Academic literature on the topic 'Fuze membran'

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Journal articles on the topic "Fuze membran"

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Brukman, Nicolas G., Berna Uygur, Benjamin Podbilewicz, and Leonid V. Chernomordik. "How cells fuse." Journal of Cell Biology 218, no. 5 (April 1, 2019): 1436–51. http://dx.doi.org/10.1083/jcb.201901017.

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Cell–cell fusion remains the least understood type of membrane fusion process. However, the last few years have brought about major advances in understanding fusion between gametes, myoblasts, macrophages, trophoblasts, epithelial, cancer, and other cells in normal development and in diseases. While different cell fusion processes appear to proceed via similar membrane rearrangements, proteins that have been identified as necessary and sufficient for cell fusion (fusogens) use diverse mechanisms. Some fusions are controlled by a single fusogen; other fusions depend on several proteins that either work together throughout the fusion pathway or drive distinct stages. Furthermore, some fusions require fusogens to be present on both fusing membranes, and in other fusions, fusogens have to be on only one of the membranes. Remarkably, some of the proteins that fuse cells also sculpt single cells, repair neurons, promote scission of endocytic vesicles, and seal phagosomes. In this review, we discuss the properties and diversity of the known proteins mediating cell–cell fusion and highlight their different working mechanisms in various contexts.
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Xu, C., K. Scott, Q. Li, J. Yang, and X. Wu. "A Quaternary Polybenzimidazole Membrane for Intermediate Temperature Polymer Electrolyte Membrane Fuel Cells." Fuel Cells 13, no. 2 (December 19, 2012): 118–25. http://dx.doi.org/10.1002/fuce.201200149.

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Kiatkittikul, P., T. Nohira, and R. Hagiwara. "Advantages of a Polyimide Membrane Support in Nonhumidified Fluorohydrogenate-Polymer Composite Membrane Fuel Cells." Fuel Cells 15, no. 4 (February 11, 2015): 604–9. http://dx.doi.org/10.1002/fuce.201400150.

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Epping Martin, K., and J. P. Kopasz. "The U.S. DOEs High Temperature Membrane Effort." Fuel Cells 9, no. 4 (August 2009): 356–62. http://dx.doi.org/10.1002/fuce.200800165.

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Leimin, X., L. Shijun, Y. Lijun, and L. Zhenxing. "Investigation of a Novel Catalyst Coated Membrane Method to Prepare Low-Platinum-Loading Membrane Electrode Assemblies for PEMFCs." Fuel Cells 9, no. 2 (April 2009): 101–5. http://dx.doi.org/10.1002/fuce.200800114.

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Yin, K. M., and C. P. Chang. "Effects of Humidification on the Membrane Electrode Assembly of Proton Exchange Membrane Fuel Cells at Relatively High Cell Temperatures." Fuel Cells 11, no. 6 (November 17, 2011): 888–96. http://dx.doi.org/10.1002/fuce.201100041.

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Zhang, H., T. Zhang, J. Wang, F. Pei, Y. He, and J. Liu. "Enhanced Proton Conductivity of Sulfonated Poly(ether ether ketone) Membrane Embedded by Dopamine-Modified Nanotubes for Proton Exchange Membrane Fuel Cell." Fuel Cells 13, no. 6 (October 2, 2013): 1155–65. http://dx.doi.org/10.1002/fuce.201300130.

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Meemuk, C., and S. Chirachanchai. "Layer-by-layer Proton Donor and Acceptor Membrane for an Efficient Proton Transfer System in a Polymer Electrolyte Membrane Fuel Cell." Fuel Cells 18, no. 2 (April 2018): 181–88. http://dx.doi.org/10.1002/fuce.201700223.

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Panchenko, U., T. Arlt, I. Manke, M. Müller, D. Stolten, and W. Lehnert. "Synchrotron Radiography for a Proton Exchange Membrane (PEM) Electrolyzer." Fuel Cells 20, no. 3 (February 17, 2020): 300–306. http://dx.doi.org/10.1002/fuce.201900055.

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QUAN QI, BAO, SPENCER W. BEASLEY, ANDREW K. WILLIAMS, and FRANCIS FRIZELLE. "DOES THE URORECTAL SEPTUM FUSE WITH THE CLOACAL MEMBRANE?" Journal of Urology 164, no. 6 (December 2000): 2070–72. http://dx.doi.org/10.1016/s0022-5347(05)66969-8.

