Relevant bibliographies by topics / Cellular

Academic literature on the topic 'Cellular'

Author: Grafiati
Published: 4 June 2021
Last updated: 28 July 2024

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Journal articles on the topic "Cellular"

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Kim, Gyeong-A., Jong-Gwon Kim, and Jae-Yun Park. "An Enhanced Handoff Mechanism for Cellular IP." KIPS Transactions:PartC 9C, no. 1 (February 1, 2002): 89–96. http://dx.doi.org/10.3745/kipstc.2002.9c.1.089.

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Hasanzadeh Mofrad, Mohammad, Sana Sadeghi, Alireza Rezvanian, and Mohammad Reza Meybodi. "Cellular edge detection: Combining cellular automata and cellular learning automata." AEU - International Journal of Electronics and Communications 69, no. 9 (September 2015): 1282–90. http://dx.doi.org/10.1016/j.aeue.2015.05.010.

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Marx, Robert E. "Commentary: Cellular Destruction vs Cellular Promotion." International Journal of Oral & Maxillofacial Implants 29, no. 1 (2014): e58. http://dx.doi.org/10.11607/jomi.te42.

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Fedyuk, R., A. Baranov, Yu Ilinsky, and Afonso Rangel Garcez de Azevedo. "PERFORMANCES OF HIGH POROUS CELLULAR CONCRETE." Construction Materials and Products 3, no. 5 (December 24, 2020): 5–14. http://dx.doi.org/10.34031/2618-7183-2020-3-5-5-14.

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The widespread use of cellular concrete for enclosing structures forces researchers to develop ways to im-prove their performance and durability. Compositions of aerated and foam concrete with the use of waste heat power engineering have been developed. The optimal formulation ratios have been identified that con-tribute to the creation of a rigid interpore matrix and water-repellent pore protection. The regularities of the synthesis of aerated concrete and foam concrete were established, which consist in optimizing the processes of structure formation through the use of a polymineral cement-ash binder and a pore-forming agent. The mix composition intensifies the process of hydration of the system, which leads to the synthesis of a poly-mineral highly porous heterodispersed matrix. The increased activity and granulometry of aluminosilicates predetermine an increase in the number of contacts and mechanical adhesion between particles during com-paction, strengthening the framework of the interpore partitions. The mechanism of the influence of the composition of the concrete mix on the microstructure of the composite is established. The calculated sound insulation of airborne noise shows sufficient characteristics for using aerated concrete blocks as enclosing structures. One of the main advantages of aerated concrete is its low thermal conductivity, which is especial-ly important from the point of view of ensuring the energy efficiency of buildings and structures. Even in spite of the high values of open porosity of the developed aerated concrete, the rigid frame makes it possible to achieve almost 2 times higher frost resistance characteristics than that of the reference specimen
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Saravanan, K. "A Review on Green Cellular Network." International Journal of Trend in Scientific Research and Development Volume-2, Issue-5 (August 31, 2018): 342–49. http://dx.doi.org/10.31142/ijtsrd15839.

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César Maruyama, Renato, and Gladis Camarini. "Properties of Cellular Concrete for Filters." International Journal of Engineering and Technology 7, no. 3 (June 2015): 223–28. http://dx.doi.org/10.7763/ijet.2015.v7.796.

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van Diest, Paul J. "Goodbye Analytical Cellular Pathology, Hello Cellular Oncology!" Analytical Cellular Pathology 25, no. 5-6 (2003): 209. http://dx.doi.org/10.1155/2003/379168.

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Sawa, Teiji, Yoshifumi Naito, Hideya Kato, and Fumimasa Amaya. "Cellular Stress Responses and Monitored Cellular Activities." Shock 46, no. 2 (August 2016): 113–21. http://dx.doi.org/10.1097/shk.0000000000000603.

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Brown, T. X. "Cellular performance bounds via shotgun cellular systems." IEEE Journal on Selected Areas in Communications 18, no. 11 (November 2000): 2443–55. http://dx.doi.org/10.1109/49.895048.

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Bouix, Remy, Philippe Viot, and Jean-Luc Lataillade. "OS13-2-3 Cellular material behavior characterization." Abstracts of ATEM : International Conference on Advanced Technology in Experimental Mechanics : Asian Conference on Experimental Mechanics 2007.6 (2007): _OS13–2–3——_OS13–2–3—. http://dx.doi.org/10.1299/jsmeatem.2007.6._os13-2-3-.

