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Journal articles on the topic 'Plant morphogenesis'

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1

Prusinkiewicz, Przemyslaw, and Anne-Gaëlle Rolland-Lagan. "Modeling plant morphogenesis." Current Opinion in Plant Biology 9, no. 1 (2006): 83–88. http://dx.doi.org/10.1016/j.pbi.2005.11.015.

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2

Lloyd, Clive. "Plant Morphogenesis: Life on a different plane." Current Biology 5, no. 10 (1995): 1085–87. http://dx.doi.org/10.1016/s0960-9822(95)00216-8.

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3

Kakkar, R. K., P. K. Nagar, P. S. Ahuja, and V. K. Rai. "Polyamines and Plant Morphogenesis." Biologia plantarum 43, no. 1 (2000): 1–11. http://dx.doi.org/10.1023/a:1026582308902.

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4

Zhuravlev, Yu N., and A. M. Omelko. "Plant morphogenesis in vitro1." Russian Journal of Plant Physiology 55, no. 5 (2008): 579–96. http://dx.doi.org/10.1134/s1021443708050014.

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5

Erland, Lauren A. E., and Praveen K. Saxena. "Melatonin in plant morphogenesis." In Vitro Cellular & Developmental Biology - Plant 54, no. 1 (2018): 3–24. http://dx.doi.org/10.1007/s11627-017-9879-5.

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6

Jackson, David. "Plant morphogenesis: Designing leaves." Current Biology 6, no. 8 (1996): 917–19. http://dx.doi.org/10.1016/s0960-9822(02)00625-5.

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7

Almeida, Marcílio de, Érika Mendes Graner, Gilvano Ebling Brondani, et al. "Plant morphogenesis: theorical bases." Advances in Forestry Science 2, no. 1 (2015): 13–22. https://doi.org/10.34062/afs.v2i1.2363.

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Comprehension of plant morphogenesis is essential for understanding organogenesis and somatic embryogenesis processes, i.e., stages of tissue and organ development of a multicellular organism, which can lead to partial or total plant regeneration. Morphogenesis comprises the integration of growth and differentiation, mediated by cell division and specialization as a result of a complex spatial and temporal hormonal control, which occurs through regulation and expression of multiple gene systems, correlative action of meristems and their derivatives and environmental variations. However, in pla
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8

Israeli, Alon, Yogev Burko, Sharona Shleizer-Burko, et al. "Coordinating the morphogenesis-differentiation balance by tweaking the cytokinin-gibberellin equilibrium." PLOS Genetics 17, no. 4 (2021): e1009537. http://dx.doi.org/10.1371/journal.pgen.1009537.

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Morphogenesis and differentiation are important stages in organ development and shape determination. However, how they are balanced and tuned during development is not fully understood. In the compound leaved tomato, an extended morphogenesis phase allows for the initiation of leaflets, resulting in the compound form. Maintaining a prolonged morphogenetic phase in early stages of compound-leaf development in tomato is dependent on delayed activity of several factors that promote differentiation, including the CIN-TCP transcription factor (TF) LA, the MYB TF CLAU and the plant hormone Gibberell
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9

Kruglova, Natalia, Anna Zinatullina, and Natalia Yegorova. "Histological Approach to the Study of Morphogenesis in Callus Cultures In Vitro: A Review." International Journal of Plant Biology 14, no. 2 (2023): 533–45. http://dx.doi.org/10.3390/ijpb14020042.

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The use of in vitro callus cultures as experimental model systems allows us to get closer to understanding the patterns and features of morphogenesis in intact plants. In this regard, the problem of realizing the morphogenetic potential of callus cells due to their pluri- and totipotency properties is of great interest. To solve this problem, it is important to use the histological approach, which involves studying the structures of developing tissues, organs and organisms in their interactions and relationships. This review article analyzes data devoted to the study of the histological featur
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10

Shi, Zhixin, David Christian, and Hei Leung. "Interactions Between Spore Morphogenetic Mutations Affect Cell Types, Sporulation, and Pathogenesis in Magnaporthe grisea." Molecular Plant-Microbe Interactions® 11, no. 3 (1998): 199–207. http://dx.doi.org/10.1094/mpmi.1998.11.3.199.

