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Journal articles on the topic 'Gene cloning'

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Published: 4 June 2021
Last updated: 26 January 2023

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1

Hain, Patricia, and Donald Lee. "Gene Cloning." Journal of Natural Resources and Life Sciences Education 32, no. 1 (2003): 134. http://dx.doi.org/10.2134/jnrlse.2003.0134b.

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2

Murray, Noreen E. "Gene cloning." European Review 4, no. 04 (October 1996): 357. http://dx.doi.org/10.1017/s106279870000212x.

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3

Murray, Noreen E. "Gene cloning." European Review 4, no. 4 (October 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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4

Chin, Lee Ping, Tan Su Hui, and Douglas B. Furtek. "Cloning and Characterization of MADS-box Gene in Oil Palm." International Journal of Engineering and Technology 1, no. 4 (2009): 314–16. http://dx.doi.org/10.7763/ijet.2009.v1.62.

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5

Al-Kanany, Fadhil N., and Rasha M. Othman. "Cloning and Expression of Pseudomonas aeruginosa AlkB Gene in E. coli." Journal of Pure and Applied Microbiology 14, no. 1 (March 31, 2020): 389–96. http://dx.doi.org/10.22207/jpam.14.1.40.

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6

Ramsden, S. "Gene Cloning and Manipulation." Journal of Medical Genetics 33, no. 5 (May 1, 1996): 440. http://dx.doi.org/10.1136/jmg.33.5.440.

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7

Kayastha, Arvind M. "Gene Cloning and Manipulation." Biochemical Education 24, no. 1 (January 1996): 40. http://dx.doi.org/10.1016/s0307-4412(96)80007-0.

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8

Bennett, A. J. "Gene cloning and manipulation." Endeavour 20, no. 1 (January 1996): 44. http://dx.doi.org/10.1016/s0160-9327(96)90084-8.

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9

Moradas-Ferreira, Pedro. "Gene cloning and sequencing." Biochemical Education 17, no. 4 (October 1989): 215. http://dx.doi.org/10.1016/0307-4412(89)90153-2.

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10

Schamhart, Denis H. J., and Alex C. C. Westerhof. "Strategies for gene cloning." Urological Research 27, no. 2 (May 1999): 83–96. http://dx.doi.org/10.1007/s002400050093.

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11

Radford, Alan. "Gene cloning and manipulation." Trends in Genetics 12, no. 5 (May 1996): 199. http://dx.doi.org/10.1016/0168-9525(96)90065-7.

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12

Petty, Elizabeth M. "Gene cloning and manipulation." American Journal of Medical Genetics 75, no. 3 (January 23, 1998): 338. http://dx.doi.org/10.1002/(sici)1096-8628(19980123)75:3<338::aid-ajmg25>3.0.co;2-p.

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13

Burdon, Thomas G. "Gene cloning: An introduction." Analytical Biochemistry 192, no. 2 (February 1991): 458. http://dx.doi.org/10.1016/0003-2697(91)90566-c.

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14

Tang, D., H. Jiang, Y. Zhang, Y. Li, X. Zhang, and T. Zhou. "Cloning and sequencing of the complicated rDNA gene family of Bos taurus." Czech Journal of Animal Science 51, No. 10 (December 5, 2011): 425–28. http://dx.doi.org/10.17221/3960-cjas.

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The rDNA genes coding for ribosomal RNA (rRNA) in animals are repeat sequences with high GC content and complicated structure. Based on the sequences of human ribosomal DNA repeat unit and transcription unit and the long and accurate PCR method with LA Taq DNA polymerase and GC buffer, we were able to amplify the complicated repeat sequences of rDNA genes in Bos taurus. Three rDNA genes and 2 internal transcribed spacer (ITS) fragments were cloned and confirmed by sequencing. The conditions for the cloning of complicated DNA sequences such as special rules of primer design, improvement of the reaction system, selection of DNA polymerase and adjustment of cycle parameters were discussed. &nbsp;
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15

ALBERTI, SAVERIO, and LEONARD A. HERZENBERG. "DNA Transfection : Gene Regulation, Gene Amplification and Gene Cloning." Juntendo Medical Journal 32, no. 4 (1986): 423–25. http://dx.doi.org/10.14789/pjmj.32.423.

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16

Brown,, Tamara. "Gene Cloning and Colony Picking." Genetic Engineering & Biotechnology News 31, no. 19 (November 2011): 22–23. http://dx.doi.org/10.1089/gen.31.19.10.

