Literatura académica sobre el tema "Membrane Modello"
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Artículos de revistas sobre el tema "Membrane Modello"
Petrauskas, Karolis. "Kompiuterinis biojutiklių su perforuota ir selektyvia membrana modeliavimas vienmačiu keturių sluoksnių modeliu". Informacijos mokslai 50 (1 de enero de 2009): 328–33. http://dx.doi.org/10.15388/im.2009.0.3217.
Texto completoDi Lullo, A. M., M. Scorza, F. Amato, M. Comegna, V. Raia, L. Maiuri, G. Ilardi, E. Cantone, G. Castaldo y M. Iengo. "An ex vivo model contributing to the diagnosis and evaluation of new drugs in cystic fibrosis". Acta Otorhinolaryngologica Italica 37, n.º 3 (junio de 2017): 207–13. http://dx.doi.org/10.14639/0392-100x-1328.
Texto completoAlfonso, M., A. Soba y G. Marshall. "Modeling the behavior of the cell membrane during electroporation using finite element method". Anales AFA 26, n.º 4 (9 de enero de 2016): 159–61. http://dx.doi.org/10.31527/analesafa.2018.26.4.159.
Texto completoSuárez Vega, Dubraska Violeta, Gladys Josefina Velazco de Maldonado y Jenair del Valle Yépez Guillén. "Histomorphometry of bone regeneration obtained with liposome-chitosan membrane system in an experimental model". Revista Virtual de la Sociedad Paraguaya de Medicina Interna 4, n.º 1 (30 de marzo de 2017): 12–34. http://dx.doi.org/10.18004/rvspmi/2312-3893/2017.04(01)12-034.
Texto completoTorrenegra, Juan David, Juan Pablo Hernandez-Ortiz y Jarol Molina. "Modelo mesoscópico de una membrana de intercambio protónico". Revista CINTEX 23, n.º 2 (31 de diciembre de 2018): 76–85. http://dx.doi.org/10.33131/24222208.320.
Texto completoAlvarado Anell, Edgar y B. I. Arévalo Rivas. "Theoretical and computacional analysis of the fixing of ossicular chain". Nova Scientia 1, n.º 1 (4 de noviembre de 2014): 107. http://dx.doi.org/10.21640/ns.v1i1.245.
Texto completoSánchez-Vargas, J. y F. J. Valdés-Parada. "Multiscale modeling of a membrane bioreactor for the treatment of oil and grease rendering wastewaters". Revista Mexicana de Ingeniería Química 20, n.º 2 (17 de marzo de 2021): 911–40. http://dx.doi.org/10.24275/rmiq/fen2368.
Texto completoBrião, Vandré Barbosa, Célia Regina Granhen Tavares, Danúbia Paula Cadore Favaretto y Marcelo Hemkemeier. "ULTRAFILTRAÇÃO DE EFLUENTE MODELO E EFLUENTE INDUSTRIAL DE LATICÍNIOS". Revista CIATEC-UPF 7, n.º 1 (19 de mayo de 2015): 1. http://dx.doi.org/10.5335/ciatec.v7i1.3367.
Texto completoDa Matta, Luciana Duarte Martins, Veronica Danielle Santos Ferreira, Rayana Vanessa da Costa Lima, Mateus Vinícius dos Santos Medeiros, Jéssika Karoline Silva do Nascimento, Luciana Guimarães Alves Filgueira y Giulianna Paiva Viana de Andrade Souza. "Metodologias ativas de aprendizagem utilizando modelo didático como ferramenta educacional para estudar interações moleculares em membranas e matriz extracelular". Revista de Ensino de Bioquímica 20, n.º 2 (2 de septiembre de 2022): 179–90. http://dx.doi.org/10.16923/reb.v20i2.917.
