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Relevant bibliographies by topics / Tissue culture in plants

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Academic literature on the topic 'Tissue culture in plants'

Author: Grafiati

Published: 4 June 2021

Last updated: 10 February 2022

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Journal articles on the topic "Tissue culture in plants"

1

Niazian, M., S. A. Sadat Noori, P. Galuszka, and S. M. M. Mortazavian. "Tissue culture-based Agrobacterium-mediated and in planta transformation methods." Czech Journal of Genetics and Plant Breeding 53, No. 4 (November 10, 2017): 133–43. http://dx.doi.org/10.17221/177/2016-cjgpb.

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Gene transformation can be done in direct and indirect (Agrobacterium-mediated) ways. The most efficient method of gene transformation to date is Agrobacterium-mediated method. The main problem of Agrobacterium-method is that some plant species and mutant lines are recalcitrant to regeneration. Requirements for sterile conditions for plant regeneration are another problem of Agrobacterium-mediated transformation. Development of genotype-independent gene transformation method is of great interest in many plants. Some tissue culture-independent Agrobacterium-mediated gene transformation methods are reported in individual plants and crops. Generally, these methods are called in planta gene transformation. In planta transformation methods are free from somaclonal variation and easier, quicker, and simpler than tissue culture-based transformation methods. Vacuum infiltration, injection of Agrobacterium culture to plant tissues, pollen-tube pathway, floral dip and floral spray are the main methods of in planta transformation. Each of these methods has its own advantages and disadvantages. Simplicity and reliability are the primary reasons for the popularity of the in planta methods. These methods are much quicker than regular tissue culture-based Agrobacterium-mediated gene transformation and success can be achieved by non-experts. In the present review, we highlight all methods of in planta transformation comparing them with regular tissue culture-based Agrobacterium-mediated transformation methods and then recently successful transformations using these methods are presented.

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van der Linde, P. C. G. "CERTIFIED PLANTS FROM TISSUE CULTURE." Acta Horticulturae, no. 530 (September 2000): 93–102. http://dx.doi.org/10.17660/actahortic.2000.530.9.

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Lee, Michael, and R. L. Phillips. "Genomic rearrangements in maize induced by tissue culture." Genome 29, no. 1 (February 1, 1987): 122–28. http://dx.doi.org/10.1139/g87-021.

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Chromosomal instability is a common occurrence in plant tissue cultures and has been documented in plants regenerated from several genotypes of maize (Zea mays L.) tissue cultures. The objective of this research was to evaluate the frequency and types of chromosomal aberrations in regenerated plants of an Oh43–A188 genetic background, which had not been examined previously for chromosome stability in culture. Organogenic callus cultures were intitated from immature embryos of F2 plants for several Oh43 ms isoline × A188 crosses. The chromosome constitution of 267 plants was investigated through meiotic analysis of plants regenerated either 3 to 4 or 8 to 9 months after culture initiation. No abnormalities were detected in 78 plants regenerated during the first period. During the second period, however, 91 of the 189 plants were cytologically abnormal. One hundred and eight aberrations were detected and most (96%) involved changes in chromosome structure such as interchanges (42%), deficiencies (35%), and heteromorphic pairs (19%). All deficiencies were intercalary. Also, most (51%) interchanges involved chromosome 6. An association between male-sterility factors and chromosome instability was not observed. Breakpoints were primarily on chromosome arms containing large blocks of heterochromatin such as knobs. Several abnormal plants from the same culture appeared to contain identical aberrations indicating the aberrations may trace to a single event. A hypothesis for the involvement of heterochromatin in chromosome breakage during in vitro culture is supported. Key words: Zea mays L., tissue culture, somaclonal variation, chromosome breakage, heterochromatin.

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Seabrook, Janet E. A., and Gerald Farrell. "City Water Can Contaminate Tissue Culture Stock Plants." HortScience 28, no. 6 (June 1993): 628–29. http://dx.doi.org/10.21273/hortsci.28.6.628.

