Littérature scientifique sur le sujet « Analyse des interactions non covalentes »
Créez une référence correcte selon les styles APA, MLA, Chicago, Harvard et plusieurs autres
Consultez les listes thématiques d’articles de revues, de livres, de thèses, de rapports de conférences et d’autres sources académiques sur le sujet « Analyse des interactions non covalentes ».
À côté de chaque source dans la liste de références il y a un bouton « Ajouter à la bibliographie ». Cliquez sur ce bouton, et nous générerons automatiquement la référence bibliographique pour la source choisie selon votre style de citation préféré : APA, MLA, Harvard, Vancouver, Chicago, etc.
Vous pouvez aussi télécharger le texte intégral de la publication scolaire au format pdf et consulter son résumé en ligne lorsque ces informations sont inclues dans les métadonnées.
Articles de revues sur le sujet "Analyse des interactions non covalentes"
Kumar, Prashant, Małgorzata Katarzyna Cabaj et Paulina Maria Dominiak. « Intermolecular Interactions in Ionic Crystals of Nucleobase Chlorides—Combining Topological Analysis of Electron Densities with Energies of Electrostatic Interactions ». Crystals 9, no 12 (11 décembre 2019) : 668. http://dx.doi.org/10.3390/cryst9120668.
Texte intégralSavoo, Nandini, Frederick P. Malan, Lydia Rhyman et Ponnadurai Ramasami. « Molecular insights of metal–metal interactions in transition metal complexes using computational methods ». Pure and Applied Chemistry 93, no 5 (1 mai 2021) : 579–89. http://dx.doi.org/10.1515/pac-2020-1212.
Texte intégralCreste, Geordie, Sihem Groni, Claire Fave, Mathieu Branca et Bernd Schöllhorn. « Comparative study of non-covalent interactions between cationic N-phenylviologens and halides by electrochemistry and NMR : the halogen bonding effect ». Faraday Discussions 203 (2017) : 301–13. http://dx.doi.org/10.1039/c7fd00082k.
Texte intégralVonderviszt, F., J. Török, S. Lakatos, F. Kilár et P. Závodszky. « Quantitative analysis of the interaction between immune complex and Clq complement subcomponent. The role of interdomain interactions in rabbit IgG in binding of Clq to immune precipitates ». Biochemical Journal 243, no 2 (15 avril 1987) : 449–55. http://dx.doi.org/10.1042/bj2430449.
Texte intégralSingh, Omkar, Kunal Sawariya et Polamarasetty Aparoy. « Graphlet signature-based scoring method to estimate protein–ligand binding affinity ». Royal Society Open Science 1, no 4 (décembre 2014) : 140306. http://dx.doi.org/10.1098/rsos.140306.
Texte intégralJungclas, Hartmut, Viacheslav V. Komarov, Anna M. Popova et Lothar Schmidt. « Molecular Interactions in Particular Van der Waals Nanoclusters ». Zeitschrift für Naturforschung A 72, no 1 (1 janvier 2017) : 17–23. http://dx.doi.org/10.1515/zna-2016-0213.
Texte intégralMaza, Susana, José L. de Paz et Pedro M. Nieto. « Synthesis of a Fluorous-Tagged Hexasaccharide and Interaction with Growth Factors Using Sugar-Coated Microplates ». Molecules 24, no 8 (22 avril 2019) : 1591. http://dx.doi.org/10.3390/molecules24081591.
Texte intégralEtxabide, Alaitz, Maite Arregi, Sara Cabezudo, Pedro Guerrero et Koro de la Caba. « Whey Protein Films for Sustainable Food Packaging : Effect of Incorporated Ascorbic Acid and Environmental Assessment ». Polymers 15, no 2 (11 janvier 2023) : 387. http://dx.doi.org/10.3390/polym15020387.
Texte intégralBjij, Imane, Pritika Ramharack, Shama Khan, Driss Cherqaoui et Mahmoud Soliman. « Tracing Potential Covalent Inhibitors of an E3 Ubiquitin Ligase Through Target-Focused Modelling ». Proceedings 22, no 1 (14 novembre 2019) : 103. http://dx.doi.org/10.3390/proceedings2019022103.
