Статті в журналах з теми "Azaspiracidi"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Azaspiracidi".
Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.
Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.
Переглядайте статті в журналах для різних дисциплін та оформлюйте правильно вашу бібліографію.
Hamilton, Brett, Mónica Díaz Sierra, Mary Lehane, Ambrose Furey, and Kevin J. James. "The fragmentation pathways of azaspiracids elucidated using positive nanospray hybrid quadrupole time-of-flight (QqTOF) mass spectrometry." Spectroscopy 18, no. 2 (2004): 355–62. http://dx.doi.org/10.1155/2004/949018.
Повний текст джерелаKilcoyne, Jane, Adela Keogh, Ger Clancy, Patricia LeBlanc, Ian Burton, Michael A. Quilliam, Philipp Hess, and Christopher O. Miles. "Improved Isolation Procedure for Azaspiracids from Shellfish, Structural Elucidation of Azaspiracid-6, and Stability Studies." Journal of Agricultural and Food Chemistry 60, no. 10 (March 2, 2012): 2447–55. http://dx.doi.org/10.1021/jf2048788.
Повний текст джерелаAbal, Paula, M. Carmen Louzao, María Fraga, Natalia Vilariño, Sara Ferreiro, Mercedes R. Vieytes, and Luis M. Botana. "Absorption and Effect of Azaspiracid-1 Over the Human Intestinal Barrier." Cellular Physiology and Biochemistry 43, no. 1 (2017): 136–46. http://dx.doi.org/10.1159/000480331.
Повний текст джерелаTrainer, Vera L., and Teri L. King. "SoundToxins: A Research and Monitoring Partnership for Harmful Phytoplankton in Washington State." Toxins 15, no. 3 (March 2, 2023): 189. http://dx.doi.org/10.3390/toxins15030189.
Повний текст джерелаKilcoyne, Jane, Pearse McCarron, Michael J. Twiner, Ciara Nulty, Sheila Crain, Michael A. Quilliam, Frode Rise, Alistair L. Wilkins, and Christopher O. Miles. "Epimers of Azaspiracids: Isolation, Structural Elucidation, Relative LC-MS Response, andin VitroToxicity of 37-epi-Azaspiracid-1." Chemical Research in Toxicology 27, no. 4 (February 7, 2014): 587–600. http://dx.doi.org/10.1021/tx400434b.
Повний текст джерелаKrock, Bernd, Urban Tillmann, Uwe John, and Allan D. Cembella. "Characterization of azaspiracids in plankton size-fractions and isolation of an azaspiracid-producing dinoflagellate from the North Sea." Harmful Algae 8, no. 2 (January 2009): 254–63. http://dx.doi.org/10.1016/j.hal.2008.06.003.
Повний текст джерелаOFUJI, Katsuya, Masayuki SATAKE, Terry MCMAHON, Kevin J. JAMES, Hideo NAOKI, Yasukatsu OSHIMA, and Takeshi YASUMOTO. "Structures of Azaspiracid Analogs, Azaspiracid-4 and Azaspiracid-5, Causative Toxins of Azaspiracid Poisoning in Europe." Bioscience, Biotechnology, and Biochemistry 65, no. 3 (January 2001): 740–42. http://dx.doi.org/10.1271/bbb.65.740.
Повний текст джерелаRossi, Rachele, Carmela Dell’Aversano, Bernd Krock, Patrizia Ciminiello, Isabella Percopo, Urban Tillmann, Vittorio Soprano, and Adriana Zingone. "Mediterranean Azadinium dexteroporum (Dinophyceae) produces six novel azaspiracids and azaspiracid-35: a structural study by a multi-platform mass spectrometry approach." Analytical and Bioanalytical Chemistry 409, no. 4 (November 7, 2016): 1121–34. http://dx.doi.org/10.1007/s00216-016-0037-4.
Повний текст джерелаLi, Jialiang, Xiaohua Li, and David R. Mootoo. "Synthetic and Computational Studies on the ABC Trioxadispiroketal Subunit of the Marine Biotoxin Azaspiracid-1." Natural Product Communications 3, no. 11 (November 2008): 1934578X0800301. http://dx.doi.org/10.1177/1934578x0800301106.
