Дисертації з теми "Glycoproteome"
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Zielinska, Dorota. "Unveiling the eukaryotic N-glycoproteome." Diss., Ludwig-Maximilians-Universität München, 2011. http://nbn-resolving.de/urn:nbn:de:bvb:19-166063.
Повний текст джерелаZielinska, Dorota [Verfasser], and Matthias [Akademischer Betreuer] Mann. "Unveiling the eukaryotic N-glycoproteome / Dorota Zielinska. Betreuer: Matthias Mann." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2011. http://d-nb.info/1047543605/34.
Повний текст джерелаHuang, Peiwu. "Method development and application for spatial proteome and glycoproteome profiling." HKBU Institutional Repository, 2020. https://repository.hkbu.edu.hk/etd_oa/788.
Повний текст джерелаMurrey, Heather Elizabeth Dougherty Dennis A. Hsieh-Wilson Linda C. "Identification and characterization of the plasticity-relevant fucose-alpha(1-2)galactose glycoproteome from mouse brain /." Diss., Pasadena, Calif. : Caltech, 2009. http://resolver.caltech.edu/CaltechETD:etd-12182008-145714.
Повний текст джерелаKalxdorf, Mathias [Verfasser]. "Mass spectrometric methods for measuring dynamic processes, drug-induced effects and target engagement on the cell surface glycoproteome / Mathias Kalxdorf." Halle, 2018. http://d-nb.info/1166140695/34.
Повний текст джерелаJi, Yanlong [Verfasser], Volker [Gutachter] Dötsch, and Thomas [Gutachter] Oellerich. "Quantitative N-glycoproteome, phosphoproteome and ubiquitinome analyses for studying B-cell receptor signaling in B-cell lymphoma / Yanlong Ji ; Gutachter: Volker Dötsch, Thomas Oellerich." Frankfurt am Main : Universitätsbibliothek Johann Christian Senckenberg, 2021. http://d-nb.info/1234680874/34.
Повний текст джерелаWeaver, Danielle. "N-linked glycosylation in Campylobacter jejuni and Campylobacter fetus and N-linked glycans as targets for antibody-based detection." Thesis, University of Manchester, 2017. https://www.research.manchester.ac.uk/portal/en/theses/nlinked-glycosylation-in-campylobacter-jejuni-and-campylobacter-fetus-and-nlinked-glycans-as-targets-for-antibodybased-detection(2b739b0d-84a3-47cc-af7a-d915b4caf37c).html.
Повний текст джерелаWu, Gang. "Glycomic and glycoproteomic studies of immune disorders." Thesis, Imperial College London, 2014. http://hdl.handle.net/10044/1/42776.
Повний текст джерелаCotton, Sofia Ribeiro. "Glycoproteomic characterization of advanced bladder cancer towards novel therapies." Master's thesis, Universidade de Aveiro, 2016. http://hdl.handle.net/10773/17366.
