Дисертації з теми "Substrats interactifs"
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Gamouh, Ahmed. "Effets comparés et interactifs des pesticides et des facteurs physiques sur la minéralisation de divers substrats carbonés dans le sol." Perpignan, 1998. http://www.theses.fr/1998PERP0314.
Battut, Alexandre. "Interaction substrates and instruments for interaction histories." Electronic Thesis or Diss., université Paris-Saclay, 2024. http://www.theses.fr/2024UPASG026.
In the digital world, as in the physical world, our interactions with objects leave traces that tell the story of the actions that shaped these objects over time. This historical data can be accessed by end users to help them better understand the steps that led to the current state of their system. These traces can also be reused for activities such as re-documenting their own history to arrange it in a way that they find more understandable. Users may also be led to share these data in collaborative environments, to better coordinate and synchronize their work. While previous work has attempted to show the benefits of cross-application histories, current implementations of interaction histories in interactive systems tend to tie history data to their source application. This prevents users from cross-referencing historical data to review and correlate events that occurred in different applications.In this thesis, I argue that designing interaction histories that can be shared among applications and users would support browsing, understanding and reusing historical data. I first ground my work in the use case of collaborative writing to explore relatable yet complex traces ecologies and interaction history use. I identify recurring practices and issues with the use of history data by interviewing knowledge workers and conducting several design activities based on these observations. I describe a first proof-of-concept system integrating two history instruments resulting from these design activities, and the first iteration of a unifying structure for historical data to be shared among applications and users. The results of user studies show that users indeed express a need for unified and customizable interaction histories.Compiling the data gathered during these research activities and based on previous works about “Dynamic Shareable Media” and the Interaction Substrates and Instruments model, I describe a framework to help create more flexible interaction histories. The goal is to describe how to design interaction history systems that would help users take control of their historical data. I introduce Steps, a structure for unifying historical data that includes descriptive core attributes to preserve the integrity of a trace across applications, and extensible contextual attributes that let users reshape their histories to suit their needs. I then introduce OneTrace, a proof-of-concept prototype based on Steps that follows my descriptive framework for cross-application histories and defines interaction histories as digital material to be shaped by digital tool use. I discuss the opportunities offered by this approach to support a shift in paradigm on how we design and interact with interaction histories
Burns, Teresa Ellen. "Asymmetric Adsorbate and Substrate Interactions in Physisorbed Systems: N2 on Graphite and Dipolar Molecules on Ionic Substrates." DigitalCommons@USU, 1994. https://digitalcommons.usu.edu/etd/2090.
Richter, Andreas. "Structure formation and fractionation in systems of colloidal rods." Phd thesis, Universität Potsdam, 2007. http://opus.kobv.de/ubp/volltexte/2007/1309/.
Sharp, Katherine Helen. "Substrate binding : interactions in ascorbate peroxidase." Thesis, University of Leicester, 2004. http://hdl.handle.net/2381/30091.
Jovelet, Cécile. "Interactions du vandetanib avec la P-glycoprotéine et passage d'une barrière physiologique : le placenta." Thesis, Paris 11, 2012. http://www.theses.fr/2012PA114825.
Overexpression of ABC transporters, especially P-glycoprotein, is involved in multidrug resistance. In this study, we demonstrate that vandetanib, a tyrosine kinase inhibitor, is both substrate and inhibitor of P-glycoprotein and is able to reverse in vitro resistance to doxorubicin, linked to overexpression of P-glycoprotein.We also studied the placental transfer of vandetanib and we show that this drug crosses the placenta
Bischofs, Ilka Bettina. "Elastic interactions of cellular force patterns." Phd thesis, [S.l. : s.n.], 2004. http://deposit.ddb.de/cgi-bin/dokserv?idn=973638915.
Hill, S. D. "Plasma torch interaction with a melting substrate." Diss., Georgia Institute of Technology, 1999. http://hdl.handle.net/1853/17261.
