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Showing 1 to 20 of 33 for “"The complement system"”.

  1. The Role of the Complement System in Mousepox Infection

    Poxviruses subvert the host immune response by producing immunomodulatory virulence factors, including a complement regulatory protein. Ectromelia virus provides a mouse model for human smallpox infection where the virus and the host's immune response have also co-evolved. Using this model, we …

    wustl Repository record for The Role of the Complement System in Mousepox Infection (opens in a new tab)

  2. Studies of EHEC and the complement system in renal diseases

    This thesis addressed the diagnosis, pathogenesis and clinical course of specific renal diseases hemolytic uremic syndrome (HUS) and dense deposit disease (DDD). HUS may be associated with infection caused by Enterohemorrhagic Escherichia coli (EHEC) or with complement dysfunction due to complement

    lund Repository record for Studies of EHEC and the complement system in renal diseases (opens in a new tab)

  3. Molecular Interactions of Human C9: The Pore Forming Protein of the Complement System

    <p>The human complement system is part of our innate immunity that acts to eliminate pathogenic organisms. Activation of complement leads to the sequential, non-enzymatic assembly of C5b, C6, C7, C8, C9 forming C5b-9<sub>n</sub> (n=12-18), a cytolytically active pore-like structure known as the

    south-carolina Repository record for Molecular Interactions of Human C9: The Pore Forming Protein of the Complement System (opens in a new tab)

  4. Genetic, molecular and functional analyses of factor I - an inhibitor of the complement system

    Factor I (FI) is a serine protease that inhibits the complement system by cleaving activated C3 and C4 complement proteins, in the presence of cofactors. Mutations in the gene coding for FI have been identified in complete FI deficient- and atypical hemolytic uremic syndrome (aHUS) patients. The

    lund Repository record for Genetic, molecular and functional analyses of factor I - an inhibitor of the complement system (opens in a new tab)

  5. Interaction Between the Metalloprotease ADAMTS-13 and the Proteins of the Alternative Pathway of the Complement System

    … in hemostasis, has been shown to interact with complement components. However results are contrasting and inconclusive. By studying 20 patients with congenital thrombotic thrombocytopenic purpura (cTTP) who can not cleave VWF multimers due to genetic ADAMTS13 deficiency, we investigated the

    the-open-u Repository record for Interaction Between the Metalloprotease ADAMTS-13 and the Proteins of the Alternative Pathway of the Complement System (opens in a new tab)

  6. Investigating the role of the complement system in the pathogenesis of sub-retinal fibrosis in neovascular age related macular degeneration

    Age related Macular Degeneration (AMD) is the leading cause of blindness in the elderly population of developed countries. Advanced AMD is categorised into two subtypes, “dry” AMD and “wet” or neovascular AMD (nAMD). nAMD is characterised by choroidal neovascularisation (CNV), which is the growth …

    qu-belfast Repository record for Investigating the role of the complement system in the pathogenesis of sub-retinal fibrosis in neovascular age related macular degeneration (opens in a new tab)

  7. Survival strategies of the human respiratory tract pathogen Haemophilus influenzae

    … one of six serotypes (a-f), of which type b is the most virulent one causing serious and sometimes life-threatening diseases (e.g., epiglottitis, septicaemia and meningitis). In contrast, non-typeable H. influenzae (NTHi) accounts for the majority of local and upper and lower respiratory tract …

    lund Repository record for Survival strategies of the human respiratory tract pathogen Haemophilus influenzae (opens in a new tab)

  8. On the immunopathogenesis of systemic lupus erythematosus - Immune complexes, type I interferon system, complement system and platelets

    Systemic lupus erythematosus (SLE) is an autoimmune rheumatic disorder characterized by inflammation in several organ systems. SLE patients have an impaired ability to clear dying cells which leads to the exposure of several nuclear antigens which might break self tolerance. Autoantibodies directed …

    lund Repository record for On the immunopathogenesis of systemic lupus erythematosus - Immune complexes, type I interferon system, complement system and platelets (opens in a new tab)

  9. Multivariate Statistical Analysis In Single Cell Transcriptomics

    With technological advances in the last decade, single cell RNA sequencing (scRNAseq) has emerged as an exciting weapon in the modern scientist’s arsenal to unravel cellular heterogeneity. The ability to measure the transcriptome in each individual cell in any given tissue poses challenges galore, …

    penn Repository record for Multivariate Statistical Analysis In Single Cell Transcriptomics (opens in a new tab)