Повний текст джерелаAlfonso, Carmen, Amparo Alfonso, Paz Otero, Paula Rodríguez, Mercedes R. Vieytes, Chris Elliot, Cowan Higgins, and Luis M. Botana. "Purification of five azaspiracids from mussel samples contaminated with DSP toxins and azaspiracids." Journal of Chromatography B 865, no. 1-2 (April 2008): 133–40. http://dx.doi.org/10.1016/j.jchromb.2008.02.020.
Повний текст джерелаKrock, Bernd, Urban Tillmann, Daniela Voß, Boris P. Koch, Rafael Salas, Matthias Witt, Éric Potvin, and Hae Jin Jeong. "New azaspiracids in Amphidomataceae (Dinophyceae)." Toxicon 60, no. 5 (October 2012): 830–39. http://dx.doi.org/10.1016/j.toxicon.2012.05.007.
Повний текст джерелаBrombacher, Stephan, Suzanne Edmonds, and Dietrich A. Volmer. "Studies on azaspiracid biotoxins. II. Mass spectral behavior and structural elucidation of azaspiracid analogs." Rapid Communications in Mass Spectrometry 16, no. 24 (2002): 2306–16. http://dx.doi.org/10.1002/rcm.863.
Повний текст джерелаNicolaou, K. C., Michael O. Frederick, Goran Petrovic, Kevin P. Cole, and Eriketi Z. Loizidou. "Total Synthesis and Confirmation of the Revised Structures of Azaspiracid-2 and Azaspiracid-3." Angewandte Chemie 118, no. 16 (April 10, 2006): 2671–77. http://dx.doi.org/10.1002/ange.200600295.
Повний текст джерелаNicolaou, K. C., Michael O. Frederick, Goran Petrovic, Kevin P. Cole, and Eriketi Z. Loizidou. "Total Synthesis and Confirmation of the Revised Structures of Azaspiracid-2 and Azaspiracid-3." Angewandte Chemie International Edition 45, no. 16 (April 10, 2006): 2609–15. http://dx.doi.org/10.1002/anie.200600295.
Повний текст джерелаNicolaou, K. C., and Jason S. Chen. "Total synthesis of complex heterocyclic natural products." Pure and Applied Chemistry 80, no. 4 (January 1, 2008): 727–42. http://dx.doi.org/10.1351/pac200880040727.
Повний текст джерелаVilariño, Natalia. "Marine toxins and the cytoskeleton: azaspiracids." FEBS Journal 275, no. 24 (October 29, 2008): 6075–81. http://dx.doi.org/10.1111/j.1742-4658.2008.06713.x.
Повний текст джерелаKrock, Bernd, Urban Tillmann, Jan Tebben, Nicole Trefault, and Haifeng Gu. "Two novel azaspiracids from Azadinium poporum, and a comprehensive compilation of azaspiracids produced by Amphidomataceae, (Dinophyceae)." Harmful Algae 82 (February 2019): 1–8. http://dx.doi.org/10.1016/j.hal.2018.12.005.
Повний текст джерелаGeisler, Lisa K., Son Nguyen, and Craig J. Forsyth. "Synthesis of the Azaspiracid-1 Trioxadispiroketal." Organic Letters 6, no. 23 (November 2004): 4159–62. http://dx.doi.org/10.1021/ol048581a.
Повний текст джерелаFrederick, Michael O., Sandra De Lamo Marin, Kim D. Janda, K. C. Nicolaou, and Tobin J. Dickerson. "Monoclonal Antibodies with Orthogonal Azaspiracid Epitopes." ChemBioChem 10, no. 10 (July 6, 2009): 1625–29. http://dx.doi.org/10.1002/cbic.200900201.
