Relevant bibliographies by topics / Primary cell culture of bivalve

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Primary cell culture of bivalve'

Author: Grafiati
Published: 8 June 2024
Last updated: 31 July 2025

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Journal articles on the topic "Primary cell culture of bivalve"

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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 (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
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Potts, Robert W. A., Alejandro P. Gutierrez, Yennifer Cortés-Araya, Ross D. Houston, and Tim P. Bean. "Developments in marine invertebrate primary culture reveal novel cell morphologies in the model bivalve Crassostrea gigas." PeerJ 8 (June 1, 2020): e9180. http://dx.doi.org/10.7717/peerj.9180.

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Cell culture provides useful model systems used in a wide range of biological applications, but its utility in marine invertebrates is limited due to the lack of immortalised cell lines. Primary cell and tissue cultures are typically used but remain poorly characterised for oysters, which can cause issues with experimental consistency and reproducibility. Improvements to methods of repeatable isolation, culture, and characterisation of oyster cells and tissues are required to help address these issues. In the current study, systematic improvements have been developed to facilitate the culture
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Odintsova, N. A., and A. V. Khomenko. "Primary cell culture from embryos of the Japanese scallop Mizuchopecten yessoensis (Bivalvia)." Cytotechnology 6, no. 1 (1991): 49–54. http://dx.doi.org/10.1007/bf00353702.

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Morgan, Siân R., Laura Paletto, Benjamin Rumney, et al. "Establishment of long-term ostracod epidermal culture." In Vitro Cellular & Developmental Biology - Animal 56, no. 9 (2020): 760–72. http://dx.doi.org/10.1007/s11626-020-00508-8.

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Abstract Primary crustacean cell culture was introduced in the 1960s, but to date limited cell lines have been established. Skogsbergia lerneri is a myodocopid ostracod, which has a body enclosed within a thin, durable, transparent bivalved carapace, through which the eye can see. The epidermal layer lines the inner surface of the carapace and is responsible for carapace synthesis. The purpose of the present study was to develop an in vitro epidermal tissue and cell culture method for S. lerneri. First, an optimal environment for the viability of this epidermal tissue was ascertained, while ma
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Odintsova, Nelly A., Vyacheslav A. Dyachuk, and Leonid P. Nezlin. "Muscle and neuronal differentiation in primary cell culture of larval Mytilus trossulus (Mollusca: Bivalvia)." Cell and Tissue Research 339, no. 3 (2010): 625–37. http://dx.doi.org/10.1007/s00441-009-0918-3.

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Dessai, Shanti Nilesh. "Primary culture of mantle cells of bivalve mollusc, Paphia malabarica." In Vitro Cellular & Developmental Biology - Animal 48, no. 8 (2012): 473–77. http://dx.doi.org/10.1007/s11626-012-9538-4.

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Le Marrec-Croq, F., D. Glaise, C. Guguen-Guillouzo, et al. "Primary cultures of heart cells from the scallp Pecten maximus (mollusca-bivalvia)." In Vitro Cellular & Developmental Biology - Animal 35, no. 5 (1999): 289–95. http://dx.doi.org/10.1007/s11626-999-0073-x.

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Сhadaeva, А. А., O. S. Povolyaeva, and S. G. Yurkov. "Primary cell culture in virology." "Veterinary Medicine" Journal 23, no. 01 (2020): 51–54. http://dx.doi.org/10.30896/0042-4846.2020.23.1.51-54.

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Dyachuk, Vyacheslav. "Extracellular matrix is required for muscle differentiation in primary cell cultures of larval Mytilus trossulus (Mollusca: Bivalvia)." Cytotechnology 65, no. 5 (2013): 725–35. http://dx.doi.org/10.1007/s10616-013-9577-z.

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Hosseini Khorami, Hajar, Sophie Breton, and Annie Angers. "In vitro proliferation of Mytilus edulis male germ cell progenitors." PLOS ONE 19, no. 2 (2024): e0292205. http://dx.doi.org/10.1371/journal.pone.0292205.

