Relevant bibliographies by topics / Potatoes Plant tissue culture

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Potatoes Plant tissue culture'

Author: Grafiati
Published: 4 June 2021
Last updated: 15 February 2022

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Journal articles on the topic "Potatoes Plant tissue culture"

1

Wan, Waylen Y., Weixing Cao, and Theodore W. Tibbitts. "Tuber Initiation in Hydroponically Grown Potatoes by Alteration of Solution pH." HortScience 29, no. 6 (June 1994): 621–23. http://dx.doi.org/10.21273/hortsci.29.6.621.

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Because tuberization in potatoes (Solarium tuberosum L.) reportedly is inhibited when stolons are immersed in liquid, this study was conducted to determine the effect of intermittent pH reductions of the nutrient solution on tuber induction of potatoes in solution culture. Tissue-culture potato plantlets were transplanted into solutions maintained at pH 5.5. The pH of the nutrient solution was changed to 3.5 and 4.0 for 10 hours on each of three dates (30, 35, and 40 days after transplanting). For the pH 3.5 treatment, tubers were observed first on day 42 and averaged 140 tubers per plant at harvest on day 54. For the pH 4.0 treatment, tubers were observed first on day 48 and averaged 40 tubers per plant at harvest. At a constant pH 5.5, tubers were observed on day 52 and averaged two tubers per plant at harvest. Plants with the intermittent pH 3.5 had smaller shoots and roots with shorter and thicker stolons compared to constant pH 5.5. With the intermittent pH 4.0, plants were of similar size, but stolons were shorter and slightly thickener compared to those from pH 5.5. Mineral composition of leaf tissues at harvest was similar for the three pH treatments. These results indicate that regulation of solution pH can be a useful technique for inducing tuberization in potatoes.
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Perry, K. L., L. Miller, and L. Williams. "Impatiens necrotic spot virus in Greenhouse-Grown Potatoes in New York State." Plant Disease 89, no. 3 (March 2005): 340. http://dx.doi.org/10.1094/pd-89-0340c.

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Impatiens necrotic spot virus (INSV; genus Tospovirus) was detected in experimental greenhouse-grown potatoes (Solanum tuberosum) and Nicotiana benthamiana in New York State in July and August of 2003 and 2004. Potato leaves exhibiting necrotic lesions with a concentric pattern similar to those induced by Tomato spotted wilt virus (1) were observed on cvs. Atlantic, Huckleberry, NY115, and Pentland Ivory. The presence of INSV was confirmed using double-antibody sandwich enzyme-linked immunosorbent assay and a rapid ‘ImmunoStrip’ assay (Agdia, Inc., Elkhart, IN). INSV-specific sequences were amplified from total RNA extracts using reverse transcription-polymerase chain reaction with ‘Tospovirus Group’ primers (Agdia, Inc.) and two independently amplified DNAs were sequenced. A common sequence of 355 nucleotides (GenBank Accession No. AY775324) showed 98% identity to coding sequences in an INSV L RNA. The virus was mechanically transmitted to potato and N. benthamiana and could be detected in asymptomatic, systemically infected potato leaves. Stems nodes and leaves were removed from infected potato plants, and sterile in vitro plantlets were established (2). None of the regenerated in vitro plantlets of cvs. Pentland Ivory (6 plantlets) or NY115 (5 plantlets) were infected with INSV. Two of ten regenerated cv. Atlantic plantlets initially tested positive, but INSV could not be detected after 6 months in tissue culture. In vitro tissue culture plantlets could not be established from infected cv. Huckleberry plants, even though they were consistently obtained from uninfected plants. Infected greenhouse plants were grown to maturity and the tubers harvested, stored for 6 months at 4°C, and replanted in the greenhouse. INSV could not be detected in plants from 26 cv. Huckleberry, 4 cv. NY115, or 4 cv. Atlantic tubers. Although this isolate of INSV was able to systemically infect potato, it was not efficiently maintained or transmitted to progeny tubers. This might explain why INSV has not been reported as a problem in potato production. Lastly, in both years, dying N. benthamiana provided the first sign of a widespread greenhouse infestation of INSV in a university facility housing ornamental and crop plants. INSV induced a systemic necrosis in N. benthamiana, and this host may be useful as a sensitive ‘trap’ plant indicator for natural infections in greenhouse production. References: (1) T. L. German. Tomato spotted wilt virus. Pages 72–73 in: Compendium of Potato Diseases. W. R. Stevenson et al., eds. The American Phytopathological Society, St. Paul, 2001. (2) S. A. Slack and L. A. Tufford. Meristem culture for virus elimination. Pages 117–128 in: Fundamental Methods of Plant Cell, Tissue and Organ Culture and Laboratory Operations. O. L. Gamborg and G. C. Philips, eds. Springer-Velag, Berlin, 1995.
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Karp, A., M. G. K. Jones, D. Foulger, N. Fish, and S. W. J. Bright. "Variability in potato tissue culture." American Potato Journal 66, no. 10 (October 1989): 669–84. http://dx.doi.org/10.1007/bf02853986.