Повний текст джерелаTillmann, Urban, C. Marcela Borel, Facundo Barrera, Rubén Lara, Bernd Krock, Gastón O. Almandoz, Matthias Witt, and Nicole Trefault. "Azadinium poporum from the Argentine Continental Shelf, Southwestern Atlantic, produces azaspiracid-2 and azaspiracid-2 phosphate." Harmful Algae 51 (January 2016): 40–55. http://dx.doi.org/10.1016/j.hal.2015.11.001.
Повний текст джерелаWU, Haiyan, Qingyun LI, Xiaofei BING, Mengmeng GUO, Haifeng GU, Yuxiu ZHAI, and Zhijun TAN. "Metabolic regulation of azaspiracids in Chlamys farreri." Journal of Fishery Sciences of China 24, no. 6 (2017): 1298. http://dx.doi.org/10.3724/sp.j.1118.2017.17025.
Повний текст джерелаOikawa, Masato, and Makoto Sasaki. "Synthetic Studies on Shellfish Toxin Azaspiracid-1." Journal of Synthetic Organic Chemistry, Japan 66, no. 9 (2008): 836–45. http://dx.doi.org/10.5059/yukigoseikyokaishi.66.836.
Повний текст джерелаNguyen, Son, Jianyan Xu, and Craig J. Forsyth. "Facile biomimetic syntheses of the azaspiracid spiroaminal." Tetrahedron 62, no. 22 (May 2006): 5338–46. http://dx.doi.org/10.1016/j.tet.2006.01.112.
Повний текст джерелаNicolaou, K., T. Koftis, S. Vyskocil, G. Petrovic, W. Tang, M. Frederick, D. Chen, T. Ling, Y. Li, and Y. Yamada. "Synthesis and Structural Elucidation of Azaspiracid-1." Synfacts 2006, no. 8 (August 2006): 0748. http://dx.doi.org/10.1055/s-2006-941937.
Повний текст джерелаAlfonso, Amparo, Mercedes R. Vieytes, Katsuya Ofuji, Masayuki Satake, K. C. Nicolaou, Michael O. Frederick, and L. M. Botana. "Azaspiracids modulate intracellular pH levels in human lymphocytes." Biochemical and Biophysical Research Communications 346, no. 3 (August 2006): 1091–99. http://dx.doi.org/10.1016/j.bbrc.2006.06.019.
Повний текст джерелаRodríguez, Laura P., Natalia Vilariño, M. Carmen Louzao, Tobin J. Dickerson, K. C. Nicolaou, Michael O. Frederick, and Luis M. Botana. "Microsphere-based immunoassay for the detection of azaspiracids." Analytical Biochemistry 447 (February 2014): 58–63. http://dx.doi.org/10.1016/j.ab.2013.10.035.
Повний текст джерелаJauffrais, Thierry, Christine Herrenknecht, Véronique Séchet, Manoella Sibat, Urban Tillmann, Bernd Krock, Jane Kilcoyne, et al. "Quantitative analysis of azaspiracids in Azadinium spinosum cultures." Analytical and Bioanalytical Chemistry 403, no. 3 (February 26, 2012): 833–46. http://dx.doi.org/10.1007/s00216-012-5849-2.
Повний текст джерелаKlontz, Karl C. "Mussel-Associated Azaspiracid Intoxication in the United States." Annals of Internal Medicine 150, no. 5 (March 3, 2009): 361. http://dx.doi.org/10.7326/0003-4819-150-5-200903030-00023.
Повний текст джерелаFlanagan, Andrew F., John Donlon, Roy Palmer, and Marian Kane. "Bioanalytical detection of azaspiracid, a newly discovered phycotoxin." Biochemical Society Transactions 28, no. 1 (February 1, 2000): A46. http://dx.doi.org/10.1042/bst028a046a.
Повний текст джерелаNzoughet, K. J., J. T. G. Hamilton, S. D. Floyd, A. Douglas, J. Nelson, L. Devine, and C. T. Elliott. "Azaspiracid: First evidence of protein binding in shellfish." Toxicon 51, no. 7 (June 2008): 1255–63. http://dx.doi.org/10.1016/j.toxicon.2008.02.016.
