Bibliografias temáticas / Membrane proteins

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Literatura científica selecionada sobre o tema "Membrane proteins"

Autor: Grafiati
Publicado: 4 de junho de 2021
Última modificação: 25 de julho de 2025

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Artigos de revistas sobre o assunto "Membrane proteins"

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Jin, Wenzhen, and Syoji T. akada. "1P103 Asymmetry in membrane protein sequence and structure : Glycine outside rule(Membrane proteins,Oral Presentations)." Seibutsu Butsuri 47, supplement (2007): S49. http://dx.doi.org/10.2142/biophys.47.s49_2.

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Kühlbrandt, Werner. "Membrane proteins." Current Opinion in Structural Biology 1, no. 4 (1991): 531–33. http://dx.doi.org/10.1016/s0959-440x(05)80073-9.

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KUHLBRANDT, W., and E. GOUAUX. "Membrane proteins." Current Opinion in Structural Biology 9, no. 4 (1999): 445–47. http://dx.doi.org/10.1016/s0959-440x(99)80062-1.

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Hurley, James H. "Membrane Proteins." Chemistry & Biology 10, no. 1 (2003): 2–3. http://dx.doi.org/10.1016/s1074-5521(03)00006-1.

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Gennis, Robert B., and Werner Kühlbrandt. "Membrane proteins." Current Opinion in Structural Biology 3, no. 4 (1993): 499–500. http://dx.doi.org/10.1016/0959-440x(93)90074-u.

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Garavito, RMichael, and Arthur Karlin. "Membrane proteins." Current Opinion in Structural Biology 5, no. 4 (1995): 489–90. http://dx.doi.org/10.1016/0959-440x(95)80033-6.

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Picard, Martin. "Membrane proteins." Biochimie 205 (February 2023): 1–2. http://dx.doi.org/10.1016/j.biochi.2023.01.018.

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Ralston, GB. "Proteins of Marsupial Erythrocyte Membranes." Australian Journal of Biological Sciences 38, no. 1 (1985): 121. http://dx.doi.org/10.1071/bi9850121.

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The proteins of erythrocyte membranes from the red kangaroo, western grey kangaroo, eastern grey wallaroo (euro), red-necked wallaby, Tammar wallaby, and brush-tail possum have been fractionated on acrylamide gels in the presence of sodium dodecyl sulfate. The pattern of proteins was remarkably similar between the different marsupial species. The pattern of Coomassie blue-staining proteins in the membranes of these species was also very similar to that of the human erythrocyte membrane. However, the glycoproteins in the marsupial erythrocyte membranes were markedly less conspicuous than those
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Corey, Robin A., Phillip J. Stansfeld, and Mark S. P. Sansom. "The energetics of protein–lipid interactions as viewed by molecular simulations." Biochemical Society Transactions 48, no. 1 (2019): 25–37. http://dx.doi.org/10.1042/bst20190149.

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Membranes are formed from a bilayer containing diverse lipid species with which membrane proteins interact. Integral, membrane proteins are embedded in this bilayer, where they interact with lipids from their surroundings, whilst peripheral membrane proteins bind to lipids at the surface of membranes. Lipid interactions can influence the function of membrane proteins, either directly or allosterically. Both experimental (structural) and computational approaches can reveal lipid binding sites on membrane proteins. It is, therefore, important to understand the free energies of these interactions
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Thoma, Johannes, and Björn M. Burmann. "Fake It ‘Till You Make It—The Pursuit of Suitable Membrane Mimetics for Membrane Protein Biophysics." International Journal of Molecular Sciences 22, no. 1 (2020): 50. http://dx.doi.org/10.3390/ijms22010050.

