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1

Chen, Na. "Synthesis of the N-oxyamide-linked glycolipids and glycopeptides." Thesis, Université Paris-Saclay (ComUE), 2015. http://www.theses.fr/2015SACLN017/document.

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Les glycoconjugués comme les glycolipides et les glycopeptides sont impliqués dans de nombreux processus biologique, physiologique et pathologique, tels que les interactions cellule-cellule, les infections virales et bactériales, les réponses immunitaires, le cancer, etc. Ces propriétés ont suscité de recherche intensive pour la synthèse de mimes de glycoconjugés pour des applications en biologie et en pharmacie. Cette thèse est consacrée à la synthèse de glycolipides et de glycopeptides liés par la liaison N-oxyamide qui possède une meilleure stabilité métabolique et une facilité de formation
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2

Oldenburg, Reid. "Immunomodulatory properties of mycobacterial phenolic glycolipids." Thesis, Sorbonne Paris Cité, 2016. http://www.theses.fr/2016USPCC234/document.

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La biosynthèse de phénol-glycolipides (PGL) par Mycobacterium tuberculosis et M. leprae favorise l’invasion des macrophages via l'interaction de la partie saccharidique des PGL avec le domaine lectine du récepteur cellulaire au complément CR3. Les PGL inhibent également la production de cytokines inflammatoires par la cellule hôte, par un mécanisme inconnu. J’ai observé que des bactéries BCG transgéniques exprimant les PGL de M. tuberculosis ou M. leprae avaient une capacité de survie accrue dans les macrophages. Cette persistance intracellulaire était dépendante de CR3 et associée à une dimin
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3

Audoin, Coralie. "Valorisation de métabolites secondaires issus de micro-algues : approches métabolomiques, isolement et caractérisation structurale." Thesis, Nice, 2013. http://www.theses.fr/2013NICE4068.

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Les microalgues présentes à la fois dans les eaux douces et salées compteraient plus de 200 000 espèces. Cette diversité en fait une source potentielle de métabolites spécialisés originaux. Parmi les principales familles de substances naturelles valorisées actuellement, on peut citer les pigments, lipides, protéines, polysaccharides, caroténoïdes. Une vision plus globale du métabolome de chacune des espèces apparaît aujourd’hui nécessaire pour mieux mettre en valeur le potentiel commercial que représente cette « microbiodiversité ». Pour cela, nous avons tout d’abord choisi d’approcher le méta
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4

Cobo, Cardenete Isidro Felipe. "Glycolipids: synthesis and multivalent systems." Doctoral thesis, Universitat Rovira i Virgili, 2012. http://hdl.handle.net/10803/284152.

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Els glicolípids i particularment els glicoesfingolípids són compostos d’interès perquè poden interaccionar amb biofactors tot inhibint o interferint en processos fisiològics de les cèl•lules. Per exemple, els glicoesfingolípids que recobreixen les membranes cel•lulars poden interaccionar en processos de reconeixement amb bactèries, virus i toxines com per exemple la toxina del Còlera la qual inicia el procés d’infecció pel reconeixement de glicolípids com el GM1. Tot i que l’ús d’antibiòtics és el tractament més emprat, la resistència als antibiòtics a zones endèmiques fa necessària la recerca
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5

Calabro, Kevin. "Valorisation dans le domaine de la cosmétique de métabolites produits par microalgues et cyanobactéries." Thesis, Université Côte d'Azur (ComUE), 2016. http://www.theses.fr/2016AZUR4100.

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Les secteurs de la parfumerie et de la cosmétique occupent une place proéminente dans la société moderne. De nombreuses entreprises se positionnent depuis plusieurs années sur les produits cosmétiques à ingrédients naturels. Les plantes, longtemps considérées comme matière première principale pour le domaine de la cosmétique, sont aujourd’hui concurrencées par les microalgues dont la biomasse devient plus facile à obtenir grâce aux avancées en biotechnologie bleue. Ainsi, Cosmo International Ingredients se positionne à travers cette thèse pour élargir son panel de matières premières valorisabl
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6

Nilsson, Ulf. "Structural requirements for glycolipid receptors recognized by uropathogenic E. coli synthetic and biological studies with fragments and analogs of globo oligosaccharides /." Lund : Organic Chemistry 2, Lund Institute of technology, University of lund, 1995. http://books.google.com/books?id=EjdsAAAAMAAJ.