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Our understanding of basic cellular processes has mostly been provided by mammalian cell culture, and by some non-mammalian vertebrate and few invertebrate cell culture models. Developing reliable culture conditions for non-model organisms is essential to allow investigation of more unusual cellular processes. Here, we investigate how cells isolated from different tissues of the marine mussel Mytilus edulis thrive and survive in vitro in the hope of establishing a suitable laboratory model for the investigation of cellular mechanisms specific to these bivalve mollusks. We found that cells diss
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Dissertations / Theses on the topic "Primary cell culture of bivalve"

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Fleurbaix, Emmanuel. "Évaluation écotoxicologique des éléments terres-rares : approches cellulaires chez différentes espèces aquatiques." Electronic Thesis or Diss., Université de Lorraine, 2021. http://www.theses.fr/2021LORR0324.

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Depuis 30 ans, l’utilisation croissante des Lanthanides dans les nouvelles technologies a entraîné des rejets importants de ces métaux vers les écosystèmes aquatiques. Dans une politique mondiale de développement durable visant à préserver la qualité des écosystèmes, la question de l’impact des Lanthanides sur les organismes aquatiques s’est naturellement posée. Néanmoins, les études restent peu nombreuses et aucun consensus ne subsiste concernant la toxicité des Lanthanides. Dans ce contexte, nous avons étudié la toxicité cellulaire des Lanthanides individuellement et en mélanges. Les effets
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Birmelin, Claudia. "Development of primary cell culture systems from marine invertebrates for use in toxicology." Thesis, University of Surrey, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.265684.

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Bohm, Maren [Verfasser]. "The role of sialic acids in avian influenza virus infection of primary cell culture / Maren Bohm." Hannover : Bibliothek der Tierärztlichen Hochschule Hannover, 2010. http://d-nb.info/1004206291/34.

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Tradewell, Miranda Lee. "The central role of calcium dysregulation in a primary cell culture model of amyotrophic lateral sclerosis." Thesis, McGill University, 2009. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=32355.

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Amyotrophic lateral sclerosis (ALS; aka Lou Gehrig Disease) is an adult-onset, rapidly progressing motor neuron disease for which there is currently very little treatment. Glutamate excitoxicity, formation of proteinaceous inclusions, proteasome impairment, and mitochondrial dysfunction have been associated with both sporadic and familial ALS, but there are many questions about how these events fit together to cause motor neuron dysfunction and death. In culture models of familial ALS due to mutations in
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Stab, II Bernd Robert. "The Effects of Cell Culture Oxygen Levels on the Replicative Senescence Processes of Primary Human Fibroblasts." Diss., Virginia Tech, 2009. http://hdl.handle.net/10919/28468.

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Serial passaging of primary human fibroblasts leads to the formation of non-dividing senescent cells by a process termed replicative senescence. This tissue culture-based methodology is currently used as a model system to determine the underlying mechanisms of in vivo cellular aging and tumor suppression. Senescence is regarded as an alternative pathway to apoptosis, where cells undergo multiple changes in metabolic and cellular signaling pathways in order to prevent proliferation but still maintain a metabolically-active cell. Whether or not this model accurately reflects in vivo processes is
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Hang, Ta-Chun. "Optimization of primary endothelial culture methods and assessment of cell signaling pathways in the context of inflammation." Thesis, Massachusetts Institute of Technology, 2012. http://hdl.handle.net/1721.1/71467.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Biological Engineering, 2012.<br>Cataloged from PDF version of thesis.<br>Includes bibliographical references.<br>Tissue engineering is a potentially valuable tool for clinical treatment of diseases where host tissues or organs need to be replaced. Progression of engineering metabolically complex organs and tissues has been severely limited by the lack of established, functional vasculature. The thesis work described herein focused on methods of establishing and studying specific endothelial cell types in vitro for potential appl
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Kraft, Robert, Allon Kahn, José L. Medina-Franco, et al. "A cell-based fascin bioassay identifies compounds with potential anti-metastasis or cognition-enhancing functions." The Company of Biologists, 2013. http://hdl.handle.net/10150/605272.