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We have previously defined four single-gene mutations, con1, con2, con4, and con7, that control various stages of spore morphogenesis in the rice blast fungus. To delineate the developmental pathway of spore morphogenesis, we investigated the interactions among these morphogenetic genes by generating strains with double mutations via transformation-mediated gene disruption. Plasmids containing portions of the inactivated CON4 and CON7 genes were introduced into strains harboring single mutation to produce double mutants. Interaction between con1 and con4 resulted in reduced vegetative growth a
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11

Alsufyani, Taghreed, Gianmaria Califano, Michael Deicke, et al. "Macroalgal–bacterial interactions: identification and role of thallusin in morphogenesis of the seaweed Ulva (Chlorophyta)." Journal of Experimental Botany 71, no. 11 (2020): 3340–49. http://dx.doi.org/10.1093/jxb/eraa066.

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Abstract Macroalgal microbiomes have core functions related to biofilm formation, growth, and morphogenesis of seaweeds. In particular, the growth and development of the sea lettuce Ulva spp. (Chlorophyta) depend on bacteria releasing morphogenetic compounds. Under axenic conditions, the macroalga Ulva mutabilis develops a callus-like phenotype with cell wall protrusions. However, co-culturing with Roseovarius sp. (MS2) and Maribacter sp. (MS6), which produce various stimulatory chemical mediators, completely recovers morphogenesis. This ecological reconstruction forms a tripartite community w
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12

Lazareva, G. G., V. V. Mironova, N. A. Omelyanchuk, et al. "Mathematical modeling of plant morphogenesis." Numerical Analysis and Applications 1, no. 2 (2008): 123–34. http://dx.doi.org/10.1134/s1995423908020043.

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13

Roberts, Keith. "Plant morphogenesis: Oligosaccharide floral messages?" Nature 314, no. 6012 (1985): 581. http://dx.doi.org/10.1038/314581a0.

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14

Ramage, Carl M., and Richard R. Williams. "Mineral nutrition and plant morphogenesis." In Vitro Cellular & Developmental Biology - Plant 38, no. 2 (2002): 116–24. http://dx.doi.org/10.1079/ivp2001269.

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15

Langdale, Jane A. "Plant Morphogenesis: More knots untied." Current Biology 4, no. 6 (1994): 529–31. http://dx.doi.org/10.1016/s0960-9822(00)00115-9.

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16

Millet, B. "Temporal Markers in Plant Morphogenesis." Biological Rhythm Research 30, no. 3 (1999): 249–58. http://dx.doi.org/10.1076/brhm.30.3.249.3054.

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17

Pałubicki, Wojtek, Andrzej Kokosza, and Agata Burian. "Formal description of plant morphogenesis." Journal of Experimental Botany 70, no. 14 (2019): 3601–13. http://dx.doi.org/10.1093/jxb/erz210.

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Abstract Plant morphogenesis may be characterized by complex feedback mechanisms between signals specifying growth and by the growth of the plant body itself. Comprehension of such feedback mechanisms is an ongoing research task and can be aided with formal descriptions of morphogenesis. In this review, we present a number of established mathematical paradigms that are useful to the formal representation of plant shape, and of biomechanical and biochemical signaling. Specifically, we discuss work from a range of research areas including plant biology, material sciences, fluid dynamics, and com
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18

Hake, Sarah, and Naomi Ori. "Plant morphogenesis and KNOX genes." Nature Genetics 31, no. 2 (2002): 121–22. http://dx.doi.org/10.1038/ng0602-121.

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19

Zhao, Feng, Wenqian Chen, and Jan Traas. "Mechanical signaling in plant morphogenesis." Current Opinion in Genetics & Development 51 (August 2018): 26–30. http://dx.doi.org/10.1016/j.gde.2018.04.001.