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7

Sather, Paula Joan. "Synthesis of cholesterol based model glycolipids." Thesis, University of British Columbia, 1990. http://hdl.handle.net/2429/29876.

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The synthesis of glycolipids containing a variable length polyethylene glycol spacer group between a glucuronic acid (glu) headgroup and a cholesterol (chol) tail glu-0CH₂(CH₂OCH₂ )nCH₂O-chol is described. The homologs (n=2,3,5) were prepared by reaction of an excess of commercially available tri, tetra and hexaethylene glycols with cholesteryl-p-toluene sulfonate. 3-O-(8-hydroxy-3,6-dioxaoctyl) cholest-5-ene (2), 3-O-(ll-hydroxy-3,6,9-trioxaundecyl)cholest-5-ene (3) and 3-O-(17-hydroxy-3,6,9,12,15-pentaoxaheptadecyl)cholest-5-ene (4) were produced, and yields were dependent on the amount of
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8

Norris-Cervetto, Edward. "Glycolipids and multidrug resistance in cancer." Thesis, University of Oxford, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.419326.

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9

Matton, Pascal. "Glycolipides fluorescents et gouttelettes glycosylées." Thesis, Paris Sciences et Lettres (ComUE), 2017. http://www.theses.fr/2017PSLEE037/document.

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Certains agents pathogènes ou cellules tumorales échappent au système immunitaire parce que les cellules immunitaires ne reconnaissent pas les peptides ou protéines présents à leur surface. Les approches thérapeutiques favorisant la reconnaissance de ces peptides ou protéines faiblement immunogènes sont donc très attractives. Pour ainsi forcer l'activation des cellules présentatrices d'antigènes, plusieurs systèmes ont été décrits, à base de liposomes ou de nanoparticules inorganiques. Nous proposons ici d'utiliser un système à base de gouttelettes d'huile. Les micro ou nanogouttelettes d'huil
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10

Chambers, Martina Natasha. "Synthesis of cellulosic glycolipids using engineered enzymes." Thesis, University of British Columbia, 2014. http://hdl.handle.net/2429/46032.

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Cellulose, a linear polymer of D-glucose units connected by β-1,4 glycosidic bonds, adopts a highly-ordered crystalline structure in solution. In cellulose I, the dominant form of cellulose in nature, the polymeric chains are aligned in the same direction. Previous attempts to synthesize cellulose I in vitro have resulted in the synthesis of cellulose II, which has the thermodynamically favored anti-parallel orientation of chains. The synthesis of soluble fragments or defined surfaces of cellulose I would enable more detailed study of carbohydrate binding domains and other proteins that intera
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11

Falconer, Robert Andrew. "Lipoamino acid based glycolipids for drug delivery." Thesis, University College London (University of London), 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.392430.

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12

Röthlisberger, Peter. "Lipoteichoic acid and glycolipids of a novel streptococcus /." [S.l.] : [s.n.], 1995. http://e-collection.ethbib.ethz.ch/show?type=diss&nr=11149.

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13

Salvadó, Molero Míriam. "Synthetic glycolipids as modulators of carbohydrate-protein interactions." Doctoral thesis, Universitat Rovira i Virgili, 2016. http://hdl.handle.net/10803/456813.

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El Capítol 1 presenta una descripció general de la glicobiologia així com el rol dels sistemes multivalents en la interacció carbohidrat-proteïna. En el Capítol 2 s’estableixen els objectius generals. El Capítol 3, fa referencia a la síntesi de glicolípids que presenten modificacions a l’anell de piranosa o a la part de l’aglicona. La avaluació tant d’aquest glicolípids com els seus corresponents sistemes multivalents es va dur a terme front glicosidases. Es va trobar, que les modificacions tant en l’anell de piranosa com en l’aglicona jugaven un paper important en la inhibició. A més a més,
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14

Minden, Hans Markus von. "Synthesis and mesomorphic properties of glycolipids and neoglycolipids." [S.l. : s.n.], 2000. http://deposit.ddb.de/cgi-bin/dokserv?idn=959565434.

