Rozprawy doktorskie na temat „Tissue culture”
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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.
Pełny tekst źródłaArunyanart, Sumay. "Chrysanthemum improvement through tissue culture". Thesis, Arunyanart, Sumay (1988) Chrysanthemum improvement through tissue culture. PhD thesis, Murdoch University, 1988. https://researchrepository.murdoch.edu.au/id/eprint/51910/.
Pełny tekst źródłaBrons, I. G. M. "Tissue culture of rat insulinoma cells". Thesis, University of Cambridge, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.303711.
Pełny tekst źródłaRathbone, Sandra. "Dynamic culture of tissue engineered ligaments". Thesis, Keele University, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.534314.
Pełny tekst źródłaCousineau, Johanne. "Isoenzyme studies and tissue culture of raspberry". Thesis, McGill University, 1992. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=70254.
Pełny tekst źródłaA high rate (70%) of adventitious shoot regeneration was observed from leaf-petiole explants of micropropagated shoot cultures of 'Comet' red raspberry cultured on modified Murashige-Skoog medium containing 1 mg/l thidiazuron (TDZ) and 0.5 mg/l 1H-indole-3-butanoic acid (IBA). Variation in the agar concentration or incubation temperature, orientation or scoring of the leaf-petiole explants and use of separate leaf or petiole explants had no effect on shoot regeneration while incubation in the dark for 1, 2, or 3 weeks prior to growth in the light depressed the number of adventitious shoots formed. Only 8 of 22 raspberry cultivars were capable of regenerating from leaf explants of greenhouse-grown plants.
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.
Pełny tekst źródłaAziz, Zaleha Biniti A. "Tissue culture of Centella asiatica : asiaticoside biosynthesis". Thesis, University of Nottingham, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.368364.
Pełny tekst źródłaTiwari, Vimlesh Kumar. "Tissue culture and transformation studies of barley". Thesis, University of Nottingham, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.334512.
Pełny tekst źródłaBrown, Andrew M. G. "Biochemistry, tissue culture and pharmacology of Tanacetum". Thesis, University of Nottingham, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.363563.
Pełny tekst źródłaEl-Shaweesh, Kamal Husein. "Tissue culture and irradiation studies in Solanum". Thesis, University of Salford, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.334320.
Pełny tekst źródłaLongden, David. "Tissue culture induced changes in tobacco somaclones". Thesis, University of Liverpool, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.306567.
Pełny tekst źródłaAl-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.
Pełny tekst źródłaMassa, Denise Marie. "Is Organic Tissue Culture of Petunia Possible?" Available to subscribers only, 2009. http://proquest.umi.com/pqdweb?did=1796330171&sid=6&Fmt=2&clientId=1509&RQT=309&VName=PQD.
Pełny tekst źródłaKhan, Saifullah. "Variation arising through tissue culture in soft fruits". Thesis, University of Edinburgh, 1997. http://hdl.handle.net/1842/28357.
Pełny tekst źródłaAfshar-Sterle, Shoukat. "Cell, tissue culture and transformation of Triticum tauschii /". Title page, abstract and contents only, 2000. http://web4.library.adelaide.edu.au/theses/09APSP/09apspa258.pdf.
Pełny tekst źródłaAkhtar, Lal Hussain. "Tissue culture and stress tolerance in Gossypium species". Thesis, Bangor University, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.296184.
Pełny tekst źródłaSipen, Philip. "Tissue Culture and Cryopreservation of Banana {Musa spp.)". Thesis, University of Nottingham, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.523611.
Pełny tekst źródła倪建春 i Kin-chun Ngai. "Demonstration of bilirubin cytotoxicity by tissue culture system". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1996. http://hub.hku.hk/bib/B31214526.
Pełny tekst źródłaAnjum, M. A. "Tissue culture and frost tolerance studies in Solanum". Thesis, University of Salford, 1994. http://usir.salford.ac.uk/14833/.
Pełny tekst źródłaTan, Chia Lock. "Tissue culture and genetic transformation of Theobroma cacao". Thesis, University of Nottingham, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.310835.