  10. Interaction of Bacillus Anthracis Exosporium Protein Bcla With Complement Factor H and Spore Persistence In The Lung

    <p>Anthrax outbreaks in the United States and Europe and its potential use as a bioweapon have made <em>Bacillus anthracis</em> an interest of study. Anthrax infections are caused by the entry of <em>B. anthracis</em> spores into the host via the respiratory system, the gastrointestinal tract, cuts …

    uthsc Repository record for Interaction of Bacillus Anthracis Exosporium Protein Bcla With Complement Factor H and Spore Persistence In The Lung (opens in a new tab)

  11. Die Untersuchung zellulärer inflammatorischer Prozesse bei Pseudoxanthoma elasticum

    The autosomal-recessive disorder Pseudoxanthoma elasticum (PXE) is characterized by progressive calcification and fragmentation of elastic fibers. The cause of PXE are mutations in the gene ATP-binding cassette subfamily C member 6 (ABCC6), encoding ABCC6, an ATP-binding transport protein. Further …

    bielefeld Repository record for Die Untersuchung zellulärer inflammatorischer Prozesse bei Pseudoxanthoma elasticum (opens in a new tab)

  12. Probabilistic Approximation and Analysis Techniques for Bio-Pathway Models

    … modeling of bio-pathway dynamics is crucial to the system-level understanding of cellular functions and behavior. Currently, a common method of representing bio-pathways is through a system of ordinary differential equations (ODEs). However, calibrating and analyzing large ODE-based pathway …

    nus Repository record for Probabilistic Approximation and Analysis Techniques for Bio-Pathway Models (opens in a new tab)

  13. The role of anaphylatoxins in asthma and airway remodelling

    … are proinflammatory polypeptides released during complement activation. They exert their biological functions by interacting with the G protein-coupled receptors, C3aR and C5aR respectively. Activation of the complement system has been implicated in the pathogenesis of many inflammatory diseases …

    kings Repository record for The role of anaphylatoxins in asthma and airway remodelling (opens in a new tab)

  14. THE ROLE OF BACTERIAL AMYLOID FIBRILS IN ESCHERICHIA COLI COMPLEMENT RESISTANCE

    … capable of causing morbidity and mortality. Of the E. coli which causes human disease, many strains which cause bacteremia have been identified as possessing virulence factors which make them more resistant to the complement system. The bacterial amyloid fibril, curli, functions in bacterial …

    temple Repository record for THE ROLE OF BACTERIAL AMYLOID FIBRILS IN ESCHERICHIA COLI COMPLEMENT RESISTANCE (opens in a new tab)

  15. Characterization of Complement C3 Dysregulation Predisposing to Two Human Disease States

    The complement system is an essential branch of the innate immune system and acts as a bridge to the adaptive immune system. It serves as the first line of defense against pathogens, as well as in the clearance of immune complexes and apoptotic cells. Deficiencies in many of the complement

    wustl Repository record for Characterization of Complement C3 Dysregulation Predisposing to Two Human Disease States (opens in a new tab)

  16. Genetic Factors Associated with Anti-Factor H Autoantibodies in Atypical Hemolytic Uremic Syndrome (aHUS)

    … acquired defects of alternative pathway (AP) of the complement system. Autoantibodies against factor H (anti-FHs), a regulator of the AP, were reported in 10% of patients, and are associated with the deficiency of factor H related 1 (FHR1), a FH homologous protein. <br></br><br></br> The aim of …

    the-open-u Repository record for Genetic Factors Associated with Anti-Factor H Autoantibodies in Atypical Hemolytic Uremic Syndrome (aHUS) (opens in a new tab)

  17. Novel Endogenous Antimicrobial Peptides

    … are an essential part of our fast innate immune system. They are ancient molecules found in all classes of life. Antimicrobial peptides rapidly kill a broad spectrum of microbes and are immunomodulatory, i.e. having additional actions influencing inflammation and other innate immune responses. …

    lund Repository record for Novel Endogenous Antimicrobial Peptides (opens in a new tab)

  18. Aspects of retransfusion of shed blood in cardiac surgery

    The use of cardiotomy suction during open heart surgery with cardiopulmonary bypass (CPB) has a long tradition and often regarded as mandatory. Recently, studies have described potentially negative effects of cardiotomy suction with activation of the complement system, enhanced inflammatory …

    lund Repository record for Aspects of retransfusion of shed blood in cardiac surgery (opens in a new tab)

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