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20

Cosgrove, Daniel J., and Enrico Coen. "Plant morphogenesis: What drives growth?" Current Biology 35, no. 8 (2025): R283—R285. https://doi.org/10.1016/j.cub.2025.02.049.

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21

Cousson, A., P. Toubart, and K. Tran Thanh Van. "Control of morphogenetic pathways in thin cell layers of tobacco by pH." Canadian Journal of Botany 67, no. 3 (1989): 650–54. http://dx.doi.org/10.1139/b89-087.

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Thin cell layer explants of tobacco were floated in vitro on the surface of liquid culture media. The initial exogenous concentrations of indolyl-3-butyric acid, and kinetin, the initial medium pH, and the explant density were varied. Various patterns of de novo and direct differentiation without any intermediate callus (flower, vegetative bud, root) as well as the absence of morphogenesis and callus formation without any subsequent organogenesis were separately controlled on 100% of the explants. On the same exogenous combination of glucose, indolyl-3-butyric acid, and kinetin, changes in ini
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22

Skaptsov, M. V., M. A. Krasnoborodkina, M. G. Kutsev, S. V. Smirnov, A. I. Shmakov та A. V. Matsyura. "УРОВНИ ПЛОИДНОСТИ И ОТНОСИТЕЛЬНОГО СОДЕРЖАНИЯ ДНК В КУЛЬТУРЕ КЛЕТОК И ТКАНЕЙ РАСТЕНИЙ IN VITRO". Biological Bulletin of Bogdan Chmelnitskiy Melitopol State Pedagogical University 6, № 3 (2016): 33–38. http://dx.doi.org/10.15421/201667.

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<p>We presented results of variations in the ploidy level and the genome size of the <em>R. acetosa</em> regenerants. These regenerants was obtained by indirect and direct morphogenesis in in vitro culture. Explants were prepared from seedlings on the three-leaf stage of plant development. More than 100 explants were used to stimulate the indirect and direct morphogenesis. Mesophilic explants were cultured on the MS nutrient medium containing auxin to callus proliferation (2 mg/L NAA, 1 mg/L BA). Cultivation of the callus was maintained for 4 weeks followed by an indirect mor
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23

Zubairova, U. S., and A. V. Doroshkov. "Wheat leaf epidermal pattern as a model for studying the influence of stress conditions on morphogenesis." Vavilov Journal of Genetics and Breeding 19, no. 6 (2015): 1–8. http://dx.doi.org/10.18699/10.18699/vj18.32-o.

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The leaf epidermis of a monocotyledonous plant is a widely used model system for studying the differentiation of plant cells, as it contains readily observable specialized cells. The approach proposed in this paper uses a growing cereal leaf to study stress-induced dynamic changes in morphogenesis. In the process of formation, the linear leaf of wheat remains in the stationary growth phase for long. This fact permits us to observe a series of successive morphogenetic events recorded in the cellular structure of the mature leaf. In studying the cellular architecture of the wheat leaf epidermis,
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24

Zubairova, U. S., and A. V. Doroshkov. "Wheat leaf epidermal pattern as a model for studying the influence of stress conditions on morphogenesis." Vavilov Journal of Genetics and Breeding 22, no. 7 (2018): 837–44. http://dx.doi.org/10.18699/vj18.32-o.

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The leaf epidermis of a monocotyledonous plant is a widely used model system for studying the differentiation of plant cells, as it contains readily observable specialized cells. The approach proposed in this paper uses a growing cereal leaf to study stress-induced dynamic changes in morphogenesis. In the process of formation, the linear leaf of wheat remains in the stationary growth phase for long. This fact permits us to observe a series of successive morphogenetic events recorded in the cellular structure of the mature leaf. In studying the cellular architecture of the wheat leaf epidermis,
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25

Dubrovna, O. V., S. I. Mykhalska, and A. H. Komisarenko. "Genetic control of plant morphogenesis in in vitro culture." Visnik ukrains'kogo tovaristva genetikiv i selekcioneriv 22, no. 1-2 (2025): 37–55. https://doi.org/10.7124/visnyk.utgis.22.1-2.1688.