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Dissertations / Theses on the topic "Cellular"

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Oshima, Masaya. "Rôles de SOX9 dans la cellule ß pancréatique humaine." Thesis, Sorbonne Paris Cité, 2017. http://www.theses.fr/2017USPCB040.

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Le pancréas est une glande amphicrine composée de cellules exocrines et de cellules endocrines. Parmi les cellules endocrines, organisées en îlot de Langerhans, les cellules ß sécrétrices d’insuline en réponse à des stimuli précis, sont essentielles pour l’homéostasie du glucose. Des perturbations tant au niveau qualitatif qu’au niveau quantitatif sont responsables de différentes pathologies telles les diabètes ou certaines formes de tumeurs endocrines. De récentes publications suggèrent que l’état de différenciation de la cellule ß pancréatique mature n’est pas immuable et montrent que le maintien d’un phénotype mature de la cellule est un processus dynamique. Différents modèles de souris mutantes (avec perte ou gain d’un facteur de transcription) montrent une perte de l’identité de la cellule ß. Cette plasticité altère la synthèse, le stockage et la sécrétion d’insuline. En plus de la perte d’identité, caractérisée par la diminution de l’expression de marqueurs de la cellule ß (MAFA, NKX6-1), les cellules ré-expriment des marqueurs de progéniteurs (NGN3, SOX9) : on parle de dédifférenciation. Cette dédifférenciation serait un mécanisme clé dans la diminution de la masse de cellules ß fonctionnelles au cours du diabète de type 2. Le but de ma thèse a été d’étudier le rôle du facteur de transcription SOX9 dans le contexte de la perte d’identité de la cellule ß humaine. SOX9 est exprimé dans les progéniteurs multipotents pancréatiques et joue plusieurs rôles cruciaux au cours du développement de l’organe. Bien qu’un rôle important de SOX9 fut attribué au cours de l’organogénèse du pancréas, il y a de plus en plus de données suggérant qu’il a des rôles additionnels dans le pancréas matures qui semble aussi importants que son rôle au cours du développement. C’est le cas notamment des cellules formant les canaux pancréatiques. D’un autre côté, pour les cellules endocrines, et plus particulièrement les cellules ß, SOX9, normalement absent de la cellule ß saine, est ré-exprimé dans ces cellules dans des conditions pathologiques (diabètes, tumeurs neuroendocrines du pancréas). Une expression ectopique de SOX9 dans les cellules ß induit un phénotype diabétique. Alors qu’il y a de plus en plus d’observation de l’expression de SOX9 dans la cellule ß, il y a très peu de connaissance sur les mécanismes moléculaires et les cibles de ce facteur de transcription dans les cellules ß humaines. Dans un premier temps, nous avons disséqué différents mécanismes impliqués dans l’induction de l’expression de SOX9. Pour cela, nous avons développé des conditions mimant des contextes pathologiques (diabètes, tumeurs neuroendocrines du pancréas VHL) en utilisant les cellules ß humaines EndoCßH1, récemment développées au sein du laboratoire. Dans un deuxième temps, nous avons développé des outils moléculaires afin d’identifier les cibles de SOX9 dans la cellule ß humaine (dominant positif, dominant négatif). Pour finir, nous avons analysé les cibles potentielles de SOX9 dans différentes conditions pathologiques
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Nicholson, Judith. "Cellulore phenomenon : promoting and policing cellular phones in Canada." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp03/MQ54266.pdf.

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Platt, Steven. "Decentralized cellular networks: Towards blockchain enabled cellular overlays." Doctoral thesis, Universitat Pompeu Fabra, 2021. http://hdl.handle.net/10803/672922.