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A first-of-its-kind, proof-of-concept drug screen with implications for two unmet medical needs.<br>The actin-bundling protein fascin is a key mediator of tumor invasion and metastasis and its activity drives filopodia formation, cell-shape changes and cell migration. Small-molecule inhibitors of fascin block tumor metastasis in animal models. Conversely, fascin deficiency might underlie the pathogenesis of some developmental brain disorders. To identify fascin-pathway modulators we devised a cell-based assay for fascin function and used it in a bidirectional drug screen. The screen utilized c
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Klingbeil, Maria Fátima Guarizo. ""Comparação de dois métodos de obtenção celular para cultura primária de queratinócitos bucais humanos"." Universidade de São Paulo, 2006. http://www.teses.usp.br/teses/disponiveis/85/85131/tde-17052007-144619/.

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Freqüentemente as condutas terapêuticas utilizadas no tratamento de patologias bucais são cirúrgicas, resultando em falhas de continuidade da mucosa bucal. A possibilidade de obtenção de epitélios transplantáveis, a partir do cultivo in vitro de células da mucosa bucal, abre novas perspectivas de utilização, não se restringindo somente ao seu local de origem, ou seja, a boca, mas também como material de reconstrução para outras regiões, tais como: uretra, córnea, superfície ocular e epitélio córneo-limbal. Os métodos utilizados para a obtenção dessas células ainda são controversos na literatur
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Song, Miyeoun. "Organ and primary culture of medaka (Oryzias latipes) testis: Test systems for the analysis of cell proliferation and differentiation." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2003. http://nbn-resolving.de/urn:nbn:de:swb:14-1059039500031-89370.

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In cultured medaka testis fragments, cells remained viable for the entire culture period (17h), and spermatids that developed from spermatocytes were viable and motile. Primary cultures were characterized over a period of two days with respect to cell viability and the distribution of adherent and suspended cells. These two cell populations were maintained in dynamic equilibrium in vitro for several days. Proliferating cells were predominant among clusters of suspended cells, as determined by BrdU labeling, and CFSE and propidium iodide PI labeling. Based on cytological criteria, the prolifera
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Geyer, Simone [Verfasser], and S. [Akademischer Betreuer] Scholpp. "Establishment of a three-dimensional cell culture system to study tubular structures - A comparative study of neuronal differentiation in zebrafish and in 2D and 3D zebrafish primary cell culture / Simone Geyer. Betreuer: S. Scholpp." Karlsruhe : KIT-Bibliothek, 2015. http://d-nb.info/1112224580/34.

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Books on the topic "Primary cell culture of bivalve"

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Kee-Woei, Ng, ed. A manual for primary human cell culture. World Scientific, 2004.

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Koller, Manfred R. Human Cell Culture: Volume IV: Primary Hematopoietic Cells. Kluwer Academic Publishers, 2002.

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Pedersen, Peter Steen. Human reabsorptive sweat duct in primary cell culture. Lægeforeningens Forlag, 1992.

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R, Koller Manfred, Palsson Bernhard, and Masters J. R. W, eds. Primary hematopoietic cells. Kluwer Academic Publishers, 1999.

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J, Schripsema, and Verpoorte R, eds. Primary and secondary metabolism of plant cell cultures III. Kluwer Academic Publishers, 1995.

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Kurz, W. G. W. 1933-, ed. Primary and secondary metabolism of plant cell cultures II. Springer-Verlag, 1989.

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Yang, Phillip Chung-Ming. Hypertrophic response in primary single-cell culture of adult rat myocardial cells. s.n.], 1989.

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(Editor), F. Koller, B. Palsson (Editor), and J. R. Masters (Editor), eds. Human Cell Culture: Primary Mesenchymal Cells (Human Cell Culture, Volume 5) (Human Cell Culture). Springer, 2000.

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Human Cell Culture: Volume IV: Primary Hematopoietic Cells (Human Cell Culture). Springer, 1999.

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Koller, Manfred R. Human Cell Culture: Primary Hematopoietic Cells. Springer, 2010.

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Book chapters on the topic "Primary cell culture of bivalve"

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O’Sullivan, Finbar, Paula Meleady, Shirley McBride, and Martin Clynes. "Primary Culture." In Animal Cell Culture Techniques. Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/978-3-642-80412-0_8.

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Martin, Bernice M. "Primary Cell Culture." In Tissue Culture Techniques. Birkhäuser Boston, 1994. http://dx.doi.org/10.1007/978-1-4612-0247-9_5.