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Kim, Irina, Elena Barsukova, Petr Fisenko, Tatyana Chekushkina, Alena Chibizova, Dmitry Volkov, and Alexey Klykov. "Applying methods of replication and recovery of potato microplants (Solanum tuberosum l.) in seed production." E3S Web of Conferences 203 (2020): 02003. http://dx.doi.org/10.1051/e3sconf/202020302003.

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Potatoes are strongly affected by pests and by pathogens of fungal, bacterial and viral nature. The most common and economically significant potato viruses are Y (PVY), X (PVX), S (PVS), M (PVM), and potato leaf twisting virus (PLRV). The development of a virus-free bio-resource collection in vitro is the basis for plant breeding development and transferring seed production to a healthier foundation. In this regard, the aim of this research was to apply methods of recovery and select optimal conditions for in vitro propagation of a collection of virus-free potato varieties. A collection of 22 healthy virus-free potato varieties was developed and kept in vitro in the FSBSI “FSC of Agricultural Biotechnology of the Far East named after A. K. Chaika". The recovery from viruses through joint use of tissue culture (apexes 2-4 mm) and chemotherapy (ribavirin) of the new potato variety Avgustin was carried out. The recovered test-tube plants, as well as the samples of six in vitro potato varieties that are in demand in plant breeding and seed production (Smak, Sante, Yantar, Zhukovsky ranny, Dachny, Adretta), were tested by enzyme immunoassay method (ELISA) for latent infection with viruses Y (PVY), X (PVX), S (PVS), M (PVM), and L (PLRV). The evaluation for Potato Spindle Tuber Viroid (PSTVd) was performed using PCR method. As a result of the study, no viral infections were detected in the recovered material and plants in vitro. The composition of nutrient medium for the microclonal propagation of potatoes that provides maximum value of the propagation rate is detected.
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Smith, MK, and RA Drew. "Current Applications of Tissue Culture in Plant Propagation and Improvement." Functional Plant Biology 17, no. 3 (1990): 267. http://dx.doi.org/10.1071/pp9900267.

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Plant tissue culture involves the culture of all types of plant cells, tissues and organs under aseptic conditions. This definition also extends to the culture of excised embryos and to protoplast culture. An overview of tissue culture techniques and their applications in plant propagation and genetic improvement of plants is presented. The areas under review include: (1) embyro culture, (2) meristem culture, (3) micropropagation, (4) somatic embryogenesis, (5) somaclonal variation, (6) in vitro selection, (7) anther culture and (8) protoplast culture. Problems and limitations of each of the techniques are also discussed. Examples are given of work that has been undertaken or that is currently in progress on the application of these techniques to the improvement of Queensland's subtropical horticultural industries. Key examples are: (1) embryo culture to facilitate incorporation of genes conferring disease-resistance from wild Cucurbita species into cultivated varieties, (2) meristem culture for virus elimination in strawberries (Fragaria × ananassa) and sweet potato (Ipomoea batatas), (3) micropropagation for rapid increase in new varieties of ginger (Zingiber officinale) and pineapple (Ananas comosus) to enable more rapid field evaluation and early release, (4) micropropagation of disease-free, genetically uniform planting material of superior female papaya (Carica papaya) selections and banana (Musa spp.) selections and (5) the use of somaclonal variation and gamma-irradiation for the genetic improvement of banana. Finally, future opportunities for the utilisation of tissue culture in plant propagation and improvement in Queensland's horticultural industries are summarised.
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Abughnia, Elmundr, Salem Hammud, Ahmed shaaban, Kheiry Keer, and Arij shaheen. "Effect of light specters (red and blue) on two-potato varieties tissue (spunta and Agria)." Journal of Misurata University for Agricultural Sciences, no. 01 (October 6, 2019): 13–26. http://dx.doi.org/10.36602/jmuas.2019.v01.01.02.