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Plant morphogenesis is the result of complex interactions of genetic, epigenetic and hormonal factors that determine the development of cells and tissues in in vitro culture. In recent decades, basic research has greatly advanced the understanding of the genetic mechanisms that control key processes of morphogenesis, such as callusogenesis, somatic embryogenesis, and de novo organogenesis. It was found that certain structural and regulatory genes play a crucial role in reprogramming cells to a totipotent state, where they are able to form various morphological structures. Hormones, such as aux
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26

Kulchin, Yuriy Nikolaevich, Olga Valerievna Nakonechnaya, Irina Victorovna Gafitskaya, et al. "Plant Morphogenesis under Different Light Intensity." Defect and Diffusion Forum 386 (September 2018): 201–6. http://dx.doi.org/10.4028/www.scientific.net/ddf.386.201.

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The innovative LED light source (Sun Box) with irradiation spectrum close to the sun spectrum in the wavelength range 440-660 nm was used in experiment for study the influence of light intensity (75, 135, 230 and 382 μmol/s*m2) on the growth and development of plants. Standard fluorescent lighting was used as a control. The experiments were carried out on plantlets ofStevia rebaudianaandSolanum tuberosum, cvs. Snegir, Rozhdestvenskiy and Kamchatskii)in vitro. The illumination intensity of 75 and 230 μmol/s*m2promoted development ofS. rebaudianaplantlets with optimal values of morphometric para
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27

Oliveri, Hadrien, and Ibrahim Cheddadi. "Hydromechanical field theory of plant morphogenesis." Journal of the Mechanics and Physics of Solids 196 (March 2025): 106035. https://doi.org/10.1016/j.jmps.2025.106035.

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28

Lamport, Derek, Li Tan, Michael Held, and Marcia Kieliszewski. "The Role of the Primary Cell Wall in Plant Morphogenesis." International Journal of Molecular Sciences 19, no. 9 (2018): 2674. http://dx.doi.org/10.3390/ijms19092674.

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Morphogenesis remains a riddle, wrapped in a mystery, inside an enigma. It remains a formidable problem viewed from many different perspectives of morphology, genetics, and computational modelling. We propose a biochemical reductionist approach that shows how both internal and external physical forces contribute to plant morphogenesis via mechanical stress–strain transduction from the primary cell wall tethered to the plasma membrane by a specific arabinogalactan protein (AGP). The resulting stress vector, with direction defined by Hechtian adhesion sites, has a magnitude of a few piconewtons
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29

Hable, Whitney E., Sherryl R. Bisgrove, and Darryl L. Kropf. "To Shape a Plant: The Cytoskeleton in Plant Morphogenesis." Plant Cell 10, no. 11 (1998): 1772. http://dx.doi.org/10.2307/3870901.

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30

Hable, Whitney E., Sherryl R. Bisgrove, and Darryl L. Kropf. "To Shape a Plant—The Cytoskeleton in Plant Morphogenesis." Plant Cell 10, no. 11 (1998): 1772–74. http://dx.doi.org/10.1105/tpc.10.11.1772.

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31

Schwab, Birgit, Ulrike Folkers, Hilmar Ilgenfritz, and Martin Hülskamp. "Trichome morphogenesis in Arabidopsis." Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences 355, no. 1399 (2000): 879–83. http://dx.doi.org/10.1098/rstb.2000.0623.

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Trichomes (plant hairs) in Arabidopsis thaliana are large non–secreting epidermal cells with a characteristic three–dimensional architecture. Because trichomes are easily accessible to a combination of genetic, cell biological and molecular methods they have become an ideal model system to study various aspects of plant cell morphogenesis. In this review we will summarize recent progress in the understanding of trichome morphogenesis.
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32

Lacalli, Thurston C., and Lionel G. Harrison. "Turing's model and branching tip growth: relation of time and spatial scales in morphogenesis, with application to Micrasterias." Canadian Journal of Botany 65, no. 7 (1987): 1308–19. http://dx.doi.org/10.1139/b87-184.