O'Donnell, Emily. "Substrate and redox partner interactions with CYP17." Thesis, University of Sheffield, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.427259.
Rahman, Nahid 1974. "Polypyrrole : an interactive substrate for bone regeneration." Thesis, Massachusetts Institute of Technology, 1998. http://hdl.handle.net/1721.1/50554.
Includes bibliographical references (leaves 59-68).
Current methods of bone repair rely on autografts (bone from a donor site) and allografts (bone from human cadaver). However, these methods are plagued with disadvantages. There is a clear and urgent need to provide alternatives for regenerating and repairing bone. Bone is known to be one of the many connective tissues in the body that are responsive to exogenous electrical stimulation. Based on this principle, this thesis explores the potential of using an electrically conducting polymer, polypyrrole, as a substrate for bone regeneration. Optically transparent thin films of polypyrrole, with a polyanionic dopant, poly(styrenesulfonate), were synthesized electrochemically and characterized by X-Ray Photoelectron Spectroscopy, UV/VIS spectroscopy, Scanning Electron Microscopy and by electrical conductivity measurements. In this study, Bone Marrow Stromal Cells (BMSC), which are the progenitor cells to bone cells (osteoblasts), were used as the in vitro model system. Their viability, proliferation and differentiation capabilities were evaluated on polypyrrole, in the absence and presence of electrical stimulation. Results indicate that polypyrrole is ideally suited as a substratum for BMSC growth and differentiation. The application of an electrical stimulus through the polypyrrole substrate was found to induce the differentiation of BMSC towards an osteogenic lineage. Thus, polypyrrole, by virtue of its conductive properties, its in vitro biocompatibility and its flexibility in altering surface characteristics, has an exciting potential as a suitable interactive substrate for bone regeneration.
by Nahid Rahman.
S.M.
Wöbking, Barbara. "Substrate interactions on the ABC transporter MsbA." Thesis, University of Cambridge, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.613410.
Rahman, Nahid S. M. Massachusetts Institute of Technology. "Polypyrrole : an interactive substrate for bone regeneration." Thesis, Massachusetts Institute of Technology, 1998. http://hdl.handle.net/1721.1/50554.
Includes bibliographical references (leaves 59-68).
Current methods of bone repair rely on autografts (bone from a donor site) and allografts (bone from human cadaver). However, these methods are plagued with disadvantages. There is a clear and urgent need to provide alternatives for regenerating and repairing bone. Bone is known to be one of the many connective tissues in the body that are responsive to exogenous electrical stimulation. Based on this principle, this thesis explores the potential of using an electrically conducting polymer, polypyrrole, as a substrate for bone regeneration. Optically transparent thin films of polypyrrole, with a polyanionic dopant, poly(styrenesulfonate), were synthesized electrochemically and characterized by X-Ray Photoelectron Spectroscopy, UV/VIS spectroscopy, Scanning Electron Microscopy and by electrical conductivity measurements. In this study, Bone Marrow Stromal Cells (BMSC), which are the progenitor cells to bone cells (osteoblasts), were used as the in vitro model system. Their viability, proliferation and differentiation capabilities were evaluated on polypyrrole, in the absence and presence of electrical stimulation. Results indicate that polypyrrole is ideally suited as a substratum for BMSC growth and differentiation. The application of an electrical stimulus through the polypyrrole substrate was found to induce the differentiation of BMSC towards an osteogenic lineage. Thus, polypyrrole, by virtue of its conductive properties, its in vitro biocompatibility and its flexibility in altering surface characteristics, has an exciting potential as a suitable interactive substrate for bone regeneration.
by Nahid Rahman.
S.M.
Zhang, Baoshe. "A study of substrate--liquid crystal interaction /." View Abstract or Full-Text, 2003. http://library.ust.hk/cgi/db/thesis.pl?PHYS%202003%20ZHANG.
