Academic literature on the topic 'Plant and cell physiology'

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Journal articles on the topic "Plant and cell physiology"

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Caboche, Michel. "Plant physiology." Trends in Cell Biology 2, no. 1 (January 1992): 32–33. http://dx.doi.org/10.1016/0962-8924(92)90144-c.

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Kylin, Anders. "Plant Physiology." Physiologia Plantarum 73, no. 1 (May 1988): 153. http://dx.doi.org/10.1111/j.1399-3054.1988.tb09206.x.

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Costa, L. M. "Plant & Cell Physiology Research Highlights." Plant and Cell Physiology 53, no. 12 (December 1, 2012): 1985–88. http://dx.doi.org/10.1093/pcp/pcs157.

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Martin, Cathie, and Mike Blatt. "Plant Physiology and The Plant Cell Go Online Only." Plant Cell 26, no. 12 (December 2014): 4561. http://dx.doi.org/10.1105/tpc.114.133579.

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Martin, Cathie, and Mike Blatt. "Plant Physiology and The Plant Cell Go Online Only." Plant Physiology 166, no. 4 (December 2014): 1677. http://dx.doi.org/10.1104/pp.114.900498.

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Schopfer, P. "Physiology and biochemistry of plant cell walls." Plant Science 123, no. 1-2 (March 1997): 211. http://dx.doi.org/10.1016/s0168-9452(96)04565-7.

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Loewus, F. A. "Physiology and biochemistry of plant cell walls." Plant Science 73, no. 1 (January 1991): 127. http://dx.doi.org/10.1016/0168-9452(91)90134-t.

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Yamaya, T. "Plant and Cell Physiology in 2012 and Beyond ..." Plant and Cell Physiology 53, no. 2 (February 1, 2012): 265–66. http://dx.doi.org/10.1093/pcp/pcs005.

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Obayashi, T., and K. Yano. "The 2013 Plant and Cell Physiology Database Issue." Plant and Cell Physiology 54, no. 2 (February 1, 2013): 169–70. http://dx.doi.org/10.1093/pcp/pct011.

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Obayashi, Takeshi, and Kentaro Yano. "Plant and Cell Physiology 2014 Online Database Issue." Plant and Cell Physiology 55, no. 1 (December 24, 2013): 1–2. http://dx.doi.org/10.1093/pcp/pct193.

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Dissertations / Theses on the topic "Plant and cell physiology"

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Lucas, W. J. "Plant physiology : transport processes in plants /." Title page, preface and contents only, 1989. http://web4.library.adelaide.edu.au/theses/09SD/09sdl933.pdf.

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Thesis (D. Sc.)--Faculty of Science, University of Adelaide, 1990.
Published works [representing] original research conducted during the various phases of [his] academic development--Pref. Includes bibliographical references.
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Liu, Xiaochuan. "The cell biology and physiology of cytoplasmic male sterility in Petunia hybrida." Thesis, University of Reading, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.328541.

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Brigham, Lindy Andersen 1951. "Root border cell differentiation." Diss., The University of Arizona, 1996. http://hdl.handle.net/10150/290689.

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The inability of a plant to run from danger or seek nutrients necessitates its capacity to change the environment of the surrounding soil for protection and sustenance. A unique plant process, the release of thousands of autonomous cells from the root cap, called root border cells, may play a role in the ability of the plant to regulate microbial populations and nutrient availability in the rhizosphere. In this study, evidence is presented showing that root border cells are a differentiated tissue, that the production of border cells is highly regulated and tied to cell turnover in the root cap and that products of border cells regulate cell division in the root cap meristem. In vivo labeling experiments demonstrate that 13% of the proteins that are abundant in preparations from border cells are undetectable in root tip cells. Differences between the two cell populations are apparent as soon as border cells separate from each other, even when they are still adhered to the root tip. Twenty-five percent of the proteins synthesized by border cells in a 1-hour period are rapidly excreted into the incubation medium. Border cells arise within the root cap meristem by cell division and their production is tightly regulated both developmentally and in response to border cell removal. Removal of border cells results in the induction of cell division in the transverse root cap meristem to 400% of the basal rate within 30 minutes. This elevated rate of mitosis is maintained for 1.5 h and falls to basal levels within 6 hours. During this time, mitosis in the root apical meristem remains constant. mRNA differential display analysis showed changes in gene expression in the root cap within 5 to 15 minutes of removal of border cells. Genes putatively involved in cell functions in three regions of the cap showed expected distribution patterns by in situ hybridization and RNA blot analysis revealed changes in their expression patterns were seen in response to border cell removal. The presence of border cells acts as an inhibitor to continued mitosis and border cell production in the root cap. Evidence from fractionation studies shows that a heat stable, protease insensitive molecule in the range of 25 to 80 kDa, produced by the border cells themselves, is responsible for this inhibition.
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Sudarmonowati, Enny. "Somatic embryogenesis and plant regeneration in cassava (Manihot esculenta, Crantz)." Thesis, University of Bath, 1990. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.278592.