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Dissertations / Theses on the topic "Fuze membran"

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Pokorná, Šárka. "Studium membránových interakcí pomocí pokročilých fluorescenčních technik: Od iontů k makromolekulám." Doctoral thesis, 2016. http://www.nusl.cz/ntk/nusl-353430.

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Advanced fluorescence techniques were used to explore tree distinct topics concerning biological membrane and their interactions. Following thesis is according to the topic divided into three parts: 1) Ionic effects were studied employing time dependent fluorescence shift experiments and molecular dynamic simulations. Combination of these two approaches are suitable to reveal characteristic like mobility and hydration of particular bilayer segment, lipid packing or ion binding sites. Halide anions were reported to adsorb to the cationic lipid bilayer specifically, altering membrane mobility and organization. Changes in observed parameters follows Hofmeister order. Their effect is mediated either by direct ionic interaction (soft, polarizable ions) as well as via alteration of water structure (hard, non-polarizable ions) in proximity of ion molecule. Further, divalent calcium was shown to bind strongly to neutral and negatively charged lipid bilayers. Several types of binding sites depending on calcium concentration were identified. 2) Two complementary lipopeptides, CPK and CPE, incorporated into distinct lipid bilayers serve as a minimal model inducing membrane fusion. Effectiveness of fusion event might be influenced by lipopeptide-membrane and lipopeptide-lipopeptide interaction. To reveal...
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Book chapters on the topic "Fuze membran"

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Koch, Christof. "Introduction." In Biophysics of Computation. Oxford University Press, 1998. http://dx.doi.org/10.1093/oso/9780195104912.003.0006.

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The brain computes! This is accepted as a truism by the majority of neuroscientists engaged in discovering the principles employed in the design and operation of nervous systems. What is meant here is that any brain takes the incoming sensory data, encodes them into various biophysical variables, such as the membrane potential or neuronal firing rates, and subsequently performs a very large number of ill-specified operations, frequently termed computations, on these variables to extract relevant features from the input. The outcome of some of these computations can be stored for later access and will, ultimately, control the motor output of the animal in appropriate ways. The present book is dedicated to understanding in detail the biophysical mechanisms responsible for these computations. Its scope is the type of information processing underlying perception and motor control, occurring at the millisecond to fraction of a second time scale. When you look at a pair of stereo images trying to fuse them into a binocular percept, your brain is busily computing away trying to find the “best” solution. What are the computational primitives at the neuronal and subneuronal levels underlying this impressive performance, unmatched by any machine? Naively put and using the language of the electronic circuit designer, the book asks: “What are the diodes and the transistors of the brain?” and “What sort of operations do these elementary circuit elements implement?” Contrary to received opinion, nerve cells are considerably more complex than suggested by work in the neural network community. Like morons, they are reduced to computing nothing but a thresholded sum of their inputs. We know, for instance, that individual nerve cells in the locust perform an operation akin to a multiplication. Given synapses, ionic channels, and membranes, how is this actually carried out? How do neurons integrate, delay, or change their output gain? What are the relevant variables that carry information? The membrane potential? The concentration of intracellular Ca2+ ions? What is their temporal resolution? And how large is the variability of these signals that determines how accurately they can encode information? And what variables are used to store the intermediate results of these computations? And where does long-term memory reside? Natural philosophers and scientists in the western world have always compared the brain to the most advanced technology of the day.
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Conference papers on the topic "Fuze membran"

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Suzuki, Sozo, Kazuo Mori, Koji Sugai, Yasuyuki Akutsu, Masaaki Ishikawa, Hideaki Sakai, and Katsuhide Hiwatashi. "ELECTRONMICROSCOPIC STUDIES ON PLATELETS AND MEGAKARYOCYTES IN GIANT PLATELET SYNDROME." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644560.