Texto completoCarles Fariña, Montserrat, Constatinos Zamboglou, Tobias Fechter, Selina Kiefer, Kathrin Reichel, Martin Werner, Cordula A. Jilg et al. "Modelo radiómico con PSMA-PET para la discriminación de pacientes con cáncer de próstata de alto riesgo". Revista de Física Médica 23, n.º 2 (15 de noviembre de 2022): 21–37. http://dx.doi.org/10.37004/sefm/2022.23.2.002.
Texto completoTesis sobre el tema "Membrane Modello"
Santarsiero, Nicola. "Analisi delle prestazioni di contattori a membrana ceramici per applicazioni di distillazione a membrana con gas di trasporto". Master's thesis, Alma Mater Studiorum - Università di Bologna, 2018.
Buscar texto completoMorgera, Francesca. "Interaction of host defence peptides with model and biological membranes". Doctoral thesis, Università degli studi di Trieste, 2010. http://hdl.handle.net/10077/3486.
Texto completoI peptidi in difesa dell’ospite (HDPs) esercitano molteplici ruoli nell’immunità, agendo sia come molecole antimicrobiche ad azione diretta sia come agenti immuno-moduatori. Il ruolo all’interfaccia tra immunità innata ed adattativa li rende molecole ideali per la futura applicazione nel trattamento di malattie infettive. Lo scopo di questo lavoro è stato quello di valutare le caratteristiche funzionali e strutturali di Catelicidine e Defensine selezionate al fine di correlare queste proprietà con l’ attività selettiva su cellule eucariotiche e procariotiche. Metodi biofisici e biochimici sono stati applicati alla catelicidina umana LL37 ed alcuni analoghi (ortologhi di primate e peptidi artificiali) con lo scopo di studiare la loro struttura e aggregazione in contatto con membrane biologiche e modello (i). Lo stesso approccio è stato anche applicato alle defensine umane hBD2 e 3 ed a loro analoghi. Inoltre, tecniche di microscopia, quali la microscopia a trasmissione elettronica (TEM), la microspettroscopia infrarossa in trasformata di fourier accoppiata ad una sorgente di sicrotrone (µSR-FTIR) e la citofluorimetria, sono state utilizzate in modo complementare al fine di studiare l’interazione a breve termine di hBD2 con cellule presentanti l’antigene, in particolare le cellule dendritiche immature (ii). (i) Lo studio strutturale e l’interazione di membrana di catelicidine ortologhe ci ha permesso di scoprire come l’evoluzione abbia lavorato sulla sequenza dei peptidi inducendo una diversa capacità di strutturare nei diversi ortologhi. Questo ha portato ad un’interazione differenziata e specifica con le membrane e a diversi meccanismi di lisi di membrana cellulare e probabilmente diversi modi di interagire con le cellule dell’ospite. (ii) Inoltre, abbiamo individuato una rapida interazione di hBD2 con le cellule presentanti l’antigene. hBD2 sembra indurre un riarrangiamento generale dei lipidi cellulari che sembra comportare un aumento nella fluidità di membrana e una ri- organizzazione del sistema endomembranoso. Queste variazioni potrebbero essere responsabili di un cambiamento morfologico delle cellule che promuoverebbe la mobilità cellulare in risposta a stimuli esterni. Questo studio dimostra l’esistenza di un posibile meccanismo alternativo di motilità cellulare rispetto alla chemotassi recettore-mediata, indicando un meccanimo di azione di hBD2 sulle iDC più complesso rispetto quanto riportato fino ad oggi.
XXII Ciclo
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Mendanha, Neto Sebastião Antônio. "Interações de terpenos com membranas de eritrócito, fibroblasto, estrato córneo e membrana modelo e interações de uma nanopartícula de ouro com membranas modelo". Universidade Federal de Goiás, 2014. http://repositorio.bc.ufg.br/tede/handle/tede/3993.
