Literatura científica selecionada sobre o tema "Primary cell culture of bivalve"
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Artigos de revistas sobre o assunto "Primary cell culture of bivalve"
Yoshino, T. P., U. Bickham e C. J. Bayne. "Molluscan cells in culture: primary cell cultures and cell lines". Canadian Journal of Zoology 91, n.º 6 (junho de 2013): 391–404. http://dx.doi.org/10.1139/cjz-2012-0258.
Texto completo da fontePotts, Robert W. A., Alejandro P. Gutierrez, Yennifer Cortés-Araya, Ross D. Houston e Tim P. Bean. "Developments in marine invertebrate primary culture reveal novel cell morphologies in the model bivalve Crassostrea gigas". PeerJ 8 (1 de junho de 2020): e9180. http://dx.doi.org/10.7717/peerj.9180.
Texto completo da fonteDessai, Shanti Nilesh. "Primary culture of mantle cells of bivalve mollusc, Paphia malabarica". In Vitro Cellular & Developmental Biology - Animal 48, n.º 8 (8 de agosto de 2012): 473–77. http://dx.doi.org/10.1007/s11626-012-9538-4.
Texto completo da fonteOdintsova, N. A., e A. V. Khomenko. "Primary cell culture from embryos of the Japanese scallop Mizuchopecten yessoensis (Bivalvia)". Cytotechnology 6, n.º 1 (maio de 1991): 49–54. http://dx.doi.org/10.1007/bf00353702.
Texto completo da fonteMorgan, Siân R., Laura Paletto, Benjamin Rumney, Farhana T. Malik, Nick White, Philip N. Lewis, Andrew R. Parker, Simon Holden, Keith M. Meek e Julie Albon. "Establishment of long-term ostracod epidermal culture". In Vitro Cellular & Developmental Biology - Animal 56, n.º 9 (outubro de 2020): 760–72. http://dx.doi.org/10.1007/s11626-020-00508-8.
Texto completo da fonteOdintsova, Nelly A., Vyacheslav A. Dyachuk e Leonid P. Nezlin. "Muscle and neuronal differentiation in primary cell culture of larval Mytilus trossulus (Mollusca: Bivalvia)". Cell and Tissue Research 339, n.º 3 (6 de fevereiro de 2010): 625–37. http://dx.doi.org/10.1007/s00441-009-0918-3.
Texto completo da fonteLe Marrec-Croq, F., D. Glaise, C. Guguen-Guillouzo, C. Chesne, A. Guillouzo, V. Boulo e G. Dorange. "Primary cultures of heart cells from the scallp Pecten maximus (mollusca-bivalvia)". In Vitro Cellular & Developmental Biology - Animal 35, n.º 5 (maio de 1999): 289–95. http://dx.doi.org/10.1007/s11626-999-0073-x.
Texto completo da fonteСhadaeva, А. А., O. S. Povolyaeva e S. G. Yurkov. "Primary cell culture in virology". "Veterinary Medicine" Journal 23, n.º 01 (janeiro de 2020): 51–54. http://dx.doi.org/10.30896/0042-4846.2020.23.1.51-54.
Texto completo da fonteRen, Daan, e Joseph D. Miller. "Primary cell culture of suprachiasmatic nucleus". Brain Research Bulletin 61, n.º 5 (setembro de 2003): 547–53. http://dx.doi.org/10.1016/s0361-9230(03)00193-x.
Texto completo da fonteDyachuk, Vyacheslav. "Extracellular matrix is required for muscle differentiation in primary cell cultures of larval Mytilus trossulus (Mollusca: Bivalvia)". Cytotechnology 65, n.º 5 (9 de maio de 2013): 725–35. http://dx.doi.org/10.1007/s10616-013-9577-z.
Texto completo da fonteTeses / dissertações sobre o assunto "Primary cell culture of bivalve"
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.
Texto completo da fonteSince 30 years ago, the growing use of Lanthanides in new technologies has contributed to important releases of these metals into aquatic ecosystems. In a global sustainable development policy aimed at preserving the quality of ecosystems, the impact of Lanthanides on aquatic organisms has naturally been questioned. However, studies on the aquatic ecotoxicology of Lanthanides are incomplete, and no consensus is established yet. In this context, we studied the cellular toxicity of Lanthanides individually and in mixtures. To determine these toxic effects, cell viability was measured on Danio rerio fibroblast-like cells (ZF4; ATCC®, CRL-2050™), Danio rerio hepatic cells (ZFL; ATCC®, CRL-2643™), Oncorhynchus mykiss epithelial cells (RTgill-W1; ATCC®, CRL-2523™), and primary culture of Corbicula fluminea digestive glands exposed to Lanthanides. Direct toxicity of Lanthanides has been observed on all cellular models. Concerning the toxicity of Lanthanides in mixtures, synergistic effects have been underlined on the three fish cell lines. In this research, we focused on the mechanisms of the detoxification of Lanthanides in the case of ZF4 cells from Danio rerio. The effects of Lanthanides were assessed in the presence of specific inhibitors of glutathione-S-transferases (ethacrynic acid) and MRP-like (MK571 and probenecid), by cell viability measurements. We decided to study these actors of the cellular detoxification due to their respective roles in phases II and III of the cellular detoxification of metals in fishes and bivalves. Regarding the results, MRP-like proteins are effectively involved in the detoxification of Lanthanides in ZF4 cells. Overall, our results highlighted the relevance of the toxic effects of Lanthanides at the cellular level for the risk assessment of these metals
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.