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Cancho, Sánchez Ester. "Dissecting the GA regulation of cell expansion in the root Arabidopsis thaliana." Thesis, University of Nottingham, 2013. http://eprints.nottingham.ac.uk/28667/.

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Gibberellins (GAs) represent an important class of hormonal signal that regulate growth and developmental processes during the plant life cycle. GA promotes growth through the targeted degradation of the nuclear localized DELLA repressor proteins via the ubiquitin proteasome pathway. Whilst DELLAs do not appear to bind directly to DNA, recent evidence suggests that they interact with several different classes of transcription factors to control the expression of downstream genes in a GA-dependent manner. In order to pinpoint the genes targeted by GA to promote root growth, several genetic approaches have been pursued in this thesis. These approaches took advantage of the previous observation that targeting expression of a steroid regulated non-degradable form of DELLA in endodermal cells (using the SCR:gai-GR transgene) blocked root elongation (Ubeda-Tomas et al., 2008, 2009). The SCR:gai-GR line was initially mutagenized to select mutants that no longer exhibit steroid-inducible root growth inhibition. Several mutant lines have been selected, characterised and subjected to next-generation sequencing to reveal whether they disrupt novel downstream components of the GA signalling pathway. The SCR:gai-GR line has also been used in transcriptomic studies and a number of novel downstream targets identified for functional characterisation. Finally, several GA-regulated genes encoding cell wall modifying enzymes belonging to the xyloglucan endotransglucosylase/ hydrolase (XTH) family have been functionally characterised. Multiple XTH mutant combinations exhibit root elongation defects and altered cell expansion dynamics, hence providing new insight into how GAs may regulate cell wall remodelling enzymes to promote root cell expansion.
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Ramakrishna, Priya. "Unraveling the role of cell wall remodeling factors in Arabidopsis root development." Thesis, University of Nottingham, 2017. http://eprints.nottingham.ac.uk/43301/.

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Lateral roots are a key component of the plant root system architecture that help anchorage in soil and acquisition of water and nutrients. In the dicot Arabidopsis, lateral roots initiate post-embryonically from a specialised set of cells at the xylem pole of the pericycle cell layer termed ‘founder cells (FC)’, overlaid by three distinct tissue layers – endodermis, cortex, epidermis. The FCs undergo a coordinated series of asymmetric cell divisions (ACD) to form a primordium that grows and emerges through these overlying layers as a mature lateral root. Different auxin signaling modules, as well as tight regulation of the cell geometry are important during early organogenesis. In this study, we were interested to identify molecular components that influence cell wall remodeling properties and cell geometry in the FC and regulates asymmetric cell division during early lateral root initiation. Transcriptomic analysis of FCs (De Smet et al., 2008) identified a candidate gene EXPANSINA1 (EXPA1) of expansin superfamily, known for their unique ability to alter linkage between the cell wall polymers and cause wall loosening. In vivo expression studies showed that EXPA1 is expressed in FCs prior asymmetric cell division. The mutant expa1-1 exhibits perturbed ACD with a delay in kinetics of primordia from Stage I to II, loss in radial expansion of FCs in response to auxin which is important for organised formative divisions. To understand if these defects are due to altered properties of the cell wall, and role of auxin in this process, we developed an optimised technique to study the chemical properties of the FC cell wall junctions based on confocal Raman spectroscopy. This showed altered interactions in expa1-1 between the major cell wall polymers xyloglucans and pectins locally in the pericycle cell wall upon auxin treatment, that could influence cell geometry during early lateral root development. Additionally, sugar monomer analysis of digested whole roots showed interesting alterations in representative global wall sugar levels in the root which although diluted due to lack of tissue specificity warrants further study. In conclusion, the combination of molecular and biochemical analyses reveals that auxin dependent regulation of EXPA1 plays an important role in lateral root FC and is required for organised asymmetric cell division.
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Lunn, Daniel. "Role of Rab GTPase proteins in cell wall deposition and potential use of RabA mutants in bioenergy crops." Thesis, University of Nottingham, 2013. http://eprints.nottingham.ac.uk/14560/.

