Relevant bibliographies by topics / Self assembly

Academic literature on the topic 'Self assembly'

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Published: 4 June 2021
Last updated: 20 July 2024

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Journal articles on the topic "Self assembly"

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PADILLA, JENNIFER E., MATTHEW J. PATITZ, ROBERT T. SCHWELLER, NADRIAN C. SEEMAN, SCOTT M. SUMMERS, and XINGSI ZHONG. "ASYNCHRONOUS SIGNAL PASSING FOR TILE SELF-ASSEMBLY: FUEL EFFICIENT COMPUTATION AND EFFICIENT ASSEMBLY OF SHAPES." International Journal of Foundations of Computer Science 25, no. 04 (June 2014): 459–88. http://dx.doi.org/10.1142/s0129054114400061.

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In this paper we demonstrate the power of a model of tile self-assembly based on active glues which can dynamically change state. We formulate the Signal-passing Tile Assembly Model (STAM), based on the model of Padilla et al. [24] to be asynchronous, allowing any action of turning a glue on or off, attaching a new tile, or breaking apart an assembly to happen in any order. Within this highly generalized model we provide three new solutions to tile self-assembly problems that have been addressed within the abstract Tile Assembly Model and its variants, showing that signal passing tiles allow for substantial improvement across multiple complexity metrics. Our first result utilizes a recursive assembly process to achieve tile-type efficient assembly of linear structures, using provably fewer tile types than what is possible in standard tile assembly models. Our second system of signal-passing tiles simulates any Turing machine with high fuel efficiency by using only a constant number of tiles per computation step. Our third system assembles the discrete Sierpinski triangle, demonstrating that this pattern can be strictly self-assembled within the STAM. This result is of particular interest in that it is known that this pattern cannot self-assemble within a number of well studied tile self-assembly models. Notably, all of our constructions are at temperature 1, further demonstrating that signal-passing confers the power to bypass many restrictions found in standard tile assembly models.
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Danino, Dganit, and Jenny E. Hinshaw. "Self-Assembly of Dynamin." Microscopy and Microanalysis 7, S2 (August 2001): 1210–11. http://dx.doi.org/10.1017/s1431927600032128.

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Dynamin is a large GTPase essential for various intracellular processes such as synaptic vesicle recycling, caveolae internalization and trafficking into and out of the Golgi. It is also involved in receptor-mediated endocytosis, and is believed to assemble at the necks of clathrin-coated pits and assist in pinching vesicles from the plasma membrane upon GTP binding and hydrolysis.Purified recombinant dynamin self-assembles into rings and spirals in low salt conditions [1]. A dynamin mutant lacking the c-terminal proline rich domain (APRD) also assembles into rings and spirals, however unlike wild type dynamin APRD constricts in the presence of GTP analogous such as GMP-PCP [2] or GTPγS. to explore differences in the behavior of the wild type and mutant dynamin we dialyzed them into different salt solutions containing various types of nucleotides and studied their assembly over time using negative staining and cryo-TEM.
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NARANTHATTA, MILI C., V. RAMKUMAR, and DILLIP KUMAR CHAND. "Self-assembly of self-assembled molecular triangles." Journal of Chemical Sciences 126, no. 5 (September 2014): 1493–99. http://dx.doi.org/10.1007/s12039-014-0702-0.

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Chen, Jinrong, Shihao Zhang, Yuhan Wang, Ruwen Xie, Lishang Liu, and Yan Deng. "In Vivo Self-Assembly Based Cancer Therapy Strategy." Journal of Biomedical Nanotechnology 16, no. 7 (July 1, 2020): 997–1017. http://dx.doi.org/10.1166/jbn.2020.2962.

