Gotowe bibliografie tematyczne / Gene cloning

Gotowa bibliografia na temat „Gene cloning”

Autor: Grafiati
Data publikacji: 4 czerwca 2021
Data aktualizacji: 26 stycznia 2023

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Artykuły w czasopismach na temat "Gene cloning"

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Hain, Patricia, i Donald Lee. "Gene Cloning". Journal of Natural Resources and Life Sciences Education 32, nr 1 (2003): 134. http://dx.doi.org/10.2134/jnrlse.2003.0134b.

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Murray, Noreen E. "Gene cloning". European Review 4, nr 04 (październik 1996): 357. http://dx.doi.org/10.1017/s106279870000212x.

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Murray, Noreen E. "Gene cloning". European Review 4, nr 4 (październik 1996): 357–70. http://dx.doi.org/10.1002/(sici)1234-981x(199610)4:4<357::aid-euro146>3.0.co;2-r.

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Chin, Lee Ping, Tan Su Hui i Douglas B. Furtek. "Cloning and Characterization of MADS-box Gene in Oil Palm". International Journal of Engineering and Technology 1, nr 4 (2009): 314–16. http://dx.doi.org/10.7763/ijet.2009.v1.62.

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Al-Kanany, Fadhil N., i Rasha M. Othman. "Cloning and Expression of Pseudomonas aeruginosa AlkB Gene in E. coli". Journal of Pure and Applied Microbiology 14, nr 1 (31.03.2020): 389–96. http://dx.doi.org/10.22207/jpam.14.1.40.

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Ramsden, S. "Gene Cloning and Manipulation". Journal of Medical Genetics 33, nr 5 (1.05.1996): 440. http://dx.doi.org/10.1136/jmg.33.5.440.

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Kayastha, Arvind M. "Gene Cloning and Manipulation". Biochemical Education 24, nr 1 (styczeń 1996): 40. http://dx.doi.org/10.1016/s0307-4412(96)80007-0.

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Bennett, A. J. "Gene cloning and manipulation". Endeavour 20, nr 1 (styczeń 1996): 44. http://dx.doi.org/10.1016/s0160-9327(96)90084-8.

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Moradas-Ferreira, Pedro. "Gene cloning and sequencing". Biochemical Education 17, nr 4 (październik 1989): 215. http://dx.doi.org/10.1016/0307-4412(89)90153-2.

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Schamhart, Denis H. J., i Alex C. C. Westerhof. "Strategies for gene cloning". Urological Research 27, nr 2 (maj 1999): 83–96. http://dx.doi.org/10.1007/s002400050093.

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Rozprawy doktorskie na temat "Gene cloning"

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Sakuntabhai, Anavaj. "Positional cloning of Darier's disease gene". Thesis, University of Oxford, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.302392.

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Glod, Frank. "PCR generated gene probes for cloning fungal polykeptide synthase genes associated with squalestatin biosynthesis". Thesis, University of Bristol, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.268525.

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Seto, Nina Oi Ling. "The copper-zinc superoxide dismutase gene from Drosophila melanogaster : attempts to clone the gene using two mixed sequence oligonucleotide probes". Thesis, University of British Columbia, 1987. http://hdl.handle.net/2429/26534.

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Superoxide dismutase is an enzyme which scavenges superoxide radicals and is thought to be a longevity determinant, as there exists a positive correlation between superoxide dismutase concentration and maximum life span potential. The cytosolic CuZn superoxide dismutase in D. melanogaster has been purified and sequenced, but the gene has not been cloned. However, when it is available the CuZn SOD gene may be reintroduced into the Drosophila genome via the P-element transformation system so its effects on the life span potential of Drosophila may be studied. This study describes attempts to clone the CuZn SOD gene from D. melanogaster using two mixed sequence oligonucleotide probes. The SI probe corresponds to amino acids 43-48 of the protein sequence and contains 128 different oligonucleotide sequences representing all possible codon combinations predicted from the amino acid sequence. The GT3 probe is targeted to amino acids 90-95 of the protein. In this probe, deoxyguanosine was placed in positions where all four nucleotides may occur to decrease probe heterogeneity. The probes were used to screen D. melanogaster Canton-S and Oregon-R genomic lambda libraries. Three positive clones isolated from the Canton-S library had identical nucleotide sequence in the GT3 probe binding region, and sequencing of the probe binding site revealed that one member of the GT3 probe had formed a 15 bp duplex with the phage DNA. Screening of the Oregon-R library produced four clones which hybridized with both GT3 and S1 probes. When these phage DNA were hybridized to polytene chromosomes by in situ hybridization, none mapped to 68AB on the third chromosome, the location of the CuZn SOD gene. These results suggest that modification of the classical strategy used in this study is necessary, and implications on probe design are discussed.
Medicine, Faculty of
Biochemistry and Molecular Biology, Department of
Graduate
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Monk, Sarah. "Positional cloning of the Darier disease gene". Thesis, University of Oxford, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.325681.