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Stock plants of `Shepody' and `Yukon Gold' potato (Solarium tuberosum L.) were grown in a greenhouse and irrigated with city water. Contamination rate of stem explant tissue cultures excised from these stock plants was 50% to 100%. A comparison of the microorganisms isolated from the contaminated cultures and from 0.22-μm filter disks through which 20 liters of city water had passed revealed the presence of similar bacterial floras. Five genera of bacteria (Listerium spp., Corynebacterium spp., Enterobacter spp., Pasteurella spp., and Actinobacillus spp.) were isolated from contaminated cultures and cultured filter disks. Watering greenhouse-grown stock plants with filtered city water decreased contamination of stem explant cultures 30% to 50%. Installing an ultraviolet light water-sterilizing unit at the greenhouse inlet point effectively reduced contamination.

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Johnson, K. "TISSUE CULTURE OF AUSTRALIAN PLANTS - A REVIEW." Acta Horticulturae, no. 447 (October 1997): 515–28. http://dx.doi.org/10.17660/actahortic.1997.447.102.

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Kunakh, V. A., D. O. Navrotska, M. O. Twardovska, and I. O. Andreev. "Peculiarities of chromosomal variability in cultured tissues of Deschampsia antarctica Desv. plants with different chromosome numbers." Visnik ukrains'kogo tovaristva genetikiv i selekcioneriv 14, no. 1 (June 20, 2016): 36–43. http://dx.doi.org/10.7124/visnyk.utgis.14.1.542.

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Aim. To clarify the details of chromosome variation in calli derived from D. antarctica plants in the initial passages of the culture in vitro. Methods. Induction of callus from root explants of plants, which were grown from seeds, and consequent subcultivation of tissue culture. Cytogenetic analysis of squashed slides stained by acetic-orcein and counting the number of chromosomes in mitotic metaphase plates. Results. There were analyzed the cultured tissues derived from D. antarctica plants with different chromosome numbers: diploid plants (2n=26), mixoploid plant with B-chromosomes (2n=26+1-3B), and mixoploid plant with near-triploid modal class (2n=36, 38). Analysis of callus tissues of all plants at 2-4 passages revealed mixoploidy, presence of polyploid and aneuploid cells. The modal class in all studied calli was composed of diploid and aneuploid cells with near-diploid chromosome number. The cytogenetic structure of cell population of cultured tissues was found to vary with characteristics of the karyotype of donor plant. The largest range of variation in the number of chromosomes (from 18 to 63 chromosomes) was found in tissue culture of diploid plant (2n=26) from the Galindez Island, and the highest frequencies of polyploid (47 %) and aneuploid cells were in the culture of mixoploid plant with near-triploid modal class from the Big Yalour Island. Conclusions. In different D. antarctica cultured tissues at the early stages of the culture, the modal class was composed of diploid cells and cells with near-diploid chromosome number irrespective of karyotype of donor plant (diploid, mixoploid poliploid).Key words: Deschampsia antarctica Desv., plant tissue culture, chromosomal variability in vitro, mixoploidy.

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Twardovska, M. O. "THE CONTENT OF PHENOLIC COMPOUNDS AND FLAVONOIDS IN Deschampsia antarctica TISSUE CULTURE." Biotechnologia Acta 14, no. 2 (February 2021): 59–66. http://dx.doi.org/10.15407/biotech14.02.059.

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Aim. The aim of the study was to determine the quantitative and qualitative content of phenolic compounds and flavonoids in Deschampsia antarctica E. Desv. tissue cultures obtained from plants originating from different islands of the maritime Antarctic. Methods. In vitro tissue culture, Folin-Ciocalteu method, spectrophotometry, HPLC analysis. Results. The quantitative content of phenolic compounds and flavonoids in D. antarctica tissue cultures obtained from plants of six genotypes (DAR12, DAR13, G/D12-2a, Y66, R30 and L57) was determined. The highest content of phenolic compounds (4.46 and 3.75 mg/g) was found in tissue cultures obtained from root and leaf explants of plant genotype L57. The highest amount of flavonoids (7.17 mg/g) was accumulated in G/D12-2a tissue culture of root origin. The content of the studied biologically active compounds (BACs) did not change with increasing number of subculture generations (from passage 10 to 19). HPLC analysis showed that in D. antarctica tissue cultures, a shift in the biosynthesis of BACs occurred towards the synthesis of more polar metabolites compared to explant donor plants. Conclusions. It was found that the transition of cells to undifferentiated growth affected the content of BACs, the amount of which decreased 2–5 times simultaneously with a significant change in their profile. This provided a basis for further biochemical studies, as well as for careful selection of tissue culture of D. antarctica to use it as a potential source of BACs.