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Nanotechnology has been widely applied in tumor imaging, diagnostic and therapy. Beside the prefabricated nanomaterials, constructing nanostructures in living cells through self-assemble provides an alternative strategy to treat cancer. In vivo self-assembly renders the conversion of compatible small molecules into assembled nanostructures with toxicity, and is expected to outperform the prefabricated nanotechnologies as the small molecules diffuse faster than their assembly form. Attributed to the specific tumor environment such as low pH, high ROS, high enzyme expression and so on, in vivo self-assembly could differentiate cancer cells from normal ones with high selectivity. The in vivo self-assembly based caner therapy has made considerable progress in the last decade with confirmed advantages such as high capacity, minimal drug resistance, high accumulation, enhanced retention and so on. This review summarized the in vivo self-assembly of nanostructures induced by the stimuli like pH, ROS, enzyme, metal ion, localized concentration, biominerization and their utilization in cancer therapy.
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Kuo, Chia Lung, and Jing Dae Huang. "Joint Design and Fabrication for Mechanical Elastic Self-deformation Micro-Assembly Technology." Materials Science Forum 505-507 (January 2006): 829–34. http://dx.doi.org/10.4028/www.scientific.net/msf.505-507.829.

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A microstructure assembled into another part using the mechanical elastic self-deformation assembly technology is proposed in the paper. To attain the self-deformation during assembling, the assembly joint on the microstructure is analytically designed as the feature with an appropriate taper and cross clearance. Take account of the accuracy, the whole process from micro-fabrication to micro-assembly is carefully planned and practiced under a micro-EDM machining center system which consists of vertical micro-EDM with dividing mechanism, and horizontal micro-machining mechanism, which is referred to as on-process micro-assembly. To illustrate the micro-assembly strategies and procedures, a micro-rotor production including assemble a tungsten carbide four-phase micro-rotor into an alumina base has been provided and discussed.
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Murugan, Arvind, Zorana Zeravcic, Michael P. Brenner, and Stanislas Leibler. "Multifarious assembly mixtures: Systems allowing retrieval of diverse stored structures." Proceedings of the National Academy of Sciences 112, no. 1 (December 22, 2014): 54–59. http://dx.doi.org/10.1073/pnas.1413941112.

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Self-assembly materials are traditionally designed so that molecular or mesoscale components form a single kind of large structure. Here, we propose a scheme to create “multifarious assembly mixtures,” which self-assemble many different large structures from a set of shared components. We show that the number of multifarious structures stored in the solution of components increases rapidly with the number of different types of components. However, each stored structure can be retrieved by tuning only a few parameters, the number of which is only weakly dependent on the size of the assembled structure. Implications for artificial and biological self-assembly are discussed.
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Braun, P. V. "Imaging of self-assembly and self-assembled materials." Microscopy and Microanalysis 8, S02 (August 2002): 316–17. http://dx.doi.org/10.1017/s1431927602100857.

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Kunkel, Meghan, Marta Lorinczi, René Rijnbrand, Stanley M. Lemon, and Stanley J. Watowich. "Self-Assembly of Nucleocapsid-Like Particles from Recombinant Hepatitis C Virus Core Protein." Journal of Virology 75, no. 5 (March 1, 2001): 2119–29. http://dx.doi.org/10.1128/jvi.75.5.2119-2129.2001.

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ABSTRACT Little is known about the assembly pathway and structure of hepatitis C virus (HCV) since insufficient quantities of purified virus are available for detailed biophysical and structural studies. Here, we show that bacterially expressed HCV core proteins can efficiently self-assemble in vitro into nucleocapsid-like particles. These particles have a regular, spherical morphology with a modal distribution of diameters of approximately 60 nm. Self-assembly of nucleocapsid-like particles requires structured RNA molecules. The 124 N-terminal residues of the core protein are sufficient for self-assembly into nucleocapsid-like particles. Inclusion of the carboxy-terminal domain of the core protein modifies the core assembly pathway such that the resultant particles have an irregular outline. However, these particles are similar in size and shape to those assembled from the 124 N-terminal residues of the core protein. These results provide novel opportunities to delineate protein-protein and protein-RNA interactions critical for HCV assembly, to study the molecular details of HCV assembly, and for performing high-throughput screening of assembly inhibitors.
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Boden, Margaret. "Self Assembly." American Scientist 95, no. 3 (2007): 260. http://dx.doi.org/10.1511/2007.65.260.

