Relevant bibliographies by topics / Betaine Phosphate

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Reports

Academic literature on the topic 'Betaine Phosphate'

Author: Grafiati
Published: 6 September 2023
Last updated: 31 July 2025

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Journal articles on the topic "Betaine Phosphate"

1

Banys, Juras, Vytautas Samulionis, Georg Voelkel, and A. Kloepperpieper. "Ultrasonic anomalies in betaine phosphate/betaine phosphite mixed crystals." Journal of the Acoustical Society of America 105, no. 2 (1999): 1294. http://dx.doi.org/10.1121/1.426166.

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2

BALASHOVA, E. V., and V. V. LEMANOV. "Dielectric Properties of Betaine Phosphite-Betaine Phosphate in Improper Ferroelastic Phase." Ferroelectrics 302, no. 1 (2004): 143–45. http://dx.doi.org/10.1080/00150190490453333.

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Freude, P., J. Totz, D. Michel, and M. Arndt. "Chemical exchange and conductivity processes in betaine phosphate and betaine phosphite." Journal of Physics: Condensed Matter 10, no. 2 (1998): 429–43. http://dx.doi.org/10.1088/0953-8984/10/2/022.

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4

Banys, J., A. Brilingas, J. Grigas, et al. "Radio and Microwave Spectroscopy of the Betaine Phosphate/Betaine Phosphite Mixed Crystals." Ferroelectrics 267, no. 1 (2002): 285–92. http://dx.doi.org/10.1080/00150190211027.

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5

Hutton, S. L., I. Fehst, R. Böhmer, and A. Loidl. "Low temperature dielectric relaxation in mixed crystals of betaine phosphate and betaine phosphite." Ferroelectrics 127, no. 1 (1992): 279–84. http://dx.doi.org/10.1080/00150199208223385.

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6

Freude, P., D. Michel, J. Totz, and A. Klöpperpieper. "Ordering behaviour at the antiferrodistortive phase transition in betaine phosphate and betaine phosphite." Ferroelectrics 208-209, no. 1 (1998): 93–103. http://dx.doi.org/10.1080/00150199808014870.

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7

Pöppl, A., G. Völkel, J. Hoentsch, S. Orlinski, and A. Klöpperpieper. "Electron spin relaxation of the PO32− radical in ferroelectric betaine phosphite and in the proton glass betaine phosphate/betaine phosphite." Chemical Physics Letters 224, no. 3-4 (1994): 233–37. http://dx.doi.org/10.1016/0009-2614(94)00549-4.

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Banys, J., C. Klimm, G. Völkel, H. Bauch, and A. Klöpperpieper. "Proton-glass behavior in a solid solution of (betaine phosphate)0.15(betaine phosphite)0.85." Physical Review B 50, no. 22 (1994): 16751–53. http://dx.doi.org/10.1103/physrevb.50.16751.

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9

Freude, P., and D. Michel. "2H NMR studies of the antiferrodistortive phase transition in betaine phosphite and betaine phosphate." physica status solidi (b) 195, no. 1 (1996): 297–310. http://dx.doi.org/10.1002/pssb.2221950133.

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10

Santos, M. L., L. C. R. Andrade, M. M. R. Costa, et al. "Detailed Structural X-Ray Study of (Betaine Phosphate)1?x(Betaine Phosphite)x Compounds." physica status solidi (b) 199, no. 2 (1997): 351–67. http://dx.doi.org/10.1002/1521-3951(199702)199:2<351::aid-pssb351>3.0.co;2-d.

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Dissertations / Theses on the topic "Betaine Phosphate"

1

Salomon, Sarah. "Rôle des bétaine lipides dans l'adaptation à la carence en phosphate chez les algues et les plantes." Electronic Thesis or Diss., Université Grenoble Alpes, 2024. http://www.theses.fr/2024GRALV026.

