Дисертації з теми "Biophysical Investigations"
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Forman, J. R. "Biophysical investigations of PKD domains : mechanosensation and pathogenesis." Thesis, University of Cambridge, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.599119.
Повний текст джерелаHands, Sarah Louise. "Biophysical investigations of the mechanism of colicin translocation." Thesis, University of Nottingham, 2005. http://eprints.nottingham.ac.uk/10102/.
Повний текст джерелаPatel, Amesh Babubhai. "Biophysical and computational investigations into receptor-ligand complexes." Thesis, University of Nottingham, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.435998.
Повний текст джерелаGarner, Thomas Peter. "Structural and biophysical investigations into ubiquitin binding proteins." Thesis, University of Nottingham, 2011. http://eprints.nottingham.ac.uk/12100/.
Повний текст джерелаYin, Daniel. "Biophysical investigations into membrane-active peptides and proteins." Thesis, University of Oxford, 2016. https://ora.ox.ac.uk/objects/uuid:25401447-e37b-4c07-a22d-29718958ac48.
Повний текст джерелаFyfe, Paul Kelman. "Biophysical investigations of photosynthetic reaction centres from Rhodobacter sphaeroides." Thesis, University of Glasgow, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.263434.
Повний текст джерелаShnoudeh, Abeer Jabra. "Biochemical and biophysical investigations of novel phosphodiesterase-5 inhibitors." Thesis, King's College London (University of London), 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.429578.
Повний текст джерелаHaggarty-Weir, Christopher Neil. "Biochemical and biophysical investigations into key malaria parasite proteins." Thesis, University of Edinburgh, 2018. http://hdl.handle.net/1842/29617.
Повний текст джерелаColledge, Vicki Louise. "Stuructural and biophysical investigations of bacillus subtillis transition-state regulators." Thesis, University of York, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.535053.
Повний текст джерелаHansen, R. K. "Biophysical and biochemical investigations of the M2 peptide of influenza A." Thesis, University of Cambridge, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.603662.
Повний текст джерелаChang, Michelle M. (Michelle Miran). "Biochemical and biophysical investigations of N-linked glycosylation pathways in archaea." Thesis, Massachusetts Institute of Technology, 2014. http://hdl.handle.net/1721.1/97981.
Повний текст джерелаCataloged from PDF version of thesis. "December 2014."
Includes bibliographical references.
Asparagine-linked glycosylation is an abundant and complex protein modification conserved among all three domains of life. Much is known about N-glycan assembly in eukaryotes and selected bacteria, in which the oligosaccharyltransferase (OTase) carries out the en bloc transfer of glycans from polyprenyl-PP-linked donors onto asparagine side chains of acceptor proteins. The first aim of this thesis is to elucidate the biochemical details of archaeal N-linked glycosylation, specifically through in vitro analysis of the polyprenyl-P-dependent pathway of the methanogenic archaeon Methanococcus voltae. The archaeal OTase, known as AglB, utilizes a-linked dolichyl-P-trisaccharide substrate as the glycosyl donor for transfer to the acceptor protein. This dolichyl-P-glycan is generated by an initial retaining glycosyltransferase (AglK) and elaborated by additional glycosyltransferases (AglC and AgIA) to afford Dol-P-GlcNAc- Glc-2,3-diNAcA-ManNAc(6Thr)A. Despite the homology to other bacterial or eukaryotic OTases that exploit polyprenyl-PP-linked substrates, the M. voltae AglB efficiently transfers disaccharide to model peptides from the Dol-P-GlcNAc-Glc-2,3-diNAcA monophosphate. While this archaeal pathway affords the same asparagine-linked P-glycosyl amide products generated in bacteria and eukaryotes, these studies provide the first biochemical evidence revealing that despite the apparent similarities of the overall pathways, there are actually two general strategies to achieve N-linked glycoproteins across the domains of life. A second focus of this thesis involves biophysical studies to probe structural features and conformational dynamics of AglB. An intramolecular LRET experimental system was developed to report on substrate binding and the resulting structural transformations in AgIB. There is a strong need for detailed studies on the mechanistic and functional significance of archaeal adaptations of N-linked glycosylation, especially exploring differences between AglB and other OTases that allow AglB to utilize these unique polyprenyl-P-linked substrates. Lastly, a cell-free expression system was established for the efficient synthesis of Alg5, a yeast dolichyl-phosphate glucosyltransferase that shares high sequence similarity to AglK, the first glycosyltransferase in the M. voltae pathway. Dol-P-Glc was generated and examined to unambiguously characterize the stereochemistry of the product of Alg5.
by Michelle M. Chang.
