Published in J Gen Virol on June 01, 2007
Experimental H-type and L-type bovine spongiform encephalopathy in cattle: observation of two clinical syndromes and diagnostic challenges. BMC Vet Res (2012) 1.14
Monitoring of clinical signs in goats with transmissible spongiform encephalopathies. BMC Vet Res (2010) 1.03
Experimental oral transmission of atypical scrapie to sheep. Emerg Infect Dis (2011) 0.89
Detection of disease-associated prion protein in the optic nerve and the adrenal gland of cattle with bovine spongiform encephalopathy by using highly sensitive immunolabeling procedures. J Histochem Cytochem (2012) 0.88
Characterization of Syrian hamster adapted prions derived from L-type and C-type bovine spongiform encephalopathies. Prion (2011) 0.88
Accumulation of L-type bovine prions in peripheral nerve tissues. Emerg Infect Dis (2010) 0.85
Relationship between clinical signs and postmortem test status in cattle experimentally infected with the bovine spongiform encephalopathy agent. BMC Vet Res (2010) 0.83
Transmission of chronic wasting disease identifies a prion strain causing cachexia and heart infection in hamsters. PLoS One (2011) 0.81
Pathogenesis of experimental bovine spongiform encephalopathy (BSE): estimation of tissue infectivity according to incubation period. Vet Res (2008) 0.78
The presence of disease-associated prion protein in skeletal muscle of cattle infected with classical bovine spongiform encephalopathy. J Vet Med Sci (2013) 0.76
Heterogeneity of abnormal prion protein (PrP(Sc)) in murine scrapie prions determined by PrP(Sc)-specific monoclonal antibodies. J Vet Med Sci (2013) 0.75
Treatment of transmissible spongiform encephalopathy by intraventricular drug infusion in animal models. J Virol (2004) 1.97
Engineering functional two- and three-dimensional liver systems in vivo using hepatic tissue sheets. Nat Med (2007) 1.96
Urinary excretion and blood level of prions in scrapie-infected hamsters. J Gen Virol (2007) 1.66
Anti-prion activity of Brilliant Blue G. PLoS One (2012) 1.48
Bovine spongiform encephalopathy infectivity in greater kudu (Tragelaphus strepsiceros). Emerg Infect Dis (2004) 1.29
Monitoring for bovine spongiform encephalopathy in sheep in Great Britain, 1998-2004. J Gen Virol (2006) 1.25
Atypical scrapie in sheep from a UK research flock which is free from classical scrapie. BMC Vet Res (2009) 1.22
Humanized knock-in mice expressing chimeric prion protein showed varied susceptibility to different human prions. Am J Pathol (2003) 1.16
Polyethylene glycol (PEG)-mediated transient gene expression in a red alga, Cyanidioschyzon merolae 10D. Plant Cell Physiol (2007) 1.14
Liver tissue engineering at extrahepatic sites in mice as a potential new therapy for genetic liver diseases. Hepatology (2005) 1.14
Cross-sequence transmission of sporadic Creutzfeldt-Jakob disease creates a new prion strain. J Biol Chem (2007) 1.11
Intraspecies transmission of L-type-like Bovine Spongiform Encephalopathy detected in Japan. Microbiol Immunol (2009) 1.10
Efficient in vitro amplification of a mouse-adapted scrapie prion protein. Neurosci Lett (2006) 1.10
A novel anti-prion protein monoclonal antibody and its single-chain fragment variable derivative with ability to inhibit abnormal prion protein accumulation in cultured cells. Microbiol Immunol (2010) 1.10
The N-terminal cleavage site of PrPSc from BSE differs from that of PrPSc from scrapie. Biochem Biophys Res Commun (2005) 1.08
Different prion disease phenotypes result from inoculation of cattle with two temporally separated sources of sheep scrapie from Great Britain. BMC Vet Res (2006) 1.06
Sulfated dextrans enhance in vitro amplification of bovine spongiform encephalopathy PrP(Sc) and enable ultrasensitive detection of bovine PrP(Sc). PLoS One (2010) 1.05
Microglial cell line established from prion protein-overexpressing mice is susceptible to various murine prion strains. J Virol (2006) 1.05