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Li, Junbai. "Self assembly." Current Opinion in Colloid & Interface Science 14, no. 2 (April 2009): 61. http://dx.doi.org/10.1016/j.cocis.2008.12.001.

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Dissertations / Theses on the topic "Self assembly"

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Fox, Michael Jacob. "Stochastic self-assembly." Thesis, Georgia Institute of Technology, 2010. http://hdl.handle.net/1853/34741.

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We present methods for distributed self-assembly that utilize simple rule-of-thumb control and communication schemes providing probabilistic performance guarantees. These methods represents a staunch departure from existing approaches that require more sophisticated control and communication, but provide deterministic guarantees. In particular, we show that even under severe communication restrictions, any assembly described by an acyclic weighted graph can be assembled with a rule set that is linear in the number of nodes contained in the desired assembly graph. We introduce the concept of stochastic stability to the self-assembly problem and show that stochastic stability of desirable configurations can be exploited to provide probabilistic performance guarantees for the process. Relaxation of the communication restrictions allows simple approaches giving deterministic guarantees. We establish a clear relationship between availability of communication and convergence properties. We consider Self-assembly tasks for the cases of many and few agents as well as large and small assembly goals. We analyze sensitivity of the presented process to communication errors as well as ill-intentioned agents. We discuss convergence rates of the presented process and directions for improving them.
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Spanton, Robert. "Stateful self-assembly." Thesis, University of Southampton, 2013. https://eprints.soton.ac.uk/355888/.

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Nature shows us many organised structures that form through interactions between their components with little external guidance. These self-assembling systems range from simple crystals to considerably more complex biological structures and organisms. Inspired by these systems, the development of programmable self assembling systems could lead to mass manufacturing processes that produce individually unique items. Current artificial self-assembling systems involve small numbers of centimetre-scale components, and have not resulted in structures anywhere near the complexity seen in natural systems. This thesis argues that to advance artificial self-assembling systems towards this complexity, the statistics of the interactions within self-assembling systems need to be empirically examined and understood. However, the pursuit of this involves the resolution of a variety of technical challenges. These are approached in this work through the development of a self-assembly toolkit that allows the collection of these statistics from a physical system with larger numbers of components than in previous works. A novel capacitive communication interface is developed for the components of this toolkit, which allows messaging between neighbouring components that are constrained to the surface of a plane. As self-assembling components reduce in size towards the microscale, the penalty for incorrect activation of a component’s binding mechanism is likely to increase. With this in mind, this capacitive communication interface is optimised to provide spatial alignment sensing, with the aim of allowing informed binding mechanism activation. The toolkit developed in this work uses components that are constrained to two degrees of freedom of motion. In pursuit of the development of programmable self-assembling components for 3D structures, a new design of alignment sensor for use in 3D is created. Simulation of this sensor, which is developed using an evolutionary algorithm, indicates that it is suited for detecting the alignment of components with three degrees of freedom. Approaches using computer vision are developed for the spatial tracking of the components of the toolkit, allowing the collection of empirical data regarding the interaction of components. The technical advances described within this work will allow the progression of data-driven self-assembly process design.
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Chen, Ho-Lin. "Robust self-assembly /." May be available electronically:, 2007. http://proquest.umi.com/login?COPT=REJTPTU1MTUmSU5UPTAmVkVSPTI=&clientId=12498.

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Dillenback, Lisa M. Keating Christine Dolan. "Self-assembly and controlled assembly of nanoparticles." [University Park, Pa.] : Pennsylvania State University, 2008. http://etda.libraries.psu.edu/theses/approved/WorldWideIndex/ETD-2613/index.html.

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Williams, Richard James. "Enzyme assisted self-assembly." Thesis, University of Manchester, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.496231.

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Self-assembling peptide systems provide a pathway for the formation of complex molecular assemblies from relatively simple designed molecules. Stimuli which have been used to trigger the self-assembly (SA) process in aqueous conditions include temperature, pH, ionic strength, and solvent exchange. Additionally, enzymes may be used to selectively control the self-assembly process; enzymes are uniquely chemo-, regio-, and enantioselective, and work naturally under mild conditions without disrupting biological Interactions.
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Mayans, Tayadella Enric. "Self-assembly of phenylalanine derivatives." Doctoral thesis, Universitat Politècnica de Catalunya, 2017. http://hdl.handle.net/10803/461917.