Ph. D.
Madani, Mobarekeh Sayed Abdollah. "Design and synthesis of new photolabile protected active substances for biophysical investigations." [S.l. : s.n.], 2003. http://deposit.ddb.de/cgi-bin/dokserv?idn=96852608X.
Повний текст джерелаSacho, Elizabeth J. Erie Dorothy A. "Biophysical and biochemical investigations of proteins involved in genomic maintenance and stability." Chapel Hill, N.C. : University of North Carolina at Chapel Hill, 2007. http://dc.lib.unc.edu/u?/etd,1431.
Повний текст джерелаTitle from electronic title page (viewed Apr. 25, 2008). " ... in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the Department of Chemistry." Discipline: Chemistry; Department/School: Chemistry.
Davidsen, Amanda. "Biophysical investigations of structural features and interactions of «Leishmania donovani» Peroxin 5." Thesis, McGill University, 2014. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=123260.
Повний текст джерелаLes parasites du genre Leishmania provoquent un large éventail de maladies, appelées collectivement leishmanioses. Ces maladies varient en termes de morbidité ; la forme cutanée se conclut généralement par une auto-guérison, alors que les manifestations cutanéo-muqueuses et viscérales nécessitent une intervention chimiothérapeutique pour éviter le décès. À l'heure actuelle, il n'existe aucun vaccin, et les méthodes actuelles d'intervention chimiothérapeutique présentent de graves conséquences. Il existe aujourd'hui un besoin urgent de trouver de nouvelles options pour lutter contre ces maladies destructrices. Un organite dans le parasite, le glycosome, a été identifié comme une cible thérapeutique intéressante. Le glycosome compartimente plusieurs enzymes de biosynthèses et voies métaboliques importantes; il a été prouvé que cet organite est nécessaire pour assurer la viabilité du parasite. Bien que l'organite soit structurellement et évolutivement lié aux peroxysomes des eucaryotes supérieurs, le mécanisme d'importation des organites diffère sensiblement. La majorité des protéines entrant dans le glycosome contient une séquence tri-peptide PTS1 C-terminal, qui est facilement reconnue et liée par le récepteur cytosolique soluble LPEX5. Le récepteur se lie au cargo PTS1 dans le cytosol, le conduisant vers la membrane glycosomale où la protéine interagit avec LPEX14, une protéine liée à la membrane périphérique. L'interaction avec LPEX14 au niveau de la membrane glycosomale, facilitée par plusieurs autres protéines de biogenèse, initie la formation d'un pore d'importation transitoire. Dans ce projet de thèse, le rôle de PEX5 dans la formation de ce pore d'importations essentiel a été analysé chez Leishmania donovani. En utilisant des techniques biophysiques, il a été constaté que l'interaction du récepteur avec un PTS1 n'a pas causé de changements majeurs dans la structure secondaire, bien qu'elle ait provoqué un changement de conformation de la protéine, précédant et éventuellement facilitant ses interactions avec LdPEX14 à une membrane glycosomale. Grâce à l'utilisation de grandes vésicules unilamellaires mimant la composition lipidique glycosomale, le domaine de LdPEX5 nécessaire pour interagir avec LdPEX14 fut ramené à 268-302. En outre, en utilisant des extractions carbonate-urée en série, il a été prouvé que le domaine identifié comme étant nécessaire pour l'interaction avec LdPEX14 au mimétique glycosomal, s'insère dans la membrane liposomale. De ce fait, l'insertion de LdPEX14 dans la membrane glycosomale pourrait tirer LdPEX5 dans la membrane dans le contexte de la formation de pores. En conclusion, cette étude a démontré que LdPEX5 possède un rôle central dans la formation du pore d'importation glycosomale transitoire.