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It has long been known that fossil fuels are a finite source of energy. With this in mind research has turned to the development of renewable energy sources. One solution is the conversion of biomass to useable energy sources. These resources are located in the cell walls of currently available agronomic crops in the form of complex biopolymers, lignocelluloses, which are highly recalcitrant. In the following thesis I explore the novel mechanism of Impacting cell wall composition using mutants involved in trafficking to the cell wall. The following work shows that Rab GTPasemutants impact on cell wall deposition, with specific sub-clades impacting particular cell wall polymers. I then go on to show these mutants have significant effect on recalcitrance and thus increase saccharification of the biomass, without impacting on agronomic properties. Finally I go on to show the same impact on cell wall composition in a presumed orthogolous Rab in tomato. These findings all have significant Implications in the fields of Intracellular trafficking, cell wall biology and bioenergy.
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Mühlenbock, Per. "Genetic and Molecular Mechanisms Controlling Reactive Oxygen Species and Hormonal Signalling of Cell Death in Response to Environmental Stresses in Arabidopsis thaliana." Doctoral thesis, Stockholms universitet, Botaniska institutionen, 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-1358.

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In the present work the regulation of environmentally induced cell death and signaling of systemic acquired acclimation (SAA) in Arabidopsis thaliana is characterized. We used the lesion simulating disease1 (lsd1) mutant as a model system that is deregulated in light acclimation and programmed cell death (PCD). In this system we identify that redox status controlling SAA and cell death is controlled by the genes LSD1, EDS1, EIN2 and PAD4 which regulate cellular homeostasis of salicylic acid (SA), ethylene (ET), auxin (IAA) and reactive oxygen species (ROS). Furthermore we propose that the roles of LSD1 in light acclimation and in biotic stress are functionally linked. The influence of SA on plant growth, short-term acclimation to high light (HL), and on the redox homeostasis of Arabidopsis leaves was also assessed. SA impaired acclimation of wild-type plants to prolonged conditions of excess excitation energy (EEE). This indicates an essential role of SA in acclimation and regulation of cellular redox homeostasis. We also show that cell death in response to EEE is controlled by specific redox changes of photosynthetic electron transport carriers that normally regulate EEE acclimation. These redox changes cause production of ET that signals through the EIN2 gene and regulon. In the lsd1 mutant, we found that propagation of cell death depends on the plant defence regulators EDS1 and PAD4 operating upstream of ET production. We conclude that the balanced activities of LSD1, EDS1, PAD4 and EIN2 regulate chloroplast dependent acclimatory and defence responses. Furthermore, we show that Arabidopsis hypocotyls form lysigenous aerenchyma in response to hypoxia and that this process involves H2O2 and ET signalling. We found that formation of lysigenous aerenchyma depends on LSD1, EDS1 and PAD4. Conclusively we show that LSD1, EDS1 and PAD4, in their functions as major plant redox and hormone regulators provide a basis for fundamental plant survival in natural contitions.
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Ries, Laure Nicolas Annick. "Regulation of genes encoding enzymes involved in plant cell wall deconstruction in Trichoderma reesei." Thesis, University of Nottingham, 2013. http://eprints.nottingham.ac.uk/13045/.

