Literature DB >> 9371069

A prion primer.

N R Cashman1.   

Abstract

By biological and medical criteria, prions are infectious agents; however, many of their properties differ profoundly from those of conventional microbes. Prions are "encoded" by alterations in protein conformation rather than in nucleic acid or amino acid sequence. New epidemic prion diseases (bovine spongiform encephalopathy and new variant Creutzfeldt-Jakob disease) have recently emerged under the active surveillance of the modern world. The risk of contracting prion disease from blood products or other biologicals is now a focus of worldwide concern. Much has been discovered about prions and prion diseases, but much remains to be done.

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Year:  1997        PMID: 9371069      PMCID: PMC1228465     

Source DB:  PubMed          Journal:  CMAJ        ISSN: 0820-3946            Impact factor:   8.262


  20 in total

1.  Cellular isoform of the scrapie agent protein participates in lymphocyte activation.

Authors:  N R Cashman; R Loertscher; J Nalbantoglu; I Shaw; R J Kascsak; D C Bolton; P E Bendheim
Journal:  Cell       Date:  1990-04-06       Impact factor: 41.582

2.  Scrapie and cellular PrP isoforms are encoded by the same chromosomal gene.

Authors:  K Basler; B Oesch; M Scott; D Westaway; M Wälchli; D F Groth; M P McKinley; S B Prusiner; C Weissmann
Journal:  Cell       Date:  1986-08-01       Impact factor: 41.582

3.  MRI abnormalities in Creutzfeldt-Jakob disease.

Authors:  A Di Rocco; S Molinari; A L Stollman; A Decker; M D Yahr
Journal:  Neuroradiology       Date:  1993       Impact factor: 2.804

4.  No propagation of prions in mice devoid of PrP.

Authors:  A Sailer; H Büeler; M Fischer; A Aguzzi; C Weissmann
Journal:  Cell       Date:  1994-07-01       Impact factor: 41.582

Review 5.  Bovine spongiform encephalopathy (BSE): causes and consequences of a common source epidemic.

Authors:  N Nathanson; J Wilesmith; C Griot
Journal:  Am J Epidemiol       Date:  1997-06-01       Impact factor: 4.897

6.  PrP-expressing tissue required for transfer of scrapie infectivity from spleen to brain.

Authors:  T Blättler; S Brandner; A J Raeber; M A Klein; T Voigtländer; C Weissmann; A Aguzzi
Journal:  Nature       Date:  1997-09-04       Impact factor: 49.962

7.  Isolation from mouse spleen of cell populations with high specific infectivity for scrapie virus.

Authors:  G C Lavelle; L Sturman; W J Hadlow
Journal:  Infect Immun       Date:  1972-03       Impact factor: 3.441

8.  Novel proteinaceous infectious particles cause scrapie.

Authors:  S B Prusiner
Journal:  Science       Date:  1982-04-09       Impact factor: 47.728

9.  Creutzfeldt-Jakob disease in mice: persistent viremia and preferential replication of virus in low-density lymphocytes.

Authors:  Y Kuroda; C J Gibbs; H L Amyx; D C Gajdusek
Journal:  Infect Immun       Date:  1983-07       Impact factor: 3.441

Review 10.  Genetics of human prion disease.

Authors:  R M Ridley; H F Baker
Journal:  Dev Biol Stand       Date:  1993
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  3 in total

1.  The quandary of Creutzfeldt-Jakob disease.

Authors:  B Larke
Journal:  CMAJ       Date:  1998-10-06       Impact factor: 8.262

Review 2.  Variant Creutzfeldt-Jakob disease: a summary of current scientific knowledge in relation to public health.

Authors:  M B Coulthart; N R Cashman
Journal:  CMAJ       Date:  2001-07-10       Impact factor: 8.262

3.  The reporting of theoretical health risks by the media: Canadian newspaper reporting of potential blood transmission of Creutzfeldt-Jakob disease.

Authors:  Kumanan Wilson; Catherine Code; Christopher Dornan; Nadya Ahmad; Paul Hébert; Ian Graham
Journal:  BMC Public Health       Date:  2004-01-05       Impact factor: 3.295

  3 in total

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