Texto completo da fonteBohm, 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.
Texto completo da fonteTradewell, 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.
Texto completo da fonteLa sclérose latérale amyotrophique (SLA, alias la maladie de Lou Gehrig) est une maladie neuromusculaire à évolution rapide qui commence à l'âge adulte, et pour laquelle il existe présentement très peu de traitements. L'excitotoxicité du glutamate, la formation d'inclusions protéiques, la déficience du protéasome et le dysfonctionnement mitochondrial ont tous été associés à la SLA sporadique et héréditaire, mais on se questionne toujours sur ce qui rassemble ces éléments qui, ensemble, mènent au dysfonctionnement neuromusculaire et au décès. Dans les modèles de culture de SLA héréditaire causée par des mutations de l'enzyme Cu/Zn-superoxyde dismutase (SOD1), les traitements réduisant le Ca2+ intra-cellulaire prolongent la viabilité et empêchent la formation d'inclusions mutantes de la SOD1. Les motoneurones sont vulnérables aux surcharges de Ca2+ causées par une régulation du Ca2+ inadéquate et par un grand apport glutamatergique. Ainsi, la perturbation de l'homéostasie du calcium joue peut-être un rôle précoce important dans la SLA. Le but de cette thèse était d'enquêter sur la façon dont les niveaux de Ca2+ à l'intérieur des organites assurant la régulation du cytosol et du calcium (mitochondrie et réticulum endoplasmique) changent dans les motoneurones d'un modèle expérimental de la SLA, ainsi que sur la façon dont ces changements sont liés à d'autres marques de pathogénie de la SLA (détérioration du fonctionnement mitochondrial et du protéasome). Afin d'atteindre cet objectif, la G93A-SOD1 causant la SLA a été introduite dans les cultures de motoneurones provenant de neurones ganglions de la racine dorsale mu
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.
Texto completo da fontePh. D.
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.
Texto completo da fonteCataloged from PDF version of thesis.
Includes bibliographical references.
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 applications in establishing functional microvascular architecture. To achieve these objectives, a model system of primary liver sinusoidal endothelial cells (LSEC) was initially studied due to the high metabolic requirements of the liver, as well as the unique phenotype that they possess. We were able to demonstrate that free fatty acids were able to rescue LSEC in culture, promote proliferation, and maintain their differentiated phenotype. Our work with lipid supplementation in serum-free conditions provides flexibility in engineering liver tissue with a functional vasculature comprised with relevant endothelial types encountered in vivo. Following up our work with LSEC, we explored the human dermal microvascular endothelial cell (HDMVEC) system to understand the signaling mechanisms involved in sprouting angiogenesis. Engineered tissues that are implanted will require integration with host vasculature. We established a method to collect large signaling data sets from a physiologically relevant in vitro culture system of HDMVEC that permitted angiogenic sprouting. We were able to find statistically significant data regarding how angiostatic cues like Platelet Factor 4 can modulate angiogenesis signaling pathways. Our results from working with both types of endothelial cell systems provide insight into potential methods for establishing specialized microvasculature for engineered tissues, both in propagation of differentiated endothelial cells in vitro and promotion of tissue/organ survival following their implantation.
by Ta-Chun Hang.
Ph.D.
Kraft, Robert, Allon Kahn, José L. Medina-Franco, Mikayla L. Orlowski, Cayla Baynes, Fabian López-Vallejo, Kobus Barnard, Gerald M. Maggiora e Linda L. Restifo. "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.
