Добірка наукової літератури з теми "Amino acids"
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Статті в журналах з теми "Amino acids"
Simon-Sarkadi, L., E. Szőke, and A. Kerekes. "Determination of free amino acid and biogenic amine contents of hungarian sparkling wines." Czech Journal of Food Sciences 22, SI - Chem. Reactions in Foods V (January 1, 2004): S287—S289. http://dx.doi.org/10.17221/10683-cjfs.
Повний текст джерелаVelíšek, J., R. Kubec, and K. Cejpek. "Biosynthesis of food constituents: Amino acids: 4. Non-protein amino acids – a review." Czech Journal of Food Sciences 24, No. 3 (November 12, 2011): 93–109. http://dx.doi.org/10.17221/3304-cjfs.
Повний текст джерелаVelíšek, J., and K. Cejpek. "Biosynthesis of food constituents: Amino acids. 3. Modified proteinogenic amino acids – a review." Czech Journal of Food Sciences 24, No. 2 (November 9, 2011): 59–61. http://dx.doi.org/10.17221/3300-cjfs.
Повний текст джерела&NA;. "Amino acids." Reactions Weekly &NA;, no. 1096 (April 2006): 4. http://dx.doi.org/10.2165/00128415-200610960-00011.
Повний текст джерелаBrosnan, John T., and Olav Rooyackers. "Amino acids." Current Opinion in Clinical Nutrition and Metabolic Care 16, no. 1 (January 2013): 56. http://dx.doi.org/10.1097/mco.0b013e32835b4ec4.
Повний текст джерелаColeman, William F. "Amino Acids." Journal of Chemical Education 83, no. 7 (July 2006): 1103. http://dx.doi.org/10.1021/ed083p1103.
Повний текст джерелаBattezzati, Alberto, and Patrizia Riso. "Amino acids:." Nutrition 18, no. 9 (September 2002): 773–74. http://dx.doi.org/10.1016/s0899-9007(02)00898-5.
Повний текст джерелаLottspeich, F. "Amino acids." Fresenius' Zeitschrift für analytische Chemie 327, no. 1 (January 1987): 23–24. http://dx.doi.org/10.1007/bf00474533.
Повний текст джерелаLewin, Ralph A. "Symbiotic algae and essential amino-acids." Algological Studies/Archiv für Hydrobiologie, Supplement Volumes 84 (April 23, 1997): 123–27. http://dx.doi.org/10.1127/algol_stud/84/1997/123.
Повний текст джерелаZhu, Xiaoli, Qianlu Yang, Junyi Huang, Iwao Suzuki, and Genxi Li. "Colorimetric Study of the Interaction Between Gold Nanoparticles and a Series of Amino Acids." Journal of Nanoscience and Nanotechnology 8, no. 1 (January 1, 2008): 353–57. http://dx.doi.org/10.1166/jnn.2008.18139.
Повний текст джерелаДисертації з теми "Amino acids"
Leung, Wai-yin David. "Synthesis and physical properties of fatty acid derivatives containing amino, amido functions and L-amino acid residues /." [Hong Kong : University of Hong Kong], 1993. http://sunzi.lib.hku.hk/hkuto/record.jsp?B13637666.
Повний текст джерелаSmith, Martin D. "Carbohydrate amino acids." Thesis, University of Oxford, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.302123.
Повний текст джерелаArdon, Helen. "Anomeric amino acids." Thesis, University of Oxford, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.363889.
Повний текст джерелаReeve, P. "Functionalising unnatural amino acids." Thesis, University of Sheffield, 2017. http://etheses.whiterose.ac.uk/19650/.
Повний текст джерелаYettella, V. Ramesh Reddy. "Riboflavin Photosensitized Oxidation of Amino Acids." The Ohio State University, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=osu1217897521.
Повний текст джерелаBarker, Sarah F. "Oxetanes : amino acids & nucleosides." Thesis, University of Oxford, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.275369.
Повний текст джерелаNewill, Philip Louis. "Generating pacidamycin related amino acids." Thesis, University of East Anglia, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.533711.
Повний текст джерела劉理雯 and Lee-man Lau. "Amino acids in soy sauce." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2000. http://hub.hku.hk/bib/B31222894.
Повний текст джерелаLin, Guoliang. "NOVEL METHANOPYRROLIDINE β– AMINO ACIDS". Diss., Temple University Libraries, 2010. http://cdm16002.contentdm.oclc.org/cdm/ref/collection/p245801coll10/id/92631.
Повний текст джерелаPh.D.
