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Complement (Immunology) --- Alexin --- Complements (Immunity) --- Blood proteins
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COMPLEMENT, physiology --- Complement (Immunology) --- Complement System Proteins --- #ABIB:aimm --- physiology. --- Complement (Immunology). --- Alexin --- Complements (Immunity) --- Blood proteins --- physiology
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From small beginnings in the early 1970s, the study of complement regulatory proteins has grown in the last decade to the point where it dominates the complement field. This growth has been fueled by the discovery of new regulators, the cloning of old and new regulators, the discovery that many of the regulators are structurally and evolutionarily related to each other and the development of recombinant forms for use in therapy. There are now more proteins known to be involved in controlling the complement system than there are components of the system and the list continues to grow. The time
Complement (Immunology) --- Complement activation. --- Activation, Complement --- Complement activators --- Enzyme activation --- Immunity --- Alexin --- Complements (Immunity) --- Blood proteins --- Activation
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The Complement FactsBook contains entries on all components of the Complement System, including C1q and Lectins, C3 Family, Serine Proteases, Serum Regulators of Complement Activation, Cell Surface Proteins, and Terminal Pathway Proteins. Domain Structure diagrams are incorporated to clearly illustrate the relationships between all the complement proteins, both within families and between families. The FactsBook also includes the cDNA sequences, marked with intron/exon boundaries, which will facilitate genetic studies.Key Features* Includes the cDNA sequences, marked with in
Complement (Immunology) --- Immunology. --- Immunobiology --- Life sciences --- Serology --- Alexin --- Complements (Immunity) --- Blood proteins --- C-reactive protein --- Complement --- Complement activation --- Receptors, cell surface --- Serine proteinases --- Complement (Immunology).
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In recent years the results of past studies on T cell dependent and T cell independent antibody responses have coalesced with discoveries regarding the roles of various primary B cell subsets and components of the innate immune system in conferring resistance to infectious pathogens. As a consequence, a new and more complete understanding of how antibody-mediated resistance to pathogens is elaborated has emerged. The recent explosion of knowledge of Toll-like receptor specificity and function has further embellished this understanding. It is now clear that there is not only extensive overlap and cross-complementarity in the action of innate and adaptive immune systems, but also specialization of function of the various B cell subsets and the types of antibodies they produce. This synergistic interaction of multiple components of these systems is perhaps best exemplified in antibody responses to bacteria. Contributions to this monograph were chosen to highlight this new perspective on antibody responses to infection, as well as to convey its practical implications, such as for contemporary vaccine design.
Immunology. --- Complement (Immunology) --- B cells. --- Immunobiology --- Life sciences --- Serology --- B lymphocytes --- Bone marrow derived cells --- Bursa equivalent cells --- Antigen presenting cells --- Lymphocytes --- Alexin --- Complements (Immunity) --- Blood proteins --- Medical virology. --- Virology. --- Medical microbiology --- Virology --- Virus diseases --- Microbiology
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Blood --- Coagulation --- Fibrinolysis --- Complement (Immunology) --- 612.12 --- Bloedstolling --- Complement systeem --- Fibrinolyse --- Thrombolytic therapy --- Alexin --- Complements (Immunity) --- Blood proteins --- Blood coagulation --- Clotting of blood --- Coagulation of blood --- Hemostasis --- Anticoagulants (Medicine) --- Coagulase --- Clotting
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Complement has long been regarded as a pivotal effector arm of the innate im-mune response, eliciting important immunoregulatory functions in the context of inflammation and also serving as a vital link between the innate and adaptive immune response. In the post-genomic era, our knowledge of the innate immune system is enriched by findings that point to novel functions that do not strictly correlate with immunological defense and surveillance, immune modulation or inflammation. Several studies indicate that complement proteins exert functions that are either more complex than previously thought, or go well beyond the innate immune character of the system. The advent of high-throughput platforms for genome and proteome-wide profiling, together with the enormous amount of raw genetic information that has accumulated in the databases, have stirred new expectations in biomedical research. They have led complementologists to revisit established biological systems, such as the complement system, from a global and integrative perspec-tive. Complement research is now faced with the challenge of trying to integrate isolated biochemical pathways into complex gene and protein regulatory cir-cuits. In this respect, scientists from around the world convened at the Third Aegean Conferences Workshop on Complement Associated Diseases, Animal Models, and Therapeutics (June 5–10, 2005), to discuss recent advances in this fast evolving field. This volume represents a collection of topics on the "novel" functions of complement, pathophysiology, protein structures, design of complement inhibitors, and complement assays discussed during the conference.
Complement (Immunology) --- Blood proteins. --- Plasma proteins --- Serum proteins --- Blood plasma --- Proteins --- Serum --- Alexin --- Complements (Immunity) --- Blood proteins --- Immunology. --- Microbiology. --- Emerging infectious diseases. --- Pathology. --- Infectious Diseases. --- Disease (Pathology) --- Medical sciences --- Diseases --- Medicine --- Medicine, Preventive --- Emerging infections --- New infectious diseases --- Re-emerging infectious diseases --- Reemerging infectious diseases --- Communicable diseases --- Microbial biology --- Biology --- Microorganisms --- Immunobiology --- Life sciences --- Serology --- Infectious diseases.
