Literatura académica sobre el tema "Complex substrates"
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Artículos de revistas sobre el tema "Complex substrates"
Kim, Ikjin, Jungmi Ahn, Chang Liu, Kaori Tanabe, Jennifer Apodaca, Tadashi Suzuki y Hai Rao. "The Png1–Rad23 complex regulates glycoprotein turnover". Journal of Cell Biology 172, n.º 2 (9 de enero de 2006): 211–19. http://dx.doi.org/10.1083/jcb.200507149.
Texto completoWu, Xi, Lanlan Li y Hui Jiang. "Doa1 targets ubiquitinated substrates for mitochondria-associated degradation". Journal of Cell Biology 213, n.º 1 (4 de abril de 2016): 49–63. http://dx.doi.org/10.1083/jcb.201510098.
Texto completoDayan, Peter. "Simple substrates for complex cognition". frontiers in Neuroscience 2, n.º 2 (15 de diciembre de 2008): 255–63. http://dx.doi.org/10.3389/neuro.01.031.2008.
Texto completoKanehara, Kazue, Wei Xie y Davis T. W. Ng. "Modularity of the Hrd1 ERAD complex underlies its diverse client range". Journal of Cell Biology 188, n.º 5 (8 de marzo de 2010): 707–16. http://dx.doi.org/10.1083/jcb.200907055.
Texto completoMin, Mingwei, Ugo Mayor y Catherine Lindon. "Ubiquitination site preferences in anaphase promoting complex/cyclosome (APC/C) substrates". Open Biology 3, n.º 9 (septiembre de 2013): 130097. http://dx.doi.org/10.1098/rsob.130097.
Texto completoKnape, Matthias J., Maximilian Wallbott, Nicole C. G. Burghardt, Daniela Bertinetti, Jan Hornung, Sven H. Schmidt, Robin Lorenz y Friedrich W. Herberg. "Molecular Basis for Ser/Thr Specificity in PKA Signaling". Cells 9, n.º 6 (25 de junio de 2020): 1548. http://dx.doi.org/10.3390/cells9061548.
Texto completoBourreau, D., P. Guillon y M. Chatard-Moulin. "Complex permittivity measurement of optoelectronic substrates". Electronics Letters 22, n.º 7 (1986): 399. http://dx.doi.org/10.1049/el:19860271.
Texto completoNeal, Sonya, Raymond Mak, Eric J. Bennett y Randolph Hampton. "A Cdc48 “Retrochaperone” Function Is Required for the Solubility of Retrotranslocated, Integral Membrane Endoplasmic Reticulum-associated Degradation (ERAD-M) Substrates". Journal of Biological Chemistry 292, n.º 8 (11 de enero de 2017): 3112–28. http://dx.doi.org/10.1074/jbc.m116.770610.
Texto completoSaunders, Reuben A., Benjamin M. Stinson, Tania A. Baker y Robert T. Sauer. "Multistep substrate binding and engagement by the AAA+ ClpXP protease". Proceedings of the National Academy of Sciences 117, n.º 45 (26 de octubre de 2020): 28005–13. http://dx.doi.org/10.1073/pnas.2010804117.
Texto completoTwomey, Edward C., Zhejian Ji, Thomas E. Wales, Nicholas O. Bodnar, Scott B. Ficarro, Jarrod A. Marto, John R. Engen y Tom A. Rapoport. "Substrate processing by the Cdc48 ATPase complex is initiated by ubiquitin unfolding". Science 365, n.º 6452 (27 de junio de 2019): eaax1033. http://dx.doi.org/10.1126/science.aax1033.
Texto completoTesis sobre el tema "Complex substrates"
Alhijjaji, Fariha. "Studies on the microbial degradation of complex substrates". Thesis, University of Sheffield, 2015. http://etheses.whiterose.ac.uk/10040/.
Texto completoSelander, Nicklas. "Catalytic Functionalization of Allylic Substrates by Palladium Pincer Complexes". Doctoral thesis, Stockholms universitet, Institutionen för organisk kemi, 2010. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-39065.