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Lam, W. F. E. "Gene cloning of human placental alkaline phosphatase". Thesis, University of Liverpool, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.384394.

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Ballance, David James. "Transformation and gene cloning in Aspergillus nidulans". Thesis, University of Bristol, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.248172.

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Hill, Russell. "Gene cloning studies in two nocardioform bacteria". Doctoral thesis, University of Cape Town, 1988. http://hdl.handle.net/11427/21896.

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Bibliography: pages 147-177.
Nocardioforms are Gram-positive, aerobic actinomycetes and are a metabolically diverse group which produce antibiotics, useful enzymes, are important in the biotransformation of organic compounds and the decomposition of organic wastes and are important medically. A gene cloning vector designated pLR591 was constructed from the broad host range, multicopy Streptomyces plasmid pIJ702 and the positive selection Escherichia coli plasmid pEcoR251. This plasmid has useful features for the construction of actinomycete genomic libraries. Cloning of DNA into the unique Bg1II endonuclease site of pLR591 inactivated the lethal EcoRI gene derived from pEcoR251, thereby selecting for recombinant plasmids containing inserted DNA. The thiostrepton resistance gene derived from pIJ702 was shown to be functional in Streptomyces lividans enabling selection of recombinant pLR591 plasmids containing foreign DNA in S. lividans. The vector pLR591 therefore functions as a positive selection Streptomyces-E. coli shuttle vector facilitating construction of actinomycete genomic libraries in E. coli and subsequent transfer of recombinant plasmids into S. lividans.
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Moser, Bernhard. "Molecular cloning, characterization and expression of the endoglucanase C gene of Cellulomonas fimi and properties of the native and recombinant gene products". Thesis, University of British Columbia, 1988. http://hdl.handle.net/2429/29036.

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In addition to substrate-associated cellulases, Cellulomonas fimi secretes endoglucanases ( endo-1, 4-β-D-glucan glucanohydrolases, EC 3.2.1.4. ) which are recovered from the cellulose-free culture supernatant of cells grown on microcrystalline cellulose. Two such enzymes, C3.1 and C3.2 with Mrs of 130'000 and 120'000, respectively, were purified to homogeneity. The two endoglucanases were shown to share the same N-terminal amino acid sequence and to hydrolyze carboxymethylcellulose ( CMC ) with similar efficiencies ( 236u/mg protein for C3.1 and 367u/mg protein for C3.2 ). The recombinant lambda vector L47.1-169 was identified from a C.fimi DNA-lambda library on the basis of hybridization with C3.1/2-specific oligonucleotide probes. The subclone pTZ18R-8 only moderately expressed CMCase activity. The 5'-terminus of cenC ( the gene coding for C3.1/2 ) was localized in the insert by Southern transfer experiments and nucleotide sequence analysis. Results from total C.fimi RNA-DNA hybrid protection analyses defined the boundaries of cenC in pTZ18R-8 and led to the tentative identification of -10 and -35 promoter sequences. To improve the expression of cenC, its entire coding sequence, except for the start codon GTG, was fused in frame to the ATG codon of a synthetic ribosomal binding site ( PTIS ) and placed under the transcriptional control of the lac p/o system. Induction of the resulting clone ( JM101[pTZP-cenC] ) led to impaired growth in liquid cultures because overproduction of CenC inhibited cell division'" and eventually led to cell death. Analysis of cell fractions by SDS-PAGE revealed a dominant ( >10% of total cell extract proteins ), clone-specific protein with a Mr of approximately 140'000 which was found exclusively in the cytoplasmic fraction. Conversely, 60% of the total CMC-hydrolyzing activity was localized in the periplasmic fraction indicating that the export of CenC is required for maximal expression of endoglucanase activity. Isolation of the cellulolytic activities from an osmotic shockate led to the purification to homogeneity of two recombinant cellulases, CenC1 and CenC2, with Mr of 130'000 and 120'000, respectively. Both enzymes hydrolyzed CMC with similar efficiencies ( 278u/mg protein for CenC1 and 390u/mg protein for CenC2 ). In addition, amino acid sequence analyses showed the two enzymes to have the same N-termini as the native enzymes and proved furthermore that the CenC leader peptide was functional in Escherichia coli.
Science, Faculty of
Microbiology and Immunology, Department of
Graduate
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Bates, Nancy Carol. "Characterization of cbg : a cloned gene encoding an extracellular [beta]-glucosidase from Cellulomonas fimi". Thesis, University of British Columbia, 1987. http://hdl.handle.net/2429/26163.