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This study was carried out in plant tissue culture laboratory which belong to bio technology research center in order to test the effect of raid and blue spectral light colors and white lighting as a control and white fluorescent lamps as a second control on plant growth stages while two potato variety ( Spunta , Agria) were used in this experiment . potato plant samples were collected and cultured in special jars contain MS media after being sterilized by Clorox solution in order to avoid the any contamination risk , while the culture stage of the explant started in sterilized condition in sited the hood cabinet, wherever the culture stage completed the cultured plants were placed in the growth room under controlled condition with raid , blue and normal light condition. The obtained results showed that the wait normal color treatment was significantly higher than the other two treatments in plant length factor for the tow used potato variety, while for the number of leaves factor the results showed that the normal light color treatment was significantly higher than the other two treatments in plant number of leaves factor followed by raid color treatment in the two used variety Spunta and Agria while the Raid color treatment scored average of leaves (23.9, 23.3 ) leaf respectively.
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Espinoza, N. O., R. Estrada, D. Silva-Rodriguez, P. Tovar, R. Lizarraga, and J. H. Dodds. "The Potato: A Model Crop Plant for Tissue Culture." Outlook on Agriculture 15, no. 1 (March 1986): 21–26. http://dx.doi.org/10.1177/003072708601500104.

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Conn, Kenneth L., George Lazarovits, and Jerzy Nowak. "A gnotobiotic bioassay for studying interactions between potatoes and plant growth-promoting rhizobacteria." Canadian Journal of Microbiology 43, no. 9 (September 1, 1997): 801–8. http://dx.doi.org/10.1139/m97-117.

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A gnotobiotic bioassay, using potato plantlets derived from single-node explants and grown in test tubes containing potato nodal cutting medium (PNCM), was found to be highly useful for investigations of direct growth promotion by a nonfluorescent Pseudomonas sp. strain PsJN. Strain PsJN was used to optimize and evaluate this bioassay for purposes of screening other rhizosphere bacteria and identification of Tn5 mutants of strain PsJN deficient in growth-promoting properties. The selection of potato cultivar used in this bioassay was critical, as growth promotion of potatoes by strain PsJN was cultivar specific. Inoculated plantlets of cultivars Norchip, Kennebec, Shepody, and Chaleur showed, in root dry weight, a five- to eight-fold increase, two- to three-fold increase, no response, and a decrease of 50%, respectively. Haulm dry weight followed similar trends but was not as consistent an indicator of growth promotion. Bioassay results were not altered to any extent by minor changes in PNCM composition or by slight changes in temperature and light conditions. A rapid method for preparation of bacterial suspensions and inoculation of explants was developed. Inoculation of three explants taken from 6-week-old stock plantlets of cv. Kennebec for each Tn5 transconjugate of strain PsJN (total of 1500 transconjugates) enabled the elimination of 93% of those isolates that retained growth-promoting activity. The remaining 7% of isolates were retested and seven were confirmed to have lost growth-promoting ability. Bacteria from different genera were also screened with this bioassay. None of these bacteria increased the growth of potato plantlets, but several inhibited root and haulm growth.Key words: plant growth-promoting rhizobacteria, gnotobiotic, tissue culture, nonfluorescent pseudomonad, bacterium, potato.
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Ehsanpour, Ali Akbar, and Zeynab Nejati. "Effect of nanosilver on potato plant growth and protoplast viability." Biological Letters 50, no. 1 (June 1, 2013): 35–43. http://dx.doi.org/10.2478/biolet-2013-0004.