Texto completoAt the time of the doctoral defense, the following papers were unpublished and had a status as follows: Paper 11: In press.
Thoresen, Mariska. "An investigation into the synergistic action of cellulose-degrading enzymes on complex substrates". Thesis, Rhodes University, 2015. http://hdl.handle.net/10962/d1017915.
Texto completoGössl, Illdiko Maria. "Supramolecular structures of dendronized polymers and DNA on solid substrates". Doctoral thesis, Humboldt-Universität zu Berlin, Mathematisch-Naturwissenschaftliche Fakultät I, 2003. http://dx.doi.org/10.18452/14893.
Texto completoComplexes of oppositely charged polyelectrolytes play an important role in both biology and material science, for instance DNA condensation in vitro, nucleosomal structure, non-viral gene transfection systems as well as layer-by-layer adsorption. Although there are theories predicting overcharging of polyelectrolyte complexes, the driving forces are still under debate and systematic experimental studies on single polyelectrolytes remain challenging. Therefore the question arose if it is possible to analyze single polyelectrolyte complexes, using DNA and dendronized polymers, with the scanning force microscope in order to investigate the complexation in detail. For the complex analysis, the polyelectrolytes were allowed to interact in solution and then to adsorb on negatively charged mica or on mica coated with a positively charged polymer. Scanning force microscopy was used to investigate the adsorbed species. DNA/dendronized polymer complexes of charge ratio of 1/1 through 1/0.7 adsorbed on mica coated with a positively charged polymer. The analysis of high resolution molecular images indicated that DNA wraps around the dendronized polymer with an estimated pitch of (2.30 ± 0.27) nm and (2.16 ± 0.27) nm for dendronized polymers of generation two and four, respectively. In the proposed model the polyelectrolyte with the smaller linear charge density is wrapped around the more highly charged dendronized polymer, resulting in a negatively overcharged complex. This overcharging is consistent within recent theories of spontaneous overcharging of complexes of one polyelectrolyte wrapping around the other. Using the complex of DNA and dendronized polymers of second generation, the influence of monovalent salt concentration on the molecular structure was studied. By increasing the salt concentration the pitch showed a minimum as predicted by the interplay of electrostatic forces and entropic interactions of polyelectrolyte adsorption. At high salt concentration (2.4 M NaCl) the release of DNA from the complex can be observed. The results showed that the DNA/dendronized polymer system can be used as a new, high potential model system to investigate single polyelectrolyte interactions. With regard to recent theories, the experimental results indicate that the overcharging of the complex is mainly driven by electrostatic forces whereas contributions of counterion entropy and bending energy seem to be negligible. This understanding may be useful for the design of single polyelectrolyte complexes for non-viral gene delivery systems and might help to optimize the transfection efficiency based on the structure of the vector system.
Zich, Judith. "Analysis of Mph1 kinase and its substrates in spindle checkpoint signalling". Thesis, University of Edinburgh, 2010. http://hdl.handle.net/1842/8253.
Texto completoKothe, Thomas. "Reductive Binding of C‒O and Nitro Substrates at a Pyrazolate-Bridged Preorganized Dinickel Scaffold". Doctoral thesis, Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2020. http://hdl.handle.net/21.11130/00-1735-0000-0005-1524-B.
Texto completoDuan, Peng-Cheng. "A Dinuclear Dihydride Complex for Bimetallic Reductive Activation and Transformation of a Range of Inert Substrates". Doctoral thesis, Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2017. http://hdl.handle.net/11858/00-1735-0000-002E-E38C-2.
Texto completoBakir, Ilyas. "Molecular studies of the γ-secretase complex activity and selectivity towards the two substrates APP and Notch". Thesis, Mälardalen University, School of Sustainable Development of Society and Technology, 2010. http://urn.kb.se/resolve?urn=urn:nbn:se:mdh:diva-9622.