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This thesis undertakes an investigation into the fit and utility of blockchain technologies within cellular networks. The core of this writing is a new 5G core network blockchain designed to be compatible with, and paired as storage for 3GPP-compliant virtual network functions. Compatibility of the blockchain design is delivered by inheriting a number of behaviors from wireless network operation, including a CSMA/CD mechanism of congestion control; a first for a blockchain design. At the carrier level, a deployment model compatible with ETSI General Autonomous Network Architecture is presented to enable decentralized service overlays. At the network edge, a novel model of transition learning allows fluid roaming of user-equipment across network boundaries. At the conclusion, the theory is combined, to reveal a model of decentralized overlays, which at the user equipment, functions in a manner similar to FM radio. A network channel radio of sorts for decentralized cellular access.
Aquesta tesi realitza una investigació sobre l’us i l’adptabilitat de les tecnologies blockchain en xarxes cel·lulars. El nucli d’aquest treball és una nova blockchain basada en la xarxa 5G dissenyada per ser compatible i utilitzada com a emmagatzematge per a la funció de xarxa virtual compatible amb 3GPP. La compatibilitat del disseny de la blockchain s’ofereix adoptant diversos comportaments de l'operació de xarxa sense fils, inclos un mecanisme CSMA/CD de control de congestió; la primera vegada que s’utilitza per a un disseny de blockchain. A nivell de transport, es presenta un model de desplegament compatible amb l’arquitectura general de xarxes autonomes ETSI per permetre superposicions de serveis descentralitzats. A la capa de xarxa, presentem un nou model de ”transition learning” que facilita una itinerància fluida de l’equip d’usuari a través dels l ́ımits de la xarxa. Per acabar, la part teórica és combina per revelar un model de capes superposades descentralitzades, on l’equip de l’usuari funciona de manera similar una radio FM. Un canal de radio amb accés descentralitzat.
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Shah, Kevan Dinesh. "Modulating cellular fate with arrayed cellular microenvironment technology." Diss., [La Jolla] : University of California, San Diego, 2009. http://wwwlib.umi.com/cr/ucsd/fullcit?p1464669.

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Thesis (M.S.)--University of California, San Diego, 2009.
Title from first page of PDF file (viewed July 7, 2009). Available via ProQuest Digital Dissertations. Includes bibliographical references (p. 57-60).
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Joest, Mathieu von. "Dissecting the non-cell autonomous impact of cellular senescence on cellular reprogramming." Electronic Thesis or Diss., Sorbonne université, 2019. https://accesdistant.sorbonne-universite.fr/login?url=https://theses-intra.sorbonne-universite.fr/2019SORUS396.pdf.

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La sénescence est une réponse suite à un stress qui entraîne l’arrêt permanent du cycle cellulaire. La sénescence s’accompagne de changements, notamment la sécrétion de facteurs réunis sous le terme de SASP (Senescence Associated Secretory Phenotype). Des études ont montré le rôle des cellules sénescentes et du SASP dans la régénération tissulaire. Cependant les mécanismes qui permettent d’influer sur la plasticité cellulaire dans ce contexte sont inconnus. La découverte de la reprogrammation cellulaire qui permet de reprogrammer une cellule différenciée en cellule souche pluripotente induite a mis en évidence la plasticité des cellules différenciées. Utilisant ce système comme une plateforme, nous avons montré que la sénescence induite après blessure permettait la reprogrammation du muscle via l’IL-6, qui est un tissu normalement réfractaire à la reprogrammation. Puis, j’ai montré in vitro que le SASP pouvait augmenter l’efficacité de reprogrammation cellulaire indépendamment de l’IL-6. Enfin, j’ai réalisé une étude protéomique afin d’identifier de nouveaux facteurs du SASP pouvant affecter la reprogrammation. J’ai identifié l’amphiréguline et démontré que son ajout augmente la reprogrammation cellulaire in vitro et in vivo. Ces travaux permettent de mieux comprendre comment la sénescence influe sur la plasticité cellulaire et de lier un nouveau facteur à la reprogrammation
Cellular senescence is a physiological response to a stress, leading to an irreversible cell cycle arrest. Entry in senescence goes along with a myriad of changes, one of the major being the secretion of various factors gathered under the term Senescence Associated Secretory Phenotype (SASP). Recent studies showed the role of senescent cells in regeneration, in particular through SASP. However, mechanisms enabling senescent cells to influence cellular plasticity in the context of tissue repair remain unknown. The discovery of cellular reprogramming, which allows the transformation of a differentiated cell into an induced pluripotent stem cell (iPSC), highlighted the plasticity of differentiated cells. This major breakthrough generated substantial hopes for regenerative medicine and understanding of diseases. I contributed to decipher the mechanisms by which senescence induces cellular plasticity. As a first step, we showed that injury-induced senescence could lead to the reprogramming of skeletal muscle, in particular by IL-6 secretion. Secondly, I decrypted more precisely how SASP influence the reprogramming in vitro and showed that this process could be IL-6 independent. Finally, I performed a proteomic study to identify factors secreted by senescent cells and to determine new factors that could affect reprogramming. I detected amphiregulin and showed that adding this protein enhanced the SASP effect on reprogramming. Indeed, Amphiregulin promotes reprogramming both in vitro and in vivo. Overall, this study not only allows us to better appreciate how senescence influences cellular plasticity after muscular injury, but also links up a new factor to cellular reprogramming
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Shangguan, D. K. "Cellular growth." Thesis, University of Oxford, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.330294.

