Gotowe bibliografie tematyczne / Tissue culture

Spis treści

  1. Artykuły w czasopismach
  2. Rozprawy doktorskie
  3. Książki
  4. Części książek
  5. Streszczenia konferencji
  6. Raporty organizacyjne

Gotowa bibliografia na temat „Tissue culture”

Autor: Grafiati
Data publikacji: 4 czerwca 2021
Data aktualizacji: 25 lipca 2025

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Artykuły w czasopismach na temat "Tissue culture"

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Jia, Zhidong, Yuan Cheng, Xinan Jiang, et al. "3D Culture System for Liver Tissue Mimicking Hepatic Plates for Improvement of Human Hepatocyte (C3A) Function and Polarity." BioMed Research International 2020 (March 4, 2020): 1–22. http://dx.doi.org/10.1155/2020/6354183.

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In vitro 3D hepatocyte culture constitutes a core aspect of liver tissue engineering. However, conventional 3D cultures are unable to maintain hepatocyte polarity, functional phenotype, or viability. Here, we employed microfluidic chip technology combined with natural alginate hydrogels to construct 3D liver tissues mimicking hepatic plates. We comprehensively evaluated cultured hepatocyte viability, function, and polarity. Transcriptome sequencing was used to analyze changes in hepatocyte polarity pathways. The data indicate that, as culture duration increases, the viability, function, polari
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McGreevy, Owen, Timothy Gilbert, Maria-Danae Jessel, et al. "A Preclinical Model of Human Liver Using Precision Cut Tissue Slice Culture." F1000Research 14 (June 10, 2025): 571. https://doi.org/10.12688/f1000research.162495.1.

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Preclinical models vary in complexity and cost. Traditional 2D cell cultures that are high throughput and cost effective, but lack the complexity of multicellular interactions. Animal models and more complex, but are costly, raise ethical concerns and are not a human model to better understand human disease or response to novel treatments. Human precision cut tissue slice (hPCTS) models bridge this gap, maintaining the architecture and microenvironment of original tissues. This study examines the viability and functionality of hPCTS using different tissue culture formats. Previous studies have
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Shrestha, Sunil, Vinod Kumar Reddy Lekkala, Prabha Acharya, Darshita Siddhpura, and Moo-Yeal Lee. "Recent advances in microarray 3D bioprinting for high-throughput spheroid and tissue culture and analysis." Essays in Biochemistry 65, no. 3 (2021): 481–89. http://dx.doi.org/10.1042/ebc20200150.

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Abstract Three-dimensional (3D) cell culture in vitro has proven to be more physiologically relevant than two-dimensional (2D) culture of cell monolayers, thus more predictive in assessing efficacy and toxicity of compounds. There have been several 3D cell culture techniques developed, which include spheroid and multicellular tissue cultures. Cell spheroids have been generated from single or multiple cell types cultured in ultralow attachment (ULA) well plates and hanging droplet plates. In general, cell spheroids are formed in a relatively short period of culture, in the absence of extracellu
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Peel, Trisha N., Tim Spelman, Brenda L. Dylla, et al. "Optimal Periprosthetic Tissue Specimen Number for Diagnosis of Prosthetic Joint Infection." Journal of Clinical Microbiology 55, no. 1 (2016): 234–43. http://dx.doi.org/10.1128/jcm.01914-16.

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ABSTRACTWe recently demonstrated improved sensitivity of prosthetic joint infection (PJI) diagnosis using an automated blood culture bottle system for periprosthetic tissue culture [T. N. Peel et al., mBio 7(1):e01776-15, 2016,https://doi.org/10.1128/mBio.01776-15]. This study builds on the prior research by examining the optimal number of periprosthetic tissue specimens required for accurate PJI diagnosis. Current guidelines recommend five to six, which is impractical. We applied Bayesian latent class modeling techniques for estimating diagnostic test properties of conventional culture techni
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Şükrüoğlu Erdoğan, Özge, Seda Kılıç Erciyas, Ayhan Bilir, et al. "Methylation Changes of Primary Tumors, Monolayer, and Spheroid Tissue Culture Environments in Malignant Melanoma and Breast Carcinoma." BioMed Research International 2019 (January 17, 2019): 1–9. http://dx.doi.org/10.1155/2019/1407167.

