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Galanin is a neuropeptide found both in the central and peripheral nervous system. The 29-amino acid peptide (named after its N-terminal glycine and C-terminal alanine) was identified in 1983 by its C-terminal amidation. This 'reverse' approach, that is to discover a substance through a distinct chemical feature, and only subsequently to characterize its biological activity, was novel and has been successful in the identification of several other peptides. After the structure of galanin was determined in 1983, functional studies were performed with material purified from natural sources until the synthetic form of the peptide became available. Galanin can act as transmitter, modulator and trophic factor, and is involved in a number of physiological processes such as hormone secretion, cardiovascular mechanisms, feeding and cognition. This peptide may also be of significance for a number of pathological processes/disorders including pain, depression, Alzheimer's disease, epilepsy, addiction and cancer. This wide diversity of actions is mediated by three galanin receptor subtypes. The studies reviewed in this volume give a fairly complete overview of the spectrum of the biological actions and functions of galanin and its receptors and on possible therapeutic applications in a number of pathological conditions.
Galanin -- Therapeutic use. --- Neuroendocrinology. --- Peptides. --- Galanin --- Neuropeptides --- Peptides --- Amino Acids, Peptides, and Proteins --- Chemicals and Drugs --- Animal Biochemistry --- Neuroscience --- Human Anatomy & Physiology --- Health & Biological Sciences --- Galanin. --- Neuropeptides. --- Brain peptides --- Life sciences. --- Neurobiology. --- Life Sciences. --- Nerve tissue proteins --- Neurotransmitters --- Neurosciences
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This volume of Methods in Enzymology covers the current methodology for the detection and assessment of constitutively active proteins. The chapters written by expert authors who are leaders in the field, provide hints and tricks not available in primary research publications.It is extensively referenced, with useful figures and tables throughout the volume. A. Expert authors who are leaders in the field B. Extensively referenced and useful figures and tables C. Provides hints and tricks to facilitate reproduction of methods
Proteins. --- Cell receptors. --- Cellular signal transduction. --- G proteins. --- Phosphotransferases (Alcohol Group Acceptor) --- Membrane Proteins --- Amino Acids, Peptides, and Proteins --- Phosphotransferases --- Chemicals and Drugs --- Transferases --- Enzymes --- Enzymes and Coenzymes --- Proteins --- Protein Kinases --- Receptors, G-Protein-Coupled --- Receptors, Cell Surface --- Human Anatomy & Physiology --- Health & Biological Sciences --- Animal Biochemistry --- Cell membrane receptors --- Cell surface receptors --- Receptors, Cell --- Proteids --- Binding sites (Biochemistry) --- Cell membranes --- Biomolecules --- Polypeptides --- Proteomics
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TECHNOLOGY & ENGINEERING --- Agriculture / Animal Husbandry --- Metabolism --- Amino Acids, Peptides, and Proteins --- Crops, Agricultural --- Animals, Domestic --- Nutritional Physiological Phenomena --- Physiological Phenomena --- Food --- Metabolic Phenomena --- Chemicals and Drugs --- Animal Population Groups --- Phenomena and Processes --- Food and Beverages --- Animals --- Eukaryota --- Technology, Industry, Agriculture --- Organisms --- Livestock --- Animal Feed --- Energy Metabolism --- Animal Nutritional Physiological Phenomena --- Proteins --- Agriculture --- Earth & Environmental Sciences --- Animal Sciences --- Animal nutrition --- Energy metabolism
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Parasitic protozoa, including some which are agents of human and veterinary diseases, display special cytoplasmic structures and organelles. Metabolic pathways have been discovered in these organelles which open up new possibilities for drug targets. This work presents reviews dealing with cytoskeletal structures such as the mastigont system found in trichomonads, the sub-pellicular microtubules in trypanosomatids and the paraflagellar rod. Further chapters cover structures involved in the synthesis, secretion and uptake of molecules, including the flagellar pocket of trypanosomatids, the reservosome of Trypanosoma and the megasome found in Leishmania, the traffic of vesicles in Entamoeba histolytica, secretory organelles and the secretory events of intestinal parasites during encystation. Reviews on special organelles, such as the kinetoplast-mitochondrion complex, the apicoplast found in Apicomplexa, the glycosomes in Kinetoplastida and the acidocalcisomes found in several protozoa complete the volume.