Methanopyrrolidine-5-carboxylic acids (MetPyr-5-acids), or 5-syn-carboxy-2- azabicyclo[2.1.1]hexanes are building blocks for β-peptides that cannot form backbone hydrogen bonds. To introduce functionality to this ring system, 6-syn-benzyloxymethyl and 6-syn-phenyl substituted derivatives have been prepared by an efficient synthetic procedure. Addition of appropriately substituted allyl amines to 3-butynone, amide protection, and irradiation afford mainly 5-acetyl-2-azabicyclo[2.1.1]hexanes. Haloform oxidation leads to the desired 6-substituted MetPyr-5-acids. A 1-ethoxycarbonyl-MetPyr-5-acid also was prepared in high yield. Condensation of ally amine with ethyl 2,4-dioxopentanoate afforded ethyl 2-(allylamino)-4-oxopent-2- enoate, and this was protected to give ethyl 2-[allyl(tert-butoxycarbonyl)amino]-4- oxopent-2-enoate. Irradiation afforded 5-syn-acetyl-1-ethoxycarbonyl-2- azabicyclo[2.1.1]hexane with high stereoselectivity and oxidation of the acetyl group afforded the desired 1-ethoxycarbonyl-MetPyr-5-acid. Resolutions of (±)-6-syn-benzyloxymethyl-MetPyr-5-acid and (±)-1- ethoxycarbonyl-MetPyr-5-acid were carried out (> 98% ee) by a classical resolution method using (S)-(-)-α-methylbenzylamine. The absolute configurations of (1S,4R,5R,6S)-(-)-6-benzyloxymethyl-MetPyr-5-acid and (1R,4S,5S)-(+)- 1- ethoxycarbonyl-MetPyr-5-acid were determined by X-ray analysis of their 5-(S)-(-)-α- methylbenzylamide. A prior X-ray analysis of N-Boc-(MetPyr)4-CO2Me indicated all amides to be trans oriented with all 5-syn-carbonyl groups directed toward Carbon-4 of the methanopyrrolidine. These structures were assigned as T4T4T4T4 or [T4]n (n = 4). The solution structure was not determined. Homooligomers of (1S,4R,5R)-5-syn-carboxy-2- azabicyclo[2.1.1]hexane (MPCA) terminally protected as N-Boc methylesters were constructed by EDC/HOBt coupling of terminal ester N-deprotected free amine units and N-Boc free acid units. To facilitate NMR analysis of the secondary structures of homooligomers, N-Boc was replaced by N-isobutyryl. NMR experiments indicated that N-isobutyryl-(MetPyr)n-CO2Me, (n = 2, 3, 4) have major favored [T4]n-1T where the orientation of the terminal ester carbonyl could not be determined.
Temple University--Theses
Lau, Lee-man. "Amino acids in soy sauce /." Hong Kong : University of Hong Kong, 2000. http://sunzi.lib.hku.hk/hkuto/record.jsp?B22401143.
Повний текст джерелаКниги з теми "Amino acids"
Boulton, Alan A., Glen B. Baker, and James D. Wood. Amino Acids. New Jersey: Humana Press, 1985. http://dx.doi.org/10.1385/0896030776.
Повний текст джерелаLubec, Gert, and Gerald A. Rosenthal, eds. Amino Acids. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-011-2262-7.
Повний текст джерелаMisch, Kelly, and William D. Martineau. Amino acids. Cleveland: Freedonia Group, 1999.
Знайти повний текст джерелаL, Hayes Teresa, Angrist Misha, Moehlenkamp Andrea, and Freedonia Group, eds. Amino acids. Cleveland: Freedonia Group, 2001.
Знайти повний текст джерелаA, Boulton A., Baker Glen B. 1947-, and Wood James D, eds. Amino acids. Clifton, N.J: Humana Press, 1985.
Знайти повний текст джерелаAngrist, Misha, Teresa L. Hayes, and Rebecca L. Friedman. World amino acids. Cleveland: Freedonia Group, 2000.
Знайти повний текст джерелаPollegioni, Loredano, and Stefano Servi, eds. Unnatural Amino Acids. Totowa, NJ: Humana Press, 2012. http://dx.doi.org/10.1007/978-1-61779-331-8.
Повний текст джерелаYoshimura, Tohru, Toru Nishikawa, and Hiroshi Homma, eds. D-Amino Acids. Tokyo: Springer Japan, 2016. http://dx.doi.org/10.1007/978-4-431-56077-7.