Повний текст джерелаA heterogenidade da natureza molecular dos tumores de bexiga tem dificultado o estabelecimento de abordagens no campo da medicina de precisão, revelando-se a necessidade de terapias mais eficientes e novas ferramentas de detecção não-invasivas. Contudo, têm-se denotado um desenvolvimento no estudo da carcinogénese de bexiga e na progressão do tumor, acompanhado de profundas alterações na glicosilação de proteínas que, dada a sua superfície celular e a natureza secretada, apresenta um potencial elevado na melhoria da gestão da doença. Segundo esta abordagem foi efectuado um estudo sobre tumores de bexiga de diferentes naturezas clinicopatológicas para O-glicanos de cadeia curta, regularmente encontrados na maioria dos tumores sólidos, recorrendo-se à imunohistoquímica. O estudo incluiu os antígenos Tn e T e os seus homólogos sialilados sialil-Tn (STn) e sialil-T (ST), geralmente associados com um mau prognóstico. Explorou-se ainda a sialilação da natureza dos antigénios T, especificamente as sialoformas sialil-3-T (S3T) e sialil-6-T (S6T), com base em combinações de tratamentos enzimáticos. Observou-se uma predominância de sialoglicanos, em comparação com as glicoformas neutras (antígenos Tn e T) em tumores de bexiga. Em particular, o antigénio STn foi associado ao estado avançado da doença e invasão muscular. Os antígenos S3T e S6T foram detectados pela primeira vez em tumores de bexiga, estando ausentes no urotélio normal, permitindo destacar a natureza específica em tumores. Verificou-se também a sobreexpressão dos glicanos em lesões avançadas, especialmente nos casos com invasão muscular.As análises glicoproteómicas dos tumores avançados de bexiga permitiram identificar diversas glicoproteínas-chave associadas ao cancro (MUC16, CD44, integrinas), denotando uma glicosilação alterada.As glicoformas da MUC16 STN positivas, características do cancro de ovário, encontram-se num subconjunto de tumores de bexiga em estado avançado, com um pior prognóstico. Em suma, os tumores de bexiga apresentam severas alterações no O-glicoma e no Oglicoproteoma devendo ser abordados de forma abrangente com o objectivo de desenvolver ferramentas de diagnóstico não invasivas e terapias dirigidas. As glicoformas aberrantes de MUC16 apresentam potencial como biomarcadores de mau prognóstico. Este trabalho estabeleceu um guia para a descoberta de glicobiomarcadores no cancro de bexiga, que pode ser utilizado para a estratificação dos pacientes e, por fim, levar à descoberta de novos alvos terapêuticos.
The heterogeneous molecular nature of bladder tumours has hampered the establishment of precision medicine approaches, more efficient therapeutics and novel non-invasive detection tools. Still, it has been long described that bladder carcinogenesis and tumour progression is accompanied by profound alterations in protein glycosylation which, given its cell surface and secreted nature, holds tremendous potential for disease management improvement. Therefore, we have screened series of bladder tumours of different clinicopathological natures for short-chain O-glycans, found in most solid tumours, by immunohistochemistry. These included the Tn and T antigens and their sialylated counterparts sialyl-Tn (STn) and sialyl-T(ST), generally associated with poor prognosis. We have also explored the nature of T antigens sialylation, namely the sialyl-3-T(S3T) and sialyl-6-T(S6T) sialoforms, based on combinations of enzymatic treatments. We observed a predominance of sialoglycans over neutral glycoforms (Tn and T antigens) in bladder tumours. In particular, the STn antigen was associated with high-grade disease and muscle invasion, in accordance with our previous observations.The S3T and S6T antigens were detected for the first time in bladder tumours, but not in healthy urothelia, highlighting their cancer-specific nature. These glycans were also overexpressed in advanced lesions, especially in cases showing muscle invasion. Glycoproteomic analyses of advanced bladder tumours identified several key cancer-associated glycoproteins (MUC16, CD44, integrins) carrying altered glycosylation. Particular interest was devoted to MUC16 STn+-glycoforms, characteristic of ovarian cancers, which were found in a subset of advanced stage bladder tumours facing worst prognosis. In summary, bladder tumours present severe O-glycome and O-glycoproteome alterations that should be comprehensively addressed envisaging novel non-invasive diagnostic tools and targeted therapeutics. Furthermore, abnormal MUC16 glycoforms holds potential as surrogate biomarkers of poor prognosis. Finally, this work established a roadmap for glycobiomarker discovery in bladder cancer, which may be used for patient stratification and ultimately lead to novel therapeutic targets.
Estrella, Ruby Poblete Graduate School of Biomedical Engineering Faculty of Engineering UNSW. "A glycoproteomic approach to the structural characterization of acidic glycoproteins." Publisher:University of New South Wales. Graduate School of Biomedical Engineering, 2009. http://handle.unsw.edu.au/1959.4/43562.
Повний текст джерелаPréhaud, Christophe. "Etude genetique et moleculaire de la glycoproteine du virus rabique cvs." Paris 6, 1988. http://www.theses.fr/1988PA066494.