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15

Wikström, Malin. "Synthesis and protein curing abilities of membrane glycolipids." Doctoral thesis, Stockholm University, Department of Biochemistry and Biophysics, 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-1361.

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<p>There are many types of membrane lipids throughout Nature. Still little is known about synthesizing pathways and how different lipids affect the embedded membrane proteins. The most common lipids are glycolipids since they dominate plant green tissue. Glycolipids also exist in mammal cells as well as in most Gram-positive bacteria. Glycosyltransferases (GTs) catalyze the final enzymatic steps for these glycolipids. In the bacteria <i>Acholeplasma laidlawii</i> and <i>Streptococcus pneumonie</i> and in the plant <i>Arabidopsis thaliana</i>, GTs for mono-/di-glycosyl-diacylglycerol (-DAG) are
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16

Wikström, Malin. "Synthesis and protein curing abilities of membrane glycolipids /." Stockholm : Department of Biochemistry and Biophysics, Stockholm University, 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-1361.

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17

Zeb, Neelofar. "Synthesis and lyotropic phase behaviour of novel glycolipids." Thesis, Imperial College London, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.336634.

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18

Comas, Theodore Christopher. "Glycolipids and markers of normal and neoplastic Macroglia /." The Ohio State University, 1999. http://rave.ohiolink.edu/etdc/view?acc_num=osu1488192447430358.

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19

Joshi-Navare, K. "Biosynthesis of novel glycolipids: basic and applied aspects." Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 2013. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/2193.

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20

Sarkar, Debasmita. "Mycobacterial glycolipids : pathways to synthesis and role in virulence." Thesis, University of Birmingham, 2012. http://etheses.bham.ac.uk//id/eprint/1790/.

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Mycobacterial diseases are responsible for numerous deaths worldwide, the major pathogens being Mycobacterium tuberculosis and Mycobacterium leprae. Also, in recent years threats from opportunistic pathogens, such as Mycobacterium marinum and Mycobacterium kansasii have been on the rise. These mycobacteria possess a unique lipid-rich cell wall with an array of mycolic acids and species-specific antigenic glycolipids, like the lipooligosaccharides. Some of these solvent extractable lipids possess immunomodulatory properties and play an important role during infection. Lipooligosaccharides (LOS)
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21

Mullin, Nicholas Paul. "Characterisation of ligand-binding to a carbohydrate-recognition domain of the macrophage mannose receptor." Thesis, University of Oxford, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.320620.

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22

Wait, Peter Robin. "The role of fast atom bombardment mass spectrometry in the structural determination of microbial glycoconjugates." Thesis, University of Greenwich, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.361086.

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23

Morales, Serna José Antonio. "Synthesis of glycolipids and glycodendritic polymers that bind HIV rgp120." Doctoral thesis, Universitat Rovira i Virgili, 2009. http://hdl.handle.net/10803/386454.

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Several viral envelope glycoprotein oligomers assembled into a viral fusion machine, form a molecular scaffold that brings the viral and target cell membranes into close apposition and allow the subsequent fusion events. The fusion pore formation and its sequential expansion are orchestrated by viral and cellular lipids and proteins. The HIV entry process is understood in some detail at the molecular level. It is coordinated by the HIV envelope glycoprotein complex, a trimer of three gp120 surface glycoproteins, each noncovalently attached to three gp41 ransmembrane glycoprotein subunits.%&/It
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24

Pierce, Eric John. "Bacterial toxins as probes for membrane glycolipids in mammalian cells." Thesis, University of Leicester, 1985. http://hdl.handle.net/2381/35129.

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Cholera toxin which binds specifically and with high affinity to a glycolipid; ganglioside GM1, has been used as a probe to study glycolipid-protein interactions in the plasma membranes of BALB/c 3T3 mouse fibroblasts and mouse lymphocytes. Evidence is presented that: i) a proportion of cholera toxin bound to GM1 of BALB/c 3T3 cells withstood extraction with Triton X-100 at 0C and remained associated with the cytoskeleton; ii) at 37C, cholera toxin-GM1 complexes were completely extracted with Triton X-100. The resulting complexes existed in a macromolecular form that did not involve other memb
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25

Xiao, X. "Investigations of heterocyst glycolipids from cyanobacteria by chromatography/mass spectrometry." Thesis, Swansea University, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.636702.