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Milan, K. L., Goutham V. Ganesh, Dhamodharan Umapathy, Md Enamul Hoque, and K. M. Ramkumar. "Primary Cell Culture." In Advanced Mammalian Cell Culture Techniques. CRC Press, 2023. http://dx.doi.org/10.1201/9781003397755-6.

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Gooch, Jan W. "Primary Cell Culture." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_14559.

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Larsen, Therese Juhlin, Naja Zenius Jespersen, and Camilla Scheele. "Adipogenesis in Primary Cell Culture." In Brown Adipose Tissue. Springer International Publishing, 2018. http://dx.doi.org/10.1007/164_2018_142.

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Darbinyan, Armine, Rafal Kaminski, Martyn K. White, Paul D. Pozniak, Nune Darbinian, and Kamel Khalili. "Isolation and Propagation of Primary Human and Rodent Embryonic and." In Neuronal Cell Culture. Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1437-2_5.

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Ng, Kee Woei, Mohan Chothirakottu Abraham, David Tai Wei Leong, Chris Morris, and Jan-Thorsten Schantz. "Primary Culture of Specific Cell Types and the Establishment of Cell Lines." In Animal Cell Culture. John Wiley & Sons, Ltd, 2011. http://dx.doi.org/10.1002/9780470669815.ch7.

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Terrance, Mystica, Tarini Gunawardena, Hong Ouyang, et al. "Primary Human Nasal Epithelial Cell Culture." In Methods in Molecular Biology. Springer US, 2023. http://dx.doi.org/10.1007/978-1-0716-3507-0_13.

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Neumann, Karl-Hermann, Ashwani Kumar, and Jafargholi Imani. "Primary Metabolism." In Plant Cell and Tissue Culture – A Tool in Biotechnology. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-49098-0_9.

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Neumann, Karl-Hermann, Jafargholi Imani, and Ashwani Kumar. "Primary Metabolism." In Plant Cell and Tissue Culture - A Tool in Biotechnology. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-93883-5_9.

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Conference papers on the topic "Primary cell culture of bivalve"

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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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Hung, Clark T., Eric D. Johnston, Fred Allen, Mitchell Litt, Solomon R. Pollack, and David F. Meaney. "Changes in Osteoblasts Under Time Averaged Microgravity Conditions." In ASME 1997 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 1997. http://dx.doi.org/10.1115/imece1997-1314.

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Abstract Subtle alterations in mechanical stimuli can promote changes in mammalian cells ranging from cell realignment and intracellular signaling to immediate early gene expression. In this study, we examined the cellular growth and phenotypic activity of primary rat osteoblasts exposed to a simulated microgravity environment. We developed a method to produce time averaged microgravity conditions in tissue culture flasks and compared the response of cells in this environment to cells grown in conditions of unit gravity, both with and without hydrostatic pressure load. Three responses were mea
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Haile, Tesfaalem, Sankara Papavinasam, and Doug Gould. "Evaluation of a Portable Online 4-Probe Sensor for Simultaneous Monitoring of Corrosion Rate and Sulfate Reducing Bacteria Activity." In CORROSION 2013. NACE International, 2013. https://doi.org/10.5006/c2013-02148.

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Abstract Corrosion is the main component of the operating and maintenance costs of petroleum industry. Microbiologically influenced corrosion (MIC) significantly contributes to the overall corrosion. Sulfate reducing bacteria (SRB) are the primary cause of MIC. A patented 4-probe sensor for simultaneous monitoring of SRB activity and corrosion was demonstrated previously. The online SRB monitoring probe (OnSM) was based on biosensor technology in which sulfide oxidase (SO) was used as the indicating element. The OnSM was previously validated using biogenic sulfide produced by SRB in continuous
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Yong Jiang, Zhe Sun, and Tong-cun Zhang. "The primary culture of vascular endothelial cell in rat." In 2011 International Symposium on Information Technology in Medicine and Education (ITME 2011). IEEE, 2011. http://dx.doi.org/10.1109/itime.2011.6132114.

