Current Molecular Medicine - Volume 4, Issue 4, 2004
Volume 4, Issue 4, 2004
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Editor's Note
Prion diseases are a group of rare and uniformly fatal neurodegenerative disorders in humans and animals.These diseases are characterized by spongiform changes within the central nervous system. In recent years,much attention has been focused on prion diseases in animals, which include bovine spongiformencephalopathy, scrapie in sheep; transmissible encephalopathy in the mink and chronic wasting disease inde Read More
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The Role of PrP in Health and Disease
Authors: E. Flechsig and C. WeissmannTransmissible spongiform encephalopathies (TSEs) such as scrapie in sheep, bovine spongiform encephalopathy (BSE) in cattle or Creutzfeldt-Jacob disease (CJD) and Gerstmann- Straussler-Scheinker syndrome (GSS) in humans, are caused by an infectious agent designated prion. The “protein only” hypothesis states that the prion consists partly or entirely of a conformational isoform of the normal host protein PrPC and that th Read More
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The Peripheral Nervous System and the Pathogenesis of Prion Diseases
Authors: Markus Glatzel, Olivier Giger, Nathalie Braun and Adriano AguzziPrion diseases are inevitably fatal neurodegenerative conditions which affect humans and a wide variety of animals. Unlike other protein aggregation diseases such as Alzheimer's, Parkinson's, and polyglutamine repeat diseases, prion diseases are unique in that they are transmissible. Therefore, prion diseases are also called transmissible spongiform encephalopathies. A number of prion diseases are caused by periphe Read More
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Impacts and Concerns for vCJD in Blood Transfusion: Current Status
Authors: I. R. MacGregor and C. V. ProwseThe impact of vCJD upon blood transfusion practice hinges on its lymphoreticular involvement. B lymphocytes play a key supporting role for the capture and replication of infectivity by follicular dendritic cells of the lymphoid tissue in animal models of transmissible spongiform encephalopathies (TSE) and tonsils, spleen and appendix in man can harbour vCJD infectivity, a situation not seen with the other human Read More
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Genetic Studies in Relation to Kuru: An Overview
Authors: L. G. Goldfarb, L. Cervenakova and D. C. GajdusekKuru is a subacute neurodegenerative disease presenting with limb ataxia, dysarthria, and a shivering tremor. The disease progress to complete motor and mental incapacity and death within 6 to 24 months. Neuropathologically, a typical pattern of neuronal loss, astrocytic and microglial proliferation, characteristic “kuru-type” amyloid plaques, and PrP deposits in the cerebral cortex and cerebellum are observed. Kuru is t Read More
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The Genetics of Scrapie in Sheep and Goats
Authors: M. Baylis and W. GoldmannScrapie, an invariably fatal disease of sheep and goats, is a transmissible spongiform encephalopathy (TSE). The putative infectious agent is the host-encoded prion protein, PrP. The development of scrapie is closely linked to polymorphisms in the host PrP gene. The pathogenesis of most TSEs involves conversion of normal, cellular PrP into a protease-resistant, pathogenic isoform called PrPSc. The conversion to PrPSc invo Read More
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Molecular Mechanisms of Neurotoxicity of Pathological Prion Protein
Authors: Joaquin Castilla, Claudio Hetz and Claudio SotoTransmissible Spongiform Encephalopathies or prion related disorders are fatal and infectious neurodegenerative diseases characterized by extensive neuronal apoptosis and accumulation of a misfolded form of the cellular prion protein (PrP), denoted PrPSc. Although the mechanism of neurodegeneration and the involvement of PrPSc is far from clear, data indicates that neuronal apoptosis might be related to activation Read More
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Sphingolipids in Inflammation: Roles and Implications
Authors: B. J. Pettus, C. E. Chalfant and Y. A. HannunSphingolipids, historically described as potential reservoirs for bioactive lipids, presently define a new family of cellular mediators, joining the well-established glycerolipid-derived mediators of signal transduction such as diacylglycerol, phosphatidylinositides, and eicosanoids. Sphingolipid metabolism is clearly involved in the regulation of cell growth, differentiation, and programmed cell death. Indeed, a majority of the gre Read More
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Fluorescence Molecular Imaging of Small Animal Tumor Models
Authors: E. E. Graves, R. Weissleder and V. NtziachristosIn vivo imaging of molecular events in small animals has great potential to impact basic science and drug development. For this reason, several imaging technologies have been adapted to small animal research, including X-ray, magnetic resonance, and radioisotope imaging. Despite this plethora of visualization techniques, fluorescence imaging is emerging as an important alternative because of its operational simplicity, Read More
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Trafficking of Natural Killer Cells
Authors: M. A. Morris and K. LeyNatural killer (NK) cells comprise a set of lymphocytes that is capable of mediating innate immune responses to viral infections, malignancies, and allogeneic bone marrow grafts. This review summarizes what is known about the mechanisms NK cells use to arrive at their sites of action. NK cells express a wide array of adhesion molecules including αLβ2, αMβ2, αXβ2, and α4β1 integrins, ICAM-1, PSGL-1, and L-selectin. Like other i Read More
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Differential TNF-Signaling in Chronic Inflammatory Disorders
Authors: Martin H. Holtmann and Markus F. NeurathTNF-α is a pleiotropic cytokine with strong proinflammatory and immunomodulatory properties. TNF-α plays a critical role in many acute or chronic inflammatory diseases and anti-TNFstrategies have proven to be clinically effective. Two TNF-specific cell surface receptors TNF-R1 and TNF-R2 have been identified and the function of these receptors and the downstream intracellular signal transduction pathways have been exte Read More
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Volume 25 (2025)
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Volume 22 (2022)
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Volume 6 (2006)
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Volume 5 (2005)
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Volume 4 (2004)
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Volume 3 (2003)
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Volume 2 (2002)
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Volume 1 (2001)
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