Includes bibliographical references (leaves 176-186). Also available in electronic version. Access restricted to campus users.
Layton, Stephanie Danielle. "Identifying Kinase/Substrate Interactions in Chlamydia trachomatis." OpenSIUC, 2014. https://opensiuc.lib.siu.edu/theses/1575.
Cubaka, Alfred. "Interactions plantes-bactéries sur des substrats contaminés en cuivre." Doctoral thesis, Universite Libre de Bruxelles, 2010. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/210068.
départ, une étude sur l'interaction entre les plantes et les bactéries sur un substrat pollué par le cuivre a été menée
dans deux directions:
1 °) une étude en conditions de laboratoire sur les capacités de C. metallidurans CH34 à interagir avec Nicotiana
plumbaginifolia (les solanacées)
2 °) une étude sur le terrain visant à examiner les interactions entre cuprophytes et bactéries résistantes aux
métaux des régions minières du Katanga.
La première partie inclut une étude in silico visant à établir un catalogue des gènes C. metallidurans CH34
potentiellement impliqués par les interactions plantes-bactéries. Ce catalogue, tout en se reposant sur le génome
proche de Ralstonia solanacearum, bactérie phytopathogène de plusieurs espèces végétales appartenant
principalement à la famille des Solanaceae, il n'a pas pris en compte les orthologues des gènes clés de la
virulence de cette phytopathogène. Les gènes correspondants de C. metallidurans étaient situées sur les deux
chromosomes et ont des orthologues dans tous les génomes séquencés des Cupriavidus / Ralstonia et dans
Enterobacter sp. 638, endophyte de peuplier. L'étude transcriptomique, à l'aide de «microarray» a montré que
certains de ces gènes étaient induits, notamment des gènes impliqués dans la mobilité flagellaire (comme motA)
et dans la synthèse des polysaccharides extracellulaires étaient surexprimés pendant le contact entre les plantes et
les bactéries, tandis que phcA (impliqué dans la détection de la densité de population et dans la conversion
phénotypique) et des gènes impliqués dans la biosynthèse de pili étaient sousexprimés dans les conditions
expérimentales testées. En outre, le contact avec les plantes semble avoir induit la surexpression des gènes
impliqués dans la réponse de cuivre et d'autres métaux. La capacité de C. metallidurans CH34 à coloniser
l'endosphere de N. plumbaginifolia a été confirmée in vitro ainsi qu'un effet de promotion de la croissance des
plantes dans certaines conditions. Mais la densité de la colonisation (104-106 c.f.u/g. poids frais) est
considérablement réduite dans des conditions non stériles et en l'absence de pression de sélection métallique.
La deuxième partie de l'étude s'est concentrée sur la microbiologie de cuprophytes (Haumaniastrum katagense et
Crepidorhopalon tenuis) dans l'arc cuprifère du Katanga: des isolats Cuprorésistants appartenant aux genres
Stenotrophomonas et Sphingomonas prédominent dans la rhizosphère alors que des isolats appartenant aux
genres Methylobacterium, Xanthomonas et Variovorax prédominent dans l'endosphere. Certaines de ces
bactéries sont plus résistantes au Cu(II), à des concentrations minimales inhibitrices (MIC) allant jusqu'à 5 mM,
que C. metallidurans CH34 (MIC: 1,5 mM) et la plupart d'entre elles résistent également aux Zn(II), Co(II) et
Cd(II). Des isolats appartenant au genre Cupriavidus/Ralstonia ont été détectés dans la rhizosphère des
cuprophytes ainsi que les séquences 16S rDNA de C. metallidurans ont été également détectées dans l'ADN
total extrait des cuprophytes. La détection via la réaction de la polymérase en chaîne (PCR) de gènes de
résistance au cuivre correspondant à des protéines periplasmiques a confirmé la présence dans les bactéries
cuprorésistantes, principalement de copA et dans une moindre mesure celle de copK. Mais les gènes homologues
de copA et de copK n'ont pas été détectés dans tous les bactéries du genre Methylobacterium dont les membres
ont été pourtant les plus résistants aux métaux. Certaines bactéries isolées sont capables d'interagir avec le
système hormonal végétal et quelques unes semblent également manifester un effet de promotion de la
croissance des plantes. Les premières tentatives d'élaboration de protocoles de reinoculation des bactéries
endophytic cuprorésistantes dans Haumaniastrum katagense ont été effectués. La biologie moléculaire et
l'écologie des interactions plantes-bactéries et des mécanismes de résistance métallique décrits dans ce travail
peuvent préparer la voie à de nouvelles applications en bioremédiation (phytostabilization / phytoextraction de
métaux toxiques).