Texte intégralHammud, Hassan H., Muhammad Yar, Imene Bayach et Khurshid Ayub. « Covalent Triazine Framework C6N6 as an Electrochemical Sensor for Hydrogen-Containing Industrial Pollutants. A DFT Study ». Nanomaterials 13, no 6 (21 mars 2023) : 1121. http://dx.doi.org/10.3390/nano13061121.
Texte intégralThèses sur le sujet "Analyse des interactions non covalentes"
Ohara, Keiichiro. « Interactions non covalentes de dérivés guanidylés avec l'ADN : synthèse, évaluation biologique et analyse par spectrométrie de masse MALDI-TOF ». Montpellier 2, 2008. http://www.theses.fr/2008MON20154.
Texte intégralWieduwilt, Erna K. « Quantum mechanics-based methods for the refinement of crystal structures and the analysis of non-covalent interactions ». Electronic Thesis or Diss., Université de Lorraine, 2021. http://www.theses.fr/2021LORR0167.
Texte intégralIn the work presented in this thesis, extremely localized molecular orbitals (ELMOs) were used as electronic LEGO building blocks to accomplish mainly two goals: (i) obtaining more accurate X-ray crystal structures for small and large systems, and (ii) analyzing non-covalent interactions in biomolecules. In fact, ELMOs are molecular orbitals that are strictly localized on small molecular fragments. Due to this strict localization, they may be computed on small molecules, stored in databases and then transferred to larger systems to reconstruct their wavefunctions and electron densities. To this end, we exploited the ELMO libraries, which contain the ELMOs for all the elementary fragments (atoms, bonds and functional groups) of the twenty natural amino acids. In situations where a higher accuracy was needed, we used the QM/ELMO embedding technique, in which the crucial part of the system under exam is treated at a higher quantum mechanical level, while the rest is described using frozen ELMOs. Concerning the first of the goals mentioned above, it is important to note that standard crystallographic refinements are based on the so-called independent atom model (IAM), which approximates the electron density as a sum of spherically averaged atomic densities. However, the element-hydrogen bond lengths resulting from IAM refinements are systematically too short. A method that solves this problem is the Hirshfeld atom refinement (HAR), a technique based on directly computing the electron density for the molecule under exam using quantum mechanical calculations. For small molecules, HAR has been proven to give element-hydrogen bond lengths that are in very good agreement with neutron reference values. However, for large systems, the applicability of the traditional HAR method is limited because the underlying fully QM calculations become computationally too expensive. Therefore, in the work presented in this thesis, the ELMO libraries and the QM/ELMO techniques have been coupled with the HAR method to refine large systems and also to obtain more accurate structures of small molecules. Furthermore, the necessity of using post-HF methods for HAR has been also evaluated. Concerning the second goal addressed in this dissertation, a similar problem as the one met in X-ray crystallography also arises in the analysis of non-covalent interactions. In fact, also the non-covalent interaction (NCI) and independent gradient model (IGM) techniques, which are commonly applied in analyses of non-covalent interactions, crucially depend on the computation of the electron density. Therefore, to analyze non-covalent interactions in large systems, both techniques had to resort to promolecular electron densities, which are the same densities used in the IAM. However, also in the cases of NCI and IGM analyses, these densities provide biased results. To overcome this drawback, we have coupled both methods with the ELMO libraries, giving rise to the NCI-ELMO and IGM-ELMO techniques, which were then applied to identify, classify and approximately quantify non-covalent interactions in polypeptides and proteins
Imani, Zeynab. « Le rôle d’interactions N-H···S proximales dans des peptides ». Thesis, université Paris-Saclay, 2021. http://www.theses.fr/2021UPASF015.