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The interactions of terpenes with membranes of erythrocyte, fibroblasts, stratum corneum and the model membranes of 1,2-dipalmitoylsn -glycero-3-phosphocholine were investigated by using the the electron paramagnetic resonance and fluorescence spectroscopic of lipophilic probes. It has been shown that when added at high concentrations to systems having a high lipid/solvent ratio, terpenes such as 1,8-cineol, α-terpineol, (+)-limonene and nerolidol are able to self-stabilize in molecular aggregates which can extract the bilayers lipids. Studies on the hemolytic and cytotoxic potential of various terpenes showed that cell damage caused by these molecules are concentration dependent and that among the studied terpenes, nerolidol and α-terpineol are the most hemolytic and cytotoxic, while (+)-limonene and 1,8-cineole are the least hemolytic and cytotoxic. However, the low correlation between these two tests indicates that the processes involved in each case are not completely dependent. It was also shown that once embedded in the membrane, terpenes increase the fluidity of lipid bilayers and decrease the temperature of the main phase transition. Differences between increased fluidity promoted by sesquiterpene nerolidol and all monoterpenes studied were observed. Meanwhile, in a comparison of the effect of the monoterpenes studied, no significant differences in their ability to increase membrane fluidity were detected. Furthermore, it was demonstrated by using confocal and atomic force microscopy and fluorescence spectroscopy that the 1,2-distearoylsn -glycero-3-(Aurora nanoparticles) is better incorporated in lipid membranes under fluid phase and that the addition of 0.1% of these conjugated nanoparticles do not produces large variations in membrane fluidity and no causes substantial morphological changes of lipid bilayers.
As intera¸c˜oes de terpenos com membranas de eritr´ocito, fibroblastos, estrato c´orneo e membrana modelo composta de 1,2-dipalmitoil-sn -glicero-3-fosfocolina foram investigadas por meio das espectroscopias de ressonˆancia paramagn´etica eletrˆ onica e de fluorescˆencia por meio do uso de sondas lipof´ılicas. Foi poss´ıvel demonstrar que quando adicionados em altas concentra¸c˜oes `a sistemas que possuem uma alta rela¸c˜ao lip´ıdio/solvente, terpenos como o 1,8-cineol, α-terpineol, (+)-limoneno e nerolidol s˜ao capazes de se estabilizar em agregados moleculares capazes de extrair os lip´ıdios das bicamadas. Estudos sobre o potencial hemol´ıtico e citot´oxico de v´arios terpenos demostraram que os danos celulares causados por estas mol´eculas s˜ao dependentes da concentra¸c˜ao e que dentre os terpenos estudados, nerolidol e terpineol s˜ao os mais hemol´ıticos e citot´oxicos enquanto limoneno e cineol s˜ao os menos hemol´ıticos e citot´oxicos. Entretanto, a baixa correla¸c˜ao entre estes dois testes indica que os processos envolvidos em cada caso n˜ao s˜ao totalmente dependentes. Ficou demonstrado ainda que uma vez incorporados nas membranas, os terpenos aumentam a fluidez das bicamadas lip´ıdicas e diminuem a temperatura de sua transi¸c˜ao de fase principal. Diferen¸cas entre o aumento de fluidez promovido pelo sesquiterpeno nerolidol e por todos os monoterpenos estudados foram verificadas. Contudo, uma compara¸c˜ao entre o efeito dos monoterpenos estudados, n˜ao aponta para diferen¸cas significativas entre suas capacidades de aumento de fluidez. Al´em disso, foi demostrado atrav´es das microscopias confocal e de for¸ca atˆomica e da espectroscopia de fluorescˆencia que a 1,2-distearoil-sn -glicero-3-(Nanopart´ıculas Aurora) ´e melhor incorporada em membranas lip´ıdicas em fase fluida e que a adi¸c˜ao de 0,1% destas nanopart´ıculas conjugadas n˜ao produz grandes varia¸c˜oes na fluidez e n˜ao provoca mudan¸cas morfol´ogicas substanciais das bicamadas lip´ıdicas.
Josyula, Ratnakar. "Structural studies of yeast mitochondrial peripheral membrane protein TIM44". Thesis, Birmingham, Ala. : University of Alabama at Birmingham, 2009. https://www.mhsl.uab.edu/dt/2009p/josyula.pdf.