Pełny tekst źródłaDeljou, Ali. "Tissue culture and genetic transformation in potato breeding". Thesis, University of Nottingham, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.339661.
Pełny tekst źródłaKermanee, Prasart. "Tissue culture and genetic manipulation of Thai rice". Thesis, University of Nottingham, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.368338.
Pełny tekst źródłaJames, 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.
Pełny tekst źródłaGe, Cheng. "Novel technologies for cell culture and tissue engineering". Thesis, University of Oxford, 2016. https://ora.ox.ac.uk/objects/uuid:ab1014cf-80a4-4675-b607-96dc52c39b17.
Pełny tekst źródłaBonfils, Anne-Christine D. (Anne-Christine Dominique) Carleton University Dissertation Biology. "Tissue culture and intergeneric somatic hybridization in Brassicaceae". Ottawa, 1992.
Znajdź pełny tekst źródłaNgai, Kin-chun. "Demonstration of bilirubin cytotoxicity by tissue culture system /". Hong Kong : University of Hong Kong, 1996. http://sunzi.lib.hku.hk/hkuto/record.jsp?B18155030.
Pełny tekst źródłaBaker, William P., Tyrone Harvard Hanks i Louis Eduardo Marin. "Tissue Culture and Cloning of Carnegiea gigantea, Cactaceae". University of Arizona (Tucson, AZ), 2015. http://hdl.handle.net/10150/554346.
Pełny tekst źródłaWilson, Christopher G. "Modeling the dynamic composition of engineered cartilage". Link to electronic thesis, 2002. http://www.wpi.edu/Pubs/ETD/Available/etd-0326102-204208/.
Pełny tekst źródłaCharles, Lara Nicole. "Culture of cells from mammalian tissue cryopreserved without cryoprotection". [College Station, Tex. : Texas A&M University, 2008. http://hdl.handle.net/1969.1/ETD-TAMU-2819.
Pełny tekst źródłaTaeb, Abdulkarim Giumaa. "Influence of culture environment on tulip micropropagation". Thesis, University of Nottingham, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.328788.
Pełny tekst źródłaGarber-Goldsman, Cheryl. "Studies of a central noradrenergic system in tissue culture". Thesis, University of Ottawa (Canada), 1985. http://hdl.handle.net/10393/4981.
Pełny tekst źródłaBatur, Sule. "Bacterial adhesion to endothelial cells in tissue culture systems". Thesis, Georgia Institute of Technology, 1991. http://hdl.handle.net/1853/25406.
Pełny tekst źródłaO'Dea, Reuben. "Multiphase modelling of tissue growth in dynamic culture conditions". Thesis, University of Nottingham, 2008. http://eprints.nottingham.ac.uk/10446/.
Pełny tekst źródłaCancino, Escalante Giovanni Orlando. "Tissue culture and Agrobacterium-mediated transformation studies in Passiflora". Thesis, University of Nottingham, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.342022.
Pełny tekst źródłaCraig, Wendy. "Tissue culture of Brassiceae : a basis for genetic improvement". Thesis, University of Nottingham, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.307757.
Pełny tekst źródłaWardrop, Julie. "Biotechnological applications of perfluorochemical liquids in plant tissue culture". Thesis, University of Nottingham, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.389475.
Pełny tekst źródłaKhalid, Norzulaani. "Somaclonal variation through tissue culture studies in Chrysanthemum morifolium". Thesis, University of Nottingham, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.329847.
Pełny tekst źródłaCastellanos, Marcos. "Tissue culture and transformation of poinsettia (Euphorbia pulcherrima Willd.)". Thesis, University of Nottingham, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.439998.
Pełny tekst źródłaGhazvini, Reza Fotouhi. "Tissue culture and frost tolerance studies in Citrus spp". Thesis, University of Salford, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.308133.
Pełny tekst źródłaWright, Rachel Claire. "Promoter probing of Listeria monocytogenes during tissue culture infection". Thesis, University of Warwick, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.409907.