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Morphogenesis following cell division in Micrasterias rotata is by outgrowth and repeated branching of a series of semicell lobes. Though successive branching events are qualitatively similar, they display changes in time and space scales, and these can be quantitated with the aid of autoradiographic patterns of labelled wall precursors that appear late in morphogenesis but which seem to represent its history. This enables us to consider branching as the conversion of a single centre of growth activity into two and to attempt to locate these centres precisely, in terms of both position and tim
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33

Holloway, David M. "The role of chemical dynamics in plant morphogenesis1." Biochemical Society Transactions 38, no. 2 (2010): 645–50. http://dx.doi.org/10.1042/bst0380645.

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In biological development, the generation of shape is preceded by the spatial localization of growth factors. Localization, and how it is maintained or changed during the process of growth, determines the shapes produced. Mathematical models have been developed to investigate the chemical, mechanical and transport properties involved in plant morphogenesis. These synthesize biochemical and biophysical data, revealing underlying principles, especially the importance of dynamics in generating form. Chemical kinetics has been used to understand the constraints on reaction and transport rates to p
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34

Owens, Lowell D., Jerry D. Cohen, and Ralph Seelke. "Gene Introduction to Induce Morphogenesis." HortScience 23, no. 3 (1988): 520. http://dx.doi.org/10.21273/hortsci.23.3.520c.

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Abstract In recent years, we have seen the development of many plant cell and tissue culture techniques that, individually or together with recombinant DNA techniques, are being used to modify crops in novel ways. Although these plant biotechnologies may employ a variety of strategies to achieve a particular crop improvement goal, there is one critical element that they all share, the necessity of regenerating a whole plant from a cultured cell, tissue, or organ. Progress has been made in this area with many plant species. For example, reports that were presented at the VI Congress of the Inte
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35

Bai, Shu-Nong. "On the Plant Developmental Unit: From Virtual Concept to Visual Plantlet." Plants 14, no. 3 (2025): 396. https://doi.org/10.3390/plants14030396.

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This study introduces the concept of the plant developmental unit (PDU) and validates its application using Wolffia Horkel ex Schleid (Araceae) as a model system for exploring fundamental processes in plant morphogenesis. Revisiting long-standing contradictions in plant biology, the author proposes viewing plants as coral-like colonies composed of multiple developmental units rather than as unitary-animal-like organisms. Utilizing the “Plant-on-Chip” culture platform, the research demonstrates Wolffia’s minimalist structure as a powerful model for investigating core regulatory mechanisms of pl
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36

Yang, Yanqiu, Weihong Huang, Endian Wu, Chentao Lin, Binqing Chen, and Deshu Lin. "Cortical Microtubule Organization during Petal Morphogenesis in Arabidopsis." International Journal of Molecular Sciences 20, no. 19 (2019): 4913. http://dx.doi.org/10.3390/ijms20194913.

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Cortical microtubules guide the direction and deposition of cellulose microfibrils to build the cell wall, which in turn influences cell expansion and plant morphogenesis. In the model plant Arabidopsis thaliana (Arabidopsis), petal is a relatively simple organ that contains distinct epidermal cells, such as specialized conical cells in the adaxial epidermis and relatively flat cells with several lobes in the abaxial epidermis. In the past two decades, the Arabidopsis petal has become a model experimental system for studying cell expansion and organ morphogenesis, because petals are dispensabl
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37

Thien, Nguyen Phuc. "Fundamentals and Applications of Red Light-Emitting Diodes (LEDs) In Vitro Plant Growth on Tomato Lycopersicon esculentum Mill." Key Engineering Materials 805 (June 2019): 141–45. http://dx.doi.org/10.4028/www.scientific.net/kem.805.141.