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A group of Escherichia coli clones harbouring recombinant pBR322 plasmid, containing Cellulomonas fimi DNA inserts, that reacted with antiserum to C.fimi culture supernatant, was screened for their ability to hydrolyze carboxymethyl cellulose (CMC) and 4-methylumbeliferyll-β-D-cellobioside (MUC). A clone, pEC62, hydrolyzed MUC but did not hydrolyze CMC. The recombinant enzyme encoded by pEC62 was shown to be a β-glucosidase (cellobiase). C.fimii itself was shown to encode an extracellular β-glucosidase in C.fimi. This is the first report of an extracellular β-glucosidase from a bacterium. Deletion analysis localized the cloned gene (cbg)to the tet promoter proximal region of the 7.0 kilobase insert of pEC62. Further analysis and sequence data showed a highly active derivative of pEC62 contained a translational gene fusion between lacZ of pUC13 and cbg. From this data, a location for the cbg start site was proposed.
Science, Faculty of
Microbiology and Immunology, Department of
Graduate
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Zhang, Ling 1962. "Molecular cloning and characterization of the chicken ornithine decarboxylase gene". Thesis, McGill University, 1994. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=22831.

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Ornithine decarboxylase (ODC) is the rate determining enzyme in the biosynthesis of polyamines which are essential for cell growth. In chickens, significantly higher bioactivity is reported in broiler than in egg layer strains of chickens (Bulfield et al., 1988). To characterize the genetic differences in growth rates and ODC levels in chickens, an ODC cDNA and genomic gene were cloned and sequenced. Sequencing of ODC cDNA revealed that this clone (pODZ3: 2,052 bp) was not a full length of ODC cDNA and contained 2 putative introns. The open reading frame (introns deleted) coded for a protein of 404 amino acids which had about 85% amino acid identity with human ODC. Sequencing of genomic ODC clone (pODG2-8: 5098 bp) represented the 3$ prime$ end of ODC gene from downstream of intron 7. Northern blotting of chicken RNA probed with the insert of pODZ3 revealed 2 hybridizable messages of 1.6 and 2.1 kb, respectively. In addition, analysis of MspI restriction fragment length polymorphism (RFLP) using the 3$ prime$ end of ODC gene as a probe suggested that two MspI RFLPs present in the lean line of broiler chickens was related to selection of high lean body mass.
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Książki na temat "Gene cloning"

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A, Lund Peter, i Minchin Steve, red. Gene cloning. New York: Taylor & Francis Group, 2007.

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Howe, Christopher. Gene Cloning and Manipulation. Wyd. 2. Leiden: Cambridge University Press, 2007.

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Gene cloning and manipulation. Cambridge [England]: Cambridge University Press, 1995.

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Brown, T. A. Gene cloning: An introduction. Wyd. 3. London: Chapman and Hall, 1995.

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Gene cloning: An introduction. Wyd. 2. London: Chapman and Hall, University and Professional Division, 1990.

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Winnacker, Ernst-L. From genes to clones: Introduction to gene technology. Weinheim: VCH, 1987.