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In this thesis studies of the structures of the heterocyst glycolipids of two species of Cyanobacteria, <I>Anabaena cylindrica</I> and <I>Aphanizomenon flos-aquae </I>have been undertaken to provide a better understanding of Cyanobacteria. Early chapters introduce the Cyanobacterium family and the preparation procedures for the heterocyst glycolipids in our studies. These chapters are separated by an introduction of chromatography and mass spectrometry with emphasis on the techniques used in these studies. The remaining chapters discuss the use of GC/EIMS, GC/CIMS, LC/APCIMS and LC/ESMS, MS/MS
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26

Colvine, James Ronald Lindsay. "Studies on mycobacterial glycolipids and inhibitors of mycolic acid biosynthesis." Thesis, University of Newcastle Upon Tyne, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.285691.

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27

Nardan, Denise. "Acid hydrolysis of neutral glycosphingolipids thesis submitted in fulfillment of the degree of Doctorate of Philosophy, Auckland University of Technology, June 2007 /." Click here to access this resource online, 2007. http://repositoryaut.lconz.ac.nz/theses/1389/.

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28

Griffiths, Susanne Lynn. "An evaluation of the role of gangliosides as the receptors for fibronectin and Escherichia coli heat-labile toxins." Thesis, University of Leicester, 1987. http://hdl.handle.net/2381/35236.

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In an attempt to evaluate the role of gangliosides as receptors for fibronectin, a series of Balb/c 3T3 variant cell lines, with a reduced ability to bind the ganglioside-specific ligand cholera toxin (CT), were examined. Initial characterisation showed that the cell lines displayed a generalised reduction in the synthesis of gangliosides more complex than GM3, but not of cell surface glycoproteins. There was no reduction in the levels of fibronectin found at the surface of the variants as compared with the parental cell line and all were able to spread and form focal contacts on fibronectin-c
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29

Sava, Georgeta Irina. "Investigations on Enterococcus faecalis glycolipids and their role in bacterial virulence." Lübeck Zentrale Hochschulbibliothek Lübeck, 2010. http://d-nb.info/1002133866/34.

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30

Patin, Emmanuel Christian Jean-Marie Bernard. "Role of mycobacterial glycolipids in survival of bacteria inside the macrophage." Thesis, London School of Hygiene and Tropical Medicine (University of London), 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.590624.

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31

Drage, Michael Gerald. "Toll-like Receptor 2-Mediated Recognition of Mycobacterial Lipoproteins and Glycolipids." Cleveland, Ohio : Case Western Reserve University, 2009. http://rave.ohiolink.edu/etdc/view?acc_num=case1244231392.

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Thesis (Ph.D.)--Case Western Reserve University, 2009<br>Title from PDF (viewed on 19 August 2009) Department of Pathology Includes abstract Includes bibliographical references Available online via the OhioLINK ETD Center
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32

Liu, Yang. "Synthesis of Glycolipids and Evaluation of Their NKT Cell Stimulatory Properties." BYU ScholarsArchive, 2010. https://scholarsarchive.byu.edu/etd/2293.

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Natural killer T (NKT) cells are a subset of T cells that modify a variety of immune responses. NKT cells recognize glycolipid antigen presented by a molecule called CD1d, a nonclassical antigen-presenting molecule. The best known subset of CD1d-dependent NKT cells expresses an invariant T cell receptor Vα (TCR-α) chain. These are referred to as type I or invariant NKT (iNKT) cells. When stimulated by a glycolipid, NKT cells rapidly release large amounts of cytokines. Cytokines released by NKT cells can induce either Th1 or Th2 responses. Th1 cytokines are effective in regulating bacterial, pa
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33

Wonjo, Justyna. "Novel glycolipids in CD1d-mediated immunity : synthesis of new agonists of CD1d." Thesis, University of Birmingham, 2012. http://etheses.bham.ac.uk//id/eprint/3551/.