Повний текст джерелаDE, PARSEVAL AYMERIC. "Le virus de l'immunodeficience feline : regulation transcriptionnelle, role de la glycoproteine cd9 dans la replication virale, et interaction de la glycoproteine de surface (gp95) avec la cellule hote." Paris 7, 2001. http://www.theses.fr/2001PA077046.
Повний текст джерелаBahloul, Chokri. "Immunisation genique : immunogenicite de la glycoproteine rabique et vaccins elargis aux lyssavirus." Paris 11, 1997. http://www.theses.fr/1997PA114831.
Повний текст джерелаRiwom, Sara Honorine. "Caracterisation biochimique de la glycoproteine erythrocytaire a activite de groupe sanguin duffy." Nantes, 1995. http://www.theses.fr/1995NANT03VS.
Повний текст джерелаBENMANSOUR, ABDENOUR. "La glycoproteine du virus rabique. Antigenicite, variabilite de la sequence et heterogeneite." Paris 11, 1991. http://www.theses.fr/1991PA112240.
Повний текст джерелаKettani, Chakib. "Les glycoproteines d'enveloppe du vih1 : importance fonctionnelle et antigenique." Strasbourg 1, 1990. http://www.theses.fr/1990STR15053.
Повний текст джерелаBRIEND, EMMANUEL. "Hgp92, une glycoproteine humaine a potentialites immunostimulantes : etude dans des modeles experimentaux murins." Paris 11, 1996. http://www.theses.fr/1996PA112381.
Повний текст джерелаSanon, Aouba Albertine M. A. "Purification et caracteristiques physico-chimiques de la n-acetyl-beta-d-hexosaminidase membranaire de trichomonas vaginalis (doctorat : interactions hotes-parasites)." Paris 11, 2000. http://www.theses.fr/2000PA114812.
Повний текст джерелаMontelimard-Laurent, Nathalie. "Vascularité leucocytoclasique à la glycoproteine extraite de Klebsiella pneumoniae avec les tests allergologiques positifs." Saint-Etienne, 2001. http://www.theses.fr/2001STET6428.
Повний текст джерелаChristophe, Olivier. "Structure du facteur willebrand et modulation de son interaction avec la glycoproteine 1b plaquettaire." Paris 7, 1994. http://www.theses.fr/1994PA077221.
Повний текст джерелаVillalba, François. "Clonage et caracterisation moleculaire d'une glycoproteine multifonctionnelle du champignon phytopathogene phytophthora parasitica var. Nicotianae." Toulouse 3, 1997. http://www.theses.fr/1997TOU30230.
Повний текст джерелаPOURTIER, ALBIN. "Description et caracterisation d'agents modulant la resistance tumorale pleiotropique mediee par la p-glycoproteine." Strasbourg 1, 1993. http://www.theses.fr/1993STR15096.
Повний текст джерелаBattini, Jean-Luc. "Etude de l'interaction de la glycoproteine d'enveloppe des retrovirus leucemogenes murins avec son recepteur cellulaire." Paris 6, 1996. http://www.theses.fr/1996PA066022.
Повний текст джерелаFélin, Murielle. "Interactions glycoproteine-lectine dans le noyau des cellules de la lignee myeloblastique leucemique humaine hl60." Paris 5, 1996. http://www.theses.fr/1996PA05S012.
Повний текст джерелаFranti, Michael. "Etude de la variabilite genetique et de l'antigenicite de la glycoproteine b de l'herpesvirus humain 7." Paris 6, 2001. http://www.theses.fr/2001PA066095.
Повний текст джерелаZENTILIN, BOYER MIREILLE. "Hypotrophie et manifestations digestives des desordres congenitaux de la glycosylation." Paris 6, 2001. http://www.theses.fr/2001PA060029.
Повний текст джерелаBenderra, Zineb. "Modulation differentielle des activites de la p-glycoproteine et la multidrug resistance associated protein dans les cellules tumorales : aspects cellulaire et pharmacologique (doctorat : ingenierie biologique." Reims, 2000. http://www.theses.fr/2000REIMP208.