Cell organelles. --- Protista. --- Protozoa, Pathogenic --- Protista --- Protozoa --- Cytology --- Cytoskeleton --- Parasites --- Cell organelles --- Proteins --- Cytoplasmic Structures --- Organisms --- Cytoplasm --- Amino Acids, Peptides, and Proteins --- Protozoan Proteins --- Organelles --- Eukaryota --- Intracellular Space --- Chemicals and Drugs --- Cellular Structures --- Cells --- Anatomy --- Biology --- Health & Biological Sciences --- Microbiology & Immunology --- Protozoa, Pathogenic. --- Protists --- Pathogenic protozoa --- Life sciences. --- Microbiology. --- Life Sciences. --- Unicellular organisms --- Eukaryotic cells --- Pathogenic microorganisms --- Medical protozoology --- Microbial biology --- Microorganisms
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Knowledge of cholesterol and its interaction with protein molecules is of fundamental importance in both animal and human biology. This book contains 22 chapters, dealing in depth with structural and functional aspects of the currently known and extremely diverse unrelated families of cholesterol-binding and cholesterol transport proteins. By drawing together this range of topics the Editor has attempted to correlate this broad field of study for the first time. Technical aspects are given considerable emphasis, particularly in relation cholesterol reporter molecules and to the isolation and study of membrane cholesterol- and sphingomyelin-rich "raft" domains. Cell biological, biochemical and clinical topics are included in this book, which serve to emphasize the acknowledged and important benefits to be gained from the study of cholesterol and cholesterol-binding proteins within the biomedical sciences and the involvement of cholesterol in several clinical disorders. It is hoped that by presenting this topic in this integrated manner that an appreciation of the fact that there is much more that needs to be taken into account, studied and understood than the widely discussed "bad and good cholesterol" associated, respectively, with the low- and high-density lipoproteins, LDL and HDL.
Carrier proteins. --- Cholesterol -- Metabolism. --- Cholesterol --- Carrier proteins --- Sterols --- Proteins --- Cholestenes --- Carrier Proteins --- Membrane Lipids --- Amino Acids, Peptides, and Proteins --- Cholestanes --- Lipids --- Steroids --- Chemicals and Drugs --- Polycyclic Compounds --- Human Anatomy & Physiology --- Chemistry --- Biology --- Biology - General --- Animal Biochemistry --- Cytology --- Biochemistry --- Health & Biological Sciences --- Physical Sciences & Mathematics --- Metabolism --- Cholesterol. --- Metabolism. --- Binding proteins --- Transport proteins --- Cholesterin --- Life sciences. --- Biochemistry. --- Proteins. --- Lipids. --- Apoptosis. --- Life Sciences. --- Biochemistry, general. --- Lipidology. --- Protein Science. --- Animal Biochemistry. --- Biological transport --- Protein binding --- Isopentenoids --- Low-cholesterol diet
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The fibroblast growth factors (FGFs) represent one of the relatively few families of extracellular signalling peptides that have been shown in recent decades to be key regulators of metazoan development. FGFs are required for multiple processes in both protostome and deuterostome groups. Given the wide range of regulatory roles attributed to the FGFs, it is perhaps not surprising that misregulation of this signalling pathway has been implicated in a number of human disease conditions. The focus of the present review is to look at the fundamental components of the FGF pathway and illustrate how this highly conserved regulatory cassette has been deployed to regulate multiple, diverse processes during vertebrate development. This review will explore examples from several vertebrate model organisms and include discussions of the role of FGF signalling in regulating the establishment of the mesoderm, neural patterning, morphogenesis, myogenesis, limb development, and the establishment of right-left asymmetry.