Morris, Janine M. "A biophysical study into the mammalian vitreous humour and investigations into replacements." Thesis, University of East Anglia, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.445210.
Повний текст джерелаLi, Shi-Jiang. "Biophysical investigations into the secondary structure of Triticum aestivum 5s ribosomal RNA /." The Ohio State University, 1985. http://rave.ohiolink.edu/etdc/view?acc_num=osu148726191911312.
Повний текст джерелаTaormina, Michael. "Developing Methods Based on Light Sheet Fluorescence Microscopy for Biophysical Investigations of Larval Zebrafish." Thesis, University of Oregon, 2014. http://hdl.handle.net/1794/18342.
Повний текст джерелаAndersson, Magnus. "Construction of force measuring optical tweezers instrumentation and investigations of biophysical properties of bacterial adhesion organelles." Doctoral thesis, Umeå : Department of Physics, Umeå Univ, 2007. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-1425.
Повний текст джерелаJameson, Katie H. "Structural and biophysical investigations of two negative regulators of DNA replication initiation in Bacillus subtilis, YabA and SirA." Thesis, University of York, 2015. http://etheses.whiterose.ac.uk/13168/.
Повний текст джерелаWolf, Justine. "Biophysical investigations of the LAH4 family peptides : enhancer of gene delivery, from peptide-peptide interactions to peptide-membrane interactions." Thesis, Strasbourg, 2018. http://www.theses.fr/2018STRAF037/document.
Повний текст джерелаThe LAH4 family consists of cationic amphiphilic peptides with propensity to fold in α-helical secondary structures. They contain histidines allowing the modulation of their interactions in a pH dependent manner in the physiological range. In membranes, at neutral or acidic pH the peptide assumes a transmembrane or an in planar configuration, respectively.In the field of gene delivery systems, peptides like LAH4 are used. They are able to firstly interact with different cargoes in order to form stable complexes, then interact with the cell membrane, and finally, promote to escape from the endosome.This PhD has been divided into three parts in order to characterize, with biophysical methods, the interactions occurring during the delivery of these gene systems: peptide-peptide interactions with a focus on the study of VF1 fibre formation; peptide-membrane interactions: with the investigation of the effect of LAH4L1 in different membranes; and peptide-DNA interactions, where the interactions of LAH4L1 with a small DNA fragment were measured
Giannetti, Anthony Michael Rees Douglas C. "Biochemical, biophysical, and cellular investigations of the interactions of transferrin receptor with transferrin and the hereditary hemochromatosis protein, HFE /." Diss., Pasadena, Calif. : California Institute of Technology, 2004. http://resolver.caltech.edu/CaltechETD:etd-05262004-173612.
Повний текст джерелаSukumaran, Madhav. "Biophysical investigations of AMPA receptor N-terminal domain structure and function reveal mechanisms underlying receptor assembly, dynamics, and allosteric potential." Thesis, University of Cambridge, 2014. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.708278.
Повний текст джерелаRoessler, Maxie M. "EPR investigations of iron-sulfur cluster relays in enzymes." Thesis, University of Oxford, 2013. http://ora.ox.ac.uk/objects/uuid:ac6fa892-f54a-490d-927b-161231f00777.
Повний текст джерелаSzwagierczak, Aleksandra. "Biochemical and biophysical characterization of the lyase isomerase PecE/PecF complex, nicastrin the transmembrane component of the gamma-secretase complex and structural investigations of the genomic islands integrases." kostenfrei, 2009. https://mediatum2.ub.tum.de/node?id=829180.
Повний текст джерелаKowalska, Kaja [Verfasser], Tad A. [Akademischer Betreuer] Holak, Bernd [Akademischer Betreuer] Reif, and Robert [Akademischer Betreuer] Huber. "Biochemical and biophysical characterization of CD44 and its binding partner, hyaluronic acid and structural investigations of the ubiquitin-like protein 5 / Kaja Kowalska. Gutachter: Bernd Reif ; Robert Huber. Betreuer: Tad A. Holak." München : Universitätsbibliothek der TU München, 2012. http://d-nb.info/1031513604/34.
Повний текст джерелаEboigbodin, Kevin Efosa. "Biophysical investigation of bacterial aggregation." Thesis, University of Sheffield, 2008. http://etheses.whiterose.ac.uk/3625/.