Texto completoPavinatto, Adriana. "Efeito de características estruturais da quitosana sobre sua interação com filmes de Langmuir como modelo de biomembrana". Universidade de São Paulo, 2010. http://www.teses.usp.br/teses/disponiveis/88/88131/tde-01032010-133328/.
Texto completoChitosans are polysaccharides used in medicine, pharmacy, dentistry and in the inhibition of microorganisms growth (eg. as bactericidal agent). In these applications their action should depend on the interaction with cell membranes, which is difficult to verify because isolating a membrane is not easy. An alternative is to investigate the interaction with membrane models, such as a Langmuir film of phospholipids, from which information on the molecular level can be obtained. This dissertation evaluates the influence of the average content of N-acetylglucosamine units (GlcNAc) of chitosan and molecular interaction with Langmuir films of dipalmitoyl phosphatidic acid (DMPA). Chitosans with different average degrees of acetylation and low molecular weight were produced with the high-intensity ultrasound procedure. Chitosans affect the surface pressure and surface potential isotherms at large areas per molecule due to electrostatic and hydrophobic interactions with DMPA. In condensed films, they are located in the subsurface with little effect on the isotherms. The chitosan with fewer GLcNAc groups induced larger changes in the isotherms and in the film elasticity, probably due to stronger electrostatic interaction owing to a larger number of amine groups in chitosan interacting with the polar heads of DMPA. The most effective sample to induce changes in the DMPA monolayers was the low molecular weight chitosan, which can be attributed to the ease of adsorption. A minimum size chain seems essential, however, for mixtures of repeating units N-acetylglucosamine (GlcNAc) and glucosamine (GlcN) did not change the surface pressure isotherms and the elasticity of the DMPA films, owing to the absence of hydrophobic interactions. We conclude that the chitosan with better prospects for biological applications relying on the cell membrane interaction should have a low degree of acetylation and low molecular weight.
Pazin, Wallance Moreira. "Anisotropia de fluorescência: aplicações em membranas modelo". Universidade de São Paulo, 2012. http://www.teses.usp.br/teses/disponiveis/59/59135/tde-26062012-145823/.
Texto completoThe study of amphiphilic aggregates is extremely important due to their cell membrane mimic, which are essential for the life of the cell. It is known that phospholipids do not have molecular structure well defined in membranes, but play an essential role in maintaining of their integrity. Zwitterionic phospholipids are one of the main components of cell membranes, and a simplified model for the membranes are the bilayers they can form in aqueous medium. The main characteristic of lipid bilayers is the self-organization of lipids, making it necessary to study natural and spontaneous process, as their structural and dynamical properties. The fluorescence spectroscopy has been used to study many processes and systems of biological interest, especially by measurement of fluorescence anisotropy, which gives information about the rotational dynamics of the fluorescent probe inserted in the systems of interest, reflecting the combined effects of flexibility, fluidity and static interactions with surrounding molecules. In this work we examined the structural and dynamic properties of phospholipid model membranes formed of 1,2-dipalmitoyl-sn-glycero-3-phosphocoline DPPC by techniques related to fluorescence spectroscopy, mainly by measurements of steady-state and time resolved anisotropy of the probes 1,6-diphenyl-1,3,5-hexatriene (DPH), 7-nitrobenz-2-oxa-1,3-diazol-yl (NBD) attached to different regions of phospholipid molecules and also the lipophilic probe 2-amino-N-hexadecyl-benzamide (Ahba). The measurements were perfomed above and below of the phase transition temperature of the phospholipid bilayers of DPPC, gel and liquid-crystalline phase, due to the difference in the lateral organization of hydrocarbon chains in these two phases. Measures of dynamic light scattering (DLS) was performed to confirm the formation of the unilamellar vesicles by extrusion of lipid suspension containing multilamellar vesicles, and the technique of differential scanning calorimetry (DSC) was used to verify if the low concentration of fluorescent probes in lipid vesicles affect its packing. From the results, we found that the behavior of the three different fluorescent probes differ in both phases of phospholipid bilayers, revealing their structural and dynamic properties, mainly because to specific locations of the fluorophores. We verify that, due to the affinity for the hydrophobic region, the motion of the DPH is restricted to the \"wobbling\" motion, limited by hydrocarbon chains. For the NBD labeled in lipids, the motion of the fluorescent analogues as a whole depends on the location of the fluorophore and on the lipid conformation in both phases of lipid bilayers. Because of the location of the fluorescent group of the probe Ahba in the interface of lipid bilayers, we found that its rotational motion increases as the bilayers becomes more fluid, showing a dependency of the motion with the microviscosity of these bilayers.