Fibroblast growth factors. --- Vertebrates -- Development. --- Vertebrates -- Growth & development. --- Fibroblast Growth Factors --- Chordata --- Intercellular Signaling Peptides and Proteins --- Animals --- Biological Factors --- Proteins --- Eukaryota --- Peptides --- Amino Acids, Peptides, and Proteins --- Organisms --- Chemicals and Drugs --- Fibroblast Growth Factor 1 --- Vertebrates --- Zoology --- Human Anatomy & Physiology --- Health & Biological Sciences --- Animal Biochemistry --- Animal Anatomy & Embryology --- Growth factors. --- Growth. --- Fibroblast Growth Factors. --- growth & development. --- Fibroblast growth factor --- Mesoderm --- Neurectoderm --- Xenopus --- Organogenesis --- Somites --- Limb --- MyoD --- Somitogenesis --- Morphogenesis --- Left-right asymmetry --- MAPK --- Sprouty --- ERK --- Map kinase phosphatase --- Signal transduction
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The Wnt/[beta]-catenin signaling pathway is a key regulator of cell fate specification, differentiation, and growth in multiple systems throughout the animal kingdom. In vertebrate posterior neural development, Wnt/[beta]-catenin signaling controls this complex multistep process. It initially induces the posterior regions of the nervous system, including the mid-hindbrain border, hindbrain, spinal cord and neural crest, and then subsequently fine-tunes the pattern of each region and determines the different cell fates within them. In this review, we explore the function of the Wnt/[beta]-catenin pathway during the formation of these specific posterior neural regions. We have examined the important transcriptional targets of the Wnt/[beta]-catenin pathway acting downstream to mediate its morphogenetic activity. Different regulatory networks are activated in different posterior neural regions, and these networks induce specific neural cell types in each region. Eludidating how each of these networks specify different cell fates is crucial for understanding the basic tenets of how Wnt morphogenetic activity induces the posterior nervous system during the earliest stages of vertebrate development.
Evolution. --- Morphogenesis. --- Neural development. --- Chordata --- Armadillo Domain Proteins --- Intercellular Signaling Peptides and Proteins --- Catenins --- Anatomy --- Transcription Factors --- Cytoskeletal Proteins --- Proteins --- Biological Factors --- Animals --- Peptides --- Chemicals and Drugs --- Eukaryota --- Amino Acids, Peptides, and Proteins --- Organisms --- Vertebrates --- beta Catenin --- Wnt Proteins --- Nervous System --- Human Anatomy & Physiology --- Health & Biological Sciences --- Neuroscience --- Cranial fossa, Posterior --- Wnt proteins. --- Growth. --- Wnt genes. --- Developmental neurobiology. --- Wnt Proteins. --- Neurogenesis. --- Cell Differentiation. --- Wnt/[beta]-catenin signaling --- vertebrate development --- neural patterning --- neural caudalization --- posterior neural cell fate specification --- neural induction
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In 1890 a case of myxedema was treated in Lisbon by the implantation of a sheep thyroid gland with the immediate improvement in the patient’s condition. A few years later, medications for the then ill-explained condition of the menopause included tablets made from cow ovaries. In the first quarter of the 20th century the identification of vitamin D, and its sunlight driven production in skin, paved the way to the elimination of rickets as a major medical problem. Twenty years or so later, Sir Vincent Wigglesworth established the endocrine basis of developmental moulting in insects, arguably the most commonly performed animal behaviour on Planet Earth. A paradigm that would unify these disparate observations arose between 1985 and 1987 beginning with the identification of the glucocorticoid receptor and the nuclear receptor super-family. What follows is a timely and positive manifestation of the capacity, productivity and value of international human scientific endeavour. Based on intrigue, lively competition and cooperation a global effort has rapidly fostered a school of biology with widespread ramifications for the understanding of metazoan animals, the human condition and the state of the planet. This book is the first this century to try and capture the spirit of this endeavour, to depict where the field is now and to identify some of the challenges and opportunities for the future.