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Epigenetic changes have major role in the normal development and programming of gene expression. Aberrant methylation results in carcinogenesis. The primary objective of our study is to determine whether primary tumor tissue and cultured tumor cells in 2D and 3D tissue culture systems have the same methylation signature forPAX5,TMPRSS2, andSBDS. These findings will play an important role in developing in vitro model system to understand the effect of methylation inhibitors on primary tumor tissue. In a previous studyPAX5,TMPRSS2, andSBDSgenes that we are investigating were reported to be methy
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Linsler, S., A. Moroldo, J. Oertel, and S. Urbschat. "P18.05.A THE GROWTH PATTERN OF MENINGIOMA CELLS IN CELL CULTURE UNDER DIFFERENT CONDITIONS." Neuro-Oncology 25, Supplement_2 (2023): ii122—ii123. http://dx.doi.org/10.1093/neuonc/noad137.413.

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Abstract BACKGROUND Cell cultures is an established method in tumor research. Thereby, the growth rate is important for the results. Depending on the experimental and clinical setting, the used tissue is exposed to different conditions. Interestingely, the different cell and tissue conditions are not well reported yet. Although, it is likely that the different conditions influence the growth pattern of cell cultures in primary cell lines. Here, the authors present their experimental analysis of cell culture of primary meningioma cells after different initial tissue conditions. MATERIAL AND MET
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Stokes, Rebecca A., Michelle C. Coleman, Artem S. Rogovskyy, Vanna M. Dickerson, and Kelley M. Thieman Mankin. "Comparison of bacteriologic culture results for skin wound swabs and skin wound biopsy specimens." Journal of the American Veterinary Medical Association 259, no. 12 (2021): 1416–21. http://dx.doi.org/10.2460/javma.20.10.0568.

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Abstract OBJECTIVE To compare bacteriologic culture results for superficial swab and tissue biopsy specimens obtained from dogs with open skin wounds. ANIMALS 52 client-owned dogs. PROCEDURES For each dog, 1 wound underwent routine preparation prior to collection of 2 specimens, 1 by superficial swab (Levine) technique and 1 by tissue biopsy. Specimens were processed for bacteriologic culture. Two observers determined whether any detected difference in culture results for the 2 types of specimen would have resulted in differing treatment plans. RESULTS Culture results of swab and tissue biopsy
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Lee, Yoonjung, Ahrang Lee, Hae Seong Jeong, et al. "The microbiology of periprosthetic joint infections as revealed by sonicate cultures in Korea: Routine use of fungal and mycobacterial cultures is necessary?" PLOS ONE 19, no. 8 (2024): e0309046. http://dx.doi.org/10.1371/journal.pone.0309046.

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Background Although sonication is a valuable diagnostic tool for periprosthetic joint infections (PJI), it is not commonly utilized. We analyzed sonicate and intraoperative tissue culture results obtained from three hospitals to define the microbial etiology of PJIs in Korea. Furthermore, we investigated necessity of conducting regular fungal and mycobacterial cultures. Methods We retrospectively analyzed data for patients with suspected orthopedic-related infections between 2017 and 2022, who had undergone prostheses removal surgery. We included 193 patients with suspected PJIs, and bacterial
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Prakash, Jitendra. "Plant Tissue Culture." Nature Biotechnology 9, no. 7 (1991): 607. http://dx.doi.org/10.1038/nbt0791-607.

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Ezzell, Carol. "Tissue culture tools." Nature 327, no. 6119 (1987): 256–58. http://dx.doi.org/10.1038/327256a0.

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Rozprawy doktorskie na temat "Tissue culture"

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Bapat, S. "Tissue culture in cereals." Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 1992. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/3020.

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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.

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Arunyanart, 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/.

