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Metabolite fingerprinting tools to detect differences between transgenic and conventional cropsMorin, Geneviève. January 2007 (has links)
No description available.
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The evolutionary ecology of tropane alkaloids /Shonle, Irene Katherine. January 1999 (has links)
Thesis (Ph. D.)--University of Chicago, Dept. of Ecology and Evolution, June 1999. / Includes bibliographical references. Also available on the Internet.
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Over-expression and analysis of two Vitis vinifera carotenoid biosynthetic genes in transgenic Arabidopsis /Brackenridge, Anika Elma. January 2006 (has links)
Thesis (MSc)--University of Stellenbosch, 2006. / Bibliography. Also available via the Internet.
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Cytokinin O-glycosyltransferases : biochemical characteristics in vitro and developmental regulation in transgenic plantsVeach, Yeonjin Kim 12 June 2002 (has links)
Graduation date: 2003
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Proteinase inhibitor II from Solanum americanum, molecular characterization and potential use in generating insect-resistant transgenic vegetablesXu, Zengfu. January 2001 (has links)
Thesis (Ph. D.)--University of Hong Kong, 2001. / Includes bibliographical references (leaves 160-187).
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Purification of Brassica juncea chitinase BJCHI1 from transgenic tobaccoFung, King-leung. January 2001 (has links)
Thesis (M. Phil.)--University of Hong Kong, 2001. / Includes bibliographical references (leaves 115-132).
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Heterotrimeric G proteins in plant signal transduction : characterisation of tobacco and arabidopsis G ̊subunits /Anderson, David John. January 2002 (has links) (PDF)
Thesis (Ph. D.)--University of Queensland, 2002. / Includes bibliographical references.
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Production of transgenic plant-derived vaccines via plastid transformation technologyLee, Yuk-ting., 李玉婷. January 2004 (has links)
published_or_final_version / abstract / toc / Botany / Master / Master of Philosophy
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Establishment of an indirect organogenesis protocol for Eucalyptus grandis species and hybrids.Hajari, Elliosha. January 2004 (has links)
The prospect of integrating transgenic eucalypts with conventional breeding programmes is of value to the Plantation Forestry and Forest Products Industries. However, significant progress in this regard has still to be reported, one constraint is the lack of appropriate high yielding regeneration culture methods for clonal material. Such was the main aim of the present study. The strategy was to develop a suitable protocol using in vitro shoots of an E. grandis x E. urophy/la clone (GU185) and thereafter to test its applicability to other clones. Explants from greenhouseestablished cuttings provided the in vitro shoots, which were multiplied via axillary bud proliferation either on semi-solid medium or using a RIT A system. To determine the best conditions for callus and shoot regeneration, parameters such as vessels (petri dishes and tubes) and types and levels of plant growth regulators were tested. The best callus production (100%) and shoot regeneration (78.9 - 100% callus with shoots) for GU185 occurred on MS, 30 g rl sucrose, 4 g rl Gelrite, 5 mg rl IAA and 0.25 mg rl BAP. Parameters tested to identify the most suitable explants for indirect organogenesis were the age of parent plants, different systems to generate in vitro shoots, elongation status of explants, 1 sI and 2nd generation in vitro shoots and the use of hyperhydric shoots. Of these, the most suitable explants for indirect organogenesis were shoots from axillary bud multiplication of 3-month-old parent plants using the semi-solid system (33 shoots/dish). Up to 90% rooting was achieved on 1f4 MS (Murashige and Skoog, 1962), 15 g rl sucrose, 0.1 mg rl biotin, 0.1 mg rl calcium pantothenate, 4 g rl Gelrite and mA. The highest rooting was obtained when regenerated shoots were first multiplied and then placed on medium without plant growth regulators for one week, before transfer to root induction medium containing 0.1 - 0.5 mg rl mA. Acclimatization success was 95% when rooted shoots were placed in pots with a rooting mix (2 perlite: 1 coir) enclosed in plastic bags and the humidity was gradually reduced over four weeks. The developed indirect organogenesis protocol appeared to have a broad general application, although the tested clones exhibited a genotype-dependent response, with GU180, GUI77 and TAG31 producing fewer shoots (9, 6 and 7 shoots/dish) than ZG14 and GU185 (24 and 18 shoots/dish). Similarly high levels of rooting were obtained for TAG3l (93.8%) and ZG14 (90%) and for hardening-off (90.7% for TAG31 and 91.4% for ZG14). / Thesis (M.Sc.)-University of KwaZulu-Natal, 2004.
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Metabolite fingerprinting tools to detect differences between transgenic and conventional cropsMorin, Geneviève. January 2007 (has links)
A concern in transgenic crops is the potential risk posed by unintended effects which could result from genetic transformation. The objective of this work was to develop an untargeted approach that could characterize transgenic crops, as well as conventional crops, at the molecular level. An experimental approach was designed and used to compare conventional and transgenic soybean varieties. Varieties were compared using their metabolite fingerprints obtained by reverse-phase high performance liquid chromatography (HPLC) and both the analytical and biological variability were assessed. Multivariate and univariate statistical analyses were applied to the data to detect significant differences between the varieties. It was found that transgenic variety PS 46 RR was the most different variety analyzed and that it differed most from Mandarin (Ottawa) and AC Dundas. The statistical analyses also determined that PS 46 RR differed more from the conventional varieties tested than 2601R did.
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