Atypical BSE in Germany--proof of transmissibility and biochemical characterization.
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A. Buschmann | M. Groschup | C. Hoffmann | K Schiebel | M. Eiden | T. Baron | A Buschmann | A Gretzschel | A-G Biacabe | C Corona | C Hoffmann | M Eiden | T Baron | C Casalone | Martin H Groschup | A. Biacabe | C. Casalone | C. Corona | K. Schiebel | A. Gretzschel
[1] A. Buschmann,et al. Characterization of BSE and scrapie strains/isolates. , 2000, Archives of virology. Supplementum.
[2] J W Wilesmith,et al. Bovine spongiform encephalopathy: epidemiological studies on the origin , 1991, Veterinary Record.
[3] J. Kamphues. [Alternatives to presently established forms of animal body removal-- tolerated, intended and feared?]. , 1997, DTW. Deutsche tierarztliche Wochenschrift.
[4] S. Simon,et al. Comparative Molecular Analysis of the Abnormal Prion Protein in Field Scrapie Cases and Experimental Bovine Spongiform Encephalopathy in Sheep by Use of Western Blotting and Immunohistochemical Methods , 2004, Journal of Virology.
[5] Anne-Gaëlle Biacabe,et al. Origin of bovine spongiform encephalopathy , 2006, The Lancet.
[6] B. Brenig,et al. Analysis of sequence variability of the bovine prion protein gene (PRNP) in German cattle breeds , 2004, Neurogenetics.
[7] C. Seabury,et al. Comparative PRNP genotyping of U.S. cattle sires for potential association with BSE , 2004, Mammalian Genome.
[8] J. Ryan,et al. Bovine spongiform encephalopathy: epidemiological studies , 1988, Veterinary Record.
[9] A. Buschmann,et al. Highly bovine spongiform encephalopathy-sensitive transgenic mice confirm the essential restriction of infectivity to the nervous system in clinically diseased cattle. , 2005, The Journal of infectious diseases.
[10] R. Eddy. Origin of BSE , 1995, The Veterinary Record.
[11] M. Groschup,et al. A comparative study of immunohistochemical methods for detecting abnormal prion protein with monoclonal and polyclonal antibodies. , 2000, Journal of comparative pathology.
[12] F. Tagliavini,et al. Identification of a second bovine amyloidotic spongiform encephalopathy: molecular similarities with sporadic Creutzfeldt-Jakob disease. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[13] T. Sata,et al. Atypical proteinase K-resistant prion protein (PrPres) observed in an apparently healthy 23-month-old Holstein steer. , 2003, Japanese journal of infectious diseases.
[14] J. Williams,et al. Sequence variation in the bovine and ovine PRNP genes. , 2003, Animal genetics.
[15] N. Hunter,et al. Molecular analysis of ovine prion protein identifies similarities between BSE and an experimental isolate of natural scrapie, CH1641. , 1999, The Journal of general virology.
[16] M. Jeffrey,et al. A novel progressive spongiform encephalopathy in cattle , 1987, Veterinary Record.
[17] Andrew F. Hill,et al. Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD , 1996, Nature.
[18] A. Humeny,et al. Identification of polymorphisms within the bovine prion protein gene (Prnp) by DNA sequencing and genotyping by MALDI-TOF-MS , 2002, Neurogenetics.
[19] A. Colchester,et al. The origin of bovine spongiform encephalopathy: the human prion disease hypothesis , 2005, The Lancet.
[20] M. D. Di Bari,et al. Molecular Analysis of Cases of Italian Sheep Scrapie and Comparison with Cases of Bovine Spongiform Encephalopathy (BSE) and Experimental BSE in Sheep , 2003, Journal of Clinical Microbiology.
[21] A. Buschmann,et al. Strain typing of German transmissible spongiform encephalopathies field cases in small ruminants by biochemical methods. , 2005, Journal of veterinary medicine. B, Infectious diseases and veterinary public health.
[22] M. Stack,et al. Differentiation of prion protein glycoforms from naturally occurring sheep scrapie, sheep-passaged scrapie strains (CH1641 and SSBP1), bovine spongiform encephalopathy (BSE) cases and Romney and Cheviot breed sheep experimentally inoculated with BSE using two monoclonal antibodies , 2002, Acta Neuropathologica.
[23] C. Drögemüller,et al. Bovine Prion Protein Gene (PRNP) Promoter Polymorphisms Modulate PRNP Expression and May Be Responsible for Differences in Bovine Spongiform Encephalopathy Susceptibility* , 2005, Journal of Biological Chemistry.
[24] L. Court. Transmissible Subacute Spongiform Encephalopathies : Prion Diseases , 1996 .
[25] M. Groschup,et al. Synthetic peptide vaccines yield monoclonal antibodies to cellular and pathological prion proteins of ruminants. , 1998, The Journal of general virology.
[26] M. Groschup,et al. Molecular analysis of bovine spongiform encephalopathy and scrapie strain variation. , 1998, The Journal of infectious diseases.
[27] J. Langeveld,et al. Discrimination between Scrapie and Bovine Spongiform Encephalopathy in Sheep by Molecular Size, Immunoreactivity, and Glycoprofile of Prion Protein , 2004, Journal of Clinical Microbiology.
[28] M. Groschup,et al. Differences in Proteinase K Resistance and Neuronal Deposition of Abnormal Prion Proteins Characterize Bovine Spongiform Encephalopathy (BSE) and Scrapie Strains , 1999, Molecular medicine.
[29] M. Groschup,et al. Generation of Monoclonal Antibodies against Human Prion Proteins in PrP0/0 Mice , 1996, Molecular medicine.
[30] J. Laplanche,et al. Distinct molecular phenotypes in bovine prion diseases , 2004, EMBO reports.
[31] P. Sarradin,et al. A newly identified type of scrapie agent can naturally infect sheep with resistant PrP genotypes. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[32] A. Chong,et al. Biochemical typing of scrapie strains , 1997, Nature.