Doctorat en Sciences
info:eu-repo/semantics/nonPublished
Linenberger, Kimberly J. "Biochemistry Students' Understandings of Enzyme-Substrate Interactions as Investigated through Multiple Representations and the Enzyme-Substrate Interactions Concept Inventory." Miami University / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=miami1321309534.
Qi, Xiaolin. "Enzyme-substrate interactions in PC1 #beta#-lactamase catalysis." Thesis, University of Newcastle Upon Tyne, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.315617.
Marsden, Catherine Jane. "Interactions between A-chain and it ribosomal substrate." Thesis, University of Warwick, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.269188.
Willenbockel, Martin [Verfasser], Frank Stefan [Akademischer Betreuer] Tautz, and Petra [Akademischer Betreuer] Tegeder. "Interacting Interactions: A Study on the Interplay of Molecule-Molecule and Molecule-Substrate Interactions at Metal-Organic Interfaces / Martin Willenbockel ; Frank Stefan Tautz, Petra Tegeder." Aachen : Universitätsbibliothek der RWTH Aachen, 2014. http://d-nb.info/1127861239/34.
Arjmandi-Tash, Omid. "Interaction of droplets and foams with solid/porous substrates." Thesis, Loughborough University, 2017. https://dspace.lboro.ac.uk/2134/24889.
Douzi, Badreddine. "La machinerie de sécrétion de type II Xcp de Pseudomonas aeruginosa : relations structure-fonction et interactome." Thesis, Aix-Marseille 1, 2011. http://www.theses.fr/2011AIX10086.
Gram-negative bacteria are characterized by a complex organization of their cell envelope composed by the inner membrane (IM) called cytoplasmic membrane, the periplasmic space containing a peptidoglycan layer and the outer membrane (OM) covered by the lipopolysaccharide matrix. Gram-negative bacteria have evolved several specialized machines called secretion systems to export their effectors from the intracellular medium to the extracellular milieu or to the host cells. Up to now, at least six secretion systems have been identified. In the opportunistic pathogen Pseudomonas aeruginosa, the type II secretion system called the Xcp secreton is the major pathway for the release of virulence factors. The Xcp secreton is a macromolecular complex composed by 12 proteins called XcpAO, XcpPC-XcpZM. This machinery is organized in 3 sub-complexes: i) the assembly platform localized in the IM implicating XcpRESFYLZM proteins ii) the OM pore composed by the oligomerization of the secretin XcpQD. The connection between the assembly platform and the secretin is performed by XcpPC anchored in the IM iii) a periplasmic pseudopilus consisting of the multimerization of the so-called major pseudopilin XcpTG. The pseudopilus is a helicoidally filament spanning the periplasmic area and pushing the substrate into the secretin pore. Four other proteins, the minor pseudopilins XcpUH-VI-WJ-XK, were found in the pseudopilus. In the present work we first focused on the study of the pseudopilus components by biochemical, biophysical and structural strategies to understand their assembly. Secondly, we investigate the protein interactome between periplasmic secreton component and secreted substrates. Thus, we revealed the presence of a quaternary complex composed by XcpUH-VI-WJ-XK located at the tip of the pseudopilus. To understand at atomic scale the regulation of the pseudopilus, we determined the structure of two components of the pseudopilus XcpTG by NMR and XcpWJ by X-ray crystallography. Using systematic protein-protein interaction studies between secreton components and purified exoproteins of Pseudomonas aeruginosa, we identified 5 proteins of the secreton able to interact with exoproteins. This interaction network allowed us to propose a model for the secretion process including the sequential steps followed by exoproteins inside the secreton to leave the cell envelop
Pauthe, Emmanuel. "Approches cinétiques et moléculaires de la reconnaissance enzyme-substrat : application à l'étude de l'activité protéolytique de la thermolysine." Compiègne, 1998. http://www.theses.fr/1998COMP1139.