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Ruan, Yiqin, and Mark H. Brand. "In Vitro Responses of Tissues from Rhododendron Plants With and Without Tissue Proliferation." HortScience 30, no. 4 (July 1995): 873D—873. http://dx.doi.org/10.21273/hortsci.30.4.873d.

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Rhododendron `Montego' shoot cultures initiated from plants with and without tissue proliferation (TP and NTP) served as explant sources for all studies (Note: in vitro TP shoot cultures produce primarily dwarf shoots, some long shoots, and stem tumors). Calli induced from TP leaves and tumors and NTP leaves were cultured on woody plant (WP) medium containing NAA and 2-iP. During the first 4 weeks of culture, calli from NTP leaves had higher relative growth rates than calli from TP leaves or tumors. However, calli from TP leaves and tumors grew faster than calli from NTP leaves for all subculture periods that followed. Shoot tips (5 mm) were excised from TP dwarf shoots, TP long shoots, and NTP shoots and were cultured on WP medium with or without 15 μM 2-iP. Shoot tips from TP dwarf and long shoots multiplied on medium without 2-iP, averaging 18.4 and 1.7 shoots per shoot tip in 12 weeks, respectively. Shoot tips from NTP shoots only multiplied when maintained on 2-iP-containing medium. When placed on 2-iP-containing medium, both types of TP shoot tips produced clusters of callus-like nodules that gave rise to highly tumorized, short shoots or leafy meristems.

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panigrahi, Sunitha, Dr k. Aruna Lakshmi, and Nida Mir. "Micro Propagation and Plant Strengthening of Tissue Cultured Plants, Inoculated with Several Bacterial Strains." International Journal of Scientific Research 2, no. 8 (June 1, 2012): 15–17. http://dx.doi.org/10.15373/22778179/aug2013/7.

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Baillie, A. M. R., K. K. Kartha, and B. G. Rossnagel. "Evaluation of 10 Canadian barley (Hordeum vulgare L.) cultivars for tissue culture response." Canadian Journal of Plant Science 73, no. 1 (January 1, 1993): 171–74. http://dx.doi.org/10.4141/cjps93-023.

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Ten Canadian barley cultivars — Abee, Deuce, Ellice, Harrington, Manley, Bonanza, Conquest, Duke, Heartland, and Samson — were evaluated for tissue-culture response. Callus was obtained from embryos 3–5 d post anthesis from all cultivars. Fertile plants were regenerated from eight. Abee cultures gave the best response in terms of the number of plants regenerated, while Bonanza and Samson cultures produced no regenerated plants. Heartland and Deuce were selected for further study to determine optimum growth-regulator concentrations for callus production and plant regeneration. Two growth regulators — 2,4-dichlorophenoxyacetic acid (2,4-D) and 2,4,5-trichlorophenoxyacetic acid (2,4,5-T) — were evaluated at five concentrations (0.5, 1.0, 2.5, 5.0 and 10 mg L−1). Maximum regeneration rates were achieved with Gamborg’s B5 medium supplemented with 2.5 mg L−1 2,4-D. Thirty-four Heartland and 19 Deuce regenerants were produced per 100 embryos cultured. Key words: Barley, growth regulators, Hordeum vulgare, regeneration, tissue culture

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Dissertations / Theses on the topic "Tissue culture in plants"

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Cubbin, Ian James. "Tissue culture studies in selected medicinal plants." Thesis, University of Sunderland, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.320538.

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Yamagishi, Masumi. "Genetic evaluation of cell and tissue culture-derived rice plants." Kyoto University, 1997. http://hdl.handle.net/2433/202414.