Texto completoAlzheimer Disease (AD) is the most common neurodegenerative disorder in the world. One of the neuropathological hallmarks of AD is the senile plaques in the brain. The plaques are mainly composed of the amyloid β (Aβ) peptide. Aβ is generated from the amyloid precursor protein, APP, when it is first cleaved by the β-secretase and subsequently the γ-secretase complex. The γ-secretase complex cleaves at different sites, called γ and ε, where the γ-cleavage site generates Aβ peptides of different lengths and ε-cleavage generates the APP intracellular domain (AICD). The two major forms of Aβ is 40 and 42 amino acids long peptides, where the latter is more prone to aggregate and is the main component in senile plaques. The γ-secretase complex is composed of four proteins; Pen-2, Aph-1, nicastrin and presenilin (PS). The PS protein harbours the catalytic site of the complex, where two aspartate residues in position 257 and 385 (Presenilin 1 numbering) are situated. Most Familial AD (FAD) mutations in the PS gene cause a change in the γ-cleavage site, leading to a shift from producing Aβ40 to the longer more toxic variant Aβ42. Frequently, this often leads to impairments of the AICD production. Another substrate for the γ-secretase complex is Notch. It is important to maintain the Notch signaling since an intracellular domain (NICD) is formed after cleavage by the γ-secretase complex in the membrane (S3-site) and this domain is involved in transcription of genes important for cell fate decisions.
It has been reported that certain APP luminal juxtamembrane mutations could drastically alter Aβ secretion, however their effect on AICD production remains unknown. In this study we want to analyse wether the juxtamembrane region is important for the AICD production. To gain more insight into the luminal juxtamembrane function for γ-secretase-dependent proteolysis, we have made a juxtamembrane chimeric construct. A four-residue sequence preceding the transmembrane domain (TMD) of APP (GSNK), was replaced by its topological counterpart from the human Notch1 receptor (PPAQ). The resulting chimeric vector C99GVP-PPAQ and the wildtype counterpart were expressed in cells lacking PS1 and PS2 (BD8) together with PS1wt. We observed that the chimeric construct did not alter production of AICD when using a cell based luciferase reporter gene assay monitoring AICD production. We also introduced a PS1 variant lacking a big portion of the large hydrophilic loop, PS1∆exon10, since our group has previously observed that this region affect Aβ production143. We found that the absence of the large hydrophilic loop in PS1 gave a 2-fold decrease in AICD-GVP formation from C99GVPwt compared to PS1wt. The activity of PS1wt and PS1Δexon10 using C99GVP-PPAQ as a substrate gave similar result as the C99GVPwt substrate, i.e. a 2-fold decrease in AICD-GVP formation when comparing PS1Δexon10 with PS1wt. From this data we therefore suggest that the four residues in the juxtramembrane domain (JMD) (GSNK) is not altering ε-cleavage of APP when changed to Notch1 counterpart, PPAQ. Furthermore, we also show that the 2-fold decrease in AICD-production by the PS1Δexon10 molecule is not changed between the two substrates C99GVPwt and C99GVP-PPAQ. This indicates that the luminal region of APP is not directly involved in the ε-site processing. If the luminal region is affecting processing in the γ-cleavage sites, remains however to be investigated.
Cowan, James. "The development and study of chelating substrates for the separation of metal ions in complex sample matrices". Thesis, University of Plymouth, 2002. http://hdl.handle.net/10026.1/1881.
Texto completoStefani, Nicola. "Energy from crops: experimental study and dynamic simulation of biogas production by anaerobic digestion of complex substrates". Doctoral thesis, Università degli studi di Trieste, 2011. http://hdl.handle.net/10077/4506.