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The aim of these studies was mainly to investigate the effects of monochromatic LEDs applied singly on the in vitro plant growth and morphogenesis. Various morphological and physiological parameters are considered that influence the growth and development of plants in vitro under red LED light as compared to those under normal light. Upon exposure to LED, in vitro-raised plants have shown significant improvements in growth and morphogenesis. In particular, red and blue lights, either alone or in combination, have a significant influence on plant growth. The present study gives an overview of t
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38

Bartholomew-Began, Sharon, and Roger V. Jean. "Phyllotaxis. A Systemic Study in Plant Morphogenesis." Bryologist 100, no. 3 (1997): 417. http://dx.doi.org/10.2307/3244517.

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39

SHIMIZU, Hiroshi, Zhiyu MA, Vui KIONG CHONG, Takahisa NISHIZU, and Naoshi KONDO. "Machine Vision System for Plant Morphogenesis Analysis." Environment Control in Biology 46, no. 4 (2008): 221–31. http://dx.doi.org/10.2525/ecb.46.221.

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40

Lee, Cheol ho. "Computer Modelling for Plant Morphogenesis Pattern Analysis." Korean Society of Science & Art 37, no. 4 (2019): 285–96. http://dx.doi.org/10.17548/ksaf.2019.09.30.285.

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41

Kilmister, C. W., and R. V. Jean. "Phyllotaxis: A Systemic Study in Plant Morphogenesis." Mathematical Gazette 79, no. 484 (1995): 248. http://dx.doi.org/10.2307/3620133.

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42

Yoshida, Saiko, Sören Strauss, and Milad Adibi. "Multidisciplinary bioimaging approach to study plant morphogenesis." PLANT MORPHOLOGY 33, no. 1 (2021): 15–23. http://dx.doi.org/10.5685/plmorphol.33.15.

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43

Moe, R., L. M. Mortensen, and S. O. Grimstad. "CONTROL OF PLANT MORPHOGENESIS WITHOUT GROWTH RETARDANTS." Acta Horticulturae, no. 319 (October 1992): 323–28. http://dx.doi.org/10.17660/actahortic.1992.319.50.

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44

Batygina, T. B., and I. V. Rudskii. "Role of stem cells in plant morphogenesis." Doklady Biological Sciences 410, no. 1 (2006): 400–402. http://dx.doi.org/10.1134/s0012496606050164.

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45

Duckett, Jeffrey G. "Plant biology: Mapping meristem morphogenesis in Marchantia." Current Biology 34, no. 19 (2024): R909—R910. http://dx.doi.org/10.1016/j.cub.2024.08.051.

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46

Sampathkumar, Arun, An Yan, Pawel Krupinski, and Elliot M. Meyerowitz. "Physical Forces Regulate Plant Development and Morphogenesis." Current Biology 24, no. 10 (2014): R475—R483. http://dx.doi.org/10.1016/j.cub.2014.03.014.

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47

Palin, Robert, and Anja Geitmann. "The role of pectin in plant morphogenesis." Biosystems 109, no. 3 (2012): 397–402. http://dx.doi.org/10.1016/j.biosystems.2012.04.006.

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48

Lubkin, Sharon. "Phyllotaxis: A systemic study in plant morphogenesis." Bulletin of Mathematical Biology 57, no. 2 (1995): 377–79. http://dx.doi.org/10.1007/bf02460623.

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49

LUBKIN, S. "Phyllotaxis: A Systemic Study in Plant Morphogenesis." Bulletin of Mathematical Biology 57, no. 2 (1995): 377–79. http://dx.doi.org/10.1016/s0092-8240(95)80011-5.

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50

Levengood, W. C. "Redox-responsive electrodes applied during plant morphogenesis." Bioelectrochemistry and Bioenergetics 19, no. 3 (1988): 461–76. http://dx.doi.org/10.1016/0302-4598(88)80025-4.

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