Повний текст джерелаMoreau, Matthew Joseph. "A biophysical and biochemical investigation of MCM." Thesis, University of Cambridge, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.612169.
Повний текст джерелаNematollahi, L. A. "NMR and biophysical investigation of death domain assemblies." Thesis, University College London (University of London), 2013. http://discovery.ucl.ac.uk/1386650/.
Повний текст джерелаDi, Marino Sara. "Biophysical investigation of biomolecules in bio-membrane models." Doctoral thesis, Universita degli studi di Salerno, 2012. http://hdl.handle.net/10556/1313.
Повний текст джерелаMany drugs are available for the treatment of systemic or superficial mycoses, but only a limited number of them are effective antifungal drugs, devoid of toxic and undesirable side effects. Therefore there remains an urgent need for a new generation of antifungal agents. The present work concerns the synthesis, the antifungal activity and the biophysical characterization of a set of linear and cyclic peptides (AMT1, cyclo-AMT1, AMT2, cyclo-AMT2, AMT3, cyclo-AMT3) including aminoacids characteristic of membrane-active antimicrobial peptides (AMP). The peptides were tested against different yeast species, and displayed general antifungal activity, with a therapeutically promising antifungal specificity against Cryptococcus neoformans. To shed light on the role played by the membrane cell in the antifungal activity an extensive biophysical study was carried out using different spectroscopic techniques. Our structural investigation provides data to exclude the ability of the peptides to penetrate the membrane of the fungal cell, highlighting their attitude to interact with the external surface of the bilayer. Taken together our data support the hypothesis that the membrane cell of the fungi may be an important platform for specific interactions of the synthesized peptides with more specific targets involved in the cell wall synthesis. Viral fusion glycoproteins present a membrane-proximal external region (MPER) which is usually rich in aromatic residues and presents a marked tendency to stably reside at the membrane interfaces, leading, through unknown mechanisms, to a destabilization of the bilayer structure. This step has been proposed to be fundamental for the fusion process between target membrane and viral envelope. In present work, we investigate the interaction between an octapeptide (C8) deriving from the MPER domain of gp36 of Feline Immunodeficiency Virus and different membrane models by combining experimental results obtained by Nuclear Magnetic Resonance, Electron Spin Resonance, Circular Dichroism and Fluorescence Spectroscopy with Molecular Dynamics simulations. Our data indicate that C8 binds to the lipid bilayer adsorbing onto the membrane surface without deep penetration. As a consequence of this interaction, the bilayer thickness decreases. The association of the peptide with the lipid membrane is driven by hydrogen bonds as well as hydrophobic interactions that the Trp side chains form with the lipid headgroups. Notably these interactions may be the key to interpret at molecular level the function played by Trp residues in all the fragments of viral envelope involved in fusion mechanism with target membrane. [edited by author]
X n.s.
Rajah, Luke. "Biophysical and microfluidic techniques for investigating protein aggregation." Thesis, University of Cambridge, 2013. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.608030.
Повний текст джерелаMayer, Jürgen. "Investigation of the biophysical basis for cell organelle morphology." Master's thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2010. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-26600.
Повний текст джерелаScaffidi, Salvatore. "Biophysical Techniques for the Investigation of Protein-Ligand Complexes." Doctoral thesis, Universitat de Barcelona, 2021. http://hdl.handle.net/10803/673608.