Pełny tekst źródłaOkyere-Boateng, George. "Tissue culture response in oil palm : (Elaeis guineensis Jacquin)". Thesis, University of Reading, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.395176.
Pełny tekst źródłaChen, Ting-yu, i 陳婷玉. "Tissue Culture of Six Paphiopedilums". Thesis, 2000. http://ndltd.ncl.edu.tw/handle/63898036664908086425.
Pełny tekst źródła國立臺灣大學
園藝學研究所
88
Protocorm explants of Paphiopedilum delenatii were cultured on 1/2-MS medium containing 0-10 mg/L NAA and 0-10 mg/L kinetin. The plain basal medium (devoid any hormones additive) were found as the best medium for shood bud formation. NAA and kinetin inhibited shoot bud development of the protocorms. Shoot buds derived maining from the epidermal cells of the protocorm explants without intermediate calli form. The method can be used to shorten the period of bud proliferation and breeding. The leaf explants of Paphiopedilum callosum album ''Oakhill'' × lawrenceanum album ''Tradition'' formed yellow calli on the medium containing 5 mg/L 2,4-D and 1 mg/L TDZ in 20 weeks those leaf-derived calli could be subcultured on the same medium but failed to produce plantlets. Difference on percentage of callus inducing and morphogenesis were among 5 species tested. Calli from leaf explants had lower regeneration and died easily in subculture period. Further investigation should be focus on the problems. The percentage of shoot bud inducing had distinction in Paphiopedilum philippinense (PH59、PH60, these two came from different parents) may resulted mainly on genetic variation. The bud formation frequency of cutting-leaf explants were higher than intact leaves. These shoot-buds formed from leaf base developed into normal plantlets on plain basal medium. Stem node explants of Paphiopedilum philippinense were cultured in light on 1/2-MS medium. After 12 weeks, shoot buds formed directly from nodes. The buds transfered into free medium after 20 weeks. Some buds became muliple shoots and developed into plantlets with roots. The percentage of bud inducing could reach 80 ﹪. Calli derived from protocorms of Paphiopedilum callosum album ''Oakhill'' × lawrenceanum album ''Tradition'' subcultured on 1/2-MS medium containing 5 mg/L 2,4-D and 1 mg/L TDZ for three years were cultured in light on 1/2-MS medium adding 0.5 mg/L BPA formed shoot buds. This proved these calli retained totipotency in long-term subculture. Cytokinins ( kinetin、zeatin、BA、2iP and BPA ) retarded browning of calli. GA3、TIBA and ABA inhibited calli growth.
CAI, ZONG-RUI, i 蔡宗叡. "Tissue culture of eucalyptus saligna". Thesis, 1991. http://ndltd.ncl.edu.tw/handle/00478117284774190243.
Pełny tekst źródłaHuang, Chien-Chen, i 黃千真. "Tissue culture of Aleurites montana". Thesis, 2013. http://ndltd.ncl.edu.tw/handle/18407499483450231338.
Pełny tekst źródła國立臺灣大學
森林環境暨資源學研究所
101
The Mature and non-mature seeds of Aleurites montana were used in this study, after arterialized with 1% sodium hypochlorite solution for 10 minutes. The seeds were cultured in MS culture medium, treated at 25℃ with a photoperiod of 16 hours and a light intensity of 28μEm-2s-1,which would result in 100% aseptic seedling. Cutting the stem of aseptic seedling into a length of 0.5~1.0 cm, cultured the samples in MS culture medium with 4mg/IBA for 4 weeks, which could induce the green callus, then taking 0.5cm3 sample from the green callus, cultured the sample in MS culture medium with 4mg/IBA, treated with a photoperiod of 16 hours, which could induce 97% multi-buds after 8 weeks. Cutting roots from the aseptic seedlings, the roots were cultured in MS culture medium with 4mg/IBA, treated with a photoperiod of 16 hours, after 4 weeks, each explants could induce 48.2 somatic embryos, if sub-cultured in the same culture medium and with the same treatment, which could produce secondary somatic embryo; putting somatic embryo in the culture medium with 0.1mg/IBA, which would promote the maturation of somatic embryo and conversion ratio. Taking 2.0mg/l green and tight callus, putting in 50ml liquid culture medium, in every 7 days, it was sub-cultured under the conditions of old liquid : new liquid = 1:5, which would increase to 3.3mg/l, and appear the formation of cell with dense cytoplasm.