Повний текст джерелаTran, Nguyet Thuy. "Developpement de nouvelles strategies analytiques pour l'etude de la glycosylation des proteines : application a l'etude et au controle de la glycoproteine recombinante de l'enveloppe du virus hiv-1 (rgp 160s-mn/lai) (doctorat : pharmacotechnie et biopharmacie)." Paris 11, 1999. http://www.theses.fr/1999PA114833.
Повний текст джерелаVillette, Hélène. "Investigations biochimiques et pharmacologiques des proprietes physiologiques de cftr : y -a-t-il une atpase associee a cftr ? (doctorat : biochimie)." Nantes, 1999. http://www.theses.fr/1999NANT05VS.
Повний текст джерелаMIZON, PASCALE. "Les glycoproteines des membranes plaquettaires : etude par cytometrie en flux." Lille 2, 1989. http://www.theses.fr/1989LIL2M305.
Повний текст джерелаEl, Bouhouti Rabia. "Utilisation de mucines gastriques de porc et de meconiums humains par des souches de differentes especes de bifidobacterium." Lille 2, 1994. http://www.theses.fr/1994LIL2P254.
Повний текст джерелаAmbrosi, Pierre. "Analyse par cytometrie en flux de douze glycoproteines de la membrane de la cellule endotheliale au repos et stimulee." Aix-Marseille 2, 1990. http://www.theses.fr/1990AIX20818.
Повний текст джерелаMASCHKE, SUSANNA. "Mise en evidence de la surexpression, dans les cellules cancereuses, d'une famille de glycoproteines ligands de la lectine endogene csl : proposition de nouveaux concepts sur la transformation maligne." Strasbourg 1, 1993. http://www.theses.fr/1993STR15022.
Повний текст джерелаJOLY, BEATRICE. "Expression fonctionnelle de la p-glycoproteine dans un modele de barriere hemato-encephalique in vitro (doctorat : toxicologie)." Paris 5, 1996. http://www.theses.fr/1996PA05N117.
Повний текст джерелаMejdoubi-Charef, Najet. "Regulation transcriptionnelle de l'expression de l'alpha-1-glycoproteine acide par le phenobarbital et par l'hormone de croissance." Paris 11, 1997. http://www.theses.fr/1997PA114825.
Повний текст джерелаDebili, Najet. "Etude de l'expression de la glycoproteine ib et du fibrinogene dans les cellules hematopoietiques normales et leucemiques." Paris 7, 1989. http://www.theses.fr/1989PA077041.
Повний текст джерелаMlambo, Shamiso Shelter. "A comparative proteomic and glycoproteomic study of platelets from patients with diabetes and non-diabetic healthy individuals." Diss., University of Pretoria, 2009. http://hdl.handle.net/2263/67808.
Повний текст джерелаDissertation (MSc)--University of Pretoria, 2018.
Pharmacology
MSc
Unrestricted
LEPAGE, ADELINE. "La glycoproteine v (gpv) plaquettaire : apparition tardive lors de la megacaryocytopoiese et etude fonctionnelle de son promoteur." Université Louis Pasteur (Strasbourg) (1971-2008), 1999. http://www.theses.fr/1999STR13149.
Повний текст джерелаMEISSONNIER, FREDERIC. "Chimioresistance pleiotropique dans le cancer du sein : detection de la gp 170 par immunohistochimie." Clermont-Ferrand 1, 1989. http://www.theses.fr/1989CLF13827.
Повний текст джерелаSavoysky, Ericka. "Etude de la structure du coronavirus enterique bovin ; clonage et sequencage du gene de la glycoproteine infectieuse e 1." Nancy 1, 1989. http://www.theses.fr/1989NAN12035.
Повний текст джерелаSCHLAIFER, DANIEL. "Contribution a l'etude de la resitance des cellules tumorales aux agents anti-cancereux : detection immunohistochimique de la p-glycoproteine ; marqueur de la resistance pleiotropique dans soixante-dix cas de tumeurs humaines." Toulouse 3, 1989. http://www.theses.fr/1989TOU31525.