Повний текст джерелаTillmann, Urban, and Alfred Wegener. "Neu entdeckte Giftalge ist Ursache der Azaspiracid-Muschelvergiftung." Biologie in unserer Zeit 39, no. 3 (June 2009): 152–53. http://dx.doi.org/10.1002/biuz.200990040.
Повний текст джерелаNicolaou, K. C., Petri M. Pihko, Nicole Diedrichs, Ning Zou, and Federico Bernal. "Synthesis of the FGHI Ring System of Azaspiracid." Angewandte Chemie 113, no. 7 (April 1, 2001): 1302–5. http://dx.doi.org/10.1002/1521-3757(20010401)113:7<1302::aid-ange1302>3.0.co;2-s.
Повний текст джерелаNicolaou, K. C., Petri M. Pihko, Nicole Diedrichs, Ning Zou, and Federico Bernal. "Synthesis of the FGHI Ring System of Azaspiracid." Angewandte Chemie 113, no. 9 (May 4, 2001): 1621. http://dx.doi.org/10.1002/1521-3757(20010504)113:9<1621::aid-ange16213>3.0.co;2-k.
Повний текст джерелаNicolaou, K. C., Wenyuan Qian, Federico Bernal, Noriaki Uesaka, Petri M. Pihko, and Jürgen Hinrichs. "Synthesis of the ABCD Ring System of Azaspiracid." Angewandte Chemie 113, no. 21 (November 5, 2001): 4192–95. http://dx.doi.org/10.1002/1521-3757(20011105)113:21<4192::aid-ange4192>3.0.co;2-0.
Повний текст джерелаNicolaou, K. C., Petri M. Pihko, Nicole Diedrichs, Ning Zou, and Federico Bernal. "Synthesis of the FGHI Ring System of Azaspiracid." Angewandte Chemie International Edition 40, no. 7 (April 1, 2001): 1262–65. http://dx.doi.org/10.1002/1521-3773(20010401)40:7<1262::aid-anie1262>3.0.co;2-9.
Повний текст джерелаNicolaou, K. C., Petri M. Pihko, Nicole Diedrichs, Ning Zou, and Federico Bernal. "Synthesis of the FGHI Ring System of Azaspiracid." Angewandte Chemie International Edition 40, no. 9 (May 4, 2001): 1573. http://dx.doi.org/10.1002/1521-3773(20010504)40:9<1573::aid-anie15733>3.0.co;2-d.
Повний текст джерелаOZAWA, MAYU. "7. Study on azaspiracid shellfish poisoning in Japan." NIPPON SUISAN GAKKAISHI 88, no. 6 (November 15, 2022): 541. http://dx.doi.org/10.2331/suisan.wa2980-7.
Повний текст джерелаNicolaou, K. C., Theocharis V. Koftis, Stepan Vyskocil, Goran Petrovic, Wenjun Tang, Michael O. Frederick, David Y. K. Chen, Yiwei Li, Taotao Ling, and Yoichi M. A. Yamada. "Total Synthesis and Structural Elucidation of Azaspiracid-1. Final Assignment and Total Synthesis of the Correct Structure of Azaspiracid-1." Journal of the American Chemical Society 128, no. 9 (March 2006): 2859–72. http://dx.doi.org/10.1021/ja054750q.
Повний текст джерелаVale, Carmen, Carolina Wandscheer, K. C. Nicolaou, Michael O. Frederick, Carmen Alfonso, Mercedes R. Vieytes, and Luis M. Botana. "Cytotoxic effect of azaspiracid-2 and azaspiracid-2-methyl ester in cultured neurons: Involvement of the c-Jun N-terminal kinase." Journal of Neuroscience Research 86, no. 13 (October 2008): 2952–62. http://dx.doi.org/10.1002/jnr.21731.
Повний текст джерелаYadav, J. S., Sipak Joyasawal, S. K. Dutta, and A. C. Kunwar. "Stereoselective synthesis of the ABCD ring framework of azaspiracids." Tetrahedron Letters 48, no. 30 (July 2007): 5335–40. http://dx.doi.org/10.1016/j.tetlet.2007.05.021.