Seminerio, Davide. "Modellazione e controllo di un sistema a celle a combustibile di tipo PEM". Master's thesis, Alma Mater Studiorum - Università di Bologna, 2022.
Buscar texto completoEineljung, Lars. "Modell av det basilära membranet". Thesis, University of Gävle, Department of Mathematics, Natural and Computer Sciences, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:hig:diva-3370.
Texto completoSyftet med detta arbete är att undersöka om det är möjligt att bygga en modell över innerörat med dess basilära membran. Om detta skulle visa sig vara möjligt, är nästa frågeställning hur en sådan modell skulle kunna fungera pedagogiskt och uppfattas av elever.
Modellen som arbetet lett fram till är konstruerad som en låda, gjord av plexiglas, vilken skall motsvara en utrullad hörselsnäcka. Som membran har en uppsättning gummiband använts. Vidare aktiveras modellen med hjälp av en högtalare som får motsvara örats trumhinna. Det har visat sig att modellens membran beter sig på ett sätt som liknar det basilära membranet i hörselsnäckan. De vibrationer som bildas på modellens membran förflyttar sig, beroende på inkommande frekvens. Detta förlopp sker även på det basilära membranet.
Modellen har testats på en niondeklass som har fått utföra laborationer med hjälp av modellen. Eleverna har observerats under arbetet och har efter laborationen fått skriva en utvärdering, i form av en laborationsrapport och en enkätundersökning. Observation och utvärdering visar att modellen har ett pedagogiskt värde, men att det krävs förkunskaper inom området för att laborationen med modellen skall bli ett givande medel för inlärning.
MANZO, GIORGIA. "Host Defence Peptides (HDPs): investigating the structure-to-function relationship through bio-physical techniques". Doctoral thesis, Università degli Studi di Cagliari, 2014. http://hdl.handle.net/11584/266428.
Texto completoBuzzá, Hilde Harb. "Avaliação da terapia fotodinâmica em um modelo tumoral em membrana corioalantóica". Universidade de São Paulo, 2016. http://www.teses.usp.br/teses/disponiveis/76/76132/tde-12042016-151204/.
Texto completoPhotodynamic Therapy (PDT) is a cancer treatment that has had great advances over the years and consists in the interaction between light and a photosensitizer compound, transforming the molecular oxygen in singlet oxygen, highly reactive and toxic to the cell. In this context, the use of Chorioallantoic Membrane (CAM) enables direct access to blood vessels, making possible to study the vascular effects involved in this therapy. The development of a tumor in this environment previously vascularized allows the study and the understanding of mechanisms that involves the growing and the destruction of tumor, improving different therapeutic modalities. The tumor cells used to develop the tumor in this model can be from several lines and ways of application, since cell culture to biopsy of some tumor. The main objective was investigating PDT in blood vessels and neoplasic cells in the tumor model in CAM. With this model studied for melanoma cells and Ehrlich, it was chosen to work with Ehrlich tumor because its facility of laboratory manipulation. After the observation the interaction between blood vessels and tumor cells, with confocal microscopy analysis, it was possible to understand and quantify the individualized effect of photosensitizers, including the pharmacodynamic of Photogem® and the Protoporphyrin IX from Aminolevulinic acid, both topic and intravenous application. From this, the tumor was illuminated and the Photdynamic Therapy effects was analyzed both tumor and blood vessels that feeds it. Still using the curcumin, photosensitizer derivated of saffron which has alone a vascular effect, was applied PDT to analysis on the Chorioallantoic Membrane and the blood vessels effect. The understanding of this effect of curcumin enables the extension of its useful as photosensitizer in the cancer treatment and vascular diseases. Therefore, with the model established, it was possible to follow all PS studying both their action in blood vessels and in the tumor region, causing damage.