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Since the pioneering work of Reches and Gazit in 2003, in which the formation of diphenylalanine (FF) nanotubes in aqueous solution was discovered, significant efforts have been made to develop a new generation of biomaterials based on the self-assembly of aromatic peptides. From recent investigations, the self-assembly of phenylalanine homopeptides can be understood by a combination of hydrogen bonding and repeated aromatic stacking interactions. In this Thesis, new phenylalanine homo-oligopeptide derivatives have been synthetized in order to test their self-assembly capability and to examine the influence of the chemical structure and the external conditions. Although, the terminal head-to-tail NH3 +···–OOC interactions in the unprotected homopeptides are shown to stabilize the peptide assemblies, chemical modulation has been introduced through the incorporation of the N- and C- protections, such as aromatic blocking groups (Chapter 4 and 5.2), azide-alkyne coupling groups (Chapter 3.2) or trifluoroacetate anion (Chapter 3.1). In Chapter 4, three FFFF-based peptides have been synthetized to study the role of the head-to-tail NH3 +···–OOC interactions in the assembly of FFFF-derivatives. Although these interactions are not possible upon the incorporation of the NFmoc and C-OBzl protections, defined hierarchical assemblies arising from p-p stacking interactions have been found. In Chapter 6, new hybrid polypeptide/polylactide conjugates have been prepared through ring opening polymerizations to reveal the effect of the constitutive polylactide block. Whereas the crystallization from the melt gave rise to spherulites from lamellar arrangements, previously reported phenylalanine-oligopeptide hierarchical morphologies have been observed from diluted solutions. We report that the homopeptide length also plays a significant role in the supramolecular organization of phenylalanine derivatives. First, in Chapter 5.2, theoretical calculations have indicated that the stability of Phe-homopeptides capped with two fluorenyl functionalities increases with the length of the Phe-segment, adopting an antiparallel b-sheet arrangement. While the existence of diverse polymorphs suggests that p-p stacking interactions involving fluorenyl groups result in different stable conformations, they are more versatile, in terms of molecular selfassociation, than hydrogen bonds. Besides, the capacity of FFF to assemble in very diverse supramolecular structures has been found to be greater than that exhibited by its homologues with an even number of Phe residues (Chapter 5.1). Additionally, spherulites from the prepared diblock copolymers with a distinctive lamellar disposition (i.e. flat-on or edge-on) and/or dendritic structures have been identified in function of the length of the PPhe block (Chapter 6). Results have evidenced not only the remarkable control exerted by the characteristics of the environment (i.e. the solvents mixture, temperature, the ionic strength, and the peptide concentration) in the organization of the assemblies, but also by the substrate (Chapter 5.3). Depending on the conditions, molecules can organize into bundled arrays of nanotubes, stacked braids, corkscrew-like, doughnut/volcano-like, spherulitic microstructures and/or triaxial ellipsoid-like nodules. Peptide···peptide interactions, peptide···surface interactions and the surface roughness have been detected as key factors for the shape, dimensions and stability of the hierarchical assemblies. The proposed mechanisms for the formation of supramolecular structures have reflected how the structural nucleation and hierarchical growing are controlled through the balance between peptide···peptide and peptide···solvent interactions, which in turn are regulated by the peptide concentration and the polarity of the solvent mixture used to dissolve the peptide, respectively. Tuning the structure of Phe-derivatives by changing the medium used in the mixture, as well as the surface, is a very attractive feature to expand the potential utility of peptide assemblies in different fields, for example as molecular carriers and delivery systems. The wide range of available surfaces offers a valuable tool for the development of bionanotechnological applications based on hierarchical peptide assemblies. Indeed, the ability of plasma treated polystyrene for stabilizing well-defined dendritic structures has been found to be particularly noticeable
En aquesta tesis, nous homooligopèptids derivats de fenilalanina ha estat sintetitzats per tal d'estudiar la seva capacitat d'autoorganització i examinar la influencia de l'estructura química i les condicions externes. Encara que les interaccions NH3+···-OOC cap-a-cua en els homopèptids desprotegits mostren estabilitzar les estructures peptídiques, s'han introduït funcionalitzacions químiques a través de la incorporació de proteccions a N- i C-, com per exemple, grups bloquejadors aromàtics, grups d'acoblament azida-alquí, l'anió trifluoroacetat o un bloc de polilàctide. Diferents capítols estan dedicats a mostrar que la llargada del bloc d'homopèptid també juga un paper rellevant en l'organització supramolecular dels derivats de fenilalanina. Els resultats publicats evidencien no només el control que exerceixen les característiques de l'ambient sinó també del substrat. Les interaccions pèptid··· pèptid, pèptid···superfície i la rugositat superficial han estat assenyalades com a factors clau que defineixen la forma, les dimensions i l'estabilitat de les estructures jerarquitzades.
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Vikramaditya, Barmeshwar. "Micromanipulation using self assembly strategies /." Diss., ON-CAMPUS Access For University of Minnesota, Twin Cities Click on "Connect to Digital Dissertations", 2001. http://www.lib.umn.edu/articles/proquest.phtml.