Texte intégralNon-covalent interactions play a key role in chemical biology phenomena such as the stabilization of protein tertiary and quaternary structure or protein-protein and protein-substrate recognition. Among these interactions, the classical amide-type NH···O=C hydrogen bond has been thoroughly studied. The study of other types of non-covalent interactions implicating peptide backbone NH groups is much rarer. This work focused on the impact of NH···S hydrogen bonding on the conformational preferences of thioether amino acid residues and their short oligomers. A panel of capped derivatives of the following non-canonical sulfur-containing amino acids was prepared: Cys(Me) (acyclic), Attc (thietane), Atlc (thiolane), Atc (thiane). These derivatives were characterized computationally, by IR/UV double resonance laser spectroscopy in the gas phase, by IR and NMR spectroscopy in solution, and in the solid state. We demonstrated the concomitant existence of inter-residue C6ˠ NH···S hydrogen bonds and C5 NH···O=C interactions in each of these four compounds. This combined stabilizing feature was also prevalent in Attc oligomers. A different intra-residue C5ˠ NH···S hydrogen bond was characterized in short oligomers of Atlc and Atc, in some cases associated with a ˠ-turn NH···O=C interaction. The significance of NH···S bonding in the combined C5-C6ˠ structural feature of Attc was evaluated by comparison with capped derivatives of other four-membered ring amino acids: Ac4c (cyclobutane), Aatc(Me) (azetidine), Aotc (oxetane). The C5–C6ˠ feature was present in the three heterocyclic residues: comparison of their IR spectra in gas phase and in solution, aided by theoretical calculations, allowed us to identify an increasing strength of NH···X hydrogen bonding from X=O to X=S to X=N
Yahia-Ouahmed, Meziane. « Caractérisation topologique d'interactions non-covalentes inter- et intramoléculaires ». Thesis, Normandie, 2017. http://www.theses.fr/2017NORMR091/document.
Texte intégralThis work aims to theoretically investigate and characterize non-covalent interactions by means of Quantum Chemical Topology (QCT) methods, which are quantum chemistry interpretative tools. Several interactions were studied from the point of view of the electron density (DFT calculations), including intramolecular interactions between halogen atoms as well as inter- and intramolecular halogen bonds. The QTAIM topological analysis complemented by the Interacting Quantum Atoms (IQA) energy decomposition revealed the physical nature of those interactions, i. e. the part of electrostatics and the part of exchange (covalency). It has been shown that exchange plays a significant role in stabilizing such interactions and enables rationalizing the different topologies observed in terms of competition between primary and secondary exchange channels. Also, the formation and breaking of a hydrogen bond during proton transfer reactions has been analyzed by utilizing an atomic decomposition of global quantities (from Conceptual DFT), the new decompositionscheme being based on the QTAIM partition and the IQA energy decomposition. This approach allows following the contribution of every atom to the reactivity of the whole system along a reaction path, introducing a new way of characterizing energy barriers and transition
Riffet, Vanessa. « Interactions non-covalentes et propriétés physico-chimiques de petits systèmes biologiques : approches théoriques ». Palaiseau, Ecole polytechnique, 2014. https://tel.archives-ouvertes.fr/tel-01084858/document.
Texte intégralThe three-dimensional structure and physico-chemical properties of biomolecules such as peptides are not only governed by their elementary composition but also various non-covalent intra-and inter-molecular interactions. The characterization, measurement and effects of these interactions are currently at the center of many researches at the interface between biology and physical chemistry. In this context, the aim of our thesis is a better understanding of these interactions in biomolecules and aggregates using the tools of quantum chemistry and molecular modeling. In this regard, due to the complexity and size of the real biological systems, chemical models have been developed. These have allowed us to study and understand the nature and effects of these interactions taken "individually" on the geometric and electronic structure of molecular systems such as small peptides and aggregates of glycine betaine. The role of non-covalent interactions on the reactivity of various physico-chemical conditions (electronic reduction, gas phase, microsolvation) is also one of the several approaches of our work. Among the systems examined, many of them included at least one ammonium, guanidinium or imidazolium charged groups, which are founded in the side chains of the amino acids lysine, arginine and histidine. We have shown that the chemical environment of these electronic charges greatly influences the structure and reactivity of the molecules that contain these groups. Eventually, we both performed a calibration of modeling methods for the study of the electronic properties of radical peptides and developed new protocols for the potential energy surface exploration starting from the AMOEBA polarizable force field, in order to optimize the conformational searches exhaustivity for flexible biological systems
Hardouin, Julie. « Etude de glutathiones S-transférases par spectrométrie de masse : séquences et interactions non covalentes ». Rouen, 2003. http://www.theses.fr/2003ROUES031.