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The use of two in vitro techniques for Chrysanthemum improvement were studied. Firstly, the direction and extent of somaclonal variation was observed using different explants from cultivars with a range of flower shape and colour. Secondly, an attempt was made to produce chimaeras from mixed calluses. Tissue culture methods were developed for callus induction and shoot regeneration from 6 cultivars of Chrysanthemum morifolium and for C. carinaturn (Syn. C. tricolour), C. parthenium (Pyrethrum) and Aster novi-belqii (Michaelmas daisy) which were included in the chimaera work. Flower col
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Jana, M. M. "Studies on plant tissue culture." Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 1998. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/3394.

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Sagare, A. P. "Tissue culture in grain legumes." Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 1996. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/3389.

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Brons, 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.

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Rathbone, Sandra. "Dynamic culture of tissue engineered ligaments." Thesis, Keele University, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.534314.

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Morwal, G. C. "Biochemical studies in plant tissue culture." Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 1994. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/2826.

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Muralidharan, E. M. "Biochemical studies in plant tissue culture." Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 1990. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/2976.

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Cousineau, 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.

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Starch gel electrophoresis and isoenzyme staining were studied in raspberry (Rubus idaeus L., R. X neglectus Peck, and R. occidentalis L.). Seven isoenzymes could be separated using one of two gel-electrophoresis buffers: tris-citric acid at pH 7.1 for aconitase (ACO), isocitrate dehydrogenase (IDH), phosphoglucomutase (PGM), and triose phosphate isomerase (TPI) and histidine-citric acid at pH 5.7 for malate dehydrogenase (MDH), phosphoglucoisomerase (PGI), and shikimate dehydrogenase (SKDH). There were no variations detected between samples obtained from micropropagated shoots, greenhouse-, o
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Książki na temat "Tissue culture"

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Laimer, Margit, and Waltraud Rücker, eds. Plant Tissue Culture. Springer Vienna, 2003. http://dx.doi.org/10.1007/978-3-7091-6040-4.

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Martin, Bernice M. Tissue Culture Techniques. Birkhäuser Boston, 1994. http://dx.doi.org/10.1007/978-1-4612-0247-9.

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S, Islam A., ed. Plant tissue culture. Science Publishers, 1996.

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Kumar, Sandeep. Plant tissue culture. Tropical Forest Research Institute, 1997.

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Tisserat, Brent. Palm tissue culture. U.S. Dept. of Agriculture, Agricultural Research Service, 1988.

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Siddiqui, Zahid Hameed, and Khalid Rehman Hakeem. Plant Tissue Culture. Apple Academic Press, 2025. https://doi.org/10.1201/9781003557944.

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Mitsuhashi, Jun. Invertebrate tissue culture methods. Springer, 2002.

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Mitsuhashi, Jun. Invertebrate tissue culture methods. Springer, 2002.

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Duray, Paul H. Tissue culture in microgravity. National Aeronautics and Space Administration, 1997.

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Gupta, S. Dutta, and Yasuomi Ibaraki, eds. Plan Tissue Culture Engineering. Springer Netherlands, 2006. http://dx.doi.org/10.1007/978-1-4020-3694-1.

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Części książek na temat "Tissue culture"

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Yoon, Jeong-Yeol. "Cell Culture." In Tissue Engineering. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-83696-2_2.

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Priyadarshan, P. M. "Tissue Culture." In PLANT BREEDING: Classical to Modern. Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-7095-3_21.

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Taylor, N. L., and K. H. Quesenberry. "Tissue Culture." In Red Clover Science. Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-015-8692-4_14.

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Wenzel, Friedel. "Tissue Culture." In Diagnostic Cytogenetics. Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/978-3-642-59918-7_1.

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Singh, Anil Kumar, Gyanendra Kumar Rai, Sreshti Bagati, and Sanjeev Kumar. "Tissue Culture." In Strawberries. CRC Press, 2019. http://dx.doi.org/10.1201/b21441-193.

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Gooch, Jan W. "Tissue Culture." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_14970.

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Rupert, E. A., and G. B. Collins. "Tissue Culture." In Agronomy Monographs. American Society of Agronomy, Crop Science Society of America, Soil Science Society of America, 2015. http://dx.doi.org/10.2134/agronmonogr25.c16.

