diaqua(sulfato)copper(II)]-μ2-glycine] into the two-dimensional polymer poly[μ2-glycine-μ4-sulfato-copper(II)]". Acta Crystallographica Section C Structural Chemistry 70, № 11 (15 жовтня 2014): 1057–63. http://dx.doi.org/10.1107/s2053229614021123.
Повний текст джерелаKensinger, Richard D., Bradley J. Catalone, Fred C. Krebs, Brian Wigdahl, and Cara-Lynne Schengrund. "Novel Polysulfated Galactose-Derivatized Dendrimers as Binding Antagonists of Human Immunodeficiency Virus Type 1 Infection." Antimicrobial Agents and Chemotherapy 48, no. 5 (May 2004): 1614–23. http://dx.doi.org/10.1128/aac.48.5.1614-1623.2004.
Повний текст джерелаKarr, Elizabeth A., W. Matthew Sattley, Melissa R. Rice, Deborah O. Jung, Michael T. Madigan, and Laurie A. Achenbach. "Diversity and Distribution of Sulfate-Reducing Bacteria in Permanently Frozen Lake Fryxell, McMurdo Dry Valleys, Antarctica." Applied and Environmental Microbiology 71, no. 10 (October 2005): 6353–59. http://dx.doi.org/10.1128/aem.71.10.6353-6359.2005.
Повний текст джерелаHayes, Anthony J., and James Melrose. "HS, an Ancient Molecular Recognition and Information Storage Glycosaminoglycan, Equips HS-Proteoglycans with Diverse Matrix and Cell-Interactive Properties Operative in Tissue Development and Tissue Function in Health and Disease." International Journal of Molecular Sciences 24, no. 2 (January 6, 2023): 1148. http://dx.doi.org/10.3390/ijms24021148.
Повний текст джерелаHempel, Ute, Carolin Preissler, Sarah Vogel, Stephanie Möller, Vera Hintze, Jana Becher, Matthias Schnabelrauch, Martina Rauner, Lorenz C. Hofbauer, and Peter Dieter. "Artificial Extracellular Matrices with Oversulfated Glycosaminoglycan Derivatives Promote the Differentiation of Osteoblast-Precursor Cells and Premature Osteoblasts." BioMed Research International 2014 (2014): 1–10. http://dx.doi.org/10.1155/2014/938368.
Повний текст джерелаSalek-Ardakani, Shahram, John R. Arrand, David Shaw, and Mike Mackett. "Heparin and heparan sulfate bind interleukin-10 and modulate its activity." Blood 96, no. 5 (September 1, 2000): 1879–88. http://dx.doi.org/10.1182/blood.v96.5.1879.
Повний текст джерелаSalek-Ardakani, Shahram, John R. Arrand, David Shaw, and Mike Mackett. "Heparin and heparan sulfate bind interleukin-10 and modulate its activity." Blood 96, no. 5 (September 1, 2000): 1879–88. http://dx.doi.org/10.1182/blood.v96.5.1879.h8001879_1879_1888.
Повний текст джерелаHaroun-Bouhedja, Ferial, Mostafa Ellouali, Corinne Sinquin, and Catherine Boisson-Vidal. "Relationship between Sulfate Groups and Biological Activities of Fucans." Thrombosis Research 100, no. 5 (December 2000): 453–59. http://dx.doi.org/10.1016/s0049-3848(00)00338-8.
Повний текст джерелаThomas, Maud, Gaëlle Chauvelon, Marc Lahaye, and Luc Saulnier. "Location of sulfate groups on sulfoacetate derivatives of cellulose." Carbohydrate Research 338, no. 8 (April 2003): 761–70. http://dx.doi.org/10.1016/s0008-6215(03)00010-7.
Повний текст джерелаPrieto, Jorge J., Maria E. Rubio, and Jaime A. Merchan. "Localization of anionic sulfate groups in the tectorial membrane." Hearing Research 45, no. 3 (May 1990): 283–93. http://dx.doi.org/10.1016/0378-5955(90)90127-b.
Повний текст джерелаBychkhov, S. M., and S. A. Kuz'mina. "Functions of the carboxyl and sulfate groups of proteoglycans." Bulletin of Experimental Biology and Medicine 119, no. 4 (April 1995): 344–46. http://dx.doi.org/10.1007/bf02445888.
Повний текст джерелаFernández-Díaz, Lurdes, Ángeles Fernández-González, and Manuel Prieto. "The role of sulfate groups in controlling CaCO3 polymorphism." Geochimica et Cosmochimica Acta 74, no. 21 (November 2010): 6064–76. http://dx.doi.org/10.1016/j.gca.2010.08.010.
Повний текст джерелаAkahane, Tooru, Sadaaki Takeuchi, and Akira Minakata. "Conductimetric titration of polyelectrolytes having sulfate and carboxyl groups." Polymer Bulletin 24, no. 4 (October 1990): 437–44. http://dx.doi.org/10.1007/bf00294098.
Повний текст джерелаStraßburger, David, Svenja Herziger, Katharina Huth, Moritz Urschbach, Rainer Haag, and Pol Besenius. "Supramolecular polymerization of sulfated dendritic peptide amphiphiles into multivalent L-selectin binders." Beilstein Journal of Organic Chemistry 17 (January 12, 2021): 97–104. http://dx.doi.org/10.3762/bjoc.17.10.
Повний текст джерелаKhil'chenko, S. R., T. S. Zaporozhets, T. N. Zvyagintseva, N. M. Shevchenko, and N. N. Besednov. "The Role of Sulfates in Fucoidan Extracted from Fucus evanescens in Proinflammatory Cytokines Production by Human Peripheral Blood Cells in vitro." Antibiotics and Chemotherapy 65, no. 5-6 (August 26, 2020): 3–10. http://dx.doi.org/10.37489/0235-2990-2020-65-5-6-3-10.
Повний текст джерелаLoy, Alexander, Kirsten Küsel, Angelika Lehner, Harold L. Drake, and Michael Wagner. "Microarray and Functional Gene Analyses of Sulfate-Reducing Prokaryotes in Low-Sulfate, Acidic Fens Reveal Cooccurrence of Recognized Genera and Novel Lineages." Applied and Environmental Microbiology 70, no. 12 (December 2004): 6998–7009. http://dx.doi.org/10.1128/aem.70.12.6998-7009.2004.
Повний текст джерелаKellner Filho, Luis C., Bruno W. Picão, Marcio L. A. Silva, Wilson R. Cunha, Patricia M. Pauletti, Gustavo M. Dias, Brent R. Copp, Camila S. Bertanha, and Ana H. Januario. "Bioactive Aliphatic Sulfates from Marine Invertebrates." Marine Drugs 17, no. 9 (September 9, 2019): 527. http://dx.doi.org/10.3390/md17090527.
Повний текст джерелаMetzger, Christoph, David Auber, Stephan Dähnhardt-Pfeiffer, and Heiko Briesen. "Agglomeration of cellulose nanocrystals: the effect of secondary sulfates and their use in product separation." Cellulose 27, no. 17 (October 9, 2020): 9839–51. http://dx.doi.org/10.1007/s10570-020-03476-0.
Повний текст джерелаShaon, Md Taohid Wasim, Md Nurul Amin, Sabbir Hossen Sabuz, and Mst Deloara Begum. "Comparative Effects of Copper Sulfate and Zinc Sulfate on Performances of Broiler Chickens." Research in Agriculture Livestock and Fisheries 7, no. 3 (December 31, 2020): 465–74. http://dx.doi.org/10.3329/ralf.v7i3.51366.
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