Повний текст джерелаRoberts, Peter J., Jon Storm-Mathisen, and Harry F. Bradford, eds. Excitatory Amino Acids. London: Palgrave Macmillan UK, 1986. http://dx.doi.org/10.1007/978-1-349-08479-1.
Повний текст джерелаLemke, Edward A., ed. Noncanonical Amino Acids. New York, NY: Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-7574-7.
Повний текст джерелаЧастини книг з теми "Amino acids"
Fowden, Leslie. "Novel amino acids from plants." In Amino Acids, 3–9. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-011-2262-7_1.
Повний текст джерелаDuguid, R. "The effect of arginine on glycolysis by oral bacteria." In Amino Acids, 81–84. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-011-2262-7_10.
Повний текст джерелаPickard, Mark R., Arun K. Sinha, Damiano Gullo, Mohamed M. Khaled, and Roger P. Ekins. "Regulatory effects of thyroid hormones on amino acid metabolism in the brain: The influence of maternal hypothyroxinemia on brain biochemistry of adult rat progeny." In Amino Acids, 828–38. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-011-2262-7_100.
Повний текст джерелаPalmer, Richard M. J., and Salvador Moncada. "The biological importance of the formation of nitric oxide from L-arginine." In Amino Acids, 839–42. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-011-2262-7_101.
Повний текст джерелаSchwenk, W. Frederick, and Morey W. Haymond. "Effects of infusion of leucine and other essential amino acids on leucine metabolism in humans." In Amino Acids, 843–49. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-011-2262-7_102.
Повний текст джерелаYoung, Gerald A., John B. Dibble, and Aleck M. Brownjohn. "The use of amino acid based CAPD fluid in chronic renal failure." In Amino Acids, 850–57. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-011-2262-7_103.
Повний текст джерелаBaccino, E., J. Caroff, J. C. Bigot, J. F. Menez, and H. H. Floch. "Is serum tryptophan a good indicator of CNS serotonin metabolism in chronic alcoholics with hepatopathy?" In Amino Acids, 858–60. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-011-2262-7_104.
Повний текст джерелаMunoz, Santiago, Marshall Stafford, Sharon Westerberg, Mackenzie Walser, and Willis Maddrey. "Effects of branched chain amino acids and ketoanalogues on brain branched chain and aromatic amino acids in experimental liver disease." In Amino Acids, 861–66. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-011-2262-7_105.
Повний текст джерелаDøskeland, Anne P., Olav K. Vintermyr, Torgeir Flatmark, Richard G. H. Cotton, and Stein O. Døskeland. "Modulation by ligands of the phosphorylation state of phenylalanine 4-monooxygenase in intact hepatocytes." In Amino Acids, 867–74. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-011-2262-7_106.
Повний текст джерелаHutson, Susan M., Stewart K. Roten, Debra L. Oliveira, and Ronald S. Kaplan. "Solubilization and functional reconstitution of the mitochondrial branched chain α-keto acid transporter." In Amino Acids, 875–80. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-011-2262-7_107.
Повний текст джерелаТези доповідей конференцій з теми "Amino acids"
Oda, Masato, Takashi Nakayama, and Takahisa Ohno. "Optical Ionization Of Amino Acids Using Amino-acid/Semiconductor Junctions." In PHYSICS OF SEMICONDUCTORS: 28th International Conference on the Physics of Semiconductors - ICPS 2006. AIP, 2007. http://dx.doi.org/10.1063/1.2730458.
Повний текст джерелаEdwards, Alison A., Mark P. Watterson, John A. Leach, George W. J. Fleet, and George E. Tranter. "TETRAHYDROFURAN BASED AMINO ACIDS." In XXIst International Carbohydrate Symposium 2002. TheScientificWorld Ltd, 2002. http://dx.doi.org/10.1100/tsw.2002.504.
Повний текст джерелаSilva, Maísa de Carvalho, Lariza Laura De Oliveira, and Renato Tinós. "Optimization of Expanded Genetic Codes via Genetic Algorithms." In XV Encontro Nacional de Inteligência Artificial e Computacional. Sociedade Brasileira de Computação - SBC, 2018. http://dx.doi.org/10.5753/eniac.2018.4440.
Повний текст джерелаSheu, Sheh-Yi, Dah-Yen Yang, Michio Tokuyama, Irwin Oppenheim, and Hideya Nishiyama. "Interaction of Adjacent Amino Acids." In COMPLEX SYSTEMS: 5th International Workshop on Complex Systems. AIP, 2008. http://dx.doi.org/10.1063/1.2897897.