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Marlow, Susan A. "Acclimatization physiology in tissue cultured plants." Thesis, Oxford Brookes University, 1990. https://radar.brookes.ac.uk/radar/items/a1e3ad31-39e0-4cd1-b236-7ae638edcdf7/1/.

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Physiological and morphological aspects of acclimatization were studied in cultured tomato (Lycopersicon esculentum Mill.), banana (Musa accuminata L.) and date palm (Phoenix dactyli/era ). The nutrient availability from agar solidified culture medium was determined to establish the nutrient status of the cultured plandets before transfer to ex vitro conditions. Analysis of the plant tissues demonstrated decreasing tissue concentrations of the major elements nitrogen, phosphorus and potassium with decreasing concentration of basal salts in the medium. The effects of agar and increasing sodium concentration in the culture medium was studied in cultured banana plants. Plandets grown on agar solidified medium with increased levels of sodium, exhibited reduced growth and stomatal movement. The use of agar as a solidifying agent was shown to reduce root growth, development and stomatal functioning in these plants. The efficiency of ion and water uptake, and translocation in in vitro and acclimatized tomato plants was assessed using [32P]-orthophosphate and [3H]_ tritiated water. The functional capacity of the root system fOlmed in vitro was established, and assessed following acclimatization treatments at 40% and 80% relative humidity. Comparative studies with tomato seedlings demonstrated reduced efficiency of ion translocation to the shoot in plandets growing in vitro. However, transport to the shoot improved during acclimatization. Ion absorption studies on in vitro and acclimatized palm plants demonstrated phosphate uptake and translocation in both plant types. A detailed examination of the tissue structure through the root/shoot junction and roots of · cultured, acclimatized and seedling tomato plants illustrated differences in the vascular development between the three plant types. However, no major abnormalities were observed which could have accounted for the reduced translocation efficiency in the cultured plants. Increased vascularization present in the root/shoot junction of the cultured plants may increase resistance to the transpiration flow through the region. The type of root system produced in vitro and the root/shoot ratio was manipulated using varying IAA and sucrose treatments. Improved root development and plantlet survival rates were achieved by reduced exposure to IAA during the root initiation phase followed by root elongation on IAA free medium supplemented with sucrose. Acclimatization at low relative humidity (40%) was achieved by producing plandets with balanced root/shoot ratios and a well developed root system.

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Shih, Sharon Min-Hsuan Biotechnology &amp Biomolecular Sciences Faculty of Science UNSW. "Transient viral infection of plant tissue culture and plants for production of virus and foreign protein." Awarded by:University of New South Wales, 2007. http://handle.unsw.edu.au/1959.4/34967.

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This work was aimed to investigate the basic viral infection protocols mainly focusing on Nicotiana benthamiana hairy root cultures and wild-type tobacco mosaic virus (TMV). The application of transgenic virus containing the gene for green fluorescent protein (GFP) for foreign protein production in plant tissue cultures and whole plants was also studied. The effect on viral accumulation of the form of plant tissue culture used, such as hairy roots, shooty teratomas and suspended cells, was investigated. Viral infection was shown to have no effect on culture growth and morphology. Hairy root cultures are a superior host for viral propagation and production in vitro. The maximum specific rate of viral accumulation occurred mainly during the root growth phase. The average maximum virus concentration in the hairy roots was 0.82 ?? 0.14 mg g-1 dry weight and virus protein represented a maximum of approximately 6% of total soluble protein in the root biomass. Proportional scale-up of TMVinfected hairy roots in shake flasks and bioreactors can be achieved without changing the average virus concentration accumulated in the hairy roots. The level of viral accumulation was much lower in N. benthamiana hairy roots infected with transgenic virus containing GFP (TMVGFPC3) compared with TMV and low levels or no GFP was detected. Viral accumulation and GFP production in whole plants was studied using different generations of transgenic TMV-GFPC3 virus. Hybrid viruses with the foreign gene GFPC3 deleted may have been formed in successive TMV-GFPC3 generations, resulting in the loss of GFP production and enhanced viral infectivity. In vitro generated RNA transcript and first generation TMV-GFPC3 were found to be more suitable for infection than the second generation TMV-GFPC3. However, the accumulation of GFP and virus concentration did not occur at the same ratio. Provided a more genetically stable transgenic viral vector is used for infection, transient viral infection of hairy roots can be a potential alternative system for foreign protein production than plants grown in the field as the containment or safety issues can be addressed.

