Mad Cow Disease and Related Spongiform Encephalopathies
暂无分享,去创建一个
[1] É. Vivier,et al. Immunoreceptor Tyrosine-based Inhibition Motifs , 2012, Current Topics in Microbiology and Immunology.
[2] A. Barrett,et al. Japanese Encephalitis and West Nile Viruses , 2012, Current Topics in Microbiology and Immunology.
[3] Li Yu,et al. [DNA methylation and cancer]. , 2005, Zhonghua nei ke za zhi.
[4] Michael W. Miller,et al. Prion disease: Horizontal prion transmission in mule deer , 2003, Nature.
[5] A. Ghani,et al. Updated projections of future vCJD deaths in the UK , 2003 .
[6] C. Farrington,et al. Deaths from variant Creutzfeldt-Jakob disease in the UK , 2003, The Lancet.
[7] D. Booth,et al. MHC typing in variant Creutzfeldt-Jakob disease , 2003, The Lancet.
[8] J. Laplanche,et al. HLA in French patients with variant Creutzfeldt-Jakob disease , 2003, The Lancet.
[9] Michael W. Miller,et al. Comparison of Abnormal Prion Protein Glycoform Patterns from Transmissible Spongiform Encephalopathy Agent-Infected Deer, Elk, Sheep, and Cattle , 2002, Journal of Virology.
[10] J. Collinge,et al. BSE prions propagate as either variant CJD‐like or sporadic CJD‐like prion strains in transgenic mice expressing human prion protein , 2002, The EMBO journal.
[11] N. Hunter,et al. Transmission of prion diseases by blood transfusion. , 2002, The Journal of general virology.
[12] A. Ghani,et al. Accumulation of prion protein in tonsil and appendix: review of tissue samples , 2002, BMJ : British Medical Journal.
[13] M. Miller,et al. Chronic wasting disease in deer and elk in North America. , 2002, Revue scientifique et technique.
[14] Jean Maccario,et al. The Incubation Period of Kuru , 2002, Epidemiology.
[15] N. T. Hobbs,et al. Evaluation of antemortem sampling to estimate chronic wasting disease prevalence in free-ranging mule deer , 2002 .
[16] R. Will,et al. First hundred cases of variant Creutzfeldt-Jakob disease: retrospective case note review of early psychiatric and neurological features , 2002, BMJ : British Medical Journal.
[17] P. Righetti,et al. Two‐dimensional mapping of three phenotype‐associated isoforms of the prion protein in sporadic Creutzfeldt‐Jakob disease , 2002, Electrophoresis.
[18] A. Ghani,et al. Estimating the human health risk from possible BSE infection of the British sheep flock , 2002, Nature.
[19] M. Miller,et al. Validation of Monoclonal Antibody F99/97.6.1 for Immunohistochemical Staining of Brain and Tonsil in Mule Deer (Odocoileus Hemionus) with Chronic Wasting Disease , 2002, Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc.
[20] M. Miller,et al. Comparison of Histological Lesions and Immunohistochemical Staining of Proteinase-resistant Prion Protein in a Naturally Occurring Spongiform Encephalopathy of Free-ranging Mule Deer (Odocoileus hemionus) with Those of Chronic Wasting Disease of Captive Mule Deer , 2002, Veterinary pathology.
[21] A. Valleron,et al. Estimation of Epidemic Size and Incubation Time Based on Age Characteristics of vCJD in the United Kingdom , 2001, Science.
[22] A. McLean,et al. The Potential Size and Duration of an Epidemic of Bovine Spongiform Encephalopathy in British Sheep , 2001, Science.
[23] J. Collinge,et al. Pathogenesis: HLA-DQ7 antigen and resistance to variant CJD , 2001, Nature.
[24] P. Righetti,et al. pH-dependent Prion Protein Conformation in Classical Creutzfeldt-Jakob Disease* , 2001, The Journal of Biological Chemistry.
[25] M. Turner. Variant Creutzfeldt-Jakob disease and blood transfusion , 2001, Current opinion in hematology.