Nuclear receptors (Biochemistry). --- Nuclear receptors (Biochemistry) --- DNA-Binding Proteins --- Transcription Factors --- Cell Physiological Processes --- Proteins --- Receptors, Cytoplasmic and Nuclear --- Cell Communication --- Cell Physiological Phenomena --- Amino Acids, Peptides, and Proteins --- Chemicals and Drugs --- Phenomena and Processes --- Biology --- Cytology --- Health & Biological Sciences --- Biochemistry. --- Biological chemistry --- Chemical composition of organisms --- Organisms --- Physiological chemistry --- Nuclear hormone receptors --- Receptors, Nuclear (Biochemistry) --- Receptors, Nuclear hormone --- Composition --- Medicine. --- Endocrinology. --- Oncology. --- Cell biology. --- Biomedicine. --- Biomedicine general. --- Cell Biology. --- Animal Biochemistry. --- Chemistry --- Medical sciences --- Hormone receptors --- Transcription factors
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An up-to-date reference on this fascinating set of complex disorders, this book features the most comprehensive strategies for diagnosing, classifying, imaging, treating, and managing amyloidosis in multiple organ systems. Beneficial to the spectrum of practitioners from residents to sub-specialists, this book is a succinct authoritative text written by leaders in the field. The authors provide instruction on all forms of amyloidosis - including primary amyloidosis (AL), secondary amyloidosis (AA), and familial amyloidosis. With essential treatment algorithms, Amyloidosis: Diagnosis and Treatment is the gold-standard for all hematologists, oncologists, and internists caring for patients with this disease.
Amyloid. --- Amyloidosis. --- Amyloidosis --- Natural Science Disciplines --- Analytical, Diagnostic and Therapeutic Techniques and Equipment --- Proteins --- Multiprotein Complexes --- Proteostasis Deficiencies --- Amino Acids, Peptides, and Proteins --- Macromolecular Substances --- Metabolic Diseases --- Disciplines and Occupations --- Amyloid --- Diagnosis --- Chemistry --- Nutritional and Metabolic Diseases --- Chemicals and Drugs --- Diseases --- Medicine --- Health & Biological Sciences --- Pathology --- Treatment --- Diagnosis. --- Treatment. --- Amyloid degeneration --- Medicine. --- Internal medicine. --- Hematology. --- Medicine & Public Health. --- Internal Medicine. --- Lymphoproliferative disorders --- Metabolism --- Disorders --- Haematology --- Internal medicine --- Blood --- Medicine, Internal
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The microcirculation is highly responsive to, and a vital participant in, the inflammatory response. All segments of the microvasculature (arterioles, capillaries, and venules) exhibit characteristic phenotypic changes during inflammation that appear to be directed toward enhancing the delivery of inflammatory cells to the injured/infected tissue, isolating the region from healthy tissue and the systemic circulation, and setting the stage for tissue repair and regeneration. The best characterized responses of the microcirculation to inflammation include impaired vasomotor function, reduced capillary perfusion, adhesion of leukocytes and platelets, activation of the coagulation cascade, and enhanced thrombosis, increased vascular permeability, and an increase in the rate of proliferation of blood and lymphatic vessels. A variety of cells that normally circulate in blood (leukocytes, platelets) or reside within the vessel wall (endothelial cells, pericytes) or in the perivascular space (mast cells, macrophages) are activated in response to inflammation. The activation products and chemical mediators released from these cells act through different well-characterized signaling pathways to induce the phenotypic changes in microvessel function that accompany inflammation. Drugs that target a specific microvascular response to inflammation, such as leukocyte-endothelial cell adhesion or angiogenesis, have shown promise in both the preclinical and clinical studies of inflammatory disease. Future research efforts in this area will likely identify new avenues for therapeutic intervention in inflammation.
Inflammation. --- Microcirculation -- Pathophysiology. --- Microcirculation -- Physiopathology. --- Microcirculation. --- Pathologic Processes --- Membrane Glycoproteins --- Biological Transport --- Blood Circulation --- Antigens, Surface --- Cardiovascular Physiological Phenomena --- Glycoproteins --- Cardiovascular Physiological Processes --- Antigens --- Metabolism --- Circulatory and Respiratory Physiological Phenomena --- Pathological Conditions, Signs and Symptoms --- Membrane Proteins --- Proteins --- Diseases --- Phenomena and Processes --- Biological Factors --- Amino Acids, Peptides, and Proteins --- Chemicals and Drugs --- Capillary Permeability --- Cell Adhesion Molecules --- Inflammation --- Microcirculation --- Medicine --- Health & Biological Sciences --- Cardiovascular Diseases --- Microcirculation disorders. --- Vasomotor function --- Leukocyte adhesion --- Vascular permeability --- Thrombosis --- Angiogenesis
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