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Slomka, Marek Jozef. "Studies of tomato golden mosaic virus in plants, protoplasts and tissue culture." Thesis, Imperial College London, 1987. http://hdl.handle.net/10044/1/46616.

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Ubaid, R. H. "Plant tissue culture and prostaglandin production from a range of Allium species." Thesis, University of Salford, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.381734.

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Sheibani, Ahmad. "Tissue culture studies of Pistacia." Thesis, University of Salford, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.238801.

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Gazis, Fotis. "Forsythia X intermedia cv. spectabilis (Zab.) in vitro propagation and raspberry ringspot virus elimination." Thesis, University of Bath, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.334617.

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Gribble, Karleen Dawn. "Towards an understanding of the physiological abnormality of tissue cultured plants known as vitrification /." [Richmond, N.S.W.] : Horticulture, University of Western Sydney, Hawkesbury, 1999. http://library.uws.edu.au/adt-NUWS/public/adt-NUWS20030513.144109/index.html.

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Thesis (Ph.D.) -- University of Western Sydney, Hawkesbury, 1999.
Thesis submitted for the degree of Doctor of Philosophy. Spine title: Towards an understanding of vitrification in tissue cultured plants. Includes bibliographical references (leaves 175-203).

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Al-Ani, Nabeel K. "Some epigenetic effects in plant tissue culture." Thesis, Aberystwyth University, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.659362.

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Books on the topic "Tissue culture in plants"

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Gilbert, Henry. Tissue culture: Plants : January 1991 - April 1993. Beltsville, Md: National Agriculture Library, 1993.

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Gilbert, Henry. Tissue culture: Plants : January 1991 - April 1993. Beltsville, Md: National Agriculture Library, 1993.

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Gilbert, Henry. Tissue culture: Plants : January 1988 - December 1990. Beltsville, Md: National Agriculture Library, 1991.

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Gilbert, Henry. Tissue culture: Plants 1984-1987 : 262 citations. Beltsville, Md: U.S. Dept. of Agriculture, National Agriculture Library, 1988.

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Gilbert, Henry. Tissue culture: Plants : January 1991 - April 1993. Beltsville, Md: National Agriculture Library, 1993.

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Gilbert, Henry. Tissue culture: Plants, January 1992 - March 1994. Beltsville, Md: National Agricultural Library, 1994.

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Gilbert, Henry. Tissue culture: Plants : January 1991 - April 1993. Beltsville, Md: National Agriculture Library, 1993.

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Laimer, Margit, and Waltraud Rücker, eds. Plant Tissue Culture. Vienna: Springer Vienna, 2003. http://dx.doi.org/10.1007/978-3-7091-6040-4.

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Kumar, Sandeep. Plant tissue culture. Jabalpur: Tropical Forest Research Institute, 1997.

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Gilbert, Henry. Tissue culture-plants, 1984-1986: 233 citations. Beltsville, Md: U.S. Dept. of Agriculture, National Agricultural Library, 1987.

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Book chapters on the topic "Tissue culture in plants"

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Preil, Walter. "Micropropagation of ornamental plants." In Plant Tissue Culture, 115–33. Vienna: Springer Vienna, 2003. http://dx.doi.org/10.1007/978-3-7091-6040-4_7.

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Maene, L. J. "Tissue Culture of Ornamental Plants." In Applications of Biotechnology in Forestry and Horticulture, 231–43. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4684-1321-2_17.

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Priyadarshan, P. M. "Tissue Culture." In PLANT BREEDING: Classical to Modern, 475–91. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-7095-3_21.

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Loyola-Vargas, Víctor M., C. De-la-Peña, R. M. Galaz-Ávalos, and F. R. Quiroz-Figueroa. "Plant Tissue Culture." In Springer Protocols Handbooks, 875–904. Totowa, NJ: Humana Press, 2008. http://dx.doi.org/10.1007/978-1-60327-375-6_50.