Texte intégralMass spectrometry coupled with the ionizations MALDI or ESI is the analytical technique in proteomic and for the study of non-covalent complexes. The goal of this work is to characterize the primary and quaternary structures of glutathiones S-transferases (GST) with mass spectrometry. Their interactions with toxins is studied to explain the detoxication processes. First, the sequences of porcine GST and post-translational modifications were determined by MALDI-TOF-MS and LC-ESI-IT/MS. Secondly, the non-covalent complexes of porcine and human GST were studied by ESI on a magnetic analyzer. The non-covalent interactions between the dimeric enzyme, the glutathion (GSH) and a cyclodepsipeptide (DTXE) were analyzed. The observation of these species needed the optimization of the sample preparation and the source parameters. This study showed the high efficiency of mass spectrometry to perform screenings of ligands, substrates and inhibitors of proteins. This approach opens up for the future studies of drugs and their metabolites linked with enzymes. The proteome has a direct link with the metabolome
Chamoun, Jean. « Contribution du couplage CE-ICP/MS dans l'étude des interactions métals-protéine non-covalentes ». Université Louis Pasteur (Strasbourg) (1971-2008), 2005. http://www.theses.fr/2005STR13090.
Texte intégralThe screening of metal/protein interactions using CE coupled to ICP/MS was investigated. The development of this new analytical tool requires, besides the hyphenation of the two techniques, both an efficient separation of the proteins and a sensitive detection of metals. The optimization of the electrophoretic separation of a protein-test mixture led to the use of a borate buffer, pH 9. 2, which both minimizes adsorption and allows the separation of all proteins’ mixture with a good migration times reproducibility. The hyphenation between capillary electrophoresis and ICP/MS was performed using a sheath flow interface. The optimization of parameters, such as coolant, auxiliary and nebulizer gases, composition and flowrate of the sheath flow solution and position of the capillary in the nebulizer was carried out in order to obtain the best detection sensitivity and separation efficiency. However, this type of interface involves important samples dilutions, which led us to develop an on-line preconcentration technique in order to improve the detection limits. The detection limits calculated for the copper and zinc contained in the carbonic anhydrase, the less efficiently concentrated protein, showed an improvement of the detection limits in CE-ICP/MS of 6 times for copper and 5 times for zinc. CE-ICP/MS was then used in the study of the interactions of three transition metals (Cd, Co and Ni) with a mixture of proteins made of metalloproteins and major blood serum proteins. These studies revealed a similar behavior of cobalt and nickel, completely different from that of cadmium. In the case of the metalloproteins, hyphenated CE-ICP/MS allowed to identify the probable nature of the interaction sites. Moreover, this method allowed studies on the relative affinity of various metals with a mixture of proteins. The dissociative aspect of the separation was also exploited in order to obtain kinetic data which allowed the access to the dissociation constants of the complexes and in certain cases, highlighted the presence of multiple interaction sites. Finally, the technique was applied to so-called “hard cations”: lanthanides and uranyl ion (UO22+). The first results showed a massive adsorption of these cations on the capillaries surface. Nevertheless, the studies, carried out on a mixture of six proteins, previously identified as uranium-targets, showed that four of them interact with the uranium, among which albumin and transferrin
Bayach, Imene. « Non-covalent interactions in natural products ». Thesis, Limoges, 2014. http://www.theses.fr/2014LIMO0050/document.
Texte intégralNatural polyphenols form non-covalent complexes in which π-stacking and H-bonding play a key stabilizing role. The dispersion-corrected DFT calculations have paved the way towards reliable description of aggregation processes of natural products. In this work, these methods are applied at i) understanding of stereo- and regio-selective oligostilbenoids biosynthesis; ii) predicting natural antioxidant aggregation within lipid bilayer membrane, which may allow rationalizing the synergism of vitamin E, vitamin C and polyphenols in their antioxidant action; and iii) modulating optical properties of chalcone derivatives
Watrelot, Aude. « Interactions non-covalentes entre les polyphénols et les pectines : Etude sur un substrat modèle : la pomme ». Thesis, Avignon, 2013. http://www.theses.fr/2013AVIG0656/document.
Texte intégralThermodynamical parameters and kinetics of interactions between polyphenols (procyanidins and anthocyanins) and pectic fractions were defined by physico-chemical methods in solution and with a solid support. Experiments confronted major anthocyanins presents in blackcurrant or B-type procyanidins from apple with various degrees of polymerization to pectic fractions from apple pectins presenting different degree of methylation and different neutral sugar side chains.Interactions between anthocyanins and pectins are influenced by the glycosyl substituent and the number of hydroxyl groups in the B-ring of anthocyanins, and by the composition of pectins. The affinity constant of procyanidins – pectins interaction in solution are the highest when both the procyanidins degree of polymerization and the pectins degree of methylation are the highest. Moreover, the ramification state of pectins limits their association with procyanidins. Those interactions are due to hydrogen bonds and hydrophobic interactions.After chemical modifications of procyanidins and immobilization on a solid support, the resonance units obtained by surface plasmon resonance between (-)-epicatechin or dimer B2 and apple pectins are similar to those obtained with the prolin-rich protein IB5 and lower than with bovine serum albumin
Didier, Dorian. « Recyclage de complexes bis(oxazolines)- cuivre chiraux pour la catalyse asymétrique : hétérogénéisation par interactions non-covalentes ». Phd thesis, Université Paris Sud - Paris XI, 2011. http://tel.archives-ouvertes.fr/tel-00856579.