Повний текст джерелаBlanco, Juan, Fabiola Arévalo, Ángeles Moroño, Jorge Correa, Susana Muñíz, Carmen Mariño, and Helena Martín. "Presence of azaspiracids in bivalve molluscs from Northern Spain." Toxicon 137 (October 2017): 135–43. http://dx.doi.org/10.1016/j.toxicon.2017.07.025.
Повний текст джерелаZhang, Zhigao, Yong Chen, Daniel Adu-Ampratwum, Antony Akura Okumu, Nathaniel T. Kenton, and Craig J. Forsyth. "Synthesis of the C22–C40 Domain of the Azaspiracids." Organic Letters 18, no. 8 (April 4, 2016): 1824–27. http://dx.doi.org/10.1021/acs.orglett.6b00557.
Повний текст джерелаGeraghty, J., C. Duffy, J. A. Aasen Bunæs, P. Hess, and B. Foley. "20. In vivo study of azaspiracids in mini pigs." Toxicon 91 (December 2014): 172–73. http://dx.doi.org/10.1016/j.toxicon.2014.08.028.
Повний текст джерелаSamdal, Ingunn A., Kjersti E. Løvberg, Lyn R. Briggs, Jane Kilcoyne, Jianyan Xu, Craig J. Forsyth, and Christopher O. Miles. "Development of an ELISA for the Detection of Azaspiracids." Journal of Agricultural and Food Chemistry 63, no. 35 (August 26, 2015): 7855–61. http://dx.doi.org/10.1021/acs.jafc.5b02513.
Повний текст джерелаOkumu, Antony A., and Craig J. Forsyth. "Synthesis of the C1–C19 Domain of Azaspiracid-34." Organic Letters 21, no. 2 (January 2, 2019): 356–59. http://dx.doi.org/10.1021/acs.orglett.8b03451.
Повний текст джерелаKellmann, Ralf, Carlos A. M. Schaffner, Toril A. Grønset, Masayuki Satake, Mathias Ziegler, and Kari E. Fladmark. "Proteomic response of human neuroblastoma cells to azaspiracid-1." Journal of Proteomics 72, no. 4 (May 2009): 695–707. http://dx.doi.org/10.1016/j.jprot.2009.02.008.
Повний текст джерелаPelin, M., S. Sosa, V. Brovedani, J. Kilcoyne, C. Nulty, P. Hess, and A. Tubaro. "In vitro effects of three azaspiracid analogues on hepatocytes." Toxicon 116 (June 2016): 85–86. http://dx.doi.org/10.1016/j.toxicon.2016.01.047.
Повний текст джерелаNzoughet, Judith K., Irene R. Grant, Paulo A. Prodöhl, John T. G. Hamilton, Luis M. Botana, and Christopher T. Elliott. "Evidence of Methylobacterium spp. and Hyphomicrobium sp. in azaspiracid toxin contaminated mussel tissues and assessment of the effect of azaspiracid on their growth." Toxicon 58, no. 8 (December 2011): 619–22. http://dx.doi.org/10.1016/j.toxicon.2011.09.012.
Повний текст джерелаAbouabdellaha, Rachid, Asmae Bennouna, Jaouad El Attar, Katrin Erler, Mina Dellal, Abdel ghani Chafik, and Abdelatif Moukrim. "Diarrhetic shellfish poisoning toxin profile of shellfish from Southern Atlantic coasts of Morocco." South Asian Journal of Experimental Biology 1, no. 2 (April 24, 2011): 101–6. http://dx.doi.org/10.38150/sajeb.1(2).p101-106.
Повний текст джерелаTriantafyllakis, Myron, Maria Tofi, Tamsyn Montagnon, Antonia Kouridaki, and Georgios Vassilikogiannakis. "Singlet Oxygen-Mediated Synthesis of Bis-spiroketals Found in Azaspiracids." Organic Letters 16, no. 11 (May 28, 2014): 3150–53. http://dx.doi.org/10.1021/ol501301w.
Повний текст джерела