Libros sobre el tema "Membrane Modello"
Les modèles moléculaires de biomembranes. Paris: Hermann, 1987.
Buscar texto completoH, Templer Richard, Leatherbarrow Robin y Royal Society of Chemistry (Great Britain). Biophysical Chemistry Group., eds. Biophysical chemistry: Membranes and proteins. Cambridge, UK: Royal Society of Chemistry, 2002.
Buscar texto completo1957-, Layton Harold Erick y Weinstein Alan M, eds. Membrane transport and renal physiology. New York: Springer, 2002.
Buscar texto completo1932-, Osa Tetsuo y Atwood J. L, eds. Inclusion aspects of membrane chemistry. Dordrecht: Kluwer Academic Publishers, 1991.
Buscar texto completoU, Raess B. y Tunnicliff Godfrey, eds. The Red cell membrane: A model for solute transport. Clifton, N.J: Humana Press, 1989.
Buscar texto completoGao, Fei. Proton exchange membrane fuel cells modeling. London: ISTE, 2011.
Buscar texto completoNorbert, Latruffe, Federation of European Biochemical Societies. y Centre national de la recherche scientifique (France), eds. Dynamics of membrane proteins and cellular energetics. Berlin: Springer-Verlag, 1988.
Buscar texto completoFrishman, Dmitrij. Structural bioinformatics of membrane proteins. Wien: Springer, 2010.
Buscar texto completo1948-, Mrak Robert E., ed. Muscle membranes in diseases of muscle. Boca Raton, Fla: CRC Press, 1985.
Buscar texto completoNATO Advanced Study Institute on Physical Methods on Biological Membranes and Their Model Systems (1982 Altavilla Milicia, Italy). Physical methods on biological membranes and their model systems. New York: Plenum Press, 1985.
Buscar texto completoCapítulos de libros sobre el tema "Membrane Modello"
Nicolescu, Radu. "Structured Grid Algorithms Modelled with Complex Objects". En Membrane Computing, 321–37. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-28475-0_22.
Texto completoManca, Vincenzo y Luca Marchetti. "Goldbeter’s Mitotic Oscillator Entirely Modeled by MP Systems". En Membrane Computing, 273–84. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-18123-8_22.
Texto completoRaff, Manfred. "Stofftransport-Modelle über Membranen". En Membranverfahren bei künstlichen Organen, 15–32. Wiesbaden: Springer Fachmedien Wiesbaden, 2019. http://dx.doi.org/10.1007/978-3-658-28053-6_3.
Texto completoMeisenheimer, Wolfgang. "Modelle für Netzwerke und Membranen". En Modelle als Denkräume, Beispiele und Ebenbilder, 332–35. Wiesbaden: Springer Fachmedien Wiesbaden, 2018. http://dx.doi.org/10.1007/978-3-658-20115-9_75.
Texto completoZhang, Gexiang, Mario J. Pérez-Jiménez, Augustín Riscos-Núñes, Sergey Verlan, Savas Konur, Thomas Hinze y Marian Gheorghe. "Introduction". En Membrane Computing Models: Implementations, 1–9. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-1566-5_1.
Texto completoZhang, Gexiang, Mario J. Pérez-Jiménez, Augustín Riscos-Núñes, Sergey Verlan, Savas Konur, Thomas Hinze y Marian Gheorghe. "P Systems Implementation on P-Lingua Framework". En Membrane Computing Models: Implementations, 11–30. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-1566-5_2.