Texte intégralLivres sur le sujet "Analyse des interactions non covalentes"
Non-Covalent Interactions in Proteins. World Scientific Publishing Co Pte Ltd, 2021.
Trouver le texte intégralKarshikoff, Andrey. Non-covalent Interactions in Proteins. Imperial College Press, 2006.
Trouver le texte intégralSamah, Posse-Ousmane. Les conditions d'admission et de séjour des travailleurs hautement qualifiés dans l'UE. Carl Grossmann Verlag, 2017. http://dx.doi.org/10.24921/2017.94115913.
Texte intégralRuiz-Villalba, Adrián, Nikolaos Frangogiannis et José Maria Pérez-Pomares. Origin and diversity of cardiac fibroblasts : developmental substrates of adult cardiac fibrosis. Sous la direction de José Maria Pérez-Pomares, Robert G. Kelly, Maurice van den Hoff, José Luis de la Pompa, David Sedmera, Cristina Basso et Deborah Henderson. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198757269.003.0012.
Texte intégralChapitres de livres sur le sujet "Analyse des interactions non covalentes"
Brandenburg, D., W. Thevis, D. Glasmacher, J. Pirrwitz, M. Fabry, E. Schaefer et L. Ellis. « Analysis of the interaction between insulin and its receptor by means of covalent and non-covalent techniques ». Dans Peptides, 574–76. Dordrecht : Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-0683-2_189.
Texte intégralSeth, Saikat Kumar, Antonio Bauzá et Antonio Frontera. « CHAPTER 9. Quantitative Analysis of Weak Non-covalent σ-Hole and π-Hole Interactions ». Dans Monographs in Supramolecular Chemistry, 285–333. Cambridge : Royal Society of Chemistry, 2018. http://dx.doi.org/10.1039/9781788013086-00285.
Texte intégralSchoenmaker, Dirk, et Willem Schramade. « Calculating Social and Environmental Value ». Dans Springer Texts in Business and Economics, 115–44. Cham : Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-35009-2_5.
Texte intégralGomendio, Montserrat, et José Ignacio Wert. « 7. Education Reforms ». Dans Dire Straits-Education Reforms, 269–98. Cambridge, UK : Open Book Publishers, 2023. http://dx.doi.org/10.11647/obp.0332.07.
Texte intégralLaplaza, Rubén, Francesca Peccati, David Arias-Olivares et Julia Contreras-García. « 14 Visualizing non-covalent interactions with NCIPLOT ». Dans Complementary Bonding Analysis, 353–78. De Gruyter, 2021. http://dx.doi.org/10.1515/9783110660074-014.
Texte intégralFrancisco, E., et A. Martín Pendás. « Energy Partition Analyses : Symmetry-Adapted Perturbation Theory and Other Techniques ». Dans Non-Covalent Interactions in Quantum Chemistry and Physics, 27–64. Elsevier, 2017. http://dx.doi.org/10.1016/b978-0-12-809835-6.00003-7.
Texte intégralHerberg, Friedrich W., et Bastian Zimmermann. « Analysis of protein kinase interactions using biomolecular interaction analysis ». Dans Protein Phosphorylation, 315–34. Oxford University PressOxford, 1999. http://dx.doi.org/10.1093/oso/9780199637294.003.0015.
Texte intégralBoto, Roberto A., et Julia Contreras-García. « Beyond QTAIM : NCI Indexes as a Tool to Reveal Intermolecular Bonds in Molecular Aggregates ». Dans Intermolecular Interactions in Crystals : Fundamentals of Crystal Engineering, 222–57. The Royal Society of Chemistry, 2017. http://dx.doi.org/10.1039/bk9781782621737-00222.