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Gutzler, Rico. "Surface-Confined Molecular Self-Assembly." Diss., lmu, 2010. http://nbn-resolving.de/urn:nbn:de:bvb:19-127201.

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Nellis, Michael. "Self assembly of complex structures." [Tampa, Fla.] : University of South Florida, 2007. http://purl.fcla.edu/usf/dc/et/SFE0002280.

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Yin, Jinsong. "Self-assembly of ordered nanostructures." Diss., Georgia Institute of Technology, 2000. http://hdl.handle.net/1853/19116.

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Books on the topic "Self assembly"

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Nagarajan, Ramanathan, ed. Self-Assembly. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2018. http://dx.doi.org/10.1002/9781119001379.

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Pelesko, John A. Self Assembly. London: Taylor and Francis, 2007.

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Chen, Xi, ed. Mechanical Self-Assembly. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-4562-3.

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McManus, Jennifer J., ed. Protein Self-Assembly. New York, NY: Springer New York, 2019. http://dx.doi.org/10.1007/978-1-4939-9678-0.

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Nilsson, Bradley L., and Todd M. Doran, eds. Peptide Self-Assembly. New York, NY: Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-7811-3.

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Publications, Key Note, ed. Self-assembly furniture. 6th ed. London: Key Note Publications, 1989.

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Publications, Key Note, ed. Self-assembly furniture. 7th ed. Hampton: Key Note Publications, 1992.

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Yamanaka, Junpei, Tohru Okuzono, and Akiko Toyotama. Colloidal Self-Assembly. Singapore: Springer Nature Singapore, 2023. http://dx.doi.org/10.1007/978-981-99-5052-2.

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Preece, Jon Andrew. From self-assembly to self-organisation. Birmingham: University of Birmingham, 1994.

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Bellucci, Stefano, ed. Self-Assembly of Nanostructures. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-0742-3.

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Book chapters on the topic "Self assembly"

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Nagarajan, Ramanathan. "Self-Assembly from Surfactants to Nanoparticles - Head vs. Tail." In Self-Assembly, 1–40. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2018. http://dx.doi.org/10.1002/9781119001379.ch1.

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Dong, Xue-Hui, Yiwen Li, Zhiwei Lin, Xinfei Yu, Kan Yue, Hao Liu, Mingjun Huang, Wen-Bin Zhang, and Stephen Z. D. Cheng. "Solution Self-Assembly of Giant Surfactants: An Exploration on Molecular Architectures." In Self-Assembly, 309–29. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2018. http://dx.doi.org/10.1002/9781119001379.ch10.

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Victorov, Alexey I. "Self-Assembly into Branches and Networks." In Self-Assembly, 41–75. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2018. http://dx.doi.org/10.1002/9781119001379.ch2.

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Smith, Timothy J., and Nicholas L. Abbott. "Self-Assembly of Responsive Surfactants." In Self-Assembly, 77–99. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2018. http://dx.doi.org/10.1002/9781119001379.ch3.