Texto completoAnaerobic digestion (AD) is a biological process which allows the removal of high organic-loading and potentially polluting substances by their transformation into biogas, a mixture of methane and carbon dioxide, prevalently. AD presents many other advantages: it has a low energy consumption and low construction costs with a relatively simple plant technology. Actually, since anaerobic bacteria work more efficiently at room temperature or higher, AD can be profitably applied in developing countries. Biogas production is a foundamental parameter of AD because it is the main index to be considered in a process economic evaluation and also because it gives a measure of its efficiency as well. Moreover, biogas production, and more frequently methane production, is often used as an index set to control the process. With the increase of energy price, the specific biogas production (SGP) of primary and residuals crops has become a goal for economic energy supply and, as a consequence, a rapid and effective method for measuring the gas produced has to be put forward, because there is not an accepted international standard yet. The effective knowledge of biogas production rate allows study of the biological process through macroscopic indicators, easily usable in industrial field, as well. The present study concerns the development and the validation of a technique for biogas production measurement and kinetic determination which adopts bench-mark laboratory-scale experiments with complex solid substrates, i.e. primary and residual energy crops. A laboratory-scale plant was designed and put up to perform this task. The equipment permits to carry out 4 contemporary tests because it is composed of 4 independent gas-lines, each of which connecting an anaerobic reactor to a gas-meter. Data from the experiments were continuously recorded by a data logger. The equipment was tested with synthetic substrate feeds of ethanol and sodium acetate. By a comparison between experimental gas production data and the theoretical ones, stoichiometrically calculated, the range of the error on methane productions resulted within ± 5%. In addition, the presence of oxygen amounts in the mixture, revealed the inconsistency of a test. These positive results allowed the implementation of different experiments to measure biogas produced from natural substrates. Apple, onion, corn straw, potato and winery wastes mixture were therefore tested in various experiments in order to calculate the SGP and SMA of the different crops. A new mathematical model for the description of complex substrate degradation was developed as well. The model was calibrated on the different biological systems and then applyed on real substrates to carry out their COD fractionation, to analyse the biological variable trends and to test the reliability of results. Finally, the reliability of a procedure for the evaluation of a two-step AD as compared to the one-step AD was tested by using apple and potato substrates.
La digestione anaerobica è un processo biologico che permette la rimozione di sostanze con alto carico organico, potenzialmente inquinanti, e la trasformazione di queste in biogas, costituito prevalentemente da metano e anidride carbonica. La digestione anaerobica ha anche ulteriori vantaggi: ha un basso consumo energetico, bassi costi di costruzione degli impianti, uniti ad una tecnologia impiantistica relativamente semplice. Inoltre, poiché i batteri anaerobici lavorano meglio a temperatura ambiente o superiore, si può applicare con profitto nei paesi in via di sviluppo. La produzione di biogas è un parametro fondamentale della digestione anaerobica perché è il principale indicatore cui fare riferimento nella valutazione economica del processo e perché allo stesso tempo fornisce anche una stima della sua efficienza. Inoltre, la produzione di biogas, o ancor più frequentemente quella di metano, è spesso usata come indice cui fare riferimento per un controllo di processo. Con l'aumento del costo energetico, risulta necessario definire correttamente ed efficacemente un metodo di misura del biogas prodotto, in particolare la produzione specifica (SGP) di biogas da biomasse primarie e residuali. Ad es, il test di attività metanogenica specifica (SMA), non ha ancora uno standard internazionale riconosciuto. La conoscenza effettiva della velocità di produzione di metano, infatti, apre la strada alla possibilità di studiare il processo biologico attraverso indicatori macroscopici, facili da applicare anche in un contesto industriale. Il presente lavoro riguarda lo sviluppo e la validazione di un metodo per effettuare la misurazione del biogas e la determinazione delle cinetiche di processo con esperimenti in scala di laboratorio effettuati su substrati complessi, ovvero biomasse primarie e residuali. Per fare ciò, è stato progettato e realizzato un impianto in scala di laboratorio. L'apparecchiatura permette di effettuare 4 prove contemporanee perché è provvista di 4 linee gas indipendenti, ciascuna delle quali connette un reattore anaerobico ad un gasometro. All'impianto è stato affiancato un sistema automatico di acquisizione dati, che permette la registrazione in continuo dei dati di produzione. L'impianto è stato verificato utilizzando alimentazioni di substrati sintetici quali etanolo e acetato di sodio. A seguito del confronto tra i dati di produzione di gas sperimentale e quelli di produzione teorica, calcolata stechiometricamente, l'errore nella risposta è risultato essere contenuto tra i valori di ± 5%. In aggiunta, la verifica del contenuto in ossigeno della miscela ha permesso di scartare le prove non conformi. Questi risultati positivi hanno consentito di passare ad esperimenti condotti su substrati naturali. Sono stati così testati, con i successivi esperimenti, mela, cipolla, patata, paglia di mais e residui solidi della lavorazione del vino, al fine di calcolarne l'SGP e l'SMA. E' anche stato sviluppato un nuovo modello matematico per simulare la degradazione di un substrato complesso. Tale modello è stato dapprima calibrato sui diversi sistemi biologici e in seguito applicato su alcuni substrati reali al fine di operare un frazionamento del COD, analizzare l'andamento delle variabili biologiche e verificare la compatibilità con i risultati sperimentali. Da ultimo, è stata verificata l'affidabilità di una procedura per la valutazione della digestione anaerobica a due fasi e il confronto con quella a fase singola, condotta con campioni di mele e di patate.