Schmidt, Matthieu. "Substrats neurophysiologiques des interactions patient- ventilateur et des sensations respiratoires correspondantes." Thesis, Paris 6, 2014. http://www.theses.fr/2014PA066487/document.
Ventilatory support must be tailored to the load capacity balance of the respiratory system to avoid patient-ventilator dysharmony as it may lead to patient-ventilator asynchronies and dyspnea. Minimizing this dysharmony is crucial. Neurally Ventilatory Assist Ventilation (NAVA) and Proportional Assist Ventilation (PAV) modes may improve patient-ventilator interaction. We showed in this work that PAV and NAVA both prevents overdistension, restores breath by breath variability of the breathing pattern and improves neuromechanical coupling and patient- ventilator asynchrony in fairly similar ways compared to pressure support ventilation. In addition the use of NAVA with non-invasive ventilation may also improve patient-ventilator interaction. We also demonstrated that dyspnea is a frequent issue in mechanically ventilated ICU patients and it can be difficult to assess when the patient is unable to report it. Surface electromyograms of extradiaphragmatic inspiratory muscles provides a simple, reliable and non-invasive indicator of respiratory muscle loading/unloading in mechanically ventilated patients. Because this EMG activity is strongly correlated to the intensity of dyspnea, it could be used as a surrogate of respiratory sensations in mechanically ventilated patients, and might, therefore, provide a monitoring tool in patients in whom detection and quantification of dyspnea is complex if not impossible. These data provide a better understanding of patient-ventilator dysharmony. Further studies are needed to evaluate the possible clinical benefits of NAVA and PAV on clinical outcomes and the impact of an early detection of dyspnea in mechanical ventilation
Ulrich, Magdalena Maria Wilhelmina. "Enzyme/substrate interactions of the vitamin K-dependent carboxylase." [Maastricht : Maastricht : Rijksuniversiteit Limburg] ; University Library, Maastricht University [Host], 1991. http://arno.unimaas.nl/show.cgi?fid=6207.
Hodge, Thomas C. "Substrate-film interaction in noble metal/polymer multichip modules." Thesis, Georgia Institute of Technology, 1996. http://hdl.handle.net/1853/10972.
Eggenhuisen, Joris Theodoor. "'The interaction between substrate evolution and turbidity current development'." Thesis, University of Leeds, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.507691.
Kinstrie, Ross Stuart. "Identification of Drosophila DYRK family substrates and interacting proteins." Thesis, University of Glasgow, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.433084.
Riley, Jane. "The interaction of topoisomerase IV with potential DNA substrates." Thesis, University of Liverpool, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.272768.
Hersch, Greg Louis. "ClpX interactions with ClpP, SspB, protein substrate and nucleotide." Thesis, Massachusetts Institute of Technology, 2005. http://hdl.handle.net/1721.1/34199.
Includes bibliographical references.
