Literature DB >> 8937784

Immunhistological evaluation of Creutzfeldt-Jakob disease with reference to the type PrPres deposition.

J Tateishi1, T Kitamoto, H Kretzschmar, P Mehraein.   

Abstract

German patients suspected of having Creutzfeldt-Jakob disease (CJD) and related diseases were studied pathologically. The immunohistochemical findings after hydrolytic autoclaving pretreatment sensitively detected the synaptic-type deposition of the protease-resistant isoform of the prion protein (PrPres which thus served to establish the consensus diagnosis of CJD.

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Year:  1996        PMID： 8937784

Source DB:  PubMed          Journal:  Clin Neuropathol        ISSN： 0722-5091            Impact factor:   1.368


  3 in total

1.  Cotranslational partitioning of nascent prion protein into multiple populations at the translocation channel.

Authors:  Soo Jung Kim; Ramanujan S Hegde
Journal:  Mol Biol Cell       Date:  2002-11       Impact factor: 4.138

Review 2.  (Ctm)PrP and ER stress: a neurotoxic mechanism of some special PrP mutants.

Authors:  Qi Shi; Xiao-Ping Dong
Journal:  Prion       Date:  2011-07-01       Impact factor: 3.931

3.  Burial of the polymorphic residue 129 in amyloid fibrils of prion stop mutants.

Authors:  Lukasz Skora; Luis Fonseca-Ornelas; Romina V Hofele; Dietmar Riedel; Karin Giller; Jens Watzlawik; Walter J Schulz-Schaeffer; Henning Urlaub; Stefan Becker; Markus Zweckstetter
Journal:  J Biol Chem       Date:  2012-12-03       Impact factor: 5.157
  3 in total

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