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This study describes the regulation of genes encoding plant cell wall-degrading enzymes in the presence of different carbon sources from the biotechnologically important fungus Trichoderma reesei. It was shown that different carbon sources influence fungal growth rate, biomass production and subsequent enzyme secretion. Several genes were identified and suggested to play a role in the development of conidia and in maintaining polarised growth. RNA-sequencing studies showed an increase in transcript levels of genes encoding enzymes involved in plant cell wall degradation (CAZy) as well as of genes encoding lipases, expansins, hydrophobins, G-protein coupled receptors and transporters when mycelia were cultivated in the presence of a lignocellulosic substrate (wheat straw). The encoded non-CAZy proteins were proposed to have accessory roles in carbohydrate deconstruction. A model for solid substrate recognition in T. reesei was described, based on the comparison with the one proposed for Aspergillus niger. Post-transcriptional regulation mediated by regulatory RNAs was identified for nearly 2% of all T. reesei genes, including genes encoding cell wall-degrading enzymes. Transcriptional regulation studies confirmed that transcription patterns of genes encoding enzymes involved in polysaccharide degradation differed between different carbon sources and that they are fine-tuned and dependent on factors such as culture conditions, consumption rate, assimilation of glucose and the presence of several transcription factors. The analysis of the structure of chromatin in the promoter and coding regions of one of these genes, cbh1, revealed different nucleosome positioning patterns under repressing (glucose) and inducing (sophorose, cellulose) conditions. CRE1, the carbon catabolite repressor in T. reesei was shown to be involved in the repression of many CAZy and non-CAZy encoding genes. Furthermore, CRE1 was also shown to be important for nucleosome positioning within the cbh1 coding region under repressing conditions and proposed to do so by interaction with (a) yet unidentified protein(s).
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Tao, Titus. "Functional characterization of ZmGRP5, a glycine-rich protein specifically expressed in the cell wall of maize silk tissue." Thesis, University of Ottawa (Canada), 2004. http://hdl.handle.net/10393/26780.

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Silk tissue is a specialized reproductive tissue of the maize plant, equivalent to the stigma and style portion of the female inflorescence. The moist and nutrient rich properties of maize silk tissue that facilitate pollen reception and the support of pollen tube growth also make maize silk a preferred site of infection by fungal pathogens such as Fusarium graminearum. The cDNA clone zmgrp5 was isolated in a previous study to identify silk tissue-specific genes. ZmGRP5, the encoded protein, was predicted to be a cell wall glycine-rich protein (GRP) and was experimentally characterized in this study. Using polyclonal antiserum, immunoblot analysis confirmed the silk tissue specificity of the protein. Additionally, subcellular fractionation studies confirmed ZmGRP5 localization in the cell wall fraction, and not in any other subcellular fractions. Interaction of ZmGRP5 with the cell wall matrix was observed to be disrupted by the addition of the reducing agent beta-ME. The reversible nature of disulfide bond formation and disruption under different redox conditions suggest that ZmGRP5 could potentially be important in the regulation of cell wall structural properties such as elasticity and rigidity in accordance with environmental and developmental changes. The variable immobilization of ZmGRP5 to the cell wall matrix could also serve as a potential mechanism of activation or inactivation of any non-structural functions. The identification of potential post-translational modifications such as phosphorylation and glycosylation, which are rarely observed in other cell wall GRPs, suggest that the functional significance of these modifications in ZmGRP5 is worthy of further study.
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Books on the topic "Plant and cell physiology"

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K, Waldron, ed. Physiology and biochemistry of plant cell walls. London: Unwin Hyman, 1990.

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Brett, C., and K. Waldron. Physiology and Biochemistry of Plant Cell Walls. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-010-9641-6.

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Cell physiology and genetics of higher plants. Boca Raton, Fla: CRC Press, 1988.

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NATO, Advanced Research Workshop on Signals for Cell Separation in Plants (1988 Turin Italy). Cell separation in plants: Physiology, biochemistry, and molecular biology. Berlin: Springer-Verlag, 1989.

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Kaspar, Anna. How plant and animal cells differ. New York: Britannica Educational Publishing, in association with Rosen Educational Services, 2015.

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Physicochemical & environmental plant physiology. 2nd ed. San Diego: Academic Press, 1999.

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Biophysical control of microfibril orientation in plant cell walls: Aquatic and terrestrial plants including trees. Dordrecht: M. Nijhoff/W. Junk, 1985.

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Penn State Symposium in Plant Physiology (2nd 1987 Pennsylvania State University). Physiology of cell expansion during plant growth: Proceedings of the second annual Penn State Symposium in Plant Physiology (May 21-23, 1987), The Pennsylvania State University. Rockville, Md: American Society of Plant Physiologists, 1987.

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service), ScienceDirect (Online, ed. Physicochemical and environmental plant physiology. 4th ed. Amsterdam: Academic Press, 2009.