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Bhojwani, Sant Saran, and Prem Kumar Dantu. "Production of Virus-Free Plants." In Plant Tissue Culture: An Introductory Text, 227–43. India: Springer India, 2013. http://dx.doi.org/10.1007/978-81-322-1026-9_16.

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Ellis, David D., and David T. Webb. "Light regimes used in conifer tissue culture." In Micropropagation of Woody Plants, 31–55. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-015-8116-5_3.

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Escobedo-Gracia-Medrano, Rosa María, Martha Josefa Burgos-Tan, José Roberto Ku-Cauich, and Adriana Quiroz-Moreno. "Using Flow Cytometry Analysis in Plant Tissue Culture Derived Plants." In Plant Cell Culture Protocols, 317–32. New York, NY: Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-8594-4_22.

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Srivastava, P. S., and B. M. Johri. "Endosperm culture." In Plant Tissue Culture Manual, 779–99. Dordrecht: Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-009-0103-2_45.

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Srivastava, P. S., and B. M. Johri. "Endosperm culture." In Plant Tissue Culture Manual, 49–69. Boston, MA: Springer US, 1992. http://dx.doi.org/10.1007/978-1-4899-3776-6_5.

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Kahn, Robert P. "Plant Quarantine and International Shipment of Tissue Culture Plants." In Tissue culture as a plant production system for horticultural crops, 147–64. Dordrecht: Springer Netherlands, 1986. http://dx.doi.org/10.1007/978-94-009-4444-2_13.

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Conference papers on the topic "Tissue culture in plants"

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Pivovarova, N. S., T. S. Shebitchenko, and A. G. Podboronova. "Obtaining tissue culture of Scutellaria baicalensis." In 2nd International Scientific Conference "Plants and Microbes: the Future of Biotechnology". PLAMIC2020 Organizing committee, 2020. http://dx.doi.org/10.28983/plamic2020.198.

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The work is devoted to the obtaining of callus culture of Scutellaria baicalensis from sterile microcuttings. Cultivation conditions were determined, growth activity was studied, and a qualitative analysis was carried out.

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Krasova, Yu V., O. V. Tkachenko, E. N. Sigida, N. V. Evseeva, G. L. Burygin, and Y. V. Lobachev. "Features of the development of wheat tissue culture during processing bacterial biomacromolecules and cells." 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/10.26907/978-5-00130-204-9-2019-236.

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Suberliak, Sofia. "Method of tissue culture for biodiversity conservation of medical plants of Carpatians." In ASPB PLANT BIOLOGY 2020. USA: ASPB, 2020. http://dx.doi.org/10.46678/pb.20.1048274.

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Echeverri Del Sarto, Julieta, María Celeste Gallia, Ana Ferrari, and Guillermina A. Bongiovanni. "TISSUE PLANT CULTURE AS A NOVEL INDUSTRIAL STRATEGY TO PRODUCE BIOPHARMACEUTICALS FROM ENDANGERED PLANTS." In 24th International Academic Conference, Barcelona. International Institute of Social and Economic Sciences, 2016. http://dx.doi.org/10.20472/iac.2016.024.030.

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Harahap, Fauziyah, Harifah Insani, Diky Setya Diningrat, Nanda Eska Anugrah Nasution, Roedhy Poerwanto, and Rifa Fadhilah Munifah Hasibuan. "Needs Assessment of Teaching Book Development Based on Plants Multiplication Research in Plant Tissue Culture Course." In 2nd Educational Sciences International Conference (ESIC 2019). Paris, France: Atlantis Press, 2020. http://dx.doi.org/10.2991/assehr.k.200417.005.

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Tkachenko, O. V., N. V. Evseeva, G. L. Burygin, K. Yu Kargapolova, Yu V. Lobachev, E. E. Kostina, and S. Yu Schegolev. "The effect of rhizospheric bacteria and their biomacromolecules on somatic plant cells and tissues by culture in vitro." 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/10.26907/978-5-00130-204-9-2019-437.