[26] S. Cousens,et al. Predictability of the UK Variant Creutzfeldt-Jakob Disease Epidemic , 2001, Science.
[27] Shu G. Chen,et al. Novel Differences between Two Human Prion Strains Revealed by Two-dimensional Gel Electrophoresis* , 2001, The Journal of Biological Chemistry.
[28] P. Scheltens,et al. Sporadic Creutzfeldt‐Jakob disease in a young Dutch valine homozygote: Atypical molecular phenotype , 2001, Annals of neurology.
[29] J. Ironside,et al. Detection of variant Creutzfeldt-Jakob disease infectivity in extraneural tissues , 2001, The Lancet.
[30] J. Collinge,et al. Tissue distribution of protease resistant prion protein in variant Creutzfeldt-Jakob disease using a highly sensitive immunoblotting assay , 2001, The Lancet.
[31] J. Ironside,et al. Use of 14–3–3 and other brain-specific proteins in CSF in the diagnosis of variant Creutzfeldt-Jakob disease , 2001, Journal of neurology, neurosurgery, and psychiatry.
[32] E. Fisher,et al. Identification of multiple quantitative trait loci linked to prion disease incubation period in mice , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[33] M. Bishop,et al. Variant Creutzfeldt-Jakob disease in an elderly patient , 2001, The Lancet.
[34] J Mackenzie,et al. Geographical distribution of variant Creutzfeldt-Jakob disease in Great Britain, 1994–2000 , 2001, The Lancet.
[35] J. Hauw,et al. Adaptation of the bovine spongiform encephalopathy agent to primates and comparison with Creutzfeldt– Jakob disease: Implications for human health , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[36] M. Alpers,et al. Increased susceptibility to Kuru of carriers of the PRNP 129 methionine/methionine genotype. , 2001, The Journal of infectious diseases.
[37] J. Grosclaude,et al. Early accumulation of PrP(Sc) in gut-associated lymphoid and nervous tissues of susceptible sheep from a Romanov flock with natural scrapie. , 2000, The Journal of general virology.
[38] J. Miller,et al. Immunohistochemical Diagnosis of Chronic Wasting Disease in Preclinically Affected Elk from a Captive Herd , 2000, Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc.
[39] L. McShane,et al. Iatrogenic Creutzfeldt–Jakob disease at the millennium , 2000, Neurology.
[40] P. Minor,et al. Vaccines and variant CJD. , 2000, Vaccine.
[41] A. Nicoll,et al. Variant Creutzfeldt-Jakob disease in UK children: a national surveillance study , 2000, The Lancet.
[42] E. Williams,et al. EPIZOOTIOLOGY OF CHRONIC WASTING DISEASE IN FREE-RANGING CERVIDS IN COLORADO AND WYOMING , 2000, Journal of wildlife diseases.
[43] H. Budka,et al. Analysis of EEG and CSF 14-3-3 proteins as aids to the diagnosis of Creutzfeldt–Jakob disease , 2000, Neurology.
[44] N. Hunter,et al. Transmission of BSE by blood transfusion in sheep , 2000, The Lancet.
[45] G. J. Raymond,et al. Evidence of a molecular barrier limiting susceptibility of humans, cattle and sheep to chronic wasting disease , 2000, The EMBO journal.
[46] J. Miller,et al. Preclinical Diagnosis of Scrapie by Immunohistochemistry of Third Eyelid Lymphoid Tissue , 2000, Journal of Clinical Microbiology.
[47] B. Ghetti,et al. Genetic influence on the structural variations of the abnormal prion protein. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[48] A. McLean,et al. Scrapie infections initiated at varying doses: an analysis of 117 titration experiments. , 2000, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.
[49] C. Farrington,et al. Incidence of variant Creutzfeldt-Jakob disease in the UK , 2000, The Lancet.
[50] R. Will,et al. Laboratory diagnosis of variant Creutzfeldt–Jakob disease , 2000, Histopathology.
[51] A. Ghani,et al. Retrospective study of prion-protein accumulation in tonsil and appendix tissues , 2000, The Lancet.