Human prion protein (PrP) 219K is converted to PrPSc but shows heterozygous inhibition in variant Creutzfeldt-Jakob disease infection. J Biol Chem (2008) 1.04
Association of an 11-12 kDa protease-resistant prion protein fragment with subtypes of dura graft-associated Creutzfeldt-Jakob disease and other prion diseases. J Gen Virol (2003) 1.03
Adenosquamous carcinoma of the pancreas: preoperative diagnosis and molecular alterations. J Gastroenterol (2003) 1.03
Biological and biochemical characterization of L-type-like bovine spongiform encephalopathy (BSE) detected in Japanese black beef cattle. Prion (2008) 1.03
Experimental H-type bovine spongiform encephalopathy characterized by plaques and glial- and stellate-type prion protein deposits. Vet Res (2011) 1.02
Alteration of the biological and biochemical characteristics of bovine spongiform encephalopathy prions during interspecies transmission in transgenic mice models. J Gen Virol (2009) 0.99
Sustained activation of M-Ras induced by nerve growth factor is essential for neuronal differentiation of PC12 cells. Genes Cells (2006) 0.99
vCJD prion acquires altered virulence through trans-species infection. Biochem Biophys Res Commun (2006) 0.96
Experimental verification of a traceback phenomenon in prion infection. J Virol (2010) 0.96
Combined assessment of beta-D-glucan and degree of candida colonization before starting empiric therapy for candidiasis in surgical patients. World J Surg (2004) 0.95
Follicular dendritic cell of the knock-in mouse provides a new bioassay for human prions. Biochem Biophys Res Commun (2002) 0.95
Protein misfolding cyclic amplification as a rapid test for assessment of prion inactivation. Biochem Biophys Res Commun (2006) 0.95
Tracing conformational transition of abnormal prion proteins during interspecies transmission by using novel antibodies. J Biol Chem (2010) 0.94
Anti-bovine prion protein RNA aptamer containing tandem GGA repeat interacts both with recombinant bovine prion protein and its beta isoform with high affinity. Prion (2008) 0.94
Intraspecies prion transmission results in selection of sheep scrapie strains. PLoS One (2010) 0.93
Phenotypic characterization of a human synovial sarcoma cell line, SW982, and its response to dexamethasone. In Vitro Cell Dev Biol Anim (2004) 0.92
Two different scrapie prions isolated in Japanese sheep flocks. Microbiol Immunol (2003) 0.92
A traceback phenomenon can reveal the origin of prion infection. Neuropathology (2009) 0.90
Neuroanatomical distribution of disease-associated prion protein in experimental bovine spongiform encephalopathy in cattle after intracerebral inoculation. Jpn J Infect Dis (2012) 0.90
Characterization and application of a novel RNA aptamer against the mouse prion protein. J Biochem (2006) 0.90
Effect of tissue deterioration on postmortem BSE diagnosis by immunobiochemical detection of an abnormal isoform of prion protein. J Vet Med Sci (2004) 0.89
The evaluation of exposure risks for natural transmission of scrapie within an infected flock. BMC Vet Res (2009) 0.89
Characterization of Syrian hamster adapted prions derived from L-type and C-type bovine spongiform encephalopathies. Prion (2011) 0.88
Detection of disease-associated prion protein in the optic nerve and the adrenal gland of cattle with bovine spongiform encephalopathy by using highly sensitive immunolabeling procedures. J Histochem Cytochem (2012) 0.88
Diagnostic and prognostic impact of beta-catenin alterations in pediatric liver tumors. Oncol Rep (2006) 0.88
Rapid PrP(Sc) detection in lymphoid tissue and application to scrapie surveillance of fallen stock in Japan: variable PrP(Sc) accumulation in palatal tonsil in natural scrapie. Microbiol Immunol (2005) 0.88
Identification of a new member of the GLWamide peptide family: physiological activity and cellular localization in cnidarian polyps. Comp Biochem Physiol B Biochem Mol Biol (2003) 0.87
Serological evidence for hepatitis e virus infection in laboratory monkeys and pigs in animal facilities in Japan. Exp Anim (2008) 0.87