Texto completo da fonteThe 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 cultured fascin-deficient mutant Drosophila neurons, whose neurite arbors manifest the 'filagree' phenotype. Taking a repurposing approach, we screened a library of 1040 known compounds, many of them FDA-approved drugs, for filagree modifiers. Based on scaffold distribution, molecular-fingerprint similarities, and chemical-space distribution, this library has high structural diversity, supporting its utility as a screening tool. We identified 34 fascin-pathway blockers (with potential anti-metastasis activity) and 48 fascin-pathway enhancers (with potential cognitive-enhancer activity). The structural diversity of the active compounds suggests multiple molecular targets. Comparisons of active and inactive compounds provided preliminary structure-activity relationship information. The screen also revealed diverse neurotoxic effects of other drugs, notably the 'beads-on-a-string' defect, which is induced solely by statins. Statin-induced neurotoxicity is enhanced by fascin deficiency. In summary, we provide evidence that primary neuron culture using a genetic model organism can be valuable for early-stage drug discovery and developmental neurotoxicity testing. Furthermore, we propose that, given an appropriate assay for target-pathway function, bidirectional screening for brain-development disorders and invasive cancers represents an efficient, multipurpose strategy for drug discovery.
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.
Texto completo da fonteKlingbeil, 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/.
Texto completo da fonteThe therapeutic procedures frequently used in oral treatments for the pathological diseases are surgical, resulting in failures of the mucosal continuity.The possibility to obtain transplantable oral epithelia from an in vitro cell culture opens new utilization perspectives not only to where it comes from, but also as a reconstructive matherial for other parts of the human body, such as: urethra, epithelia corneo-limbal, cornea, ocular surface. Many researchers still use controversial methods for obtaining cells. It was therefore evaluated and compared the efficiency in both methods: enzimatic and direct explant to obtain oral keratinocytes from human oral mucosa. Fragments of intra oral epithelial tissues from healthy human subjects, undergoing dental surgeries, were donated to the research project. The keratinocytes were cultivated over a feeder-layer from a previously irradiated 3T3 Swiss albino fibroblasts. In this study it was compared the time needed in the cell obtaintion, the best cell amount between both methods, the life-span, the cell capacity to form an in vitro epithelia and its morphologic structure. The results in the accessment of both methods have shown the possibility to obtain keratinocytes from a small oral fragment, but at the same time we may verify the advantages and peculiar restrictions for each one of both analyzed methods.
Geyer, Simone [Verfasser], e 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.
Texto completo da fonteLivros sobre o assunto "Primary cell culture of bivalve"
Schantz, Jan-Thorsen. A manual for primary human cell culture. Hackensack, NJ: World Scientific, 2004.
Encontre o texto completo da fonteKoller, Manfred R. Human Cell Culture: Volume IV: Primary Hematopoietic Cells. Dordrecht: Kluwer Academic Publishers, 2002.
Encontre o texto completo da fonteR, Koller Manfred, Palsson Bernhard e Masters John R. W, eds. Primary mesenchymal cells. Dordrecht: Kluwer Academic Publishers, 2001.
Encontre o texto completo da fonteR, Koller Manfred, Palsson Bernhard e Masters J. R. W, eds. Primary hematopoietic cells. Dordrecht: Kluwer Academic Publishers, 1999.
Encontre o texto completo da fonte1936-, Neumann K. H., Barz W. 1935- e Reinhard Ernst 1926-, eds. Primary and secondary metabolism of plant cell cultures. Berlin: Springer-Verlag, 1985.
Encontre o texto completo da fonteW, Masters John R., ed. Human cancer in primary culture: A handbook. Dordrecht: Kluwer Academic Publishers, 1991.
Encontre o texto completo da fonteJ, Schripsema, e Verpoorte R, eds. Primary and secondary metabolism of plant cell cultures III. Dordrecht: Kluwer Academic Publishers, 1995.
Encontre o texto completo da fonteYang, Phillip Chung-Ming. Hypertrophic response in primary single-cell culture of adult rat myocardial cells. [New Haven: s.n.], 1989.
Encontre o texto completo da fonte(Editor), F. Koller, B. Palsson (Editor) e J. R. Masters (Editor), eds. Human Cell Culture: Primary Mesenchymal Cells (Human Cell Culture, Volume 5) (Human Cell Culture). Springer, 2000.
Encontre o texto completo da fonteHuman Cell Culture: Volume IV: Primary Hematopoietic Cells (Human Cell Culture). Springer, 1999.
Encontre o texto completo da fonteCapítulos de livros sobre o assunto "Primary cell culture of bivalve"
O’Sullivan, Finbar, Paula Meleady, Shirley McBride e Martin Clynes. "Primary Culture". In Animal Cell Culture Techniques, 115–28. Berlin, Heidelberg: Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/978-3-642-80412-0_8.
Texto completo da fonteMartin, Bernice M. "Primary Cell Culture". In Tissue Culture Techniques, 113–36. Boston, MA: Birkhäuser Boston, 1994. http://dx.doi.org/10.1007/978-1-4612-0247-9_5.
Texto completo da fonteGooch, Jan W. "Primary Cell Culture". In Encyclopedic Dictionary of Polymers, 917. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_14559.
Texto completo da fonteMilan, K. L., Goutham V. Ganesh, Dhamodharan Umapathy, Md Enamul Hoque e K. M. Ramkumar. "Primary Cell Culture". In Advanced Mammalian Cell Culture Techniques, 18–20. Boca Raton: CRC Press, 2023. http://dx.doi.org/10.1201/9781003397755-6.