Texto completoZhang, Gexiang, Mario J. Pérez-Jiménez, Augustín Riscos-Núñes, Sergey Verlan, Savas Konur, Thomas Hinze y Marian Gheorghe. "P Systems Implementation on GPUs". En Membrane Computing Models: Implementations, 163–215. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-1566-5_6.
Texto completoZhang, Gexiang, Mario J. Pérez-Jiménez, Augustín Riscos-Núñes, Sergey Verlan, Savas Konur, Thomas Hinze y Marian Gheorghe. "P Systems Implementation on FPGA". En Membrane Computing Models: Implementations, 217–43. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-1566-5_7.
Texto completoZhang, Gexiang, Mario J. Pérez-Jiménez, Augustín Riscos-Núñes, Sergey Verlan, Savas Konur, Thomas Hinze y Marian Gheorghe. "Applications of Software Implementations of P Systems". En Membrane Computing Models: Implementations, 31–69. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-1566-5_3.
Texto completoZhang, Gexiang, Mario J. Pérez-Jiménez, Augustín Riscos-Núñes, Sergey Verlan, Savas Konur, Thomas Hinze y Marian Gheorghe. "Applications of Hardware Implementation of P Systems". En Membrane Computing Models: Implementations, 245–76. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-1566-5_8.
Texto completoActas de conferencias sobre el tema "Membrane Modello"
Salamanca, Jacobo M. y Fernando Tadeo. "Energía osmótica: modelado y simulación de ósmosis por presión retardada". En Actas de las XXXVII Jornadas de Automática 7, 8 y 9 de septiembre de 2016, Madrid. Universidade da Coruña, Servizo de Publicacións, 2022. http://dx.doi.org/10.17979/spudc.9788497498081.0616.
Texto completoYang, E. H., Y. Hishinuma, J. Su, T. B. Xu, R. Morgan y Z. Chang. "Active Membrane Using Electrostructure Graft Elastomer for Deployable and Lightweight Mirrors". En ASME 2007 International Mechanical Engineering Congress and Exposition. ASMEDC, 2007. http://dx.doi.org/10.1115/imece2007-43541.
Texto completoLolies, T., N. Gourdain, M. Charlotte y H. Belloc. "Wall Modeled Immersed Boundary Lattice Boltzmann Method for the Fluid-Structure Interaction of Ram-Air Parachutes and Paragliders". En 10th edition of the conference on Textile Composites and Inflatable Structures. CIMNE, 2021. http://dx.doi.org/10.23967/membranes.2021.037.
Texto completoKumar, Karthik, Ali Besharatian, Luis P. Bernal, Rebecca L. Peterson y Khalil Najafi. "A Multiphysics Reduced Order Model of Valve Pumping in a 4-Stage Vacuum Micropump". En ASME 2012 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/imece2012-87681.
Texto completoGonzález, Marina, Marco Granero y Mariana Baroni. "ESTUDO DA DINÂMICA DA MEMBRANA NEURAL ATRAVÉS DE UM MODELO MATEMÁTICO (MODELO HODGKIN HUXLEY)." En IX Simpósio de Engenharia Biomédica. Uberlândia - MG, Brazil: Galoa, 2016. http://dx.doi.org/10.17648/seb-2016-53332.
Texto completoSolasi, Roham, Xinyu Huang, Yue Zou, Matthew Feshler, Kenneth Reifsnider y David Condit. "Mechanical Response of 3-Layered MEA During RH and Temperature Variation Based on Mechanical Properties Measured Under Controlled T and RH". En ASME 2006 4th International Conference on Fuel Cell Science, Engineering and Technology. ASMEDC, 2006. http://dx.doi.org/10.1115/fuelcell2006-97094.
