Academic literature on the topic 'Régression de cycle C4→C3'
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Journal articles on the topic "Régression de cycle C4→C3"
Sherry, A. D., P. Zhao, A. J. Wiethoff, F. M. H. Jeffrey, and C. R. Malloy. "Effects of aminooxyacetate on glutamate compartmentation and TCA cycle kinetics in rat hearts." American Journal of Physiology-Heart and Circulatory Physiology 274, no. 2 (February 1, 1998): H591—H599. http://dx.doi.org/10.1152/ajpheart.1998.274.2.h591.
Full textHattersley, PW, and NE Stone. "Photosynthetic Enzyme Activities in the C3-C4 Intermediate Neurachne minor S. T . Blake (Poaceae)." Functional Plant Biology 13, no. 3 (1986): 399. http://dx.doi.org/10.1071/pp9860399.
Full textKrall, JP, GE Edwards, and MSB Ku. "Quantum Yield of Photosystem II and Efficiency of CO2 Fixation in Flaveria (Asteraceae) Species under Varying Light and CO2." Functional Plant Biology 18, no. 4 (1991): 369. http://dx.doi.org/10.1071/pp9910369.
Full textSalgia, Ravi, Benjamin J. Solomon, Alice Tsang Shaw, D. Ross Camidge, Tracey L. Evans, Dong-Wan Kim, Yuankai Shi, et al. "Visual effects in anaplastic lymphoma kinase (ALK)-positive advanced non-small cell lung cancer (NSCLC) patients treated with crizotinib." Journal of Clinical Oncology 30, no. 15_suppl (May 20, 2012): 7596. http://dx.doi.org/10.1200/jco.2012.30.15_suppl.7596.
Full textBalcaen, A., E. Claeys, V. Fievez, P. Boeckx, O. van Cleemput, and S. de Smet. "Stable carbon isotope analysis of faecal and blood samples of sheep in relation to the diet." Proceedings of the British Society of Animal Science 2003 (2003): 159. http://dx.doi.org/10.1017/s1752756200013181.
Full textMason, Graeme F., Douglas L. Rothman, Kevin L. Behar, and Robert G. Shulman. "NMR Determination of the TCA Cycle Rate and α-Ketoglutarate/Glutamate Exchange Rate in Rat Brain." Journal of Cerebral Blood Flow & Metabolism 12, no. 3 (May 1992): 434–47. http://dx.doi.org/10.1038/jcbfm.1992.61.
Full textStitt, Mark, Gian Luca Borghi, and Stéphanie Arrivault. "Targeted metabolite profiling as a top-down approach to uncover interspecies diversity and identify key conserved operational features in the Calvin–Benson cycle." Journal of Experimental Botany 72, no. 17 (June 22, 2021): 5961–86. http://dx.doi.org/10.1093/jxb/erab291.
Full textZhang, Xuecai, Paulino Pérez-Rodríguez, Juan Burgueño, Michael Olsen, Edward Buckler, Gary Atlin, Boddupalli M. Prasanna, Mateo Vargas, Félix San Vicente, and José Crossa. "Rapid Cycling Genomic Selection in a Multiparental Tropical Maize Population." G3 Genes|Genomes|Genetics 7, no. 7 (July 1, 2017): 2315–26. http://dx.doi.org/10.1534/g3.117.043141.
Full textAngelo, Courtney L., and Curtis C. Daehler. "Temperature is the major driver of distribution patterns for C4 and C3 BEP grasses along tropical elevation gradients in Hawai‘i, and comparison with worldwide patterns." Botany 93, no. 1 (January 2015): 9–22. http://dx.doi.org/10.1139/cjb-2014-0075.
Full textHäusler, Rainer E., Heinz‐Josef Hirsch, Fritz Kreuzaler, and Christoph Peterhänsel. "Overexpression of C4‐cycle enzymes in transgenic C3 plants: a biotechnological approach to improve C3‐photosynthesis." Journal of Experimental Botany 53, no. 369 (April 1, 2002): 591–607. http://dx.doi.org/10.1093/jexbot/53.369.591.
Full textDissertations / Theses on the topic "Régression de cycle C4→C3"
Karkour, Belkacem. "Les cyclopropanols chiraux et leur potentialité synthétique." Paris 11, 1987. http://www.theses.fr/1987PA112378.