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Petrova, Siyana. "Cellular Landscapes." Thesis, KTH, Arkitektur, 2018. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-229656.

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Global climate change has been a point of concern over the past century. Some of its major consequences, which are already present, include melting of glaciers, increasing sea water level, temperature rise and excessive acidity of sea water. The natural fluctuations harm the ecology and the biological species will face increased extinction risk. The raise of the water level will cause sinking and gradually vanishing of the land’s surface as a natural resource and place for habitation. It has been estimated that if Greenland ice sheet melts completely, the water would be enough to cover the land with up to 6 meters. The project investigates the consequences of the rising sea levels due to the climate change and what impact this will have on the topography and the natural landscape. It proposes a utopian vision for a large scale strategy for agriculture which does not rely on the use of land. The structure comprises of inflatable spherical modules, which float on the water surface. It is a dynamic and expandable system, with minimal environmental footprint, designed for low-lying areas vulnerable to flooding and land shortage. The more the land surface is vanishing due to the increasing sea levels, the more the structure will stretch to compensate for the loss of farmland.
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Al, Kindi Adil Hashim 1976. "Cellular cardiomyoplasty : optimizing cellular dosage and retention by microencapsulation." Thesis, McGill University, 2008. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=111585.

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Cellular Cardiomyoplasty (cell therapy for myocardial regeneration) targets the basic pathophysiology of heart failure and represents a novel technique for augmenting the function of the failing heart. Previous studies have demonstrated massive mechanical losses in the first few minutes. Thus, efforts to reduce mechanical losses may prove more beneficial than those directed against biological losses alone. We believe that "Wash-out" into the disrupted blood vessels is responsible for these early losses.
In the first part of this study we hypothesized that by increasing the size of the injectate, the amount of immediate losses can be reduced achieving better retention. Using Alginate-poly-L-lysine-Alginate (APA) miscrocapsules of two different sizes (200mum&400mum) and comparing retention with bare microspheres (10mum) of similar size to MSCs, we demonstrated that immediate retention rate increased by four folds. The retention rate for group 1 (microspheres only) was 4.28+/-3.46% which was significantly lower than that for groups 2 (microspheres in 200mum microcapsules) at 16.45+/-12.66% and group 3 (microspheres in 400mum microcapsules) at 12.93+/-6.28% for Group (p<0.05). There was no difference between group 2 and 3.
In the second part, we investigated the potential of gradually increasing the cell load on functional improvement and engraftment using conventional intramuscular delivery. Five groups of rats received escalating doses of MSCs after surgically induced ischemia (gp1 no cells, gp2 0.5x 10 6, gp3 1.5x106, gp4 3x106,gp5 5x106 MSCs). At 7 weeks, we observed significant improvement in cardiac function in groups 3 to 5 compared to post-infarction baseline. This was not observed in groups 1 & 2. However, in groups 3 to 5, we observed no functional advantage for increasing the cell load beyond a minimal therapeutic dose. This is consistent with our hypothesis that small cells are washed out into the circulation.
We also showed the ability of Alginate-Poly-l-lysine-Alginate (APA) microcapsules to sustain the viability of encapsulated MSCs in-vitro. Finally, the ability of encapsulated MSCs to improve the function of the heart in-vivo was tested.
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Hosu, Basarab Gabriel. "Quantitative biological studies at cellular and sub-cellular level." Diss., Columbia, Mo. : University of Missouri-Columbia, 2007. http://hdl.handle.net/10355/4689.

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Thesis (Ph. D.)--University of Missouri-Columbia, 2007.
The entire dissertation/thesis text is included in the research.pdf file; the official abstract appears in the short.pdf file (which also appears in the research.pdf); a non-technical general description, or public abstract, appears in the public.pdf file. Title from title screen of research.pdf file (viewed Mar. 23, 2009). Vita. Includes bibliographical references.
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Childs, Peter Geoffrey. "Cellular mechanotransduction : development of a nanovibrational bioreactor for cellular stimulation." Thesis, University of the West of Scotland, 2016. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.739388.