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The glycolipid α-galactosyl ceramide, α-GalCer, has been shown to stimulate the proliferation of murine spleen cells and activate the immune system. Stimulation occurs through binding of the glycolipid to the protein CD1d. Subsequent presentation of the CD1d−glycolipid complex to invariant Natural Killer T cells (iNKT cells) initiates the proliferation of a host of cytokines leading to an immune response The therapeutic potential of α-GalCer is currently being explored; however the induction of both Th1 and Th2 cytokines by this agent is likely to limit its therapeutic application. Significant
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34

Jemmett, Philip N. "Towards an understanding of the biological activity of glycolipids : a physicochemical study." Thesis, University of Birmingham, 2018. http://etheses.bham.ac.uk//id/eprint/8191/.

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Monolayers composed of N-palmitoyl sphingomyelin (SM) or dipalmitoylphosphatidylcholine (DPPC) have been investigated at the air|water interface. Bilayers of these molecules have also been investigated at the Au(111)|water interface. Monolayer studies revealed differences in molecular area between the two molecules, despite identical headgroups, suggesting the sphingosine backbone of SM allows a more densely packed monolayer structure. Polarisation modulated infrared reflection-absorption spectroscopy studies of the corresponding bilayers revealed that the alkyl chain orientation is comparable
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35

Custer, Jenny Elise. "Phospholipids and Glycolipids of the Oral Bacterium Streptococcus mutans UA159." University of Cincinnati / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1307442038.

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36

Dubey, P. "Biosynthesis of novel glycolipids (Sophorolipids): exploring the mechanism of assembling and biological properties." Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 2017. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/5873.

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37

Belkai, Sonia. "Recherche d'acteurs lysosomaux impliqués dans la présentation de lipides mycobactériens par CD1b aux lymphocytes T." Electronic Thesis or Diss., Université de Toulouse (2023-....), 2024. http://www.theses.fr/2024TLSES176.

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Les lipides peuvent être antigéniques et présentés en surface des cellules présentatrices d'antigènes (CPA). Ces lipides, généralement amphiphiles, sont présentés par les protéines CD1 (CD1a à CD1d), des protéines proches structurellement de la protéine du CMH de classe 1, avec pour principale différence le site de liaison des antigènes. Cette présentation mène à une réponse immunitaire spécifique médiée par des lymphocytes T non conventionnels. Mycobacterium tuberculosis (Mtb), agent causal de la tuberculose, possède dans son enveloppe des lipides antigènes présentés par les protéines CD1, et
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38

Kadri, Nabil. "Graines de Pinus SP : caractérisation physico-chimique et activité anticancéreuse." Thesis, Montpellier 2, 2014. http://www.theses.fr/2014MON20143/document.

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Les graines de pin (Pinus halepensis Mill., Pinus pinea L., Pinus pinaster et Pinus canariensis) sont les quatre espèces les plus disponibles dans le bassin méditerranéen. Elles sont très utilisées par les populations Nord-africaines en médecine traditionnelle et en gastronomie où elles agrémentent les plats traditionnels (salades, riz, poissons …etc), car elles sont bien connues pour leur excellent goût salé. Cependant, la composition biochimique, les valeurs nutritionnelles, et les mécanismes d'actions cellulaires et moléculaires via lesquels ces graines exercent leurs effets thérapeutiques
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39

Ces, Oscar. "The phase behaviour of glycolipids employing a novel high-pressure X-ray beamline." Thesis, Imperial College London, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.416049.

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40

Muindi, K. M. "Cellular lipids and immunity : characterisation of glycolipids binding the antigen presenting molecule CD1." Thesis, University of Oxford, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.670089.

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41

Torres-L{u00F3}pez, Beatriz Virginia. "Affinity purification of blood group A-active glycolipids on immobilized Helix pomatia lectin." Diss., Virginia Polytechnic Institute and State University, 1988. http://hdl.handle.net/10919/77851.

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Lectin affinity chromatography has proven to be a powerful method to separate oligosaccharides based on their stereochemical structures. This technique has not been used for the separation of glycolipids since mixtures of these compounds form micelles in aqueous solution. Since N-acetylgalactosamine (GalNAc) is commonly found in glycolipids, three GalNAc-specific lectins were selected to develop a lectin affinity chromatographic method for glycolipids. To circumvent the difficulty of working with micelles, the autoradiographic detection of ¹²⁵l-labeled lectins binding to glycolipids on thin-la
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42

Mahon, Robert Norman III. "Direct Inhibition of CD4+ T-cell Activation by Mycobacterium tuberculosis Cell Wall Glycolipids." Case Western Reserve University School of Graduate Studies / OhioLINK, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=case1275668686.