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Au cours de l’évolution, les organismes ont développé différentes stratégies afin de s’adapter aux stress rencontrés dans leur milieu. La disponibilité en nutriments représente une part importante de ces stress et peut conduire à des changements métaboliques conséquents. Le phosphore est un nutriment essentiel à la croissance des organismes ; il est assimilé sous la forme de phosphate inorganique (Pi) et se retrouve souvent limitant dans les écosystèmes. Chez les plantes, la carence en phosphate affecte grandement la croissance et génère un remodelage massif des lipides membranaires afin de re
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2

Huang, Bing. "Réponses physiologiques et biochimiques à une limitation nutritive en phosphore ou en azote sur la réorientation métabolique des lipides polaires chez différentes espèces de microalgues marines." Thesis, Le Mans, 2018. http://www.theses.fr/2018LEMA1021/document.

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Les bétaïne lipides (BL) sont des lipides polaires qui se distinguent des phospholipides (PL)par l’absence de phosphore (P). La réorientation métabolique induite par une limitation en P chez des microalgues produisant des BL (Tisochrysis lutea et Diacronema lutheri, Haptophytes) ou en produisant peu (Phaeodactylum tricornutum, Bacillariophyte) a été comparée à celle induite par une limitation en azote (N). Le devenir et le flux de carbone dans différentes voies de biosynthèse ont été étudiés par une approche pluridisciplinaire.La limitation nutritive en P ou en N affecte différemment le métabo
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Ramanuja, M. N. "1H-NMR Study of Proton Glasses - Nuclear Spin Lattice Relaxation in BPxBPI(1-x) and BPxGPI(1-x) - Effects of Disorder on the Proton Group Dynamics." Thesis, 2007. https://etd.iisc.ac.in/handle/2005/4693.

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Mixed systems made from a combination of ferroelectric (FE) and antiferroelectric (AFE) compounds, exhibit various effects of disorder in different temperature regions. The kind of effects observed, depend on the technique and the window of observation employed. Model systems, like Potassium Ammonium dihydrogen phosphate (KADP), Rubidium Ammonium dihydrogen phosphate (RADP) and BPxBPI(1-x) , with H-bonding networks, have been well studied by dielectric techniques. These investigations have revealed disorder effects like deviations from Curie Weiss law, progressive broadening of dielectric loss
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Book chapters on the topic "Betaine Phosphate"

1

Singh, Rani. "Homocystinuria." In Pediatric Nutrition In Chronic Diseases And Developmental Disorders. Oxford University PressNew York, NY, 2005. http://dx.doi.org/10.1093/oso/9780195165647.003.0037.

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Abstract Homocystinuria can result from hereditary or acquired enzymatic deficiencies in either the remethylaton pathway of homocysteine to methionine or the trans-sulfuration of homocysteine to cysteine. Homocysteine occupies a central position in methyl metabolism, specifically methyl cycling involving methionine, homocysteine, and cysteine (Fig. 37–1). One fate of homocysteine is remethylation to synthesize methionine using the methyl donor from either 5-methyl-tetrahydrofolate (THF), with methyl cobalamin as coenzyme, or using the methyl donor from betaine, which is catalyzed by betaine-ho
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Reports on the topic "Betaine Phosphate"

1

Droby, Samir, Michael Wisniewski, Ron Porat, and Dumitru Macarisin. Role of Reactive Oxygen Species (ROS) in Tritrophic Interactions in Postharvest Biocontrol Systems. United States Department of Agriculture, 2012. http://dx.doi.org/10.32747/2012.7594390.bard.

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To elucidate the role of ROS in the tri-trophic interactions in postharvest biocontrol systems a detailed molecular and biochemical investigation was undertaken. The application of the yeast biocontrol agent Metschnikowia fructicola, microarray analysis was performed on grapefruit surface wounds using an Affymetrix Citrus GeneChip. the data indicated that 1007 putative unigenes showed significant expression changes following wounding and yeast application relative to wounded controls. The expression of the genes encoding Respiratory burst oxidase (Rbo), mitogen-activated protein kinase (MAPK)
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Journal articles
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