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Abstract Potato tissue culture is sensitive to ethylene accumulation in the culture vessel. Ag inhibits ethylene action but no information on nanosilver application in potato tissue culture has been published so far. In our study, potato cv. White Desiree was treated with nanosilver (0, 1.0, 1.5, and 2.0 ppm) in vitro. Leaf surface was increased, while stem length and root length decreased. Nanosilver caused also a decrease in the number of isolated protoplasts and in the viability of isolated protoplasts when applied either directly or indirectly.
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Bailey, E., N. Deighton, S. A. Clulow, B. A. Goodman, and E. E. Benson. "Changes in free radical profiles during the callogenesis of responsive and recalcitrant potato genotypes." Proceedings of the Royal Society of Edinburgh. Section B. Biological Sciences 102 (1994): 243–46. http://dx.doi.org/10.1017/s0269727000014160.

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Changes of the in vitro morphogenetic state may be achieved for some potato genotypes, but others are unresponsive (recalcitrant). Although the biochemical basis for somatic recalcitrance is unknown, evidence suggests that two different aspects of oxidative stress may be involved. Phenolic oxidation is a major problem in manipulating cultures of woody plant species (Thorpe & Harry 1990) and lipid peroxidation has been associated with recalcitrance in monocotyledonous plants (Cutler et al. 1989; Benson et al. 1992). Both oxidative phenomena are believed to be free-radical mediated, but to date there is no reported direct evidence for the formation of free radicals during plant tissue culture callogenesis. The objectives of the present study were twofold; to assess the feasibility of using electron paramagnetic resonance (EPR) spectroscopy to detect free radicals directly in plant tissue cultures and to investigate free radical activity during dedifferentiation of responsive and unresponsive potato genotypes.
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Dissertations / Theses on the topic "Potatoes Plant tissue culture"

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Snider, Karen Teten. "Factors affecting variability in anther culture and in regeneration of androgenic embryos of Solanum phureja." Thesis, This resource online, 1992. http://scholar.lib.vt.edu/theses/available/etd-09122009-040345/.

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Hamidoghli, Yousef. "Production and identification of interspecific potato somatic hybrids." Thesis, University of the West of Scotland, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.283091.

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Kandasamy, Kodi Isparan. "Tissue culture studies on the interactions between the yam anthracnose pathogen and Dioscorea alata L." Thesis, Imperial College London, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.321759.

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Brown, Greta Suzanne. "The Effects of Estrogen on the Growth and Tuberization of Potato Plants (Solanum tuberosum cv. 'Iwa') Grown in Liquid Tissue Culture Media." Thesis, University of Canterbury. Biological Sciences, 2006. http://hdl.handle.net/10092/1376.

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Mammalian estrogens and estrogen-like compounds known as xeno-estrogens are being found in and excreted into the environment in ever increasing amounts. The xeno-estrogen DDE has been found at high concentrations of 1-5 mg/kg of soil (Aislabie et. al, 1997). These estrogens and xeno-estrogens are having a devastating effect on animal-life, yet little is known or understood on the effects of estrogens on plant-life. Thus it is important to determine what effects (if any) estrogens may have on plants. Other research has shown that estrogen has an effect on plants grown in vitro (Janeczko and Skoczowski, 2005). This research aims to help increase the amount of information on what effects estrogens may have on plants. In this study, the effects of mammalian estrogens (17-β-estradiol, estrone and estriol) on the growth and tuberization of potato plants (Solanum tuberosum L. cv 'Iwa') grown in liquid tissue culture medium are presented. It was found that at even 0.1 mg/L of estrogen, root growth of the plants was diminished and at 10 mg/L of estrogen, plant deformity was apparent and callus growth induced. Acid phosphatase activity of the plants was increased with the addition of 0.1 mg/L and 1 mg/L of estrogen but then decreased with the addition of 10 mg/L of estrogen. Tuber production was slightly reduced in plants treated with estrogen compared to the control.
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Arvin, Javad. "Tissue culture in potatoes and in vitro selection for salinity tolerance." Thesis, University of Reading, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.315388.

