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Journal articles on the topic 'Animal cell culture'

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Published: 4 June 2021
Last updated: 13 February 2022

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1

Hall, P. "Animal Cell Culture." Journal of Clinical Pathology 43, no. 9 (September 1, 1990): 785. http://dx.doi.org/10.1136/jcp.43.9.785-a.

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2

McCarthy, Kevin J. "Animal cell culture." Transgenic Research 4, no. 2 (March 1995): 153. http://dx.doi.org/10.1007/bf01969419.

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3

Harris, Ian. "Animal cell culture." Biochemical Education 21, no. 4 (October 1993): 226. http://dx.doi.org/10.1016/0307-4412(93)90121-f.

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4

Shephard, Elizabeth A. "Animal cell culture." Endeavour 17, no. 4 (January 1993): 202. http://dx.doi.org/10.1016/0160-9327(93)90076-f.

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5

Mazie, J. C. "Animal cell culture." Biochimie 72, no. 12 (December 1990): 898. http://dx.doi.org/10.1016/0300-9084(90)90012-6.

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6

Märkl, Ing Herbert. "Animal cell culture technology." Journal of Biotechnology 34, no. 3 (May 1994): vii. http://dx.doi.org/10.1016/0168-1656(94)90056-6.

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7

Chatterton, Jean M. W., Susan McDonagh, and Darrel O. Ho-Yen. "Toxoplasma tachyzoites from cell culture are more appropriate in some situations." Journal of Clinical Pathology 63, no. 5 (April 1, 2010): 438–40. http://dx.doi.org/10.1136/jcp.2009.072066.

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BackgroundLaboratories traditionally culture toxoplasma tachyzoites in animals for testing and experimental use. This article considers why available cell culture methods are not used more often.AimTo compare HeLa cell culture and animal culture for production of toxoplasma tachyzoites.MethodsIn 2000 HeLa culture replaced animal culture for continuous production of toxoplasma tachyzoites in the Scottish Toxoplasma Reference Laboratory. The performance of animal culture (1994–1998) was compared with HeLa culture (2004–2008). A PubMed search was carried out for 1998 and 2008 to assess the culture methods used in laboratories.ResultsAnimal culture was able to produce higher yields of tachyzoites (109 from a cotton rat peritoneal harvest compared to 107 from a 75 cm2 cell culture flask) but significantly more HeLa cultures were successful (93% versus 84%; p=0.025). There was no difference in the quality of tachyzoites from animal and HeLa cultures as demonstrated by the high levels of success in the dye test. HeLa culture offered significant advantages in flexibility and control. A review of the literature showed no significant change in the method of culture used in laboratories between 1998 and 2008 (p=0.36).ConclusionThe availability of cell culture methods and the increasingly stringent regulations on the use of animals have not resulted in a decline in the use of animal culture. Animals are necessary for certain experiments but many studies could use cell-culture-derived parasites.
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8

Al-Rubeai, Mohamed, and A. Nicholas Emery. "Flow Cytometry in Animal Cell Culture." Nature Biotechnology 11, no. 5 (May 1993): 572–79. http://dx.doi.org/10.1038/nbt0593-572.

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9

Merten, Otto-Wilhelm. "Animal cell culture: A practical approach." Trends in Biochemical Sciences 11, no. 10 (October 1986): 412. http://dx.doi.org/10.1016/0968-0004(86)90170-2.

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10

Gooch, Keith J., and John A. Frangos. "Shear sensitivity in animal cell culture." Current Opinion in Biotechnology 4, no. 2 (April 1993): 193–96. http://dx.doi.org/10.1016/0958-1669(93)90124-f.

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11

Raxworthy, MJ. "Animal Cell Culture: A Practical Approach." Biochemical Education 15, no. 1 (January 1987): 53. http://dx.doi.org/10.1016/0307-4412(87)90173-7.

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12

Hassell, T., S. Gleave, and M. Butler. "Growth inhibition in animal cell culture." Applied Biochemistry and Biotechnology 30, no. 1 (July 1991): 29–41. http://dx.doi.org/10.1007/bf02922022.

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13

Gray, Tim. "Animal cell culture: A practical approach." Food and Chemical Toxicology 26, no. 8 (January 1988): 736–37. http://dx.doi.org/10.1016/0278-6915(88)90078-6.

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14

Yoshino, T. P., U. Bickham, and C. J. Bayne. "Molluscan cells in culture: primary cell cultures and cell lines." Canadian Journal of Zoology 91, no. 6 (June 2013): 391–404. http://dx.doi.org/10.1139/cjz-2012-0258.