XXIII Ciclo
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Libros sobre el tema "Complex substrates"
Gasparini, Evel. Il matriarcato slavo. Editado por Marcello Garzaniti y Donatella Possamai. Florence: Firenze University Press, 2010. http://dx.doi.org/10.36253/978-88-8453-999-1.
Texto completoGoldstein, Alan S. Catalytic oxidations of organic substrates by transition metal salts. 1991.
Buscar texto completoEstimation of complex permittivity of composite multilayer material at microwave frequency using waveguide measurements. Hampton, VA: National Aeronautics and Space Administration, Langley Research Center, 2003.
Buscar texto completoAng, Xiaolu Lulu Lim. Substrates of the SCF-beta-TRCP E3 ubiquitin ligase complex: Mechanisms of recognition and delivery to the proteasome. 2009.
Buscar texto completoGarvey, Marjorie A. TMS: neurodevelopment and perinatal insults. Editado por Charles M. Epstein, Eric M. Wassermann y Ulf Ziemann. Oxford University Press, 2012. http://dx.doi.org/10.1093/oxfordhb/9780198568926.013.0022.
Texto completoAmzica, Florin y Fernando H. Lopes da Silva. Cellular Substrates of Brain Rhythms. Editado por Donald L. Schomer y Fernando H. Lopes da Silva. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190228484.003.0002.
Texto completoGuo, Yong y Claudia F. Lucchinetti. Taking a Microscopic Look at Multiple Sclerosis. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199341016.003.0005.
Texto completoGuo, Lucie Y. Aph-1 is a substrate-binding site within the γ-secretase complex. 2010.
Buscar texto completoLiaw, Ean-Tun. Characterization of substrate-velocity relationships for the cellulase enzyme complex from Trichoderma viride. 1989.
Buscar texto completoVaghi, M. M. y T. W. Robbins. Task-Based Functional Neuroimaging Studies of Obsessive-Compulsive Disorder: A Hypothesis-Driven Review. Editado por Christopher Pittenger. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190228163.003.0022.
Texto completoCapítulos de libros sobre el tema "Complex substrates"
Semenov, S., V. M. Starov, M. G. Velarde y R. G. Rubio. "Evaporation of Sessile Droplets of Liquid on Solid Substrates". En Understanding Complex Systems, 285–300. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-34070-3_26.
Texto completoStymne, Sten, Gareth Griffiths y Keith Stobart. "Desaturation of Fatty Acids on Complex-lipid Substrates". En The Metabolism, Structure, and Function of Plant Lipids, 405–12. Boston, MA: Springer New York, 1987. http://dx.doi.org/10.1007/978-1-4684-5263-1_74.
Texto completoChen, Z., W. Wang y B. Cotterell. "The Evaluation of the Fracture Strain of ITO Films on Polymeric Substrates". En Properties of Complex Inorganic Solids 2, 409–16. Boston, MA: Springer US, 2000. http://dx.doi.org/10.1007/978-1-4615-1205-9_30.
Texto completoEssaaidi, Mohamed y Otman Mrabet. "Dielectric Substrates Anisotropy Effects on the Characteristics of Microstrip Structures". En Advances in Electromagnetics of Complex Media and Metamaterials, 449–60. Dordrecht: Springer Netherlands, 2002. http://dx.doi.org/10.1007/978-94-007-1067-2_27.