Повний текст джерелаGonçalves, M., S. A. Barros, Vânia Frade, and João Moura. "Fluorescence Derivatisation of Amino Acids." In The 9th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2005. http://dx.doi.org/10.3390/ecsoc-9-01478.
Повний текст джерелаMartinelli, E., G. Pennazza, M. Santonico, A. D'Amico, C. Di Natale, R. Paolesse, D. Monti, M. Mascini, and D. Compagnone. "Gas sensitivity of amino acids monolayers." In 2008 IEEE Sensors. IEEE, 2008. http://dx.doi.org/10.1109/icsens.2008.4716573.
Повний текст джерелаIordache, A., E. Horj, A. R. Ani, C. Mesaros, S. Morar, O. Cozar, M. Culea, Madalin Bunoiu, and Iosif Malaescu. "Amino Acids Profiles in Biological Media." In Proceedings of the Physics Conference. AIP, 2010. http://dx.doi.org/10.1063/1.3482230.
Повний текст джерелаChyba, Christopher F. "Extraterrestrial amino acids and terrestrial life." In Physical orgin of homochirality in life. AIP, 1996. http://dx.doi.org/10.1063/1.51255.
Повний текст джерелаCroitoriu, Alexandra, Loredana E. Nita, Alina G. Rusu, Andrei Cimponeriu, and Aurica P. Chiriac. "Supramolecular Gels Based on Amino Acids." In 2021 International Conference on e-Health and Bioengineering (EHB). IEEE, 2021. http://dx.doi.org/10.1109/ehb52898.2021.9657568.
Повний текст джерелаMelnic, Maria, and Olesea Gliga. "About chemical composition of the nematode Ditylenchus Dipsaci." In Xth International Conference of Zoologists. Institute of Zoology, Republic of Moldova, 2021. http://dx.doi.org/10.53937/icz10.2021.40.
Повний текст джерелаЗвіти організацій з теми "Amino acids"
Singh, Anjali. Amino Acids: Building Blocks of Proteins. ConductScience, June 2022. http://dx.doi.org/10.55157/cs20220612.
Повний текст джерелаAdnani-Gleason, Z. Polymerization of Amino Acids on Kaolinite. Portland State University Library, January 2000. http://dx.doi.org/10.15760/etd.2372.
Повний текст джерелаSpielvogel, Bernard F., Barbara R. Shaw, and Robert G. Ghirardelli. Boron Analogues of Amino Acids and Derivatives. Fort Belvoir, VA: Defense Technical Information Center, July 1989. http://dx.doi.org/10.21236/ada211311.
Повний текст джерелаSpielvogel, Bernard F., and Andrew T. McPhail. Studies on Syntheses of Amine-Carboxyboranes (Boron Analogues of Amino Acids) and Derivatives. Fort Belvoir, VA: Defense Technical Information Center, August 1987. http://dx.doi.org/10.21236/ada184838.
Повний текст джерелаCotman, C. W. Excitatory Amino Acids as Transmitters in the Brain. Fort Belvoir, VA: Defense Technical Information Center, April 1989. http://dx.doi.org/10.21236/ada210685.
Повний текст джерелаvan Krimpen, M. M., P. G. van Wikselaar, and L. H. de Jonge. Degradation of free amino acids in liquidfeeding conditions. Wageningen: Wageningen Livestock Research, 2019. http://dx.doi.org/10.18174/473960.
Повний текст джерелаAnderson, Olin D., Gad Galili, and Ann E. Blechl. Enhancement of Essential Amino Acids in Cereal Seeds: Four Approaches to Increased Lysine Content. United States Department of Agriculture, October 1998. http://dx.doi.org/10.32747/1998.7585192.bard.
Повний текст джерелаSchultz, Peter G. In Vivo Incorporation of Unnatural Amino Acids into Proteins. Fort Belvoir, VA: Defense Technical Information Center, December 2000. http://dx.doi.org/10.21236/ada392129.
Повний текст джерелаTirrell, David A. Genetic Engineering of Artificial Proteins Containing Non-Natural Amino Acids. Fort Belvoir, VA: Defense Technical Information Center, May 2001. http://dx.doi.org/10.21236/ada394071.
Повний текст джерелаDeCarli, J. P. II, G. Carta, and C. H. Byers. Large-scale separation of amino acids by continuous displacement chromatography. Office of Scientific and Technical Information (OSTI), October 1989. http://dx.doi.org/10.2172/5912255.
Повний текст джерела