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Ortiz-Medina, Estela. "Potato tuber protein and its manipulation by chimeral disassembly using specific tissue explantation for somatic embryogenesis." Thesis, McGill University, 2006. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=103001.

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Potato is a major part of the human diet in many countries of the world, providing substantial levels of carbohydrate, protein, and vitamins. This study examined the tuber protein content. In the first part of the research, total soluble protein (TSP) and patatin concentration were determined in periderm, cortex, and pith, in tubers of 20 important potato cultivars. TSP concentration was greater in periderm and lesser in cortex and pith tissues. Patatin was present in all tuber tissues but with the opposite pattern, less in periderm and greater in cortex and pith tissues. For intercultivar comparisons, a means of converting the specific tissue-based TSP and patatin data (dry weight) into a uniform weight whole tuber basis was developed. This relied on conversion factor values that were generated from percent weight tissue proportion and percent dry matter for each tissue layer. Cultivars with relatively more or less TSP and patatin in each tissue layer, and on a whole tuber basis, were identified. In the second part of the study, disassembly of chimeral (Russet Burbank) and putatively chimeral (Alpha, Bintje, Red Gold) tubers into their component genotypes was evaluated as a strategy for the production of intraclones with altered protein content. Explants were selected from tissue with greater or lesser protein levels and somatic embryogenesis was used to produce regenerants from each tissue source. Russeting was used as a phenotypic marker and TSP as a biochemical marker. Russet Burbank was confirmed as a periclinal chimera, although chimeral instability was evident, since some non-chimeral regenerants showed displacement of LI tunic cells with the russeting mutation into the pith. Red Gold was "uncovered" as an LII periclinal chimera (Red-Gold-Red). The value of chimeral disassembly in explaining an important component of somatic variation was clearly seen with this cultivar. The inconsistent TSP distribution in Russet Burbank intraclones proved that TSP was not distributed in a periclinal chimeral manner, as initially hypothesized. However, there was clear variation in protein content in the tubers of non-chimeral regenerants. Periclinal chimeral disassembly and somatic embryogenesis are potentially useful technologies for the production of improved intraclones of potato.
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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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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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Owen, Henry R. "Use of monoploid solanum phureja in cell and tissue culture techniques for potato improvement." Diss., This resource online, 1987. http://scholar.lib.vt.edu/theses/available/etd-07282008-135528/.

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James, V. J. "Regulation of xenobiotic catabolism in plant tissue culture." Thesis, Cardiff University, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.380205.

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Books on the topic "Potatoes Plant tissue culture"

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Lynch, Dermot. Disease elimination by tissue culture and testing of potato breeding clones: Final report. [Regina, Sask.]: Saskatchewan Agriculture and Food, 1995.

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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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Trivedi, Pravin Chandra. Plant tissue culture & biotechnology. Jaipur: Pointer Publishers, 2006.

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Lindsey, K., ed. Plant Tissue Culture Manual. Dordrecht: Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-009-0181-0.

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Lindsey, K., ed. Plant Tissue Culture Manual. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-0303-9.

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Dutta Gupta, S., and Yasuomi Ibaraki, eds. Plant Tissue Culture Engineering. Berlin/Heidelberg: Springer-Verlag, 2006. http://dx.doi.org/10.1007/1-4020-3694-9.

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Lindsey, K., ed. Plant Tissue Culture Manual. Boston, MA: Springer US, 1992. http://dx.doi.org/10.1007/978-1-4899-3776-6.

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Lindsey, K., ed. Plant Tissue Culture Manual. Boston, MA: Springer US, 1992. http://dx.doi.org/10.1007/978-1-4899-3778-0.