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Martin, Bernice M. "Culture Changes." In Tissue Culture Techniques. Birkhäuser Boston, 1994. http://dx.doi.org/10.1007/978-1-4612-0247-9_8.

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Reddy, Jayarama. "Types of Plant Tissue Culture-Organ Culture." In Plant Tissue Culture. CRC Press, 2023. http://dx.doi.org/10.1201/9781032712611-8.

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Loyola-Vargas, Víctor M., C. De-la-Peña, R. M. Galaz-Ávalos, and F. R. Quiroz-Figueroa. "Plant Tissue Culture." In Springer Protocols Handbooks. Humana Press, 2008. http://dx.doi.org/10.1007/978-1-60327-375-6_50.

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Streszczenia konferencji na temat "Tissue culture"

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Magni, Giada, Martina Banchelli, Leonardo Ciaccheri, et al. "In vitro analysis on the interaction between cell culture medium and blue LED light." In Optical Interactions with Tissue and Cells XXXVI, edited by Joel N. Bixler, Norbert Linz, and Alex J. Walsh. SPIE, 2025. https://doi.org/10.1117/12.3043442.

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Bhatia, Sangeeta N., Martin L. Yarmush, and Mehmet Toner. "Engineered Substrates for Controlling Cell-Cell Interactions." In ASME 1997 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 1997. http://dx.doi.org/10.1115/imece1997-1319.

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Abstract Biomaterials have been previously engineered to serve a variety of different functions: precise degradation in vivo (Kimura, 1993), modulation of cell physiology via binding to specific ligands (Hubbell et al, 1992), and selective permeability of certain solutes (Lysaght et al, 1994). However, in complex tissues, where cell-cell interactions strongly influence tissue function, biomaterials which modulate this fundamental parameter have not been available. In this study, we describe a technique which allows control over cell-cell interactions by using semiconductor-based microfabricati
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Sathisrajan, N., H. M. A. Chandeep, S. C. Rathnayake, Samitha Vidhanaarachchi, and V. R. M. Vidhanaarachchi. "Advanced Plant Growth Recognition Model with Deep Learning for the Coconut Tissue Culture." In 2024 9th International Conference on Information Technology Research (ICITR). IEEE, 2024. https://doi.org/10.1109/icitr64794.2024.10857788.

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Yongkun Yu and Qingpeng Sun. "Aloe tissue culture technology." In 2011 International Conference on Remote Sensing, Environment and Transportation Engineering (RSETE). IEEE, 2011. http://dx.doi.org/10.1109/rsete.2011.5965875.

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Li, Nan-Yu, Hao-Ru Tang, Cong Ge, Fan Mo, Yi-Hu Xiao, and Ya Luo. "Tissue culture of Lavandula angustifolia L." In 2018 INTERNATIONAL CONFERENCE ON BIOTECHNOLOGY AND BIOENGINEERING (8TH ICBB). Author(s), 2019. http://dx.doi.org/10.1063/1.5092392.

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Pivovarova, N. S., T. S. Shebitchenko, and A. G. Podboronova. "Obtaining tissue culture of Scutellaria baicalensis." In 2nd International Scientific Conference "Plants and Microbes: the Future of Biotechnology". PLAMIC2020 Organizing committee, 2020. http://dx.doi.org/10.28983/plamic2020.198.

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The work is devoted to the obtaining of callus culture of Scutellaria baicalensis from sterile microcuttings. Cultivation conditions were determined, growth activity was studied, and a qualitative analysis was carried out.
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Boepple, Kathrin, Meng Dong, Emma Davis, et al. "Abstract 5040: Perfusion air culture of tissue slices: A new method to cultivate tumor tissue with minimal culture-dependent tissue stress." In Proceedings: AACR Annual Meeting 2018; April 14-18, 2018; Chicago, IL. American Association for Cancer Research, 2018. http://dx.doi.org/10.1158/1538-7445.am2018-5040.