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Hanczyc, Martin M., and Pierre-Alain Monnard. "Self-Assembly and Primitive Membrane Formation: Between Stability and Dynamism." In Self-Assembly, 101–36. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2018. http://dx.doi.org/10.1002/9781119001379.ch4.

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Thompson, Matthew P., and Nathan C. Gianneschi. "Programming Micelles with Biomolecules." In Self-Assembly, 137–78. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2018. http://dx.doi.org/10.1002/9781119001379.ch5.

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Leon, Lorraine, and Matthew Tirrell. "Protein Analogous Micelles." In Self-Assembly, 179–205. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2018. http://dx.doi.org/10.1002/9781119001379.ch6.

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Dong, Xuehui, Aaron Huang, Allie Obermeyer, and Bradley D. Olsen. "Self-Assembly of Protein−Polymer Conjugates." In Self-Assembly, 207–55. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2018. http://dx.doi.org/10.1002/9781119001379.ch7.

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Li, Ting, Rebecca J. McMurray, and Monica Olvera de la Cruz. "Multiscale Modeling and Simulation of DNA-Programmable Nanoparticle Assembly." In Self-Assembly, 257–75. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2018. http://dx.doi.org/10.1002/9781119001379.ch8.

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Yong, Xin, Emily J. Crabb, Nicholas M. Moellers, Isaac Salib, Gerald T. McFarlin, Olga Kuksenok, and Anna C. Balazs. "Harnessing Self-Healing Vesicles to Pick Up, Transport, and Drop Off Janus Particles." In Self-Assembly, 277–307. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2018. http://dx.doi.org/10.1002/9781119001379.ch9.

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Conference papers on the topic "Self assembly"

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Bhalla, Navneet, Peter J. Bentley, and Marco Dorigo. "Self-assembly." In GECCO '14: Genetic and Evolutionary Computation Conference. New York, NY, USA: ACM, 2014. http://dx.doi.org/10.1145/2598394.2605366.

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Fochtman, Tyler, and Matthew Patitz. "Tile Assembly Simulator: A Software Package for Tile-Based Algorithmic Self-Assembly." In 2013 IEEE Conference on Self-Adaptive and Self-Organizing Systems Workshops (SASOW). IEEE, 2013. http://dx.doi.org/10.1109/sasow.2013.29.

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Wang, Yunlong, Ulrike Pfeil, and Harald Reiterer. "Supporting Self-Assembly." In MM '16: ACM Multimedia Conference. New York, NY, USA: ACM, 2016. http://dx.doi.org/10.1145/2985766.2985775.

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Wang, Yunlong, Ulrike Pfeil, and Harald Reiterer. "Supporting Self-Assembly." In MM '16: ACM Multimedia Conference. New York, NY, USA: ACM, 2016. http://dx.doi.org/10.1145/2985766.2988528.

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Welsby, Andrew. "System Self Assembly." In C&C '15: Creativity and Cognition. New York, NY, USA: ACM, 2015. http://dx.doi.org/10.1145/2757226.2757378.

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Arbuckle, D., and A. A. G. Requicha. "Active self-assembly." In IEEE International Conference on Robotics and Automation, 2004. Proceedings. ICRA '04. 2004. IEEE, 2004. http://dx.doi.org/10.1109/robot.2004.1307263.

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Nguyen, Nguyen, Eric Jankowski, and Sharon Glotzer. "Self-Assembly and Self-Tuning Behavior of Self-Propelled Particles." In 2011 5th IEEE International Conference on Self-Adaptive and Self-Organizing Systems (SASO). IEEE, 2011. http://dx.doi.org/10.1109/saso.2011.39.

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Kladitis, Paul E., and Victor M. Bright. "Novel Resistive Point Heater for MEMS Remote Solder Self-Assembly." In ASME 2000 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2000. http://dx.doi.org/10.1115/imece2000-1087.