Lactoferrin induces cell surface retention of prion protein and inhibits prion accumulation. J Neurochem (2008) 0.87
Long-term survival in patients with para-aortic lymph node metastasis with systematic retroperitoneal lymphadenectomy followed by adjuvant chemotherapy in endometrial carcinoma. Int J Gynecol Cancer (2010) 0.86
Long-term results of seton drainage on complex anal fistulae in patients with Crohn's disease. J Gastroenterol (2002) 0.86
Distinct origins of dura mater graft-associated Creutzfeldt-Jakob disease: past and future problems. Acta Neuropathol Commun (2014) 0.86
Assessment of prion inactivation by fenton reaction using protein misfolding cyclic amplification and bioassay. Biosci Biotechnol Biochem (2007) 0.86
Biological and biochemical characterization of sheep scrapie in Japan. J Clin Microbiol (2002) 0.85
Deciphering the pathogenesis of sporadic Creutzfeldt-Jakob disease with codon 129 M/V and type 2 abnormal prion protein. Acta Neuropathol Commun (2013) 0.85
Conformational change in hamster scrapie prion protein (PrP27-30) associated with proteinase K resistance and prion infectivity. J Vet Med Sci (2008) 0.85
Glycosylphosphatidylinositol anchor-dependent stimulation pathway required for generation of baculovirus-derived recombinant scrapie prion protein. J Virol (2011) 0.85
Differential gene expression profiles between neuroblastomas with high telomerase activity and low telomerase activity. J Pediatr Surg (2003) 0.85
Accumulation of L-type bovine prions in peripheral nerve tissues. Emerg Infect Dis (2010) 0.85
Expression of cellular prion-related protein by murine Langerhans cells and keratinocytes. J Dermatol Sci (2002) 0.85
Bacterial translocation in patients with Crohn's disease undergoing surgery. Dis Colon Rectum (2002) 0.84
Sensitive detection of scrapie prion protein in soil. Biochem Biophys Res Commun (2010) 0.84
Isolation of two distinct prion strains from a scrapie-affected sheep. Arch Virol (2009) 0.84
Establishment and characterization of SV40 large T antigen-immortalized cell lines derived from fetal bovine brain tissues after prolonged cryopreservation. Cell Biol Int (2006) 0.84
Assessment of prion inactivation by combined use of Bacillus-derived protease and SDS. Biosci Biotechnol Biochem (2007) 0.84
Comparative analysis of K-ras point mutation, telomerase activity, and p53 overexpression in pancreatic tumours. Oncol Rep (2003) 0.84
The N-terminal sequence of prion protein consists an epitope specific to the abnormal isoform of prion protein (PrP(Sc)). PLoS One (2013) 0.84
Expression profiling of favorable and unfavorable neuroblastomas. Pediatr Surg Int (2003) 0.83
Immunohistochemical detection of disease-associated prion protein in the intestine of cattle naturally affected with bovine spongiform encephalopathy by using an alkaline-based chemical antigen retrieval method. J Vet Med Sci (2010) 0.83
Prion infection correlates with hypersensitivity of P2X7 nucleotide receptor in a mouse microglial cell line. FEBS Lett (2007) 0.83
Transmissibility studies of vacuolar changes in the rostral colliculus of pigs. BMC Vet Res (2009) 0.83
Relationship between clinical signs and postmortem test status in cattle experimentally infected with the bovine spongiform encephalopathy agent. BMC Vet Res (2010) 0.83
Quantitative analysis of wet-heat inactivation in bovine spongiform encephalopathy. Biochem Biophys Res Commun (2013) 0.82
Fusion of Doppel to octapeptide repeat and N-terminal half of hydrophobic region of prion protein confers resistance to serum deprivation. Microbiol Immunol (2006) 0.82
Prion inactivation by the Maillard reaction. Biochem Biophys Res Commun (2007) 0.82
The influence of PRNP polymorphisms on human prion disease susceptibility: an update. Acta Neuropathol (2015) 0.82
Changes in the agr locus affect enteritis caused by methicillin-resistant Staphylococcus aureus. J Clin Microbiol (2009) 0.82
Prion in saliva of bovine spongiform encephalopathy-infected cattle. Emerg Infect Dis (2012) 0.82