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Relevant bibliographies by topics / Membrane cofactor protein; Glycoproteins / Dissertations / Theses

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Dissertations / Theses on the topic 'Membrane cofactor protein; Glycoproteins'

Author: Grafiati

Published: 4 June 2021

Last updated: 12 February 2022

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1

Pollard, Alison Jane. "Characterisation of CD46 isoforms in human peripheral blood cells : localisation of complement regulatory proteins throughout the male reproductive tract." Thesis, University of Liverpool, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.365911.

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2

Richards, Anna. "Genetic factors predisposing to the haemolytic uraemic syndrome." Thesis, University of Newcastle Upon Tyne, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.289212.

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3

Simpson, Karen Lesley. "Expression of complement regulatory proteins in human development and reproduction." Thesis, University of Bristol, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.294904.

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4

Turner, C. E. "Capping of the major rat thymocyte glycoproteins : Their interactions with other membrane proteins and the cytoskeleton." Thesis, University of Oxford, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.376955.

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5

Crombie, Andrea Rene. "Lysosomal integral membrane protein II, a member of the CD36 gene family : comparative analysis of structure-function relationships /." Access full-text from WCMC, 1998. http://proquest.umi.com/pqdweb?did=733079741&sid=9&Fmt=2&clientId=8424&RQT=309&VName=PQD.

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6

Holmlund, Camilla. "Identification and investigations of leucine-rich repeats and immunoglobulin-like domains protein 2 (LRIG2)." Doctoral thesis, Umeå : Department of Radiation Sciences, Oncology, Umeå university, 2010. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-33784.

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7

Alvares, Stacy M. "The role of membrane microdomains in the phosphorylation of the epithelial transmembrane protein, GP140/CDCP1 /." Thesis, Connect to this title online; UW restricted, 2007. http://hdl.handle.net/1773/5022.

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8

Oran, Alp E. "Defining sites of interaction in the Ã-chain of C3 for factor H, membrane cofactor protein (MCP), and complement receptor 1 (CR1)." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp01/MQ29260.pdf.

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9

Chang, Eddie. "The role of perforin and chemokines in the pathogenesis of chronic corneal inflammation induced by herpes simplex virus type-1 infection." free to MU Campus, others may purchase, 2003. http://wwwlib.umi.com/cr/mo/fullcit?p3091911.

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10

Wilson, Cheryl Anne. "The Membrane Integration of the Hemagglutinin-Neuraminidase Glycoprotein of Newcastle Disease Virus: A Thesis." eScholarship@UMMS, 1989. http://escholarship.umassmed.edu/gsbs_diss/295.

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The hemagglutinin-neuraminidase (HN) molecule of Newcastle disease virus (NDV) is an integral membrane glycoprotein that is oriented with its N-terminus in the cytoplasm and its C-terminus external to the infected cell. Single spanning membrane proteins with this type of topology (N-terminus in, C-terminus out) have been classified as Type II glycoproteins, in contrast to the more common Type I glycoproteins, which are oriented in the opposite direction. (C-terminus in, N-terminus out). The membrane integration of HN protein was investigated using a wheat germ translation system to synthesize

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11

Wenham, Matt. "The role of Adaptor Protein 3 in cytotoxic T lymphocytes." Thesis, University of Oxford, 2009. http://ora.ox.ac.uk/objects/uuid:1a5c1fd6-c8cc-454f-81a5-b9a5a18c1540.

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Cytotoxic T lymphocytes (CTL) kill virally infected and tumourigenic cells via the regulated secretion of specialised secretory lysosomes. These secretory lysosomes contain cytolytic effector molecules, such as perforin and granzymes, which are able to induce apoptosis in target cells. Secretion occurs at the contact point between the CTL and its target, in a highly structured region termed the immunological synapse (IS). Upon formation of the IS, CTL undergo polarisation of their microtubule cytoskeleton and movement of the microtubule organising centre (MTOC) to the IS. Secretory lysosomes a

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12

Melanson, Vanessa R. "Characterization of the Interaction Between the Attachment and Fusion Glycoproteins Required for Paramyxovirus Fusion: a Dissertation." eScholarship@UMMS, 2005. https://escholarship.umassmed.edu/gsbs_diss/24.

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The first step of viral infection requires the binding of the viral attachment protein to cell surface receptors. Following binding, viruses penetrate the cellular membrane to deliver their genome into the host cell. For enveloped viruses, which have a lipid bilayer that surrounds their nucleocapsids, entry into the host cell requires the fusion of viral and cellular membranes. This process is mediated by viral glycoproteins located on the surface of the virus. For many enveloped viruses, such as influenza, Ebola, and human immunodeficiency virus, the fusion protein is responsible for mediatin

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13

Guo, Beichu. "Interaction of PKCbeta with CARMA1 mediates B cell receptor-induced NF-kappaB activation /." Thesis, Connect to this title online; UW restricted, 2003. http://hdl.handle.net/1773/8348.