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Books on the topic "Cellular"

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J, Delves Peter, ed. Cellular immunology labfax. Oxford: BIOS Scientific, 1994.

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David, Dellafiora, ed. Cellular. [London]: Open Hand Press, 1999.

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Sibinga, C. Th Smit, and L. F. M. H. De Leij, eds. Cellular Engineering and Cellular Therapies. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4757-3718-9.

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Th, Smit Sibinga C., and Leij, L. F. M. H. de., eds. Cellular engineering and cellular therapies. Boston: Kluwer Academic Publishers, 2003.

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1939-, Van Dyke Knox, and Castranova Vincent, eds. Cellular chemiluminescence. Boca Raton, Fla: CRC Press, 1987.

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Cossart, Pascale, Patrice Boquet, Staffan Normark, and Rino Rappuoli, eds. Cellular Microbiology. Washington, DC, USA: ASM Press, 2004. http://dx.doi.org/10.1128/9781555817633.

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Chopard, Bastien, Stefania Bandini, Alberto Dennunzio, and Mira Arabi Haddad, eds. Cellular Automata. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-14926-9.

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Mauri, Giancarlo, Samira El Yacoubi, Alberto Dennunzio, Katsuhiro Nishinari, and Luca Manzoni, eds. Cellular Automata. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-99813-8.

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Macario, R. C. V. Cellular Radio. London: Macmillan Education UK, 1997. http://dx.doi.org/10.1007/978-1-349-14433-4.

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Kao, Race L., ed. Cellular Cardiomyoplasty. Totowa, NJ: Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-511-8.

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Book chapters on the topic "Cellular"

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Bährle-Rapp, Marina. "cellular." In Springer Lexikon Kosmetik und Körperpflege, 94. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_1733.

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Dold, Albrecht. "Cellular Decomposition and Cellular Homology." In Lectures on Algebraic Topology, 85–122. Berlin, Heidelberg: Springer Berlin Heidelberg, 1995. http://dx.doi.org/10.1007/978-3-642-67821-9_5.

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Deutsch, Andreas. "Cellular Swarms in Cellular Automata." In The Art of Theoretical Biology, 104–5. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-33471-0_52.

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de Leij, L. F. M. H., M. J. A. van Luyn, and M. C. Harmsen. "Cellular Engineering and Cellular Therapies — An Overview." In Cellular Engineering and Cellular Therapies, 3–10. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4757-3718-9_1.

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Roddie, P. H. "From Research to Clinical Application-The Quality Concept." In Cellular Engineering and Cellular Therapies, 111–17. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4757-3718-9_10.

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Drayer, A. L., and E. Vellenga. "Factors Controlling Expansion and Maturation of Haematopoietic Progenitor Cells." In Cellular Engineering and Cellular Therapies, 119–31. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4757-3718-9_11.

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Slaper-Cortenbach, I., E. Simonetti, C. Arts, Ph G. de Groot, A. van Dijk, S. Ebeling, and A. Hagenbeek. "Cell Processing for Gene and Cell Therapy Protocols: Limitations and Opportunities!" In Cellular Engineering and Cellular Therapies, 133–38. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4757-3718-9_12.

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de Vries, J., G. J. Adema, C. J. A. Punt, and C. G. Figdor. "State of the Art in Dendritic Cell Vaccination." In Cellular Engineering and Cellular Therapies, 153–59. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4757-3718-9_13.

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Solomon, S. R., and A. J. Barrett. "Reconstituting T Cell Immunity Following Hematopoietic Stem Cell Transplantation." In Cellular Engineering and Cellular Therapies, 161–69. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4757-3718-9_14.

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Haisma, H. J., and M. G. Rots. "State of the Art in Gene Therapy." In Cellular Engineering and Cellular Therapies, 171–87. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4757-3718-9_15.

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Conference papers on the topic "Cellular"

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Kawaguchi, Yoichiro. "Cellular." In ACM SIGGRAPH 96 Visual Proceedings: The art and interdisciplinary programs of SIGGRAPH '96. New York, New York, USA: ACM Press, 1996. http://dx.doi.org/10.1145/253607.253649.

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Schubel, J. J. "Cellular telecommunications handoff between cellular systems." In 36th IEEE Vehicular Technology Conference. IEEE, 1986. http://dx.doi.org/10.1109/vtc.1986.1623476.