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Membrane proteins evolved to reside in the hydrophobic lipid bilayers of cellular membranes. Therefore, membrane proteins bridge the different aqueous compartments separated by the membrane, and furthermore, dynamically interact with their surrounding lipid environment. The latter not only stabilizes membrane proteins, but directly impacts their folding, structure and function. In order to be characterized with biophysical and structural biological methods, membrane proteins are typically extracted and subsequently purified from their native lipid environment. This approach requires that lipid
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Teses / dissertações sobre o assunto "Membrane proteins"

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Gill, Katrina Louise. "Protein-protein interactions in membrane proteins." Thesis, University of Newcastle Upon Tyne, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.400016.

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Hedin, Linnea E., Kristoffer Illergård, and Arne Elofsson. "An Introduction to Membrane Proteins." Stockholms universitet, Institutionen för biokemi och biofysik, 2011. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-69241.

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alpha-Helical membrane proteins are important for many biological functions. Due to physicochemical constraints, the structures of membrane proteins differ from the structure of soluble proteins. Historically, membrane protein structures were assumed to be more or less two-dimensional, consisting of long, straight, membrane-spanning parallel helices packed against each other. However, during the past decade, a number of the new membrane protein structures cast doubt on this notion. Today, it is evident that the structures of many membrane proteins are equally complex as for many soluble protei
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Kota, Jhansi. "Membrane chaperones : protein folding in the ER membrane /." Stockholm : Karolinska institutet, 2007. http://diss.kib.ki.se/2007/978-91-7357-102-9/.

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Whitehead, L. "Computer simulation of biological membranes and membrane bound proteins." Thesis, University of Southampton, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.297412.

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Armstrong, James P. "Artificial membrane-binding proteins." Thesis, University of Bristol, 2014. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.686615.

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Membrane functionalization is a promising strategy for augmenting cell performance in regenerative medicine. To this end, the design, construction, characterisation and cell affinity of protein-polymer surfactant nanoconstructs are presented. Nanoconstructs of eGFP were synthesised that exhibited near-native structure and function, as well as effective and persistent membrane affinity. Human mesenchymal stem cells were labelled for up to ten days in culture, without affecting cell viability or differentiation capacity. This "cell priming" technology has been used to address the issue of hypoxi
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Zhang, Xiao Xiao. "Identification of membrane-interacting proteins and membrane protein interactomes using Nanodiscs and proteomics." Thesis, University of British Columbia, 2011. http://hdl.handle.net/2429/39413.

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The insoluble nature of membrane proteins has complicated the identification of their interactomes. The Nanodisc has allowed the membrane and membrane proteins to exist in a soluble state. In this thesis, we combined Nanodisc and proteomics and applied the technique to discover the interactome of membrane proteins. Using the SecYEG and MalFGK membrane complex incorporated into Nanodisc, we identified, Syd, SecA, and MalE. These interactions were identified with high specificity and confidence from total soluble protein extracts. The protein YidC was also tested but no interactors were detected
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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.

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Rapp, Mikaela. "The Ins and Outs of Membrane Proteins : Topology Studies of Bacterial Membrane Proteins." Doctoral thesis, Stockholm : Department of Biochemistry and Biophysics, Stockholm University, 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-1330.

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Berger, Bryan William. "Protein-surfactant solution thermodynamics applications to integral membrane proteins /." Access to citation, abstract and download form provided by ProQuest Information and Learning Company; downloadable PDF file 15.42 Mb., 304 p, 2006. http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&res_dat=xri:pqdiss&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&rft_dat=xri:pqdiss:3200533.

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Keegan, Neil. "From engineered membrane proteins to self-assembling protein monolayers." Thesis, University of Newcastle Upon Tyne, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.419991.

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Livros sobre o assunto "Membrane proteins"

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Ghirlanda, Giovanna, and Alessandro Senes, eds. Membrane Proteins. Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-583-5.

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Azzi, Angelo, Lanfranco Masotti, and Arnaldo Vecli, eds. Membrane Proteins. Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-71543-3.

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C, Goheen Steven, and Bio-Rad Laboratories, eds. Membrane proteins: Proceedings of the Membrane Protein Symposium. Bio-Rad Laboratories, 1987.