Повний текст джерелаUna vez que se identifica y caracteriza una proteina, comienza el largo camino para desarrollar un fármaco. En este proceso, los métodos biofísicos tienen un papel importante que jugar y hoy en día se combinan firmemente en varias etapas. En este escenario, utilizando técnicas biofísicas, el principal objetivo de este trabajo se basa en la identificación y caracterización de pequeñas moléculas con capacidad para unirse a varias proteínas. Fbw7 es una ligasa E3 con un papel importante en el cáncer. Sin embargo, hasta ahora no se han identificado ligandos de moléculas pequeñas de Fbw7. En esta tesis hemos realizado un programa FBDD para identificar fragmentos capaces de unirse a esta ligasa E3. Estos fragmentos podrían emplearse como puntos de partida para dilucidar la mejor estrategia para apuntar a Fbw7 y construir nuevas moléculas PROTAC. Debido a la escasa solubilidad en agua de los retinoides, la evolución ha ajustado su unión a proteínas celulares para abordar funciones fisiológicas especializadas mediante la modulación de la captación, el almacenamiento y la entrega a sitios específicos . En esta tesis, hemos desenredado las relaciones estructura-función de estas clases de proteínas y hemos revelado pistas para diseñar transportadores selectivos. Dado el modo de unión de los fragmentos a un objetivo de interés, la optimización de los fragmentos puede resultar laboriosa, difícil y requiere mucho tiempo. En esta tesis, se ha hecho un ensayo sobre pequeñas moléculas que se unen a Brd4 (BD1), identificadas por la plataforma de evolución de fragmentos automatizada desarrollada por nuestro grupo, y se ha validado la plataforma.
Mayer, Jürgen. "Investigation of the biophysical basis for cell organelle morphology." Master's thesis, Max-Planck-Institut für Molekulare Zellbiologie und Genetik, 2008. https://tud.qucosa.de/id/qucosa%3A25225.
Повний текст джерелаDonovan, Alexandra. "Comparative Biophysical Analysis of APOE3 and APOE4| A Mechanistic Investigation." Thesis, California State University, Long Beach, 2017. http://pqdtopen.proquest.com/#viewpdf?dispub=10606132.
Повний текст джерелаApolipoprotein E is an exchangeable apolipoprotein whose isoforms are associated with various disease risk profiles. Individuals bearing the APOE ϵ4 allele are at increased risk for developing Alzheimer’s disease compared to those bearing the APOE ϵ3 allele. The two isoforms differ in amino acid at position 112: apoE3 bears a Cys while apoE4 bears an Arg. It is hypothesized that the Cys to Arg substitution in apoE4 causes a decrease in stability in comparison to apoE3, which is exaggerated at endosomal pH <6.0. In our study, changes in secondary structure were monitored using circular dichroism at pH 7.4 and pH 3.5. Chemical denaturation indicated that both apoE3 and apoE4 retained their helical secondary structure at the lower pH, with a biphasic and monophasic guanidine HCl denaturation profile, respectively. Tertiary structure was monitored at both pH’s through fluorescence spectral characteristics and mobility of a fluorescent probe attached to each of the 7 major amphipathic α-helices of apoE3 and apoE4. The data showed decreases in fluorescence emission (FE), changes in fluorescence polarization (FP), and fluctuations in probe mobility, which were interpreted as likely formation of a molten globule. Formation of a molten globule appeared to occur during denaturation primarily for apoE4, and thermodynamic parameters of apoE4 showed a lower stability than apoE3, with a larger effect of pH. Taken together, our results suggest that the acidic pH in the endosomal compartments could interact with the native structure of apoE4 to generate a molten globule state that is able to bind endosomal membranes, other proteins, or itself. This study offers mechanistic insight into the impact of the single residue difference between apoE3 and apoE4 with regard to folding/unfolding behavior, and with regard to its physiological and pathological implications.
Teevan, Claire Patricia. "A biophysical investigation into the surface properties of Candida albicans." Thesis, University of Essex, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.243396.
Повний текст джерелаStollar, Elliott Jonathan. "Biophysical and crystallographic investigation of homeodomain stability, dynamics, and recognition." Thesis, University of Cambridge, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.615778.
Повний текст джерелаMulaj, Mentor. "Biophysical Investigation of Amyloid Formation and Their Prion-like Self-replication." Scholar Commons, 2016. http://scholarcommons.usf.edu/etd/6332.
Повний текст джерелаNauseef, Jones Trevor. "An investigation of the molecular and biophysical properties of metastatic cells." Diss., University of Iowa, 2015. https://ir.uiowa.edu/etd/3150.
Повний текст джерелаMirheydari, Mona Sadat. "INVESTIGATION OF THE BIOPHYSICS OF LIPID DROPLETS." Kent State University / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=kent1498862985023767.
Повний текст джерелаSiahpoosh, Yasmin(Yasmin H. ). "Investigating mechanisms of biophysical diversity between phasic and tonic motor neurons." Thesis, Massachusetts Institute of Technology, 2020. https://hdl.handle.net/1721.1/130197.