Lo, Kuo~Jui, i 羅國瑞. "Tissue Culture of Taraxacum formosanum". Thesis, 2001. http://ndltd.ncl.edu.tw/handle/69730092196932460564.
Pełny tekst źródła中國醫藥學院
中國藥學研究所
89
Summary Taraxacum spp (Compositae) were first recorded in Sin-Sho-Pen-Tsao of the Tang Dynasty under inferior category.Taraxacum formosanum is one of the trantional Chinese medicinal herbs used in the treatment of matitis, tonsillits, cholestasis and cleaning the waste of the liver. Due to limited geographical distribution and indiscriminate collection, T. formosanum is now rarely found in its natural habitat. Over development of land for many use and introduction of alien species of T. officinale also resulted in reduction population of T. formosanum. The purpose of this study was to establish the tissue culture techniques for mass propagation of Taraxacum formosanum. The results of the present investigation are summarized as: 1.Nearly 100% germination rate was obtained, when seeds of T. formosanum were cultured on a medium containing half-strength MS basic salts supplemented with 0.5mg/l BA, 3% sucrose and 1.0% Difco agar. 2.A medium containing half-strength MS salts, 1.0 mg/l NAA, 0.5 mg/l BA, 3% sucrose and 1% Difco agar can induce callus from T. formosanum seed. 3.A medium containing half-strength MS salts, 0.5 mg/l NAA, 1.0 mg/l kinetin, 3% sucrose and 1.0% Difco agar (pH=5.7) was the most suitable medium for inducing callus formation of T. formosanum. The cultures were maintained at 25±1℃ under dark. 4.Addition of 10%(v/v) coconut milk (CM) or potato homogenate is not good for callus growth of T. formosanum. 5.Adding (500,1000,2000 mg/l) peptone or casein hydrolysate(CH) is not good for callus growth of T. formosanum. 6.Adventitious buds can be induced from leaves when cultured on a medium containing half-strength MS basic salts, 0.5mg/l BA, 3% sucrose and 1% Difco agar (pH=5.7). The cultures were maintained at 25±1℃ under a photoperiod of 14-h light (2000 lux fluorecent light) and 10-h dark cycle. 7.For rooting of adventitious buds, which are induced on leaves, buds were cultured on a medium containing 1/4~1/2 MS basic salts, 0.5mg/l NAA, 3~5% sucrose and 1% Difco agar (pH=5.7). The cultures were maintained at 25±1℃ under a photoperiod of 14-h light (2000 lux fluorecent light) and 10-h dark cycle. 8.The plantlets of T. formosanum produced from tissus culture could be transplanted into a mixture of vermiculite and peat moss (1:1), and grown successfully under outdoor conditions.
Hung, Ming-Hung, i 洪銘宏. "Tissue culture of Taxus mairei". Thesis, 1996. http://ndltd.ncl.edu.tw/handle/15619472501620853743.
Pełny tekst źródła高毓瑩. "Tissue Culture of Zelkova Serrate". Thesis, 1995. http://ndltd.ncl.edu.tw/handle/85438558056548564320.
Pełny tekst źródła劉祖惠. "The tissue culture of Dieffenbachia". Thesis, 1990. http://ndltd.ncl.edu.tw/handle/83314905429411437685.
Pełny tekst źródła王上仁. "Tissue culture of Cotyledon tomentosa". Thesis, 2018. http://ndltd.ncl.edu.tw/handle/3trs28.
Pełny tekst źródłaSHEN, MIN-JUAN, i 沈敏娟. "Tissue culture of ginkgo biloba". Thesis, 1992. http://ndltd.ncl.edu.tw/handle/99777319907932899101.
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