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Prions : food and drug safety

Author: T Kitamoto
Publisher: Tokyo : Springer, ©2005.
Edition/Format:   eBook : Document : Conference publication : EnglishView all editions and formats
Summary:
"This volume is a collection of current work on prion research that was presented at the 2004 symposium. Topics included range from basic research to clinical aspects of prion diseases, making the book a valuable resource for researchers and clinicians, and encouraging further developments by the next generation of researchers."--Jacket.
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Genre/Form: Electronic books
Congresses
Additional Physical Format: Print version:
Prions.
Tokyo : Springer, ©2005
(DLC) 2005928946
(OCoLC)61714777
Material Type: Conference publication, Document, Internet resource
Document Type: Internet Resource, Computer File
All Authors / Contributors: T Kitamoto
ISBN: 4431255397 9784431255390 4431294023 9784431294023 1280613262 9781280613265 6610613265 9786610613267
OCLC Number: 75392348
Description: 1 online resource (xv, 271 pages) : illustrations
Contents: Pathology of variant Creutzfeldt-Jakob disease --
Clinical aspects of variant CJD --
Dura mater related Creutzfeldt-Jakob disease in Japan: relationship between sites of grafts and clinical features --
Treatment options in patients with prion disease: the role of long term cerebroventricular infusion of pentosan polysulphate --
Human prion diseases: novel diagnostic principles --
History and state of the art of PrP-res "typing" in Creutzfeldt-Jakob disease --
Chronic wasting disease in cervids in North America --
Bovine spongiform encephalopathy (BSE) in Japan --
The role of host PrP in control of incubation time --
The role of the immune system in TSE agent neuroinvasion --
Prion protein interactions and TSE interactions in cell culture models --
Semi-classical quantization of protein dynamics: novel NMR relaxation formalism and its application to prion --
Surveillance of chronic wasting disease (CWD) in Japan --
Unexpected high incidence of visceral AA-amyloidosis in slaughtered cattle in Japan --
A novel BSE screening kit with simplified preparation methods for EIA --
Detection of recombinant bovine prion protein by fluorescence correlation spectroscopy --
PrPSc distribution of a natural case of bovine spongiform encephalopathy --
Report of the first oral inoculation of BSE prion into cattle in Japan --
The development of the intracerebral inoculation method and BSE experimental transmission to calves --
Comparative analyses of three mouse-adapted scrapie strains G1, obihiro, and I3/I5 and pathogenesis of G1 strain-induced polyuria in ICR mice --
Dose effect on detection of PrPSc in follicular dendritic cells of knock-in mice for rapid bioassay --
Cell surface retention of PrPC by anti-PrP antibody prevents protease-resistant PrP formations --
Prion-conformation-specific human antibodies established from phage display library --
Partial characterization of monoclonal antibodies which bind to disease-associated prion protein in immunoprecipitaion assay --
Production and characterization of monoclonal antibodies specific for prion protein --
In vitro selection of anti-mouse prion protein RNA aptamers --
Detection of the prion protein in a liquid phase capture assay using magnetic beads coupled to protein A --
New pretreatment method for immunohistochemistry for abnormal prion protein --
Cellular prion protein suppresses the apoptosis in a neuronal cell line established from type-1 prion protein gene-deficient mice --
Cellular prion protein suppresses the apoptotic cell death by mediating the intracellular H2O2 in primary culture and immortalized neuronal cells. Targeting of cytosolic PrPC via a novel 14-3-3-Tom 70-mitochondrial BCL-2 pathway induces mitochondrial apoptosis --
Microtubule-dependent intracellular trafficking of cellular prion protein --
Hsp90 modifies the conformation of recombinant mouse prion protein in vitro --
Purification and characterization of a novel ATP-dependent robust protein-unfoldase, unfoldin --
Nucleic acid and prion protein interaction produces spherical amyloids which in vivo can function as coats of spongiform encephalopathy agent --
Species barrier in yeast [psi+] prion transmission --
Molecular memory of [psi+] prion strains in s. cerevisiae is dependent on the the primary structure of the Sup35 prion domain --
Expression of a splice variant of prion protein during hypoxia in human glioblastoma cell line T98G --
PRNP promoter region polymorphism in Creutzfeldt-Jakob disease --
Tubulovesicular structures are consistently found in prion diseases including vCJD and FFI --
Autophagy is a common ultrastructural feature of neuropathology of prion diseases --
Type 1 and type 2 human PrPSc have different aggregation sizes in methionine homozygotes with sporadic, iatrogenic and variant Creutzfeldt-Jakob disease --
A pitfall in diagnosis of human prion diseases using detection of protease-resistant prion protein in urine: contamination with bacterial outer membrane proteins --
Comparative analysis of chronological data of total tau protein in CSF, serial studies of MRI (DWI and FLAIR) and staging of clinical features in patients with sporadic CJD --
Duration between initial manifestation of CJD and detection of PSD, specific findings on MRI, CSF 14-3-3 protein, or CSF high NSE --
Biochemical analysis of peripheral tissue involvement in transmissible spongiform encephalopathies --
Involvement of the peripheral nervous system in human prion diseases including dural graft-associated Creutzfeldt-Jakob disease --
MM2 type sporadic Creutzfeldt-Jakob disease: clinicoradiologic features and clinical diagnosis --
Early clinical and radiological diagnosis of sporadic Creuzfeldt-Jakob's disease (sCJD): a case study of pathologically proved sCJD MV2 --
Familial Creutzfeldt-Jakob disease with a point mutation (met to arg) at codon 232: two different phenotypes --
Familial Creutzfeldt-Jakob disease with five octapeptide repeat insert --
A case of Creutzfeldt-Jakob disease with a noverl insertion mutation and codon 219 lysine/lysine polymorphism in the prion protein gene --
Inhibition of prion propagation in scrapie-infected cell lines using mouse monoclonal antibodies against prion protein --
The inhibitory effect of the ScFv of an anti-prion protein antibody secreted from N2a58 cells on abnormal prion protein accumulation in scrapie-infected cells, ScN2a --
Mucosal immunogenicity of prion protein fused with heat-labile enterotoxin B subunit --
Identification of drugs that enhance the stimulatory effect of PrP on the fibrinolytic system --
Screening study of prion binding agents and their inhibitory effect on the conversion of prion protein --
Can forage grasses inhibit prion replication? --
Inhibition of abnormal PrP formation by amyloid-imaging probes in vitro --
Treatment with anti-malaria agents, quinacrine and quinine, for Creutzfeldt-Jakob disease patients --
Effect of oral administration of pentosan polysulfate for patients with Creutzfeldt-Jakob disease (CJD) and new design for low molecular-weight of pentosan polysulfate.
Responsibility: T. Kitamoto (ed.).

Abstract:

Prion diseases recently have attracted interest not only scientifically but also socially because of the bovine spongiform encephalopathy (BSE) epidemic and the outbreak of variant Creutzfeldt-Jakob  Read more...

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