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Physicochemical and environmental plant physiology. San Diego: Academic Press, Inc., 1991.

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Book chapters on the topic "Plant and cell physiology"

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Duca, Maria. "Plant Cell Physiology." In Plant Physiology, 13–37. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-17909-4_2.

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Mohr, Hans, and Peter Schopfer. "The Cell as an Energetic System." In Plant Physiology, 39–62. Berlin, Heidelberg: Springer Berlin Heidelberg, 1995. http://dx.doi.org/10.1007/978-3-642-97570-7_4.

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Mohr, Hans, and Peter Schopfer. "The Cell as a Morphological System." In Plant Physiology, 21–37. Berlin, Heidelberg: Springer Berlin Heidelberg, 1995. http://dx.doi.org/10.1007/978-3-642-97570-7_3.

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Mohr, Hans, and Peter Schopfer. "The Cell as a Metabolic System." In Plant Physiology, 63–85. Berlin, Heidelberg: Springer Berlin Heidelberg, 1995. http://dx.doi.org/10.1007/978-3-642-97570-7_5.

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Mohr, Hans, and Peter Schopfer. "The Cell as a Dividing System." In Plant Physiology, 87–92. Berlin, Heidelberg: Springer Berlin Heidelberg, 1995. http://dx.doi.org/10.1007/978-3-642-97570-7_6.

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Mohr, Hans, and Peter Schopfer. "The Cell as a Polar System." In Plant Physiology, 93–97. Berlin, Heidelberg: Springer Berlin Heidelberg, 1995. http://dx.doi.org/10.1007/978-3-642-97570-7_7.

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Mohr, Hans, and Peter Schopfer. "The Cell as a Growing System." In Plant Physiology, 99–109. Berlin, Heidelberg: Springer Berlin Heidelberg, 1995. http://dx.doi.org/10.1007/978-3-642-97570-7_8.

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Mohr, Hans, and Peter Schopfer. "The Cell as an Oscillatory System." In Plant Physiology, 111–20. Berlin, Heidelberg: Springer Berlin Heidelberg, 1995. http://dx.doi.org/10.1007/978-3-642-97570-7_9.

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Mohr, Hans, and Peter Schopfer. "The Cell as a Gene-Physiological System." In Plant Physiology, 121–32. Berlin, Heidelberg: Springer Berlin Heidelberg, 1995. http://dx.doi.org/10.1007/978-3-642-97570-7_10.

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Beilby, Mary J., and Michelle T. Casanova. "The Whole Plant and Cell-to-Cell Transport." In The Physiology of Characean Cells, 165–94. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-40288-3_4.

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Conference papers on the topic "Plant and cell physiology"

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Cosgrove, D. J. "How cell wall structure, mechanics and extensibility relate to the plant cell growth." In IX Congress of society physiologists of plants of Russia "Plant physiology is the basis for creating plants of the future". Kazan University Press, 2019. http://dx.doi.org/10.26907/978-5-00130-204-9-2019-26.

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Mokshina, N. E., O. V. Gorshkov, and T. A. Gorshkova. "Thickening of Plant Cell Walls: Scenarios and Directing." In IX Congress of society physiologists of plants of Russia "Plant physiology is the basis for creating plants of the future". Kazan University Press, 2019. http://dx.doi.org/10.26907/978-5-00130-204-9-2019-21.

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Baranova, E. N. "The effect of edaphic stress factors on plant cell compartments." In IX Congress of society physiologists of plants of Russia "Plant physiology is the basis for creating plants of the future". Kazan University Press, 2019. http://dx.doi.org/10.26907/978-5-00130-204-9-2019-57.

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Kucherova, E. V., A. A. Aleksandrova, and Zh M. Okhlopkova. "Introduction to cell culture Artemísiavulgáris L." In IX Congress of society physiologists of plants of Russia "Plant physiology is the basis for creating plants of the future". Kazan University Press, 2019. http://dx.doi.org/10.26907/978-5-00130-204-9-2019-254.

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Pavlova, M. A., E. N. Terebova, and E. F. Markovskaya. "The accumulation of heavy metals and the properties of the leaf cell wall and the root cell wall of the White Sea plants." In IX Congress of society physiologists of plants of Russia "Plant physiology is the basis for creating plants of the future". Kazan University Press, 2019. http://dx.doi.org/10.26907/978-5-00130-204-9-2019-332.