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14

Louie, Sarah. "Wnt signaling regulated by Frizzled and HIPK1 /." Thesis, Connect to this title online; UW restricted, 2004. http://hdl.handle.net/1773/6267.

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15

Wessels, Miriam [Verfasser]. "The intracellular lectin vesicular integral-membrane protein (VIP36) as a potential sorting receptor for the glycoproteins dipeptidyl peptidase IV and sucrase-isomaltase in the early secretory pathway / Miriam Wessels." Hannover : Technische Informationsbibliothek und Universitätsbibliothek Hannover (TIB), 2011. http://d-nb.info/1013471717/34.

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16

Corey, Elizabeth Ann. "Characterization of the Relationship Between Measles Virus Fusion, Receptor Binding, and the Virus-Specific Interaction Between the Hemagglutinin and Fusion Glycoproteins: a Dissertation." eScholarship@UMMS, 2006. https://escholarship.umassmed.edu/gsbs_diss/221.

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Measles (MV) virions, like those of other enveloped viruses, enter cells by fusing their lipid membranes with those of the target host cells. Additionally, infected tissues often possess giant multinucleate cells, known as syncytia, which are formed by fusion of infected cells with uninfected neighbors. Expression of both the MV attachment (H) and fusion (F) proteins is required for membrane fusion. MV H mediates receptor binding in order to bring the two membranes into close proximity prior to F activation and is thought to trigger F activation through a specific interaction between the two p

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17

Ljuslinder, Ingrid. "Studies of LRIG1 and the ERBB receptor family in breast and colorectal cancer." Doctoral thesis, Umeå : Umeå university, 2009. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-25678.

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18

Nilsson, Jonas. "The LRIG-family : identification of novel regulators of ErbB signaling with clinical implications in astrocytoma /." Doctoral thesis, Umeå : Department of Radiation Sciences, 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-783.

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19

Pari, François Michel. "Etude d'une proteine de la membrane plasmique de l'oligodendrocyte en culture." Université Louis Pasteur (Strasbourg) (1971-2008), 1988. http://www.theses.fr/1988STR13098.

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Des anticorps diriges contre des antigenes partiellemnt accessibles a la surface de la membrane oligodendrogliale constituent des outils biologiques utiles pour l'etude des mecanismes biochimiques de la myelinisation. Deux glycoproteines (g2 et g3) derivant de la membrane oligodendrogliale, sont utilisees comme marqueurs d'oligodendrocytes. Une glycoproteine de 53 kda a ete identifiee a la surface de l'oligodendrocyte isolee, un serum polyclonal a ete obtenu. Une etude immunocytochimique a confirme sa presence a la surface de la membrane plasmique, elle est egalement trouvee en surface sur les

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20

Tejle, Katarina. "Leishmania donovani Lipophosphoglycan : Modulation of Macrophage and Dendritic Cell Function." Doctoral thesis, Linköping : Univ, 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-6527.

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21

MILLET, BOTTI JOELLE. "Dynamique de l'interaction fibronectine-matrice extracellulaire dans l'adhesion des fibroblastes au cours du developpement embryonnaire chez le poulet." Paris 7, 1988. http://www.theses.fr/1988PA077120.

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22

Démares, Marie-José. "Etude de l'expression du facteur H du complément par les leucocytes humains." Rouen, 1987. http://www.theses.fr/1987ROUES053.

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23

Lackman, J. (Jarkko). "Glycosylation and dimerization of the human δ-opioid receptor polymorphic variants". Doctoral thesis, Oulun yliopisto, 2018. http://urn.fi/urn:isbn:9789526221342.

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Abstract Cellular signaling by G protein-coupled receptors (GPCRs) governs a wide array of physiological functions throughout the body. The human δ-opioid receptor (hδOR) is a GPCR that modulates the sensation of pain and mood and has great potential for the treatment of pain and a variety of neurological disorders. A common single-nucleotide polymorphism (SNP) in the extracellular N-terminal tail of hδOR changes Phe to Cys at position 27. Using various biochemical and cell biological methods, the study demonstrates that several events during receptor biosynthesis and cell surface delivery are

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24

Chang, Wen-Pin. "Functional charaterization of symaptic proteins in calcium triggered exocytosis." 2008. http://www4.utsouthwestern.edu/library/ETD/etdDetails.cfm?etdID=392.

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