Texto completoSchlage, Pascal, Fabian E. Egli y Ulrich auf dem Keller. "Time-Resolved Analysis of Matrix Metalloproteinase Substrates in Complex Samples". En Methods in Molecular Biology, 185–98. New York, NY: Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-6863-3_9.
Texto completoDelan-Forino, Clémentine y David Tollervey. "Mapping Exosome–Substrate Interactions In Vivo by UV Cross-Linking". En Methods in Molecular Biology, 105–26. New York, NY: Springer New York, 2019. http://dx.doi.org/10.1007/978-1-4939-9822-7_6.
Texto completoBeloglazova, Natalia, Sofia Lemak, Robert Flick y Alexander F. Yakunin. "Analysis of Nuclease Activity of Cas1 Proteins Against Complex DNA Substrates". En Methods in Molecular Biology, 251–64. New York, NY: Springer New York, 2015. http://dx.doi.org/10.1007/978-1-4939-2687-9_16.
Texto completoVarfolomeev, Sergey, Bella Grigorenko, Sofya Lushchekina, Patrick Masson, Galina Mahaeva y Alexander Nemuchin. "Human cholinesterases". En ORGANOPHOSPHORUS NEUROTOXINS, 69–126. ru: Publishing Center RIOR, 2020. http://dx.doi.org/10.29039/21_069-126.
Texto completoVarfolomeev, Sergey, Bella Grigorenko, Sofya Lushchekina y Alexander Nemuchin. "Human cholinesterases". En Organophosphorous Neurotoxins, 63–120. ru: Publishing Center RIOR, 2020. http://dx.doi.org/10.29039/chapter_5e4132b5f22366.15634219.
Texto completoMäkelä, Miia R. y Kristiina Hildén. "Efficient Extraction Method for High Quality Fungal RNA from Complex Lignocellulosic Substrates". En Methods in Molecular Biology, 69–73. New York, NY: Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-7804-5_6.
Texto completoActas de conferencias sobre el tema "Complex substrates"
Olson Reichhardt, C. J., D. Ray y C. Reichhardt. "Active matter transport on complex substrates". En SPIE NanoScience + Engineering, editado por Kishan Dholakia y Gabriel C. Spalding. SPIE, 2014. http://dx.doi.org/10.1117/12.2063481.
Texto completoBie, Youqin. "Replicated mirros with magnetic steel as substrates". En 15th Int'l Optics in Complex Sys. Garmisch, FRG, editado por F. Lanzl, H. J. Preuss y G. Weigelt. SPIE, 1990. http://dx.doi.org/10.1117/12.34914.
Texto completoNakayama, Hideyuki. "Surface Undulation Appearing by Continuous Temperature Elevation of Supercooled Liquids on Metal Substrates". En SLOW DYNAMICS IN COMPLEX SYSTEMS: 3rd International Symposium on Slow Dynamics in Complex Systems. AIP, 2004. http://dx.doi.org/10.1063/1.1764079.
Texto completoModi, Mitul, Deepak Kulkarni, Andy Bao, Ibrahim Bekar y Steve Cho. "Analytical Homogenization for Microelectronic Substrates". En ASME 2007 International Mechanical Engineering Congress and Exposition. ASMEDC, 2007. http://dx.doi.org/10.1115/imece2007-43460.
Texto completoKotlikov, E. N., Yu A. Novikova y Yu N. Tsarev. "DEFINITION OF REFRACTIVE INDICES OF MgBaF4 FILMS ON Si SUBSTRATES". En MODELING AND SITUATIONAL QUALITY MANAGEMENT OF COMPLEX SYSTEMS. St. Petersburg State University of Aerospace Instrumentation, 2020. http://dx.doi.org/10.31799/978-5-8088-1449-3-2020-1-80-85.