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Vazquez Rueda, Martin G., Federico Hahn, and Jose L. Zapata. "Adaptive image segmentation applied to plant reproduction by tissue culture." In AeroSense '97, edited by Steven K. Rogers. SPIE, 1997. http://dx.doi.org/10.1117/12.271476.

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Yang, Yanli, Qi Chu, Meizhang Gu, Hanhan Ji, and Song Gu. "Simulation analysis and experiment of unpowered roller conveying for culture bottle in tissue culture plant." In 2021 6th International Conference on Automation, Control and Robotics Engineering (CACRE). IEEE, 2021. http://dx.doi.org/10.1109/cacre52464.2021.9501338.

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"Alterations of differential gene expression during the morphogenesis induction in wheat tissue culture (transcriptome analysis)." In Plant Genetics, Genomics, Bioinformatics, and Biotechnology. Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences, 2019. http://dx.doi.org/10.18699/plantgen2019-029.

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Lugovtsova, S. Yu, N. A. Neshumayeva, and N. V. Zobova. "INFLUENCE OF TOXIC METABOLITES FUSARIUM SPOROTRICHIOIDES ON THE PROCESSES OF REGENERATION OF AVENA SATIVA IN THE TISSUE CULTURE." In The All-Russian Scientific Conference with International Participation and Schools of Young Scientists "Mechanisms of resistance of plants and microorganisms to unfavorable environmental". SIPPB SB RAS, 2018. http://dx.doi.org/10.31255/978-5-94797-319-8-1308-1312.

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Reports on the topic "Tissue culture in plants"

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Scott, C. D., and D. K. Dougall. Plant cell tissue culture: A potential source of chemicals. Office of Scientific and Technical Information (OSTI), August 1987. http://dx.doi.org/10.2172/5938126.

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Harris, David T. Tissue Culture Hood for Immunotoxicology of JP-8 Fuel. Fort Belvoir, VA: Defense Technical Information Center, July 2000. http://dx.doi.org/10.21236/ada383524.

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Ostry, M. E., and K. T. Ward. Bibliography of Populus cell and tissue culture. St. Paul, MN: U.S. Department of Agriculture, Forest Service, North Central Forest Experiment Station, 1991. http://dx.doi.org/10.2737/nc-gtr-146.

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Peehl, Donna M. Development of a Novel Tissue slice Culture Model of Human Prostate Cancer. Fort Belvoir, VA: Defense Technical Information Center, February 2005. http://dx.doi.org/10.21236/ada435857.

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Peehl, Donna M. Development of a Novel Tissue Slice Culture Model of Human Prostate Cancer. Fort Belvoir, VA: Defense Technical Information Center, February 2004. http://dx.doi.org/10.21236/ada425981.

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Kraybill, William H. Lectin Enzyme Assay Detection of Viruses, Tissue Culture, and a Mycotoxin Simulant. Fort Belvoir, VA: Defense Technical Information Center, September 1988. http://dx.doi.org/10.21236/ada276469.

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Peehl, Donna M. Development of a Novel Tissue Slice Culture Model of Human Prostate Cancer. Fort Belvoir, VA: Defense Technical Information Center, February 2003. http://dx.doi.org/10.21236/ada417612.

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Peehl, Donna M. Discovery of Hyperpolarized Molecular Imaging Biomarkers in a Novel Prostate Tissue Slice Culture Model. Fort Belvoir, VA: Defense Technical Information Center, June 2013. http://dx.doi.org/10.21236/ada580953.

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Kurhanewicz, John. Discovery of Hyperpolarized Molecular Imaging Biomarkers in a Novel Prostate Tissue Slice Culture Model. Fort Belvoir, VA: Defense Technical Information Center, June 2013. http://dx.doi.org/10.21236/ada584506.

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Ronen, Sabrina. Discovery of Hyperpolarized Molecular Imaging Biomarkers in a Novel Prostate Tissue Slice Culture Model. Fort Belvoir, VA: Defense Technical Information Center, June 2013. http://dx.doi.org/10.21236/ada585099.

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