ClpXP and related ATP-dependent proteases are implements of cytosolic protein destruction. They couple chemical energy, derived from ATP hydrolysis, to the selection, unfolding, and degradation of protein substrates with the appropriate degradation signals. The ClpX component of ClpXP is a hexameric enzyme that recognizes protein substrates and unfolds them in an ATP-dependent reaction. Following unfolding, ClpX translocates the unfolded substrate into the ClpP peptidase for degradation. The best characterized degradation signal is the ssrA-degradation tag, which contains a binding site for ClpX and an adjacent binding site for the SspB adaptor protein. I show that the close proximity of these binding elements causes SspB binding to mask signals needed for ssrA-tag recognition by ClpX. The SspB dimer overcomes this signal masking by tethering itself and bound substrate to ClpX, via docking sites located in the dimeric N-terminal domain of ClpX. Because this N-domain dimer binds only a single SspB subunit, the ClpX hexamer can accommodate just one SspB dimer per hexamer. Other adaptor proteins that use these same tethering sites must compete with SspB for access to ClpXP. Substrates bearing ssrA tags with increased spacing between the SspB and ClpX binding elements are degraded more efficiently at low concentrations by ClpXP.
(cont.) This mechanism in which the adaptor first obstructs and then stimulates substrate recognition may have evolved to permit an additional level of regulation of substrate choice. SspB binding to ssrA-tagged substrate is a highly dynamic process, allowing rapid transfer of substrates from SspB to ClpX. Although the ClpX hexamer is composed of six identical polypeptides, individual subunits assume at least three distinct conformations. Using a hexamer that was engineered to prevent nucleotide hydrolysis, I show that some nucleotide-binding sites in ClpX release ATP rapidly, others release ATP slowly, and at least two sites remain nucleotide free. Occupancy of both the slow sites by ATP and the fast sites by either ATP or ADP is required to bind the degradation tags of protein substrates. The ability of ClpX to retain binding of substrate with ATP or ADP in the fast sites suggests that nucleotide hydrolysis in the fast sites, but not in the slow sites, will allow repeated unfolding attempts without substrate release over multiple ATPase cycles. My results rule out ATPase models including ClpX6eATP6 or ADP6 and also suggest that the enzyme hydrolyzes only a fraction of bound ATP in a single turnover event. Short peptide motifs of ClpX, known as IGF loops, interact with ClpP and change conformation as a response to nucleotide binding by ClpX.
(cont.) As ClpX varies its nucleotide content during the ATP hydrolysis cycle, it also varies its affinity for ClpP. Processing of substrates is coupled to the ATP-hydrolysis cycle of ClpX and appears to modulate ClpX's affinity for ClpP by changing how long each ClpX subunit spends in each nucleotide state.
by Greg Louis Hersch.
Ph.D.
Jones, Darran Dafydd. "Protein-domain interactions and substrate channelling in multienzyme complexes." Thesis, University of Cambridge, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.621518.
Gullekson, Corinne. "Effect of Cell-Substrate Interactions on Epithelial Cell Mechanics." Thesis, Université d'Ottawa / University of Ottawa, 2018. http://hdl.handle.net/10393/38174.
Leckey, Jill J. "Exercise-nutrient interactions: Effects on substrate metabolism and performance." Thesis, Australian Catholic University, 2017. https://acuresearchbank.acu.edu.au/download/8abaa0b1b76c3014cfc2aad93fc50c5008eef9e6b6e8bbe177c3a02c38715a1e/5618185/Leckey_2017_Exercise_nutrient_interactions_effects_on_substrate_metabolism.pdf.
Zhang, Xinchen. "Interaction of PEG-ylated Lipid Nanoparticles with Silica Substrates." Thesis, Uppsala universitet, Institutionen för kemi - BMC, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-296349.
Schafe, Glenn E. "Neuroanatomical substrates of conditioned taste aversion : forebrain-brainstem interactions /." Thesis, Connect to this title online; UW restricted, 1997. http://hdl.handle.net/1773/9068.
Aref, Amirreza. "Nanotechnology applied to stem cell-substratum interactions." Thesis, Cranfield University, 2008. http://dspace.lib.cranfield.ac.uk/handle/1826/4448.