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Abstract MEMS structures can be assembled using the surface tension of molten solder (solder self-assembly). Until this novel development, solder self-assembly was performed at the wafer or chip level where the whole chip needed to be heated to melt the micro sized solder droplets used to assemble devices. In this paper we present the design, testing, and modeling of a resistive point heater that is used to assemble an individual device on a chip without affecting neighboring devices. The point heater was packaged in 14 and 24 pin ceramic dual inline packages and tested in air, nitrogen, and formic-acid/nitrogen vapor. The lowest power needed to liquify a 63Sn/37Pb, 8 mil diameter equivalent volume solder droplet and assemble a device in formic-acid/nitrogen vapor was found to be 714 mW. The average power, of several trials, required to liquify a solder droplet is 998 mW at 141 mA and 7.08 V. A steady-state heat transfer model predicts 986.4 mW is required to keep the droplet at 181 °C (the observed minimum temperature at which 63Sn/37Pb solder is in liquid state). Growth of pure Sn platey crystals, varified by X-ray flourescence, was noted on the point heater assembly and surroundings during assembly in formic-acid/nitrogen vapor.
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JOHNSON, JOHN E. "VIRUS ASSEMBLY AND MATURATION." In Folding and Self-Assembly of Biological Macromolecules Conference. WORLD SCIENTIFIC, 2004. http://dx.doi.org/10.1142/9789812703057_0013.

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Frei, Regina, Giovanna Di Marzo Serugendo, and Jose Barata. "Designing Self-Organization for Evolvable Assembly Systems." In 2008 Second IEEE International Conference on Self-Adaptive and Self-Organizing Systems (SASO). IEEE, 2008. http://dx.doi.org/10.1109/saso.2008.20.

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Reports on the topic "Self assembly"

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CURRO, JOHN G., JOHN DWANE MCCOY, AMALIE L. FRISCHKNECHT, and KUI YU. Molecular Self-Assembly. Office of Scientific and Technical Information (OSTI), November 2001. http://dx.doi.org/10.2172/789581.

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Lavin, Judith, Richard Alan Kemp, and Constantine A. Stewart. Photovoltaic self-assembly. Office of Scientific and Technical Information (OSTI), October 2010. http://dx.doi.org/10.2172/1011215.

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Furst, Eric M. Directed Self-Assembly of Nanodispersions. Office of Scientific and Technical Information (OSTI), November 2013. http://dx.doi.org/10.2172/1105006.

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De Yoreo, J., W. D. Wilson, and T. Palmore. Solvent mediated self-assembly of solids. Office of Scientific and Technical Information (OSTI), December 1997. http://dx.doi.org/10.2172/674420.

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Cheng, Shengfeng, Steven James Plimpton, Jeremy B. Lechman, and Gary Stephen Grest. Drying/self-assembly of nanoparticle suspensions. Office of Scientific and Technical Information (OSTI), October 2010. http://dx.doi.org/10.2172/993324.

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Parviz, Babak A. Meso-Scale Self-Assembly Pilot Study. Fort Belvoir, VA: Defense Technical Information Center, April 2007. http://dx.doi.org/10.21236/ada466178.

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Schunk, Peter Randall, William Michael Brown, Steven James Plimpton, Jeremy B. Lechman, Gary Stephen Grest, Matthew K. Petersen, and Pieter J. in't Veld. Nanoparticle flow, ordering and self-assembly. Office of Scientific and Technical Information (OSTI), October 2008. http://dx.doi.org/10.2172/1028914.

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Harris, J. S., Kiehl Jr., and R. A. Patterned Self-Assembly in Non-Stoichiometric Semiconductors. Fort Belvoir, VA: Defense Technical Information Center, November 2001. http://dx.doi.org/10.21236/ada398657.

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Hsu, Julia W. P. Nanolithography Directed Materials Growth and Self-Assembly. Office of Scientific and Technical Information (OSTI), October 2006. http://dx.doi.org/10.2172/1137213.

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SUGAMA, T., R. SABATINI, and K. GAWLIK. SELF-ASSEMBLY CE OXIDE/ORGANOPOLYSILOXANE COMPOSITE COATINGS. Office of Scientific and Technical Information (OSTI), January 2005. http://dx.doi.org/10.2172/15011205.

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