Texte intégralChowdhry, Babur Z., et Stephen E. Harding. « Protein-ligand interactions and their analysis ». Dans Protein-Ligand Interactions : hydrodynamics and calorimetry, 1–18. Oxford University PressOxford, 2000. http://dx.doi.org/10.1093/oso/9780199637492.003.0001.
Texte intégralKhanmohammadi, Azadeh. « Investigation of Non-Covalent Interactions of Copper (II) Complexes with Small Biomolecules ». Dans Copper - From the Mineral to the Final Application [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.106216.
Texte intégralActes de conférences sur le sujet "Analyse des interactions non covalentes"
Direm, Amani, Brahim El Bali, Mohammed Lachkar, Esra Çetiner, Koray Sayin et Michal Dusek. « Towards quantitative analysis of the non-covalent interactions in a newly synthesized phenanthroline-based nickel(II) complex : A combined experimental and computational study ». Dans 6th International Electronic Conference on Medicinal Chemistry. Basel, Switzerland : MDPI, 2020. http://dx.doi.org/10.3390/ecmc2020-07512.
Texte intégralHosszu, Alexandra, et Mihai alexandru Botezatu. « LEARNING ABOUT INTERACTIONS AND EMOTIONAL SUPPORT THROUGH CHATBOTS ». Dans eLSE 2020. University Publishing House, 2020. http://dx.doi.org/10.12753/2066-026x-20-106.
Texte intégralMilenković, Dejan A., Marko N. Živanović, Milan S. Dekić, Marijana Stanojević Pirković et Jelena R. Đorović Jovanović. « CYTOTOXIC ACTIVITY AND MOLECULAR DOCKING STUDY OF 4- SUBSTITUTED FLAVYLIUM SALT ». Dans 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac,, 2021. http://dx.doi.org/10.46793/iccbi21.466m.
Texte intégralGanapathy, Harish, V. Emlin, Anant Narendra Parikh et V. Sajith. « Experimental Investigation on Surface Particle Interactions During Pool Boiling of Nanofluids ». Dans ASME 2011 9th International Conference on Nanochannels, Microchannels, and Minichannels. ASMEDC, 2011. http://dx.doi.org/10.1115/icnmm2011-58180.
Texte intégralDirem, Amani, zina Boutobba, Koray Sayın, Brahim El Bali, Mohammed Lachkar et Nourredine Benali-Cherif. « A combined experimental and theoretical study of an oxalato-bridged copper(II) complex : Crystal structure and <em>Hirshfeld</em> ; surface analysis of the non-covalent interactions ». Dans 6th International Electronic Conference on Medicinal Chemistry. Basel, Switzerland : MDPI, 2020. http://dx.doi.org/10.3390/ecmc2020-07402.
Texte intégralBalogh, Lajos P., et Mohamed K. Khan. « Biodistribution of Dendrimer Nanocomposites for Nano-Radiation Therapy of Cancer ». Dans ASME 2006 Multifunctional Nanocomposites International Conference. ASMEDC, 2006. http://dx.doi.org/10.1115/mn2006-17025.
Texte intégralJosserand, E., et F. Billon. « Application of Mixed Equivalent Solid and Explicit Hole Models to Analysis of Thick Perforated Plates ». Dans ASME 2008 Pressure Vessels and Piping Conference. ASMEDC, 2008. http://dx.doi.org/10.1115/pvp2008-61885.
Texte intégralPrieto Sanz, Helena. « Do text discussions improve the academic skills of students of HE ? Andorra University case. » Dans Sixth International Conference on Higher Education Advances. Valencia : Universitat Politècnica de València, 2020. http://dx.doi.org/10.4995/head20.2020.11211.
Texte intégralTsarau, Andrei, Marnix van den Berg, Wenjun Lu, Raed Lubbad et Sveinung Løset. « Modelling Results With a New Simulator for Arctic Marine Structures - SAMS ». Dans ASME 2018 37th International Conference on Ocean, Offshore and Arctic Engineering. American Society of Mechanical Engineers, 2018. http://dx.doi.org/10.1115/omae2018-78593.
Texte intégralPerre, Patrick, et Ian Turner. « A physical interpretation of the use of fractional operators for modelling the drying process ». Dans 21st International Drying Symposium. Valencia : Universitat Politècnica València, 2018. http://dx.doi.org/10.4995/ids2018.2018.7885.
Texte intégral