Markevich, Alexander. "Modification of electronic properties of graphene by interaction with substrates and dopants." Thesis, University of Exeter, 2012. http://hdl.handle.net/10871/10726.
Molloy, Claire Ann. "Interaction between oestradiol and the IGF-I signal transduction pathway in breast cancer cells." Thesis, University of Newcastle Upon Tyne, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.265214.
BERGERAT, AGNES. "Caracterisation des interactions de la methylase dam d'e. Coli avec ses substrats." Paris 6, 1990. http://www.theses.fr/1990PA066406.
ESSIA, NGANG JEAN-JUSTIN. "Interaction s. Cerevisiae l. Casei en fermentation alcoolique de substrats de sucrerie." Amiens, 1991. http://www.theses.fr/1991AMIES006.
Fransson, Linda. "Enzyme substrate solvent interactions : a case study on serine hydrolases." Doctoral thesis, KTH, Biokemi, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-4867.
QC 20100722
Meyer, Andrew James. "A calorimetric study of host-guest and protein-substrate interactions." Thesis, University of Leicester, 1997. http://hdl.handle.net/2381/30009.
Yap, Jessica. "Identification of Plasmodium falciparum protein kinase substrates and interacting proteins." Honors in the Major Thesis, University of Central Florida, 2012. http://digital.library.ucf.edu/cdm/ref/collection/ETH/id/644.
B.S.
Bachelors
Burnett School of Biomedical Sciences
Molecular and Microbiology
Öhlund, Thomas. "Metal Films for Printed Electronics : Ink-substrate Interactions and Sintering." Doctoral thesis, Mittuniversitetet, Avdelningen för naturvetenskap, 2014. http://urn.kb.se/resolve?urn=urn:nbn:se:miun:diva-23420.
Al-Hamdani, Y. S. "Theoretical approach towards accurate molecular interactions with low dimensional substrates." Thesis, University College London (University of London), 2016. http://discovery.ucl.ac.uk/1531128/.
Lack, Barbara Anne. "Metal interactions with neural substrates and their role in neurodegeneration." Thesis, Rhodes University, 2003. http://hdl.handle.net/10962/d1005709.
Russ, Jennifer Lynn. "Studies of Solution Paramagnetic-Substrate Nuclear and Electron Intermolecular Interactions." Diss., Virginia Tech, 2006. http://hdl.handle.net/10919/27050.
Ph. D.
Bach, Kristensen Jan. "Enzymatic hydrolysis of lignocellulose : substrate interactions and high solids loadings." Forest & Landscape, 2008. http://www.sl.kvl.dk/upload/nr_42_phd_jan__web.pdf.
Panse, Vikram G. "Interaction Of Chaperone SecB With Protein Substrates: A Biophysical Study." Thesis, Indian Institute of Science, 2000. https://etd.iisc.ac.in/handle/2005/242.
Panse, Vikram G. "Interaction Of Chaperone SecB With Protein Substrates: A Biophysical Study." Thesis, Indian Institute of Science, 2000. http://hdl.handle.net/2005/242.
Ben, Arfi Rim. "Adsorption, interaction et conformation de molécules modèles d’agent de couplage sur substrats métalliques." Mulhouse, 2007. http://www.theses.fr/2007MULH0886.
The understanding of mechanisms governing the growth, the structure and the conformation of coupling agents onto different metal substrates is determinant for an optimal use in any application. A variety of analytical techniques were used to characterize the different substrates : wettability, ellipsometry, atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS)and the polarization infrared reflection absorption spectroscopy (PM-IRRAS). Observations suggest that the structure of organic films is controlled by varying the concentration of the solution and the assembly time. The packing density, the organization and the conformation of the molecular chain depend on the nature of the metal substrate and on the roughness of the surface. All results presented in this work demonstrate the interest of multi-techniques and multi-scales approach in the characterization of ultra-thin organic films