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Mikshina, P. V., and T. A. Gorshkova. "Tertiary cell wall of plant fibers: physiological and biochemical view of the organization and functioning." In IX Congress of society physiologists of plants of Russia "Plant physiology is the basis for creating plants of the future". Kazan University Press, 2019. http://dx.doi.org/10.26907/978-5-00130-204-9-2019-287.

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Gordeeva, E. P., A. R. Nazipova, P. V. Mikshina, and T. A. Gorshkova. "Ramnogalacturonan I in the tertiary cell walls of fibers of various plants." In IX Congress of society physiologists of plants of Russia "Plant physiology is the basis for creating plants of the future". Kazan University Press, 2019. http://dx.doi.org/10.26907/978-5-00130-204-9-2019-130.

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Deineko, E. V., A. A. Zagorskaya, T. V. Marenkova, N. V. Permyakova, Yu V. Sidorchuk, P. A. Belavin, E. A. Uvarova, et al. "Higher plant cell cultures - a promising platform for the production of recombinant proteins for medical use." In IX Congress of society physiologists of plants of Russia "Plant physiology is the basis for creating plants of the future". Kazan University Press, 2019. http://dx.doi.org/10.26907/978-5-00130-204-9-2019-147.

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Golovatskaya, I. F., M. V. Nechaeva, and E. V. Boiko. "20E-dependent regulation of growth and secondary metabolism of cell culture Lychnis chalcedonica L." In IX Congress of society physiologists of plants of Russia "Plant physiology is the basis for creating plants of the future". Kazan University Press, 2019. http://dx.doi.org/10.26907/978-5-00130-204-9-2019-124.

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Meychik, N. R., Yu I. Nikolaeva, and M. A. Kushunina. "Ion-exchange properties of root cell walls and their significance for some physiological processes." In IX Congress of society physiologists of plants of Russia "Plant physiology is the basis for creating plants of the future". Kazan University Press, 2019. http://dx.doi.org/10.26907/978-5-00130-204-9-2019-285.

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Reports on the topic "Plant and cell physiology"

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HLADEK, K. L. T Plant Cell Investigation. Office of Scientific and Technical Information (OSTI), September 2001. http://dx.doi.org/10.2172/807319.

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Hossein Ghezel-Ayagh. DIRECT FUEL/CELL/TURBINE POWER PLANT. Office of Scientific and Technical Information (OSTI), May 2004. http://dx.doi.org/10.2172/825367.

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Hossein Ghezel-Ayagh. DIRECT FUEL CELL/TURBINE POWER PLANT. Office of Scientific and Technical Information (OSTI), November 2004. http://dx.doi.org/10.2172/835263.

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Hossein Ghezel-Ayagh. DIRECT FUEL CELL/TURBINE POWER PLANT. Office of Scientific and Technical Information (OSTI), May 2003. http://dx.doi.org/10.2172/821186.

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Hossein Ghezel-Ayagh. DIRECT FUEL CELL/TURBINE POWER PLANT. Office of Scientific and Technical Information (OSTI), May 2003. http://dx.doi.org/10.2172/821188.

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Hossein Ghezel-Ayagh. DIRECT FUEL CELL/TURBINE POWER PLANT. Office of Scientific and Technical Information (OSTI), May 2003. http://dx.doi.org/10.2172/821189.

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HLADEK, K. L. T plant cell investigation phase II report. Office of Scientific and Technical Information (OSTI), December 2002. http://dx.doi.org/10.2172/808832.

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Cosgrove, D. J. [Feedback control mechanisms of plant cell expansion]. Office of Scientific and Technical Information (OSTI), January 1992. http://dx.doi.org/10.2172/6846257.

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Keairns, Dale, and Richard Newby. Analysis of Natural Gas Fuel Cell Plant Configurations. Office of Scientific and Technical Information (OSTI), May 2011. http://dx.doi.org/10.2172/1490257.

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Newby, Richard, and Dale Keairns. Analysis of Integrated Gasification Fuel Cell Plant Configurations. Office of Scientific and Technical Information (OSTI), February 2011. http://dx.doi.org/10.2172/1490263.

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