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Gaojun Song and Hongwu Liu. "Dynamic resource allocation in relay-aided celluar OFDMA systems [celluar read cellular]." In Symposium on ICT and Energy Efficiency and Workshop on Information Theory and Security (CIICT 2012). Institution of Engineering and Technology, 2012. http://dx.doi.org/10.1049/cp.2012.1861.

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Ngo, Angela, Disha Sardana, and Ivica Ico Bukvic. "Sonifying 2d Cellular Behavior Using Cellular Stethoscope." In ICAD 2022: The 27th International Conference on Auditory Display. icad.org: International Community for Auditory Display, 2022. http://dx.doi.org/10.21785/icad2022.015.

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This paper presents an approach to sonifying 2D cellular data. Its primary goal is attaining listener comprehension parity between original visual data and its sonified counterpart for the purpose of understanding cell behavior, including movement, mitosis (or division), and cell death. Here, we present the initial findings of the automated sonification prototype named “Cellular Stethoscope” that was assessed through a 19-subject pilot study to assess its ability to accurately reflect the cell behavior captured in the video footage. The resulting system is envisioned to serve as a foundation for a complementing and potentially more efficient approach to studying cell behavior when subjected to various pharmaceutical interventions.
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Lomas, Andy. "Cellular forms." In ACM SIGGRAPH 2014 Studio. New York, New York, USA: ACM Press, 2014. http://dx.doi.org/10.1145/2619195.2656282.

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Montalvo, Tony, and Aarno Parssinen. "Cellular Transceivers." In 2008 International Solid-State Circuits Conference - (ISSCC). IEEE, 2008. http://dx.doi.org/10.1109/isscc.2008.4523125.

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Bollard, C., and B. Burkhardt. "Cellular therapies." In ISCAYAHL 2020. © Georg Thieme Verlag KG, 2020. http://dx.doi.org/10.1055/s-0040-1701875.

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Haron, Anis, Yong Soon Xuan, and Wong Chee Onn. "Cellular Music." In MM '18: ACM Multimedia Conference. New York, NY, USA: ACM, 2018. http://dx.doi.org/10.1145/3240508.3264577.

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Perdang, J. M., and A. Lejeune. "Cellular Automata." In Workshop on Cellular Automata Models for Astrophysical Phenomena. WORLD SCIENTIFIC, 1993. http://dx.doi.org/10.1142/9789814535908.

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Kawaguchi, Yoichiro. "Cellular GROWTH." In ACM SIGGRAPH 99 Electronic art and animation catalog. New York, New York, USA: ACM Press, 1999. http://dx.doi.org/10.1145/312379.312411.

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Reports on the topic "Cellular"

1

Orhai, Max. Cellular Automata as Cellular Spaces. Portland State University Library, January 2014. http://dx.doi.org/10.15760/honors.90.

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Glaser, M. Cellular energy metabolism. Office of Scientific and Technical Information (OSTI), June 1991. http://dx.doi.org/10.2172/5714213.

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TRIVELPIECE, CORY. FUNCTIONALIZED CELLULAR MAGMATICS. Office of Scientific and Technical Information (OSTI), October 2021. http://dx.doi.org/10.2172/1827955.

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Abelson, Harold, Gerald J. Sussman, Thomas F. Knight, and Jr. Amorphous and Cellular Computing. Fort Belvoir, VA: Defense Technical Information Center, August 2001. http://dx.doi.org/10.21236/ada408046.

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Campisi, Judith. Cellular Senescence and Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, August 2004. http://dx.doi.org/10.21236/ada442901.

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Neilsen, M. K. Continuum representations of cellular solids. Office of Scientific and Technical Information (OSTI), September 1993. http://dx.doi.org/10.2172/10190111.

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Meyer, David A. Knot Invariants and Cellular Automata. Fort Belvoir, VA: Defense Technical Information Center, May 1993. http://dx.doi.org/10.21236/ada264199.

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Albrecht-Buehler, Guenter. Cellular Detection of Infrared Sources. Fort Belvoir, VA: Defense Technical Information Center, April 1998. http://dx.doi.org/10.21236/ada344432.

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Campisi, Judith. Cellular Senescene and Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, August 2006. http://dx.doi.org/10.21236/ada466555.

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Campisi, Judith. Cellular Senescene and Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, August 2005. http://dx.doi.org/10.21236/ada466569.

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