Texto completo da fonteLarsen, Therese Juhlin, Naja Zenius Jespersen e Camilla Scheele. "Adipogenesis in Primary Cell Culture". In Brown Adipose Tissue, 73–84. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/164_2018_142.
Texto completo da fonteDarbinyan, Armine, Rafal Kaminski, Martyn K. White, Paul D. Pozniak, Nune Darbinian e Kamel Khalili. "Isolation and Propagation of Primary Human and Rodent Embryonic and". In Neuronal Cell Culture, 51–61. New York, NY: Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1437-2_5.
Texto completo da fonteNg, Kee Woei, Mohan Chothirakottu Abraham, David Tai Wei Leong, Chris Morris e Jan-Thorsten Schantz. "Primary Culture of Specific Cell Types and the Establishment of Cell Lines". In Animal Cell Culture, 205–30. Chichester, UK: John Wiley & Sons, Ltd, 2011. http://dx.doi.org/10.1002/9780470669815.ch7.
Texto completo da fonteTerrance, Mystica, Tarini Gunawardena, Hong Ouyang, Julie Avolio, Wenming Duan, Sowmya Thanikachalam e Theo J. Moraes. "Primary Human Nasal Epithelial Cell Culture". In Methods in Molecular Biology, 213–23. New York, NY: Springer US, 2023. http://dx.doi.org/10.1007/978-1-0716-3507-0_13.
Texto completo da fonteNeumann, Karl-Hermann, Ashwani Kumar e Jafargholi Imani. "Primary Metabolism". In Plant Cell and Tissue Culture – A Tool in Biotechnology, 209–31. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-49098-0_9.
Texto completo da fonteNeumann, Karl-Hermann, Jafargholi Imani e Ashwani Kumar. "Primary Metabolism". In Plant Cell and Tissue Culture - A Tool in Biotechnology, 161–79. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-93883-5_9.
Texto completo da fonteTrabalhos de conferências sobre o assunto "Primary cell culture of bivalve"
Yong Jiang, Zhe Sun e 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.
Texto completo da fonteZhilnikova, M. V., O. S. Troitskaya, D. D. Novak, A. A. Nushtaeva e 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.
Texto completo da fonteShimba, Kenta, Atsushi Saito, Akimasa Takeuchi, Yuzo Takayama, Kiyoshi Kotani e 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.
Texto completo da fonteEric, Sceusi, Asif Rashid, Yunfei Zhou, Shaija Samuel, Fan Fan, Ling Xia, Xiang-Cang Ye 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.
Texto completo da fonteSimental, Alfred, Steve Lee, Pedro A. De Andrade Filho, Nathaniel R. Peterson, Saied Mirshahidi, Penelope Duerksen-Hughes e Xiangpeng Yuan. "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.
Texto completo da fontePraveen, Kesavan Nair, Nicole Streiner, Martin Vo, Kenna Anderes, Koichi Yokota e 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.
Texto completo da fonteGoji, Hiroshi, Manami Shimomura, Yasushi Uemura, Tetsuya Nakatsura, M. Mamunur Rahman e 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.
Texto completo da fonteSchlaermann, Philipp, e Thomas F. Meyer. "Abstract 2028: A novel human gastric primary cell culture system for modelling Helicobacter pylori infection in vitro". In Proceedings: AACR Annual Meeting 2014; April 5-9, 2014; San Diego, CA. American Association for Cancer Research, 2014. http://dx.doi.org/10.1158/1538-7445.am2014-2028.
Texto completo da fonteMuñoz, Juan José Augusto Moyano, Sandra A. Drigo, Tiago Goss, Hellen Kuasne, Fabio Marchi, Gustavo Guimaraes, Ademar Lopes, Cristovam S. Neto e Silvia R. Rogatto. "Abstract 3248: Establishment and characterization of primary penile carcinoma cell culture versus xenograft by using transcriptome analysis". 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.am2015-3248.
Texto completo da fonteShimomura, Manami, Ruriko Sakamoto, Kaori Yoshida, Ikuyo Ueda, Masahito Yonemura, Yoshihisa Shimada e Tetsuya Nakatsura. "Abstract 5437: Novel drug sensitivity test using three-dimensional primary lung cancer cell culture on microfabricated surface". 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.am2011-5437.
Texto completo da fonteRelatórios de organizações sobre o assunto "Primary cell culture of bivalve"
Heifetz, Yael, e Michael Bender. Success and failure in insect fertilization and reproduction - the role of the female accessory glands. United States Department of Agriculture, dezembro de 2006. http://dx.doi.org/10.32747/2006.7695586.bard.
Texto completo da fonte