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The ABCs of gene cloning. New York: Chapman & Hall, 1997.

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Wong, Dominic W. S. The ABCs of Gene Cloning. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-77982-9.

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Winnacker, Ernst-L. From genes to clones: Introduction to gene technology. Weinheim: VCH Verlagsgesellschaft, 1987.

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Canada. Library of Parliament, Science and Technology Division. Gene therapy, genetic alteration and cloning. Ottawa: Library of Parliament, 2000.

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Części książek na temat "Gene cloning"

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Peck, Stewart B., Carol C. Mapes, Netta Dorchin, John B. Heppner, Eileen A. Buss, Gustavo Moya-Raygoza, Marjorie A. Hoy i in. "Gene Cloning". W Encyclopedia of Entomology, 1587. Dordrecht: Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6359-6_1044.

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Wong, Tuck Seng, i Kang Lan Tee. "Gene Cloning". W A Practical Guide to Protein Engineering, 63–86. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-56898-6_5.

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Kriegler, Michael. "Expression Cloning". W Gene Transfer and Expression, 114–35. London: Palgrave Macmillan UK, 1990. http://dx.doi.org/10.1007/978-1-349-11891-5_7.

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Liu, Xue-Ting, i Ailin Tao. "Allergen Gene Cloning". W Allergy Bioinformatics, 105–19. Dordrecht: Springer Netherlands, 2015. http://dx.doi.org/10.1007/978-94-017-7444-4_7.

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Cortes, Mauricio, James R. Mensch, Miriam Domowicz i Nancy B. Schwartz. "Proteoglycans: Gene Cloning". W Methods in Molecular Biology, 3–21. Totowa, NJ: Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-498-8_1.

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McKenzie, Edward. "Hpa2 Gene Cloning". W Advances in Experimental Medicine and Biology, 787–805. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-34521-1_34.

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Wong, Dominic W. S. "Animal Cloning". W The ABCs of Gene Cloning, 213–17. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-77982-9_23.

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Gu, Weikuan, i Daniel Goldowitz. "Gene Discovery: From Positional Cloning to Genomic Cloning". W Gene Discovery for Disease Models, 1–9. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9780470933947.ch1.

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Habener, Joel F. "Approaches to Gene Cloning". W Molecular Cloning of Hormone Genes, 1–9. Totowa, NJ: Humana Press, 1987. http://dx.doi.org/10.1007/978-1-4612-4824-8_1.

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Wong, Dominic W. S. "Gene-Vector Construction". W The ABCs of Gene Cloning, 123–29. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-77982-9_10.

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Streszczenia konferencji na temat "Gene cloning"

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Zhang, Dong-Jie, i Di Liu. "Cloning and Expression Analysis of Wild Boar Osteopontin Gene". W 2009 3rd International Conference on Bioinformatics and Biomedical Engineering (iCBBE 2009). IEEE, 2009. http://dx.doi.org/10.1109/icbbe.2009.5162510.

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Shengjun Lv, Hongliang Xu, Pengchao Wang, Wenhui Li, Yaxuan Li i Yingkao Hu. "Cloning, phylogenetic and expression analysis of soybean ferritin gene". W 2011 International Conference on Remote Sensing, Environment and Transportation Engineering (RSETE). IEEE, 2011. http://dx.doi.org/10.1109/rsete.2011.5966091.

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Ding, Shan-shan, Yong Leng i Zhen-hui Song. "Cloning and Sequence Analysis of Rongchang Porcine Interferen-gamma Gene". W 2012 International Conference on Biomedical Engineering and Biotechnology (iCBEB). IEEE, 2012. http://dx.doi.org/10.1109/icbeb.2012.2.

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Fang, GuiJie, i XianFeng Qiao. "Molecular Cloning and Analysis of Hubei White Swine Myostatin Gene". W 2010 2nd International Conference on Information Engineering and Computer Science (ICIECS). IEEE, 2010. http://dx.doi.org/10.1109/iciecs.2010.5678159.