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Ou, Ri-Ming, Fang-Hua Niu, Yu-Jie Yang, and Zhi-Hui Li. "The Tissue Culture Technique of Sloanea hemsleyana." In 2015 International Conference on Medicine and Biopharmaceutical. WORLD SCIENTIFIC, 2016. http://dx.doi.org/10.1142/9789814719810_0182.

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Suganuma, Lisa, Hiromichi Fujie, Hiroki Sudama, et al. "Nanostructure Processed on Culture Plate Improves Cell Adhesion." In ASME 2011 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2011. http://dx.doi.org/10.1115/sbc2011-53753.

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Ligaments and tendons have superior functions, but their healing capacities are limited. We have been developing a novel tissue-engineering technique for the repair of ligaments and tendons which involve stem cell-based self-assembled tissues (scSAT) derived from synovium[1]. For biological reconstruction of soft tissues, it is required for the scSAT to have high tensile strength. Our previous study indicted that, when the scSAT was cultured under high cell density condition, the tensile strength of the scSAT become higher than that cultured under low density condition[2]. However, the scSAT h
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Matsumoto, Takuya, and Seiji Aoyagi. "Removing mesenchymal cells from gland tissue on micro-patterned tissue culture dish." In 2012 International Symposium on Micro-NanoMechatronics and Human Science (MHS). IEEE, 2012. http://dx.doi.org/10.1109/mhs.2012.6492441.

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Raporty organizacyjne na temat "Tissue culture"

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Scott, C. D., and D. K. Dougall. Plant cell tissue culture: A potential source of chemicals. Office of Scientific and Technical Information (OSTI), 1987. http://dx.doi.org/10.2172/5938126.

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Ostry, M. E., and K. T. Ward. Bibliography of Populus cell and tissue culture. U.S. Department of Agriculture, Forest Service, North Central Forest Experiment Station, 1991. http://dx.doi.org/10.2737/nc-gtr-146.

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Harris, David T. Tissue Culture Hood for Immunotoxicology of JP-8 Fuel. Defense Technical Information Center, 2000. http://dx.doi.org/10.21236/ada383524.

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Ketchum, Jesse. Preserving Giant Sequoias: Cloning, Tissue Culture, and Genomic Conservation. ResearchHub Technologies, Inc., 2025. https://doi.org/10.55277/researchhub.cbld6y7g.

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Reisch, Bruce, Pinhas Spiegel-Roy, and Aliza Vardi. Tissue Culture and Gene Transfer for Genetic Improvement of Grapes. United States Department of Agriculture, 1991. http://dx.doi.org/10.32747/1991.7599656.bard.

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Labrune, Elsa, Bruno Salle, and Jacqueline Lornage. An update on in vitro folliculogenesis: a new technique for post-cancer fertility. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, 2022. http://dx.doi.org/10.37766/inplasy2022.8.0111.

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Review question / Objective: The present review intends to summarize the progress of in vitro folliculogenesis in humans. It focuses on the culture media and then, according to the culture stage, on the different culture systems developed with comments on the results obtained. Condition being studied: This review focuses on the progress of in vitro folliculogenesis in humans. Eligibility criteria: Inclusion criteria : all original English-language articles on in vitro folliculogenesis from ovarian tissue in humans; exclusion criteria: non-English papers, works on animals, in vitro maturation a
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Peehl, Donna M. Development of a Novel Tissue slice Culture Model of Human Prostate Cancer. Defense Technical Information Center, 2005. http://dx.doi.org/10.21236/ada435857.

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Peehl, Donna M. Development of a Novel Tissue Slice Culture Model of Human Prostate Cancer. Defense Technical Information Center, 2003. http://dx.doi.org/10.21236/ada417612.

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Kraybill, William H. Lectin Enzyme Assay Detection of Viruses, Tissue Culture, and a Mycotoxin Simulant. Defense Technical Information Center, 1988. http://dx.doi.org/10.21236/ada276469.

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Peehl, Donna M. Development of a Novel Tissue Slice Culture Model of Human Prostate Cancer. Defense Technical Information Center, 2004. http://dx.doi.org/10.21236/ada425981.

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