Повний текст джерелаSalphati, Laurent. "P-glycoproteine et cytochrome p450 3a : interactions potentielles et roles complementaires dans l'absorption et la disposition des drogues." Paris 11, 1998. http://www.theses.fr/1998PA114805.
Повний текст джерелаCLERGET-RASLAIN, CLERGET BRIGITTE, and P. A. CAZENAVE. "Relations entre structure, antigenicite et fonctions de la glycoproteine d'enveloppe gp160 du virus de l'immunodeficience humaine vih-1." Paris 6, 1993. http://www.theses.fr/1993PA066533.
Повний текст джерелаBeitia, Ortiz de Zárate Igor. "Etude du transport intracellulaire de la Glycoproteine B de HSV-1 et de son impact sur l'infection virale." Paris 7, 2006. http://www.theses.fr/2006PA077071.
Повний текст джерелаHerpes simplex virus type 1 (HSV-1) is a human pathogen which infects neurons and can reach the central nervous System (CNS), causing encephalitis. Glycoprotein B (gB), a main component of HSV-1 necessary for entry into host cells, has been involved in neuroinvasion. Its cytoplasmic domain contains highly conserved motifs, similar to motifs involved in intracellular sorting of transmembrane proteins. To determine their role in the intracellular transport and maturation of gB, we deleted or mutated these motifs, and characterized the subsequent modifications in transfected and infected cells. We identified a region that includes the di-acidic motif ERTE, which is essential for the maturation and cell surface expression of gB, and for complementation of a gB-null virus. Two other motifs, YTQV and LL, participate in the retrograde transport of gB from the cell surface to the TGN. Whereas YTQV is essential for internalization of gB from the cell surface, LL most likely participates in a further step of this transport, since mutation of the LL motif does not prevent internalization of gB, but delays its accumulation in the TGN, while enhancing its recycling to the cell surface. Modification of these motifs leads to a decrease in virus infectivity and to changes in the phenotype of infection in cell culture (disruption of the LL motif enhances syncytium formation and the opposite is observed when the YTQV motif is modified). Altogether, these results favor a model in which HSV-1 gets its glycoproteins and final envelope at the TGN, and suggest that retrograde transport of gB, albeit non essential, might play an important role in cell-to-cell spread and infectivity of the virus
Négrier, Claude. "L'apport de la biologie moléculaire à l'étude des thrombocytopathies." Lyon 1, 1998. http://www.theses.fr/1998LYO1T047.
Повний текст джерелаMunteanu, Albani Dalila. "L'inter-alpha-inhibiteur au cours des etats septiques (doctorat : sciences pharmaceutiques)." Lille 2, 1999. http://www.theses.fr/1999LIL2P008.
Повний текст джерелаZidane, Mohamed. "Purification et caracterisation d'une glycoproteine pachymatismine extraite d'une eponge marine pachymatisma johnstonii (bow. ) : etude pharmacologique sur un carcinome bronchopulmonaire non-a-petites cellules." Nantes, 1996. http://www.theses.fr/1996NANT07VS.
Повний текст джерелаLecureur-Rolland, Valérie. "Expression, regulation et activite dans les cellules hepatiques de deux transporteurs membranaires de molecules cationiques : la p-glycoproteine et le transporteur de cations organiques (oct1)." Paris 5, 1997. http://www.theses.fr/1997PA05N100.
Повний текст джерелаSOLLY, SOUNKARY-KARINE. "Etude de l'expression et de la regulation de la myeline/oligodendrocyte glycoproteine (mog), une proteine myelinique du systeme nerveux central." Paris 6, 1996. http://www.theses.fr/1996PA066394.
Повний текст джерелаMOLLET, LUCILE. "Caracterisation des lymphocytes cd8 f o r tcd57+, analyse biochimique de la glycoproteine inhibitrice des fonctions de cytotoxicite qu'ils produisent." Paris 6, 1998. http://www.theses.fr/1998PA066571.
Повний текст джерела