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In vitro cell culture systems from molluscs have significantly contributed to our basic understanding of complex physiological processes occurring within or between tissue-specific cells, yielding information unattainable using intact animal models. In vitro cultures of neuronal cells from gastropods show how simplified cell models can inform our understanding of complex networks in intact organisms. Primary cell cultures from marine and freshwater bivalve and gastropod species are used as biomonitors for environmental contaminants, as models for gene transfer technologies, and for studies of innate immunity and neoplastic disease. Despite efforts to isolate proliferative cell lines from molluscs, the snail Biomphalaria glabrata (Say, 1818) embryonic (Bge) cell line is the only existing cell line originating from any molluscan species. Taking an organ systems approach, this review summarizes efforts to establish molluscan cell cultures and describes the varied applications of primary cell cultures in research. Because of the unique status of the Bge cell line, an account is presented of the establishment of this cell line, and of how these cells have contributed to our understanding of snail host – parasite interactions. Finally, we detail the difficulties commonly encountered in efforts to establish cell lines from molluscs and discuss how these difficulties might be overcome.
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15

NAGAMINE, Kenichi, and Masato SHIRAISHI. "Cultured mammalian cells for production of bioactive macromolecules. Cell attachment factors for animal cell culture." Journal of the agricultural chemical society of Japan 63, no. 2 (1989): 196–99. http://dx.doi.org/10.1271/nogeikagaku1924.63.196.

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16

Merten, Otto-Wilhelm. "Concentrating mammalian cells I. large-scale animal cell culture." Trends in Biotechnology 5, no. 8 (August 1987): 230–37. http://dx.doi.org/10.1016/0167-7799(87)90053-9.

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17

Chisti, Yusuf. "Science and technology of animal cell culture." Biotechnology Advances 26, no. 5 (September 2008): 501. http://dx.doi.org/10.1016/j.biotechadv.2008.04.006.

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18

Griffin, Gilly. "Book Review: Bioprocesses Including Animal Cell Culture." Alternatives to Laboratory Animals 17, no. 4 (June 1990): 412. http://dx.doi.org/10.1177/026119299001700414.

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19

Lavery, M., and A. W. Nienow. "Oxygen transfer in animal cell culture medium." Biotechnology and Bioengineering 30, no. 3 (August 20, 1987): 368–73. http://dx.doi.org/10.1002/bit.260300307.

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20

Beuvery, E. Coen. "Animal cell culture: Towards the 21st century." Cytotechnology 18, no. 1-2 (1995): 1–2. http://dx.doi.org/10.1007/bf00744312.

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21

Scheirer, Winfried. "Laboratory management of animal cell culture processes." Trends in Biotechnology 5, no. 9 (September 1987): 261–65. http://dx.doi.org/10.1016/0167-7799(87)90103-x.

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22

Griffiths, J. B. "Animal cell culture processes - batch or continuous?" Journal of Biotechnology 22, no. 1-2 (January 1992): 21–30. http://dx.doi.org/10.1016/0168-1656(92)90129-w.

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23

Kremkow, Benjamin G., and Kelvin H. Lee. "Sequencing technologies for animal cell culture research." Biotechnology Letters 37, no. 1 (September 12, 2014): 55–65. http://dx.doi.org/10.1007/s10529-014-1660-9.

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24

Skottman, Heli, and Outi Hovatta. "Culture conditions for human embryonic stem cells." Reproduction 132, no. 5 (November 2006): 691–98. http://dx.doi.org/10.1530/rep.1.01079.

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Human embryonic stem cell (hESC) lines have been derived and cultured in variable conditions. The idea behind derivation of hESC lines is to use them in human cell transplantation after differentiation, but already now these cells are widely used for research purposes. Despite similarities among the established lines, important differences have been reported between them, and it has been difficult to compare the results obtained using different lines. Recent optimization of hESC culture conditions has moved from cultures on mouse embryonic fibroblasts (MEFs) in fetal bovine serum-containing medium towards feeder-free culture methods using more defined animal substance-free cultures. The aim has been to establish robust and cost-effective systems for culturing these cells and eliminate the risk of infection transmitted by animal pathogens and immunoreactions caused by animal substances in cell cultures before clinical treatment. It is important to take these modifications into account when carrying out research using these cells. It is known that culture conditions influence gene expression and, hence, probably many properties of the cells. Optimization and standardization of culture methods is needed for research as well as for clinical purposes.
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25

Matsumura, Masatoshi. "Application of Membrane Separation in Animal Cell Culture." membrane 18, no. 6 (1993): 347–56. http://dx.doi.org/10.5360/membrane.18.347.