Texto completoLykotrafitis, George y He Li. "Two-Component Coarse-Grain Model for Erythrocyte Membrane". En ASME 2011 International Mechanical Engineering Congress and Exposition. ASMEDC, 2011. http://dx.doi.org/10.1115/imece2011-62133.
Texto completoMamouri, Sina Jahangiri, Volodymyr V. Tarabara y André Bénard. "A Wall Film Model for Membrane Fouling". En ASME 2018 5th Joint US-European Fluids Engineering Division Summer Meeting. American Society of Mechanical Engineers, 2018. http://dx.doi.org/10.1115/fedsm2018-83298.
Texto completoCreasy, M. Austin y Donald J. Leo. "Modeling Bilayer Systems as Electrical Networks". En ASME 2010 Conference on Smart Materials, Adaptive Structures and Intelligent Systems. ASMEDC, 2010. http://dx.doi.org/10.1115/smasis2010-3791.
Texto completoSirota, Lea y Yoram Halevi. "A Combined Modal-Wave Based Control of Membranes Using Irrational Transfer Functions". En ASME 2014 Conference on Smart Materials, Adaptive Structures and Intelligent Systems. American Society of Mechanical Engineers, 2014. http://dx.doi.org/10.1115/smasis2014-7628.
Texto completoInformes sobre el tema "Membrane Modello"
Marquart, Grant. Biomimetic Model Membranes to Study Protein-membrane Interactions and their Role in Alzheimer?s Disease. Portland State University Library, enero de 2015. http://dx.doi.org/10.15760/honors.154.
Texto completoElbaum, Michael y Peter J. Christie. Type IV Secretion System of Agrobacterium tumefaciens: Components and Structures. United States Department of Agriculture, marzo de 2013. http://dx.doi.org/10.32747/2013.7699848.bard.
Texto completoVilla, Daniel, Charles Morrow, Johan Vanneste, Emily Gustafson, NREL Sertac Akar, Craig Turchi y Tzahi Cath. Multi-configuration Membrane Distillation Model (MCMD). Office of Scientific and Technical Information (OSTI), octubre de 2018. http://dx.doi.org/10.2172/1489619.
Texto completoShirley, David Noyes, Thomas W. Hunt, W. Michael Brown, Joseph S. Schoeniger, Alexander Slepoy, Kenneth L. Sale, Malin M. Young, Jean-Loup Michel Faulon y Genetha Anne Gray. Model-building codes for membrane proteins. Office of Scientific and Technical Information (OSTI), enero de 2005. http://dx.doi.org/10.2172/920776.
Texto completoHurst, J. K. [Membrane-based photochemical systems as models for photosynthetic cells]. Office of Scientific and Technical Information (OSTI), enero de 1992. http://dx.doi.org/10.2172/6675105.
Texto completoDas, Digendra K. Enhancement of the Computational Efficiency of Membrane Computing Models. Fort Belvoir, VA: Defense Technical Information Center, abril de 2007. http://dx.doi.org/10.21236/ada469153.
Texto completoEpel, Bernard y Roger Beachy. Mechanisms of intra- and intercellular targeting and movement of tobacco mosaic virus. United States Department of Agriculture, noviembre de 2005. http://dx.doi.org/10.32747/2005.7695874.bard.
Texto completoSieder, Isolde. Electrostatic Interactions at Membrane-water Interfaces and Distribution of 2, 4, 6-Trichlorophenol in a Membrane Model System. Portland State University Library, enero de 2000. http://dx.doi.org/10.15760/etd.6963.
Texto completoGiannelis, Emmanuel P. Nanobiohybrids: New Model Systems for Membranes and Sensors. Fort Belvoir, VA: Defense Technical Information Center, septiembre de 2004. http://dx.doi.org/10.21236/ada427213.
Texto completoGiannelis, Emmanuel P. Nanobiohybrids: New Model Systems for Membranes and Sensors. Fort Belvoir, VA: Defense Technical Information Center, junio de 2005. http://dx.doi.org/10.21236/ada434611.
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