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H, White Stephen, ed. Membrane protein structure: Experimental approaches. Oxford University Press, 1994.

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Graham, J. M. Membrane analysis. BIOS Scientific Publishers, 1997.

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1940-, Hille Bertil, Fambrough Douglas M, and Society of General Physiologists, eds. Proteins of excitable membranes. Society of General Physiologists and Wiley-Interscience, 1987.

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Kleinschmidt, Jörg H. Lipid-protein Interactions: Methods and protocols. Humana Press, 2013.

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J, Kenny A., and Turner A. J. 1947-, eds. Mammalian ectoenzymes. Elsevier, 1987.

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Stefan, Bröer, and Wagner Carsten A, eds. Membrane transporter diseases. Kluwer Academic/Plenum Publishers, 2003.

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C, Froehner Stanley, and Bennett Vann, eds. Cytoskeletal regulation of membrane function. Rockefeller University Press, 1997.

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Capítulos de livros sobre o assunto "Membrane proteins"

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Broger, Clemens, Reinhard Bolli, and Angelo Azzi. "Spin Labeling of Membranes and Membrane Proteins." In Membrane Proteins. Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-71543-3_15.

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Bolli, Reinhard, Clemens Broger, and Angelo Azzi. "Purification of Cytochrome c Reductase and Oxidase by Affinity Chromatography." In Membrane Proteins. Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-71543-3_1.

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Spisni, A., G. Farruggia, and L. Franzoni. "Polypeptide-Lipid Interactions as Studied by 13C NMR." In Membrane Proteins. Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-71543-3_10.

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Masotti, L., J. Von Berger, and N. Gesmundo. "Conformational Changes in Polypeptides and Proteins Brought About by Interactions with Lipids." In Membrane Proteins. Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-71543-3_11.

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Müller, Michele, and Angelo Azzi. "Two Examples of Selective Fluorescent Labeling of SH-Groups with Eosin-5-Maleimide: The ADP/ATP Translocator and the Cytochrome c Oxidase Subunit III of Bovine Heart Mitochondria." In Membrane Proteins. Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-71543-3_12.

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Montecucco, C. "Hydrophobic Photolabeling with 125I-TID of Red Blood Cell Membranes." In Membrane Proteins. Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-71543-3_13.

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Brandolin, Gérard, Marc R. Block, François Boulay, and Pierre V. Vignais. "Use of Fluorescent Probes of the Adenine Nucleotide Carrier for Binding Studies and Analysis of Conformational Changes." In Membrane Proteins. Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-71543-3_14.

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Nałȩcz, M. J., and A. Azzi. "Functional Reconstitution of the Mitochondrial Cytochrome b-c1 Complex: Effect of Cholesterol." In Membrane Proteins. Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-71543-3_16.

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Nałȩcz, M. J., A. Szewczyk, and L. Wojtczak. "Changes of the Membrane Surface Potential Measured by Amphiphilic Fluorescent and ESR Probes." In Membrane Proteins. Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-71543-3_17.

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Capitanio, N., and S. Papa. "Reconstitution of Cytochrome c Oxidase." In Membrane Proteins. Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-71543-3_18.

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Trabalhos de conferências sobre o assunto "Membrane proteins"

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Daufin, G., J. P. Escudier, H. Carrère, S. Bérot, L. Fillaudeau, and M. Decloux. "Application of Membrane Processes in Food and Dairy Industry." In CORROSION 2000. NACE International, 2000. https://doi.org/10.5006/c2000-00313.

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Abstract Membrane processes have become major tools in food processing for more than 25 years. The food industry represents a significant part of the turnover of the membrane manufacturing industry worldwide. The main applications of membrane operations are in the dairy industry (whey protein concentration, milk protein standardization, etc.) far before beverages (wine, beer, fruit juices, etc.) and egg products. Among the very numerous applications on an industrial scale a few striking particular separations which represent the last advances in food processing are reported. Clarification of f
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Russo, Michael J., Simon H. Friedman, Jens O. M. Karlsson, and Mehmet Toner. "A Two-Compartment Membrane Limited Model of Molecular Transport Through Nano-Scale Pores With a Metal-Actuated Switch." In ASME 1997 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 1997. http://dx.doi.org/10.1115/imece1997-1306.