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It is evident that a defective or deregulated complement system results in kidney diseases. An important role of complement effector and regulatory proteins in pathological settings of the kidney has been demonstrated. A large panel of distinct human kidney diseases is caused by defective complement control. Genetic analyses have identified mutations in complement regulators that are associated with these diseases. Mutations have been identified in the fluid phase alternative pathway regulator Factor H and the membrane regulator Membrane Cofactor Protein MCP (CD46). The functional characterization of the mutant proteins allows to define the pathophysiological events on a molecular level. These new concepts and data on disease mechanisms allowed establishing new diagnostic and promising therapeutic approaches for several human kidney diseases. Molecular biology, clinics and therapy are discussed in this volume.
Kidneys --- Complement (Immunology) --- Diseases --- Etiology. --- Alexin --- Complements (Immunity) --- Blood proteins --- Abdomen --- Urinary organs --- Nephrology --- Immunology. --- Cytology. --- Nephrology. --- Human physiology. --- Internal medicine. --- Microbiology. --- Cell Biology. --- Human Physiology. --- Internal Medicine. --- Medical Microbiology. --- Internal medicine --- Cell biology --- Cellular biology --- Biology --- Cells --- Cytologists --- Immunobiology --- Life sciences --- Serology --- Microbial biology --- Microorganisms --- Medicine, Internal --- Medicine --- Human biology --- Medical sciences --- Physiology --- Human body --- Cell biology. --- Medical microbiology.
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Although the complement system-a vital part of the body's defense against bacteria-was discovered more than a century ago, its study has undergone a renaissance with the identification of its regulatory molecules and the realization that these molecules can be used therapeutically. In Complement Methods and Protocols, B. Paul Morgan and a team of expert laboratorians present a comprehensive set of readily reproducible methods to study this critical system. These cutting-edge techniques are suitable both for the basic scientist interested in understanding complement's mechanisms of activation and for the clinical scientist wishing to quantify its activation, and range from the purification of its components to generating complement-deficient mice by gene deletion. Additional techniques presented include procedures for the analysis of complement function, for the study of its regulators, for detection of its activation in vivo, and for the identification of its autoantibodies. Comprehensive and cutting-edge, Complement Methods and Protocols offers today's basic and clinical investigators powerful tools for the analysis of the role of complement in human pathophysiology and disease, as well as its therapeutic regulation.
Complement (Immunology) -- Laboratory manuals. --- Electronic books. -- local. --- Immunology. --- Complement (Immunology) --- Immunoproteins --- Blood Proteins --- Proteins --- Amino Acids, Peptides, and Proteins --- Chemicals and Drugs --- Complement System Proteins --- Biology --- Health & Biological Sciences --- Microbiology & Immunology --- Immunobiology --- Life sciences --- Serology --- Alexin --- Complements (Immunity) --- Blood proteins --- Complement system proteins --- analysis
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Innate Immunity has long been regarded as the non-specific arm of immune response, acting immediately and in a generic way, to defend the host from infections. In the post genomic era, our knowledge of the innate immune system is enriched by findings on the specificity of innate immune reactions as well as to novel functions that do not strictly correlate with immunological defense and surveillance, immune modulation or inflammation. Several studies indicate that molecules involved in innate immunity exert functions that are either more complex than previously thought, or go well beyond the innate immune character of the system. The advent of high-throughput platforms for genome and proteome-wide profiling, together with the enormous amount of raw genetic information that has accumulated in the databases, have stirred new expectations in biomedical research. They have led scientists to revisit established biological systems from a global and integrative perspective. Innate Immunity research is now faced with the challenge of trying to integrate isolated biochemical pathways into complex gene and protein regulatory circuits. In this respect, scientists from around the world convened at the 4th International Conference on Innate Immunity (June 4 - 9, 2006), in Corfu, Greece to discuss recent advances in this fast evolving field. This volume represents a collection of topics on natural killer cells, mast cells, phagocytes, toll like receptors, complement, host defense in plants and invertebrates, evasion strategies of microorganisms, pathophysiology, protein structures, design of therapeutics, and experimental approaches discussed during the conference.
Natural immunity --- Killer cells --- Complement (Immunology) --- Alexin --- Complements (Immunity) --- Blood proteins --- K cells --- Natural killer cells --- NK cells --- Immunocompetent cells --- Cell-mediated cytotoxicity --- Disease resistance --- Host resistance --- Innate immunity --- Innate resistance --- Native immunity --- Natural resistance --- Nonspecific immunity --- Resistance to disease --- Immunity --- Immunology. --- Microbiology. --- Emerging infectious diseases. --- Infectious Diseases. --- Emerging infections --- New infectious diseases --- Re-emerging infectious diseases --- Reemerging infectious diseases --- Communicable diseases --- Microbial biology --- Biology --- Microorganisms --- Immunobiology --- Life sciences --- Serology --- Infectious diseases.
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