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Zhilnikova, M. V., O. S. Troitskaya, D. D. Novak, A. A. Nushtaeva, and O. A. Koval. "ESTABLISHMENT AND CHARACTERIZATION OF PRIMARY UVEAL MELANOMA CELL CULTURE." In X Международная конференция молодых ученых: биоинформатиков, биотехнологов, биофизиков, вирусологов и молекулярных биологов — 2023. Novosibirsk State University, 2023. http://dx.doi.org/10.25205/978-5-4437-1526-1-320.

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The primary human uveal melanoma (UM) cell culture was established and key surface and intracellular markers of oncotransformed melanocytes were characterized. Based on the primary cell culture, genetically modified cell culture of UM expressing fluorescent protein mKate2 and luciferase Luc2 was created.
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Shimba, Kenta, Atsushi Saito, Akimasa Takeuchi, Yuzo Takayama, Kiyoshi Kotani, and Yasuhiko Jimbo. "Bidirectional synaptic connection between primary and stem cell-derived neurons in co-culture device." In 2013 35th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC). IEEE, 2013. http://dx.doi.org/10.1109/embc.2013.6611087.

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Eric, Sceusi, Asif Rashid, Yunfei Zhou, et al. "Abstract 5199: Primary culture of human midgut carcinoid cell lines and isolation of a putative carcinoid stem cell population." In Proceedings: AACR 102nd Annual Meeting 2011‐‐ Apr 2‐6, 2011; Orlando, FL. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1538-7445.am2011-5199.

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Simental, Alfred, Steve Lee, Pedro A. De Andrade Filho, et al. "Abstract 60: Characterization of papillary thyroid carcinoma primary cell culture derived cancer stem-like cells." In Abstracts: AACR-AHNS Head and Neck Cancer Conference: Optimizing Survival and Quality of Life through Basic, Clinical, and Translational Research; April 23-25, 2017; San Diego, CA. American Association for Cancer Research, 2017. http://dx.doi.org/10.1158/1557-3265.aacrahns17-60.

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Praveen, Kesavan Nair, Nicole Streiner, Martin Vo, Kenna Anderes, Koichi Yokota, and Takeshi Ikeya. "Abstract 5270: Evaluation of Cell-able spheroid culture system for culturing patient derived primary tumor cells." In Proceedings: AACR 103rd Annual Meeting 2012‐‐ Mar 31‐Apr 4, 2012; Chicago, IL. American Association for Cancer Research, 2012. http://dx.doi.org/10.1158/1538-7445.am2012-5270.

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Goji, Hiroshi, Manami Shimomura, Yasushi Uemura, Tetsuya Nakatsura, M. Mamunur Rahman, and Manabu Itoh. "Abstract 329: Establishment of three-dimensional primary tumor cell culture method and novel drug sensitivity test." In Proceedings: AACR 106th Annual Meeting 2015; April 18-22, 2015; Philadelphia, PA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.am2015-329.

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Reports on the topic "Primary cell culture of bivalve"

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Ampornaramveth, Ruchanee. IL-1β mediate cementoblasts and osteoclast precursors interaction. Chulalongkorn University, 2016. https://doi.org/10.58837/chula.res.2016.17.

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An injury of the periodontium followed by an inflammatory response often leads to root resorption. Resorption is accomplished by osteoclasts and their generation may depend on an interaction with the cells in direct contact with the root, the cementoblasts. Our study aimed to investigate the role of human cementoblasts in the formation of osteoclasts and the effect of IL-1β hereupon. Extracted teeth from healthy volunteers were subjected to sequential digestion by type I collagenase and trypsin. The effect of enzymatic digestion on the presence of cells on the root surface was analyzed by hist
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Heifetz, Yael, and Michael Bender. Success and failure in insect fertilization and reproduction - the role of the female accessory glands. United States Department of Agriculture, 2006. http://dx.doi.org/10.32747/2006.7695586.bard.

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The research problem. Understanding of insect reproduction has been critical to the design of insect pest control strategies including disruptions of mate-finding, courtship and sperm transfer by male insects. It is well known that males transfer proteins to females during mating that profoundly affect female reproductive physiology, but little is known about the molecular basis of female mating response and no attempts have yet been made to interfere with female post-mating responses that directly bear on the efficacy of fertilization. The female reproductive tract provides a crucial environm
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