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Giant platelet syndrome are characterized morphologically by many giant platelets associated with several functional abnormalities in the peripheral blood. However, the mechanism of large platelet production has not yet been clarified. In 1981, we reported acase with Bernard-Soulier syndrome(BSS) in whom giant platelets were considered to be formed by fusion of two or three platelets in the circulating blood. We examined the ultrastructure of platelets and megakaryocytes in another case with BSS (29 year-old female) and a case with May-Hegglin anomaly (31 year-old male). Whole blood and bone marrow specimens were fixed with glutaraldehyde-osmium solution. Thin sections were prepared and stained with uranyl acetate and lead cytrate. Membrane systems of platelets and megakaryocytes in a case with BSS was investigated by staining of surface coating with ruthenium red.In a case with BSS, most platelets were very large and similar in morphology to those in formerly reported case. Giant platelets contained several-fold increased number of α-granules and mitochondria. Typical dense bodies were also observed. Contents of ATP/ADP, platelet factor-4(PF-4), B-thromboglobulin(B-TG) and platelet factor-3 availability(PF-3) were increased. Disorganization of microtubules was recognized. Some giant platelet contained membrane systems similar to demarcation membranes(DM) in megakaryocytes, characteristically. In mature megakaryocytes, areas divided by DM similar in size to those in normal megakaryocytes were observed. Several of these areas appeared to fuse together to form the giant platelets containing many granules and remnants of DM. In a case with May-Hegglin anomaly, typical Dohle’s bodies were shown in neutrophilic granulocytes. Giant platelets in this case also contained large number of α-granules and some of them contained membrane systems similar to DM. Areas similar in morphology to these giant platelets were clearly noted in the cytoplasm of mature megakaryocytes.In these cases, most giant platelets in the peripheral blood may be formed in the cytoplasm of megakaryocytes by fusion of several areas divided by DM, each of which may become normal sized platelets in normal megakaryocytes.
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Gao, Wei, William S. Oates, Paul R. Miles, and Ralph C. Smith. "Application of the Maximum Entropy Method to Multifunctional Materials for Data Fusion and Uncertainty Quantification." In ASME 2018 Conference on Smart Materials, Adaptive Structures and Intelligent Systems. American Society of Mechanical Engineers, 2018. http://dx.doi.org/10.1115/smasis2018-7960.

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Bayesian statistics is a quintessential tool for model validation in many applications including smart materials, adaptive structures, and intelligent systems. It typically uses either experimental data or high-fidelity simulations to infer model parameter uncertainty of reduced order models due to experimental noise and homogenization of quantum or atomistic behavior. When heterogeneous data is available for Bayesian inference, open questions remain on appropriate methods to fuse data and avoid inappropriate weighting on individual data sets. To address this issue, we implement a Bayesian statistical method that begins with maximizing entropy. We show how this method can weight heterogeneous data automatically during the inference process through the error covariance. This Maximum Entropy (ME) method is demonstrated by quantifying uncertainty in 1) a ferroelectric domain structure model and 2) a finite deforming electrostrictive membrane model. The ferroelectric phase field model identifies continuum parameters from multiple density functional theory calculations. In the case of the electrostrictive membrane, parameters are estimated from both mechanical and electric displacement experimental measurements.
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Varner, Victor D., Dmitry A. Voronov, and Larry A. Taber. "Mechanics of Embryonic Head Fold Morphogenesis." In ASME 2008 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2008. http://dx.doi.org/10.1115/sbc2008-193032.

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Head fold morphogenesis constitutes the first discernible epithelial folding event in the embryonic development of the chick. It arises at Hamburger and Hamilton (HH) stage 6 (approximately 24 hours into a 21-day incubation period) and establishes the anterior extent of the embryo [1]. At this stage, the embryonic blastoderm is composed of three germ layers (endoderm, mesoderm, and ectoderm), which are organized into a flat layered sheet that overlies the fibrous vitelline membrane (VM). Within this blastodermal sheet, a crescent-shaped head fold develops just anterior to the elongating notochord, spanning across the embryonic midline at the rostral end of neural plate. At the crest of this fold, the bilateral precardiac plates fuse in a cranial to caudal direction and give rise to the primitive heart tube and foregut [2, 3]. An understanding of head fold morphogenesis may thus offer insight into how embryonic tissues are arranged to make ready for proper cardiac formation.
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Reports on the topic "Fuze membran"

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Joe Suriano. GE Final technical report for Design and Development of high performance polymer fule cell membranes. Office of Scientific and Technical Information (OSTI), April 2010. http://dx.doi.org/10.2172/977060.

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