Texto completoWanga, Shanshan, Peixiang Ma, Feng Qu y Yulin Deng. "Application of Biologically Functionalized Chromatography to Simulate the Interaction Between MAO and Substrates". En 2007 IEEE/ICME International Conference on Complex Medical Engineering. IEEE, 2007. http://dx.doi.org/10.1109/iccme.2007.4382057.
Texto completoVermeer, C., BA M. Soute y MM W. Ulrich. "IN VITRO CARBOXYLATION OF EXOGENOUS PROTEIN SUBSTRATES BY VITAMIN K-DEPENDENT CARBOXYLASE". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643994.
Texto completoWiatrowska, Aneta, Karolina Fiaczyk, Piotr Kowalczewski, Mateusz Lysien, Lukasz Witczak, Jolanta Gadzalinska, Iwona Gradzka-Kurzaj, Ludovic Schneider, Lukasz Kosior y Filip Granek. "Printing of Micrometer-Size Features on Complex Substrates for System Integration". En 2022 IEEE 9th Electronics System-Integration Technology Conference (ESTC). IEEE, 2022. http://dx.doi.org/10.1109/estc55720.2022.9939386.
Texto completoXiuqin Jia, Shengfu Lu, Ning Zhong, Yiyu Yao, Kuncheng Li y Yanhui Yang. "Common and distinct neural substrates of forward-chaining and backward-chaining syllogistic reasoning". En 2009 ICME International Conference on Complex Medical Engineering - CME 2009. IEEE, 2009. http://dx.doi.org/10.1109/iccme.2009.4906618.
Texto completoSoukup, L., M. Šícha, L. Jastrabík y M. Novák. "Thin film deposition on internal walls of cavities and complex hollow substrates". En The XXII. international conference on phenomena in ionized gases (ICPIG). AIP, 1996. http://dx.doi.org/10.1063/1.50122.
Texto completoInformes sobre el tema "Complex substrates"
Rine, Kristin, Roger Christopherson y Jason Ransom. Harlequin duck (Histrionicus histrionicus) occurrence and habitat selection in North Cascades National Park Service Complex, Washington. National Park Service, abril de 2022. http://dx.doi.org/10.36967/nrr-2293127.
Texto completoHenson, B. F., S. J. Buelow y J. M. Robinson. Modification of heterogeneous chemistry by complex substrate morphology. Office of Scientific and Technical Information (OSTI), diciembre de 1998. http://dx.doi.org/10.2172/562542.
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 completoChoudhary, Ruplal, Victor Rodov, Punit Kohli, Elena Poverenov, John Haddock y Moshe Shemesh. Antimicrobial functionalized nanoparticles for enhancing food safety and quality. United States Department of Agriculture, enero de 2013. http://dx.doi.org/10.32747/2013.7598156.bard.
Texto completoIrudayaraj, Joseph, Ze'ev Schmilovitch, Amos Mizrach, Giora Kritzman y Chitrita DebRoy. Rapid detection of food borne pathogens and non-pathogens in fresh produce using FT-IRS and raman spectroscopy. United States Department of Agriculture, octubre de 2004. http://dx.doi.org/10.32747/2004.7587221.bard.
Texto completoChen, Junping, Zach Adam y Arie Admon. The Role of FtsH11 Protease in Chloroplast Biogenesis and Maintenance at Elevated Temperatures in Model and Crop Plants. United States Department of Agriculture, mayo de 2013. http://dx.doi.org/10.32747/2013.7699845.bard.
Texto completoMorrison, Mark y Joshuah Miron. Molecular-Based Analysis of Cellulose Binding Proteins Involved with Adherence to Cellulose by Ruminococcus albus. United States Department of Agriculture, noviembre de 2000. http://dx.doi.org/10.32747/2000.7695844.bard.
Texto completoGuy, Charles, Gozal Ben-Hayyim, Gloria Moore, Doron Holland y Yuval Eshdat. Common Mechanisms of Response to the Stresses of High Salinity and Low Temperature and Genetic Mapping of Stress Tolerance Loci in Citrus. United States Department of Agriculture, mayo de 1995. http://dx.doi.org/10.32747/1995.7613013.bard.
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