[52] James W Ironside,et al. The pulvinar sign on magnetic resonance imaging in variant Creutzfeldt-Jakob disease , 2000, The Lancet.
[53] J. Lowe. Evidence of a CJD epidemic may still be missed , 2000, BMJ : British Medical Journal.
[54] M. Beekes,et al. Early accumulation of pathological PrP in the enteric nervous system and gut-associated lymphoid tissue of hamsters orally infected with scrapie , 2000, Neuroscience Letters.
[55] M. Haltia,et al. Human prion diseases , 2000, Annals of medicine.
[56] S. Prusiner,et al. Compelling transgenetic evidence for transmission of bovine spongiform encephalopathy prions to humans. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[57] H. Budka,et al. Disease associated prion protein may deposit in the peripheral nervous system in human transmissible spongiform encephalopathies , 1999, Acta Neuropathologica.
[58] E. Williams,et al. PrP genotypes of captive and free-ranging Rocky Mountain elk (Cervus elaphus nelsoni) with chronic wasting disease. , 1999, The Journal of general virology.
[59] E A Hoover,et al. Oral transmission and early lymphoid tropism of chronic wasting disease PrPres in mule deer fawns (Odocoileus hemionus). , 1999, The Journal of general virology.
[60] Y. Agid,et al. Incubation period of Creutzfeldt–Jakob disease in human growth hormone recipients in France , 1999, Neurology.
[61] P Brown,et al. Classification of sporadic Creutzfeldt‐Jakob disease based on molecular and phenotypic analysis of 300 subjects , 1999, Annals of neurology.
[62] R. Somerville. Host and transmissible spongiform encephalopathy agent strain control glycosylation of PrP. , 1999, The Journal of general virology.
[63] H. Budka,et al. A novel phenotype in familial Creutzfeldt‐Jakob disease: Prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease‐resistant prion protein , 1999, Annals of neurology.
[64] S. Prusiner,et al. Prion protein conformation in a patient with sporadic fatal insomnia. , 1999, The New England journal of medicine.
[65] A. Alpérovitch,et al. Codon 129 prion protein genotype and sporadic Creutzfeldt-Jakob disease , 1999, The Lancet.
[66] J. Collinge,et al. Strain-specific prion-protein conformation determined by metal ions , 1999, Nature Cell Biology.
[67] A. Ghani,et al. Predicting the size of the epidemic of the new variant of Creutzfeldt‐Jakob disease , 1999 .
[68] T. Sato,et al. Creutzfeldt-Jakob disease with florid-type plaques after cadaveric dura mater grafting. , 1999, Archives of neurology.
[69] J Collinge,et al. Investigation of variant Creutzfeldt-Jakob disease and other human prion diseases with tonsil biopsy samples , 1999, The Lancet.
[70] M. Zeidler,et al. Geographical distribution of variant CJD in the UK (excluding Northern Ireland) , 1999, The Lancet.
[71] J. Ironside. Prion diseases in man , 1998, The Journal of pathology.
[72] P. Brown,et al. Phenotype-genotype studies in kuru: implications for new variant Creutzfeldt-Jakob disease. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[73] R. Anderson,et al. Estimation of the number of people incubating variant CJD , 1998, The Lancet.
[74] J. Zajicek,et al. Prion immunoreactivity in appendix before clinical onset of variant Creutzfeldt-Jakob disease , 1998, The Lancet.
[75] H. Budka,et al. Different patterns of truncated prion protein fragments correlate with distinct phenotypes in P102L Gerstmann-Sträussler-Scheinker disease. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[76] P. Cortelli,et al. Molecular Pathology of Fatal Familial Insomnia , 1998, Brain pathology.
[77] E. Granieri,et al. Case-control study of risk factors of Creutzfeldt-Jakob disease in Europe during 1993-95 , 1998, The Lancet.
[78] S. Cousens,et al. Transmissions to mice indicate that ‘new variant’ CJD is caused by the BSE agent , 1997, Nature.