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26

Lydersen, Bjorn K., Gordon G. Pugh, Martin S. Paris, Bhavender P. Sharma, and Lee A. Noll. "Ceramic Matrix for Large Scale Animal Cell Culture." Nature Biotechnology 3, no. 1 (January 1985): 63–67. http://dx.doi.org/10.1038/nbt0185-63.

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27

Balls, Michael. "Book Review: Animal Cell Culture: A Practical Approach." Alternatives to Laboratory Animals 13, no. 4 (June 1985): 304. http://dx.doi.org/10.1177/026119298501300415.

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28

Clothier, Richard. "Book Review: Trends in Animal Cell Culture Technology." Alternatives to Laboratory Animals 19, no. 4 (October 1991): 450. http://dx.doi.org/10.1177/026119299101900413.

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29

Croughan, Matthew Shane, Jean-Fran�ois P. Hamel, and Daniel I. C. Wang. "Effects of microcarrier concentration in animal cell culture." Biotechnology and Bioengineering 32, no. 8 (October 5, 1988): 975–82. http://dx.doi.org/10.1002/bit.260320805.

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30

Perry, Steven D., and Daniel I. C. Wang. "Fiber bed reactor design for animal cell culture." Biotechnology and Bioengineering 34, no. 1 (June 5, 1989): 1–9. http://dx.doi.org/10.1002/bit.260340102.

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31

MURAKAMI, Hiroki. "Technology of animal cell culture and substance production." Kagaku To Seibutsu 24, no. 1 (1986): 34–42. http://dx.doi.org/10.1271/kagakutoseibutsu1962.24.34.

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32

Jang, Juno, Soo-Jin Moon, Sung-Hwan Hong, and Ik-Hwan Kim. "Colorimetric pH measurement of animal cell culture media." Biotechnology Letters 32, no. 11 (July 6, 2010): 1599–607. http://dx.doi.org/10.1007/s10529-010-0341-6.

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33

Croughan, Matthew, Sean Delfosse, and Kirilynn Svay. "Microbial contamination in industrial animal cell culture operations." Pharmaceutical Bioprocessing 2, no. 1 (February 2014): 23–25. http://dx.doi.org/10.4155/pbp.13.67.

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34

Nienow, Alvin W. "Reactor Engineering in Large Scale Animal Cell Culture." Cytotechnology 50, no. 1-3 (March 2006): 9–33. http://dx.doi.org/10.1007/s10616-006-9005-8.

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35

Ryder, Oliver A., and Manabu Onuma. "Viable Cell Culture Banking for Biodiversity Characterization and Conservation." Annual Review of Animal Biosciences 6, no. 1 (February 15, 2018): 83–98. http://dx.doi.org/10.1146/annurev-animal-030117-014556.

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36

Spier, R. E. "Animal cells in culture are microorganisms." Cytotechnology 8, no. 2 (June 1992): 89–92. http://dx.doi.org/10.1007/bf02525490.

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37

FUJIYOSHI, NOBUO. "New trends of animal cell engineering.(1).2.Present situation of animal cell high-density culture." Kagaku To Seibutsu 31, no. 1 (1993): 61–65. http://dx.doi.org/10.1271/kagakutoseibutsu1962.31.61.

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38

Zhang, Lei, Mingsheng Li, Zhongren Ma, and Yuping Feng. "Synthesis of DEAE-Soybean Starch Microspheres for Adhere Animal Cell Culture." Journal of Agricultural Science 9, no. 8 (July 18, 2017): 91. http://dx.doi.org/10.5539/jas.v9n8p91.

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The present study outlines the synthesis of a new microcarrier for anchorage-dependent animal cell cultures. The new microcarriers were synthesized from the cross-linking soybean starch microspheres followed by modification with 2-diethylaminoethyl (DEAE). Furthermore, 5 g/100 mL of wet microspheres DEAE-soybean starch microspheres were applied in the adhere cell culture, with an inoculation density 2.0 × 105 cells/mL of BHK-21, Marc-145, and MDCK cells. The cells were shown to grow well in the DEAE-soybean starch microcarrier, with BHK-21 cells showing a higher cell density after 144 h (2.5 × 106 cells/mL) compared to cells grown on the commercial product Cytodex 1 (2.2 × 106 cells/mL). These starch microcarriers have a potential application in anchorage-dependent animal cells culture, due to its low cost and its simple process.
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39

Nema, Rajeev, and Sarita Khare. "An animal cell culture: Advance technology for modern research." Advances in Bioscience and Biotechnology 03, no. 03 (2012): 219–26. http://dx.doi.org/10.4236/abb.2012.33030.