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Mo, Fan, Ya Luo, Cong Ge, Qin Mo, Yajie Ling, Shu Luo i Haoru Tang. "Cloning and expression analysis of FaPR-1 gene in strawberry". W 2017 INTERNATIONAL CONFERENCE ON BIOTECHNOLOGY AND BIOENGINEERING (ICBB-2017). Author(s), 2018. http://dx.doi.org/10.1063/1.5034261.

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Xiaojue Peng, Chao Yu, Shaobo Li, Youlin Zhu i Zuyu Chen. "Cloning and expressing an OsDCL3b gene from Oryza sativa indica". W 2011 International Conference on Remote Sensing, Environment and Transportation Engineering (RSETE). IEEE, 2011. http://dx.doi.org/10.1109/rsete.2011.5964037.

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Sakaguchi, Keishi, Noriyuki Sueyoshi i Makoto Ito. "cDNA CLONING, EXPRESSION, AND GENE KNOCKDOWN OF ZEBRAFISH LACTOSYLCERAMIDE SYNTHASE". W XXIst International Carbohydrate Symposium 2002. TheScientificWorld Ltd, 2002. http://dx.doi.org/10.1100/tsw.2002.715.

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Xie, Fangjie, Shanshan Tan, Jie Li i Mengyao Li. "Cloning and sequence analysis of BjuCYP1 gene in Brassica juncea". W 2ND INTERNATIONAL CONFERENCE ON FRONTIERS OF BIOLOGICAL SCIENCES AND ENGINEERING (FSBE 2019). AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0000361.

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Wang, Shuixing, Chen Zhen, Lianying Liu i Lingwei Wu. "Streptomyces ST66 Amylomaltase Gene Cloning and Expression and Production of Cycloamylose". W 2009 3rd International Conference on Bioinformatics and Biomedical Engineering (iCBBE). IEEE, 2009. http://dx.doi.org/10.1109/icbbe.2009.5163428.

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Yin, Heng, Xiaoming Zhao i Yuguang Du. "Cloning and Molecular Characterization of a SKP1 Gene from Brassica napus". W 2009 3rd International Conference on Bioinformatics and Biomedical Engineering (iCBBE). IEEE, 2009. http://dx.doi.org/10.1109/icbbe.2009.5162512.

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Raporty organizacyjne na temat "Gene cloning"

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Bertani, Giuseppe. Cloning and Gene Fusion for a Metalloprotein. Fort Belvoir, VA: Defense Technical Information Center, wrzesień 1987. http://dx.doi.org/10.21236/ada190914.

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Zamir, Dani, Steven Tanksley i Robert Fluhr. Cloning a Fusarium Resistance Gene in Tomato Based on Knowledge of its Map Position. United States Department of Agriculture, lipiec 1995. http://dx.doi.org/10.32747/1995.7604934.bard.

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The objectives of this project were to develop the tools and methodologies for positional cloning of genes in tomato and apply them for the cloning a Fusarium resistance gene - I2.. The feasibility of positional cloning of disease resistance genes was demonstrated for Pto which confers resistance to pseudomonas (Martin et al. 1993). The Fusarium resistance gene was mapped genetically and physically and was found to be in close proximity to TG 105 (Segal et al. 1992). To obtain fine mapping of gene I2, and additional target genes in future projects, a high density linkage map was developed (Tanksley et al. 1992; Broun and Tanksley 1993). In addition two permanent mapping populations were constructed: a recombinant inbred (Paran et al. 1995; Zamir et al. 1993) and an introgression line population (Eshed et al. 1992; Eshed and Zamir 1994). Using these resources we determined that the I2 locus shows complete co-segregation, down to a resolution of a few Kb, with SL8 which shows architectural similarity with other plant resistance genes. Transformation and complementation analysis is in progress (Ori et al. in preparation).
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Athwal, Raghbir S. Cloning and Characterization of a Cell Senescence Gene for Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, lipiec 2005. http://dx.doi.org/10.21236/ada452288.

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Conti, Claudio J. Identification and Cloning a Novel Tumor Suppressor Gene in Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, grudzień 1999. http://dx.doi.org/10.21236/ada382956.

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Kaiser, Ivan I. Crotoxin: Structural Studies, Mechanism of Action and Cloning of Its Gene. Fort Belvoir, VA: Defense Technical Information Center, marzec 1987. http://dx.doi.org/10.21236/adb110940.