[79] Andrew F. Hill,et al. The same prion strain causes vCJD and BSE , 1997, Nature.
[80] R. Higgo,et al. New variant Creutzfeldt-Jakob disease: psychiatric features , 1997, The Lancet.
[81] M. Zeidler,et al. New variant Creutzfeldt-Jakob disease: neurological features and diagnostic tests , 1997, The Lancet.
[82] S. Cousens,et al. Sporadic Creutzfeldt-Jakob disease in the United Kingdom: analysis of epidemiological surveillance data for 1970-96 , 1997, BMJ.
[83] S. Gore. Commentary: Age related exposure of patients to the agent of BSE should not be downplayed , 1997, BMJ.
[84] P. Lansbury,et al. Molecular assessment of the potential transmissibilities of BSE and scrapie to humans , 1997, Nature.
[85] R. B. Petersen,et al. Typing prion isoforms , 1997, Nature.
[86] C. Donnelly,et al. Transmission dynamics and epidemiology of BSE in British cattle , 1997, Nature.
[87] D. Gajdusek,et al. Kuru: Forty Years Later, A Historical Note , 1997, Brain pathology.
[88] S. Prusiner,et al. Evidence for the Conformation of the Pathologic Isoform of the Prion Protein Enciphering and Propagating Prion Diversity , 1996, Science.
[89] Andrew F. Hill,et al. Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD , 1996, Nature.
[90] J. Hauw,et al. BSE transmission to macaques , 1996, Nature.
[91] J Q Trojanowski,et al. Molecular basis of phenotypic variability in sporadc creudeldt‐jakob disease , 1996, Annals of neurology.
[92] A. Hofman,et al. Risk factors for Creutzfeldt‐Jakob disease , 1996, Neurology.
[93] A. Hofman,et al. A new variant of Creutzfeldt-Jakob disease in the UK , 1996, The Lancet.
[94] M. Palmer,et al. Unaltered susceptibility to BSE in transgenic mice expressing human prion protein , 1995, Nature.
[95] S. Gore. More than happenstance: Creutzfeldt-Jakob disease in farmers and young adults , 1995 .
[96] J. Collinge,et al. Sporadic Creutzfeldt-Jakob disease in a 16-year-old in the UK , 1995, The Lancet.
[97] S. Love,et al. Sporadic Creutzfeldt-Jakob disease in a 18-year-old in the UK , 1995, The Lancet.
[98] R. Castellani,et al. Regional distribution of protease‐resistant prion protein in fatal familial insomnia , 1995, Annals of neurology.
[99] R. Petersen,et al. Fatal Familial Insomnia and Familial Creutzfeldt‐Jakob Disease: Clinical, Pathological and Molecular Features , 1995, Brain pathology.
[100] R. Marsh,et al. Distinct PrP properties suggest the molecular basis of strain variation in transmissible mink encephalopathy , 1994, Journal of virology.
[101] P. Brown,et al. Human spongiform encephalopathy: The national institutes of health series of 300 cases of experimentally transmitted disease , 1994, Annals of neurology.
[102] J. Miller,et al. Intracerebral transmission of scrapie to cattle. , 1994, The Journal of infectious diseases.
[103] H. Fraser,et al. Transmission of bovine spongiform encephalopathy and scrapie to mice. , 1992, The Journal of general virology.
[104] S. Prusiner. Genetic and infectious prion diseases. , 1993, Archives of neurology.
[105] E. Williams,et al. Neuropathology of Chronic Wasting Disease of Mule Deer (Odocoileus hemionus) and Elk (Cervus elaphus nelsoni) , 1993, Veterinary pathology.
[106] E. Williams,et al. Spongiform encephalopathies in Cervidae. , 1992, Revue scientifique et technique.
[107] J. Ryan,et al. Bovine spongiform encephalopathy: epidemiological features 1985 to 1990 , 1992, Veterinary Record.
[108] P. Brown,et al. Survival of scrapie virus after 3 years' interment , 1991, The Lancet.
[109] E J Snyder,et al. The electroencephalogram (EEG). , 1990, Biomedical instrumentation & technology.