Full textThe aim of this thesis is the preparation and study of the synthetic potential of chiral cyclopropanols. The 1-hydroxy 2-methyl cyclopropanecarboxaldehyde available from 2-methylsuccinate, is used to prepare 1-(vinylcarbinol} cyclopropanols which, undergo acid induced C3 C4 regiospecific ring expansion into 2-vinyl cyclobutanones (BF3-Et20) or C3 -+ C4 --+- C5 ring expansion into cyclopenten-2- ones (CH3S03H-P205). The thermal rearrangement of 2-methyl vinylcyclopropanes leads by an ene-reaction to ring-opened products ; therefore the limitation of the thermal vinylcyclopropane-cyclopentene ring enlargement is removed by this new approach. (R)(+) and (S)(-). Dimethyl 2-methylsuccinates, now available from enantiose lective hydrolysis by porcine pancreatic lipase, undergo acyloin type cyclization into (R) and (S) 3-methyl-1,2-disiloxycyclobutene, respectively. Base-induced stereoselective C4 C3 ring contraction of these cyclobutenes provides 1-hydroxycyclopropanecarboxaldehydes which are used to prepare optically active 1-alkenylcyclopropanols. Then, acid-induced regio- and stereospecific C3---+ C4 ring enlargement leads to 2-vinylcyclobutanones with high enantiomeric excesses. These compounds are used to synthetize (S) 5-methyl cyclohexen-2-one and abutenolide ; i. E. The quercus lactone b2-Vinylcyclobutanones are efficient precursors of 5-, 6- and 8-membered rings. Therefore, this new methodology, which does not involve cyclopropylcarbiny1 cations as proven by the stereospecificity of the rearrangements, allows one to prepare from chiral succinates natural compounds bearing different frameworks
Ollivier, Jean. "Les cyclopropanols précurseurs de composés cyclopentaniques : application à la synthèse totale de produits naturels." Paris 11, 1986. http://www.theses.fr/1986PA112003.
Full textThe aim of this thesis is the synthetic applications of two peculiar cyclopropanols : l) The l-ethoxycyclopropanol, is converted into propargylic cyclopropanols upon treatment with acetylenic magnesium bromide or lithium. Hydride reduction and O-silylation lead to l-siloxy l-vinylcyclopropanes which undergo thermal C3 ---> C5 ring enlargement into l-siloxycyclopentenes ; then , these enol ethers are regiospecifically alkylated into 2, 3-disubstituted cyclopentanones. This scheme is illustrated by the total synthesis of ± ll-deoxyprostaglandin E₂ methyl ester. 2) The l-hydroxycyclopropanecarboxaldehyde tetrahydropyranyl and silylated ethers provide l-siloxy-l-vinylcyclopropanes which, after thermal rearrangement lead directly to 2,3-disubstituted cyclopentanones and cyclopentenones upon hydrolysis or dehydrosilylation, so avoiding the quite delicate enol ether alkylation. Dicranenones, new fatty acids structurally similar to prostanoids and jasmanoids, having antimicrobial activity, are prepared from this new synthon
Book chapters on the topic "Régression de cycle C4→C3"
Monson, Russell K. "Evidence for Inefficient C4-Cycle Function in C3-C4 Intermediate Flaveria Species: Implications for C4 Evolution." In Progress in Photosynthesis Research, 641–44. Dordrecht: Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-017-0516-5_136.
Full textBrugnoli, E., M. C. De Tullio, M. C. Monteverdi, M. Lauteri, and A. Scartazza. "Xanthophyll Cycle Components and Energy Dissipation in Sun and Shade Leaves of C3 and C4 Plants." In Photosynthesis: from Light to Biosphere, 3043–46. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-009-0173-5_713.
Full textConference papers on the topic "Régression de cycle C4→C3"
Jafarpour, Marjan, and Rosimah Nulit. "An overview of over-expression of C4-cycle enzymes into C3 plants." In 2011 National Postgraduate Conference (NPC). IEEE, 2011. http://dx.doi.org/10.1109/natpc.2011.6136448.
Full textHormozi, Mohammad R., Farid Biglari, and Kamran M. Nikbin. "Study of Sensitivity of Damage Parameters c1, c2, c3 and c4 on FB2 Material Under Low Cycle Fatigue Test." In ASME 2012 Pressure Vessels and Piping Conference. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/pvp2012-78810.
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