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Lindsey, K., ed. Plant Tissue Culture Manual. Dordrecht: Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-009-0103-2.

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Book chapters on the topic "Potatoes Plant tissue culture"

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Visser, Richard G. F. "Regeneration and transformation of potato by Agrobacterium tumefaciens." In Plant Tissue Culture Manual, 301–9. Dordrecht: Springer Netherlands, 1991. http://dx.doi.org/10.1007/978-94-009-0103-2_16.

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Jones, M. G. K. "In vitro Culture of Potato." In Plant Cell and Tissue Culture, 363–78. Dordrecht: Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-017-2681-8_15.

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Spychalla, James P., and Michael W. Bevan. "Agrobacterium-mediated transformation of potato stem and tuber tissue, regeneration and PCR screening for transformation." In Plant Tissue Culture Manual, 379–96. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-009-0103-2_22.

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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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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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Haberlandt, G. "Culturversuche mit isolierten Pflanzenzellen." In Plant Tissue Culture, 1–24. Vienna: Springer Vienna, 2003. http://dx.doi.org/10.1007/978-3-7091-6040-4_1.

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Lucca, Paolo, and Ingo Potrykus. "Genetic engineering technology against malnutrition." In Plant Tissue Culture, 167–74. Vienna: Springer Vienna, 2003. http://dx.doi.org/10.1007/978-3-7091-6040-4_10.

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Zoglauer, Kurt, U. Behrendt, A. Rahmat, H. Ross, and Taryono. "Somatic embryogenesis — the gate to biotechnology in conifers." In Plant Tissue Culture, 175–202. Vienna: Springer Vienna, 2003. http://dx.doi.org/10.1007/978-3-7091-6040-4_11.

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Wilhelm, Eva. "Tissue culture of broad-leafed forest tree species." In Plant Tissue Culture, 203–16. Vienna: Springer Vienna, 2003. http://dx.doi.org/10.1007/978-3-7091-6040-4_12.

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Laimer, M. "The development of transformation of temperate woody fruit crops." In Plant Tissue Culture, 217–42. Vienna: Springer Vienna, 2003. http://dx.doi.org/10.1007/978-3-7091-6040-4_13.

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Conference papers on the topic "Potatoes Plant tissue culture"

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Simbolon, Napit, Revandy Damanik, and Hot Setiado. "Effect of Sucrose And Atonic Against Tunas Culture Potatoes (Solanum tuberosum L.) Through Tissue Culture Technique." In The 3rd International Conference Community Research and Service Engagements, IC2RSE 2019, 4th December 2019, North Sumatra, Indonesia. EAI, 2020. http://dx.doi.org/10.4108/eai.4-12-2019.2293868.

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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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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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Seelye, Jared T., Gourab Sen Gupta, and John Seelye. "Investigations into a low-cost TDS sensor for sterile plant tissue culture media." In 2017 IEEE International Instrumentation and Measurement Technology Conference (I2MTC). IEEE, 2017. http://dx.doi.org/10.1109/i2mtc.2017.7969839.

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Zhou, Hong, Xiating Yu, and Junlin Yu. "Non-destructive growth measurement of tissue-culture orchid plant based on machine vision." In 2011 International Conference on Electrical and Control Engineering (ICECE). IEEE, 2011. http://dx.doi.org/10.1109/iceceng.2011.6057913.

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Vazquez Rueda, Martin G., and Federico Hahn. "Pattern matching and adaptive image segmentation applied to plant reproduction by tissue culture." In AeroSense '99, edited by Kevin L. Priddy, Paul E. Keller, David B. Fogel, and James C. Bezdek. SPIE, 1999. http://dx.doi.org/10.1117/12.342894.

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adil, Muhammad. "Production of high valued medicinal compounds using plant cell tissue and organ culture." In 5th International Electronic Conference on Medicinal Chemistry. Basel, Switzerland: MDPI, 2019. http://dx.doi.org/10.3390/ecmc2019-06308.

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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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Reports on the topic "Potatoes Plant tissue culture"

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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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