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Kaiser, Ivan I. Crotoxin: Structural Studies, Mechanism of Action and Cloning of its Gene. Fort Belvoir, VA: Defense Technical Information Center, marzec 1988. http://dx.doi.org/10.21236/adb122454.

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Kaiser, Ivan I. Crotoxin: Structural Studies, Mechanism of Action and Cloning of Its Gene. Fort Belvoir, VA: Defense Technical Information Center, grudzień 1989. http://dx.doi.org/10.21236/adb148335.

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Dubcovsky, Jorge, Tzion Fahima i Ann Blechl. Positional cloning of a gene responsible for high grain protein content in tetraploid wheat. United States Department of Agriculture, wrzesień 2003. http://dx.doi.org/10.32747/2003.7695875.bard.

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High Grain Protein Content (GPC) is a desirable trait in breadmaking and pasta wheat varieties because of its positive effects on quality and nutritional value. However, selection for GPC is limited by our poor understanding of the genes involved in the accumulation of protein in the grain. The long-term goal of this project is to provide a better understanding of the genes controlling GPC in wheat. The specific objectives of this project were: a) to develop a high-density genetic map of the GPC gene in tetraploid wheat, b) to construct a T. turgidum Bacterial Artificial Chromosome (BAC) library, c) to construct a physical map of the GPC gene and identify a candidate for the GPC gene. A gene with a large effect on GPC was detected in Triticum turgidum var. dicoccoides and was previously mapped in the short arm of chromosome 6B. To define better the position of the Gpc-B1 locus we developed homozygous recombinant lines with recombination events within the QTL region. Except for the 30-cM region of the QTL these RSLs were isogenic for the rest of the genome minimizing the genetic variability. To minimize the environmental variability the RSLs were characterized using 10 replications in field experiments organized in a Randomized Complete Block Design, which were repeated three times. Using this strategy, we were able to map this QTL as a single Mendelian locus (Gpc-B1) on a 2.6-cM region flanked by RFLP markers Xcdo365 and Xucw67. All three experiments showed that the lines carrying the DIC allele had an average absolute increase in GPC of 14 g/kg. Using the RFLP flanking markers, we established the microcolinearity between a 2.l-cM region including the Gpc-B1 gene in wheat chromosome 6BS and a 350-kb region on rice chromosome 2. Rice genes from this region were used to screen the Triticeae EST collection, and these ESTs were used to saturate the Gpc-B1 region with molecular markers. With these new markers we were able to map the Gpc-B1 locus within a 0.3-cM region flanked by PCR markers Xucw83 and Xucw71. These flanking markers defined a 36-kb colinear region with rice, including one gene that is a potential candidate for the Gpc-B1 gene. To develop a physical map of the Gpc-B1 region in wheat we first constructed a BAC library of tetraploid wheat, from RSL#65 including the high Gpc-B1 allele. We generated half- million clones with an average size of l3l-kb (5.1 X genome equivalents for each of the two genomes). This coverage provides a 99.4% probability of recovering any gene from durum wheat. We used the Gpc-BI flanking markers to screen this BAC library and then completed the physical map by chromosome walking. The physical map included two overlapping BACs covering a region of approximately 250-kb, including two flanking markers and the Gpc-B1 gene. Efforts are underway to sequence these two BACs to determine if additional wheat genes are present in this region. Weare also developing new RSLs to further dissect this region. We developed PCR markers for flanking loci Xucw79andXucw71 to facilitate the introgression of this gene in commercial varieties by marker assisted selection (httQ://maswheat.ucdavis.edu/ orotocols/HGPC/index.hlm). Using these markers we introgressed the Gpc-B1 gene in numerous pasta and common wheat breeding lines.
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Athwal, Raghbir S. Cloning and Characterization of a Cell Senescence Gene for Breast Cancer Cells. Fort Belvoir, VA: Defense Technical Information Center, lipiec 2004. http://dx.doi.org/10.21236/ada443043.

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Glesne, D. A., i E. Huberman. Cloning, characterization, and regulation of the human type II IMP dehydrogenase gene. Office of Scientific and Technical Information (OSTI), styczeń 1997. http://dx.doi.org/10.2172/505306.

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