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43

Long, Xiangtian. "Synthesis and Evaluation of Stimulatory Properties of Glycolipids for Natural Killer T Cells." BYU ScholarsArchive, 2009. https://scholarsarchive.byu.edu/etd/2133.

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Natural killer T cells (NKT cells) are a subset of T cells. They regulate a wide range of diseases including infection, tumor growth, and autoimmune diseases, through recognizing glycolipid antigens in the context of CD1d. An understanding of the scope of glycolipid antigens would facilitate use of this cell type in controlling immune responses. Till today, a lysosomal glycolipid, isoglobotrihexosylceramide (iGb3), is the only natural glycolipid that has been found to be recognized by both human and mouse NKT cells. To elucidate the molecular basis of this specific recognition, iGb3 variants w
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44

Arcens, Dounia. "Conception de nouveaux monomères glycolipidiques par voie chimio-enzymatique pour la synthèse de polymères amphiphiles et leur auto-assemblage dans l’eau : vers des applications de vectorisation." Thesis, Bordeaux, 2017. http://www.theses.fr/2017BORD0838/document.

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Ces travaux de thèse portent sur la conception par voie chimio-enzymatique de polymères amphiphiles issus de glycolipides, capables de s’auto-assembler en phase aqueuse et susceptibles de répondre à des applications de vectorisation de principes actifs. Après une étude préalable des paramètres influents lors de la synthèse enzymatique, huit monomères glycolipidiques porteurs de fonctions esters vinyliques,méthacrylate ou [alpha]-méthylstyrène ont été synthétisés à partir de dérivés d’huile de ricin et de glucose. Les monomères porteurs d’une fonction ester vinylique comme groupement polymérisa
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FURUKAWA, KOICHI, KOJI KIKKAWA, TETSUYA OKAJIMA та ін. "STRONG ANTIBODY REACTION AGAINST GLYCOSPHINGOLIPIDS INJECTED IN LIPOSOMEEMBEDDED FORMS IN β3GN-T5 KNOCKOUT MICE". Nagoya University School of Medicine, 2011. http://hdl.handle.net/2237/15356.

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Dockery, Keith Foorest. "Investigations on Glycolipid Production by Pseudomonas Putida grown on Toluene in Batch and Continuous Culture Conditions." PDXScholar, 1994. https://pdxscholar.library.pdx.edu/open_access_etds/4969.

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Utilization of toluene by Pseudomonas putida as its sole carbon and energy source affects morphology, outer membrane protein composition, and glycolipid production. Two strains of P. putida were found to utilize toluene and to coexist in continuous and batch culture. The two strains were designated translucent and opaque, based upon their readily identifiable coloration when grown on Luria agar. The translucent strain was the dominant strain in continuous culture conditions. The outer membrane proteins of P. putida were separated by sodium dodecyl sulphate polyacrylamide gel electrophoresis. W
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Milkereit, 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.

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Gorbea, Carlos M. "Glycolipids in mouse F9 teratocarcinoma cells : some changes associated with retinoic acid-induced differentiation /." Thesis, This resource online, 1991. http://scholar.lib.vt.edu/theses/available/etd-08142009-040425/.

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Aydt, Alexander Paul, Robin Polt, Alexander Paul Aydt, and Robin Polt. "Creating a C-12 Series of Glycolipids for Use as Micelles in Drug Delivery." Thesis, The University of Arizona, 2017. http://hdl.handle.net/10150/624907.

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Micelles are critically important molecules with a variety of uses. They have historically been used in the multibillion dollar soap industry. More recently, their efficacy in drug delivery has been demonstrated (1). Normal oxygen-linked glycosides are susceptible to hydrolysis (2). We are seeking to develop a series of carbon-linked glycolipids of varying chain lengths and functional groups in order to observe trends in their micelle properties, including Critical Micelle Concentration (CMC). Presented here are the C-12 Glycoside series.
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Sava, Georgeta Irina [Verfasser]. "Investigations on Enterococcus faecalis glycolipids and their role in bacterial virulence / Georgeta Irina Sava." Lübeck : Zentrale Hochschulbibliothek Lübeck, 2010. http://d-nb.info/1002133866/34.

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