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Abstract We have previously demonstrated that we can reversibly alter the transport selectivity of the plasma membrane to small molecules (∼1000 Da) by treating cells with H5, a genetic mutant of the pore-forming protein Staphylococcus aureus α-toxin, designed to be equipped with a metal-actuated switch. Toward the development of a plasma membrane permeabilization technique for both clinical and basic research applications, we have developed a simple model of molecular transport through the H5 pore. This model in combination with hindered transport models predicts the rate of transport of our
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Börsch, Michael. "Single-Molecule FRET for structural biology of active membrane proteins." In Multiphoton Microscopy in the Biomedical Sciences XXV, edited by Ammasi Periasamy, Peter T. So, and Karsten König. SPIE, 2025. https://doi.org/10.1117/12.3046317.

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Mora-Mendoza, J. L., R. García-Esquivel, A. A. Padilla-Viveros, et al. "Study of Internal MIC in Pipelines of Sour Gas, Mixed with Formation Waters." In CORROSION 2001. NACE International, 2001. https://doi.org/10.5006/c2001-01246.

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Abstract Microorganisms isolated from sour gas transmission pipelines from/to offshore platforms located in Mexico, have been associated with localized corrosion process. The microorganisms, isolated under an oxygen-free atmosphere, grew in a culture media rich in lactate/sulfate and reduced sulfate to hydrogen sulfide. When carbon steel was exposed to their activity, severe corrosion rates were measured and pitting damage was observed on sample surfaces. The 16S rRNA sequential analysis procedure showed that both samples are identified as Citrobacter amalonaticus. At present, these bacteria h
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Cheung, K. H., H. Y. Lai, and Ji-Dong Gu. "Reduction of Chromate by Marine Bacillus Megaterium TKW3." In CORROSION 2006. NACE International, 2006. https://doi.org/10.5006/c2006-06521.

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abstract Hexavalent chromium (Cr6+) is an important corrosion inhibitor and is also highly toxic pollutant, which can be detoxified and precipitated through reduction to Cr3+. Bacillus megaterium TKW3 isolated from contaminated sediments was capable of reducing Cr6+ in concomitance with metalloids (Se4+, Se6+ and As5+). Notwithstanding the approximately 50% inhibition, it is firstly reported that bacteria reduced Cr6+ and Se4+ [to elemental Se] simultaneously. No significant difference was observed among electron donors (glucose, maltose and mannitol) on Cr6+ reduction of B. megaterium TKW3. T
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Merchant, Fatima A., and Mehmet Toner. "Spatial and Dynamic Characterization of the Interaction of Staphylococcus Aureus Alpha-Toxin With Cell Membranes." In ASME 1997 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 1997. http://dx.doi.org/10.1115/imece1997-1305.

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Abstract Genetically engineered pore-forming proteins such as the H5 mutant of the staphylococcal aureus α-toxin, have been specially designed to achieve controlled and reversible plasma membrane permeabilization. Hence, quantitative information regarding the dynamics of poration is critical for designing applications employing α-toxins for the permeabilization of cell membranes. We have employed immunofluorescence imaging techniques in conjunction with viability assays to elucidate the spatial and temporal interactions of α-toxin with living cells. This information would aid in the design and
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Lapetina, Eduardo G., Bryan R. Reep, and Luis Molina Y. Vedia. "NOVEL GTP-BINDING PROTEINS OF CYTOSOLIC AND MEMBRANE FRACTIONS OF HUMAN PLATELETS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644629.