[110] Jurg Ott,et al. Linkage of a prion protein missense variant to Gerstmann–Sträussler syndrome , 1989, Nature.
[111] J. Ryan,et al. Bovine spongiform encephalopathy: epidemiological studies , 1988, Veterinary Record.
[112] R. Brookmeyer,et al. Methods for projecting course of acquired immunodeficiency syndrome epidemic. , 1988, Journal of the National Cancer Institute.
[113] M. Jeffrey,et al. A novel progressive spongiform encephalopathy in cattle , 1987, Veterinary Record.
[114] P. Smith,et al. A retrospective study of Creutzfeldt-Jakob disease in England and Wales 1970-1979. II: Epidemiology. , 1986, Journal of neurology, neurosurgery, and psychiatry.
[115] R. Will,et al. A retrospective study of Creutzfeldt-Jakob disease in England and Wales 1970-79. I: Clinical features. , 1984, Journal of neurology, neurosurgery, and psychiatry.
[116] E. Williams,et al. SPONGIFORM ENCEPHALOPATHY OF ROCKY MOUNTAIN ELK1 , 1982, Journal of wildlife diseases.
[117] S. Prusiner,et al. Kuru with incubation periods exceeding two decades , 1982, Annals of neurology.
[118] S. Prusiner. Novel proteinaceous infectious particles cause scrapie. , 1982, Science.
[119] G. Clements. Aspects of Slow and Persistent Virus Infections , 1981 .
[120] D. Gajdusek,et al. Degenerative disease of the central nervous system in New Guinea; the endemic occurrence of kuru in the native population. , 1957, The New England journal of medicine.
[121] P E SARTWELL,et al. The distribution of incubation periods of infectious disease. , 1950, American journal of hygiene.
[122] Y. Kawaoka. Biology of Negative Strand RNA Viruses: The Power of Reverse Genetics , 2004, Current Topics in Microbiology and Immunology.
[123] A. Hilgendorf. Adenoviruses: Model and Vectors in Virus-Host Interactions , 2004, Current Topics in Microbiology and Immunology.
[124] J. Ironside,et al. Prion protein accumulation in eyes of patients with sporadic and variant Creutzfeldt-Jakob disease. , 2003, Investigative ophthalmology & visual science.
[125] A. Alpérovitch,et al. Predicting the size of the vCJD epidemic in France. , 2002, Comptes rendus biologies.
[126] S. Bird,et al. UK dietary exposure to BSE in beef mechanically recovered meat: by birth cohort and gender. , 2002, Journal of cancer epidemiology and prevention.
[127] S. Simon,et al. Screening slaughtered cattle for BSE. , 2001, Nature.
[128] C. Rice,et al. The Hepatitis C Viruses , 2000, Current Topics in Microbiology and Immunology.
[129] S. Czinn,et al. Gastroduodenal Disease and Helicobacter pylori , 1999, Current Topics in Microbiology and Immunology.
[130] M. Miller,et al. SPONGIFORM ENCEPHALOPATHY IN FREE-RANGING MULE DEER (ODOCOILEUS HEMIONUS), WHITE-TAILED DEER (ODOCOILEUS VIRGINIANUS) AND ROCKY MOUNTAIN ELK (CERVUS ELAPHUS NELSONI) IN NORTHCENTRAL COLORADO , 1997, Journal of wildlife diseases.
[131] C. Mclean. Comparative neuropathology of kuru and new variant CJD , 1997 .
[132] J. Bell,et al. A new variant of Creutzfeldt-Jakob disease: neuropathological and clinical features. , 1996, Cold Spring Harbor symposia on quantitative biology.
[133] L. Hoinville. A review of the epidemiology of scrapie in sheep. , 1996, Revue scientifique et technique.
[134] T. Thorne. Report of the committee on wildlife diseases. , 1993 .
[135] L. Du Pasquier. Origin and evolution of the vertebrate immune system. , 1992, APMIS : acta pathologica, microbiologica, et immunologica Scandinavica.