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17

Smith, M. "Recent Advances in Gene Cloning." Forestry Chronicle 61, no. 5 (October 1, 1985): 423–24. http://dx.doi.org/10.5558/tfc61423b1-5.

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18

Ishihama, A. "Viruses as gene cloning vectors." Uirusu 36, no. 1 (1986): A1. http://dx.doi.org/10.2222/jsv.36.a1.

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19

ISHIURA, Masahiro. "Gene cloning from animal cells." Seibutsu Butsuri 26, no. 6 (1986): 268–81. http://dx.doi.org/10.2142/biophys.26.268.

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20

Chelly, Jamel, and Anthony P. Monaco. "Cloning the Wilson disease gene." Nature Genetics 5, no. 4 (December 1993): 317–18. http://dx.doi.org/10.1038/ng1293-317.

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21

Kunkel, Louis M. "Cloning of the DMD Gene*." American Journal of Human Genetics 76, no. 2 (February 2005): 205–14. http://dx.doi.org/10.1086/428143.

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22

Davies, Kevin. "Cloning the Menkes disease gene." Nature 361, no. 6407 (January 1993): 98. http://dx.doi.org/10.1038/361098a0.

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23

Nakahama, Kazuo, Koji Yoshimura, Ryuji Marumoto, Masakazu Kikuchi, In Sook Lee, Toshiharu Hase, and Hiroshi Matsubara. "Cloning and sequencing ofSerratiaprotease gene." Nucleic Acids Research 14, no. 14 (1986): 5843–55. http://dx.doi.org/10.1093/nar/14.14.5843.

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24

Lu, Quinn. "Seamless cloning and gene fusion." Trends in Biotechnology 23, no. 4 (April 2005): 199–207. http://dx.doi.org/10.1016/j.tibtech.2005.02.008.

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25

Taouis, Mohammed, Jin-Wen Chen, Christian Daviaud, Joelle Dupont, Michel Derouet, and Jean Simon. "Cloning the chicken leptin gene." Gene 208, no. 2 (February 1998): 239–42. http://dx.doi.org/10.1016/s0378-1119(97)00670-7.

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26

Bettgenhaeuser, Jan, and Simon G. Krattinger. "Rapid gene cloning in cereals." Theoretical and Applied Genetics 132, no. 3 (October 19, 2018): 699–711. http://dx.doi.org/10.1007/s00122-018-3210-7.

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27

Kawai, Shuji, Hiroyuki Honda, Takaaki Tanase, Masahito Taya, Shinji Iijima, and Takeshi Kobayashi. "Molecular Cloning ofRuminococcus albusCellulase Gene." Agricultural and Biological Chemistry 51, no. 1 (January 1987): 59–63. http://dx.doi.org/10.1080/00021369.1987.10867974.

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28

Tryggvason, Karl. "Cloning of Alport Syndrome Gene." Annals of Medicine 23, no. 3 (January 1991): 237–39. http://dx.doi.org/10.3109/07853899109148055.

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29

Boehm, Thomas. "Positional Cloning and Gene Identification." Methods 14, no. 2 (February 1998): 152–58. http://dx.doi.org/10.1006/meth.1997.0574.

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30

Zhu, Yanfei, Yanying Qu, and Melkamu Teshome Ayana. "Cloning Method for Stress-Resistant Gene of Conringia planisiliqua under Drought Stress." Journal of Healthcare Engineering 2021 (June 15, 2021): 1–10. http://dx.doi.org/10.1155/2021/3517002.

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The low temperature, drought, high salt, and other environments influence crop production and development directly, so the gene cloning method has become an effective biological means. In order to effectively improve the cloning effect, a gene cloning method for Conringia planisiliqua based on mRNA differential display technology was proposed. Based on mRNA differential display technology, the gene of Conringia planisiliqua was transcribed. The present study expects gene cloning to be better than the traditional method. This will lay the basis for gene cloning and functional verification of the transcription and disease-resistant proteins in Conringia planisiliqua. According to homologous identification results, the homologous drought-resistant genes were determined and screened. The data of Conringia planisiliqua in the existing biological database were used to extract ESTs data of Conringia planisiliqua. Then, the heating environment was established and the concept of integral function was introduced to express the influence of growth environment of different genomes. The mass, momentum, energy, and turbulent flow situation of stress-resistant gene of Conringia planisiliqua during the growth were satisfied. Finally, the data search was carried out in the NCBI database and gene cloning was achieved by ESTs data sequence. Experimental results show that the proposed method can effectively reduce the gene data fitting and improve the quantity of gene fragments cloned in a cycle, so the overall cloning effect is better.
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31

Thompson, Michael A., Eunpyo Moon, Ung-Jin Kim, Jingping Xu, Michael J. Siciliano, and Richard M. Weinshilboum. "Human Indolethylamine N-Methyltransferase: cDNA Cloning and Expression, Gene Cloning, and Chromosomal Localization." Genomics 61, no. 3 (November 1999): 285–97. http://dx.doi.org/10.1006/geno.1999.5960.