Повний текст джерелаCataloged from student-submitted PDF of thesis.
Includes bibliographical references (pages 65-67).
Neurons exhibit striking diversity in core neuronal properties (intrinsic biophysical and synaptic properties), which are the building blocks of brain function and computation. Despite the central role of these properties in brain function, the underlying molecular and biophysical mechanisms which generate this diversity remain incompletely understood. In the Drosophila larval motor system, phasic (1s) and tonic (1b) motor neurons (MNs) differ in their intrinsic biophysical properties, providing an ideal system to examine electrophysiological diversity across neuronal populations. To address this question, we combined in vivo whole-cell patch-clamp physiology with biophysical modeling. First, we characterized biophysical diversity between 1s and 1b MNs. To explore molecular mechanisms underlying such diversity, single-neuron PatchSeq RNA profiling experiments were carried out to correlate biophysical properties with differences in ion channel gene expression profiles. These experiments suggest that cyclic nucleotide- gated like (CNGL) ion channels are upregulated in 1b MNs several folds, which indicates that CNGL could be a candidate ion channel that might specify diversity in electrical properties . To test this hypothesis, we misoverexpress CNGL in 1s MNs so that we could investigate how this ion channel contributes to the diversity between them. We developed an analysis toolset in MATLAB that can be used to analyze whole-cell patch-clamp physiology data and obtain excitability properties. Using the Izhikevich model, we were able to quantify and predict the spiking properties of 1s and 1b MNs. Using a ball and stick model, we were able to reproduce the tonic firing pattern of 1b neurons and tested tonic firing patterns in different compartments of 1b neurons. Taken together, this thesis work laid the foundation to begin characterizing biophysical mechanisms of intrinsic diversity of Drosophila neurons by combining experimental data with modeling.
by Yasmin Siahpoosh.
M. Eng.
M.Eng. Massachusetts Institute of Technology, Department of Electrical Engineering and Computer Science
DeGrazia, Henry. "A biophysical investigation of the mechanisms of the catabolite gene activator protein." Diss., Georgia Institute of Technology, 1988. http://hdl.handle.net/1853/25641.
Повний текст джерелаFiorentini, S. "ADVANCED COMPUTATIONAL METHODS FOR THE INVESTIGATION OF BIOPHYSICAL PROPERTIES OF MACROMOLECULAR PROTEINS." Doctoral thesis, Università degli Studi di Milano, 2011. http://hdl.handle.net/2434/155491.
Повний текст джерелаBottomley, Matthew James. "Biophysical studies of intracellular signal transduction proteins : investigating the structure-function relationship." Thesis, University College London (University of London), 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.286570.
Повний текст джерелаJonnalagadda, Umesh Sai. "Investigation of the biophysical role of the acoustic environment for cartilage tissue engineering." Thesis, University of Southampton, 2017. https://eprints.soton.ac.uk/425931/.
Повний текст джерелаZhang, Ruojing. "The Investigation of Biophysical and Biological Function of PRPS from Nostoc PCC 7120." Miami University / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=miami1617630241200474.
Повний текст джерелаGashua, Ibrahim Babale. "An investigation of the molecular structure, composition and biophysical properties of gum Arabic." Thesis, University of Wolverhampton, 2016. http://hdl.handle.net/2436/608784.
Повний текст джерелаShanmugam, Nirukshan. "Biophysical investigation of the amyloidogenic potential of human and viral necroptosis-associated proteins." Thesis, The University of Sydney, 2021. https://hdl.handle.net/2123/25455.
Повний текст джерелаMilkereit, Götz Eckart. "Investigation of colloidal, biophysical and liquid crystalline properties of synthetic alkyl glycosides and glycolipids." [S.l.] : [s.n.], 2006. http://deposit.ddb.de/cgi-bin/dokserv?idn=980736676.
Повний текст джерелаZhang, Lei. "Biophysical and biochemical investigation of the structure of chloroplast twin arginine transport component Hcf106." Miami University / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=miami1429539744.
Повний текст джерелаMartin, William R. "Computational Investigation of the Prothrombinase Complex." Cleveland State University / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=csu1544528008896018.
Повний текст джерела