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We have assessed the binding of (α-32P)GTP to platelet proteins from cytosolic and membrane fractions. Proteins were separated by SDS-PAGE and electrophoretically transferred to nitrocellulose. Incubation of the nitrocellulose blots with (α-32p)GTP indicated the presence of specific and distinct GTP-binding proteins in cytosol and membranes. Binding was prevented by 10-100 nM GTP or GTPyS and by 100 nM GDP; binding was unaffected by 1 nM-1 μM ATP. One main GTP-binding protein (29.5 KDa) was detected in the membrane fraction while three others (29, 27, and 21 KDa) were detected in the soluble f
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Maiti, Sudipta. "Plasmonics for Membrane Proteins?" In International Conference on Fibre Optics and Photonics. OSA, 2014. http://dx.doi.org/10.1364/photonics.2014.s3d.1.

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Park, Jeong-Man. "Interactions between membrane proteins." In Third tohwa university international conference on statistical physics. AIP, 2000. http://dx.doi.org/10.1063/1.1291595.

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Sikorski, Aleksander F. "Membrane rafts organizing proteins?" In International Conference on Cell Science and Regenerative Medicine. United Research Forum, 2024. https://doi.org/10.51219/urforum.2024.aleksander-f-sikorski.

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Relatórios de organizações sobre o assunto "Membrane proteins"

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Woolf, Thomas B., Paul Stewart Crozier, and Mark Jackson Stevens. Molecular dynamics of membrane proteins. Office of Scientific and Technical Information (OSTI), 2004. http://dx.doi.org/10.2172/919637.

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Shirley, David Noyes, Thomas W. Hunt, W. Michael Brown, et al. Model-building codes for membrane proteins. Office of Scientific and Technical Information (OSTI), 2005. http://dx.doi.org/10.2172/920776.

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Smith, H. G. Surface-Bound Membrane-Mimetic Assemblies: Electrostatic Attributes of Integral Membrane Proteins. Defense Technical Information Center, 1988. http://dx.doi.org/10.21236/ada204381.

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Smith, H. G. Surface-Bound Membrane-Mimetic Assemblies: Electrostatic Attributes of Integral Membrane Proteins. Defense Technical Information Center, 1991. http://dx.doi.org/10.21236/ada237229.

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Williams, Timothy J., Ramesh Balakrishnan, Brian K. Radak, et al. Free Energy Landscapes of Membrane Transport Proteins. Office of Scientific and Technical Information (OSTI), 2017. http://dx.doi.org/10.2172/1483996.

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Creutz, Carl E. Repair of Nerve Cell Membrance Damage by Calcium-Dependent, Membrane-Binding Proteins. Defense Technical Information Center, 2013. http://dx.doi.org/10.21236/ada596750.

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Creutz, Carl E. Repair of Nerve Cell Membrane Damage by Calcium-Dependent, Membrane-Binding Proteins. Defense Technical Information Center, 2011. http://dx.doi.org/10.21236/ada560549.

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Barkan, Alice, and Zach Adam. The Role of Proteases in Regulating Gene Expression and Assembly Processes in the Chloroplast. United States Department of Agriculture, 2003. http://dx.doi.org/10.32747/2003.7695852.bard.

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Chloroplasts house many biochemical processes that are essential for plant viability. Foremost, among these is photosynthesis, which requires the protein-rich thylakoid membrane system. The activation of chloroplast genes encoding thylakoid membrane proteins and the targeting and assembly of these proteins together with their nuclear-encoded partners are essential for the elaboration of the thylakoid membrane. Several nuclear-encoded proteins that regulate chloroplast gene expression and that mediate the targeting of proteins to the thylakoid membrane have been identified in recent years, and
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Moczydlowski, Edward G. Intra-membrane molecular interactions of K+ channel proteins :. Office of Scientific and Technical Information (OSTI), 2013. http://dx.doi.org/10.2172/1092995.

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Schiffer, M., C. H. Chang, and F. J. Stevens. The functions of tryptophan residues in membrane proteins. Office of Scientific and Technical Information (OSTI), 1994. http://dx.doi.org/10.2172/10172497.

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