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32

Zhao, Weiguo, Rongfang Li, Dandan Chen, Dominic Kwame Kotoka, Renjie Sun, Yuanliang Deng, Feng Li, Jiao Qian, Rongjun fang, and Long Li. "Cloning and expression pattern analysis of MmPOD12 gene in mulberry under abiotic stresses." Journal of Experimental Biology and Agricultural Sciences 4, VIS (January 2, 2017): 698–705. http://dx.doi.org/10.18006/2016.4(vis).698.705.

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33

de Jong, Rob N., Mark A. Daniëls, Rob Kaptein, and Gert E. Folkers. "Enzyme Free Cloning for high throughput gene cloning and expression." Journal of Structural and Functional Genomics 7, no. 3-4 (December 2006): 109–18. http://dx.doi.org/10.1007/s10969-006-9014-z.

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34

Yosef, Ido, Noga Bloushtain, Michal Shapira, and Udi Qimron. "Restoration of Gene Function by Homologous Recombination: from PCR to Gene Expression in One Step." Applied and Environmental Microbiology 70, no. 12 (December 2004): 7156–60. http://dx.doi.org/10.1128/aem.70.12.7156-7160.2004.

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ABSTRACT We have developed a simple method for single-step cloning of any PCR product into a plasmid. A novel selection principle has been applied, in which activation of a drug selection marker is achieved following homologous recombination. In this method a DNA fragment is amplified by PCR with standard oligonucleotides that contain flanking tails derived from the host plasmid and the complete λPR or rrnA1 promoter regions. The resulting PCR product is then electroporated into an Escherichia coli strain harboring both the phage λ Red functions and the host plasmid. Upon homologous recombination of the PCR fragment into the plasmid, expression of a drug selection marker is fully induced due to restoration of its truncated promoter, thus allowing appropriate selection. Recombinant plasmid vectors encoding β-galactosidase and neomycin phosphotransferase were constructed by using this method in two well-known Red systems. This cloning strategy significantly reduces both the time and costs associated with cloning procedures.
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35

Son, Lo Thanh, Le Van Son, Nguyen Vu Thanh Thanh, and Chu Hoang Mau. "Cloning and Designing Vector Carrying GmEXP1 Gene Isolated from Local Soybean Cultivar Sonla, Vietnam." International Journal of Bioscience, Biochemistry and Bioinformatics 4, no. 3 (2014): 191–94. http://dx.doi.org/10.7763/ijbbb.2014.v4.337.

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36

Shoemaker, C. B., and L. D. Mitsock. "Murine erythropoietin gene: cloning, expression, and human gene homology." Molecular and Cellular Biology 6, no. 3 (March 1986): 849–58. http://dx.doi.org/10.1128/mcb.6.3.849-858.1986.

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The gene for murine erythropoietin (EPO) was isolated from a mouse genomic library with a human EPO cDNA probe. Nucleotide sequence analysis permitted the identification of the murine EPO coding sequence and the prediction of the encoded amino acid sequence based on sequence conservation between the mouse and human EPO genes. Both the coding DNA and the amino acid sequences were 80% conserved between the two species. Transformation of COS-1 cells with a mammalian cell expression vector containing the murine EPO coding region resulted in secretion of murine EPO with biological activity on both murine and human erythroid progenitor cells. The transcription start site for the murine EPO gene in kidneys was determined. This permitted tentative identification of the transcription control region. The region included 140 base pairs upstream of the cap site which was over 90% conserved between the murine and human genes. Surprisingly, the first intron and much of the 5'- and 3'-untranslated sequences were also substantially conserved between the genes of the two species.
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37

Shoemaker, C. B., and L. D. Mitsock. "Murine erythropoietin gene: cloning, expression, and human gene homology." Molecular and Cellular Biology 6, no. 3 (March 1986): 849–58. http://dx.doi.org/10.1128/mcb.6.3.849.