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40

Tekkatte, Chandana, Gency Ponrose Gunasingh, K. M. Cherian, and Kavitha Sankaranarayanan. "“Humanized” Stem Cell Culture Techniques: The Animal Serum Controversy." Stem Cells International 2011 (2011): 1–14. http://dx.doi.org/10.4061/2011/504723.

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Cellular therapy is reaching a pinnacle with an understanding of the potential of human mesenchymal stem cells (hMSCs) to regenerate damaged tissue in the body. The limited numbers of these hMSCs in currently identified sources, like bone marrow, adipose tissue, and so forth, bring forth the need for theirin vitroculture/expansion. However, the extensive usage of supplements containing xenogeneic components in the expansion-media might pose a risk to the post-transplantation safety of patients. This warrants the necessity to identify and develop chemically defined or “humanized” supplements which would makein vitrocultured/processed cells relatively safer for transplantation in regenerative medicine. In this paper, we outline the various caveats associated with conventionally used supplements of xenogenic origin and also portray the possible alternatives/additives which could one day herald the dawn of a new era in the translation ofin vitrocultured cells to therapeutic interventions.
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41

Sanderson, C. S., J. P. Barford, and G. W. Barton. "A structured, dynamic model for animal cell culture systems." Biochemical Engineering Journal 3, no. 3 (June 1999): 203–11. http://dx.doi.org/10.1016/s1369-703x(99)00021-2.

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42

Oyeleye, O. O., S. T. Ogundeji, S. I. Ola, and O. G. Omitogun. "Basics of animal cell culture: Foundation for modern science." Biotechnology and Molecular Biology Reviews 11, no. 2 (October 31, 2016): 6–16. http://dx.doi.org/10.5897/bmbr2016.0261.

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43

Arifin, Mohd Azmir, Maizirwan Mel, Nurhusna Samsudin, Yumi Zuhanis Has-Yun Hashim, Hamzah Mohd Salleh, Iis Sopyan, and Norshariza Nordin. "Ultraviolet/ozone treated polystyrene microcarriers for animal cell culture." Journal of Chemical Technology & Biotechnology 91, no. 10 (December 29, 2015): 2607–19. http://dx.doi.org/10.1002/jctb.4855.

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44

Mozdziak, Paul E., James N. Petitte, and Susan D. Carson. "An introductory undergraduate course covering animal cell culture techniques." Biochemistry and Molecular Biology Education 32, no. 5 (September 2004): 319–22. http://dx.doi.org/10.1002/bmb.2004.494032050381.

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45

Yao, Tatsuma, and Yuta Asayama. "Animal-cell culture media: History, characteristics, and current issues." Reproductive Medicine and Biology 16, no. 2 (March 21, 2017): 99–117. http://dx.doi.org/10.1002/rmb2.12024.

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46

Croughan, Matthew Shane, Elizabeth S. Sayre, and Daniel I. C. Wang. "Viscous reduction of turbulent damage in animal cell culture." Biotechnology and Bioengineering 33, no. 7 (February 20, 1989): 862–72. http://dx.doi.org/10.1002/bit.260330710.

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47

Jöbses, I., D. Martens, and J. Tramper. "Lethal events during gas sparging in animal cell culture." Biotechnology and Bioengineering 37, no. 5 (March 5, 1991): 484–90. http://dx.doi.org/10.1002/bit.260370510.

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48

Nayve, Fidel Rey P., Masamichi Motoki, Masatoshi Matsumura, and Hiroshi Kataoka. "Selective removal of ammonia from animal cell culture broth." Cytotechnology 6, no. 2 (June 1991): 121–30. http://dx.doi.org/10.1007/bf00373029.

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49

Sanderson, C. "Optimisation of animal cell culture media using dynamic simulation." Computers & Chemical Engineering 19, no. 1 (June 11, 1995): S681—S686. http://dx.doi.org/10.1016/0098-1354(95)00139-s.

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50

Sanderson, C. S., G. W. Barton, and J. P. Barford. "Optimisation of animal cell culture media using dynamic simulation." Computers & Chemical Engineering 19 (June 1995): 681–86. http://dx.doi.org/10.1016/0098-1354(95)87114-4.

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