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The gene for murine erythropoietin (EPO) was isolated from a mouse genomic library with a human EPO cDNA probe. Nucleotide sequence analysis permitted the identification of the murine EPO coding sequence and the prediction of the encoded amino acid sequence based on sequence conservation between the mouse and human EPO genes. Both the coding DNA and the amino acid sequences were 80% conserved between the two species. Transformation of COS-1 cells with a mammalian cell expression vector containing the murine EPO coding region resulted in secretion of murine EPO with biological activity on both murine and human erythroid progenitor cells. The transcription start site for the murine EPO gene in kidneys was determined. This permitted tentative identification of the transcription control region. The region included 140 base pairs upstream of the cap site which was over 90% conserved between the murine and human genes. Surprisingly, the first intron and much of the 5'- and 3'-untranslated sequences were also substantially conserved between the genes of the two species.
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38

Hesketh, John E., and Kristine Partridge. "Gene cloning: Studies of nutritional regulation of gene expression." Proceedings of the Nutrition Society 55, no. 1B (March 1996): 575–81. http://dx.doi.org/10.1079/pns19960050.

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39

Schneider-Hirsch, Stefan, Uta-Maria Bauer, Reinhard Heiermann, Martin Rentrop, and Alfred Maelicke. "Cloning of the Human Ncnf Gene." Journal of Receptors and Signal Transduction 18, no. 1 (January 1998): 1–13. http://dx.doi.org/10.3109/10799899809039161.

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40

Nagamine, Kentaro, Pärt Peterson, Hamish S. Scott, Jun Kudoh, Shinsei Minoshima, Maarit Heino, Kai J. E. Krohn, et al. "Positional cloning of the APECED gene." Nature Genetics 17, no. 4 (December 1997): 393–98. http://dx.doi.org/10.1038/ng1297-393.

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41

Mirsky, Steve, and John Rennie. "What Cloning Means for Gene Therapy." Scientific American 276, no. 6 (June 1997): 121–23. http://dx.doi.org/10.1038/scientificamerican0697-121.

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42

He, Xiao-Ping, Zhao-Shen Li, Zhen-Xing Tu, Xue Pan, Yan-Fang Gong, Jun Gao, and Jing Jin. "Molecular cloning of human canstatin gene." World Chinese Journal of Digestology 12, no. 10 (2004): 2329. http://dx.doi.org/10.11569/wcjd.v12.i10.2329.

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43

Card, Charles O., Geoffrey G. Wilson, Karin Weule, Joseph Hasapes, Antal Kiss, and Richard J. Roberts. "Cloning and characterization of theHpallmethylase gene." Nucleic Acids Research 18, no. 6 (1990): 1377–83. http://dx.doi.org/10.1093/nar/18.6.1377.

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44

Hammond, E. M., and R. J. A. Grand. "CLONING OF AN APOPTOSIS SPECIFIC GENE." Biochemical Society Transactions 24, no. 4 (November 1, 1996): 572S. http://dx.doi.org/10.1042/bst024572s.

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45

Cooper, D. N., and J. Schmidtke. "HUMAN GENE CLONING AND DISEASE ANALYSIS." Lancet 329, no. 8527 (January 1987): 273. http://dx.doi.org/10.1016/s0140-6736(87)90090-0.

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46

Zan, Y. H., C. B. Dai, and R. Guo. "Synthesis and cloning of hirudin gene." Toxicon 35, no. 4 (April 1997): 494. http://dx.doi.org/10.1016/s0041-0101(97)84761-7.

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47

de Klein, A., A. Van Agthoven, D. Bootsma, and G. Grosveld. "Cloning of the mouse “bcr” gene." Leukemia Research 10, no. 7 (January 1986): 873. http://dx.doi.org/10.1016/0145-2126(86)90314-0.

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48

Radford, Alan. "Gene cloning — an introduction (3rd edn)." Trends in Genetics 12, no. 5 (May 1996): 199. http://dx.doi.org/10.1016/0168-9525(96)81438-7.

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49

Iijima, Shinji, Takeshi Uozumi, and Teruhiko Beppu. "Molecular Cloning ofThermus flavusMalate Dehydrogenase Gene." Agricultural and Biological Chemistry 50, no. 3 (March 1986): 589–92. http://dx.doi.org/10.1080/00021369.1986.10867438.

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50

Robertson, Debra. "“Gene,” another landmark in farmyard cloning." Nature Biotechnology 15, no. 9 (September 1997): 833. http://dx.doi.org/10.1038/nbt0997-833.

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